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trans-(CO)3Fe(PF3)2 | 16454-87-8

中文名称
——
中文别名
——
英文名称
trans-(CO)3Fe(PF3)2
英文别名
carbon monoxide;iron;trifluorophosphane
trans-(CO)3Fe(PF3)2化学式
CAS
16454-87-8;17594-22-8;17594-23-9;53275-22-2
化学式
C3F6FeO3P2
mdl
——
分子量
315.816
InChiKey
BNAPQDQTYIAXJW-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

计算性质

  • 辛醇/水分配系数(LogP):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Stereochemical nonrigidity in iron carbonyl fluorophosphine compounds
    摘要:
    DOI:
    10.1021/ic50075a009
  • 作为产物:
    参考文献:
    名称:
    羰基铁三卤化磷衍生物的立体化学
    摘要:
    衍生物的Fe(CO)的红外光谱5 - Ñ(PF 3)ñ和Fe(CO)4(PCL 3)已经研究了在该区域4200-400cm -1特别是从由于statellites的VIE的点13合作组。已经显示出这些衍生物包含对于铁原子周围的三角双锥体结构几何上预期的所有异构体。分离这些异构体是不可能的。然而,已经制备了仅包含一种异构体的反应混合物。
    DOI:
    10.1016/s0022-328x(00)83732-8
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文献信息

  • IR laser pyrolysis and the isotopic labelling of organometallic compounds
    作者:Neil J. Bristow、Barry D. Moore、Martyn Poliakoff、Graham J. Ryott、James J. Turner
    DOI:10.1016/s0022-328x(00)98693-5
    日期:1984.1
    A homogeneous gas phase pyrolysis technique involving SF6 sensitization and a continuous wave (CW) CO2 laser, is described for preparing small quantities (∼ 100 mg) of organometallic compounds. Several reactions have been successfully carried out and the synthesis of Os(CO)5 from H2Os(CO)4 and CO is discussed in detail. With IR laser pyrolysis, room temperature reactors and sub-atmospheric pressures
    描述了一种涉及SF 6敏化和连续波(CW)CO 2激光的均相气相热解技术,用于制备少量(〜100 mg)的有机金属化合物。已成功进行了数个反应,并详细讨论了由H 2 Os(CO)4和CO合成Os(CO)5的方法。通过IR激光热解,可以将室温反应器和低于大气压的压力用于通常需要高压和高温的反应。
  • Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: Fe: Org.Verb.B1, 1.1.4.4.3.1, page 148 - 168
    作者:
    DOI:——
    日期:——
  • Sulfur hexafluoride sensitized infrared photodecomposition of iron pentacarbonyl
    作者:Tetsuro Majima、Tadahiro Ishii、Yoshiyasu Matsumoto、Michio Takami
    DOI:10.1021/ja00189a007
    日期:1989.3
  • Phosphorus Trifluoride Substitution Compounds of Iron Pentacarbonyl
    作者:Ronald J. Clark
    DOI:10.1021/ic50020a011
    日期:1964.10
  • Ultraviolet laser photolysis: Primary photochemistry of Fe(CO)<sub>5</sub> in PF<sub>3</sub>
    作者:Gilbert Nathanson、Barbara Gitlin、Alan M. Rosan、James T. Yardley
    DOI:10.1063/1.440841
    日期:1981.1
    We have studied the photolysis of mixtures of Fe(CO)5 and PF3 with a KrF laser operating at 248 nm. The product yields of Fe(CO)2(PF3)3, Fe(CO)3(PF3)2, and Fe(CO)4PF3 have been measured as a function of laser fluence and mixture composition. A simple kinetic model appears to explain semiquantitatively the observed dependence of product yield upon mixture composition. This model has allowed us to determine that the primary photochemical yields at 248 nm for the fragments Fe(CO)2, Fe(CO)3, and Fe(CO)4 over the fluence range 0.1–200 mJ/cm2 are 0.55, 0.35, and 0.10, respectively, independent of laser fluence. This fragmentation results from a simple one-photon absorption process. We have found that CO ligands are exchanged readily in collisions of the above fragments with Fe(CO)5, with a bimolecular rate constant relative to that for trapping by PF3 of kM/kT=4. We have also found that these primary photofragments react with Fe(CO)5 to form unobserved products with a rate constant (relative to that for trapping by PF3) of kQ/kT=7.
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