Issue 13, 1973

Fluorescence quenching of 2-piperidinoanthraquinone

Abstract

Fluorescence solvent shift data indicate the first excited singlet state of 2-piperidinoanthraquinone [2-PA] to be considerably more polar than its ground state. Amines quench the fluorescence of [2-PA] in cyclohexane by electron transfer. Alcohols also quench the fluorescence but by a different mechanism involving hydrogen bonding between the alcohol and the ground state of [2-PA] to form a complex that is itself fluorescent.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1973, 1742-1743

Fluorescence quenching of 2-piperidinoanthraquinone

A. K. Davies, G. A. Gee, J. F. Mckellar and G. O. Phillips, J. Chem. Soc., Perkin Trans. 2, 1973, 1742 DOI: 10.1039/P29730001742

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