NO863433L - Polymerer til behandling av overflater. - Google Patents

Polymerer til behandling av overflater.

Info

Publication number: NO863433L
Authority: NO; Norway
Prior art keywords: phenyl; groups; group; substituents; alkyl
Prior art date: 1984-12-28

Application number

NO863433A

Other languages

English (en)

Norwegian (no)

Other versions

NO863433D0 (no

Inventor

Jorma Virtanen

Paavo Kinnunen

Arvo Kulo

Original Assignee

Ksv Chemicals Oy

Priority date (The priority date 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 date listed.)

1984-12-28

Filing date

1986-08-27

Publication date

1986-10-21

1986-08-27 Application filed by Ksv Chemicals Oy filed Critical Ksv Chemicals Oy

1986-08-27 Publication of NO863433D0 publication Critical patent/NO863433D0/no

1986-10-21 Publication of NO863433L publication Critical patent/NO863433L/no

Links

229920000642 polymer Polymers 0.000 title claims description 10
238000004381 surface treatment Methods 0.000 title description 3
150000001875 compounds Chemical class 0.000 claims description 27
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 25
125000000217 alkyl group Chemical group 0.000 claims description 16
-1 -SH Chemical group 0.000 claims description 14
125000004093 cyano group Chemical group *C#N 0.000 claims description 12
238000004817 gas chromatography Methods 0.000 claims description 9
125000003545 alkoxy group Chemical group 0.000 claims description 8
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 8
229910000077 silane Inorganic materials 0.000 claims description 8
125000004432 carbon atom Chemical group C* 0.000 claims description 7
125000001424 substituent group Chemical group 0.000 claims description 7
239000001257 hydrogen Substances 0.000 claims description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 6
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 6
150000004756 silanes Chemical class 0.000 claims description 6
229910052710 silicon Inorganic materials 0.000 claims description 6
125000003342 alkenyl group Chemical group 0.000 claims description 5
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 5
125000006850 spacer group Chemical group 0.000 claims description 5
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 4
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 4
239000011521 glass Substances 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
238000004587 chromatography analysis Methods 0.000 claims description 3
229910044991 metal oxide Inorganic materials 0.000 claims description 3
125000005581 pyrene group Chemical group 0.000 claims description 3
230000027756 respiratory electron transport chain Effects 0.000 claims description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
125000005037 alkyl phenyl group Chemical group 0.000 claims description 2
125000005577 anthracene group Chemical group 0.000 claims description 2
235000010290 biphenyl Nutrition 0.000 claims description 2
239000004305 biphenyl Substances 0.000 claims description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
229910052794 bromium Inorganic materials 0.000 claims description 2
239000000460 chlorine Substances 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims description 2
229910052731 fluorine Inorganic materials 0.000 claims description 2
239000011737 fluorine Substances 0.000 claims description 2
230000005660 hydrophilic surface Effects 0.000 claims description 2
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
239000010453 quartz Substances 0.000 claims description 2
238000004519 manufacturing process Methods 0.000 claims 1
239000000178 monomer Substances 0.000 claims 1
229920001296 polysiloxane Polymers 0.000 claims 1
239000000047 product Substances 0.000 description 18
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 16
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
239000000203 mixture Substances 0.000 description 8
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 8
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 7
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
238000000034 method Methods 0.000 description 6
239000011541 reaction mixture Substances 0.000 description 6
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 5
239000007789 gas Substances 0.000 description 5
239000005055 methyl trichlorosilane Substances 0.000 description 5
JLUFWMXJHAVVNN-UHFFFAOYSA-N methyltrichlorosilane Chemical compound C[Si](Cl)(Cl)Cl JLUFWMXJHAVVNN-UHFFFAOYSA-N 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
230000003993 interaction Effects 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
230000001681 protective effect Effects 0.000 description 4
