Loughborough University
Browse

Versatile routes to selenoether functionalised tertiary phosphines

Download (125.48 kB)
journal contribution
posted on 2014-09-30, 12:53 authored by Tom J. Cunningham, Mark ElsegoodMark Elsegood, Paul KellyPaul Kelly, Martin SmithMartin Smith, Paul M. Staniland
New selenoether functionalised tertiary phosphines, based on aryl (2a, 2b) or alkyl (4) backbones, have been synthesised and characterised. P,Se-chelation has been achieved upon complexation to square-planar PtII (3a) or PdII (3b) metal centres. For 3a and 3b, weak non-covalent M◊ ◊ ◊ Se contacts were established using single crystal X-ray crystallography.

History

School

  • Science

Department

  • Chemistry

Published in

DALTON TRANSACTIONS

Volume

39

Issue

22

Pages

5216 - 5218 (3)

Citation

CUNNINGHAM, T.J. ... et al, 2010. Versatile routes to selenoether functionalised tertiary phosphines. Dalton Transactions, 39 (22), pp. 5216 - 5218.

Publisher

© The Royal Society of Chemistry

Version

  • AM (Accepted Manuscript)

Publisher statement

This work is made available according to the conditions of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) licence. Full details of this licence are available at: https://creativecommons.org/licenses/by-nc-nd/4.0/

Publication date

2010

Notes

This article was published in the journal, Dalton Transactions [© The Royal Society of Chemistry]. The definitive version is available at: http://dx.doi.org/10.1039/c0dt00004c

ISSN

1477-9226

Language

  • en

Usage metrics

    Loughborough Publications

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC