Issue 1, 1994

Photolysis of 4-methoxyphenyl aryl alkylphosphonates

Abstract

UV irradiation of bis(4-methoxyphenyl) methylphosphonate 1a in methanol gave 4,4′-dimethoxybiphenyl 2a as the main product through an intramolecular excimer. With 4-cyanophenyl-4-methoxyphenyl methylphosphonate 1b 4-cyano-4′-methoxybiphenyl 2c and 4-cyano-2-(4′-methoxyphenyl)phenyl methylphosphonate 4b were obtained through an intramolecular exciplex. 3-Cyanophenyl-4-methoxyphenyl methylphosphonate 1c gave only 3-cyano-4′-methoxybiphenyl 2f. Methyl 4-methoxyphenyl 4-chlorobenzylphosphonate 5a gave methyl 4-Chlorobenzyl-2-(4′-methoxyphenyl)phosphonate and methyl 2-(4′-methoxyphenyl)benzylphosphonate.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1994, 141-146

Photolysis of 4-methoxyphenyl aryl alkylphosphonates

M. Nakamura, K. Sawasaki, Y. Okamoto and S. Takamuku, J. Chem. Soc., Perkin Trans. 1, 1994, 141 DOI: 10.1039/P19940000141

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