Facile C-H bond cleavage via a proton-coupled electron transfer involving a C-H...Cu(II) interaction.
Facile C-H bond cleavage via a proton-coupled electron transfer involving a C-H...Cu(II) interaction.
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DOI:
10.1021/ja101599e
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发表时间:
2010-09-08
影响因子:
15
通讯作者:
Stack, T. Daniel P.
中科院分区:
文献类型:
--
作者:
Ribas, Xavi;Calle, Carlos;Poater, Albert;Casitas, Alicia;Gomez, Laura;Xifra, Rauel;Parella, Teodor;Benet-Buchholz, Jordi;Schweiger, Arthur;Mitrikas, George;Sola, Miguel;Llobet, Antoni;Stack, T. Daniel P.
The present study provides mechanistic details of a mild aromatic C-H activation effected by a copper(II) center ligated in a triazamacrocylic ligand, affording equimolar amounts of CuIII-aryl species and CuI as reaction products. At low-temperatures the CuII complex 1 forms a 3-center 3-electron C-H⋯CuII interaction, identified by pulse-EPR spectroscopy and supported by density functional theory (DFT) calculations. C-H bond cleavage is coupled with copper oxidation, as a CuIII-aryl product 2 is formed. This reaction proceeds to completion at 273 K within minutes through either a copper disproportionation reaction or, alternatively, an even faster reaction with one-equivalent of TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl), quantitatively yielding 2. Kinetic studies of both reactions strongly implicate a rate-limiting proton coupled electron transfer (PCET) as the key C-H activation step, a mechanism that does not conform to either the C-H activation mechanism in a NiII analogue or to any previously proposed C-H activation mechanisms.
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影响因子:
4.4
作者:
BECKE, AD
通讯作者:
BECKE, AD
影响因子:
2.9
作者:
Barone, V;Cossi, M
通讯作者:
Cossi, M
影响因子:
2.3
作者:
BROOKHART, M;GREEN, MLH
通讯作者:
GREEN, MLH
影响因子:
4.6
作者:
Chmielewski, PJ;Latos-Grazynski, L;Schmidt, I
通讯作者:
Schmidt, I
DOI:
10.1021/ci00011a011
发表时间:
1993-01-01
期刊:
JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES
影响因子:
--
作者:
KRYGOWSKI, TM
通讯作者:
KRYGOWSKI, TM