239000002904 solvent Substances 0.000 description 4
239000000758 substrate Substances 0.000 description 4
125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 3
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 3
238000010521 absorption reaction Methods 0.000 description 3
125000003118 aryl group Chemical group 0.000 description 3
239000010410 layer Substances 0.000 description 3
239000011777 magnesium Substances 0.000 description 3
229910052749 magnesium Inorganic materials 0.000 description 3
230000014759 maintenance of location Effects 0.000 description 3
239000010703 silicon Substances 0.000 description 3
238000005292 vacuum distillation Methods 0.000 description 3
ZJQQRRMYJSBNOH-UHFFFAOYSA-N (3,4-dimethoxyphenyl)-dimethoxy-methylsilane Chemical compound COC1=CC=C([Si](C)(OC)OC)C=C1OC ZJQQRRMYJSBNOH-UHFFFAOYSA-N 0.000 description 2
KJLUORISKYXZLZ-UHFFFAOYSA-N 4-[dimethoxy(methyl)silyl]-2,6-dimethylbenzonitrile Chemical compound CO[Si](C)(OC)C1=CC(C)=C(C#N)C(C)=C1 KJLUORISKYXZLZ-UHFFFAOYSA-N 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
238000005411 Van der Waals force Methods 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
238000000576 coating method Methods 0.000 description 2
239000012043 crude product Substances 0.000 description 2
LNBLBKMIENYAGP-UHFFFAOYSA-N dichloro-(3,5-dimethylphenyl)-methylsilane Chemical compound CC1=CC(C)=CC([Si](C)(Cl)Cl)=C1 LNBLBKMIENYAGP-UHFFFAOYSA-N 0.000 description 2
JJQZDUKDJDQPMQ-UHFFFAOYSA-N dimethoxy(dimethyl)silane Chemical compound CO[Si](C)(C)OC JJQZDUKDJDQPMQ-UHFFFAOYSA-N 0.000 description 2
229910001873 dinitrogen Inorganic materials 0.000 description 2
239000000284 extract Substances 0.000 description 2
FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 2
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 2
150000003961 organosilicon compounds Chemical class 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 2
150000003377 silicon compounds Chemical class 0.000 description 2
229920005573 silicon-containing polymer Polymers 0.000 description 2
239000000126 substance Substances 0.000 description 2
WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 description 2
PYOKUURKVVELLB-UHFFFAOYSA-N trimethyl orthoformate Chemical compound COC(OC)OC PYOKUURKVVELLB-UHFFFAOYSA-N 0.000 description 2
LMFRTSBQRLSJHC-UHFFFAOYSA-N 1-bromo-3,5-dimethylbenzene Chemical compound CC1=CC(C)=CC(Br)=C1 LMFRTSBQRLSJHC-UHFFFAOYSA-N 0.000 description 1
BVTLTBONLZSBJC-UHFFFAOYSA-N 2,4,6-tris(ethenyl)-2,4,6-trimethyl-1,3,5,2,4,6-trioxatrisilinane Chemical compound C=C[Si]1(C)O[Si](C)(C=C)O[Si](C)(C=C)O1 BVTLTBONLZSBJC-UHFFFAOYSA-N 0.000 description 1
125000003762 3,4-dimethoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 description 1
KBTMGSMZIKLAHN-UHFFFAOYSA-N 4-bromo-1,2-dimethoxybenzene Chemical compound COC1=CC=C(Br)C=C1OC KBTMGSMZIKLAHN-UHFFFAOYSA-N 0.000 description 1
LAYDFDMDUCVHBO-UHFFFAOYSA-N 4-bromo-2,6-dimethylbenzonitrile Chemical compound CC1=CC(Br)=CC(C)=C1C#N LAYDFDMDUCVHBO-UHFFFAOYSA-N 0.000 description 1
NHMXBWJNWMUZEM-UHFFFAOYSA-N 5-[dimethoxy(phenyl)silyl]benzene-1,3-dicarbonitrile Chemical compound C=1C(C#N)=CC(C#N)=CC=1[Si](OC)(OC)C1=CC=CC=C1 NHMXBWJNWMUZEM-UHFFFAOYSA-N 0.000 description 1
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
SJUPTFDROKFGMI-UHFFFAOYSA-N C[SiH](OC)OC.C(#N)C=1C=C(C=C(C1)C#N)C1=CC=CC=C1 Chemical compound C[SiH](OC)OC.C(#N)C=1C=C(C=C(C1)C#N)C1=CC=CC=C1 SJUPTFDROKFGMI-UHFFFAOYSA-N 0.000 description 1
238000003747 Grignard reaction Methods 0.000 description 1
239000007818 Grignard reagent Substances 0.000 description 1
235000011114 ammonium hydroxide Nutrition 0.000 description 1
229940095564 anhydrous calcium sulfate Drugs 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
230000033228 biological regulation Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
FDCBKHMYMQKXGF-UHFFFAOYSA-N chloro-methoxy-methylsilane Chemical compound CO[SiH](C)Cl FDCBKHMYMQKXGF-UHFFFAOYSA-N 0.000 description 1
238000013375 chromatographic separation Methods 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
125000001891 dimethoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
125000005805 dimethoxy phenyl group Chemical group 0.000 description 1
GYZSPRZBAAJGON-UHFFFAOYSA-N dimethoxy-methyl-(6-pyren-1-ylhexyl)silane Chemical compound C1=C2C(CCCCCC[Si](C)(OC)OC)=CC=C(C=C3)C2=C2C3=CC=CC2=C1 GYZSPRZBAAJGON-UHFFFAOYSA-N 0.000 description 1
LIKFHECYJZWXFJ-UHFFFAOYSA-N dimethyldichlorosilane Chemical compound C[Si](C)(Cl)Cl LIKFHECYJZWXFJ-UHFFFAOYSA-N 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
239000012259 ether extract Substances 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 1
