Premium
Mechanistic Insights on Concentrated Lithium Salt/Nitroalkane Electrolyte Based on Analogy with Fluorinated Alcohols
Author(s) -
Shida Naoki,
Imada Yasushi,
Okada Yohei,
Chiba Kazuhiro
Publication year - 2020
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201901576
Subject(s) - chemistry , electrosynthesis , lithium perchlorate , lithium (medication) , electrolyte , cyclic voltammetry , perchlorate , salt (chemistry) , dimethoxymethane , dimethoxyethane , inorganic chemistry , redox , propylene carbonate , organic chemistry , alcohol , electrochemistry , catalysis , ion , electrode , medicine , endocrinology
Fluorinated alcohols such as 1,1,1,3,3,3‐hexafluoro2‐propanol (HFIP) and 2,2,2‐trifluoroethanol (TFE) have emerged as powerful solvents in oxidation chemistry including hole catalysis. In this paper, we describe the similarity of lithium salt/nitroalkane electrolytes with fluorinated alcohols in electrosynthesis. Based on the results from electrosynthesis, Raman and nuclear magnetic resonance spectroscopy and cyclic voltammetry (CV), we have demonstrated that the combination of lithium cation, perchlorate or sulfonimide anions, and nitroalkanes make up an ideal solution to stabilize radical cations, just like fluorinated alcohols. The CV results suggested that the radical cation of 1,4‐dimethoxybenzene is better stabilized in 1.0 m LiClO 4 than in a neat HFIP solution. A mechanistic proposal for this electrolyte system described herein will give new directions for designing reaction systems for a wide range of oxidation chemistries.