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  4. On the reactivity of the iminodiphosphane C6H4(o-CN)N=PPh2-PPh2: Fragmentation versus isomerisation
 
research article

On the reactivity of the iminodiphosphane C6H4(o-CN)N=PPh2-PPh2: Fragmentation versus isomerisation

Fei, ZF  
•
Scopelliti, R  
•
Dyson, PJ  
2004
European Journal of Inorganic Chemistry

The reactivity of the iminodiphosphane C6H4(o-CN)N= PPh2-PPh2, which contains an N=P-P unit, has been investigated. Reaction with small molecules, [viz. H2O/O-2, H2O2, CH3OH, C6H4(o-CN)NH2] and elemental sulfur result in cleavage of the P-P bond to give aminophosphane-derivatised compounds. The products from these reactions have been characterized spectroscopically, including two by single-crystal X-ray diffraction. The reactivity of the iminodiphosphane towards the transition metal complexes [M(cod)Cl-2] (M = Pd or Pt) has also been investigated. In the reactions, the immodiphosphane rearranges to form the more common diphosphonylamine (P-N-P) unit which chelates to the metal centres, Three different compounds were isolated from these reactions and they have all been fully characterised by spectroscopy and single-crystal X-ray diffraction. (C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.

  • Details
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Type
research article
DOI
10.1002/ejic.200300529
Author(s)
Fei, ZF  
Scopelliti, R  
Dyson, PJ  
Date Issued

2004

Published in
European Journal of Inorganic Chemistry
Issue

3

Start page

530

End page

537

Subjects

ligands (ph2p)(2)nh dppa

•

mixed-metal clusters

•

n-p backbone

•

coordination chemistry

•

crystal-structure

•

polyfunctional molecules

•

complexes

•

platinum(ii)

•

aminophosphines

•

palladium(ii)

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LCOM  
Available on Infoscience
November 9, 2005
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/219897
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