Skip to content Skip to navigation
University of Warwick
  • Study
  • |
  • Research
  • |
  • Business
  • |
  • Alumni
  • |
  • News
  • |
  • About

University of Warwick
Publications service & WRAP

Highlight your research

  • WRAP
    • Home
    • Search WRAP
    • Browse by Warwick Author
    • Browse WRAP by Year
    • Browse WRAP by Subject
    • Browse WRAP by Department
    • Browse WRAP by Funder
    • Browse Theses by Department
  • Publications Service
    • Home
    • Search Publications Service
    • Browse by Warwick Author
    • Browse Publications service by Year
    • Browse Publications service by Subject
    • Browse Publications service by Department
    • Browse Publications service by Funder
  • Statistics
  • Help & Advice
University of Warwick

The Library

  • Login

Anodic oxidation of the dye materials methylene blue, acid blue 25, reactive blue 2 and reactive blue 15 and the characterisation of novel intermediate compounds in the anodic oxidation of methylene blue

Tools
- Tools
+ Tools

UNSPECIFIED. (2002) Anodic oxidation of the dye materials methylene blue, acid blue 25, reactive blue 2 and reactive blue 15 and the characterisation of novel intermediate compounds in the anodic oxidation of methylene blue. JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY, 77 (7). pp. 756-760. ISSN 0268-2575

Full text not available from this repository.
Official URL: http://dx.doi.org/10.1002/jctb.642

Abstract

Anodic oxidation of the dye molecules, methylene blue, acid blue 25, reactive blue 2 and reactive blue 15 in chloride solution leads to colour destruction but UV and TOC data show that the oxidation reactions do not lead to complete destruction of the organic molecules. Analysis of the anodic oxidation products of [3,7-bis (dimethylamino) phenothiazinium] chloride (methylene blue) in a chloride solution provides evidence for formation of seven neutral and two charged intermediates. The main intermediate is identified by its X-ray diffraction crystal structure and accurate mass spectrometry as the novel leuco dye 4,6-dichloro-7-dimethylamino-3H-phenothiazin-3-one, C14H10C12N2OS (I) formed by replacement of one of the dimethylamino groups of methylene blue with oxygen accompanied by regiospecific chlorination of the carbocyclic systems. The mass spectra of other intermediates formed are interpreted in terms of the structure of I. (C) 2002 Society of Chemical Industry.

Item Type: Journal Article
Subjects: T Technology > TP Chemical technology
Q Science > QD Chemistry
Journal or Publication Title: JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY
Publisher: JOHN WILEY & SONS LTD
ISSN: 0268-2575
Date: July 2002
Volume: 77
Number: 7
Number of Pages: 5
Page Range: pp. 756-760
Identification Number: 10.1002/jctb.642
Publication Status: Published
URI: http://wrap.warwick.ac.uk/id/eprint/10843

Data sourced from Thomson Reuters' Web of Knowledge

Request changes to a record

Actions (login required)

View Item View Item
twitter

Email us: publications@warwick.ac.uk
Contact Details
About Us