WO2004103559A2 - Coordination complex system comprising building blocks and use thereof as a catalyst - Google Patents

Coordination complex system comprising building blocks and use thereof as a catalyst Download PDF

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Publication number
WO2004103559A2
WO2004103559A2 PCT/EP2004/050906 EP2004050906W WO2004103559A2 WO 2004103559 A2 WO2004103559 A2 WO 2004103559A2 EP 2004050906 W EP2004050906 W EP 2004050906W WO 2004103559 A2 WO2004103559 A2 WO 2004103559A2
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Prior art keywords
functional group
template
building blocks
building block
ligand
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
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PCT/EP2004/050906
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French (fr)
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WO2004103559A3 (en
Inventor
Joost Nicolaas Hendrik Reek
Ruifang Chen
Paul Clemens Jozef Kamer
Vincent Friso Slagt
Petrus Wilhelmus Nicolaas Maria Van Leeuwen
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Universiteit Van Amsterdam
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Universiteit Van Amsterdam
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Filing date
Publication date
Application filed by Universiteit Van Amsterdam filed Critical Universiteit Van Amsterdam
Priority to EP04741642A priority Critical patent/EP1633476A2/en
Priority to US10/557,706 priority patent/US8216968B2/en
Priority to JP2006530218A priority patent/JP2007505153A/en
Priority to KR1020057022241A priority patent/KR101049492B1/en
Publication of WO2004103559A2 publication Critical patent/WO2004103559A2/en
Publication of WO2004103559A3 publication Critical patent/WO2004103559A3/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • B01J31/2495—Ligands comprising a phosphine-P atom and one or more further complexing phosphorus atoms covered by groups B01J31/1845 - B01J31/1885, e.g. phosphine/phosphinate or phospholyl/phosphonate ligands
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    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/60—Reduction reactions, e.g. hydrogenation
    • B01J2231/64—Reductions in general of organic substrates, e.g. hydride reductions or hydrogenations
    • B01J2231/641—Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes
    • B01J2231/645—Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes of C=C or C-C triple bonds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/02—Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0238—Complexes comprising multidentate ligands, i.e. more than 2 ionic or coordinative bonds from the central metal to the ligand, the latter having at least two donor atoms, e.g. N, O, S, P
    • B01J2531/0241—Rigid ligands, e.g. extended sp2-carbon frameworks or geminal di- or trisubstitution
    • B01J2531/025—Ligands with a porphyrin ring system or analogues thereof, e.g. phthalocyanines, corroles
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/02—Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0286—Complexes comprising ligands or other components characterized by their function
    • B01J2531/0291—Ligands adapted to form modular catalysts, e.g. self-associating building blocks as exemplified in the patent document EP-A-1 479 439
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/20—Complexes comprising metals of Group II (IIA or IIB) as the central metal
    • B01J2531/26—Zinc
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82—Metals of the platinum group
    • B01J2531/822—Rhodium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82—Metals of the platinum group
    • B01J2531/824—Palladium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2540/00—Compositional aspects of coordination complexes or ligands in catalyst systems
    • B01J2540/60—Groups characterized by their function
    • B01J2540/68—Associating groups, e.g. with a second ligand or a substrate molecule via non-covalent interactions such as hydrogen bonds
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals

Definitions

  • the invention relates to a coordination complex system comprising a ligand having at least two donor moieties, which are complexed to at least a metal selected from a transition metal and lanthanide, to a catalyst system comprising said coordination complex system, to the use of said coordination complex system, and to a set and the use thereof of self-complementary building blocks for making a ligand two donor moieties for complexation to a metal.
  • the present invention provides in such tool, and further provides new effective supramolecular techniques to construct ligands, particularly bidentate ligands, which can be formed by just mixing monomeric compounds.
  • a phosphorus monodentate ligand building block equipped with a zinc (II) porphyrin moiety can selectively bind monodentate building block that have a nitrogen donor atom.
  • Zn-N selective etal-ligand interactions
  • a matrix of new self-assembled mono- and bidentate ligands can be created easily.
  • This novel supramolecular strategy to prepare new assembled ligands was successfully applied in a combinatorial fashion and clearly simplifies the construction of catalyst libraries, for instance based on sophisticated phosphite-phosphine chelating ligands.
  • Other objectives such as immobilizing well-defined binding sites based on different binding motives on, for instance, silica support that can be non-covalently functionalized with catalysts that have ligands with the complementary motive will become clear herein below.
  • the ligation around the metal center, the chiral environment, the presence of a substrate binding site and the local polarity around the catalysts can be controlled. These are key parameters that direct catalyst properties as activity and selectivity.
  • catalysts can be immobilized reversibly on dendrimers, silica, monolayers in an easy manner, enabling the rapid accumulation of information on the impact of catalyst immobilization on its performance. This leads to an extremely versatile modular approach, in which the environment of the catalysts can be controlled by reversible connection to supports, chiral environments, substrate binding-sites, mono- layers and aggregates, thereby creating a new set of selective catalysts systems.
  • non-covalent anchoring also enables controlled de-functionalization of support, which enables the separation and re-use of support and catalyst. This can be relevant for multi-purpose reactors since the support can stay in the reactor while the catalyst (the same in the case of deactivation and a different one in the case a new reaction is required) can be replaced.
  • non-covalent has the common meaning as used by the skilled person, i.e. any chemical or physical bonding that is not covalent.
  • Non-covalent bonding for example, includes bonding via ionic interactions, hydrogen bonding, and reversible metal-ligand interactions.
  • the spatial orientation of donor atoms coordinating to the catalytically active transition metal is of crucial importance for the properties in catalysis.
  • these donor atoms were attached covalently to a ligand backbone thereby, depending on the rigidity of the backbone, enforcing (or supporting) certain coordination geometries around metal.
  • this rigid conventional approach has been replaced by a non-covalent approach to control the ligation by assembly of ligands direct via complementary building blocks or by building blocks noncovalently bonded to each other via a template.
  • the invention pertains to a coordination complex system comprising a ligand having at least two donor moieties, which are complexed to at least a metal selected from a transition metal and lanthanide, characterized in that the ligand comprises at least two building blocks, each having at least one functional group and at least one donor moiety, wherein one building block is non-covalently bonded through its functional group to a complementary functional group of another building block or of a template, wherein the template comprises at least one other functional group that is non-covalently bonded to a complementary functional group of another building block, and wherein all building block-template-building block structures are the same when the template contains more than two functional groups.
  • the dynamic character of the system may lead to special reactivity of the catalyst system and it also enables the formation of dynamic combinatorial catalyst systems based on transition metal from which the catalyst can be selected by adding a selector, for instance a transition state analogue.
  • At least one of the building blocks is immobilized onto an inorganic support, a polymeric organic support, or a hybrid support.
  • the building blocks preferably have a molecular weight less than 5,000, more preferably less than 2,500.
  • the chiral environment will also be controlled by assembly and it was shown that zinc (II) porphyrins in combination with pyridyl-phosphine building blocks are suitable for this approach.
  • the pyridine is selectively coordinated to the zinc and the phosphine donor is still available for coordination to the catalytically active transition metal.
  • the coordination complex system comprises a ligand having at least two donor moieties, which are complexed to at least a metal selected from a transition metal and lanthanide, characterized in that the ligand comprises 2 to 6 building blocks each having at least one functional group and at least one donor moiety, wherein at least one building block is non-covalently bonded through its functional group to a complementary functional group of a template .
  • the system may further comprise a co-factor that is non-covalently bonded to a functional group of the ligand.
  • a co-factor may be covalently bonded to another building block, or to the template or support.
  • the template contains more than two functional groups all building block-template-building block structures are the same. For instance, when the template contains 8 functional groups and two functional groups form a pair whereas the six other functional groups form three similar other pairs, two building blocks are non-covalently attached to each of these pairs, and not to one functional group of the first pair and one functional group of another pair when such bonding gives rise to different spatial orientations
  • the properties of the assembly may be different from the prior art catalysts, which for instance can result in higher reaction rates in the palladium catalyzed Heck reaction and the rhodium catalyzed hydroformylation.
  • using bis-zinc-porphyrin systems as templates resulted in chelating bidentate ligands of which the catalytic performance (in activity and (enantio-) selectivity) strongly depended on the components of the assembly.
  • FIG. 1 Examples of some of the hydrogen bond building blocks that can be used are shown in Chart I .
