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

Young Mo Sung; Bartosz Szyszko; Radomir Mysliborski; Marcin Stepien; Juwon Oh; Minjung Son; Lechoslaw Latos Grazynski; Dongho Kim

doi:10.1039/c4cc03855j

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

Young Mo Sung, Bartosz Szyszko, Radomir Mysliborski, Marcin Stepien, Juwon Oh, Minjung Son, Lechoslaw Latos Grazynski, Dongho Kim

Department of Chemistry

Research output: Contribution to journal › Article › peer-review

18 Scopus citations

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.

Original language	English
Pages (from-to)	8367-8369
Number of pages	3
Journal	Chemical Communications
Volume	50
Issue number	61
DOIs	https://doi.org/10.1039/c4cc03855j
State	Published - 3 Jul 2014

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10.1039/c4cc03855j

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title = "The effect of π-conjugation in the macrocyclic ring on the photophysical properties of a series of thiaaceneporphyrinoids",

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.",

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AU - Sung, Young Mo

AU - Szyszko, Bartosz

AU - Mysliborski, Radomir

AU - Stepien, Marcin

AU - Oh, Juwon

AU - Son, Minjung

AU - Grazynski, Lechoslaw Latos

AU - Kim, Dongho

PY - 2014/7/3

Y1 - 2014/7/3

N2 - 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.

AB - 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.

UR - https://www.scopus.com/pages/publications/84903952365

U2 - 10.1039/c4cc03855j

DO - 10.1039/c4cc03855j

M3 - Article

C2 - 24943403

AN - SCOPUS:84903952365

SN - 1359-7345

VL - 50

SP - 8367

EP - 8369

JO - Chemical Communications

JF - Chemical Communications

IS - 61

ER -

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

Abstract

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