Excited states of metal-metal bonded diimine complexes vary from extremely long lived to very reactive with formation of radicals or zwitterions
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Physical and Theoretical Chemistry,Inorganic Chemistry
Reference37 articles.
1. Halide-Dependent Change of the Lowest-Excited-State Character from MLCT to XLCT for the Complexes Re(X)(CO)3(α-diimine) (X = Cl, Br, I; α-diimine = bpy, iPr-PyCa, iPr-DAB) Studied by Resonance Raman, Time-Resolved Absorption, and Emission Spectroscopy
2. Studies of intramolecular electron and energy transfer using the fac-(diimine)ReI(CO)3 chromophore
3. The Remarkable Properties of α-Diimine Rhenium Tricarbonyl Complexes in Their Metal-to-Ligand Charge-Transfer (MLCT) Excited States
4. Photochemistry of metal-metal bonded complexes. 5. Cleavage of the M-M bond in (OC)5M-M(CO)3L by irradiation into a low-lying M .fwdarw. L charge-transfer band
5. Competitive radiative decay and metal-metal bond cleavage from the lowest excited state of triphenyltin- and triphenylgermanium tricarbonyl(1,10-phenanthroline)rhenium
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