期刊
DALTON TRANSACTIONS
卷 51, 期 26, 页码 10148-10159出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2dt01484j
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资金
- US National Institutes of Health [R35 GM139545-01]
- US National Science Foundation [CHE-1900141]
- Ohio State University Graduate School
This paper presents a practical method for the synthesis and isolation of cobalt(I) bis-phosphine complexes and their use in Co(I)-catalyzed reactions. These complexes exhibit good catalytic activity in low-valent cobalt-catalyzed reactions and can be used in various reactions with sensitive substrates. Additionally, these complexes are useful for synthesizing rare cationic complexes, which show excellent catalytic performance.
Although cobalt(I) bis-phosphine complexes have been implicated in many selective C-C bond-forming reactions, until recently relatively few of these compounds have been fully characterized or have been shown to be intermediates in catalytic reactions. In this paper we present a new practical method for the synthesis and isolation of several cobalt(I)-bis-phosphine complexes and their use in Co(I)-catalyzed reactions. We find that easily prepared (in situ generated or isolated) bis-phosphine and (2,6-N-aryliminoethyl) pyridine (PDI) cobalt(II) halide complexes are readily reduced by 1,4-bis-trimethylsilyl-1,4-dihydropyrazine or commercially available lithium nitride (Li3N), leaving behind only innocuous volatile byproducts. Depending on the structures of the bis-phosphines, the cobalt(I) complex crystallizes as a phosphine-bridged species [(P similar to P)Co-I[mu-(P similar to P)]Co-I(X)(P similar to P)] or a halide bridged species [(P similar to P)Co-I[mu-(X)](2)Co-I(P similar to P)]. Because the side-products are innocuous, these methods can be used for the in situ generation of catalytically competent Co(I) complexes for a variety of low-valent cobalt-catalyzed reactions of even sensitive substrates. These complexes are also useful for the synthesis of rare cationic [(P similar to P)Co-I-eta(4)-diene](+) X- or [(P similar to-P)Co-I-eta(6)-arene](+) X- complexes, which are shown to be excellent single-component catalysts for the following regioselective reactions of dienes: heterodimerizations with ethylene or methyl acrylate, hydroacylation and hydroboration. The reactivity of the single-component catalysts with the in situ generated species are also documented.
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