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Structure property relationship of linear and angular pyrazine-based structural isomers with terminal D-A groups and evaluation of their photophysical properties

Authors
Meti, PuttavvaPark, Dong-JinGong, Young-Dae
Issue Date
Sep-2019
Publisher
ELSEVIER SCI LTD
Keywords
Pyrazine; Intramolecular charge transfer; Fluorescence; Solvatochromism
Citation
DYES AND PIGMENTS, v.168, pp 357 - 368
Pages
12
Indexed
SCI
SCIE
SCOPUS
Journal Title
DYES AND PIGMENTS
Volume
168
Start Page
357
End Page
368
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/7728
DOI
10.1016/j.dyepig.2019.04.057
ISSN
0143-7208
1873-3743
Abstract
A series of pyrazine-based linear and angular shaped push-pull chromophores were synthesized by Sonogashira reaction and were further investigated by X-ray analysis. The photophysical properties were comprehensively studied both experimentally and through quantum chemical methods. The drastic influence of the electrondonor and acceptor on the absorption and emission spectra of the linear and angular scaffolds was established. Quantum chemical computations provided a reliable theoretical rationalization of the observed spectral features. These results suggest that extending the conjugation of a pyrazine acceptor in a linear direction can dramatically improve the intramolecular charge transfer interactions.
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