Intrinsically thermochromic fluorans

Farid Azizian; Amanda J. Field; B. Mark Heron; Colin Kilner

doi:10.1039/c1cc15854f

Intrinsically thermochromic fluorans

Farid Azizian, Amanda J. Field, B. Mark Heron, Colin Kilner

Research output: Contribution to journal › Article › peer-review

35 Citations (Scopus)

Abstract

A Suzuki coupling strategy has been employed to access a series of novel fluorans substituted with a phenolic moiety. These fluorans display good thermochromism in methyl stearate and obviate the need for traditional complex formulations containing acidic colour developers.

Original language	English
Pages (from-to)	750-752
Number of pages	3
Journal	Chemical Communications
Volume	48
Issue number	5
Early online date	24 Nov 2011
DOIs	https://doi.org/10.1039/c1cc15854f
Publication status	Published - 18 Jan 2012
Externally published	Yes

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title = "Intrinsically thermochromic fluorans",

abstract = "A Suzuki coupling strategy has been employed to access a series of novel fluorans substituted with a phenolic moiety. These fluorans display good thermochromism in methyl stearate and obviate the need for traditional complex formulations containing acidic colour developers.",

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Intrinsically thermochromic fluorans

Abstract

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