Two new di-zinc-aryl complexes, [LZn Ph ] and [LZn (C F ) ], coordinated by a diphenol tetraamine macrocyclic ligand have been prepared and fully characterised, including by single-crystal X-ray diffraction experiments. The complexes' reactivities with monomers including carbon dioxide, cyclohexene oxide, phthalic anhydride, isopropanol and phenol were investigated using both experimental studies and density functional theory calculations. In particular, [LZn Ph ] readily inserts carbon dioxide to form a carboxylate, at 1 bar pressure, whereas [LZn (C F ) ] does not react. Under these conditions [LZn Ph ] shows moderate activity in the ring-opening copolymerisation of cyclohexene oxide/carbon dioxide (TOF=20 h ), cyclohexene oxide/phthalic anhydride (TOF=33 h ) and the ring-opening polymerisations of rac-lactide (TOF=99 h ) and ϵ-caprolactone (TOF=5280 h ).
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http://dx.doi.org/10.1002/chem.201701013 | DOI Listing |
Chemistry
May 2017
Department of Chemistry, Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford, OX2 3TA, UK.
Two new di-zinc-aryl complexes, [LZn Ph ] and [LZn (C F ) ], coordinated by a diphenol tetraamine macrocyclic ligand have been prepared and fully characterised, including by single-crystal X-ray diffraction experiments. The complexes' reactivities with monomers including carbon dioxide, cyclohexene oxide, phthalic anhydride, isopropanol and phenol were investigated using both experimental studies and density functional theory calculations. In particular, [LZn Ph ] readily inserts carbon dioxide to form a carboxylate, at 1 bar pressure, whereas [LZn (C F ) ] does not react.
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