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    • 2. 发明申请
    • PHOTOCHROMIC AND ELETROCHROMIC COMPOUNDS AND METHODS OF SYNTHESIZING AND USING SAME
    • 光致变色和非光致变色化合物及其合成和使用方法
    • US20110003966A1
    • 2011-01-06
    • US12828756
    • 2010-07-01
    • Neil R. BrandaAndrea PetersAnthony J. Wigglesworth
    • Neil R. BrandaAndrea PetersAnthony J. Wigglesworth
    • C08G75/00C07D495/04C07D409/08
    • C07D495/04C08G61/02C08G61/126C09K9/02C09K2211/1458G03H2001/0264G03H2260/52Y10T428/1041
    • This invention relates to novel photochromic and electrochromic monomers and polymers based on 1,2-dithienylcyclopentene derivatives and method of using and synthesizing same. The compounds are reversibly interconvertible between different isomeric forms under suitable photochromic or electrochromic conditions. The electrochromic conversion may be catalytic. The application also relates to ultra-high density homopolymers prepared using ring-opening methathesis polymerization (ROMP) where the central ring of the 1,2-bis(3-thienyl)-cyclopentene is incorporated directly into the polymer backbone. The monomer units may be readily functionalized to enable the synthesis of polymers with diverse structural and electronic properties. The compounds have many potential applications including high-density optical information storage systems, photoregulated molecular switches, reversible holographic systems, ophthalmic lenses, actinometry and molecular sensors, photochromic inks, paints and fibers and optoelectronic systems such as optical waveguides, Bragg reflectors and dielectric mirrors.
    • 本发明涉及基于1,2-二噻吩环戊烯衍生物的新型光致变色和电致变色单体和聚合物及其使用和合成方法。 在合适的光致变色或电致变色条件下,化合物在不同的异构体形式之间是可逆的相互转化的。 电致变色可能是催化的。 本申请还涉及使用开环错译聚合(ROMP)制备的超高密度均聚物,其中1,2-双(3-噻吩基) - 环戊烯的中心环直接并入聚合物主链。 单体单元可以容易地官能化以使得能够合成具有不同结构和电子性质的聚合物。 这些化合物具有许多潜在的应用,包括高密度光学信息存储系统,光调节分子开关,可逆全息系统,眼用透镜,光化学测量和分子传感器,光致变色油墨,油漆和纤维以及光电子系统,例如光波导,布拉格反射器和电介质反射镜 。
    • 3. 发明申请
    • PHOTOCHROMIC AND ELECTROCHROMIC COMPOUNDS AND SYNTHESIS AND USE THEREOF
    • 光致变色和电化学化合物及其合成及其用途
    • US20100190868A1
    • 2010-07-29
    • US11915530
    • 2006-05-25
    • Neil R. BrandaBettina WuestenbergVincent LemieuxMichael AdamsSimon Gauthier
    • Neil R. BrandaBettina WuestenbergVincent LemieuxMichael AdamsSimon Gauthier
    • A61K47/22C07D333/22C07D409/06C07C47/00C07C49/00G01N33/00
    • C07D333/18C07D333/22C07D333/24C07D333/28C07D333/78C07D409/08C07D409/14C09K9/02C09K2211/1007C09K2211/1092Y10T436/14Y10T436/142222
    • Novel photochromic and electrochromic hexadiene compounds are described. The compounds are reversibly convertible between ring-open and ring-closed isomeric forms as indicated in structures I(o) and I(c) below. (See formula in original abstract of application) The conversion between the different isomeric forms may be induced by light or electricity. In one embodiment the compounds may include a charge transfer moiety including electron donor and acceptor groups. The electron donor and acceptor are linearly conjugated in the ring-open form to enable electron transfer but are electrically insulated in the ring-closed form. Methods for synthesizing the compounds from photochemically and/or electrically inert precursors are also described. For example, the photoresponsive compounds may be synthesized by reacting diene precursors with dienophiles in a condensation reaction. The compounds may be utilized in reactivity-gated photochromic or electrochromic applications. In one embodiment of the invention, compounds of the invention may be used in a method to selectively release a releasable agent, such as a small molecule. According to this method, a photochemically inert precursor compound is reacted with the releasable agent to form a carrier compound comprising a switching moiety, the switching moiety being reversibly convertible between a thermally unstable form and a thermally stable form. The switching moiety may be selectively converted between the first and second forms to cause controlled release of the releasable agent from the carrier compound.
