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(C2F5)2POSnBu3 | 1159100-60-3

中文名称
——
中文别名
——
英文名称
(C2F5)2POSnBu3
英文别名
tributylstannyl bis(pentafluoroethyl)phosphinite;Bis(1,1,2,2,2-pentafluoroethyl)-tributylstannyloxyphosphane;bis(1,1,2,2,2-pentafluoroethyl)-tributylstannyloxyphosphane
(C2F5)2POSnBu3化学式
CAS
1159100-60-3
化学式
C16H27F10OPSn
mdl
——
分子量
575.058
InChiKey
LTMJDVGNWPJHMR-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    320.7±52.0 °C(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    9.06
  • 重原子数:
    29
  • 可旋转键数:
    13
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    11

反应信息

  • 作为反应物:
    描述:
    (C2F5)2POSnBu3氢溴酸 作用下, 反应 0.33h, 生成 bis(pentafluoroethyl)phosphinous acid
    参考文献:
    名称:
    Bis(perfluoralkyl)phosphinous acids and derivatives and use thereof
    摘要:
    这项发明涉及双(全氟烷基)膦酸、双(全氟烷基)硫膦酸及其衍生物,其合成和用途,特别是用于合成用于催化过程的空气稳定金属配合物。
    公开号:
    US20110124873A1
  • 作为产物:
    参考文献:
    名称:
    Bis(perfluoralkyl)phosphinous acids and derivatives and use thereof
    摘要:
    这项发明涉及双(全氟烷基)膦酸、双(全氟烷基)硫膦酸及其衍生物,其合成和用途,特别是用于合成用于催化过程的空气稳定金属配合物。
    公开号:
    US20110124873A1
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文献信息

