二苯基膦基鋰

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	[Li+].C1=CC=C(C=C1)[P-]C2=CC=CC=C2;
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。

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]

二苯基膦基鋰可以在水中水解，生成二苯基膦：^[4]

(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.

[1] 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.

[2] R. Goldsberry Kim Cohn. Diphenyl(trimethylsilyl)phosphine and Dimethyl(trimethylsilyl)‐phosphine. Inorganic Syntheses. 1972, 13: 26–32. doi:10.1002/9780470132449.ch7.

[3] George W. Luther, III, Gordon Beyerle. Lithium Diphenylphosphide and Diphenyl(Trimethylsilyl)Phosphine. Inorganic Syntheses. 1977, 17: 186–188. doi:10.1002/9780470132487.ch51.

[Bianco-4] 4.0 ^4.1 V. D. Bianco, S. Doronzo. Diphenylphosphine. Inorganic Syntheses. 1976, 16: 161–188. doi:10.1002/9780470132470.ch43.

[5] W. Levason, C. A. Mcauliffe. Cis‐2‐Diphenylarsinovinyldiphenylphosphine and 2‐Diphenylarsinoethyldiphenylphosphine. Inorganic Syntheses. 1976, 16: 188–192. doi:10.1002/9780470132470.ch50.

[6] 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.

[7] 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.

[8] 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.

[9] 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.

[10] 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.

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