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Flexible kappa(4)-PNN ' O-tetradentate ligands: synthesis, complexation and structural studies

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posted on 29.09.2014, 14:29 authored by Sean E. Durran, Mark ElsegoodMark Elsegood, Shelly R. Hammond, Martin SmithMartin Smith
The three-step synthesis of new, air-stable, PNN′O-tetradentate ligands 3a·HH–3c·HH by Schiff base condensation of the 1° amines 2a–2c with 2-Ph2PC6H4(CHO) in refluxing EtOH is described. The racemic ligand 3d·HH, isolated in 79% yield, was successfully prepared from 2-C6H4(OH){C(O)NHCH2CH(Me)NH2} 2d and 2-Ph2PC6H4(CHO) in absolute EtOH... cont'd.

Funding

We should like to thank the EPSRC for funding, Johnson Matthey for the generous loan of precious metal salts and the EPSRC Mass Spectrometry Service Centre at Swansea. We also wish to acknowledge the use of the EPSRC’s Chemical Database Service at Daresbury.

History

School

  • Science

Department

  • Chemistry

Published in

DALTON TRANSACTIONS

Volume

39

Issue

30

Pages

7136 - 7146 (11)

Citation

DURRAN, S.E. ... et al, 2010. Flexible kappa(4)-PNN ' O-tetradentate ligands: synthesis, complexation and structural studies. Dalton Transactions, 39 (30), pp. 7136 - 7146.

Publisher

© Royal Society of Chemistry

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

2010

Notes

This article was published in the journal Dalton Transactions [© Royal Society of Chemistry]. The definitive version is available at: http://dx.doi.org/10.1039/c0dt00200c

ISSN

1477-9226

Language

en

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