Canadian journal of chemistry

Intramolecular excimer fluorescence from folded ground state rotamers of N, N'dimethyl-N, N'-dipyrenylurea protophanes

FD Lewis, TL Kurth

Index: Lewis, Frederick D.; Kurth, Todd L. Canadian Journal of Chemistry, 2003 , vol. 81, # 6 p. 770 - 776

Full Text: HTML

Citation Number: 17

Abstract

The molecular structure, absorption, and fluorescence spectra of N, N'-dimethyl-N, N'-di-1- pyrenylurea and N, N'-dimethyl-N, N'-di-2-pyrenylurea have been investigated and compared to the properties of N, N, N'-trimethyl-N'-pyrenylurea model compounds. Di-1- pyrenylurea exists as a mixture of folded (E, E) syn-and anti-rotamers that interconvert via flipping of one of the pyrene rings to an unfolded (E, Z) rotamer geometry. The symmetric ...

Related Articles:

First examples of fluorinated and chlorinated polycyclic aromatic hydrocarbon (PAH) dications from benzo [a] pyrene, pyrene, and their alkyl-substituted derivatives

[Vollmann et al. Justus Liebigs Annalen der Chemie, 1937 , vol. 531, p. 1,139]

More Articles...