  • Two identical building blocks can be assembled around a template resulting in a bidentate ligand with properties that depend on the template.
  • a representative example is a building block comprising urea functionalities and benz- amidine, which can be used to form complexes with small anionic templates. The orientation of two urea units will strongly depend on the template.
  • the catalytic performance of the assemblies can also be used as diagnostic tool by studying several reactions that are known to be sensitive to geometry changes (such as hydroformylation, carbonylation and allylic substitution) .
  • Employing cationic transition or lanthanide metal complexes e.g.
  • the coordination complex system preferably has a molar ratio between the ligand and the metal of between 0.2 and 100.
  • the invention further relates to a catalyst system comprising the above-mentioned coordination complex system and the use of the coordination complex system as a catalyst, preferably for hydroformylation, hydrogenation, transfer hydrogenation, hydrocyanation, polymerization, isomerization, carbonylation, cross-coupling, metathesis, CH activation, allylic substitution, aldol condensation, and Michael addition.
  • L x and L 2 are coordination moieties of the building blocks, M is transition or lanthanide metal.
  • A) is an embodiment using a template; B) is an embodiment using self- complementary building blocks .
  • the templates may include calix-arenes and rigid multi- aromatic systems.
  • Bisporphyrin templates with two different metals are also suitable templates: nitrogen donor will coordinate selectively to the zinc atom and tin porphyrins are known to strongly coordinate carboxylate groups.
  • Systems functionalized with two orthogonal binding sites can be prepared in which the catalyst and either the substrate molecule or a chiral cofactor can be fixed in a well-defined way using non-covalent interactions.
  • the binding of the transition (or lanthanide) metal will be based on hydrogen bonding (ionic interactions) and the (guest) cofactor will be bound using metal-ligand interactions (such as pyridine-zinc coordination) .
  • the binding on the porphyrin can be used for several types of guests including amino acids.
  • Several analogues with different hydrogen bond functional groups thereby changing the position of the catalysts with respect to the binding site can be made.
  • the invention therefore also relates to the use of at least two building blocks each having at least one functional group, wherein a functional group of one building block is complementary to a functional group of another building block or of a template to form through their functional groups a non-covalent bond between the building blocks or between the building blocks and the template, to obtain a ligand that with the metal forms the coordination complex system.
  • Another aspect of the invention relates to the use of a set of self-complementary building blocks for making a ligand having at least two donor moieties for complexation to a metal selected from a transition metal and lanthanide, wherein the ligand comprises the set of building blocks, each building block having at least one functional group that is complementary to a functional group of another building block or of a template, and at least one donor moiety, wherein the building blocks are non-covalently bonded to each other or to the template through their complementary functional groups.
  • the invention further pertains to the set comprising self-complementary building blocks, and optionally templates for making a ligand.
  • the set may also comprise metals for coordination, for the above-mentioned use.
  • metals for coordination for the above-mentioned use.
  • 3 B ⁇ tetraarylporphyrins as well as trans-A 2 B 2 tetraarylporphyrins can easily be made by well- established synthetic procedures.
  • reactive groups for further functionalization amines and isothiocyanate groups can be introduced, which are both reactive and easily accessible.
  • porphyrins can be prepared (large quantities) and used as synthons for the synthesis of building blocks required for different ways of non-covalent immobilization.
  • Examples of approaches of making tailor-made catalysts on a support are mixing trialkoxy-functionalized porphyrin with commercially available silica, immobilization via a sol-gel process, pre-assembly of the transition metal complex prior to immobilization, and post-modification of the immobilized porphyrins with the catalysts.
  • Synthetically easily accessible porphyrins which are expected to form well-defined aggregates such as micelles and vesicles due to their amphiphilic character, can also be made according to this approach.
  • Amphiphiles that form well-defined aggregates can be used for the assembly of catalysts. These amphiphiles can be prepared via ion-pairing by mixing a bis- anion with cationic amphiphiles.
  • 1-Octene was purified over neutral alumina prior to its use. Solvents were dried prior to their use. Hexane, pentane, diethyl ether, THF (tetrahydrofuran) , toluene and benzene were distilled from sodium/benzophenone or calcium hydride (dichloromethane, triethylamine) . All solutions and solvents not stated above were degassed under argon prior to their use. All reactions were performed under Schlenk conditions using argon or purified nitrogen as inert atmosphere. Water and CDC1 3 were degassed and stored under nitrogen. Chemicals were purchased from Aldrich Chemical Co. and Acros Chimica and were used without further purification. The piperidine was filtered over neutral alumina prior to use.
  • This compound was prepared as described for Bl, using freshly prepared (S) -3, 3' -bis (trimethylsilyl) -2, 2' -bisnaphthol phosphorochloridite (ref. Buisman, G. J. H.; van der Veen, L.
  • This compound was prepared as described for Bl, using freshly prepared (R) -2, 2' -bisnaphthol phosphorochloridite. Yield (78 %) as a white solid.
  • the porphyrin was purified using column chromatography (basic alumina, CH 2 C1 2 , upgrade 2 % methanol in CH 2 C1 2 ) , giving 1.09 g of 5- (3-hydroxyphenyl) - 10, 15, 20-tris (phenyl) .
  • the zinc porphyrin was prepared by refluxing 5- (3-hydroxyphenyl) -10, 15, 20-tris (phenyl) in the presence of excess Zn(OAc) 2 .
  • This compound was prepared as described for B14, using 5- (3-hydroxyphenyl) -10, 15, 20-tris (phenyl) -zinc (II) porphyrin. Yield (47 %) as a purple-red solid.
  • This compound was prepared as described for B16, using freshly prepared (R) -2, 2' -bisnaphthol phosphorochloridite. Yield (46 %) as a purple-red solid.
  • This compound was prepared as described for B16, using freshly prepared (S) -3, 3' -bis (trimethylsilyl) -2,2' - bisnaphthol phosphorochloridite. Yield (51 %) as a purple-red solid.
  • This compound was formed after oxidation with air of B4.
  • T13 This compound was prepared as described for T12, using the free base analogue of Til (Biemans, H. A. M.; Rowan, A. E.; Verhoeven, A,; Vanoppen, P.; Latterini, L.; Foeke a, J. ; Schenning, A. P. H. J. ; Meijer, E. W.; De Schryver, F. C; Nolte, R. J. M., J. Am . Chem . Soc. , 1998, 120, 11054) as starting material (89 %) as a purple solid.
  • T25 was obtained after refluxing a suspension of T24 and silica in toluene for 5 hours.
  • Rh (acac) (CO) 2 ligand to rhodium is 10, 1 ml of 1-octene, 1 ml of decane, 20 ml of toluene, 80 " C, 50 bar of CO/H 2 , 20 h .
  • ligand to rhodium is 10 , 1 ml of 1-octene, 1 ml of decane, 20 ml of toluene , 80 ° C, 50 bar of CO/H 2 .

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Abstract

The invention relates to a coordination complex system comprising a ligand having at least two donor moieties, which are complexed to at least a metal selected from a transition metal and lanthanide, characterized in that the ligand comprises at least two building blocks, each having at least one functional group and at least one donor moiety, wherein one building block is non-covalently bonded through its functional group to a complementary functional group of another building block or of a template, wherein the template comprises at least one other functional group that is noncovalently bonded to a complementary functional group of another building block, and wherein all building blockemplate-building block structures are the same when the template contains more than two functional groups.

Description

COORDINATION COMPLEX SYSTEM COMPRISING BUILDING BLOCKS
The invention relates to a coordination complex system comprising a ligand having at least two donor moieties, which are complexed to at least a metal selected from a transition metal and lanthanide, to a catalyst system comprising said coordination complex system, to the use of said coordination complex system, and to a set and the use thereof of self-complementary building blocks for making a ligand two donor moieties for complexation to a metal.
During the past decades combinatorial chemistry has evolved in an incredible manner and has been applied especially in pharmacy for drug discovery and optimization and for making homogeneous catalysts. The development of homogeneous catalysts using combinatorial techniques involves two distinct challenges: 1) devising strategies and methods for the preparation of large • libraries of ligands and/or catalyst displaying high degrees of structural diversity, 2) developing high-throughput screening techniques for the reaction of interest. A lot of effort has been put in the development of new screening techniques for homogeneous catalyst libraries and various methods have proven successful. In the search for new transition metal catalysts the preparation of catalyst libraries has mainly been focused on variation of ligands, which are based on commercially available ligands or are prepared via conventional synthetic pathways and/or divergent methods using parallel synthesis.
The synthesis of large libraries of new ligands indeed yields a major challenge and so far only a limited number of methodologies have been reported. Until now, library synthesis of ligands is based on combinatorial organic synthesis followed by metal co plexation. This approach utilizes advanced solid and solution phase combinatorial synthetic methodologies including parallel synthesis, split-pool techniques, encoding/deconvolution and polymer-supported reagents. Methods such as split pool techniques are much faster than traditional serial approaches and enable the preparation of relatively large numbers of compounds but often lack control over the purity and mixtures of compounds entering the assay screen. In contrast, the methods based on parallel or array syntheses yield intermediate sized libraries of pure compounds. Although these combinatorial techniques to construct ligand libraries have proven to be valuable, the preparation and evaluation of truly large numbers of potentially (enantio) -selective catalysts has not been reported and the application is still limited to a few catalytic reactions. Moreover, the preparation of important multidentate ligands, like promising diphosphorus ligands, faces synthetic challenges, especially when sophisticated chiral entities are required for asymmetric catalysis. There is a need to develop new tools to efficiently deal with these synthetic challenges.
The present invention provides in such tool, and further provides new effective supramolecular techniques to construct ligands, particularly bidentate ligands, which can be formed by just mixing monomeric compounds. For instance, a phosphorus monodentate ligand building block equipped with a zinc (II) porphyrin moiety, can selectively bind monodentate building block that have a nitrogen donor atom. These selective etal-ligand interactions (Zn-N) are utilized for the assembly of ligand systems and yield novel transition metal catalysts. Upon variation of the phosphorus monodentate compounds a matrix of new self-assembled mono- and bidentate ligands can be created easily. This novel supramolecular strategy to prepare new assembled ligands was successfully applied in a combinatorial fashion and clearly simplifies the construction of catalyst libraries, for instance based on sophisticated phosphite-phosphine chelating ligands.
There is an increasing demand for metal catalysts and the number of tailor-made transition metal catalysts for various chemical transformations is ever increasing, however, the practical use of these homogenous catalysts is limited by the cumbersome separation from the product-phase. So far, many different methods of catalyst recycling have been studied, including two-phase catalysis, supported aqueous phase catalysis, fluorous phase catalysis, the use of ionic liquids and supercritical fluids. An amply studied approach to facilitate catalyst-product separation is the attachment of homogeneous catalysts to dendritic, polymeric organic, inorganic or hybrid supports.
In most supported catalysts reported so far the catalyst has been covalently linked to the support. An interesting alternative approach is the anchoring of the catalyst to the support. Only a few examples have been reported for non-covalent bonding, for example, the immobilization via ionic interactions. Cationic transition metal catalysts have been immobilized on heteropoly acids and silica support via ion-pairing. This appeared to be a viable approach for cationic rhodium catalysts that are active in hydrogenation reactions, but the concept is obviously limited to charged catalysts.
The problem of all these approaches is the cumbersome independent syntheses of the various catalysts systems that are necessary for the different systems to be catalyzed. In D. de Groot et al . , J. Am. Chem. Soc, 2001, 123, 8453-58 a method was disclosed wherein phosphine ligands for complexation with palladium were non-covalently assembled to a template of urea adamantly-functionalized pol (propylene imine) dendrimer. However, the templates are unevenly distributed over the support. Such method is unsuitable for making catalyst systems in a controlled manner, and therefore catalyst systems are obtained with unpredictable properties .
It is therefore an objective of the present invention to obtain a method enabling a flexible and versatile synthesis of tailor-made catalytic systems for metal-catalyzed reactions. Other objectives such as immobilizing well-defined binding sites based on different binding motives on, for instance, silica support that can be non-covalently functionalized with catalysts that have ligands with the complementary motive will become clear herein below.
The implementation of supramolecular strategies simplifies the preparation of new catalysts materials significantly since the components will find their way by assembly. Apart from this advantage, the dynamic nature of the non-covalent interactions leads to materials with new catalytic properties, e.g. the catalyst may adapt its structure during the catalytic cycle adjusting its properties for the next step. Sets of (mostly known) orthogonal interactions based on metal-ligand interactions, hydrogen bonding consisting of different binding motives, polar/ionic interactions (for examples see chart I, wherein A denotes acceptor and D denotes donor) with which the components can be functionalized may be employed. By means of assembly, the ligation around the metal center, the chiral environment, the presence of a substrate binding site and the local polarity around the catalysts can be controlled. These are key parameters that direct catalyst properties as activity and selectivity. Moreover, by functionalization of several supports catalysts can be immobilized reversibly on dendrimers, silica, monolayers in an easy manner, enabling the rapid accumulation of information on the impact of catalyst immobilization on its performance. This leads to an extremely versatile modular approach, in which the environment of the catalysts can be controlled by reversible connection to supports, chiral environments, substrate binding-sites, mono- layers and aggregates, thereby creating a new set of selective catalysts systems. The approach of non-covalent anchoring also enables controlled de-functionalization of support, which enables the separation and re-use of support and catalyst. This can be relevant for multi-purpose reactors since the support can stay in the reactor while the catalyst (the same in the case of deactivation and a different one in the case a new reaction is required) can be replaced.
The term "non-covalent" has the common meaning as used by the skilled person, i.e. any chemical or physical bonding that is not covalent. Non-covalent bonding, for example, includes bonding via ionic interactions, hydrogen bonding, and reversible metal-ligand interactions.
The spatial orientation of donor atoms coordinating to the catalytically active transition metal is of crucial importance for the properties in catalysis. Conventionally, these donor atoms were attached covalently to a ligand backbone thereby, depending on the rigidity of the backbone, enforcing (or supporting) certain coordination geometries around metal. In this invention this rigid conventional approach has been replaced by a non-covalent approach to control the ligation by assembly of ligands direct via complementary building blocks or by building blocks noncovalently bonded to each other via a template. Thus the invention pertains to a coordination complex system comprising a ligand having at least two donor moieties, which are complexed to at least a metal selected from a transition metal and lanthanide, characterized in that the ligand comprises at least two building blocks, each having at least one functional group and at least one donor moiety, wherein one building block is non-covalently bonded through its functional group to a complementary functional group of another building block or of a template, wherein the template comprises at least one other functional group that is non-covalently bonded to a complementary functional group of another building block, and wherein all building block-template-building block structures are the same when the template contains more than two functional groups. The dynamic character of the system may lead to special reactivity of the catalyst system and it also enables the formation of dynamic combinatorial catalyst systems based on transition metal from which the catalyst can be selected by adding a selector, for instance a transition state analogue.
In an embodiment of the invention at least one of the building blocks is immobilized onto an inorganic support, a polymeric organic support, or a hybrid support. The building blocks preferably have a molecular weight less than 5,000, more preferably less than 2,500. The chiral environment will also be controlled by assembly and it was shown that zinc (II) porphyrins in combination with pyridyl-phosphine building blocks are suitable for this approach. The pyridine is selectively coordinated to the zinc and the phosphine donor is still available for coordination to the catalytically active transition metal.
In another embodiment the coordination complex system comprises a ligand having at least two donor moieties, which are complexed to at least a metal selected from a transition metal and lanthanide, characterized in that the ligand comprises 2 to 6 building blocks each having at least one functional group and at least one donor moiety, wherein at least one building block is non-covalently bonded through its functional group to a complementary functional group of a template .
The system may further comprise a co-factor that is non-covalently bonded to a functional group of the ligand. Such co-factor may be covalently bonded to another building block, or to the template or support.
When the template contains more than two functional groups all building block-template-building block structures are the same. For instance, when the template contains 8 functional groups and two functional groups form a pair whereas the six other functional groups form three similar other pairs, two building blocks are non-covalently attached to each of these pairs, and not to one functional group of the first pair and one functional group of another pair when such bonding gives rise to different spatial orientations
(configurations) of the various building block-template- building block moieties. It should further be noted that if not all building blocks are the same and two different building blocks are used for attachment to one pair of functional groups, the same two different building blocks are used for attachment to the other pairs.
