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Modification of Titanium Isopropoxide with Aromatic Aldoximes
Author(s) -
Baumann Stefan O.,
Bendova Maria,
Puchberger Michael,
Schubert Ulrich
Publication year - 2011
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.201000881
Subject(s) - chemistry , oxime , benzaldehyde , monomer , medicinal chemistry , titanium , molar ratio , derivative (finance) , ligand (biochemistry) , dissolution , polymer chemistry , organic chemistry , catalysis , receptor , polymer , biochemistry , financial economics , economics
Dimeric [Ti(O i Pr) 2 (benzaldoximate) 2 ] 2 was obtained upon reaction of titanium isopropoxide with two molar equivalents of benzaldehyde ( E )‐ or ( Z )‐oxime or m ‐anisaldoxime. Two isomers were formed differing by the mutual orientation of the oximate ligands. Reaction with perillaldoxime or trans ‐cinnamaldoxime resulted in the corresponding derivatives with functional ligands. The degree of substitution was higher when o ‐ or p ‐anisaldoxime were employed in the same molar ratio, and dimeric Ti 2 (O i Pr) 3 ( o ‐anisaldoximate) 5 with a bridging oximate ligand and monomeric Ti(oximate) 4 (oximate = o ‐anisaldoximate or p ‐anisaldoximate) were obtained. Dissolution of the p ‐anisaldoximate derivative upon heating in [D 6 ]DMSO led to deoximation reactions.