239000005350 fused silica glass Substances 0.000 description 1
150000004795 grignard reagents Chemical class 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
239000002035 hexane extract Substances 0.000 description 1
AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
238000004811 liquid chromatography Methods 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
GBMDVOWEEQVZKZ-UHFFFAOYSA-N methanol;hydrate Chemical compound O.OC GBMDVOWEEQVZKZ-UHFFFAOYSA-N 0.000 description 1
BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 1
SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
125000005575 polycyclic aromatic hydrocarbon group Polymers 0.000 description 1
230000001376 precipitating effect Effects 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
125000005372 silanol group Chemical group 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000002344 surface layer Substances 0.000 description 1
239000012756 surface treatment agent Substances 0.000 description 1
ICEYAVKJMMRQIX-UHFFFAOYSA-N trichloro-[3-(3,5-dimethoxyphenyl)propyl]silane Chemical compound COC1=CC(CCC[Si](Cl)(Cl)Cl)=CC(OC)=C1 ICEYAVKJMMRQIX-UHFFFAOYSA-N 0.000 description 1
150000003751 zinc Chemical class 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- 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
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/281—Sorbents specially adapted for preparative, analytical or investigative chromatography
- B01J20/286—Phases chemically bonded to a substrate, e.g. to silica or to polymers
- 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
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/30—Processes for preparing, regenerating, or reactivating
- B01J20/32—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
- B01J20/3202—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the carrier, support or substrate used for impregnation or coating
- B01J20/3204—Inorganic carriers, supports or substrates
- 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
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/30—Processes for preparing, regenerating, or reactivating
- B01J20/32—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
- B01J20/3214—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the method for obtaining this coating or impregnating
- B01J20/3217—Resulting in a chemical bond between the coating or impregnating layer and the carrier, support or substrate, e.g. a covalent bond
- B01J20/3219—Resulting in a chemical bond between the coating or impregnating layer and the carrier, support or substrate, e.g. a covalent bond involving a particular spacer or linking group, e.g. for attaching an active group
- 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
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/30—Processes for preparing, regenerating, or reactivating
- B01J20/32—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
- B01J20/3231—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the coating or impregnating layer
- B01J20/3242—Layers with a functional group, e.g. an affinity material, a ligand, a reactant or a complexing group
- B01J20/3244—Non-macromolecular compounds
- B01J20/3246—Non-macromolecular compounds having a well defined chemical structure
- B01J20/3257—Non-macromolecular compounds having a well defined chemical structure the functional group or the linking, spacer or anchoring group as a whole comprising at least one of the heteroatoms nitrogen, oxygen or sulfur together with at least one silicon atom, these atoms not being part of the carrier as such
- 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
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- B01J20/30—Processes for preparing, regenerating, or reactivating
- B01J20/32—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
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- B01J20/3242—Layers with a functional group, e.g. an affinity material, a ligand, a reactant or a complexing group
- B01J20/3244—Non-macromolecular compounds
- B01J20/3246—Non-macromolecular compounds having a well defined chemical structure
- B01J20/3257—Non-macromolecular compounds having a well defined chemical structure the functional group or the linking, spacer or anchoring group as a whole comprising at least one of the heteroatoms nitrogen, oxygen or sulfur together with at least one silicon atom, these atoms not being part of the carrier as such
