Preparation of two stereoisomers of the macrocyclic electron donor tetramethoxycarbonyl[5.5]-tetrathiafulvalenophane with bridges containing two sulfur atoms

O. Neiland, V. Khodorkovskii, M. Utinans, I. Sudmale

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Isomers of a macrocycle containing two tetrathiafulvalene structural units joined by propylenedithio bridges are prepared. The electrochemical oxidation potentials are determined. Possible conformations of tetramethoxycarbonyl[5.5]tetrathiafulvalenophane are analyzed using the AM1 method.

Original languageEnglish
Pages (from-to)795-798
Number of pages4
JournalChemistry of Heterocyclic Compounds
Volume35
Issue number7
DOIs
StatePublished - 1 Jan 1999

ASJC Scopus subject areas

  • Organic Chemistry

Fingerprint

Dive into the research topics of 'Preparation of two stereoisomers of the macrocyclic electron donor tetramethoxycarbonyl[5.5]-tetrathiafulvalenophane with bridges containing two sulfur atoms'. Together they form a unique fingerprint.

Cite this