A Simple Manganese(I) Catalyst for the Efficient and Selective Hydrophosphination of Olefins with PH₃, Primary, and Secondary Phosphanes


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Date

2024-04-05

Publication Type

Journal Article

ETH Bibliography

yes

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Abstract

A tridentate ligand L with a P,NH,N donor motif was synthesized in few steps from commercially available precursors. Upon reaction with [MnBr(CO)₅], an octahedral 18-electron complex [Mn(CO)₃(L)]Br (1) is obtained in which L adopts a facial arrangement. After deprotonation of the NH group in the cationic complex unit, a neutral Mn(I) amido complex [Mn(CO)₂(L-H)] (2) is formed under loss of CO. Rearrangement of L-H leads to a trigonal bipyramidal structure in which the P and N donor centers are in trans position. Further deprotonation of 2 results in a dep-blue anionic complex fragment [Mn(CO)₂(L-2H)]⁻ (3). DFT calculations and a QTAIM analysis show that the amido complex 2 contains a Mn-N bond with partial double bond character and 3 an aromatic MnN₂C₂ ring. The anion [Mn(CO)₂(L-2H)]⁻ reacts with Ph₂PH to give a phosphido complex, which serves as phosphide transfer reagent to activated olefins. But the catalytic activity is low. However, the neutral amido complex 2 is an excellent catalyst and with loadings as low as 0.04 mol %, turn over frequencies of >40’000 h⁻¹ can be achieved. Furthermore, secondary and primary alkyl phosphines as well as PH₃ can be added in a catalytic hydrophosphination reaction to a wide range of activated olefins such as α,β-unsaturated aldehydes, ketones, esters, and nitriles. But also, vinyl pyridine and some styrene derivatives are converted into the corresponding phosphanes.

Publication status

published

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Volume

30 (20)

Pages / Article No.

Publisher

Wiley-VCH

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Edition / version

Methods

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Subject

Manganese(I) Catalyzed; Hydrophosphination; Michael addition; Catalytic studies; Mechanistic studies

Organisational unit

03447 - Grützmacher, Hansjörg (emeritus) / Grützmacher, Hansjörg (emeritus) check_circle
02024 - Small Molecule Crystallography Center check_circle

Notes

Funding

181966 - Coordinated radicals and catalyzed dehydrogenation reactions II (SNF)
ETH-46 21-1 - Lewis-acid promoted synthesis of primary and secondary phosphanes (ETHZ)

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