2018
DOI: 10.1039/c8ra01330f
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Solvent-tuned charge-transfer properties of chiral Pt(ii) complex and TCNQ˙ anion adducts

Abstract: A new couple of charge transfer adducts comprising of one chiral Pt(ii) complex cation together with one TCNQ˙− anion have been prepared, and solvent-induced variances of absorption, luminescence as well as chiral spectra have been investigated.

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Cited by 2 publications
(1 citation statement)
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“…Chiral sorting corresponds to enantiomeric self-recognition or enantiomeric self-discrimination, and these processes have been documented for supramolecular systems, metal complexes, and organic systems, including macrocyclic compounds. Chiral sorting phenomena are most often demonstrated for solid state, while examples of enantiomeric self-recognition well documented for solutions of metal complexes are less common. Another important issue in the synthesis of elaborate enantiopure metal complexes or supramolecular assemblies is chirality transfer, e.g., the transmission of chiral information from enantiopure ligands to metal centers. While there are many chiral transition metal complexes with well-defined stable configurations, the control over chirality of lanthanide complexes, in particular polynuclear complexes, , is more difficult due to the lack of spatial preferences, lability, and high-coordination numbers of these ions.…”
Section: Introductionmentioning
confidence: 99%
“…Chiral sorting corresponds to enantiomeric self-recognition or enantiomeric self-discrimination, and these processes have been documented for supramolecular systems, metal complexes, and organic systems, including macrocyclic compounds. Chiral sorting phenomena are most often demonstrated for solid state, while examples of enantiomeric self-recognition well documented for solutions of metal complexes are less common. Another important issue in the synthesis of elaborate enantiopure metal complexes or supramolecular assemblies is chirality transfer, e.g., the transmission of chiral information from enantiopure ligands to metal centers. While there are many chiral transition metal complexes with well-defined stable configurations, the control over chirality of lanthanide complexes, in particular polynuclear complexes, , is more difficult due to the lack of spatial preferences, lability, and high-coordination numbers of these ions.…”
Section: Introductionmentioning
confidence: 99%