JP6208137B2 - ジアリールエテン化合物およびそれらの使用 - Google Patents

ジアリールエテン化合物およびそれらの使用 Download PDF

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JP6208137B2
JP6208137B2 JP2014532194A JP2014532194A JP6208137B2 JP 6208137 B2 JP6208137 B2 JP 6208137B2 JP 2014532194 A JP2014532194 A JP 2014532194A JP 2014532194 A JP2014532194 A JP 2014532194A JP 6208137 B2 JP6208137 B2 JP 6208137B2
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mmol
synthesis
group
butyl
och
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JP2015501292A (ja
JP2015501292A5 (enExample
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ブランダ,ニール・ロビン
フィンデン,ジェレミー・グラハム
ゴーチエ,シモン・ジェイムズ
ハイエク,アリ
ホープ−ロス,カイル・アンドリュー
シニア,ジェイムズ・ダニエル
スパンツレスク,アンドリーア
スビリドブ,セルゲイ
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Switch Materials Inc
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Switch Materials Inc
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/22Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/78Benzo [b] furans; Hydrogenated benzo [b] furans
    • C07D307/79Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
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    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
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    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
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    • C07D333/06Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
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    • C07D333/26Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
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    • C07D495/14Ortho-condensed systems
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    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
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    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/12Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
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    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/0803Compounds with Si-C or Si-Si linkages
    • C07F7/081Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
    • C07F7/0812Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
    • C07F7/0814Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring said ring is substituted at a C ring atom by Si
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    • C09K9/00Tenebrescent materials, i.e. materials for which the range of wavelengths for energy absorption is changed as a result of excitation by some form of energy
    • C09K9/02Organic tenebrescent materials
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B1/00Optical elements characterised by the material of which they are made; Optical coatings for optical elements
    • G02B1/04Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00Optical elements other than lenses
    • G02B5/20Filters
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00Optical elements other than lenses
    • G02B5/20Filters
    • G02B5/22Absorbing filters
    • G02B5/223Absorbing filters containing organic substances, e.g. dyes, inks or pigments
    • GPHYSICS
    • G02OPTICS
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    • G02B5/00Optical elements other than lenses
    • G02B5/20Filters
    • G02B5/22Absorbing filters
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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Polymers & Plastics (AREA)
  • Health & Medical Sciences (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
  • Furan Compounds (AREA)
  • Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
  • Optical Filters (AREA)
  • Electrochromic Elements, Electrophoresis, Or Variable Reflection Or Absorption Elements (AREA)
JP2014532194A 2011-09-30 2012-09-28 ジアリールエテン化合物およびそれらの使用 Expired - Fee Related JP6208137B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201161541841P 2011-09-30 2011-09-30
US61/541,841 2011-09-30
US201261675460P 2012-07-25 2012-07-25
US61/675,460 2012-07-25
PCT/CA2012/000910 WO2013044371A1 (en) 2011-09-30 2012-09-28 Photochromic and electrochromic diarylcyclopentene derivatives as optical filters

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2017171192A Division JP6480997B2 (ja) 2011-09-30 2017-09-06 ジアリールエテン化合物およびそれらの使用

Publications (3)

Publication Number Publication Date
JP2015501292A JP2015501292A (ja) 2015-01-15
JP2015501292A5 JP2015501292A5 (enExample) 2015-11-19
JP6208137B2 true JP6208137B2 (ja) 2017-10-04

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Application Number Title Priority Date Filing Date
JP2014532194A Expired - Fee Related JP6208137B2 (ja) 2011-09-30 2012-09-28 ジアリールエテン化合物およびそれらの使用
JP2017171192A Expired - Fee Related JP6480997B2 (ja) 2011-09-30 2017-09-06 ジアリールエテン化合物およびそれらの使用
JP2019021745A Pending JP2019123713A (ja) 2011-09-30 2019-02-08 ジアリールエテン化合物およびそれらの使用
JP2020185146A Pending JP2021042212A (ja) 2011-09-30 2020-11-05 ジアリールエテン化合物およびそれらの使用
JP2022077367A Pending JP2022110051A (ja) 2011-09-30 2022-05-10 ジアリールエテン化合物およびそれらの使用

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JP2017171192A Expired - Fee Related JP6480997B2 (ja) 2011-09-30 2017-09-06 ジアリールエテン化合物およびそれらの使用
JP2019021745A Pending JP2019123713A (ja) 2011-09-30 2019-02-08 ジアリールエテン化合物およびそれらの使用
JP2020185146A Pending JP2021042212A (ja) 2011-09-30 2020-11-05 ジアリールエテン化合物およびそれらの使用
JP2022077367A Pending JP2022110051A (ja) 2011-09-30 2022-05-10 ジアリールエテン化合物およびそれらの使用

