DFT studies of two-electron oxidation, photochemistry, and radical transfer between metal centres in the formation of platinum(iv) and palladium(iv) selenolates from diphenyldiselenide and metal(ii) reactants
Author:
Affiliation:
1. School of Natural Sciences – Chemistry
2. University of Tasmania
3. Hobart
4. Australia
5. Department of Chemistry
6. University of Western Ontario
7. London
8. Canada N6A 5B
Abstract
Excitation by light to the M–M antibonding orbital of [MIIIMe2(2,2′-bipyridine)(SePh)]2 releases 2[MIIIMe2(bipy)(SePh)]˙; the doublets react to give MIVMe2(bipy)(SePh)2 and MIIMe2(bipy).
Funder
Australian Research Council
National Computational Infrastructure
Publisher
Royal Society of Chemistry (RSC)
Subject
Inorganic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2020/DT/D0DT02978E
Reference23 articles.
1. Oxidative addition of E–E bonds (E = Group 16 element) to platinum(II): a route to platinum(IV) thiolate and selenolate complexes
2. Oxidation of Complexes by (O2CPh)2 and (ER)2 (E = S, Se), Including Structures of Pd(CH2CH2CH2CH2)(SePh)2(bpy) (bpy = 2,2‘-Bipyridine) and MMe2(SePh)2(L2) (M = Pd, Pt; L2 = bpy, 1,10-Phenanthroline) and C···O and C···E Bond Formation at Palladium(IV)
3. SnBrMe3 and dichalcogenides (ER)2 as oxidants: Synthesis of platinum(IV) complexes, and C⋯C and C⋯E coupling from pallada(IV)cyclopentane complexes and PdMe2(EPh){(pz)3BH} {E=O2C, S, Se; [(pz)3BH]−=tris(pyrazol-1-yl)borate}
4. Reversible oxidative addition of a diaryl diselenide to a diorganopalladium(II) complex, carbon–selenium bond formation at palladium(IV), and structural studies of palladium(II) and platinum(IV) selenolates
5. Fine-Tuning the Basicity of Metal Complexes: Reversible Oxidative Addition of Se−Se Bonds to Platinum(II) Precursors
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