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• W2049551452 abstract "We present a combined density functional theory (DFT)/time-dependent density functional theory (TDDFT) study of the geometry, electronic structure, and absorption and emission properties of the tetranuclear “cubane” Cu4I4py4 (py = pyridine) system. The geometry of the singlet ground state and of the two lowest triplet states of the title complex were optimized, followed by TDDFT excited-state calculations. This procedure allowed us to characterize the nature of the excited states involved in the absorption spectrum and those responsible for the dual emission bands observed for this complex. In agreement with earlier experimental proposals, we find that while in absorption the halide-to-pyridine charge-transfer excited state (XLCT*) has a lower energy than the cluster-centered excited state (CC*), a strong geometrical relaxation on the triplet cluster-centered state surface leads to a reverse order of the excited states in emission." @default.
• W2049551452 created "2016-06-24" @default.
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• W2049551452 date "2006-11-23" @default.
• W2049551452 modified "2023-10-11" @default.
• W2049551452 title "Electronic Transitions Involved in the Absorption Spectrum and Dual Luminescence of Tetranuclear Cubane [Cu₄I₄(pyridine)₄] Cluster: a Density Functional Theory/Time-Dependent Density Functional Theory Investigation" @default.
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• W2049551452 doi "https://doi.org/10.1021/ic061147f" @default.
• W2049551452 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/17173412" @default.
• W2049551452 hasPublicationYear "2006" @default.
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