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Substitution Reactions at Dipp BIAN Supported Fluoroantimony Cations Yielding Cyanoantimony and Azidoantimony Cations
Author(s) -
Suter Riccardo,
Frazee Christopher,
Burford Neil,
McDonald Robert,
Ferguson Michael J.
Publication year - 2017
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201703951
Subject(s) - chemistry , cationic polymerization , antimony , medicinal chemistry , substituent , ligand (biochemistry) , acenaphthene , coordination complex , stereochemistry , inorganic chemistry , organic chemistry , metal , biochemistry , receptor , pyrene
This work presents new cationic coordination complexes of antimony with the 1,2‐bis[(2,6‐diisopropylphenyl)imino]acenaphthene ( Dipp BIAN) ligand system. The fluoroantimony complexes [ SbF ( Dipp BIAN)][OTf] 2 and [ SbF 2 ( Dipp BIAN)][OTf] have been successfully isolated and characterized. The fluorine substituent in the Lewis acidic complex [ SbF ( Dipp BIAN)][OTf] 2 can be selectively replaced without degradation of the Sb‐ Dipp BIAN interaction to give the first dicationic azido and cyano derivatives, [ Sb(CN) ( Dipp BIAN)][OTf] 2 and [ Sb(N 3 ) ( Dipp BIAN)][OTf] 2 , which have been isolated and structurally characterized.
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