Issue 2, 1997

Charge–transfer excitation of electron donor–acceptor complexes of arylcyclopropanes

Abstract

Electron-transfer (ET) reactions of mono- and di-arylcyclopropanes 1 and 2 have been investigated by employing charge-transfer (CT) excitation of their electron donor–acceptor (EDA) complexes with tetracyanoethylene (TCNE) or p-chloranil (CA). For the TCNE complexes, no reaction is observed following photoexcitation within their CT bands. Picosecond absorption spectroscopic experiments with phenylcyclopropane 1a and 1,1-diphenylcyclopropane 2a reveal that the photogenerated ion radical pairs [1a˙+, TCNE˙-] and [2a˙+, TCNE˙-] are too short-lived to undergo chemical reaction. For the CA complexes, net chemical change is observed in the CT excitation of the 2a–CA complex though the efficiency is very low. The other arylcyclopropane–CA complexes are found to be unreactive. Factors concerned with the reactivity of 1 and 2 upon their CT-excitation are discussed.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1997, 303-308

Charge–transfer excitation of electron donor–acceptor complexes of arylcyclopropanes

Y. Takahashi, H. Ohaku, N. Nishioka, H. Ikeda, T. Miyashi, D. A. Gormin and E. F. Hilinski, J. Chem. Soc., Perkin Trans. 2, 1997, 303 DOI: 10.1039/A604565K

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