Issue 94, 2014

Reversible mechanochromism in dipyridylamine-substituted unsymmetrical benzothiadiazoles

Abstract

We report the design and synthesis of push–pull benzothiadiazoles (BTDs) of type D1–π–A–π–D2 and D1–π–A–D2. These BTDs show strong charge transfer interaction. BTD 3 shows reversible mechanochromism with color contrast between yellow (crystalline state) and orange (amorphous state). Photophysical and computational studies reveal that the planar orientation of the pyridyl and BTD unit in 2 results in no change in solid state emission whereas non-planar orientation of the dipyridylamine and BTD unit in 3 results in efficient mechanochromism.

Graphical abstract: Reversible mechanochromism in dipyridylamine-substituted unsymmetrical benzothiadiazoles

Supplementary files

Article information

Article type
Communication
Submitted
06 Sep 2014
Accepted
13 Oct 2014
First published
14 Oct 2014

RSC Adv., 2014,4, 52526-52529

Reversible mechanochromism in dipyridylamine-substituted unsymmetrical benzothiadiazoles

P. Gautam, R. Maragani, S. M. Mobin and R. Misra, RSC Adv., 2014, 4, 52526 DOI: 10.1039/C4RA09921D

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