Synthesis and structure of sterically hindered o-benzoquinone carboxylic acid

被引：2

作者：

Zherebtsov, Maxim A. ^{[1
,2
]}

Arsenyev, Maxim, V ^{[1
,2
]}

Baranov, Evgeny, V ^{[1
]}

Chesnokov, Sergey A. ^{[1
]}

Cherkasov, Vladimir K. ^{[1
,2
]}

机构：

[1] Russian Acad Sci, GA Razuvaev Inst Organometall Chem, Nizhnii Novgorod 603950, Russia

[2] NI Lobachevsky State Univ Nizhny Novgorod, Nizhnii Novgorod 603950, Russia

来源：

MENDELEEV COMMUNICATIONS | 2021年 / 31卷 / 02期

基金：

俄罗斯基础研究基金会;

关键词：

catechol; pyrocatechuic acid; oxidation; X-ray; o-quinone; cyclic voltammetry; MACROCYCLIC CHELATOR; MECHANISM; CATECHOL; QUINONE; REDUCTION; COMPLEXES; OXIDATION; ROUTE; GUEST;

D O I：

10.1016/j.mencom.2021.03.042

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

2,4-Di-tert-butyl-5,6-dioxocyclohexa-1,3-diene-1-carboxylic acid, an oxidized analogue of sterically hindered pyrocatechuic acid, was obtained from 4,6-di-tert-butyl-2,3dihydroxybenzaldehyde in four stages. The electrochemical reduction of this compound proceeds in two stages: the first reduction wave (Ered1 = ?0.24 V) is irreversible, while the second stage is partially reversible (E1/2, red2 = ?0.65 V). The molecular structure of the o-quinone carboxylic acid in the crystalline state was comfirmed by single-crystal X-ray analysis.

引用

页码：268 / 270

页数：3

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