Nature of the lowest triplet states of 4′-substituted N-phenylphenothiazine derivatives

Literature Information

Publication Date 2000-09-08
DOI 10.1039/B005058J
Impact Factor 3.676
Authors

Paweł Borowicz, Jerzy Herbich, Andrzej Kapturkiewicz, Romana Anulewicz-Ostrowska, Jacek Nowacki, Günter Grampp


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Abstract

The nature of the lowest triplet state of the donor–acceptor N-phenylphenothiazine derivatives has been studied by means of phosphorescence and EPR spectroscopy in various low temperature glasses. The triplet excitation of N-phenylphenothiazine and N-(p-anisyl)-phenothiazine is localised within the phenothiazine subunit. On the contrary, the 77 K phosphorescence of the molecules containing an electron acceptor group (i.e. –CN, –COCH3 or –COC6H5 at the 4′ position) is similar to that for benzonitrile, acetophenone or benzophenone, respectively, although the energy levels of their T1 states are higher than that of phenothiazine. With increasing temperature, however, their phosphorescence becomes similar to that characteristic for phenothiazine. This finding has been explained in terms of the excited-state intramolecular energy transfer accompanied by the planarisation of the phenothiazine kernel. The results of crystallographic investigations support this hypothesis.

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Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
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