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Synthesis and structure of bis(dialkylamino)carbeniumdithiocarboxylates

✍ Scribed by Akira Nagasawa; Isao Akiyama; Shigeru Mashima; Juzo Nakayama


Book ID
102228886
Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
447 KB
Volume
6
Category
Article
ISSN
1042-7163

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✦ Synopsis


Abstract

2‐Chloro and 2‐phenoxy substituted 1,1‐bis(diethylamino)ethylenes (4a and 4c) react with elemental sulfur at room temperature to give the inner salt, bis(diethylamino)carbeniumdithiocarboxylate (1a), in excellent yields with extrusion of hydrogen chloride and phenol, respectively, thus providing a new and convenient synthesis of the structurally interesting inner salt. X‐ray single crystal structure analysis of 1a reveals that the NCN and SCS planes are nearly vertical to each other with a dihedral angle of 82.0° and that the positive and negative charges are delocalized over the NCN and SCS moieties, respectively. Results of solid‐state ^13^C NMR of 1a are also briefly described.


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Synthesis and characterization of 1,3-bi
✍ Keil, D. ;Hartmann, H. 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 539 KB

## Abstract By condensation of squaric acid (1) with 2‐(dialkylamino)‐substituted thiazoles 8 a novel type of heterocyclic‐substitued squaraines of the general structure 9 was prepared in moderate yield mostly. The squaraines 9 obtained are sparingly soluble in the most organic solvents and exhibit