The properties of the assembly may be different from the prior art catalysts, which for instance can result in higher reaction rates in the palladium catalyzed Heck reaction and the rhodium catalyzed hydroformylation. Moreover, using bis-zinc-porphyrin systems as templates resulted in chelating bidentate ligands of which the catalytic performance (in activity and (enantio-) selectivity) strongly depended on the components of the assembly. These results show that dynamic non-covalent interactions are sufficient to impose spatial orientation of ligands and that the assemblies are stable under catalytic conditions. The metal-ligand interactions are used to make new ligand assemblies. Moreover, different hydrogen bond building blocks can be used to make bidentate ligands by assembly. Examples of some of the hydrogen bond building blocks that can be used are shown in Chart I . One should note that these building blocks could be used for several concepts according to this invention. Two identical building blocks can be assembled around a template resulting in a bidentate ligand with properties that depend on the template. A representative example is a building block comprising urea functionalities and benz- amidine, which can be used to form complexes with small anionic templates. The orientation of two urea units will strongly depend on the template. The catalytic performance of the assemblies can also be used as diagnostic tool by studying several reactions that are known to be sensitive to geometry changes (such as hydroformylation, carbonylation and allylic substitution) . Employing cationic transition or lanthanide metal complexes (e.g. asymmetric hydrogenation, hydrovinyl- ation) is of special interest since the counter-ion will be fixed at a certain distance from the metal. This is believed to give special effects in catalysis and in the formation of the cationic complexes . The coordination complex system preferably has a molar ratio between the ligand and the metal of between 0.2 and 100.
The invention further relates to a catalyst system comprising the above-mentioned coordination complex system and the use of the coordination complex system as a catalyst, preferably for hydroformylation, hydrogenation, transfer hydrogenation, hydrocyanation, polymerization, isomerization, carbonylation, cross-coupling, metathesis, CH activation, allylic substitution, aldol condensation, and Michael addition.
For many reactions bidentate ligands with different donor atoms offer a higher level of control of the selectivity. For this purpose approaches are required that enable the selective assembly of different building blocks.
This is done by making sets of building blocks with functional groups that associate with the complementary functional groups attached to either another building block, enabling direct formation of the ligand, or to a template equipped with a plurality of the same or different functional groups. Complementary binding motives of a series of ligands (phosphines, phosphites) utilized are shown in Chart I. By just mixing the proper compounds chelating mono- and bi- dentates were formed, facilitating the easy formation of. different combinations. In addition the same building blocks can be assembled onto a template with the same complementary binding functional groups (Figure 1) .
Figure imgf000010_0001
Fig. 1. Lx and L2 are coordination moieties of the building blocks, M is transition or lanthanide metal. A) is an embodiment using a template; B) is an embodiment using self- complementary building blocks .
In that case the shape of the template will also affect the catalytic performance of the supramolecular system. The templates may include calix-arenes and rigid multi- aromatic systems. Bisporphyrin templates with two different metals are also suitable templates: nitrogen donor will coordinate selectively to the zinc atom and tin porphyrins are known to strongly coordinate carboxylate groups.
Systems functionalized with two orthogonal binding sites can be prepared in which the catalyst and either the substrate molecule or a chiral cofactor can be fixed in a well-defined way using non-covalent interactions. In a straightforward example based on porphyrins the binding of the transition (or lanthanide) metal will be based on hydrogen bonding (ionic interactions) and the (guest) cofactor will be bound using metal-ligand interactions (such as pyridine-zinc coordination) . The binding on the porphyrin can be used for several types of guests including amino acids. Several analogues with different hydrogen bond functional groups thereby changing the position of the catalysts with respect to the binding site can be made. It was found that the dynamic binding of both the catalysts as the substrate molecule is an efficient strategy towards host-guest catalysis. In a slightly different approach chiral cofactors were assembled using metal-building block interactions, for instance based on selective bipyridine- etal complexation, such as in:
Figure imgf000011_0001
One of these components may be functionalized with chiral information, whereas the other contains the catalytically active phosphine-metal complex. A major advantage over the conventional approaches is that large libraries of chiral catalysts can be assembled easily, (compared to covalent synthesis) which is important considering the fact that new substrates generally require novel modified catalysts. The invention therefore also relates to the use of at least two building blocks each having at least one functional group, wherein a functional group of one building block is complementary to a functional group of another building block or of a template to form through their functional groups a non-covalent bond between the building blocks or between the building blocks and the template, to obtain a ligand that with the metal forms the coordination complex system. Another aspect of the invention relates to the use of a set of self-complementary building blocks for making a ligand having at least two donor moieties for complexation to a metal selected from a transition metal and lanthanide, wherein the ligand comprises the set of building blocks, each building block having at least one functional group that is complementary to a functional group of another building block or of a template, and at least one donor moiety, wherein the building blocks are non-covalently bonded to each other or to the template through their complementary functional groups.
The invention further pertains to the set comprising self-complementary building blocks, and optionally templates for making a ligand. The set may also comprise metals for coordination, for the above-mentioned use. As an example 3Bι tetraarylporphyrins as well as trans-A2B2 tetraarylporphyrins can easily be made by well- established synthetic procedures. As reactive groups for further functionalization amines and isothiocyanate groups can be introduced, which are both reactive and easily accessible. Thus for instance porphyrins can be prepared (large quantities) and used as synthons for the synthesis of building blocks required for different ways of non-covalent immobilization.
Examples of approaches of making tailor-made catalysts on a support are mixing trialkoxy-functionalized porphyrin with commercially available silica, immobilization via a sol-gel process, pre-assembly of the transition metal complex prior to immobilization, and post-modification of the immobilized porphyrins with the catalysts. Synthetically easily accessible porphyrins, which are expected to form well-defined aggregates such as micelles and vesicles due to their amphiphilic character, can also be made according to this approach. Amphiphiles that form well-defined aggregates can be used for the assembly of catalysts. These amphiphiles can be prepared via ion-pairing by mixing a bis- anion with cationic amphiphiles.
An extension to functionalized block copolymers (based on porphyrins, carbosilane dendrimers and polystyrene units) is also possible to give interesting systems with control over aggregation and microphase separation by differences in polarity (i.e. amphiphilic systems), incompatibilities in conformational flexibility and in volume filling characteristics of the component blocks. Several examples of building blocks according to the invention are given in Chart II. Some of the templates are given in Chart III. On the basis of these examples the skilled person can easily envisage other building blocks and templates. The number of ligands (made from building blocks, and optionally, templates, that is accessible for the non-covalent anchoring is virtually infinite, and several building blocks and templates are commercial available. In Chart IV examples are given of building blocks that are non-covalently bonded to a support (in the example a silica support) . An important class of compounds, related to porphyrins, which is suitable for the approaches described in this patent comprise the bis (salicylaldimine) metal complexes. The great advantage of the building blocks is the synthetic availability and the structural variations possible. The axial coordination to bis (salicylaldimine) -zinc is two orders of magnitude larger then to the zinc-porphyrin analogue.
The invention is further clarified and exemplified by the following examples.
General
1-Octene was purified over neutral alumina prior to its use. Solvents were dried prior to their use. Hexane, pentane, diethyl ether, THF (tetrahydrofuran) , toluene and benzene were distilled from sodium/benzophenone or calcium hydride (dichloromethane, triethylamine) . All solutions and solvents not stated above were degassed under argon prior to their use. All reactions were performed under Schlenk conditions using argon or purified nitrogen as inert atmosphere. Water and CDC13 were degassed and stored under nitrogen. Chemicals were purchased from Aldrich Chemical Co. and Acros Chimica and were used without further purification. The piperidine was filtered over neutral alumina prior to use.
For the size exclusion chromatography Bio-Beads® S-Xl Beads (Gel Permeation Gel 200-400 mesh, Bio-Rad Laboratories,
Hercules, USA) were used, p- (Diphenylphosphino)benzylamine (COD)PdMeCl, [ (allyl) PdCl] 2 and [ (crotyl) PdCl] 2 were prepared according to literature procedures.
Synthesis of building blocks
With exception of the compounds given below, all reagents were purchased from commercial suppliers and used without further purification. Diisopropylethylamine and triethylamine were distilled from CaH2 under argon. The following compounds (building blocks or templates) were synthesized according to published procedures: Building blocks
B4-B6 (Buhling, A.; Kamer, P. C. J. ; van Leeuwen, P. W. N. M. ;
J. Mole . Catal . A, 1995, 98, 69-80); B8 (Hayashi, T.; Mise, T.; Fukushima, M. ; Kagotani, M. ; Nagashima, N.; Hamada, Y.;
Matsumoto, A.; Kawakami, S.; Konishi, M.; Yamamoto, K. ;
Kumada, M. , Bull . Chem . Soc. Jpn . 1980, 53, 1138); Bll-13
(Buhling, A.; Kamer, P. C. J.; van Leeuwen, P. W. N. M. ; J.
