Journal
CHEMPLUSCHEM
Volume 78, Issue 5, Pages 413-418Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cplu.201300009
Keywords
coordination chemistry; iridium; ligand effects; N; O ligands
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Funding
- National Science Foundation of China (NSFC) [20975074, 21072218, 20902066]
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Three biscyclometalated iridium(III) complexes with three different ancillary ligands have been investigated with respect to the final products of acid-induced transformation in coordinating or non-coordinating solvents. All of these complexes, represented as [Ir(LC boolean AND N)2LO boolean AND O] and [Ir(LC boolean AND N)2LN boolean AND O], are susceptible to acid attack, followed by the departure of the ancillary ligand, LO boolean AND O or LN boolean AND O. Depending on the coordinating ability of the solvent molecule and whether or not a coordinating anion exists, the final product will be either a solvento complex or a dichloro-bridged iridium(III) dimer. Although coexistence of the solvento complex and dichloro-bridged iridium(III) dimer was observed under certain conditions, the conversion of the solvento complex into the dichloro-bridged iridium(III) dimer has been proven.
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