Issue 14, 1971
From the journal:

Journal of the Chemical Society D: Chemical Communications

Crystal structure of the yellow 1:2 molecular complex lumiflavin–bisnaphthalene-2,3-diol

Benes L. Trus,   Joe L. Wells,   Robert M. Johnstone,   Charles J. Fritche, Jun.  and  Richard E. Marsh  

Abstract

In the first molecular complex of the physiologically active neutral form of isoalloxazine studied, lumiflavin–bisnaphthalene-2,3-diol, each flavin is sandwiched between two naphthalenediol molecules with extensive overlap but a moderately large (3·44 Å) spacing, indicating at most weak charge-transfer interaction and in agreement with the yellow colour of the complex, nearly the same as that of the parent lumiflavin.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/C29710000751
Article type
Paper

J. Chem. Soc. D, 1971, 751-752

Permissions

Request permissions

Crystal structure of the yellow 1:2 molecular complex lumiflavin–bisnaphthalene-2,3-diol

B. L. Trus, J. L. Wells, R. M. Johnstone, C. J. Fritche and R. E. Marsh, J. Chem. Soc. D, 1971, 751 DOI: 10.1039/C29710000751

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