## Abstract magnified image A series of novel 1,3‐dissubstitutedpyridyl(thiazolyl)methyl‐2‐substituted‐methylideneimidazolidine derivatives **2** and **4** were designed and synthesized __via__ the __N__‐alkylation of the disubstituted heterocyclic ketene aminal derivative **1**. When **1** (R = C
Synthesis and analytical characterization of novel pyridyl-substituted 1,1′-ethenedithiolato complexes
✍ Scribed by Karsten Schubert; Helmar Goerls; Wolfgang Weigand
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 161 KB
- Volume
- 16
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.20103
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✦ Synopsis
Abstract
Some 1,1′‐ethenedithiolato complexes of nickel(II), palladium(II), and platinum(II) with different phosphine ligands, such as PPh~3~, PEt~3~, and dppe were prepared. Starting from 2‐, 3‐ as well as 4‐pyridyl methyl ketone, the complexes 1–15 were obtained in an one‐pot synthesis through reaction with carbon disulfide, using potassium‐tert‐butylate as a base. They were characterized by ^1^H, ^13^C, and ^31^P NMR, mass spectra, infrared spectra, and UV–VIS spectra. The molecular structures of the (Ph~3~P)~2~Pd^II^ complex 9 containing the 3‐pyridyl‐ethenedithiolato ligand and of the (Et~3~P)~2~Pt^II^ complex 12 containing the 4‐pyridyl‐ethenedithiolato ligand were determined. © 2005 Wiley Periodicals, Inc. Heteroatom Chem 16:369–378, 2005; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20103
📜 SIMILAR VOLUMES
## Abstract The reactions of hexachlorocyclotriphosphazene N~3~P~3~Cl~6~ (1) with 1‐naphthol and 1‐naphthylamine have been examined. The reaction of 1 with sodium 1‐naphthoxy gave the hexakis(1‐naphthoxy)cyclotriphosphazene (2) in high yield. Geminal 2,2‐di(1‐naphthylamino)‐4,4,6,6‐tetrachlorocyclo