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由阴离子铼(I)β-二酮腙生成的异四核 Re-Zn-Zn-Re 配合物。

Heterotetrametallic Re-Zn-Zn-Re Complex Generated by an Anionic Rhenium(I) β-Diketiminate.

机构信息

Department of Chemistry , University of California, Berkeley , Berkeley , California 94720 , United States.

Chemical Sciences Division , Lawrence Berkeley National Laboratory , Berkeley , California 94720 , United States.

出版信息

J Am Chem Soc. 2019 Jan 16;141(2):800-804. doi: 10.1021/jacs.8b12494. Epub 2019 Jan 8.

Abstract

We report the synthesis of an anionic rhenium(I) compound, Na[Re(η-Cp)(BDI)] (1; Cp = cyclopentadienide, BDI = N, N'-bis(2,6-diisopropylphenyl)-3,5-dimethyl-β-diketiminate) and initial investigations of its use as a strong chemical reductant and metalloligand. Chemical oxidation of 1 gives a rare example of a rhenium(II) compound Re(η-Cp)(BDI) (2), while protonation of 1 yields the rhenium(III) hydride complex Re(H)(η-Cp)(BDI) (3). The reaction of 1 with ZnCl generated both 2 and the zinc(I) compound [ZnRe(η-Cp)(BDI)] (4), which features a linear, tetrametallic Re(I)-Zn(I)-Zn(I)-Re(I) core. Computational studies of 4 were performed to characterize the metal-metal bonding interactions; the results indicate a dative interaction from rhenium to zinc and covalent bonding between the two zinc centers. One-electron oxidation of 4 yielded both 2 and the triflate-bridged zinc(II) complex [(μ-OTf)ZnRe(η-Cp)(BDI)] (5, OTf = trifluoromethanesulfonate).

摘要

我们报告了一种阴离子铼(I)化合物 Na[Re(η-Cp)(BDI)](1;Cp = 环戊二烯基,BDI = N,N'-双(2,6-二异丙基苯基)-3,5-二甲基-β-二酮亚胺基)的合成及其作为强化学还原剂和金属配体的初步研究。1 的化学氧化得到了一个罕见的铼(II)化合物 Re(η-Cp)(BDI)(2)的例子,而 1 的质子化则得到了铼(III)氢化物配合物 Re(H)(η-Cp)(BDI)(3)。1 与 ZnCl 的反应同时生成了 2 和锌(I)化合物 [ZnRe(η-Cp)(BDI)](4),其具有线性的四配位 Re(I)-Zn(I)-Zn(I)-Re(I)核心。对 4 进行了计算研究以表征金属-金属键合相互作用;结果表明,铼到锌的配位作用和两个锌中心之间的共价键合。4 的单电子氧化生成了 2 和三氟甲磺酸桥接的锌(II)配合物 [(μ-OTf)ZnRe(η-Cp)(BDI)](5,OTf = 三氟甲磺酸根)。

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