Issue 4, 1979

The fluorescence of some dipolar NN-dialkyl-4-(dichloro-1,3,5-triazinyl)anilines. Part 1. Solvent effects and solvent exciplex formation

Abstract

The fluorescence emissions of the title compounds occur from highly charge-transfer excited states and, in cyclohexane solution, the fluorescence quantum yields ϕF are high. In aprotic solvents of low to moderate polarity ϕF is much reduced, mainly by an increase in the non-radiative rate constant kNR with solvent polarity increase. The decay channel is thought to be intersystem crossing from the singlet to the triplet intramolecular charge transfer excited state. The formation of a 1 : 1 solvent exciplex between acetonitrile and the excited dipolar triazine system in aliphatic hydrocarbon solvents has been investigated and found to be diffusion controlled.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1979, 484-489

The fluorescence of some dipolar NN-dialkyl-4-(dichloro-1,3,5-triazinyl)anilines. Part 1. Solvent effects and solvent exciplex formation

D. J. Cowley and P. J. Healy, J. Chem. Soc., Perkin Trans. 2, 1979, 484 DOI: 10.1039/P29790000484

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements