Issue 4, 1996

Unusual reactivity of acenaphthenone as an electron donor in sensitized photooxygenation

Abstract

Acenaphthenone (ANO) is an effective electron donor and undergoes stepwise photooxygenation sensitized by 9,10-dicyanoanthracene, affording hydroxylactone and anhydride derivatives; the electron transfer mechanism via an enol intermediacy was verified by the enhancement effect of biphenyl, fluorescence quenching, exciplex emission and chemically induced dynamic nuclear polarization (CIDNP).

Article information

Article type
Paper

Chem. Commun., 1996, 493-494

Unusual reactivity of acenaphthenone as an electron donor in sensitized photooxygenation

S. Wu, J. Liu and Z. Jiang, Chem. Commun., 1996, 493 DOI: 10.1039/CC9960000493

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.

Social activity

Spotlight

Advertisements