Literature DB >> 15903325

Synthesis, electronic properties, and electrochemiluminescence of donor-substituted phenylethynylanthronitriles.

Arumugasamy Elangovan1, Kuo-Ming Kao, Shu-Wen Yang, Yu-Ling Chen, Tong-Ing Ho, Yuhlong Oliver Su.   

Abstract

A new series of pi-conjugated donor-acceptor compounds (1-6) with inherent redox centers have been prepared and studied with respect to their electronic properties. The photophysical characteristics of these compounds have been studied in relation to their structures. Cyclic voltammetry and UV-vis spectroelectrochemistry were used to probe the ground-state electronic properties of the neutral and charged species. The observed electronic absorption properties of the neutral and charged molecules are explained with the help of frontier orbital structures and electrostatic potential maps obtained from density functional theory (DFT, B3LYP/6-31G) calculations. Electrochemiluminescence (ECL) of this series of donor-substituted phenylethynylanthronitriles with different donors was also studied. The structure-property relationship of all of the compounds is discussed.

Entities:  

Year:  2005        PMID: 15903325     DOI: 10.1021/jo0477953

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

1.  4-(9-Anthryl)-2-methylbutyn-2-ol.

Authors:  Irena Bylińska; Artur Sikorski; Wiesław Wiczk
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-01-23

2.  Hydroquinone-benzonitrile system: intramolecular charge-transfer and computational studies.

Authors:  Kuangsen Sung; Pin-Mei Huang; Chi-Han Zhou
Journal:  J Fluoresc       Date:  2007-07-14       Impact factor: 2.217

3.  Blue-red emitting materials based on a pyrido[2,3-b]pyrazine backbone: design and tuning of the photophysical, aggregation-induced emission, electrochemical and theoretical properties.

Authors:  Deepak M Kapse; Pooja S Singh; Mohammed Ghadiyali; Sajeev Chacko; Rajesh M Kamble
Journal:  RSC Adv       Date:  2022-03-01       Impact factor: 3.361

  3 in total

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