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Synthesis and photochromic properties of spiro[naphthopyran-7′H-benzocyclohepta-5′,8′-dienes]

Crossley, Daniel L., Gabbutt, Christopher D., Heron, B. Mark, Kay, Paul and Mogstad, Martin (2012) Synthesis and photochromic properties of spiro[naphthopyran-7′H-benzocyclohepta-5′,8′-dienes]. Dyes and Pigments, 95 (1). pp. 62-68. ISSN 0143-7208

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A series of spironaphthopyrans has been synthesised by the acid-catalysed condensation between either a substituted 1-naphthol or 2-naphthol and the propargylic alcohol derived from the addition of lithium trimethylsilylacetylide to a 7H-benzocycloheptan-7-one with subsequent in situ silyl group removal. The photochromism of the novel spironaphthopyrans was characterised by a bathochromically shifted λmax coupled with a relatively quick initial fade of the photogenerated species relative to the comparable diphenyl substituted model compounds. After initial fading a relatively intense residual colour persisted for the spironaphthopyrans.

Item Type: Article
Subjects: Q Science > Q Science (General)
Q Science > QD Chemistry
Schools: School of Applied Sciences
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Depositing User: Sharon Beastall
Date Deposited: 18 Sep 2012 12:02
Last Modified: 28 Aug 2021 11:21


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