    • 描述了新的光致变色和电致变色己二烯化合物。 如下文结构I(o)和I(c)所示,化合物在开环和闭环异构体形式之间是可逆转化的。 (参见原始应用摘要中的公式)不同异构形式之间的转换可能是由光或电引起的。 在一个实施方案中,化合物可以包括电子转移部分,包括电子给体和受体基团。 电子给体和受体以开环形式线性共轭以使电子转移,但以闭环形式电绝缘。 还描述了从光化学和/或电惰性前体合成化合物的方法。 例如,光响应化合物可以通过二烯前体与缩合反应中的亲二烯体反应来合成。 化合物可用于反应性门控的光致变色或电致变色应用中。 在本发明的一个实施方案中,本发明的化合物可用于选择性释放可释放剂如小分子的方法。 根据该方法,将光化学惰性的前体化合物与可释放剂反应形成包含切换部分的载体化合物,该切换部分在热不稳定形式和热稳定形式之间可逆地转化。 切换部分可以在第一和第二形式之间选择性地转化以引起可释放试剂从载体化合物的受控释放。
    • 6. 发明授权
    • Photochromic and electrochromic compounds and methods of synthesizing and using same
    • 光致变色和电致变色化合物及其合成和使用方法
    • US07777055B2
    • 2010-08-17
    • US10523965
    • 2003-08-11
    • Neil R. BrandaAndrea PetersAnthony J. Wigglesworth
    • Neil R. BrandaAndrea PetersAnthony J. Wigglesworth
    • C07D333/50C07D409/14
    • C07D495/04C08G61/02C08G61/126C09K9/02C09K2211/1458G03H2001/0264G03H2260/52Y10T428/1041
    • This invention relates to novel photochromic and electrochromic monomers and polymers based on 1,2-dithienylcyclopentene derivatives and method of using and synthesizing same. The compounds are reversibly interconvertible between different isomeric forms under suitable photochromic or electrochromic conditions. The electrochromic conversion may be catalytic. The application also relates to ultra-high density homopolymers prepared using ring-opening methathesis polymerization (ROMP) where the central ring of the 1,2-bis(3-thienyl)-cyclopentene is incorporated directly into the polymer backbone. The monomer units may be readily functionalized to enable the synthesis of polymers with diverse structural and electronic properties. The compounds have many potential applications including high-density optical information storage systems, photoregulated molecular switches, reversible holographic systems, ophthalmic lenses, actinometry and molecular sensors, photochromic inks, paints and fibers and optoelectronic systems such as optical waveguides, Bragg reflectors and dielectric mirrors.
    • 本发明涉及基于1,2-二噻吩环戊烯衍生物的新型光致变色和电致变色单体和聚合物及其使用和合成方法。 在合适的光致变色或电致变色条件下,化合物在不同的异构体形式之间是可逆的相互转化的。 电致变色可能是催化的。 本申请还涉及使用开环错译聚合(ROMP)制备的超高密度均聚物,其中1,2-双(3-噻吩基) - 环戊烯的中心环直接并入聚合物主链。 单体单元可以容易地官能化以使得能够合成具有不同结构和电子性质的聚合物。 这些化合物具有许多潜在的应用,包括高密度光学信息存储系统,光调节分子开关,可逆全息系统,眼用透镜,光化学测量和分子传感器,光致变色油墨,油漆和纤维以及光电子系统,例如光波导,布拉格反射器和电介质反射镜 。
    • 7. 发明授权
    • Photochromic and electrochromic compounds and methods of synthesizing and using same
    • 光致变色和电致变色化合物及其合成和使用方法
    • US08450503B2
    • 2013-05-28
    • US12828756
    • 2010-07-01
    • Neil R. BrandaAndrea PetersAnthony J. Wigglesworth
    • Neil R. BrandaAndrea PetersAnthony J. Wigglesworth
    • C07D333/50C07D409/02
    • C07D495/04C08G61/02C08G61/126C09K9/02C09K2211/1458G03H2001/0264G03H2260/52Y10T428/1041
    • This invention relates to novel photochromic and electrochromic monomers and polymers based on 1,2-dithienylcyclopentene derivatives and method of using and synthesizing same. The compounds are reversibly interconvertible between different isomeric forms under suitable photochromic or electrochromic conditions. The electrochromic conversion may be catalytic. The application also relates to ultra-high density homopolymers prepared using ring-opening methathesis polymerization (ROMP) where the central ring of the 1,2-bis(3-thienyl)-cyclopentene is incorporated directly into the polymer backbone. The monomer units may be readily functionalized to enable the synthesis of polymers with diverse structural and electronic properties. The compounds have many potential applications including high-density optical information storage systems, photoregulated molecular switches, reversible holographic systems, ophthalmic lenses, actinometry and molecular sensors, photochromic inks, paints and fibers and optoelectronic systems such as optical waveguides, Bragg reflectors and dielectric mirrors.
    • 本发明涉及基于1,2-二噻吩环戊烯衍生物的新型光致变色和电致变色单体和聚合物及其使用和合成方法。 在合适的光致变色或电致变色条件下,化合物在不同的异构体形式之间是可逆的相互转化的。 电致变色可能是催化的。 本申请还涉及使用开环错译聚合(ROMP)制备的超高密度均聚物,其中1,2-双(3-噻吩基) - 环戊烯的中心环直接并入聚合物主链。 单体单元可以容易地官能化以使得能够合成具有不同结构和电子性质的聚合物。 这些化合物具有许多潜在的应用,包括高密度光学信息存储系统,光调节分子开关,可逆全息系统,眼用透镜,光化学测量和分子传感器,光致变色油墨,油漆和纤维以及光电子系统,如光波导,布拉格反射器和电介质镜 。