三氟甲硒醇四甲基銨

三氟甲硒醇四甲基銨
識別
CAS號	75264-92-5
SMILES	FC(F)(F)[Se-].C[N+](C)(C)C;
性質
外觀	無色固體
熔點	215—217 °C（488—490 K）（分解）
	若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。

三氟甲硒醇四甲基銨是一種化合物，化學式為[(CH₃)₄N]SeCF₃，它可由四甲基氟化銨和SeCF₂反應製得。^[2]四甲基氟化銨、三甲基三氟甲基硅烷和紅硒的反應也能製得標題化合物。^[1]它和(TDAE)Br₂（TDAE為四(二甲氨基)乙烯）反應，可以得到(TDAE)(SeCF₃)₂。^[3]它和氟硼酸銀或氯化亞金反應，可以得到[M(SeCF₃)₂]⁻（M=Ag或Au）配合物。^[4]它可用於有機物的三氟甲硒基化反應。^[5]

參考文獻

^ ^1.0 ^1.1 ^1.2 Wieland Tyrra, Dieter Naumann, Yurii L Yagupolskii. Stable trifluoromethylselenates(0), [A]SeCF3—synthesis, characterizations and properties. Journal of Fluorine Chemistry. 2003-10, 123 (2): 183–187 [2020-04-30]. doi:10.1016/S0022-1139(03)00118-0. （原始內容存檔於2018-06-25）（英語）.
^ Darmadi, Alexius; Haas, Alois; Koch, Bernd. Simplified synthesis and reactors of selenocarbonyl difluoride. Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie, 1980. 35B (5): 526-529. ISSN: 0340-5087
^ Tyrra, Wieland; Naumann, Dieter; Pohl, Herbert; Pantenburg, Ingo. Trifluoromethylselenate(0), [SeCF₃]^-, and trifluoromethyltellurate(0), [TeCF₃]^- - crystalline products of the reduction of the bis(trifluoromethyl)dichalcogen compounds, E2(CF3)2 (E = Se, Te), with tetrakis(dimethylamino)ethene (TDAE). Zeitschrift fuer Anorganische und Allgemeine Chemie, 2003. 629 (6): 1039-1043. ISSN: 0044-2313
^ Dieter Naumann, Wieland Tyrra, Silke Quadt, Sigrid Buslei, Ingo Pantenburg, Mathias Schäfer. Bis(trifluoromethylselenato(0))metallates(I) of Silver and Gold, [M(SeCF3)2]− (M = Ag, Au). Zeitschrift für anorganische und allgemeine Chemie. 2005-10, 631 (13-14): 2733–2737 [2020-04-30]. ISSN 0044-2313. doi:10.1002/zaac.200500115 （德語）.
^ Qiu-Yan Han, Cheng-Long Zhao, Tao Dong, Jin Shi, Kai-Li Tan, Cheng-Pan Zhang. Metal-free oxidative trifluoromethylselenolation of electron-rich (hetero)arenes with the readily available [Me 4 N][SeCF 3 ] reagent. Organic Chemistry Frontiers. 2019, 6 (15): 2732–2737 [2020-04-30]. ISSN 2052-4129. doi:10.1039/C9QO00631A （英語）.

[Tyrra-1] 1.0 ^1.1 ^1.2 Wieland Tyrra, Dieter Naumann, Yurii L Yagupolskii. Stable trifluoromethylselenates(0), [A]SeCF3—synthesis, characterizations and properties. Journal of Fluorine Chemistry. 2003-10, 123 (2): 183–187 [2020-04-30]. doi:10.1016/S0022-1139(03)00118-0. （原始內容存檔於2018-06-25）（英語）.

[2] Darmadi, Alexius; Haas, Alois; Koch, Bernd. Simplified synthesis and reactors of selenocarbonyl difluoride. Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie, 1980. 35B (5): 526-529. ISSN: 0340-5087

[3] Tyrra, Wieland; Naumann, Dieter; Pohl, Herbert; Pantenburg, Ingo. Trifluoromethylselenate(0), [SeCF₃]^-, and trifluoromethyltellurate(0), [TeCF₃]^- - crystalline products of the reduction of the bis(trifluoromethyl)dichalcogen compounds, E2(CF3)2 (E = Se, Te), with tetrakis(dimethylamino)ethene (TDAE). Zeitschrift fuer Anorganische und Allgemeine Chemie, 2003. 629 (6): 1039-1043. ISSN: 0044-2313

[4] Dieter Naumann, Wieland Tyrra, Silke Quadt, Sigrid Buslei, Ingo Pantenburg, Mathias Schäfer. Bis(trifluoromethylselenato(0))metallates(I) of Silver and Gold, [M(SeCF3)2]− (M = Ag, Au). Zeitschrift für anorganische und allgemeine Chemie. 2005-10, 631 (13-14): 2733–2737 [2020-04-30]. ISSN 0044-2313. doi:10.1002/zaac.200500115 （德語）.

[5] Qiu-Yan Han, Cheng-Long Zhao, Tao Dong, Jin Shi, Kai-Li Tan, Cheng-Pan Zhang. Metal-free oxidative trifluoromethylselenolation of electron-rich (hetero)arenes with the readily available [Me 4 N][SeCF 3 ] reagent. Organic Chemistry Frontiers. 2019, 6 (15): 2732–2737 [2020-04-30]. ISSN 2052-4129. doi:10.1039/C9QO00631A （英語）.

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