Mole . Ca tal . A 1995, 98, 69); B20, B21 (Kellner, K.; Hanke, W.; Tzschach, A., Zeltschrift fur Chem . 1984, 24, 193); B33
( Liebigs Ann . Chem . 1962, 659, 49) T2-T6 (Cooper, J. B. ;
Brewer, C. T.; Brewer G., Inorg. Chi . Acta 1987, 225, 25. and ' Adler, A. D.; Longo, F. R. ; Kampas, F.; Kim, J. , J. Inorg.
Nucl . Chem . , 1970, 32, 2443); T7-T10 (Thesis P. Kaiser, 2002, University of Koln, Germany). Til (Biemans, H. A. M. ; Rowan,
A. E.; Verhoeven, A.; Vanoppen, P.; Latterini, L.; Foekema,
J. ; Schenning, A. P. H. J. ; Meijer, E. W.; De Schryver, F. C;
Nolte, R. J. M, J. Am . Chem . Soc. 1998, 120, 11054); T12 (Arnold D. P.; Kennard, C. H. L.; Mak, T. C. W., Polyhedron 1991, 10, 509; Arnold, D. P., Polyhedron 1990, 3, 1331;
Arnold, D. P., Polyhedron 1986, 5, 1957), B25 (D. de Groot et al., J. Am . Chem . Soc . 2001, 123, 8453-58).
The following compounds are commercially available:
B7, B9, Tl, T14-T23 (ex Aldrich) .
Synthesis of Bl
3-Hydroxypyridine (1.44 g, 15.1 mmole), azeotropic- ally dried with toluene (3x5 ml), and triethylamine (2.3 ml,
16.6 mmole) were dissolved in THF (40 ml) and the solution was cooled to -40° C. Freshly prepared (S) -2,2' -bisnaphthol phosphorochloridite (ref. Buisman, G. J. H.; van der Veen, L. A.; Klootwijk,- A.; de Lange, W. G. J. ; Kamer, P. C. J. ; van Leeuwen, P. W. N. M. ; Vogt, D., Organometallics 1997, 16, 2929) (5.3 g) was dissolved in THF (20 ml) and added dropwise. The cooling bath was removed and the solution was allowed to warm to room temperature, stirring was continued for 1 hour. The reaction mixture was filtered and the solvent evaporated. A mixture of toluene/hexane 1/3 (40 ml) was added to extract the product. After filtration the solvent was removed in vacuo, giving Bl (5.4 g) as a white solid:
Synthesis of B2
This compound was prepared as described for Bl, using freshly prepared (S) -3, 3' -bis (trimethylsilyl) -2, 2' -bisnaphthol phosphorochloridite (ref. Buisman, G. J. H.; van der Veen, L.
A.; Klootwijk, A.; de Lange, W. G. J. ; Kamer, P. C. J.; van
•Leeuwen, P. W. N. M.; Vogt D., Organometallics 1997, 16,
2929) . (Yield (66 %) as a white solid.
Synthesis of B3
3-Hydroxypyridine (0.95 g) , azeotropically dried with toluene (3x2 ml), and triethylamine (1.4 ml, 10 mmole) were dissolved in THF (20 ml) and the solution was cooled to 0° C. Freshly prepared 3, 3' -5, 5' -tetra- tert-butyl-1, 1' -bisphenol phosphorochloridite (4.75 g, 10 mmole) was dissolved in THF (20 ml) and added drop wise, stirring was continued for 10 minutes. The cooling bath was removed and the solution was allowed to warm to room temperature, stirring was continued for 1 hour. The reaction mixture was filtered and the solvent evaporated. A mixture of toluene/hexane 1/3 (40 ml) was added to extract the product. After filtration the solvent was removed in vacuo, giving B3 (3.4 g) as a white solid. Synthesis of BIO
This compound was prepared as described for Bl, using freshly prepared (R) -2, 2' -bisnaphthol phosphorochloridite. Yield (78 %) as a white solid.
Synthesis of 5- (3-hydroxyphenyl) -10 , 15 , 20-tris (phenyl) (zinc (II) ) porphyrin
3-Hydroxybenzaldehyde (6.35 g) and benzaldehyde (15.8 ml) were dissolved in 750 ml of propionic acid and heated till reflux. Under an air flow and vigorous stirring pyrrole (14.4 ml, 208 mmole) was added and the solution was refluxed for 1 hour. The reaction mixture was cooled to 60° C and 100 ml of methanol were added. The reaction was stored overnight at 4° C, allowing the porphyrin to precipitate. The reaction mixture was filtered and washed several times with methanol until the filtrate was colorless. The porphyrin was purified using column chromatography (basic alumina, CH2C12, upgrade 2 % methanol in CH2C12) , giving 1.09 g of 5- (3-hydroxyphenyl) - 10, 15, 20-tris (phenyl) . The zinc porphyrin was prepared by refluxing 5- (3-hydroxyphenyl) -10, 15, 20-tris (phenyl) in the presence of excess Zn(OAc)2.
Synthesis of B14
5- (2-hydroxyphenyl) -10, 15, 20-tris (phenyl) -zinc (II) porphyrin (1.59 g) , azeotropically dried with toluene (3x5 ml), and diisopropylethylamine (4.0 ml, 23.0 mmole) were dissolved in THF (80 ml) and the solution was cooled to 0° C. Freshly prepared (S) -2, 2 ' -bisnaphtol phosphorochloridite (0.73 g, 2.09 mmole) was dissolved in THF (20 ml) and added dropwise, stirring was continued for 15 minutes. The cooling bath was removed and the solution was allowed to warm to room temperature, stirring was continued for 30 minutes. The reaction mixture was filtered and the solvent evaporated. The crude product was purified by flash column chromatography under argon (basic alumina; CH2C12) to remove the excess of hydroxyl porphyrin, giving B14 (0.887 g) as a purple-red solid.
Synthesis of B15
This compound was prepared as described for B14, using 5- (3-hydroxyphenyl) -10, 15, 20-tris (phenyl) -zinc (II) porphyrin. Yield (47 %) as a purple-red solid.
Synthesis of B16
5- (2-Hydroxyphenyl) -10, 15, 20-tris (phenyl) -zinc (II) porphyrin (1.59 g, 2.30 mmole) azeotropically dried with toluene (3x5 ml), and diisopropylethylamine (4.0 ml, 23.0 mmole) were dissolved in THF (80 ml) and the solution was cooled to -40° C. Freshly prepared (S) -2, 2' -bisnaphthol phosphorochloridite (0.73 g, 2.09 mmole) was dissolved in THF (20 ml) and added dropwise, and stirring was continued for 15 minutes. The cooling bath was removed and the solution was allowed to warm to room temperature, stirring was continued for 30 minutes. The reaction mixture was filtered and the solvent evaporated. The crude product was purified by flash column chromatography under argon (basic alumina; CH2C12) to remove the excess of hydroxyporphyrin, giving B16 (0.887 g) as a purple-red solid.
Synthesis of B17
This compound was prepared as described for B16, using freshly prepared (R) -2, 2' -bisnaphthol phosphorochloridite. Yield (46 %) as a purple-red solid.
Synthesis of B18
This compound was prepared as described for B16, using 5- (3-hydroxyphenyl) -10, 15, 20-tris (phenyl) -zinc (IT) porphyrin and freshly prepared (S) -2, 2' -bisnaphthol phosphorochloridite. Yield (39 %) as a purple-red solid. Synthesis of B19
This compound was prepared as described for B16, using freshly prepared (S) -3, 3' -bis (trimethylsilyl) -2,2' - bisnaphthol phosphorochloridite. Yield (51 %) as a purple-red solid.
Synthesis of B22
This compound was formed after oxidation with air of B4.
Synthesis of B23
5- (3-Hydroxyphenyl) -10, 15, 20-tris (phenyl) -zinc (II) porphyrin (1.23 g) azeotropically dried with toluene (3x3 ml), and diisopropylethylamine (3.1 ml) were dissolved in THF (80 ml) and the solution was cooled to -40° C. Freshly prepared PC13 (44 μl) was dissolved in THF (10 ml) and added dropwise, and stirring was continued for 15 minutes. The cooling bath was removed and the solution was allowed to warm to room temperature, stirring was continued for 2 hours. The reaction mixture was filtered and the solvent evaporated. The crude product was purified by flash column chromatography under argon (silica; toluene) to remove the excess of hydroxyporphyrin, giving B23 (0.341 g) as a purple-red solid.
