Bis(trifluormethyl)selen(IV)-Oxid | 78334-30-2

• 分子结构分类: 有机化合物 - 有机卤素化合物 - 卤代烷
• 英文名称: Bis(trifluormethyl)selen(IV)-Oxid
• 英文别名: bis(trifluoromethyl) selenoxide；Trifluoro(trifluoromethylseleninyl)methane
• CAS: 78334-30-2
• 化学式: C₂F₆OSe
• 分子量: 232.972
• InChiKey: OOQFWLYNKYXLHH-UHFFFAOYSA-N

物化性质

• 沸点：
  -74.9±40.0 °C(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.61
• 重原子数：
  10
• 可旋转键数：
  0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  bis(trifluoromethyl)selenide 在 间氯过氧苯甲酸 作用下， 以98%的产率得到Bis(trifluormethyl)selen(IV)-Oxid
  参考文献：
  名称：

  Fluorocarbon-selenium chemistry: Accomplishments and quests

  摘要：

  DOI：

  10.1016/s0022-1139(00)81949-1

文献信息

• Cesium Fluoride Catalyzed Trifluoromethylation of Esters, Aldehydes, and Ketones with (Trifluoromethyl)trimethylsilane
  作者：Rajendra P. Singh、Ganfeng Cao、Robert L. Kirchmeier、Jean'ne M. Shreeve

  DOI：10.1021/jo982494c

  日期：1999.4.1

  low reactivity of carboxylic esters toward (trifluoromethyl)trimethylsilane (TMS-CF(3)) was investigated. A universal cesium fluoride catalyzed procedure for nucleophilic trifluoromethylation was developed. At room temperature (25 degrees C), with catalytic amounts of cesium fluoride, carboxylic esters were found to react to give the silyl ether intermediates, which afforded the trifluoromethyl ketones

  研究了羧酸酯对（三氟甲基）三甲基硅烷（TMS-CF（3））的低反应性。建立了通用的氟化铯催化亲核三氟甲基化反应的方法。在室温（25摄氏度）下，催化量的氟化铯被发现与羧酸酯反应生成甲硅烷基醚中间体，在水解后得到三氟甲基酮。磺酸酯，亚磺酸酯和亚硒酸酯也显示出良好的反应活性，得到了新颖的三氟甲基化化合物。三氟甲基化方法也适用于醛和酮，将其转化为三氟甲基甲硅烷基醚中间体，并在酸水解后以优异的产率得到三氟甲基化的醇。乙二醇二甲醚用作固体或高沸点底物的溶剂，
• Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: F: PerFHalOrg.SVol.3, 6.3.2, page 215 - 245
  作者：

  DOI：——

  日期：——
• Contributions to bis(perfluoroalkyl) chalkogenide chemistry: preparation of (Rf)2SeO [Rf = C2F5, (CF3)2CF, n-C4F9], (Rf′)2TeX2 [X = F, Cl: Rf′ = n-C3F7, (CF3)2CF, n-C4F9; X = Br: Rf′ = n-C3F7, n-C4F9], (CF3)2Te(NSO)2 and (C2F5)2Te(OH)NO3
  作者：S. Gockel、A. Haas、V. Probst、Roland Boese、Iris Müller

  DOI：10.1016/s0022-1139(99)00292-4

  日期：2000.3

  The reaction between perfluoroalkyl iodides with a threefold excess of a 1 : 1 molar mixture of Se and Cu is a new method for the preparation of corresponding monoselenides (la-c) and diselenides (2a-d). They are oxidised with HOF without a solvent to bis(perfluoroalkyl) selenium(IV) oxides (3a-d). Halogenation of (R-f)(2)Te with XeF2, Cl-2 or Br-2 yielded (R-f)(2)TeF2(7a-c), (R-f)(2)TeCl2 (8a-c) and (R-f')(2)TeBr2 (9a, 9c). Oxidation of (C2F5)(2)Te with cone. HNO3 gave (C2F5)(2)TeCOH)NO3 (4). When (CF3)(2)TeCl2 is treated with AgNSO metathesis took place forming (CF3)(2)Te(NSO)(2), (6). Two (C6F5)(2)Te(VI) derivatives with the general formula (C6F5)(2)TeX4. with X = CF3C(O)O (5) and F are made from (C6F5)(2)TeO2 and CF3C(O)OH or SP4, respectively. The monotelluride (n-C6F13)(2)Te was synthesised similarly from n-C6F13I, Te and Cu. X-ray structures for 3d, 8a, and 8b are provided. (C) 2000 Elsevier Science S.A. All rights reserved.
• Haas, Alois; Tebbe, Klaus, Zeitschrift fur Naturforschung, Teil B: Anorganische Chemie, Organische Chemie, 1984, vol. 39, # 7, p. 897 - 902
  作者：Haas, Alois、Tebbe, Klaus

  DOI：——

  日期：——
• Haas, A.; Tebbe, K., Zeitschrift fur Naturforschung, 1984, vol. 39b, p. 897 - 902
  作者：Haas, A.、Tebbe, K.

  DOI：——

  日期：——