JPH1045732A5 - - Google Patents

Info

Publication number
JPH1045732A5
JPH1045732A5 JP1996219073A JP21907396A JPH1045732A5 JP H1045732 A5 JPH1045732 A5 JP H1045732A5 JP 1996219073 A JP1996219073 A JP 1996219073A JP 21907396 A JP21907396 A JP 21907396A JP H1045732 A5 JPH1045732 A5 JP H1045732A5
Authority
JP
Japan
Prior art keywords
following formula
formula
group
isomers
represent
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.)
Granted
Application number
JP1996219073A
Other languages
Japanese (ja)
Other versions
JP4006654B2 (en
JPH1045732A (en
Filing date
Publication date
Application filed filed Critical
Priority to JP21907396A priority Critical patent/JP4006654B2/en
Priority claimed from JP21907396A external-priority patent/JP4006654B2/en
Publication of JPH1045732A publication Critical patent/JPH1045732A/en
Publication of JPH1045732A5 publication Critical patent/JPH1045732A5/ja
Application granted granted Critical
Publication of JP4006654B2 publication Critical patent/JP4006654B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Description

【００２６】
得られた１，２−ビス（５−メチル−２−フェニルチアゾール）ヘキサフルオロシクロペンテンの融点は、１４８〜１５０℃であり、また、その核磁気共鳴スペクトルによる分析値（ＣＤＣｌ３ 、δ値、ｐｐｍ）は、２００ＭＨｚにおいて、次のとおりである。１．６０〜２．１５（ｓ，６Ｈ）、７．４５〜７．９９（ｍ，１０Ｈ）。また、その元素分析値（％）を表２に示す。
【表２】
[0026]
The melting point of the obtained 1,2-bis(5-methyl-2-phenylthiazole)hexafluorocyclopentene was 148-150°C, and its nuclear magnetic resonance spectroscopy ( CDCl3 , δ value, ppm) at 200 MHz was as follows: 1.60-2.15 (s, 6H), 7.45-7.99 (m, 10H). The elemental analysis values (%) are shown in Table 2 .
[Table 2]

Claims (1)

下記式（１）
（式中、Ｒ１ 、Ｒ２ は、それぞれアルキル基、アルコキシ基またはアリール基を示す。）
で表されるジアリールエテン誘導体及びそれらの異性体。The following formula (1)
(In the formula, R 1 and R 2 each represent an alkyl group, an alkoxy group, or an aryl group. )
Diarylethene derivatives represented by the following formula (I) and their isomers.
JP21907396A 1996-08-02 1996-08-02 Diarylethene derivative and photochromic material using the same Expired - Fee Related JP4006654B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21907396A JP4006654B2 (en) 1996-08-02 1996-08-02 Diarylethene derivative and photochromic material using the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21907396A JP4006654B2 (en) 1996-08-02 1996-08-02 Diarylethene derivative and photochromic material using the same

Publications (3)

Publication Number Publication Date
JPH1045732A JPH1045732A (en) 1998-02-17
JPH1045732A5 true JPH1045732A5 (en) 2004-07-22
JP4006654B2 JP4006654B2 (en) 2007-11-14

Family

ID=16729845

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21907396A Expired - Fee Related JP4006654B2 (en) 1996-08-02 1996-08-02 Diarylethene derivative and photochromic material using the same

Country Status (1)

Country Link
JP (1) JP4006654B2 (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100557552B1 (en) * 2001-06-29 2006-03-03 주식회사 하이닉스반도체 Photoresist monomers, polymers thereof and photoresist compositions containing them
US7755826B2 (en) 2003-07-07 2010-07-13 The University Of Hong Kong Photochromic diarylethene-containing coordination compounds and the production thereof
EP1648864B1 (en) 2003-07-07 2015-08-19 The University of Hong Kong Photochromic diarylethene-containing coordination compounds and the production thereof
JP4929513B2 (en) 2006-12-15 2012-05-09 国立大学法人九州大学 Light-driven actuator element
CN121449595A (en) * 2019-09-16 2026-02-03 香港大学 Light-responsive coordination compound with light-controlled electron transport and conductive properties, organic electronic device with light conversion performance, and manufacture of organic resistive memory device
CN116425791A (en) 2021-11-30 2023-07-14 香港大学 Photochromic germanol fused diarylethenes and their preparation
CN114656646B (en) * 2022-04-19 2023-02-17 江西科技师范大学 Synthetic method of diarylene COFs material and application of diarylene COFs material in light-operated adsorption
CN117551258B (en) * 2024-01-10 2024-03-15 西南石油大学 A kind of biologically derived light-responsive epoxy resin and preparation method thereof

Similar Documents

Publication Publication Date Title
CA2204200A1 (en) Phenyl alkyl ketone substituted by cyclic amine and a process for the preparation thereof
EP1178072A3 (en) Aromatic liquid-crystalline polyester solution composition
EP1335000A3 (en) Phthalocyanine compounds
EP1826196A3 (en) Vinyl ether compounds
RU93046499A (en) METHOD FOR INCREASING THE RELATIVE DENSITY OF POLYAMIDS
JPH1045732A5 (en)
JP2009511649A5 (en)
JP2004075986A5 (en)
EP1411927A4 (en) PROCESS FOR PREPARING SELECTIVE SUBSTITUTE CORROLES AND SUBSTITUTED NEW CORROLES
RU94019411A (en) KHINUK LIDINA ETHERS, INTERMEDIATE COMPOUNDS FOR THEIR SYNTHESIS, PHARMACEUTICAL COMPOSITION AND METHOD OF TREATMENT
JP2004509756A5 (en)
EP1262508A3 (en) Novel polyhydroxyalkanoate that comprises unit having substituted or unsubstituted (phenylmethyl) sulfanyl structure in side chain thereof and process for producing the same
JPH1112272A5 (en)
JPH0912569A5 (en)
EP2269694A3 (en) Antituberculous composition comprising oxazole compounds
RU95115049A (en) CAMPTOTECINE DERIVATIVES, THEIR PRODUCTION AND ANTI-TUMOR COMPOSITION
KR950032226A (en) Silacyclohexanone Compound and Manufacturing Method of Silacyclohexane Type Liquid Crystal Compound Using the Same
EP0024017A3 (en) N-pyrimidinylmethyl-haloacetanilides, process for their preparation and their use as herbicides; intermediates and their preparation
RU92004582A (en) ETHANOL ADDUDES, METHOD OF THEIR PRODUCTION AND USE AS A MEANS OF INHALATION IN DISEASES
JPH1060307A5 (en)
IE821475L (en) Benzoyl-phenyl-piperidine derivatives
EP0223184A3 (en) Cephalosporins, process for their preparation and their use as medicaments
JP2002294094A5 (en)
JPH11228520A5 (en)
JP2000226349A5 (en)