Selective P4 Activation by a Highly Reduced Cobaltate: Synthesis of Dicobalt Tetraphosphido Complexes.
Selective P4 Activation by a Highly Reduced Cobaltate: Synthesis of Dicobalt Tetraphosphido Complexes.
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DOI：
10.1002/chem.201603296
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发表时间：
2017-05
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影响因子：
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通讯作者：
Stefan Pelties;Thomas M. Maier;D. Herrmann;B. de Bruin;C. Rebreyend;Stefanie Gärtner;I. Shenderovich;Robert Wolf
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文献类型：
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作者：
Stefan Pelties;Thomas M. Maier;D. Herrmann;B. de Bruin;C. Rebreyend;Stefanie Gärtner;I. Shenderovich;Robert Wolf
Although the chemistry of transition metal polyphosphide anions has attracted significant attention, there are few reports of studies in which such species have been synthesized directly from white phosphorus. [K(OEt2 )2 {Co(BIAN)(cod)}] (1, BIAN=1,2-bis(2,6-diisopropylphenylimino)acenaphthene, cod=1,5-cyclooctadiene), which is readily prepared by ligand exchange from [K(thf)x {Co(cod)2 }], reacts with P4 to afford [{K(thf)}2 {(BIAN)Co}2 (μ-η4 :η4 -P4 )] (2 a) in 61 % yield (isolated product). [{K(OEt2 )}2 {(BIAN)Co}2 (μ-η4 :η4 -P4 )] (2 b) and [K([18]crown-6)(MeCN)]2 [{(BIAN)Co}2 (μ-η4 :η4 -P4 )] (2 c) were obtained by recrystallizing 2 a from diethyl ether and acetonitrile (and using [18]crown-6 in case of 2 c). Oxidation of 2 a with [Cp2 Fe]BArF4 (one equivalent) and subsequent recrystallization of the product from different solvents gave [K(OEt2 ){(BIAN)Co}2 (μ-η4 :η4 -P4 )] (3 a) and [K(dme)4 ][{(BIAN)Co}2 (μ-η4 :η4 -P4 )] (3 b; dme=1,2-dimethoxyethane). Neutral [{(BIAN)Co}2 (μ-η4 :η4 -P4 )] (4) was obtained in moderate yield by oxidizing 2 a with two equivalents of [Cp2 Fe]BArF4 . The new complexes were characterized by NMR, EPR (in the case of 3 a), and UV/Vis spectroscopy, and elemental analysis. The molecular structures revealed by X-ray crystallography display planar cyclic or open-chain P44- units sandwiched between {(BIAN)Co} fragments.
Although the chemistry of transition metal polyphosphide anions has attracted significant attention, there are few reports of studies in which such species have been synthesized directly from white phosphorus. [K(OEt2 )2 {Co(BIAN)(cod)}] (1, BIAN=1,2-bis(2,6-diisopropylphenylimino)acenaphthene, cod=1,5-cyclooctadiene), which is readily prepared by ligand exchange from [K(thf)x {Co(cod)2 }], reacts with P4 to afford [{K(thf)}2 {(BIAN)Co}2 (μ-η4 :η4 -P4 )] (2 a) in 61 % yield (isolated product). [{K(OEt2 )}2 {(BIAN)Co}2 (μ-η4 :η4 -P4 )] (2 b) and [K([18]crown-6)(MeCN)]2 [{(BIAN)Co}2 (μ-η4 :η4 -P4 )] (2 c) were obtained by recrystallizing 2 a from diethyl ether and acetonitrile (and using [18]crown-6 in case of 2 c). Oxidation of 2 a with [Cp2 Fe]BArF4 (one equivalent) and subsequent recrystallization of the product from different solvents gave [K(OEt2 ){(BIAN)Co}2 (μ-η4 :η4 -P4 )] (3 a) and [K(dme)4 ][{(BIAN)Co}2 (μ-η4 :η4 -P4 )] (3 b; dme=1,2-dimethoxyethane). Neutral [{(BIAN)Co}2 (μ-η4 :η4 -P4 )] (4) was obtained in moderate yield by oxidizing 2 a with two equivalents of [Cp2 Fe]BArF4 . The new complexes were characterized by NMR, EPR (in the case of 3 a), and UV/Vis spectroscopy, and elemental analysis. The molecular structures revealed by X-ray crystallography display planar cyclic or open-chain P44- units sandwiched between {(BIAN)Co} fragments.