Loughborough University
Browse
Manuscript (LUPIN, MBSmith).pdf (336.74 kB)

Intramolecular hydrogen-bonded tertiary phosphines as 1,3,5-triaza-7-phosphaadamantane (PTA) analogues

Download (336.74 kB)
journal contribution
posted on 2014-09-29, 14:19 authored by Allen T. Ekubo, Mark ElsegoodMark Elsegood, Andrew Lake, Martin SmithMartin Smith
New cationic trialkylphosphines [P(CH2NH2R){CH2N(R)CH2N(R)CH2}]+ (R ) C6H5CH2, a; 4-FC6H4CH2, b), as their Cl- (1a, 1b), SbF6 - (2a, 2b), and PF6 - (3a, 3b) salts, are described. The phosphine framework is conformationally locked, in the solid state, through pairs of intramolecular N-H · · · N hydrogen bonds which are maintained in the RuII and RhIII complexes 4 and 5. Phosphines 1a-3b can be considered as charged variants of the well-known PTA ligand.

Funding

We thank the EPSRC, Loughborough University, and Niger Delta University, Bayelsa State, Nigeria, for funding (A.T.E., A.J.L.). Rhodia UK Ltd. (Dr. Ranbir Padda) and Johnson Matthey are gratefully acknowledged for their kind donations of THPC and precious metal salts, respectively. We wish to acknowledge the use of the EPSRC Chemical Database Service at Daresbury.

History

School

  • Science

Department

  • Chemistry

Published in

INORGANIC CHEMISTRY

Volume

48

Issue

6

Pages

2633 - 2638 (6)

Citation

EKUBO, A.T. ... et al, 2009. Intramolecular hydrogen-bonded tertiary phosphines as 1,3,5-triaza-7-phosphaadamantane (PTA) analogues. Inorganic Chemistry, 48 (6), pp. 2633 - 2638.

Publisher

© American Chemical Society

Version

  • SMUR (Submitted Manuscript Under Review)

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

2009

Notes

This document is the unedited Author’s version of a Submitted Work that was subsequently accepted for publication in Inorganic Chemistry, copyright © American Chemical Society after peer review. To access the final edited and published work see: http://dx.doi.org/10.1021/ic801709z

ISSN

0020-1669

Language

  • en

Usage metrics

    Loughborough Publications

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC