Regular and red-shifted fluorescence of the donor–acceptor compound 5-(1H-pyrrole-1-yl)thiophenecarbonitrile (TCN) is efficiently quenched by internal modes of thiophene
Author:
Affiliation:
1. Interdisciplinary Center for Scientific Computing
2. Im Neuenheimer Feld 205
3. 69120 Heidelberg
4. Germany
5. Institute of Physical and Theoretical Chemistry
6. Max-von-Laue-Straße 7
7. 60438 Frankfurt
Abstract
The photochemical properties of thiophene analogs of N-pyrrolobenzonitrile (PBN), notably the two isomers 5-(1H-pyrrole-1-yl)thiophene-2-carbonitrile (2-TCN) and 5-(1H-pyrrole-1-yl)thiophene-3-carbonitrile (3-TCN) have been investigated.
Publisher
Royal Society of Chemistry (RSC)
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Link
http://pubs.rsc.org/en/content/articlepdf/2017/CP/C7CP01460K
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