Jump to main content
Jump to site search

Issue 4, 2001
Previous Article Next Article

Novel organosulfur donors containing hydroxy functionalities: synthesis of bis[2,2-bis(hydroxymethyl)propane-1,3-diyldithio]tetrathiafulvalene and related materials

Author affiliations

Abstract

The synthesis of four novel organosulfur donors carrying two or more hydroxymethyl groups are described. TTF nuclei are fused to 1,4-dithiepine and/or 1,4-dithiine rings and in two cases both outer rings carry functionality capable of introducing hydrogen bonding; for the two chiral organosulfur donor molecules both racemic and enantiopure forms are prepared.

Graphical abstract: Novel organosulfur donors containing hydroxy functionalities: synthesis of bis[2,2-bis(hydroxymethyl)propane-1,3-diyldithio]tetrathiafulvalene and related materials [ ]

Back to tab navigation

Supplementary files

Article information


Submitted
21 Sep 2000
Accepted
22 Dec 2000
First published
01 Feb 2001

J. Chem. Soc., Perkin Trans. 1, 2001, 407-414
Article type
Paper

Novel organosulfur donors containing hydroxy functionalities: synthesis of bis[2,2-bis(hydroxymethyl)propane-1,3-diyldithio]tetrathiafulvalene and related materials

T. Ozturk, N. Saygili, S. Ozkara, M. Pilkington, C. R. Rice, D. A. Tranter, F. Turksoy and J. D. Wallis, J. Chem. Soc., Perkin Trans. 1, 2001, 407
DOI: 10.1039/B007660K

Search articles by author

Spotlight

Advertisements