Substitution Effect on the Coloration Quantum Yield of a Photochromic Bisbenzothienylethene
Introduction of isopropyl substituents to 2 and 2′ positions of benzothiophene rings of bis(1-benzothiophen-3-yl)hexa-fluorocyclopentene increased the population of anti-parallel conformation, and enhanced the quantum yield of the cyclization reaction.
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Veröffentlicht in: | Chemistry letters 1999-01, Vol.28 (1), p.63-64 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Introduction of isopropyl substituents to 2 and 2′ positions of benzothiophene rings of bis(1-benzothiophen-3-yl)hexa-fluorocyclopentene increased the population of anti-parallel conformation, and enhanced the quantum yield of the cyclization reaction. |
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ISSN: | 0366-7022 1348-0715 |
DOI: | 10.1246/cl.1999.63 |