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Tetranuclear Copper(II) Complexes with Macrocyclic and Open‐Chain Disiloxane Ligands as Catalyst Precursors for Hydrocarboxylation and Oxidation of Alkanes and 1‐Phenylethanol
Author(s) -
Zaltariov MirelaFernanda,
Alexandru Mihaela,
Cazacu Maria,
Shova Sergiu,
Novitchi Ghenadie,
Train Cyrille,
Dobrov Anatolie,
Kirillova Marina V.,
Alegria Elisabete C. B. A.,
Pombeiro Armando J. L.,
Arion Vladimir B.
Publication year - 2014
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.201402578
Subject(s) - disiloxane , chemistry , catalysis , copper , cyclohexane , ligand (biochemistry) , medicinal chemistry , solvent , polymer chemistry , crystallography , organic chemistry , biochemistry , receptor
Two new tetranuclear copper(II) complexes [Cu 4 (μ 4 ‐O)( L 1 )Cl 4 ] ( 1 ) and [Cu 4 (μ 4 ‐O)( L 2 ) 2 Cl 4 ] ( 2 ), where H 2 L 1 is a macrocyclic ligand resulting from [2+2] condensation of 2,6‐diformyl‐4‐methylphenol (DFF) and 1,3‐bis(aminopropyl)tetramethyldisiloxane, and HL 2 is a 1:2 condensation product of DFF with trimethylsilyl p ‐aminobenzoate, have been prepared. The structures of the products were established by X‐ray diffraction. The complexes have been characterised by FTIR, UV/Vis spectroscopy, ESI mass‐spectrometry and magnetic susceptibility measurements. The latter revealed that the tetranuclear complexes can be described as two ferromagnetically coupled dinuclear units, in which the two copper(II) ions interact antiferromagnetically. The compounds act as homogeneous catalyst precursors for a number of single‐pot reactions, including (i) hydrocarboxylation, with CO, H 2 O and K 2 S 2 O 8 , of a variety of linear and cyclic( n = 5–8) alkanes into the corresponding C n +1 carboxylic acids, (ii) peroxidative oxidation of cyclohexane, and (iii) solvent‐free microwave‐assisted oxidation of 1‐phenylethanol.