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Reversible Hydride Migration from C 5 Me 5 to Rh I Revealed by a Cooperative Bimetallic Approach
Author(s) -
Alférez Macarena G.,
Moreno Juan J.,
Hidalgo Nereida,
Campos Jesús
Publication year - 2020
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.202008442
Subject(s) - bimetallic strip , cyclopentadienyl complex , rhodium , chemistry , intramolecular force , catalysis , hydride , reactivity (psychology) , organometallic chemistry , activation barrier , stereochemistry , crystallography , medicinal chemistry , metal , organic chemistry , medicine , alternative medicine , pathology
The use of cyclopentadienyl ligands in organometallic chemistry and catalysis is ubiquitous, mostly due to their robust spectator role. Nonetheless, increasing examples of non‐innocent behaviour are being documented. Here, we provide evidence for reversible intramolecular C−H activation at one methyl terminus of C 5 Me 5 in [( η ‐C 5 Me 5 )Rh(PMe 3 ) 2 ] to form a new Rh−H bond, a process so far restricted to early transition metals. Experimental evidence was acquired from bimetallic rhodium/gold structures in which the gold center binds either to the rhodium atom or to the activated Cp* ring. Reversibility of the C−H activation event regenerates the Rh I and Au I monometallic precursors, whose cooperative reactivity towards polar E−H bonds (E=O, N), including the N−H bonds in ammonia, can be understood in terms of bimetallic frustration.