TCE ForumWhats NewSearchOrders


The Chemical Educator

ISSN: 1430-4171 (electronic version)

Table of Contents

Abstract Volume 13 Issue 3 (2008) pp 158-160

Solid State Isomerization

David E. Berry* and Kelli L. Fawkes

Department of Chemistry, University of Victoria, Victoria, British Columbia, Canada, V8W 3V6, berryde@uvic.ca, fawkesk@uvic.ca
Received June 20, 2007. Accepted December 27, 2007.

Published online: 1 June 2008

Abstract. A two-step synthesis of trans,trans,trans-[RuCl2(CNBut)2(PPh3)2] is described in which the first step uses a microwave reflux to make [RuCl2(PPh3)3] and the second step is the room temperature addition of t-butylisocyanide to a solution of the isolated [RuCl2(PPh3)3]. The final product is isomerized to the cis,cis,trans-isomer in the solid state. The progression of this reaction at a fixed temperature within the 140 C150 C range can be monitored by solution 1H NMR spectroscopy.

Key Words: Laboratories and Demonstrations; organometallic chemistry; isomerization; solid state reactions; green chemistry; reaction kinetics

(*) Corresponding author. (E-mail: fawkesk@uvic.ca)

Article in PDF format (62 KB) HTML format

Supporting Materials:

An example procedure as written for an undergraduate student is given. Notes for the instructor are obtainable from either of the authors. (42 KB).


Issue date: June 1, 2008

The Chemical Educator 1996-2017