meso-Tris(oligo-2,5-thienylene)-substituted subporphyrins exhibit remarkably red-shifted and intensified absorption bands with increasing number of thienyl subunits. A dimeric subporphyrin obtained from homocoupling of a monobrominated tris(2-thienyl)-substituted subporphyrin exhibits a split Soret-like band due to the exciton coupling.
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Hayashi et al. (2010) studied this question.
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