二苯基膦基鋰
外觀
二苯基膦基鋰 | |
---|---|
![]() | |
別名 | 二苯基磷化鋰 |
識別 | |
CAS號 | 4541-02-0 ![]() |
PubChem | 3478053 |
ChemSpider | 2719164 |
SMILES |
|
性質 | |
化學式 | C12H10LiP |
摩爾質量 | 192.12 g·mol−1 |
外觀 | 淺黃色固體 |
溶解性 | 醚類 |
危險性 | |
GHS危險性符號![]() ![]() ![]() | |
GHS提示詞 | 危險 |
H-術語 | H302, H312, H314, H332, H400, H410 |
P-術語 | P260, P261, P264, P270, P271, P273, P280, P301+312, P301+330+331, P302+352, P303+361+353, P304+312, P304+340, P305+351+338 |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
二苯基膦基鋰是一種化合物,化學式為(C6H5)2PLi,它是對空氣敏感的固體,可用於製備其它含二苯基膦基團的化合物。其乙醚配合物是紅色的。
![](http://upload.wikimedia.org/wikipedia/commons/thumb/0/0c/DOXDUP.png/220px-DOXDUP.png)
合成
[編輯]二苯基膦基鋰可由二苯基氯化膦、[2]三苯基膦[3][4]或四苯基二膦被金屬鈉還原得到:
- (C6H5)2PCl + 2 Li → (C6H5)2PLi + LiCl
- (C6H5)3P + 2 Li → (C6H5)2PLi + LiC6H5
- (C6H5)4P2 + 2 Li → 2 (C6H5)2PLi
它也可由二苯基膦脫氫得到。
反應
[編輯]- (C6H5)2PLi + H2O → (C6H5)2PH + LiOH
它和鹵代烴反應,生成叔膦:[5]
- (C6H5)2PLi + RX → (C6H5)2PR + LiX
例如,它和1,6-二氯己烷在四氫呋喃中反應,可以得到1,6-雙(二苯基膦基)己烷。[6]
它可用作甲基季銨鹽的脫甲基試劑。[7]它和金屬鹵化物(或有機金屬鹵化物[8][9])反應,生成過渡金屬膦配合物。[10]
參考文獻
[編輯]- ^ Ruth A. Bartlett, Marilyn M. Olmstead, Philip P. Power. Structural Characterization of the Solvate Complexes of the Lithium Diorganophosphides [{Li(Et2O)PPh2}∞], [{Li(THF)2PPh2}∞], and [{Li(THF)P(C6H11)2}∞]. Inorg. Chem. 1986, 25: 1243–1247. doi:10.1021/ic00228a034.
- ^ R. Goldsberry Kim Cohn. Diphenyl(trimethylsilyl)phosphine and Dimethyl(trimethylsilyl)‐phosphine. Inorganic Syntheses. 1972, 13: 26–32. doi:10.1002/9780470132449.ch7.
- ^ George W. Luther, III, Gordon Beyerle. Lithium Diphenylphosphide and Diphenyl(Trimethylsilyl)Phosphine. Inorganic Syntheses. 1977, 17: 186–188. doi:10.1002/9780470132487.ch51.
- ^ 4.0 4.1 V. D. Bianco, S. Doronzo. Diphenylphosphine. Inorganic Syntheses. 1976, 16: 161–188. doi:10.1002/9780470132470.ch43.
- ^ W. Levason, C. A. Mcauliffe. Cis‐2‐Diphenylarsinovinyldiphenylphosphine and 2‐Diphenylarsinoethyldiphenylphosphine. Inorganic Syntheses. 1976, 16: 188–192. doi:10.1002/9780470132470.ch50.
- ^ Cao, Guangxiu; Ma, Huailing; Li, Guanliang; Li, Jiqin. Study on synthesis of 1,6-bis(diphenylphosphinel)hexane. Huaxue Yanjiu Yu Yingyong, 2006. 18 (12): 1464-1468.
- ^ Plenat, Francoise; Cahyono, Bambang; Cristau, Henri-Jean. Lithium diphenylphosphide: a new demethylation reagent for methylammonium salts. Comptes Rendus de l'Academie des Sciences, Serie IIb: Mecanique,Physique, Chimie, Astronomie, 1995. 320 (10): 539-543. ISSN: 1251-8069.
- ^ Alcalde, Maria Isabel; de la Mata, Javier; Gómez, Manuel; Royo, pascual; Sánchez, Fernando. Half-sandwich isocyanide, phosphine, methyl and phosphanido pentamethylcyclopentadienylniobium (V) complexes. Journal of Organometallic Chemistry. 1995, 492 (2): 151–155. ISSN 0022-328X. doi:10.1016/0022-328X(94)05289-N.
- ^ Cano, Ana; Cuenca, Tomás; Galakhov, Mikhail; Rodríguez, Gema M.; Royo, Pascual; Cardin, Christine J.; Convery, Maire A. Fulvalene titanium and zirconium complexes: synthesis and NMR study of phosphanido-, alkyl-, and alkynyl-derivatives. X-ray crystal structures of [{Ti(η5−C5H5)(μ−PPH2)}2{μ−(η5−C5H4−η5−C5H4)}] and [{Zr(η5−C5H5)(μ−C≡CSiMe3)}2{μ−(η5−C5H4−η5−C5H4)}]. Journal of Organometallic Chemistry. 1995, 493 (1-2): 17–25. ISSN 0022-328X. doi:10.1016/0022-328X(94)05288-M.
- ^ Issleib, Kurt; Froehlich, Hans Otto. Alkali metal-phosphorus compounds and their reactive behavior. XIII. Preparation and properties of zinc and cuprous diphenylphosphide. Chemische Berichte, 1962. 95: 375-380. ISSN: 0009-2940.