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Journal ArticleDOI

The thermodynamic driving force for CH activation at iridium

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TLDR
In this article, the relationship between the intermolecular oxidative addition reaction of carbon-hydrogen bonds in organic molecules to transition metal centres, and the dissociation energies of the CH, MH, and MR bonds that undergo changes during this process is discussed.
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This article is published in Polyhedron.The article was published on 1988-01-01. It has received 60 citations till now. The article focuses on the topics: Bond energy & Hydrogen bond.

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Citations
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Journal ArticleDOI

Activation of c-h bonds by metal complexes

TL;DR: In this article, it was shown that the same alkylhydridoplatinum(IV) complex is the intermediate in the reaction of ethane with platinum(II) σ-complexes.
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Complementary Strategies for Directed C(sp3 )-H Functionalization: A Comparison of Transition-Metal-Catalyzed Activation, Hydrogen Atom Transfer, and Carbene/Nitrene Transfer.

TL;DR: This Review discusses the strengths and weaknesses of three main approaches: transition-metal-catalyzed C-H activation, 1,n-hydrogen atom transfer, and transition- Metal-Catalyzed carbene/nitrene transfer, for the directed functionalization of unactivated C(sp3 )-H bonds.
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Selectivities in Hydrocarbon Activation: Kinetic and Thermodynamic Investigations of Reversible 1,2-RH-Elimination from (silox)2(tBu3SiNH)TiR (silox = tBu3SiO)

TL;DR: In this article, a first-order process for 1,2-RH/D-elimination from 2-R was shown to achieve 24.8 °C in the presence of C2H4, butadiene, HC2H, and HC2tBu.
References
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Principles and applications of organotransition metal chemistry

TL;DR: A perspective survey of organotransition metal complexes according to ligand substitution processes can be found in this paper, with a focus on transition metal complexes with metal carbon-bonded ligands.
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C-H and H-H Activation in Transition Metal Complexes and on Surfaces.

TL;DR: In this paper, the breaking of the H-H bond in H2 and a C-H link in CH4 on both discrete transition metal complexes and on Ni and Ti surfaces is studied, and the essential continuity and similarity of the physical and chemical processes in two cases is demonstrated.
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Aliphatic hydroxylation catalyzed by iron porphyrin complexes

TL;DR: Hydroxylation et oxydation de cyclohexane, cycloheptane et cis-decaline, selectivite et stereospecificite, and stereos pecificite are described.
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