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Dynamic Behavior of an N ‐Metalated β‐Enaminoimine Complex − Preparation of N ‐Phosphanylenamine and β‐Enaminoimine Derivatives
Author(s) -
Maraval Alexandrine,
Owsianik Krzysztof,
Arquier Damien,
Igau Alain,
Coppel Yannick,
Donnadieu Bruno,
Zablocka Maria,
Majoral JeanPierre
Publication year - 2003
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.200390128
Subject(s) - chemistry , transmetalation , intramolecular force , imine , coordination complex , proton , nuclear magnetic resonance spectroscopy , hydrogen bond , chelation , bent molecular geometry , crystal structure , medicinal chemistry , crystallography , stereochemistry , organic chemistry , molecule , catalysis , physics , quantum mechanics , metal
Variable‐temperature NMR spectroscopy of the β‐enaminoimine complex 2 showed a dynamic process which was attributed to an internal fluxional aldimido N ‐zirconated π‐linear/σ‐bent structure. Such an internal rearrangement has been previously proposed to occur in these systems but never observed. We have prepared a variety of ( N ‐phosphanyl‐β‐enamino)imine ligands using the hydrozirconation/transmetalation reaction of malonodinitrile compounds RCH(CN) 2 (R = H, PPh 2 ). In addition to their potential uses in coordination chemistry, these systems are good tools for the study of intramolecular hydrogen bonding. The X‐ray crystal structure of 14 at 180 K shows an unsymmetrical system with the N(H) proton localized on one of the two chelating nitrogen atoms, consistent with the existence in solution of a low barrier proton transfer process with a double‐well potential. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)