Synthesis of B27
0.50 g (0.616 mmole) of 4 , 5-di (diphenylphosphine) -2- pentyl~7~bromopentyl-9, 9-dimethyl-xanthene were dissolved in 15 ml of THF. Under argon the solution was transferred into a 100 ml autoclave. After addition of 20 ml of liquid NH3, the autoclave was stirred and heated at 70° C overnight. THF was removed in vacuo and the residue was dissolved in 20 ml of DCM (dichloromethane) and hydrolyzed with 10 ml of water. The organic layer was separated and dried over MgS04. White solids were obtained after removing the solvent in vacuo. Yield 0.41 g.
Synthesis of B24 To a solution of 0.25 g of B27 in 10 ml DCM, 0.038 ml ethyl isocyanatoacetate were added. After stirring overnight at room temperature the solvent was evaporated. The product was recrystallized from DCM/pentane and a white solid was obtained and dissolved in 5 ml THF to which a solution of 15.0 mg NaOH (0.375 mmole) in 4 ml water was added. After stirring overnight the THF was evaporated and the reaction mixture was neutralized by addition of 2 ml 0.44 M aqueous HCI. The solvent was decanted and the crude product was washed with water. After recrystallization from chloroform 0.136 g of a white powder was obtained.
Synthesis of B28
3-Aminopyridine (0.82 g, 8.7 mmole), azeotropically dried with toluene (3x2 ml) , and triethylamine (1 ml, 8 mmole) were dissolved in THF (40 ml) and the solution was cooled to 0°
C. Freshly prepared (S) -2, 2' -bisnaphtol phosphorochloridite
(ref. Buisman, G. J. H. ; van der Veen, L. A.; Klootwijk, A. ; de Lange, W. G. J.; Kamer, P. C. J. ; van Leeuwen, P. W. N. M.;
Vogt D., Organometallics 1997, 16, 2929) (from 1 g of (S)- (-) 2,2' -bisphenol and 0.76 g of PC13 and 1.4 g of Et3N) was dissolved in THF (20 ml) and added dropwise. The cooling bath was removed and the solution was allowed to warm to room temperature, and stirring was continued for 2.5 hour. The reaction mixture was filtered and the solvent evaporated, giving B28 (1.3 g) as a white solid.
Synthesis of B29
199 mg (0.856 mmole) of hydroxymethyldiphenylphosphine oxide
(prepared as described by R.S. Marmor in J. Org. Chem . 1969, 34, 748) were azeotropically dried on toluene (3x2 ml) and subsequently dissolved in 10 ml of THF and 1 ml of Et3N. At 0° C a solution of 250 mg (0.713 mmole) of freshly prepared (S)- 2,2'-bisnaphtol phosphorochloridite in 10 ml of THF was slowly added to the reaction mixture. The resulting mixture was stirred for 24 h at room temperature. The mixture was filtered and the solvents were removed under reduced pressure. After intense washing with EtOAc (ethylacetate) , the product was obtained pure as a white solid (yield: 224 mg) .
Synthesis of B30
182.6 mg (1.427 mmole) of N-acetyl-2-imidazolidone (prepared as described by H.K. Hall in J. Am . Chem . Soc . 1958, 80, 6409) was azeotropically dried on toluene (3x2ml) and suspended in 20 ml of THF and 2 ml of Et3N. A solution of 500 mg (1.43 mmole) of freshly prepared (R) -2, 2' -binaphtol phosphochlorodite in 10 ml of THF was slowly added at 0° C. The resulting mixture was stirred for 18 h at room temperature. Upon removing the THF under reduced pressure, after filtration, the product was obtained as a white solid. The product was purified upon rapid extraction in hexane/methanol (Yield: 253 mg) .
Synthesis of B31
97 mg (1.31 mmole) of methyl •urea was azeotropically dried over acetonitrile (3x3 ml) and kept under vacuum overnight in the presence of P20s. A solution of 309.4 mg (0.882 mmole) of freshly prepared (R) -2, 2' -bisnaphtol phosphochlorodite in 10 ml of THF was slowly added to a solution of the methyl-urea in 10 ml of THF and 1 ml of Et3N at 0° C. A white precipitate was immediately formed. The resulting mixture was stirred for 18 h at room temperature, filtered and concentrated to dryness under reduced pressure. The product was obtained as a colorless solid. The product was purified by dissolution in toluene and addition of a small amount of hexane. (Yield: 301 mg) .
Synthesis of B32 200 mg (1.341 mmole) of 3-methoxyphenylisocyanate were dropwise added to a suspension of 202.8 mg (1.341 mmole) of (1R,2S) - (-) -norephedrin in 20 ml of dichloromethane at room temperature. The resulting mixture was further stirred for 18 h at room temperature. Solvents were removed under reduced pressure. A dichloromethane solution of the product was washed (3x5 ml) with a 10% aqueous HCI solution, dried on MgS04 and isolated under reduced pressure. (Yield: 352 mg) .
The obtained product 1- (IR, 2S) -2—hydroxy—l-methyl-2- phenylethyl-3- (3-methoxyphenylurea) was dried on toluene (3x3ml) and dissolved in 10 ml of THF and 1 ml of Et3N was added. To this clear solution, a solution of (R)-2,2'~ bisnaphtol phosphochlorodite in 10 ml of THF was slowly added at 0° C. The resulting mixture was stirred for 18 h at room temperature, filtered and concentrated to dryness. The product was obtained at a colorless solid. (Yield: 299 mg) .
Synthesis of 112
According to a similar procedure as described by Arnold D. P.; Kennard, C. H. L. ; Mak, T. C. W. , Polyhedron 1991, 10, 509; Arnold, D. P., Polyhedron 1990, 9, 1331;
Arnold, D. P., Polyhedron 1986, 5, 1957, potassium carbonate (800 mg) and 5, 10, 15, 20-tetrakisphenyl dichlorotin (IV) porphyrin (280 mg) were dissolved in a mixture of 150 ml of THF and 40 ml of water and heated at reflux for 3 hours. The organic solvent was removed and the aqueous layer was extracted with 100 ml of dichloromethane. The organic layer was washed with water (2x80 ml) and then dried over anhydrous sodium sulfate, filtered and then the solvent was removed to give the crude product, which was then recrystallized from hexane/dichloromethane (1/1) to give T12 (242 mg, 91%) as a metallic purple crystalline solid.
Synthesis of T13 This compound was prepared as described for T12, using the free base analogue of Til (Biemans, H. A. M.; Rowan, A. E.; Verhoeven, A,; Vanoppen, P.; Latterini, L.; Foeke a, J. ; Schenning, A. P. H. J. ; Meijer, E. W.; De Schryver, F. C; Nolte, R. J. M., J. Am . Chem . Soc. , 1998, 120, 11054) as starting material (89 %) as a purple solid.
Synthesis of T24
DAB-dendr- (NH2)4 (N,N,N! ,N'-tetrakis (3-aminopropyl) - 1, -butanediamine; 0.12 g (Aldrich)) was dissolved in dichloromethane (5 ml), 3- (triethoxysilyl)propylisocyanate (0.34 g) was added and the mixture was stirred for 2 hours. After evaporation of the solvent the compound was isolated (Yield 76.9 %) .
Synthesis of T25
T25 was obtained after refluxing a suspension of T24 and silica in toluene for 5 hours.
Synthesis of 126 T26 was prepared using a similar procedure as for
T25.
Synthesis of T27-T32, T38
We used a modified procedure taken from 0' Conner, M.J.; West, B.O., Aust . J. Chem . , 1967, 20, 2077: To a solution of the salicylaldehyde (2 eq) and ortho- phenylenediamine (1 eq) in methanol (40 ml) was added a solution of zinc acetate dihydrate (> 1 eq) and triethylamine (2-4 ml) . The mixture was stirred at room temperature for 18 h. The product was subsequently isolated by filtration and dried. Typical isolated yield 57 - 100 % Typical example T27 :
4, 5-Dichloro-o-phenylenediamine (0.38 g, 2.15 mmole), 3, 5-di-tert-butyl-salicylaldehyde (1.04 g, 4.44 mmole) were mixed in MeOH (50 ml). Then a solution of Zn (OAc) 2.2H20 (0.60 g, 2.73 mmole) in MeOH (5 ml) was added followed by addition of neat NEt3 (3 ml) . The mixture was stirred for 18 h at room temperature, and the precipitated product collected by filtration. Drying in vacuo afforded 0.83 g of an orange solid (1.23 mmole, 57 %) .