- B01J20/3259—Non-macromolecular compounds having a well defined chemical structure the functional group or the linking, spacer or anchoring group as a whole comprising at least one of the heteroatoms nitrogen, oxygen or sulfur together with at least one silicon atom, these atoms not being part of the carrier as such comprising at least two different types of heteroatoms selected from nitrogen, oxygen or sulfur with at least one silicon atom
- 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
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/30—Processes for preparing, regenerating, or reactivating
- B01J20/32—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
- B01J20/3231—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the coating or impregnating layer
- B01J20/3242—Layers with a functional group, e.g. an affinity material, a ligand, a reactant or a complexing group
- B01J20/3244—Non-macromolecular compounds
- B01J20/3246—Non-macromolecular compounds having a well defined chemical structure
- B01J20/3257—Non-macromolecular compounds having a well defined chemical structure the functional group or the linking, spacer or anchoring group as a whole comprising at least one of the heteroatoms nitrogen, oxygen or sulfur together with at least one silicon atom, these atoms not being part of the carrier as such
- B01J20/3261—Non-macromolecular compounds having a well defined chemical structure the functional group or the linking, spacer or anchoring group as a whole comprising at least one of the heteroatoms nitrogen, oxygen or sulfur together with at least one silicon atom, these atoms not being part of the carrier as such comprising a cyclic structure not containing any of the heteroatoms nitrogen, oxygen or sulfur, e.g. aromatic structures
- 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
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/30—Processes for preparing, regenerating, or reactivating
- B01J20/32—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
- B01J20/3231—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the coating or impregnating layer
- B01J20/3242—Layers with a functional group, e.g. an affinity material, a ligand, a reactant or a complexing group
- B01J20/3244—Non-macromolecular compounds
- B01J20/3246—Non-macromolecular compounds having a well defined chemical structure
- B01J20/3257—Non-macromolecular compounds having a well defined chemical structure the functional group or the linking, spacer or anchoring group as a whole comprising at least one of the heteroatoms nitrogen, oxygen or sulfur together with at least one silicon atom, these atoms not being part of the carrier as such
- B01J20/3263—Non-macromolecular compounds having a well defined chemical structure the functional group or the linking, spacer or anchoring group as a whole comprising at least one of the heteroatoms nitrogen, oxygen or sulfur together with at least one silicon atom, these atoms not being part of the carrier as such comprising a cyclic structure containing at least one of the heteroatoms nitrogen, oxygen or sulfur, e.g. an heterocyclic or heteroaromatic structure
- 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
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/30—Processes for preparing, regenerating, or reactivating
- B01J20/32—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
- B01J20/3231—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the coating or impregnating layer
- B01J20/3242—Layers with a functional group, e.g. an affinity material, a ligand, a reactant or a complexing group
- B01J20/3268—Macromolecular compounds
- B01J20/3272—Polymers obtained by reactions otherwise than involving only carbon to carbon unsaturated bonds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/12—Organo silicon halides
- C07F7/121—Preparation or treatment not provided for in C07F7/14, C07F7/16 or C07F7/20
- C07F7/122—Preparation or treatment not provided for in C07F7/14, C07F7/16 or C07F7/20 by reactions involving the formation of Si-C linkages
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2991—Coated
- Y10T428/2993—Silicic or refractory material containing [e.g., tungsten oxide, glass, cement, etc.]
- Y10T428/2995—Silane, siloxane or silicone coating
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2991—Coated
- Y10T428/2998—Coated including synthetic resin or polymer
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31—Surface property or characteristic of web, sheet or block
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31—Surface property or characteristic of web, sheet or block
- Y10T428/315—Surface modified glass [e.g., tempered, strengthened, etc.]
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
- Y10T428/31609—Particulate metal or metal compound-containing
- Y10T428/31612—As silicone, silane or siloxane

