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Coordination chemistry of copper(I) complexes with bis(phosphine) ligands

Thomas, JM and Madarasi, PK and Sivasankar, C and Samuelson, AG (2019) Coordination chemistry of copper(I) complexes with bis(phosphine) ligands. [Book Chapter]

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Official URL: https://doi.org/10.1016/B978-0-12-815052-8.00007-5

Abstract

The simple mixing of copper(I) compounds with bisphosphines led to the formation of copper(I) complexes with chelating or bridging bisphosphines. A wide vasriety of mononuclear, dinuclear, and polynuclear complexes result. The bisphosphine plays a key role in determining the nuclearity, coordination number, and structure of the complexes formed. Significant deviations from the expected tetrahedral or trigonal coordination geometries are often dictated by the substituents on the phosphorus. The plasticity of the coordination sphere of copper(I) permits distortions from ideal geometries. Limitless variation of substituents on phosphorus, including the possibility of having chiral phosphines, has played a key role in the utility of these copper(I) complexes. Although catalytic reactions promoted by copper(I) complexes do not involve redox transformations, they are useful in chiral transformations.

Item Type: Book Chapter
Publication: Copper(I) Chemistry of Phosphines, Functionalized Phosphines and Phosphorus Heterocycles
Publisher: Elsevier
Additional Information: The copyright for this article belongs to Elsevier.
Keywords: 1D coordination polymers; Adamantanoid frameworks; Bisphosphines; C-C bond formation; C-N bond formation; C-Si bond formation; Catalysis; Copper(I); Cytotoxicity; Dppe; Polynuclear; Radioactive tracers
Department/Centre: Division of Chemical Sciences > Inorganic & Physical Chemistry
Date Deposited: 29 Nov 2022 07:03
Last Modified: 29 Nov 2022 07:03
URI: https://eprints.iisc.ac.in/id/eprint/78108

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