학술논문

Remarkable discrimination in the triplet lifetimes of the diastereomers of 1,4-bis(p-methoxyphenyl)-2,3-diphenylbutan-1-4-dione
Document Type
Academic Journal
Source
Journal of the American Chemical Society. Nov 12, 1997, Vol. 119 Issue 45, p11094, 2 p.
Subject
Stereochemistry -- Research
Conformational analysis -- Usage
Energy transfer -- Analysis
Chirality -- Research
Molecular structure -- Analysis
Chemistry
Language
ISSN
0002-7863
Abstract
Synthesis of the diastomers of 1,4-bis(p-methoxyphenyl)-2,3-dyphenylbutan-1,4-dione (compound 1) revealed that the diastereomeric discrimination in the lifetimes for compound 1-meso and compound 1-rac is a direct result of conformational control. The efficiency of this discrimination in solution makes compound 1 a potential probe for studying the chirality of supramolecular structures. Photochemical probes with a stereocenter that affects their photophysics are desirable to the study of the dynamics and local mobility of supramolecular structures.