Tetraethylphosphonium azide, [P(C 2 H 5 ) 4 ] ם [N 3 ] מ , was prepared from tetraethyl phosphonium bromide and silver azide. Single crystals of [P(C 2 H 5 ) 4 ] ם [N 3 ] מ were grown from dichloromethane/THF (10:1) solution. The structure was determined by single-crystal X-ray diffraction a
The synthesis of tetraphenylarsonium azide, [Ph4As]+[N3]−, and the attempted preparation of tetraphenylarsonium azidodithiocarbonate, [Ph4As]+[SCSN3]−
✍ Scribed by Margaret-Jane Crawford; Thomas M. Klapötke
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 142 KB
- Volume
- 10
- Category
- Article
- ISSN
- 1042-7163
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✦ Synopsis
Tetraphenylarsonium azide was prepared from the reaction of tetraphenylarsonium chloride monohydrate and sodium azide in aqueous solution. [Ph 4 As] ם [N 3 ] מ crystallizes in the orthorhombic space group P nma with Z ס 4 and unit cell dimensions a ס 16.539(2), b ס 10.879(2), and c ס 12.671(2) A ˚. The preparation of the compound [Ph 4 As] ם [SCSN 3 ] מ was also attempted; however, it was found that at temperatures Ն0ЊC, this compound always decomposed into the tetraphenylarsonium thiocyanate, [Ph 4 As] ם [SCN]
📜 SIMILAR VOLUMES
## Abstract The kinetics and controllability of the Ti[OCH~2~CCl~3~]~4~‐initiated atom transfer radical polymerization (ATRP) of __n__‐butyl acrylate were investigated. Then, with Ti[OCH~2~CCl~3~]~4~ as the initiator, poly(ϵ‐caprolactone)‐__block__‐poly(__n__‐butyl acrylate) (PCL‐__b__‐PBA) copolym