Issue 21, 2003

Formation of gold-like metal-lustrous inclusion crystals from 1-phenyl-2,5-bis[5-(tricyanoethenyl)-2-thienyl]pyrrole host and an electron-donating aromatic guest

Abstract

A novel π-conjugated organic compound, 1-phenyl-2,5-bis[5-(tricyanoethenyl)-2-thienyl]pyrrole, which bears two powerful electron-withdrawing tricyanoethenyl substitutents, readily yielded gold-like metal-lustrous inclusion crystals with a series of aromatic guest molecules such as toluene, p-xylene, anisole, dimethoxybenzenes and indene. All the inclusion compounds have a common stoichiometric ratio (host/guest) of 2 ∶ 1. X-Ray structural analyses demonstrate that the structural feature for toluene included crystal is similar to those containing p-xylene, anisole, dimethoxybenzenes and indene.

Graphical abstract: Formation of gold-like metal-lustrous inclusion crystals from 1-phenyl-2,5-bis[5-(tricyanoethenyl)-2-thienyl]pyrrole host and an electron-donating aromatic guest

Supplementary files

Article information

Article type
Paper
Submitted
10 Mar 2003
Accepted
08 Sep 2003
First published
01 Oct 2003

Org. Biomol. Chem., 2003,1, 3845-3850

Formation of gold-like metal-lustrous inclusion crystals from 1-phenyl-2,5-bis[5-(tricyanoethenyl)-2-thienyl]pyrrole host and an electron-donating aromatic guest

K. Ogura, R. Zhao, T. Mizuoka, M. Akazome and S. Matsumoto, Org. Biomol. Chem., 2003, 1, 3845 DOI: 10.1039/B302689B

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.

Social activity

Spotlight

Advertisements