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cis-dihydrido-trans-bis(trimethylphosphite)dicarbonyliron | 77482-07-6

中文名称
——
中文别名
——
英文名称
cis-dihydrido-trans-bis(trimethylphosphite)dicarbonyliron
英文别名
——
cis-dihydrido-trans-bis(trimethylphosphite)dicarbonyliron化学式
CAS
77482-07-6
化学式
C8H20FeO8P2
mdl
——
分子量
362.037
InChiKey
CWCTWPWEQPGDHB-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:
    描述:
    三甲氧基磷cis-dihydrido-trans-bis(trimethylphosphite)dicarbonyliron甲醇 为溶剂, 以99%的产率得到dicarbonyltris(trimethylphosphite)iron
    参考文献:
    名称:
    Ligand substitution processes on carbonylmetal derivatives. 2. Reaction of tetracarbonylhydridoferrates with phosphites
    摘要:
    Ligand substitution processes m KHFe(CO)4 (1) have been evidenced by reaction with various phosphites. The nature of the reaction products strongly depends on (i) the nature of the solvent, (ii) the Tolman cone angle of the phosphite, and (iii) the reaction conditions. In protic media (H2O-THF), phosphites with small cone angles, such as P(OMe)3, P(OEt)3, and P(OPh)3, react (2 equiv) with 1 at room temperature to give the corresponding complexes H2Fe(CO)2[P(OR)3]2 in > 90% yield, whereas a phosphite with a larger cons angle (P[O-o-C6H4Ph]3) reacts only at a higher temperature to afford the disubstituted Fe(CO)3[P{O-o-C6H4Ph}3]2 derivative in 94% yield. When the reaction with phosphites having small cone angles is conducted with a 3-fold excess of phosphite at 65-degree-C, the trisubtituted derivatives Fe(CO)2[P(OR)3]3 are formed in 75-96% yield. In aprotic medium (THF), 1 reacts with phosphites (2 equiv) at room temperature to yield the monosubstituted anionic hydrides K+[HFe(CO)3{P(OR)3}]-, which can be isolated in > 90% yield. In refluxing THF the reaction of 1 with P(OMe)3 (3 equiv) demonstrates the first synthesis of the hydridoferrate K+[HFe(CO)2{P(OMe)3}2]-. Protonation of K+[HFe(CO)3{P(OR)3}]-with trifluoroacetic acid in THF at -10-degrees-C provides an excellent route for the high-yield synthesis of the monosubstituted dihydrides H2Fe(CO)3[P(OR)3]. In situ reaction of the latter with another phosphane PZ3 (Z = Ph, OPh) leads to the mixed dihydrides H2Fe(CO)2[P(OR)3][PZ3] (R = Me, Et; Z = Ph, OPh), which are reported for the first time. Finally, reaction of H2Fe(CO)2[P(OEt)3]2 with KH under sonication allows the generation of the highly reduced derivative K2[Fe(CO)2{P(OEt)3}2], the first disubstituted analogue of the Collman reagent.
    DOI:
    10.1021/om00045a015
  • 作为产物:
    描述:
    Dicarbonyl-formaldehyd-bis(trimethylphosphit)eisen(0) 在 H2 作用下, 以 乙醚 为溶剂, 以23%的产率得到cis-dihydrido-trans-bis(trimethylphosphite)dicarbonyliron
    参考文献:
    名称:
    Berke, Heinz; Birk, Reiner; Huttner, Gottfried, Zeitschrift fur Naturforschung, Teil B: Anorganische Chemie, Organische Chemie, 1984, vol. 39, # 10, p. 1380 - 1388
    摘要:
    DOI:
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文献信息

  • Brunet, Jean-Jacques; Kindela, Fadjai Banda; Labroue, Daniel, Inorganic Chemistry, 1990, vol. 29, # 20, p. 4152 - 4153
    作者:Brunet, Jean-Jacques、Kindela, Fadjai Banda、Labroue, Daniel、Neibecker, Denis
    DOI:——
    日期:——
  • Brookhart, Maurice; Chandler, Wayne A.; Pfister, Anne C., Organometallics, 1992, vol. 11, # 3, p. 1263 - 1274
    作者:Brookhart, Maurice、Chandler, Wayne A.、Pfister, Anne C.、Santini, Catherine C.、White, Peter S.
    DOI:——
    日期:——
  • Berke, Heinz; Bankhardt, Willi; Huttner, Gottfried, Chemische Berichte, 1981, vol. 114, # 8, p. 2754 - 2768
    作者:Berke, Heinz、Bankhardt, Willi、Huttner, Gottfried、Seyerl, Joachim v.、Zsolnai, Laszlo
    DOI:——
    日期:——
  • Berke, Heinz; Huttner, Gottfried; Zsolnai, Laszlo, Zeitschrift fur Naturforschung, Teil B: Anorganische Chemie, Organische Chemie, 1981, vol. 36, # 8, p. 938 - 944
    作者:Berke, Heinz、Huttner, Gottfried、Zsolnai, Laszlo
    DOI:——
    日期:——
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