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Issue 61, 2014
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The effect of π-conjugation in the macrocyclic ring on the photophysical properties of a series of thiaaceneporphyrinoids

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Abstract

In a series of thiaaceneporphyrinoids, their conformers exhibit macrocyclic π-conjugation pathways controlled by a dihedral angle between the porphyrin framework and acene planes. Conformational equilibria significantly affect the photophysical properties of these macrocycles.

Graphical abstract: The effect of π-conjugation in the macrocyclic ring on the photophysical properties of a series of thiaaceneporphyrinoids

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Publication details

The article was received on 20 May 2014, accepted on 10 Jun 2014 and first published on 10 Jun 2014


Article type: Communication
DOI: 10.1039/C4CC03855J
Author version available: Download Author version (PDF)
Citation: Chem. Commun., 2014,50, 8367-8369
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    The effect of π-conjugation in the macrocyclic ring on the photophysical properties of a series of thiaaceneporphyrinoids

    Y. M. Sung, B. Szyszko, R. Myśliborski, M. Stępień, J. Oh, M. Son, L. Latos-Grażyński and D. Kim, Chem. Commun., 2014, 50, 8367
    DOI: 10.1039/C4CC03855J

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