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Analytical Chemistry (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Inorganic Chemistry (AREA)
Graft Or Block Polymers (AREA)
Treatments Of Macromolecular Shaped Articles (AREA)
Silicon Polymers (AREA)

NO863433A 1984-12-28 1986-08-27 Polymerer til behandling av overflater. NO863433L (no)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
FI845161A FI845161A0 (fi)	1984-12-28	1984-12-28	Ytbehandlingsmedel.
PCT/FI1985/000102 WO1986004063A1 (en)	1984-12-28	1985-12-20	Surface treatment agents and polymers

Publications (2)

Publication Number	Publication Date
NO863433D0 NO863433D0 (no)	1986-08-27
NO863433L true NO863433L (no)	1986-10-21

Family

ID=8520118

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO863433A NO863433L (no)	1984-12-28	1986-08-27	Polymerer til behandling av overflater.

Country Status (9)

Country	Link
US (1)	US4756971A (da)
EP (2)	EP0207977A1 (da)
JP (1)	JPS62501557A (da)
AU (1)	AU5315786A (da)
DK (1)	DK407486A (da)
FI (2)	FI845161A0 (da)
HU (1)	HUT42494A (da)
NO (1)	NO863433L (da)
WO (1)	WO1986004063A1 (da)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5013585A (en) *	1989-06-13	1991-05-07	Shin-Etsu Chemical Co., Ltd.	Method for the preparation of surface-modified silica particles
US5457564A (en) *	1990-02-26	1995-10-10	Molecular Displays, Inc.	Complementary surface confined polymer electrochromic materials, systems, and methods of fabrication therefor
US5818636A (en) *	1990-02-26	1998-10-06	Molecular Displays, Inc.	Complementary surface confined polmer electrochromic materials, systems, and methods of fabrication therefor
US5653875A (en) *	1994-02-04	1997-08-05	Supelco, Inc.	Nucleophilic bodies bonded to siloxane and use thereof for separations from sample matrices
US5624881A (en) *	1994-09-27	1997-04-29	Syracuse University	Chemically active ceramic compositions with a pyrogallol moiety
US5668079A (en) *	1994-09-27	1997-09-16	Syracuse University	Chemically active ceramic compositions with an hydroxyquinoline moiety
US5612275A (en) *	1994-09-27	1997-03-18	Syracuse University	Chemically active ceramic compositions with a phospho-acid moiety
US5616533A (en) *	1994-09-27	1997-04-01	Syracuse University	Chemically active ceramic compositions with a thiol and/or amine moiety
US20050214827A1 (en) *	1996-07-08	2005-09-29	Burstein Technologies, Inc.	Assay device and method
US6331275B1 (en)	1996-07-08	2001-12-18	Burstein Technologies, Inc.	Spatially addressable, cleavable reflective signal elements, assay device and method
US6342349B1 (en)	1996-07-08	2002-01-29	Burstein Technologies, Inc.	Optical disk-based assay devices and methods
CA2260361A1 (en)	1996-07-08	1998-01-15	Burstein Laboratories, Inc	Cleavable signal element device and method
BR9808653A (pt) *	1997-02-28	2001-07-31	Burstein Lab Inc	Laboratório em um disco
TW546301B (en)	1997-02-28	2003-08-11	Sumitomo Chemical Co	Silicon-containing compound and organic electroluminescence device using the same
EP1097378A2 (en) *	1998-07-21	2001-05-09	Burstein Laboratories Inc.	Optical disc-based assay devices and methods
WO2002094410A1 (en) *	2001-05-18	2002-11-28	University Of South Florida	Sol-gel dendron separation and extraction capillary column
KR100427258B1 (ko) *	2001-08-11	2004-04-14	광주과학기술원	플로린을 함유한 실록산 단량체와 이의 제조방법
JP4959333B2 (ja) *	2003-05-09	2012-06-20	エーエスエムアメリカインコーポレイテッド	化学的不活性化を通じたリアクタ表面のパシベーション
US7914847B2 (en)	2003-05-09	2011-03-29	Asm America, Inc.	Reactor surface passivation through chemical deactivation
US20050106068A1 (en) *	2003-11-18	2005-05-19	Abdul Malik	Sol-gel dendron separation and extraction capillary column
US20050242038A1 (en) *	2004-04-30	2005-11-03	Wu Chen	Novel stationary phases for use in high-performance liquid chromatography
US7314505B1 (en) *	2005-06-20	2008-01-01	Sandia Corporation	Stationary phase deposition based on onium salts
US8293658B2 (en) *	2010-02-17	2012-10-23	Asm America, Inc.	Reactive site deactivation against vapor deposition
US9223203B2 (en)	2011-07-08	2015-12-29	Asm International N.V.	Microcontact printed films as an activation layer for selective atomic layer deposition
JP5833492B2 (ja) *	2012-04-23	2015-12-16	信越化学工業株式会社	ケイ素化合物、ポリシロキサン化合物、これを含むレジスト下層膜形成用組成物及びパターン形成方法
US9596755B2 (en)	2014-10-15	2017-03-14	Rogers Corporation	Magneto-dielectric substrate, circuit material, and assembly having the same
FI126130B (en) *	2015-03-20	2016-07-15	Inkron Oy	Siloxane monomers with high refractive index, polymerization thereof and their use
FI127462B (en) *	2016-07-14	2018-06-29	Inkron Oy	Siloxane monomers, their polymerization and uses thereof
WO2018222315A1 (en) *	2017-06-01	2018-12-06	Dow Silicones Corporation	Polysiloxane comprising substituents having multiple aryl groups
CN110168670A (zh)	2017-11-07	2019-08-23	罗杰斯公司	具有改善的热导率的介电层
US11198263B2 (en)	2018-03-22	2021-12-14	Rogers Corporation	Melt processable thermoplastic composite comprising a multimodal dielectric filler
KR20220105642A (ko)	2019-11-22	2022-07-27	로저스코포레이션	조사를 통해 가교된 성형된 유전성 컴포넌트 및 이의 제조 방법
WO2023239594A1 (en)	2022-06-08	2023-12-14	Rogers Corporation	Y-type hexaferrite, method of manufacture, and uses thereof