Synthesis of T33-T37
Modified reaction procedure as described for T27- T32: salicylaldehyde and salicylidene (l-iminophenylene-2- amine) (Munoz-Hernandez, M.A.; Keizer, T.S.; Parkin, S.;
Patrick, B. ; Atwood, D.A., Organometallics, 2000, 19, 4416) were mixed in a 1:1 ratio and a solution of zinc acetate dihydrate ( 1 eq) and triethylamine was added. The mixture was stirred at room temperature for 18 h. The product was subsequently isolated by filtration and dried. Typical isolated yield 57 - 100 %
Formation of the ligands and complexes by assembly of the building blocks
The ligands and complexes were formed by just mixing in solution the building blocks, templates, and metal precursors in the required ratios. In the following table 1 some examples of complexes that have been prepared in this manner are listed (see Charts II and III for structures) . 'Table 1
Figure imgf000025_0001
Figure imgf000026_0001
Figure imgf000027_0001
Figure imgf000028_0001
Figure imgf000029_0001
Figure imgf000030_0001
Figure imgf000031_0001
Figure imgf000032_0001
Examples of coordina tion complexes based on assembled building blocks in catalysis are given in the following tables .
Table 2. Rhodium catalyzed hydroformylation of 1-octene using coordination complexes of Table la
Entry of temp. T.0.F.c 1/b d isomerse [%] catalyst in (°C) table 1 b
1 120 1.3*103 7.0 19.8
2 80 3.0*103 2.0 26.0
5 80 2.7*103 2.9 1.9
4 80 2.8*103 2.9 2.8
3 80 2.8*103 2.9 2.9
6 80 3.0*103 2.9 3.4
9 80 3.5*103 2.4 1.1
8 80 3.5*103 2.3 1.2
7 80 3.6*103 2.3 0.7
10 80 3.6*103 2.4 1.0
(a) [Rh(acac) (CO)2] = 0.084 mmole/1 in toluene, pressure = 20 bar (CO/H2 = 1/1) , 1-octene/rhodium = 5160, in none of the reactions hydrogenation was observed, (b) [phosphorus] = 2.1 mmole/1, [porphyrin] = 2.1 mmole/1, (c) T.O.F. = average turn over frequency = (mole aldehyde) (mole Rh)-1!!"1, the reaction was stopped after 1 hour (d) 1/b = linear/branched, (e) percent isomerization to 2-, 3- and 4-octene based on converted 1-octene .
Table 3. Hydrogenation of dimethyl itactonate using coordination complexes of Table la
Entry of conversion (%)c e.e. (%)d catalyst in Table lb
_ __ 33 (R)
12 6.2 21 (R)
13 4.3 31 (R)
14 18.8 50 (R)
15 2.5 2 (R)
16 3.1 40 (R)
(a) [Rh(nbd)2(BPh4) ] = 1.0 mmole/1, [dimethyl itaconate] = 100 mmole/1, pressure = 5 bar hydrogen, T = 40° C, (b) [phosphite] = 3.0 mmole/1, [porphyrin] = 3.0 mmole/1, (c) the reaction was stopped after 17 hours (d) e.e. = percent enantiomeric excess.
Table 4. Rhodium-catalyzed hydroformylation of styrene using coordination complexes of Table 1
Entry of T.0.F.° b/1 d e.e.e (%)
Catalyst in Table l
1 0.02 >100 6.0 (S)
30 0.15 >100 33.2 (S)
31 0.02 >100 6.3 (R)
32 0.14 >100 32.6 (R)
(a) [Rh] = 0.084 mmole/1 in toluene, pressure = 20 bar (C0/H2 = 1/1), styrene/rhodium = 7000, in none of the reactions hydrogenation was observed, T = 25° C. (b) [phosphite] = 2.1 mmole/1, [1] = 2.1 mmole/1, [2] = 1.1 mmole/1. (c) T.O.F. = average turn over frequency = (mole aldehyde) (mole Rh)~1h""1, the reaction was stopped after 64 hours, (d) b/1 = branched/linear, (e) e.e.= enantiomeric excess (%) . Table 5. Rhodium-catalyzed hydrogenation of dimethyl itaconate using coordination complexes of Table 1
Entry of conversion e.e. (% catalyst in Table lb
1 7.5 31 (S)
30 9.5 8 (S)
31 6.9 32 (R)
32 10:2 7 (R)
(a) [Rh (nbd) 2BPh] = 0.10 mmole/1, substrate/rhodium 200, T = 40° C. (b) [phosphite] = 0.60 mmole/1, [1] = 0.60 mmole/1, [2] = 0.30 mmole/1 in toluene (c) the reaction was stopped after 15 hours (d) e.e.= enantiomeric excess (%).
Table 6. Palladium catalyzed allylic alkylation using coordination complexes of Table la
Entry of conversion e.e.d (%) catalyst in (%)c
Table lb
1 >99 31 (S)
30 >99 45 (S)
31 >99 32 (R)
32 >99 44 (R)
(a) [[Pd(allyl)Cl]2] = 0.10 mmole/1, 1, 3-diphenyl-allyl acetate/rhodium = 100, T = 25° C. (b) [phosphite] = 0.60 mmole/1, [1] = 0.60 mmole/1, [2] = 0.30 mmole/1. (c) the reaction was stopped after 63 hours, (d) e.e.= enantiomeric excess (%) . Table 7. Hydroformylation of 1-octene using coordination complexes of Table la
Entry of T.0.F.c 1/b d 2-octenee linear6 (%) catalyst in (no3) (%)
Table lb
43 2.4 2.1 0.8 66.9
43f 2.3 2.1 1.0 66.3
39 2.0 2.6 0.8 71.4
39 f 2.0 2.5 0.4 70.9
41 0.03 2.4 2.4 68.1
41 f 0.3 2.1 1.7 67.4
(a) [Rh(acac) (CO)2] = 0.084 mmole/1 in toluene, pressure = 20 bar (C0/H = 1/1) , 1-octene/rhodium = 5160, in none of the reactions hydrogenation was observed, (b) [phosphine] = 0.84 mmole/1, (c) T.O.F. = average turn over frequency = (mole aldehyde) (mole Rh.)-1]!"1, the reaction was stopped after 1 hour (80° C) , (d) 1/b = linear/branched ratio, (e) percent selectivity to 2-octene and percent selectivity to linear aldehyde based on converted 1- octene. (f) Building block/template ratio = 4.
Table 7. Hydroformylation of styrene using coordination complexes of Table la
Entry of T.O.F. b/r Branched (%) catalyst in
Table lb
171 2900 2.6 72
103 398 10.4 91
103e 375 10.5 91
151 3010 2.7 73
172 1060 3.6 78
172e 1730 5.0 83
104 449 9.3 90
104e 461 9.4 90
(a) [Rh(acac) (CO)2] = 0.83 mmole/1 , pressure = 20 bar (CO/H2 = 1/1) , T= 80° C (b) phosphite / rhodium = 25, phosphite/phosphine = 1, (c) T.O.F. = average turn over frequency = (mole aldehyde) (mole Rh)-1^1, the reaction was stopped after 1 hour, (d) b/1 = branched/linear, (e) in the presence of triphenylphosphine.
Table 8. Allylic alkylation of 1, 3-diphenyl-allyl acetate using coordination complexes of Table la
Entry of conversion e.e.b (%) catalyst in (%)
Table lb
173 56 97 (S)
51 100 60 (R)
57 100 0
63 100 44 (S)
174 54 96 (R)
52 100 60 (S)
175 73 42 (S)
53 40 70 (S) (a) [[Pd(allyl)Cl]2] = 0.100 mmole/1, [phosphite] = 0.6 mmole/1, [phosphine] = 0.6 mmole/1, the reaction was stopped after 43 hours, T = -20° C (b) e.e. = enantiomeric excess .
