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{Fe(CO)4(vdpp-P)} | 105954-74-3

中文名称
——
中文别名
——
英文名称
{Fe(CO)4(vdpp-P)}
英文别名
tetracarbonyl(1,1-bis(diphenylphoshino)ethene-P)iron
{Fe(CO)4(vdpp-P)}化学式
CAS
105954-74-3
化学式
C30H22FeO4P2
mdl
——
分子量
564.297
InChiKey
SWXQOZLPECKIIX-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:
    {Fe(CO)4(vdpp-P)} 、 di(rhodium)tetracarbonyl dichloride 以 not given 为溶剂, 生成
    参考文献:
    名称:
    The systematic synthesis of heterobimetallic complexes with only one bridging Ph2PCH2PPh2(dppm) ligand: crystal structures of [(OC)4Fe(µ-dppm)RhCl(CO)] and [(OC)3Fe(µ-dppm)(µ-CO)PtBr2]
    摘要:
    [(OC)4Fe(dppm-P)](dppm = Ph2PCH2PPh2)与[RH2Cl2(CO)4]反应生成[(OC)4Fe(µ-dppm)RhCl(CO)],其中含有一个 Fe-Rh 键,但没有桥接羰基;与[PtBr2(环辛烷-1,5-二烯)]反应生成的[(OC)3Fe(µ-dppm)(µ-CO)PtBr2]显示出其中一个羰基配体的桥联作用。
    DOI:
    10.1039/c39860000013
  • 作为产物:
    描述:
    五羰基铁1,1-双(二苯基膦)乙烯 在 (CH3)3NO*2H2O 作用下, 以 四氢呋喃甲醇 为溶剂, 以70%的产率得到tricarbonyl(1,1,-bis(diphenylphosphino)ethene)iron
    参考文献:
    名称:
    Syntheses of iron-containing heterometallic complexes using tridentate phosphine ligands; the crystal structure of [(OC)3Fe{(Ph2P)2CHCH2PPh2}Ru3(CO)9{Ph2PC(CH2)PPh2}]
    摘要:
    Treatment of [Fe(CO)3(dppee)] [dppee = 1,1 -bis(diphenylphosphino)ethene] with PPh2H gives the addition product [Fe(CO)3{(Ph2P)2CHCH2PPh2}] 1. The unco-ordinated phosphine group of complex 1 reacts with [{RhCl(CO)2}2] to give [(OC)4Fe{Ph2PCH(PPh2)CH2PPh2}RhCl] 3 via [(OC)3Fe-{(Ph2P)2CHCH2PPh2}Rh(CO)Cl2Rh(CO)2] 2. Complex 1 reacts with [Ru3(CO)10(dppee)] to give the heterometallic complex [(OC)3Fe{(Ph2P)2CHCH2PPh2}Ru3(CO)9(dppee)] 4 the structure of which has been determined by X-ray crystallography.
    DOI:
    10.1039/dt9920002939
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文献信息

  • Reactions of metal carbonyl cluster complexes with multidentate phosphine ligands; preparation of 1,1-bis(diphenylphosphino)ethene derivatives, and the x-ray crystal structures of Fe(CO)3(dppee) and Os3(CO)10(dppee) (dppee = Ph2PC(CH2)PPh2)
    作者:Jennifer A. Clucas、Richard H. Dawson、P.Ann Dolby、Marjorie M. Harding、Keith Pearson、Anthony K. Smith
    DOI:10.1016/0022-328x(86)80228-5
    日期:1986.9
    A number of metal cluster carbonyl complexes containing the 1,1-bis(diphenylphosphino)ethene (dppee) ligand have been prepared and characterised, as have the mononuclear iron complexes Fe(CO)4(dppee) and Fe(CO)3(dppee). The crystal structures of Fe(CO)3(dppee) and Os3(CO)10(dppee) have been determined.
    已经制备并表征了许多含有1,1-双(二苯基膦基乙烯(dppee)配体属簇羰基配合物,以及单核配合物Fe(CO)4(dppee)和Fe(CO)3(dppee) )。已经确定了Fe(CO)3(dppee)和Os 3(CO)10(dppee)的晶体结构。
  • Organo–platinum–iron complexes containing one bridging Ph<sub>2</sub>PCH<sub>2</sub>PPh<sub>2</sub>ligand. Crystal structures of [(OC)<sub>3</sub>Fe(µ-dppm)(µ-CO)Pt(PPh<sub>3</sub>)], [(OC)<sub>2</sub>Fe(µ-dppm){µ-C(O)C<sub>2</sub>H<sub>2</sub>}Pt(PPh<sub>3</sub>)], and [(OC)<sub>3</sub>Fe(µ-dppm)(µ-CMeCH<sub>2</sub>)Pt(PPh<sub>3</sub>)][BF<sub>4</sub>]
    作者:Xavier L. R. Fontaine、Grant B. Jacobsen、Bernard L. Shaw、Mark Thornton-Pett
    DOI:10.1039/dt9880000741
    日期:——
    MeCO2CCH) also reacted with complex (1), at 80 °C, to give complexes of type [(OC)2Fe(µ-dppm)µ-C(O)CRCH}Pt(PPh3)]. At 20 °C, MeCCH and 4-MeC6H4CCH reacted with (1) to give isolable complexes of type [(OC)2Fe(µ-dppm)µ-C(O)CHCR}Pt(PPh3)] which isomerised in solution, at rates dependent on the steric bulk of R, to complexes of type [(OC)2Fe(µ-dppm)µ-C(O)CRCH}Pt(PPh3)]. The mechanism of the alkyne-insertion
    用[Pt(反式-PhCH CHPh)(PPh 3)2 ]处理[Fe(CO)4(dppm- P)](dppm = Ph 2 PCH 2 PPh 2),得到双属[[OC)3 Fe(µ -dppm)(μ-CO)Pt(PPh 3)](1)的分离产率为75%。还通过在PPh 3存在下通过四氢硼酸还原[(OC)3 Fe(μ-dppm)(μ-CO)PtCl 2 ]来制备配合物(1)。它的结构是通过X射线晶体学确定的:晶体是三斜晶的,空间群为P,其中a = 1 177.3(2),b = 1 198.4(1),c = 1 776.5(1)pm,α= 103.34(1),β= 107.81(1),γ= 91.76(1)°,和Z = 2;对于5 422个观察到的反射,最终R因子0.0257。结构表明,羰基配体之一几乎对称地桥接了Fe–Pt键。用HBF 4 ·OEt 2对配合物(1)进行质子化反应得到氢化物[[OC)4
  • Jacobsen, Grant B.; Shaw, Bernard L.; Thornton-Pett, Mark, Journal of the Chemical Society, Dalton Transactions, 1987, p. 2751 - 2756
    作者:Jacobsen, Grant B.、Shaw, Bernard L.、Thornton-Pett, Mark
    DOI:——
    日期:——
  • Jacobsen, Grant B.; Shaw, Bernard L.; Thornton-Pett, Mark, Journal of the Chemical Society, Dalton Transactions, 1987, p. 1509 - 1514
    作者:Jacobsen, Grant B.、Shaw, Bernard L.、Thornton-Pett, Mark
    DOI:——
    日期:——
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