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL72963C (da) *	1948-01-05
US2546330A (en) *	1948-12-11	1951-03-27	Dow Chemical Co	Synthesis of aromatic silane
US2626270A (en) *	1949-02-01	1953-01-20	Dow Corning	t-butylsilanes
DE834002C (de) *	1950-09-19	1952-03-13	Dow Corning	Verfahren zur Oberflaechenbehandlung von Glas u. dgl.
DE1114492B (de) *	1958-11-17	1961-10-05	Union Carbide Corp	Verfahren zur Herstellung von Cyanphenyl-alkoxysilanen
US3312727A (en) *	1965-02-03	1967-04-04	Dow Corning	Organosilicon compounds
US3795313A (en) *	1970-05-22	1974-03-05	Du Pont	Chromatographic packing with chemically bonded organic stationary phases
US3722181A (en) *	1970-05-22	1973-03-27	Du Pont	Chromatographic packing with chemically bonded organic stationary phases
US3853726A (en) *	1970-07-04	1974-12-10	B Vainshiein	Method of producing organochlorosilanes
DE2132569C3 (de) *	1970-07-04	1975-06-12	Boris Iosifowitsch Wainstein	Verfahren zur Herstellung von Organochlorsilanen
US3651117A (en) *	1970-09-08	1972-03-21	Union Carbide Corp	Esterification of halosilanes
US4164509A (en) *	1970-11-24	1979-08-14	Deutsche Gold- Und Silber-Scheideanstalt Vormals Roessler	Process for preparing finely divided hydrophobic oxide particles
US3899328A (en) *	1973-05-07	1975-08-12	Xerox Corp	Active matrix and intrinsic photoconductive polymer of a linear polysiloxane
US4044037A (en) *	1974-12-24	1977-08-23	Union Carbide Corporation	Sulfur containing silane coupling agents
DE2930516A1 (de) *	1979-07-27	1981-02-12	Merck Patent Gmbh	Trennmaterial fuer die chromatographie mit organisch modifizierter oberflaeche, verfahren zur herstellung solcher trennmaterialien und ihre verwendung
US4242227A (en) *	1979-07-31	1980-12-30	The Dow Chemical Company	Chromatographic column packing having a bonded organosiloxane coating
US4276061A (en) *	1979-07-31	1981-06-30	The Dow Chemical Company	Chromatographic column packing having a bonded organosiloxane coating
EP0028665B1 (en) *	1979-11-02	1983-05-18	Chisso Corporation	Process for the production of diaralkyldichlorosilanes and their use in manufacture of polysiloxane
DE3104326A1 (de) *	1981-02-07	1982-08-19	Basf Ag, 6700 Ludwigshafen	"verfahren zur herstellung von aromatischen silanen"
SU1056050A1 (ru) *	1982-07-02	1983-11-23	Предприятие П/Я А-7629	Неподвижна фаза дл газовой хроматографии органических и кремнийорганических соединений
SU1073248A1 (ru) *	1982-10-29	1984-02-15	Московский Ордена Трудового Красного Знамени Институт Тонкой Химической Технологии Им.М.В.Ломоносова	Карбазол- и антраценсодержащие полисилоксаны в качестве основы электрофотографических слоев и способ их получени
SU1078324A1 (ru) *	1982-12-30	1984-03-07	Государственный научно-исследовательский институт химии и технологии элементоорганических соединений	Способ разделени органических и кремнийорганических соединений
US4539061A (en) *	1983-09-07	1985-09-03	Yeda Research And Development Co., Ltd.	Process for the production of built-up films by the stepwise adsorption of individual monolayers

