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Title: Photoassociation and photoinduced charge transfer in bridged diaryl compounds. 6. Intramolecular triplet excimers of dicarbazolylalkanes and their comparison to an intermolecular triplet excimer of carbazole

Journal Article · · Journal of Physical Chemistry; (United States)
DOI:https://doi.org/10.1021/j100061a004· OSTI ID:7267382
;  [1]
  1. Univ. of Akron, OH (United States)

A time-resolved emission study of intramolecular triplet excimer formation has been carried out for dicarbazolylmethane (DCM) and dicarbazolylpropane (DCP) in fluid solution at room temperature. The triplet excimer formation was deduced from the comparison of the phosphorescence with the corresponding emission from the intermolecular triplet excimer of carbazole. It has been found that whereas the triplet excimer formation in DCP is evident in both polar and nonpolar solvents, the excimer formation in DCM is observed only in polar solvents at longer delay times. The result indicates that the conformation favored by the triplet excimer is more readily attainable in DCP than in DCM. The enhancement of the triplet excimer formation by polar solvent, which is also observed for carbazole, suggests that the triplet excimers are stabilized (at least in part) by charge resonance interactions. Comparison of the temporal characteristics of the normal delayed fluorescence of DCP with those of the corresponding excimer phosphorescence suggests that the delayed fluorescence at long delay times is produced by bimolecular annihilation of the intramolecular triplet excimers. This in turn implies that the excited singlet-state species produced by bimolecular annihilation of the triplet excimers is unstable and rearranges into monomeric (i.e., non-interacting) conformation prior to its decay by emission of radiation. 16 refs., 7 figs.

DOE Contract Number:
FG02-89ER14024
OSTI ID:
7267382
Journal Information:
Journal of Physical Chemistry; (United States), Vol. 98:10; ISSN 0022-3654
Country of Publication:
United States
Language:
English