P-Functionalized tetrathiafulvalenes from 1,3-dithiole-2-thiones?
Author:
Affiliation:
1. Institut für Anorganische Chemie
2. Rheinische Friedrich-Wilhelms-Universität Bonn
3. 53121 Bonn
4. Germany
5. Departamento de Química Orgánica
6. Facultad de Química
7. Universidad de Murcia
8. Campus de Espinardo
9. 30100 Murcia
Abstract
Synthesis of mono- and bisphosphanylated 1,3-dithiole-2-thiones is presented, including phosphite-mediated reductive C,C coupling reactions. Computational studies point to a spirothiaphosphirane and a S-heterocyclic carbene as key intermediates.
Funder
Rheinische Friedrich-Wilhelms-Universität Bonn
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,General Chemistry,Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2020/NJ/D0NJ02984J
Reference24 articles.
1. Bis-1,3-dithiolium chloride: an unusually stable organic radical cation
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3. Crystal structure of the radical-cation radical-anion salt from 2,2′-bi-1,3-dithiole and 7,7,8,8-tetracyanoquinodimethane
4. Preparation of Tetrathiafulvalenes (TTF) and their Selenium Analogs -Tetraselenafulvalenes (TSeF)
5. Bis- and tetrakis-(diphenylphosphino) tetrathiafulvalenes as precursors of redox-active organic—inorganic polymeric networks
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