  • Chlorobis(pentafluoroethyl)phosphane: Improved Synthesis and Molecular Structure in the Gas Phase
    作者:Stuart A. Hayes、Raphael J. F. Berger、Norbert W. Mitzel、Julia Bader、Berthold Hoge
    DOI:10.1002/chem.201003048
    日期:2011.3.28
    low‐frequency vibrational modes and therefore large‐amplitude motions. The conformer calculated to be most stable was also found to be most abundant by GED and comprised 61(5) % of the total. The molecular structure parameters determined by GED were in good agreement with those calculated at the MP2/TZVPP level of theory; the only significant difference was a discrepancy of about 3° in the C‐P‐C angle, which
    (C 2 F 5)2 PC1现在可以通过从技术产品(C 2 F 5)3 PF 2开始的显着改进的合成方案访问。(C 2 F 5)3 PF 2的第一步是在120°C的无溶剂反应中用NaBH 4还原。用过量的氢氧化钠水溶液处理产物P(C 2 F 5)3,得到相应的次膦酸盐Na +(C 2 F 5)2PO -选择下五氟乙烷的解放。随后用PhPCl 4氯化导致(C 2 F 5)2 PCl选择性形成,通过分步冷凝将其分离,总产率为66%。(C 2 F 5)2的气体电子衍射(GED)图记录了PC1,并发现它由两个一致性模型进行描述。对势能表面的量子化学研究表明,可能存在许多低能构象体,每个构象体都有许多低频振动模式,因此具有大振幅运动。通过GED还发现,计算出的最稳定的构象异构体最丰富,占总数的61(5)%。通过GED测定的分子结构参数与在理论上在MP2 / TZVPP水平上计算的参数相吻合。唯一的显
  • Bis(perfluoralkyl)phosphinous acids and derivatives and use thereof
    申请人:Hoge Berthold
    公开号:US20110124873A1
    公开(公告)日:2011-05-26
    The invention relates to bis(perfluoroalkyl)phosphinous acids, bis(perfluoroalkyl)thiophosphinous acids and derivatives, the synthesis thereof and the use thereof, in particular for the synthesis of air-stable metal complexes for catalytic processes.
    这项发明涉及双(全氟烷基)膦酸、双(全氟烷基)硫膦酸及其衍生物,其合成和用途,特别是用于合成用于催化过程的空气稳定金属配合物。
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氯(双五氟乙基)膦 5-萘-2-基-1,3-噁唑 1-氯-2-[2-氯乙基(甲基)磷基]乙烷 1-丁基-1-甲基吡咯烷鎓三(五氟乙基)三氟磷酸盐 1,1,1,3,3,3-六氟-2-(2,2,2-三氟-1-羟基-1-(三氟甲基)乙基磷酰基)-2-丙醇 bis(pentafluoroethyl)phosphinyl amide 1-butylpyridinium bis(pentafluoroethyl)phosphinate N,N-butylmethylpyrrolidinium bis(pentafluoroethyl)-phosphinate bis(pentafluoroethyl)phosphinate anion triethylmethylammonium bis(pentafluoroethyl)-phosphinate bis(dimethylamino)chlorocarbenium bis(pentafluorethyl)phosphinate 1-methyl-1-propargylpyrrolidinium bis(pentafluoro-ethyl)phosphinate N,N-dimethylpyrrolidinium bis(pentafluoroethyl)-phosphinate 1-butyl-3-methylimidazolium bis(pentafluoroethyl)phosphinate propargyl bis(pentafluoroethyl)phosphinate 1,3-dimethylimidazolium bis(pentafluoroethyl)phosphinate 1-propargyl-3-methylimidazolium bis(pentafluoroethyl)-phosphinate 1-ethyl-3-methylimidazolium bis(nonafluorobutyl)-phosphinate tetrabutylammonium tris(pentafluoroethyl)trifluorophosphate bis-(2,2-dichloro-1-hydroxy-ethyl)-phosphinic acid 2,2,3,3,4,4,5,5-octafluoropentyl bis(pentafluoroethyl) phosphinate 2-methyl-1,1,3,3-tetramethylisouronium bis(pentafluoroethyl)phosphinate ethyl bis(nonafluorobutyl)phosphinate fluorobis(pentafluoroethyl)phosphane tetraethylammonium bis(nonafluorobutyl)tetrafluorophosphate tetraethylammonium tris(pentafluoroethyl)trifluorophosphate tris(pentafluoroethyl)phosphane ethyl bis(pentafluoroethyl)phosphinate N,N,N',N'-tetramethyl-N''-ethylguanidinium bis(pentafluoroethyl)phosphinate 3-bromopropyl bis(pentafluoroethyl)phosphinate Tetramethylammonium tris(pentafluorophosphate Bis-(2-chlor-ethyl)-thiophosphinsaeure-ethylester ethyl bis(pentafluoroethyl)phosphinite Bis-heptafluorpropyl-fluorphosphin trimethylsilyl bis(pentafluoroethyl)phosphinite tris(undecafluoroisopentyl)phosphine oxide 1-(Bis-undecafluoropentyl-phosphinoyl)-1,1,2,2,3,3,4,4,5,5,5-undecafluoro-pentane Bis-(2-chlor-ethyl)-chlorphosphin 1,1,1,3,3,3,1',1',1',3',3',3'-dodecafluoro-2,2'-phosphanediyl-bis-propan-2-ol Bis-<2-chlor-aethyl>-chlormethyl-phosphinoxid Tri(β-chlorethyl)phosphinoxid cis-[(C2F5)2P(methyl)]4Pt Perfluorhexylphosphinsaeure bis-(2,2,2-trichloro-1-hydroxy-ethyl)-phosphinic acid ethyl ester bis(pentafluoroethyl)phosphinyl bromide (S)-4-benzyl-2-(2-(bis(pentafluoroethyl)phosphino)phenyl)-4,5-dihydrooxazole (S)-2-(2-(bis(pentafluoroethyl)phosphino)phenyl)-4-phenyl-4,5-dihydrooxazole tetra(n-butyl)phosphonium tris(pentafluoroethyl)trifluorophosphate silver bis(heptafluoropropyl)phosphinate Tris(2,2,3,3,4,4,5,5-octafluoropentyl)phosphine