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1,3-Bisarylbutadienes: Novel Thermally Irreversible Photochromic System
Novel thermally irreversible photochromic compounds 1O , 2O and 3O based on 1,3-bisarylbutadiene system were synthesized. The closed ring-forms 1C and 2C showed absorption maximum at 445 nm, while the closed ring-form 3C , a methyl group of 2C on C-5 of thienyl ring was replaced with a formyl group,...
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Published in: | Molecular crystals and liquid crystals (Philadelphia, Pa. : 2003) Pa. : 2003), 2005-06, Vol.431 (1), p.433-439 |
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cited_by | cdi_FETCH-LOGICAL-c346t-75143015bcbdec8c8e39abf81162d7e6661de210792f5cc88b5d6f4e9074f20f3 |
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container_end_page | 439 |
container_issue | 1 |
container_start_page | 433 |
container_title | Molecular crystals and liquid crystals (Philadelphia, Pa. : 2003) |
container_volume | 431 |
creator | Yokoyama, Yasushi Shrestha, Sujen Man Yokoyama, Yayoi |
description | Novel thermally irreversible photochromic compounds
1O
,
2O
and
3O
based on 1,3-bisarylbutadiene system were synthesized. The closed ring-forms
1C
and
2C
showed absorption maximum at 445 nm, while the closed ring-form
3C
, a methyl group of
2C
on C-5 of thienyl ring was replaced with a formyl group, showed the absorption maximum at 500 nm. |
doi_str_mv | 10.1080/15421400590947018 |
format | article |
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1O
,
2O
and
3O
based on 1,3-bisarylbutadiene system were synthesized. The closed ring-forms
1C
and
2C
showed absorption maximum at 445 nm, while the closed ring-form
3C
, a methyl group of
2C
on C-5 of thienyl ring was replaced with a formyl group, showed the absorption maximum at 500 nm.</description><identifier>ISSN: 1542-1406</identifier><identifier>EISSN: 1563-5287</identifier><identifier>DOI: 10.1080/15421400590947018</identifier><language>eng</language><publisher>Taylor & Francis Group</publisher><subject>bathochromic shift ; bisarylbutadiene ; fatigue resistivity ; photochromism ; thermal irreversibility</subject><ispartof>Molecular crystals and liquid crystals (Philadelphia, Pa. : 2003), 2005-06, Vol.431 (1), p.433-439</ispartof><rights>Copyright Taylor & Francis Group, LLC 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c346t-75143015bcbdec8c8e39abf81162d7e6661de210792f5cc88b5d6f4e9074f20f3</citedby><cites>FETCH-LOGICAL-c346t-75143015bcbdec8c8e39abf81162d7e6661de210792f5cc88b5d6f4e9074f20f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Yokoyama, Yasushi</creatorcontrib><creatorcontrib>Shrestha, Sujen Man</creatorcontrib><creatorcontrib>Yokoyama, Yayoi</creatorcontrib><title>1,3-Bisarylbutadienes: Novel Thermally Irreversible Photochromic System</title><title>Molecular crystals and liquid crystals (Philadelphia, Pa. : 2003)</title><description>Novel thermally irreversible photochromic compounds
1O
,
2O
and
3O
based on 1,3-bisarylbutadiene system were synthesized. The closed ring-forms
1C
and
2C
showed absorption maximum at 445 nm, while the closed ring-form
3C
, a methyl group of
2C
on C-5 of thienyl ring was replaced with a formyl group, showed the absorption maximum at 500 nm.</description><subject>bathochromic shift</subject><subject>bisarylbutadiene</subject><subject>fatigue resistivity</subject><subject>photochromism</subject><subject>thermal irreversibility</subject><issn>1542-1406</issn><issn>1563-5287</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqF0M1Kw0AQB_BFFKzVB_CWBzC6s98RL1q0FooK1nNINrM0su3Kbqzm7U2pt4KeZg7zG2b-hJwDvQRq6BVIwUBQKgtaCE3BHJARSMVzyYw-3PaC5cOAOiYnKb1TyoQGMyJTuOD5XZuq2Pv6s6uaFteYrrOnsEGfLZYYV5X3fTaLETcYU1t7zF6WoQt2GcOqtdlrnzpcnZIjV_mEZ791TN4e7heTx3z-PJ1Nbue55UJ1uZYgOAVZ27pBa6xBXlS1MwCKNRqVUtAgA6oL5qS1xtSyUU5gQbVwjDo-JrDba2NIKaIrP2K7Gq4vgZbbJMq9JAZzszPt2oXhn68QfVN2Ve9DdLFa2zaV_C-u_-V7quy-O_4D80p2MA</recordid><startdate>20050601</startdate><enddate>20050601</enddate><creator>Yokoyama, Yasushi</creator><creator>Shrestha, Sujen Man</creator><creator>Yokoyama, Yayoi</creator><general>Taylor & Francis Group</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20050601</creationdate><title>1,3-Bisarylbutadienes: Novel Thermally Irreversible Photochromic System</title><author>Yokoyama, Yasushi ; Shrestha, Sujen Man ; Yokoyama, Yayoi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c346t-75143015bcbdec8c8e39abf81162d7e6661de210792f5cc88b5d6f4e9074f20f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>bathochromic shift</topic><topic>bisarylbutadiene</topic><topic>fatigue resistivity</topic><topic>photochromism</topic><topic>thermal irreversibility</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yokoyama, Yasushi</creatorcontrib><creatorcontrib>Shrestha, Sujen Man</creatorcontrib><creatorcontrib>Yokoyama, Yayoi</creatorcontrib><collection>CrossRef</collection><jtitle>Molecular crystals and liquid crystals (Philadelphia, Pa. : 2003)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yokoyama, Yasushi</au><au>Shrestha, Sujen Man</au><au>Yokoyama, Yayoi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>1,3-Bisarylbutadienes: Novel Thermally Irreversible Photochromic System</atitle><jtitle>Molecular crystals and liquid crystals (Philadelphia, Pa. : 2003)</jtitle><date>2005-06-01</date><risdate>2005</risdate><volume>431</volume><issue>1</issue><spage>433</spage><epage>439</epage><pages>433-439</pages><issn>1542-1406</issn><eissn>1563-5287</eissn><abstract>Novel thermally irreversible photochromic compounds
1O
,
2O
and
3O
based on 1,3-bisarylbutadiene system were synthesized. The closed ring-forms
1C
and
2C
showed absorption maximum at 445 nm, while the closed ring-form
3C
, a methyl group of
2C
on C-5 of thienyl ring was replaced with a formyl group, showed the absorption maximum at 500 nm.</abstract><pub>Taylor & Francis Group</pub><doi>10.1080/15421400590947018</doi><tpages>7</tpages></addata></record> |
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identifier | ISSN: 1542-1406 |
ispartof | Molecular crystals and liquid crystals (Philadelphia, Pa. : 2003), 2005-06, Vol.431 (1), p.433-439 |
issn | 1542-1406 1563-5287 |
language | eng |
recordid | cdi_crossref_primary_10_1080_15421400590947018 |
source | Taylor and Francis Science and Technology Collection |
subjects | bathochromic shift bisarylbutadiene fatigue resistivity photochromism thermal irreversibility |
title | 1,3-Bisarylbutadienes: Novel Thermally Irreversible Photochromic System |
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