Publication | Closed Access
Multiple Photoluminescence from 1,2‐Dinaphthyl‐<i>ortho</i>‐Carborane
156
Citations
35
References
2013
Year
Naphthyl-substituted Ortho-carboranesOrganic Charge-transfer CompoundPhotoluminescenceDerivativesMultiple PhotoluminescencePhotochemistryCarboranyl σ OrbitalEngineeringPhosphorescenceOrganic ChemistryChemistryNaphthyl π OrbitalLuminescence PropertyPhotophysical PropertyBiomolecular Engineering
Naphthyl-substituted ortho-carboranes, which were prepared following the reaction between acetylene and decarborane, showed unique multiple photoluminescence behavior associated with intramolecular charge transfer (see picture). On the basis of theoretical calculations, the photoluminescence is shown to originate from the overlap between the naphthyl π orbital and the carboranyl σ orbital.
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