A Crystalline Bismuth(II) Radical Anion: Synthesis, Characterization, and Reactivity.

IF 16.9
Sotirios Pavlidis, Christian Teutloff, Ana Guilherme Buzanich, Konstantin B Krause, Franziska Emmerling, Robert Bittl, Josh Abbenseth
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Abstract

We report the synthesis of a planarized tris-amidobismuthane supported by a rigid, bulky NNN pincer ligand, which enforces a T-shaped geometry at the bismuth center. The Bi(NNN) complex features a low-lying LUMO with distinct Bi(6p) orbital character as shown by DFT calculations. Cyclic voltammetry reveals a fully reversible one-electron reduction at E1/2 = -1.85 V versus Fc0/+ in THF. Chemical reduction with KC8 in the presence of 4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo[8.8.8]hexacosane (222-crypt) enables the isolation of an unprecedented Bi(II) radical anion in high isolated yields. Multi-frequency EPR, X-ray absorption spectroscopy and SQUID magnetometry complemented by theoretical calculations confirm localization of the unpaired electron on the bismuth center. Preliminary reactivity studies display radical reactivity as shown by single-electron transfer chemistry and radical coupling reactions.

晶体铋(II)自由基阴离子:合成、表征和反应性。
我们报道了一种由刚性、笨重的NNN钳形配体支撑的平面化三氨基甲烷的合成,该配体在铋中心形成了t形几何结构。DFT计算表明,Bi(NNN)配合物具有明显的Bi(6p)轨道特征的低洼LUMO。循环伏安法显示,在E1/2 = -1.85 V时,与f0 /+相比,THF具有完全可逆的单电子还原。在4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo[8.8.8] hexocosane (222-crypt)存在下,用KC8化学还原可以分离出前所未有的Bi(II)自由基阴离子,分离收率很高。多频EPR、x射线吸收光谱和SQUID磁强计结合理论计算证实了未配对电子在铋中心的定位。初步的反应性研究显示了单电子转移化学和自由基偶联反应显示的自由基反应性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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