Issue 1, 2011
From the journal:

Chemical Communications

Gold(i) “click” 1,2,3-triazolylidenes: synthesis, self-assembly and catalysis†‡

Kelly J. Kilpin,a   Ursula S. D. Paul,b   Ai-Lan Lee*b  and  James D. Crowley*a  

* Corresponding authors

a Department of Chemistry, University of Otago, PO Box 56, Dunedin, New Zealand
E-mail: jcrowley@chemistry.otago.ac.nz
Fax: +64 3 479 7906
Tel: +64 3 479 7731

b School of Engineering and Physical Sciences, Chemistry – William H. Perkin Building, Heriot-Watt University, Edinburgh EH14 4AS, UK
E-mail: A.Lee@hw.ac.uk
Tel: +44 (0)131-4518030

Abstract

Novel gold(I) “click” carbene(1,2,3-triazolylidene) complexes have been synthesised, characterised and exploited for the self-assembly of a metallomacrocycle and as precatalysts for gold(I)-catalysed reactions.

Graphical abstract: Gold(i) “click” 1,2,3-triazolylidenes: synthesis, self-assembly and catalysis

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C0CC02185G
Article type
Communication
Submitted
29 6月 2010
Accepted
04 8月 2010
First published
23 8月 2010

Chem. Commun., 2011,47, 328-330

Permissions

Request permissions

Gold(I) “click” 1,2,3-triazolylidenes: synthesis, self-assembly and catalysis

K. J. Kilpin, U. S. D. Paul, A. Lee and J. D. Crowley, Chem. Commun., 2011, 47, 328 DOI: 10.1039/C0CC02185G

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