翻訳と辞書
Words near each other
・ "O" Is for Outlaw
・ "O"-Jung.Ban.Hap.
・ "Ode-to-Napoleon" hexachord
・ "Oh Yeah!" Live
・ "Our Contemporary" regional art exhibition (Leningrad, 1975)
・ "P" Is for Peril
・ "Pimpernel" Smith
・ "Polish death camp" controversy
・ "Pro knigi" ("About books")
・ "Prosopa" Greek Television Awards
・ "Pussy Cats" Starring the Walkmen
・ "Q" Is for Quarry
・ "R" Is for Ricochet
・ "R" The King (2016 film)
・ "Rags" Ragland
・ ! (album)
・ ! (disambiguation)
・ !!
・ !!!
・ !!! (album)
・ !!Destroy-Oh-Boy!!
・ !Action Pact!
・ !Arriba! La Pachanga
・ !Hero
・ !Hero (album)
・ !Kung language
・ !Oka Tokat
・ !PAUS3
・ !T.O.O.H.!
・ !Women Art Revolution


Dictionary Lists
翻訳と辞書 辞書検索 [ 開発暫定版 ]
スポンサード リンク

phosphaalkyne : ウィキペディア英語版
phosphaalkyne
In chemistry, phosphaalkynes (IUPAC name: alkylidynephosphanes) are organophosphorus compounds that have a phosphorus-carbon triple bond.〔"Cyaphide (C≡P): The Phosphorus Analogue of Cyanide (C≡N)" Robert J. Angelici Angew. Chem. Int. Ed. 2007, 46, 330 – 332 〕
Two types of phosphaalkynes are recognized. One type of phosphaalkyne is a heavier analogue of nitriles (R-C≡N), i.e. P replaces N in a nitrile. Another type of phosphaalkyne feature pentavalent, three coordinate phosphorus. Such species can also be described as ylides or phosphinocarbenes. The phosphorus version of the isonitriles R-P+≡C, which would be called isophosphaalkynes, has not been observed.
In 1950, H. Albers reported the first indication of the existence of the parent compound of phosphaalkynes (type A), H-C≡P. This compound was identified by infrared absorption spectrometry, and its synthesis was improved by Manfred Regitz in 1987. The synthesis of the first kinetically stable phosphaalkyne, which has a tert-butyl group as a substituent R (tert-Butylphosphaacetylene), was reported in 1981 by Gerd Becker and Werner Uhl. These phosphaalkynes undergo 1,2-addition reactions and cycloadditions .
In 2000, Guy Bertrand reported the first structure of the type B phosphaalkyne. Its P-C-R bond angle is 152.6 degrees, so this type of phosphaalkyne may be best described by a phosphorus vinyl ylide structure (B2).
==Cyaphide ion==
The cyaphide ion P≡C as the phosphorus cyanide cousin is not known as a salt and only observed in the gas phase. In silico measurements reveal that the -1 charge in this ion is location mainly on carbon (0.65). On the other hand the molecule does exist as a terminal ligand in the ruthenium transition metal complex trans-(), which is stabilized by dppe.〔"Making the True "CP" Ligand." Cordaro et al. Angew. Chem. Int. Ed. 2006, 45, 6159 - 6162 〕 Recently, the synthesis and electronic structure of the first cyaphide-alkynyl complexes has been reported.〔"Synthesis and electronic structure of the first cyaphide-alkynyl complexes." Trathen et al. Dalton Trans. 2014, 43, 9004 - 9007 〕 The novel complexes trans-() (R = CO2Me, C6H4OMe) are the first complexes to incorporate cyaphide as part of a conjugated system.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
ウィキペディアで「phosphaalkyne」の詳細全文を読む



スポンサード リンク
翻訳と辞書 : 翻訳のためのインターネットリソース

Copyright(C) kotoba.ne.jp 1997-2016. All Rights Reserved.