Journal
INORGANIC CHEMISTRY
Volume 61, Issue 1, Pages 32-36Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.1c03391
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- Ministry of Science, ICT & Future Planning [NRF-2019R1A2C1001989]
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Two dinuclear palladium complexes were selectively synthesized from chiral Schiff base tridentate ligands using acetonitrile and ethanol, with one complex being the first example connected only by a bridging acetonitrile. Theoretical calculations supported the formation of these complexes.
From the chiral Schiff base tridentate ligand LPh, unusual acetonitrile-bridged dinuclear palladium complex 1 and organopalladium complex 1' were synthesized selectively by using acetonitrile and ethanol, respectively. The chiral tridentate Schiff base ligand was bound to the palladium metal center with different chelation modes ([ONO] for 1 and [CNO] for 1'). Complex 1 constitutes the first example of dinuclear metal complexes connected only by a bridging acetonitrile, in which an exceptionally short C N bond distance [0.945(12) angstrom] of bridged acetonitrile was observed. To study the influence of a phenyl group attached to an imine, the phenyl-free ligand LH was prepared and used. In that case, an acetonitrile bridge was not observed. Theoretical calculation studies supporting the formation of 1 and 1' are favored.
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