N-oxyl-mediated electrooxidation in ionic liquid. A prominent approach to totally closed system

Manabu Kuroboshi, Junko Fujisawa, Hideo Tanaka

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

N-Oxyl-mediated electrooxidation of sec-alcohols in ionic liquids was performed successfully to give the corresponding ketones. By use of ionized N-oxyl, [TEMPOmim] [Tf2N], both the ionic liquids and the N-oxyl compound could be recovered and reused for the electrooxidation of alcohols.

Original languageEnglish
Pages (from-to)846-848
Number of pages3
JournalElectrochemistry
Volume72
Issue number12
Publication statusPublished - Dec 2004

Fingerprint

Ionic Liquids
Electrooxidation
Ionic liquids
Alcohols
Ketones

Keywords

  • Electrooxidation of alcohol
  • Ionic liquid
  • N-Oxyl

ASJC Scopus subject areas

  • Electrochemistry

Cite this

N-oxyl-mediated electrooxidation in ionic liquid. A prominent approach to totally closed system. / Kuroboshi, Manabu; Fujisawa, Junko; Tanaka, Hideo.

In: Electrochemistry, Vol. 72, No. 12, 12.2004, p. 846-848.

Research output: Contribution to journalArticle

@article{c9b41d10d2634b9fb979d079a92d7024,
title = "N-oxyl-mediated electrooxidation in ionic liquid. A prominent approach to totally closed system",
abstract = "N-Oxyl-mediated electrooxidation of sec-alcohols in ionic liquids was performed successfully to give the corresponding ketones. By use of ionized N-oxyl, [TEMPOmim] [Tf2N], both the ionic liquids and the N-oxyl compound could be recovered and reused for the electrooxidation of alcohols.",
keywords = "Electrooxidation of alcohol, Ionic liquid, N-Oxyl",
author = "Manabu Kuroboshi and Junko Fujisawa and Hideo Tanaka",
year = "2004",
month = "12",
language = "English",
volume = "72",
pages = "846--848",
journal = "Electrochemistry",
issn = "1344-3542",
publisher = "Electrochemical Society of Japan",
number = "12",

}

TY - JOUR

T1 - N-oxyl-mediated electrooxidation in ionic liquid. A prominent approach to totally closed system

AU - Kuroboshi, Manabu

AU - Fujisawa, Junko

AU - Tanaka, Hideo

PY - 2004/12

Y1 - 2004/12

N2 - N-Oxyl-mediated electrooxidation of sec-alcohols in ionic liquids was performed successfully to give the corresponding ketones. By use of ionized N-oxyl, [TEMPOmim] [Tf2N], both the ionic liquids and the N-oxyl compound could be recovered and reused for the electrooxidation of alcohols.

AB - N-Oxyl-mediated electrooxidation of sec-alcohols in ionic liquids was performed successfully to give the corresponding ketones. By use of ionized N-oxyl, [TEMPOmim] [Tf2N], both the ionic liquids and the N-oxyl compound could be recovered and reused for the electrooxidation of alcohols.

KW - Electrooxidation of alcohol

KW - Ionic liquid

KW - N-Oxyl

UR - http://www.scopus.com/inward/record.url?scp=11844272634&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=11844272634&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:11844272634

VL - 72

SP - 846

EP - 848

JO - Electrochemistry

JF - Electrochemistry

SN - 1344-3542

IS - 12

ER -