Kongkiatkrai Pornwimon, Anusanti Thana, Chantarojsiri Teera
Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Mahidol University, Bangkok, 10400, Thailand.
ACS Org Inorg Au. 2024 Oct 20;4(6):620-627. doi: 10.1021/acsorginorgau.4c00051. eCollection 2024 Dec 4.
Carbon dioxide (CO) is an abundant and useful C feedstock for electrocarboxylation, a process that incorporates a carboxyl moiety into an organic molecule. In this work, three first-row transition metal CO reduction electrocatalysts, NiPDI (), NiTPA (), and Fe(salenCl) (), were explored as electrocarboxylation catalysts with benzyl chloride as a substrate. The cyclic voltammograms of all three catalysts showed current enhancements in the presence of benzyl chloride under a CO atmosphere. Introduction of DMAP as additives showed further current enhancement. Electrolyses with one-compartment cell generated a moderate yield of phenylacetic acid. Addition of MgBr was proven to be crucial to the formation of the carboxylate product. While the yield of carboxylation was moderate, this work showed an example of electrocarboxylation of benzyl chloride without using a metal electrode or sacrificial anode, which could lead to a more sustainable carboxylation methodology.
二氧化碳(CO)是用于电羧化反应的一种丰富且有用的碳原料,电羧化反应是将羧基部分引入有机分子的过程。在这项工作中,研究了三种第一行过渡金属CO还原电催化剂,NiPDI()、NiTPA()和Fe(salenCl)(),以苄基氯为底物作为电羧化催化剂。在CO气氛下,所有三种催化剂的循环伏安图在苄基氯存在下均显示出电流增强。引入DMAP作为添加剂显示出进一步的电流增强。用单室电解槽进行电解产生了中等产率的苯乙酸。事实证明,添加MgBr对羧酸盐产物的形成至关重要。虽然羧化产率中等,但这项工作展示了一个不使用金属电极或牺牲阳极的苄基氯电羧化的例子,这可能会导致一种更可持续的羧化方法。