Table 9. Rhodium-catalyzed hydrogenation of dimethyl itaconate using coordination complexes of Table la
Entry of conversion e.e.d (%) catalyst in (%)c
Table lb
123 2 24 (S)
105 4 18 (S)
111 5 13 (S)
117 1 17 (S)
141 100 66 (S)
147 22 5 (S)
129 1 35 (S)
153 6 6 (S)
107 19 18 (S)
113 13 25 (S)
119 9 19 (S)
143 13 24 (S)
149 15 21 (S)
125 0 -
131 10 19 (S)
155 19 16 (S) a [Rh(nbd)2BPh4] = 1.0 mmole/1, [porphyrin] = 3.0 mmole/1, [phosphorous (a-i) ] = 3.0 mmole/1, T = 40° C, the reaction was stopped after 18 hours (b) ee = enantiomeric excess. Table 10 Hydroformylation of 1-octene using rhodium catalysts using coordination complexes of Table la
Entry of temp. T.0.F.c 1/b d isomers6 catalyst (°C) (%) in Table lb
162 80 3.4*103 1.9 16.1
163 80 2. mo3 2.3 11.2
164 80 2.4*103 2.7 14.1
165 80 3.4*103 2.1 14.7
166 80 3.2*103 2.1 14.4
167 80 1.9*103 3.4 10.4
168 80 ι.ι*ιo3 15.1 11.9
168 30 25 22.8 10.3
169 80 2. mo3 2.5 11.3
170 80 1.4*103 2.9 10.4
(a) [Rh (acac) (CO) 2] = 0. 084 mmole/1 in toluene, pressure = 20 bar (CO/H2 = 1/1 ) , 1-octene/rhodium = 5160 . (b) [4 ] = 2. 1 mmole/1, [a] = 6.3 mmole/1 [b-i] = 3. 1 mmole/1. (c) T . O . F. = average turn over frequency = (mole aldehyde) (mole Rh) "1!}-1, the reaction was stopped after 1 hour ( 80° C) and 17 hours (30° C) . (d) 1/b = linear /branched ratio , (e) percent selectivity to isomerization to 2-, 3- and 4-octene based on converted 1-octene .
Table 11. Recycling of catalyst entry 186 and catalyst performance in the allylic amination
Entry of Time Conv. Linear Linear Branched catalyst in (min. ) (%) trans cis (%)
Table lb (%) (%)
186 30 91 51 12 37 recycle 1' 30 85 51 13 36 recycle 2' 30 85 50 13 37 recycle 3' 30 72 51 14 35 CH2C12 (5 ml) ; [crotyl acetate] = 0.2 M; [piperidine] = 0. 4 M; ligand/Pd= 2 ; [Pd] = 0 . 002 M; r . t .
Table 12. Recycling of catalyst assembly 187 and catalyst performance in Hydroformylation of 1-octene
Cycle Conv. (%) 1-aldehyde b-aldehyde 1/bi ratio Isomers (%) (%) (%)
1 89.3 64.6 32.2 2.0 3.2
2 89.8 62.7 33.0 1.9 4.3
3 88.7 66.9 30.4. 2.2 2.7
4 87.9 60.9 33.8 1.8 5.3
5 85.4 61.3 34.0 1.8 4.7
6 82.2 63.4 33.4 1.9 3.2
7 81.3 67.0 30.5 2.2 2.5
8 81.4 67.7 30.7 2.2 1.6
0 . 01 mmole Rh (acac) (CO) 2, ligand to rhodium is 10, 1 ml of 1-octene, 1 ml of decane, 20 ml of toluene, 80 " C, 50 bar of CO/H2, 20 h .
Table 13. Recycling of catalyst assembly 183 and catalyst performance in hydroformylation of 1-octene
Cycle Conv. TOF 1-aldehyde b-aldehyde isomers 1/b a
(%) (h"1) (%) (%) (%) ratio
1 39.4 17.0 87.7 3.4 8.9 25.9
2 39.9 17.1 87.7 3.6 8.7 24.4
3 39.0 16.9 87.4 3.5 9.1 25.0
4 40.0 17.1 87.9 3.5 8.6 25.0
5 39.6 17.0 87.4 3.6 9.0 24.3
6 39.0 16.9 87.4 3.4 9.2 25.7
7b 42.2 17.7 86.1 3.7 10.2 23.3
8C 41.4 18.4 87.5 3.3 9.2 26.5
9d 45.3 20.4 87.9 3.1 9.0 27.9
10e 54.6 19.2 65.6 2.5 31.9 25.9 llf 40.5 17.1 86.1 3.9 10.0 22.2 a: 0 .01 mmole Rh (acac) ( Cθ) 2, ligand to rhodium is 10 , 1 ml of 1-octene, 1 ml of decane, 20 ml of toluene , 80 ° C, 50 bar of CO/H2. b: 40 bar of CO/H2 ; ; c: 30 bar of CO/H, ; d: 20 bar of CO/H2; e: 10 bar of C0/H2; V 50 bar of CO/H2; g 100 ° C; h: 120 ° C .

Claims

Claims :
1. A coordination complex system comprising a ligand having at least two donor moieties, which are complexed to at least a metal selected from a transition metal and lanthanide, characterized in that the ligand comprises at least two building blocks, each having at least one functional group and at least one donor moiety, wherein one building block is noncovalently bonded through its functional group to a complementary functional group of another building block or of a template, wherein the template comprises at least one other functional group that is non-covalently bonded to a complementary functional group of another building block, and wherein all building block-template-building block structures are the same when the template contains more than two functional groups.
2. The coordination complex system of claim 1 wherein at least one the building blocks is immobilized onto an inorganic support, a polymeric organic support, or a hybrid support.
3. The coordination complex system of claim 1 or 2 wherein the building blocks have a molecular weight less than 5,000.
4. The coordination complex system of any one of claims 1-3 wherein the system further comprises a co-factor that is non-covalently bonded to a functional group of the ligand.
5. The coordination complex system of any one of claims 1-4 wherein the molar ratio between the ligand and the metal is between 0.2 and 100.
6. The coordination complex system comprising a ligand having at least two donor moieties, which are complexed to at least a metal selected from a transition metal and lanthanide, characterized in that the ligand comprises 2 to 6 building blocks each having at least one functional group and at least one donor moiety, wherein at least one building block is noncovalently bonded through its functional group to a complementary functional group of a template.
7. A catalyst system comprising the coordination complex system of any one of claims 1-6.
8. Use of the coordination complex system of any one of claims 1-6 as a catalyst, preferably for hydroformylation, hydrogenation, transfer hydrogenation, hydrocyanation, polymerization, isomerization, carbonylation, cross-coupling, metathesis, CH activation, allylic substitution, aldol condensation, and Michael addition.
9. Use of at least two building blocks each having at least one functional group, wherein a functional group of one building block is complementary to a functional group of another building block or of a template to form through their functional groups a non-covalent bond between the building block and the template, or between the at least two building blocks, directly or through the template, to obtain with the metal the coordination complex system of any one of claims 1- 7.
10. Use of a set of self-complementary building blocks for making a ligand having at least two donor moieties for complexation to a metal selected from a transition metal and lanthanide, wherein the ligand comprises the set of building blocks, each building block having at least one functional group that is self-complementary to a functional group of another building block or a template, and at least one donor moiety, wherein the building blocks are non-covalently bonded to each other or to the template through their complementary functional groups.
11. A set comprising self-complementary building blocks for making a ligand, and optionally templates and/or metals for coordination, for use as claimed in claim 10.
PCT/EP2004/050906 2003-05-22 2004-05-24 Coordination complex system comprising building blocks and use thereof as a catalyst Ceased WO2004103559A2 (en)

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US8283276B2 (en) 2007-11-22 2012-10-09 Universiteit Van Amsterdam Coordination complex system comprising tautomeric ligands
EP2559484A1 (en) 2011-08-18 2013-02-20 Universiteit van Amsterdam Coordination complex system comprising a second bulding block without donor moiety

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EP1816132A1 (en) 2006-01-26 2007-08-08 Engelhard Corporation Process for the production of phosphorous compounds
WO2008031889A3 (en) * 2006-09-15 2009-04-16 Basf Se Pnicogen-containing pseudochelating ligands
US8283276B2 (en) 2007-11-22 2012-10-09 Universiteit Van Amsterdam Coordination complex system comprising tautomeric ligands
EP2559484A1 (en) 2011-08-18 2013-02-20 Universiteit van Amsterdam Coordination complex system comprising a second bulding block without donor moiety

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