1,5-雙(二苯基膦基)戊烷

1,5-雙(二苯基膦基)戊烷
英文名	1,5-Bis(diphenylphosphino)pentane
別名	DPPP
識別
CAS號	27721-02-4
PubChem	2733414
ChemSpider	2015213
SMILES	C1=CC=C(C=C1)P(CCCCCP(C2=CC=CC=C2)C3=CC=CC=C3)C4=CC=CC=C4;
性質
化學式	C29H30P2
摩爾質量	440.5 g·mol−1
外觀	白色無定形粉末
熔點	41—44 °C（314—317 K）
危險性
	GHS危險性符號;
GHS提示詞	警告
H-術語	H315, H319, H335
	若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。

1,5-雙(二苯基膦基)戊烷是一種有機磷化合物，化學式為C₂₉H₃₀P₂。它可由1,5-二溴戊烷和二苯基膦基鋰反應，^[2]或和二苯基膦在氫氧化銫存在下反應製得。^[3]它可以被二氟化氙氧化為1,5-雙(二苯基二氟磷基)戊烷。^[4]它和碘化亞銅反應，得到雙核配合物[CuIPh₂P(CH₂)₅PPh₂]₂。^[5]

參考文獻[編輯]

^ Shatunov, V.V.; Korlyukov, A.A.; Lebedev, A.V.; Sheludyakov, V.D.; Kozyrkin, B.I.; Orlov, V.Yu. The synthesis and deep purification of GaEt3. Reversible complexation of adducts MAlk3 (M = Al, Ga, In; Alk = Me, Et) with phenylphosphines. Journal of Organometallic Chemistry (Elsevier BV). 2011, 696 (10): 2238–2251. ISSN 0022-328X. doi:10.1016/j.jorganchem.2010.11.044.
^ Chou, Ta Shue; Yuan, Jeh Jing; Tsao, Chung Huang. Ultrasonic acceleration of the reductive cleavage of phosphorus-carbon bonds with lithium metal. A simple preparation of tertiary phosphines. Journal of Chemical Research, Synopses. 1985, (1): 18–19. ISSN 0308-2342. .
^ Honaker, Matthew T.; Salvatore, Ralph Nicholas. A MILD AND EFFICIENT CsOH-PROMOTED SYNTHESIS OF DITERTIARY PHOSPHINES. Phosphorus, Sulfur, and Silicon and the Related Elements (Informa UK Limited). February 1, 2004, 179 (2): 277–283. ISSN 1042-6507. doi:10.1080/10426500490262261.
^ Michael H. Holthausen, Rashi R. Hiranandani, Douglas W. Stephan. Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines. Chemical Science. 2015, 6 (3): 2016–2021 [2022-03-02]. ISSN 2041-6520. PMC 5496503 . PMID 28717457. doi:10.1039/C5SC00051C （英語）.
^ Zhang, Xiayi; Song, Li; Hong, Mingwei; Shi, Hongsheng; Xu, Kaijie; Lin, Qizhong; Zhao, Yi; Tian, Yuan; Sun, Jiafeng; Shu, Kangying; Chai, Wenxiang. Luminescent dinuclear copper(I) halide complexes double bridged by diphosphine ligands: Synthesis, structure characterization, properties and TD-DFT calculations. Polyhedron (Elsevier BV). 2014, 81: 687–694. ISSN 0277-5387. doi:10.1016/j.poly.2014.07.034.

[1] Shatunov, V.V.; Korlyukov, A.A.; Lebedev, A.V.; Sheludyakov, V.D.; Kozyrkin, B.I.; Orlov, V.Yu. The synthesis and deep purification of GaEt3. Reversible complexation of adducts MAlk3 (M = Al, Ga, In; Alk = Me, Et) with phenylphosphines. Journal of Organometallic Chemistry (Elsevier BV). 2011, 696 (10): 2238–2251. ISSN 0022-328X. doi:10.1016/j.jorganchem.2010.11.044.

[2] Chou, Ta Shue; Yuan, Jeh Jing; Tsao, Chung Huang. Ultrasonic acceleration of the reductive cleavage of phosphorus-carbon bonds with lithium metal. A simple preparation of tertiary phosphines. Journal of Chemical Research, Synopses. 1985, (1): 18–19. ISSN 0308-2342. .

[3] Honaker, Matthew T.; Salvatore, Ralph Nicholas. A MILD AND EFFICIENT CsOH-PROMOTED SYNTHESIS OF DITERTIARY PHOSPHINES. Phosphorus, Sulfur, and Silicon and the Related Elements (Informa UK Limited). February 1, 2004, 179 (2): 277–283. ISSN 1042-6507. doi:10.1080/10426500490262261.

[4] Michael H. Holthausen, Rashi R. Hiranandani, Douglas W. Stephan. Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines. Chemical Science. 2015, 6 (3): 2016–2021 [2022-03-02]. ISSN 2041-6520. PMC 5496503 . PMID 28717457. doi:10.1039/C5SC00051C （英語）.

[5] Zhang, Xiayi; Song, Li; Hong, Mingwei; Shi, Hongsheng; Xu, Kaijie; Lin, Qizhong; Zhao, Yi; Tian, Yuan; Sun, Jiafeng; Shu, Kangying; Chai, Wenxiang. Luminescent dinuclear copper(I) halide complexes double bridged by diphosphine ligands: Synthesis, structure characterization, properties and TD-DFT calculations. Polyhedron (Elsevier BV). 2014, 81: 687–694. ISSN 0277-5387. doi:10.1016/j.poly.2014.07.034.

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