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Reversible mechanochromism and enhanced AIE in tetraphenylethene substituted phenanthroimidazoles
Journal article   Peer reviewed

Reversible mechanochromism and enhanced AIE in tetraphenylethene substituted phenanthroimidazoles

Rajneesh Misra, Thaksen Jadhav, Bhausaheb Dhokale and Shaikh M. Mobin
Chemical communications (Cambridge, England), Vol.50(65), pp.9076-9078
21/08/2014
PMID: 24983656

Abstract

Chemistry Chemistry, Multidisciplinary Physical Sciences Science & Technology
Tetraphenylethene (TPE) substituted phenanthroimidazoles 3a and 3b were designed and synthesized by the Suzuki cross-coupling reaction. They show reversible mechanochromic behavior with contrast colors between sky-blue and yellow green. The powder XRD studies show that destruction of a crystalline state into an amorphous state is responsible for mechanochromism. Hydrogen bonding interaction of a cyano-group in 3b results in enhanced AIE and improved thermal stability.

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