Issue 12, 1982

Photophysics of 1,1′-binaphthyl and its formation of a complex with N-(1-propyl)-2,5-dimethylpyrrole

Abstract

Fluorescence lifetimes for 1,1′-binaphthyl in cyclohexane, benzene, propan-1-ol and acetonitrile have been measured and found to lie between 2.5 and 3.5 ns. The conformational changes which occur in the excited singlet state of 1,1′-binaphthyl are so rapid that they elude detection by sub-nanosecond fluorescence spectroscopy. 1,1′-Binaphthyl forms an exciplex with N-(1-propyl)-2,5-dimethylpyrrole. This is weakly fluorescent in non-polar solvents. The kinetics of formation of the exciplex were examined. The radiative decay rate constant for the exciplex appears to be relatively small. It is suggested that the pyrrole complexes with one of the naphthalene rings of the 1,1′-binaphthyl to give a complex which resembles that formed between the pyrrole and naphthalene.

Article information

Article type
Paper

J. Chem. Soc., Faraday Trans. 1, 1982,78, 3477-3484

Photophysics of 1,1′-binaphthyl and its formation of a complex with N-(1-propyl)-2,5-dimethylpyrrole

X. Luo, G. S. Beddard, G. Porter and R. S. Davidson, J. Chem. Soc., Faraday Trans. 1, 1982, 78, 3477 DOI: 10.1039/F19827803477

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