Country Status (7)

Country Link
US (4) US9227986B2 (enExample)
EP (2) EP3385354A1 (enExample)
JP (5) JP6208137B2 (enExample)
KR (2) KR102038447B1 (enExample)
CN (2) CN103890133A (enExample)
CA (1) CA2832149C (enExample)
WO (1) WO2013044371A1 (enExample)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20130271811A1 (en) 2010-12-15 2013-10-17 Switch Materials, Inc. Variable transmittance optical filter with substantially co-planar electrode system
US9176357B2 (en) 2010-12-15 2015-11-03 Switch Materials, Inc. Variable transmittance optical devices
CA2832149C (en) 2011-09-30 2017-12-12 Switch Materials Inc. Photochromic and electrochromic diarylcyclopentene derivatives
US9910301B2 (en) 2012-02-23 2018-03-06 Switch Materials, Inc. Switchable optical filter apparatus with light
WO2013152425A1 (en) 2012-04-09 2013-10-17 Switch Materials , Inc. Switching materials, and compositions and methods for making same
US9588358B2 (en) 2012-05-29 2017-03-07 Switch Materials, Inc. Optical filter comprising a variable transmittance layer
US9810963B2 (en) 2013-03-07 2017-11-07 Switch Materials, Inc. Seal and seal system for a layered device
US10254617B2 (en) 2013-12-19 2019-04-09 Switch Materials Inc. Switchable objects and methods of manufacture
WO2015135867A1 (de) * 2014-03-12 2015-09-17 Ludwig-Maximilians-Universität München Terminal substituierte oligothiophene und ihre verwendung in optischen signalübertragungssystemen und/oder als farbpigmente
US9708528B2 (en) 2014-06-13 2017-07-18 The University Of Hong Kong Robust photochromic compounds with silicon- or phosphorus-containing heterocyclic ring and the production thereof
EP3221420B1 (en) * 2014-11-17 2021-02-17 Switch Materials, Inc. Photochromic-electrochromic compositions
US20180231887A1 (en) * 2015-08-24 2018-08-16 Toyo Gosei Co., Ltd. Method for manufacturing device, and composition
CN107011317B (zh) * 2016-05-24 2020-03-20 北京大学 光致异构化合物及包含其的器件
EP3284764A1 (en) 2016-08-18 2018-02-21 Basf Se Composition especially for printing or coating comprising polyurethane polymers
EP3284799A1 (en) 2016-08-18 2018-02-21 Basf Se Composition especially for printing or coating comprising (meth)acrylate polymers
WO2018033620A1 (en) 2016-08-18 2018-02-22 Basf Se Composition especially for printing or coating comprising polyurethane polymers
EP3284800A1 (en) 2016-08-18 2018-02-21 Basf Se Composition for preparing an electrochromic layer
WO2018033621A1 (en) 2016-08-18 2018-02-22 Basf Se Composition for preparing an electrochromic layer
CN106371258B (zh) * 2016-10-21 2019-08-06 北京华逸高科科技有限公司 电致变色薄膜的制备方法及电致变色器件
CN107118757A (zh) * 2017-04-24 2017-09-01 上海电力学院 一种基于呋喃的二芳基乙烯有机光致变色材料及其制备方法和应用
CN108359439B (zh) * 2018-02-06 2019-07-26 厦门大学 光致变色化合物及其制备方法和光致变色制品
DE102018004790A1 (de) * 2018-06-14 2019-12-19 Rodenstock Gmbh Photochrome annellierte Naphthopyran-Systeme mit speziellen Substituenten zur Realisierung sehr schneller Aufhellgeschwindigkeiten
KR101989876B1 (ko) * 2019-04-02 2019-06-17 주식회사 제이텍 표면 보호 테이프용 점착제 조성물 및 이의 제조방법
EP3947596A4 (en) * 2019-04-03 2022-09-21 Solutia Canada Inc. Photochromic and electrochromic diarylethene compounds with improved photostability and solubility
US20230341276A1 (en) * 2020-02-07 2023-10-26 Chromatic Technologies, Inc. Roofing Membrane Bond Indicator
CN111430564B (zh) 2020-03-19 2022-06-03 武汉天马微电子有限公司 一种显示面板以及显示装置
KR102693003B1 (ko) * 2020-04-29 2024-08-09 삼성디스플레이 주식회사 표시 패널
DE102021110210A1 (de) 2021-04-22 2022-10-27 Delo Industrie Klebstoffe Gmbh & Co. Kgaa Verfahren zum Herstellen eines optischen Moduls und optisches Modul
JP7770645B2 (ja) * 2021-08-30 2025-11-17 日産自動車株式会社 フォトクロミック化合物
CN116397242B (zh) * 2023-03-31 2025-06-20 平湖市浙江工业大学新材料研究院 一种基于萘二并噻二唑受体结构的薄膜材料的制备方法及其应用
CN119060013A (zh) * 2024-08-26 2024-12-03 华中科技大学 一种烷氧基三苯胺修饰的二噻吩基乙烯衍生物及其及应用

Family Cites Families (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3635544A (en) 1963-12-23 1972-01-18 American Cyanamid Co Photochromic polymer matrix
JPS6422872A (en) 1987-07-16 1989-01-25 Yamaha Corp Photochromic compound
GB8916860D0 (en) 1989-07-24 1989-09-06 Traqson Ltd Novel photoactive compounds
EP0773948A4 (en) 1992-04-03 1998-09-02 California Inst Of Techn HIGHLY ACTIVE RUTHENIUM OR OSMIUM METAL CARBEN COMPLEXES FOR OLEFIN METHETHESE REACTIONS AND THEIR SYNTHESIS
US5312940A (en) 1992-04-03 1994-05-17 California Institute Of Technology Ruthenium and osmium metal carbene complexes for olefin metathesis polymerization
JPH06240242A (ja) 1993-02-15 1994-08-30 Nippon Telegr & Teleph Corp <Ntt> 重合体フォトクロミック組成物
JP3264573B2 (ja) 1994-01-14 2002-03-11 株式会社三協精機製作所 小型モータ
JP3395854B2 (ja) 1994-02-02 2003-04-14 日立化成工業株式会社 酸化銅の化学還元液およびこれを用いた多層プリント配線板の製造方法
JPH07311979A (ja) 1994-03-24 1995-11-28 Sanyo Electric Co Ltd 光記録媒体及びその再生方法
JP3132630B2 (ja) 1994-08-25 2001-02-05 科学技術振興事業団 チオフェン誘導体の重合体とその製造法
JP3491704B2 (ja) 1994-10-21 2004-01-26 入江  正浩 ジチエニルエテン系化合物及び該化合物からなるフォトクロミック材料
JPH10152679A (ja) 1996-11-22 1998-06-09 Mita Ind Co Ltd 光メモリ素子と、それを用いた電子写真感光体、エレクトロルミネッセンス素子、液晶表示素子、および空間光変調素子
FR2772266B1 (fr) 1997-12-12 2000-02-04 Oreal Utilisation d'agent de coloration photochrome dans une composition cosmetique, et composition cosmetique le comprenant
EP0933375A1 (en) 1997-12-17 1999-08-04 Amersham Life Science Ltd Photochromic compounds
JP3538019B2 (ja) * 1998-03-11 2004-06-14 独立行政法人 科学技術振興機構 フォトクロミック結晶材料
JPH11256147A (ja) 1998-03-13 1999-09-21 Dainippon Printing Co Ltd コレステリック液晶性フォトクロミック高分子材料及びそれを用いた光機能性媒体
US6479604B1 (en) 1998-08-17 2002-11-12 Korea Research Institute Of Chemical Technology Diarylethene compound, photochromic diarylethene type copolymer and method for the production of the same
US6884553B2 (en) 1999-03-11 2005-04-26 Mitsubishi Chemical Corporation Near-field optical recording medium and near-field optical recording method
DE10042603B4 (de) 1999-08-31 2010-04-29 Kyocera Corp. Photochrome Verbindung und ihre Verwendung in optischen Funktionsvorrichtungen
US7041763B2 (en) 2000-07-14 2006-05-09 Simon Fraser University Photochromic polymers and methods of synthesizing same
FR2813697A1 (fr) 2000-09-04 2002-03-08 Dixet Support securise de donnees a lecture optique
CN1152110C (zh) 2000-12-13 2004-06-02 中国科学院感光化学研究所 杂环取代俘精酸酐类光致变色材料及其合成方法
JP4025920B2 (ja) 2001-03-05 2007-12-26 入江  正浩 フォトクロミック材料
KR100424862B1 (ko) 2001-03-06 2004-03-31 한국화학연구원 이속사졸기로 치환된 신규한 광변색성 디아릴에텐계 화합물
JP3870703B2 (ja) 2001-03-14 2007-01-24 ダイソー株式会社 新規ホトクロミック化合物、およびその製造法と用途
WO2002102923A1 (fr) 2001-06-15 2002-12-27 Mitsubishi Chem Corp Materiau photochrome et chromodosimetre utilisant ledit materiau
KR100501829B1 (ko) 2001-07-30 2005-07-20 한국화학연구원 디아릴에텐 유도체와 이를 이용한 광변색 박막
KR100482654B1 (ko) 2001-09-18 2005-04-13 한국화학연구원 광변색 나노 캡슐 및 그의 제조방법
