Department of Chemistry and Biochemistry, Center for Biomolecular Structure and Dynamics, University of Montana, Missoula, MT 59812, United States.
Department of Chemistry and Biochemistry, New Mexico State University, Las Cruces, NM 88003, United States.
J Inorg Biochem. 2024 Jul;256:112552. doi: 10.1016/j.jinorgbio.2024.112552. Epub 2024 Apr 9.
In this work, we report the generation and characterization of two new Co(III)-peroxo complexes 2 and 3. 2 is best described as a mononuclear Co-(O) complex that exhibits an O-isotope sensitive OO bond stretching vibration at 845(-49) cm, indicating a relatively weak peroxo moiety compared to those of other Co-(O) complexes reported previously. Complex 3 is a Co-peroxo-arylboronate species having a rare {CoOOBO} five-membered metallocycle, which is structurally characterized using X-ray crystallography. Investigations of the reaction mechanism using density functional theory calculations show that 2 likely undergoes a nucleophilic attack to an arylboronic acid, which is generated by hydrolysis of the BPh anion in wet acetonitrile solution, to first form a Co-peroxo-arylboronic acid adduct, followed by the loss of one benzene molecule to generate the five-membered metallocycle. The entire reaction is thermodynamically favorable. Taken together, the conversion of 2 to 3 represents the discovery of a novel nucleophilic reactivity that can be carried out by mononuclear Co(III)-peroxo complexes.
在这项工作中,我们报告了两种新型 Co(III)-过氧配合物 2 和 3 的生成和表征。2 最好被描述为单核 Co-(O) 配合物,其在 845(-49) cm 处表现出对 O 同位素敏感的 OO 键伸缩振动,表明与以前报道的其他 Co-(O) 配合物相比,过氧部分相对较弱。配合物 3 是一种 Co-过氧芳基硼酸物种,具有罕见的{CoOOBO}五元金属环,通过 X 射线晶体学进行结构表征。使用密度泛函理论计算研究反应机理表明,2 可能首先经历亲核攻击芳基硼酸,芳基硼酸由 BPh 阴离子在湿乙腈溶液中的水解生成,然后形成 Co-过氧芳基硼酸加合物,随后失去一个苯分子生成五元金属环。整个反应在热力学上是有利的。总之,2 到 3 的转化代表了单核 Co(III)-过氧配合物可以进行的新型亲核反应性的发现。