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Cationic Homoleptic Vanadium( II ), ( IV ), and ( V ) Complexes Arising from Protonolysis of [V(NEt 2 ) 4 ]
Author(s) -
Choukroun Robert,
Moumboko Pierre,
Chevalier Sandrine,
Etienne Michel,
Donnadieu Bruno
Publication year - 1998
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/(sici)1521-3773(19981204)37:22<3169::aid-anie3169>3.0.co;2-0
Subject(s) - protonolysis , vanadium , cationic polymerization , homoleptic , counterion , chemistry , inorganic chemistry , boron , oxidation state , salt (chemistry) , catalysis , polymer chemistry , ion , organic chemistry , metal
At least three different cationic species arise in the classic protonolysis of [V IV (NEt 2 ) 4 ] with a borate ammonium salt. The unexpected formation of the vanadium( V ) species [V(NEt 2 ) 4 ][B(C 6 H 5 ) 4 ] (shown in the picture without its counterion) underlines the problem of deducing the true oxidation state of vanadium species in Ziegler–Natta reactions.

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