KR20030025622A (ko) 2001-09-21 2003-03-29 한국화학연구원 비닐기 함유 디아릴에텐 단량체 및 이를 이용하여 제조한광활성 고분자
CN1206308C (zh) * 2002-02-06 2005-06-15 清华大学 二芳基乙烯类光致变色化合物及其制备方法和用途
KR20030085251A (ko) 2002-04-29 2003-11-05 한국화학연구원 광변색 형광 중합체와 그 제조방법
AU2003257320A1 (en) * 2002-08-09 2004-02-25 Simon Fraser University Photochromic and electrochromic compounds and methods of synthesizing and using same
JP2004277416A (ja) 2003-02-27 2004-10-07 Masahiro Irie ジアリールエテン系化合物、フォトクロミック材料および光機能素子
JP2005326503A (ja) 2004-05-12 2005-11-24 Tokai Rubber Ind Ltd 調光材用着色部材
FR2882282B1 (fr) 2005-02-21 2008-10-17 Snecma Moteurs Sa Procede pour le corroyage d'un lopin metallique, chemise pour la mise en oeuvre du procede et ensemble d'une chemise et d'un couvercle pour la mise en oeuvre du procede
EP1888553A4 (en) 2005-05-25 2010-03-10 Switch Materials Inc ELECTROCHROMIC AND PHOTOCHROMIC COMPOUNDS AND SYNTHESIS AND USE THEREOF
US20070115762A1 (en) 2005-11-21 2007-05-24 Wisnudel Marc B Optical article having anti-theft feature and a system and method for inhibiting theft of same
JP5216954B2 (ja) * 2006-03-10 2013-06-19 国立大学法人京都大学 ジアリールエテン化合物の製造方法
JP2008162895A (ja) * 2006-12-26 2008-07-17 Masahiro Irie ジアリールエテン系化合物
KR100938491B1 (ko) 2007-10-24 2010-01-25 한국생명공학연구원 생체분자 표지용 수용성 광변색 화합물 및 이를 이용한생체분자의 검출방법
EP2440967B1 (en) * 2009-06-11 2018-03-21 Switch Materials, Inc. Variable transmittance optical filter and uses thereof
CN101851232B (zh) 2010-05-31 2012-01-25 江西科技师范学院 光致变色异噁唑噻吩混联型全氟环戊烯化合物及合成方法和应用
WO2012000020A1 (en) * 2010-06-28 2012-01-05 Wood, Stephen Raymond Temporary fence base
CN102079742B (zh) * 2010-11-01 2012-11-14 江西科技师范学院 光致变色萘环-噻吩混联型全氟环戊烯化合物及合成方法和应用
US9176357B2 (en) * 2010-12-15 2015-11-03 Switch Materials, Inc. Variable transmittance optical devices
US20130271811A1 (en) * 2010-12-15 2013-10-17 Switch Materials, Inc. Variable transmittance optical filter with substantially co-planar electrode system
WO2012128293A1 (ja) 2011-03-24 2012-09-27 リンテック株式会社 粘着剤組成物、及び粘着シート
CA2832149C (en) 2011-09-30 2017-12-12 Switch Materials Inc. Photochromic and electrochromic diarylcyclopentene derivatives
WO2013152425A1 (en) * 2012-04-09 2013-10-17 Switch Materials , Inc. Switching materials, and compositions and methods for making same

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US10072023B2 (en) 2018-09-11
US20180339995A1 (en) 2018-11-29
WO2013044371A1 (en) 2013-04-04
EP3385354A1 (en) 2018-10-10
US9227986B2 (en) 2016-01-05
JP2022110051A (ja) 2022-07-28
CN103890133A (zh) 2014-06-25
JP2018048316A (ja) 2018-03-29
CA2832149A1 (en) 2013-04-04
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JP2019123713A (ja) 2019-07-25
JP2021042212A (ja) 2021-03-18
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US11124524B2 (en) 2021-09-21
CN108690045B (zh) 2022-08-30
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US20190256526A1 (en) 2019-08-22
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