1984
- 1984-12-28 FI FI845161A patent/FI845161A0/fi not_active Application Discontinuation
1985
- 1985-12-20 EP EP86900671A patent/EP0207977A1/en not_active Ceased
- 1985-12-20 US US06/907,687 patent/US4756971A/en not_active Expired - Fee Related
- 1985-12-20 JP JP86500609A patent/JPS62501557A/ja active Pending
- 1985-12-20 AU AU53157/86A patent/AU5315786A/en not_active Abandoned
- 1985-12-20 HU HU86761A patent/HUT42494A/hu unknown
- 1985-12-20 EP EP88115789A patent/EP0310904A1/en not_active Withdrawn
- 1985-12-20 WO PCT/FI1985/000102 patent/WO1986004063A1/en not_active Ceased
1986
- 1986-08-22 FI FI863399A patent/FI863399A7/fi not_active Application Discontinuation
- 1986-08-27 NO NO863433A patent/NO863433L/no unknown
- 1986-08-27 DK DK407486A patent/DK407486A/da not_active Application Discontinuation

Also Published As

Publication number	Publication date
HUT42494A (en)	1987-07-28
US4756971A (en)	1988-07-12
EP0310904A1 (en)	1989-04-12
WO1986004063A1 (en)	1986-07-17
NO863433D0 (no)	1986-08-27
JPS62501557A (ja)	1987-06-25
EP0207977A1 (en)	1987-01-14
FI863399A0 (fi)	1986-08-22
DK407486A (da)	1986-10-27
AU5315786A (en)	1986-07-29
FI863399A7 (fi)	1986-08-22
FI845161A0 (fi)	1984-12-28
DK407486D0 (da)	1986-08-27

Publication	Publication Date	Title
NO863433L (no)	1986-10-21	Polymerer til behandling av overflater.
Mallegol et al.	2005	Practical and efficient synthesis of tris (4-formylphenyl) amine, a key building block in materials chemistry
Kussmaul et al.	2011	Enhancement of dielectric permittivity and electromechanical response in silicone elastomers: molecular grafting of organic dipoles to the macromolecular network
US7635741B2 (en)	2009-12-22	Multifunctional monomers and their use in making cross-linked polymers and porous films
JPH0459317B2 (da)	1992-09-21
JP4447923B2 (ja)	2010-04-07	多官能性モノマー並びにそれらの架橋ポリマー及び多孔質フィルムの製造における使用
Richter et al.	1983	Nonextractable cyanopropyl polysiloxane stationary phases for capillary chromatography
Markides et al.	1984	Cyanosilicones as stationary phases in gas chromatography: III. Synthesis, characterization and evaluation
US5286890A (en)	1994-02-15	Aromatic amine terminated silicone monomers, oligomers, and polymers therefrom
Ohshita et al.	2004	Synthesis of poly {[bis (diethynylphenyl) silylene] phenylene} s with highly heat-resistant properties and an application to conducting materials
JP4889097B2 (ja)	2012-02-29	ポリシクロオレフィン官能性ポリシロキサン
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DE69315916T2 (de)	1998-08-27	(Alpha, Omega)Phenylethinylsiloxanmonomere und daraus hergestellte Oligomere und Polymere
SU1073248A1 (ru)	1984-02-15	Карбазол- и антраценсодержащие полисилоксаны в качестве основы электрофотографических слоев и способ их получени
Hu et al.	2004	Synthesis and properties of novel conjugated poly (silylacetylene silazane) s
US5116973A (en)	1992-05-26	Caprolactam silane compound and a method of manufacturing the same
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DE4027253A1 (de)	1992-03-05	Neue arylmethylole, deren herstellung und verwendung
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