Publication details

Synthesis and properties of pi-conjugated donor-acceptor macrocycles derived from phenanthrylene building blocks

Authors

PHULWALE Bhimrao Vaijnath MISHRA Sushil Kumar MAZAL Ctibor

Year of publication 2018
Type Article in Periodical
Magazine / Source Tetrahedron
MU Faculty or unit

Faculty of Science

Citation
Web https://www.sciencedirect.com/science/article/pii/S0040402018305428?via%3Dihub
Doi http://dx.doi.org/10.1016/j.tet.2018.05.025
Keywords Macrocycles; Phenanthrene; Donor-acceptor; Solvatochromism; Intramolecular charge transfer; Sonogashira cross-coupling
Description Phenanthrylene-ethynylidene macrocycles combining electron donor and electron acceptor subunits in their shape-persistent fully conjugated core were synthesized. The donor subunits consisted of two 9,10-dialkoxyphenanthrenes linked either with 1,2-ethynylidene or 2,5-thienylene bridge. The acceptors were 9,10-phenanthroquinone and dibenzoquinoxaline and dibenzophenazines derived from it. Solvatochromic photoluminescence from intramolecular-charge-transfer (ICT) excited state was observed mainly in non-polar solvents. In more polar solvents, the excited states favor non-radiative relaxation. DFT calculated HOMO/LUMO energies of the macrocycles correlate well with spectroscopic and electrochemical data. In the series of substituted dibenzophenazine acceptors a good correlation with Hammett substituent constants sigma(-)(p) was found. (C) 2018 Elsevier Ltd. All rights reserved.
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