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An ab initio conformational study on...
Journal article

An ab initio conformational study on 2,3-dihydrobilin-1,19(21H,24H)-dione, a model compound for open-chain tetrapyrroles

Abstract

The molecule 2,3-dihydrobilin-1,19(21H,24H)-dione (DHB) was studied as a model of the fully conjugated linear open-chain tetrapyrroles phycocyanobilin (PCB), phycoerythrobilin (PEB) and phytochrome (PC) as well as biliverdin (BV) and bilirubin (BR). The rotations around the single bonds of the exocyclic methine bridges were investigated for all possible cis and trans, E and Z isomers of DHB. The geometries and energies of conformers were …

Authors

Marai CNJ; Chass GA; Doust AB; Scholes GD

Journal

Computational and Theoretical Chemistry, Vol. 680, No. 1-3, pp. 219–225

Publisher

Elsevier

Publication Date

July 2004

DOI

10.1016/j.theochem.2004.04.040

ISSN

2210-271X