Issue 40, 2005
From the journal:

Chemical Communications

Identification of new N–Sb topologies: understanding the sequential dehydrochloride coupling of primary amines and trichloropnictines

Neil Burford,*a   Ezra Edelstein,a   Jeff C. Landry,a   Michael J. Fergusonb  and  Robert McDonaldb  

* Corresponding authors

a Department of Chemistry, Dalhousie University, Halifax, Nova Scotia, Canada
E-mail: Neil.Burford@dal.ca
Fax: 1-902-494-1310
Tel: 1-902-494-3190

b X-ray Crystallography Laboratory, Chemistry Department, University of Alberta, Edmonton, AB, Canada

Abstract

Subtle steric strain imposed by 2,6-dimethylphenyl substituents on N–Sb frameworks has enabled identification of the first acyclic dipnictadiazane and the first six-membered cyclotristibatriazane providing insight into the dehydrohalide coupling reaction of amines with halopnictines.

Graphical abstract: Identification of new N–Sb topologies: understanding the sequential dehydrochloride coupling of primary amines and trichloropnictines

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B509481J
Article type
Communication
Submitted
04 Jul 2005
Accepted
17 Aug 2005
First published
13 Sep 2005

Chem. Commun., 2005, 5074-5076

Permissions

Request permissions

Identification of new N–Sb topologies: understanding the sequential dehydrochloride coupling of primary amines and trichloropnictines

N. Burford, E. Edelstein, J. C. Landry, M. J. Ferguson and R. McDonald, Chem. Commun., 2005, 5074 DOI: 10.1039/B509481J

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