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末端镍(III)-氧加合物的表征与反应活性

Characterization and reactivity of a terminal nickel(III)-oxygen adduct.

作者信息

Pirovano Paolo, Farquhar Erik R, Swart Marcel, Fitzpatrick Anthony J, Morgan Grace G, McDonald Aidan R

机构信息

School of Chemistry and CRANN/AMBER Nanoscience Institute, The University of Dublin, Trinity College, College Green, Dublin 2 (Ireland).

出版信息

Chemistry. 2015 Feb 23;21(9):3785-90. doi: 10.1002/chem.201406485. Epub 2015 Jan 22.

Abstract

High-valent terminal metal-oxygen adducts are hypothesized to be the potent oxidizing reactants in late transition metal oxidation catalysis. In particular, examples of high-valent terminal nickel-oxygen adducts are scarce, meaning there is a dearth in the understanding of such oxidants. A monoanionic Ni(II)-bicarbonate complex has been found to react in a 1:1 ratio with the one-electron oxidant tris(4-bromophenyl)ammoniumyl hexachloroantimonate, yielding a thermally unstable intermediate in high yield (ca. 95%). Electronic absorption, electronic paramagnetic resonance, and X-ray absorption spectroscopies and density functional theory calculations confirm its description as a low-spin (S = 1/2), square planar Ni(III)-oxygen adduct. This rare example of a high-valent terminal nickel-oxygen complex performs oxidations of organic substrates, including 2,6-di-tert-butylphenol and triphenylphosphine, which are indicative of hydrogen atom abstraction and oxygen atom transfer reactivity, respectively.

摘要

高价末端金属-氧加合物被认为是晚期过渡金属氧化催化中强效的氧化反应物。特别是,高价末端镍-氧加合物的例子很少,这意味着对这类氧化剂的了解不足。已发现一种单阴离子Ni(II)-碳酸氢盐配合物与单电子氧化剂三(4-溴苯基)铵六氯锑酸盐以1:1的比例反应,高产率(约95%)生成一种热不稳定的中间体。电子吸收光谱、电子顺磁共振光谱、X射线吸收光谱以及密度泛函理论计算证实其为低自旋(S = 1/2)的平面正方形Ni(III)-氧加合物。这种高价末端镍-氧配合物的罕见例子能够对有机底物进行氧化反应,包括2,6-二叔丁基苯酚和三苯基膦,分别表明了氢原子夺取和氧原子转移反应活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34f0/4401485/b084c5ca34f6/nihms-676940-f0002.jpg

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