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[(1,2-bis(diphenyiphosphlno)ethane)Ni(μ-1,3-propanedithiolato)Fe(CN)2(CO)2] | 1174416-02-4

中文名称
——
中文别名
——
英文名称
[(1,2-bis(diphenyiphosphlno)ethane)Ni(μ-1,3-propanedithiolato)Fe(CN)2(CO)2]
英文别名
[(dppe)Ni(μ-pdt)Fe(CN)2(CO)2];(CO)2(CN)2Fe(pdt)Ni(C2H4(PPh2)2);(CO)2(CN)2Fe(pdt)Ni(dppe)
[(1,2-bis(diphenyiphosphlno)ethane)Ni(μ-1,3-propanedithiolato)Fe(CN)2(CO)2]化学式
CAS
1174416-02-4
化学式
C33H30FeN2NiO2P2S2
mdl
——
分子量
727.23
InChiKey
TXXZGCQWPVZPJA-UHFFFAOYSA-L
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:
    [(1,2-bis(diphenyiphosphlno)ethane)Ni(μ-1,3-propanedithiolato)Fe(CN)2(CO)2]三(五氟苯基)硼烷二氯甲烷 为溶剂, 以82%的产率得到(CO)2(CNB(C6F5)3)2Fe(pdt)Ni(C2H4(PPh2)2)
    参考文献:
    名称:
    Hydrogen Activation by Biomimetic [NiFe]-Hydrogenase Model Containing Protected Cyanide Cofactors
    摘要:
    Described are experiments demonstrating incorporation of cyanide cofactors and hydride substrate into [NiFe]-hydrogenase (H(2)ase) active site models. Complexes of the type (CO)(2)(CN)(2)Fe(pdt)Ni(dxpe) (dxpe = dppe, 1; dxpe = dcpe, 2) bind the Lewis acid B(C6F5)(3) (BAr3F) to give the adducts (CO)(2)(CNBAr3F)(2)Fe(pdt)Ni(dxpe), (1(BAr3F)(2), 2(BAr3F)(2)). Upon decarbonylation using amine oxides, these adducts react with H-2 to give hydrido derivatives [(CO)(CNBAr3F)(2)Fe(H)(pdt)Ni-(dxpe)](-) (dxpe = dppe, [H3(BAr3F)(2)](-); dxpe = dcpe, [H4(BAr3F)(2)](-)). Crystallographic analysis shows that Et4N[H3(BAr3F)(2)] generally resembles the active site of the enzyme in the reduced, hydride-containing states (Ni-C/R). The Fe-H center dot center dot center dot Ni center is unsymmetrical with r(Fe-H) = 1.51(3) angstrom and r(Ni-H) = 1.71(3) angstrom. Both crystallographic and F-19 NMR analyses show that the CNBAr3F- ligands occupy basal and apical sites. Unlike cationic Ni-Fe hydrides, [H3(BAr3F)(2)](-) and [H4(BAr3F)(2)](-) oxidize at mild potentials, near the Fc(+/0) couple. Electrochemical measurements indicate that in the presence of base, [H3(BAr3F)(2)](-) catalyzes the oxidation of H-2. NMR evidence indicates dihydrogen bonding between these anionic hydrides and R3NH+ salts, which is relevant to the mechanism of hydrogenogenesis. In the case of Et4N[H3(BAr3F)(2)], strong acids such as HCl induce H-2 release to give the chloride Et4N[(CO)(CNBAr3F)(2)Fe(Cl)(pdt)Ni-(dppe)].
    DOI:
    10.1021/ja404580r
  • 作为产物:
    描述:
    1,2-双(二苯基膦)乙烷氯化镍 、 cis,cis,cis-[Fe(CN)2(CO)2(1,3-propanedithiolato)](2-) 以 二氯甲烷 为溶剂, 生成 [(1,2-bis(diphenyiphosphlno)ethane)Ni(μ-1,3-propanedithiolato)Fe(CN)2(CO)2]
    参考文献:
    名称:
    氢化酶中Ni-Fe位点的类似物的合成与结构
    摘要:
    二硫键桥接Ni-Fe络合物[(dppe)Ni II(μ-SEt)2 Fe II(CN)2(CO)2 ] 6和[(dppe)Ni II(μ-pdt)Fe II(CN)2(CO )2 ] [dppe = 1,2-双(二苯基膦基)乙烷和pdt = 1,3-丙二硫醇酯]已经合成,并且在结构上被表征为Ni-Fe氢化酶活性位点的结构类似物。合成从关键中间体fac- [Fe(CN)2(CO)3 I] -开始。[(dppe)Ni II(μ-SEt)2 Fe II(CN)2(CO)2 ] 6,其中设有一个近似平面diethanethiolate桥接镍-铁菱形,和2CN的布置-配体是顺式到彼此。相比之下,[(DPPE)的Ni II(μ-PDT)的Fe II(CN)2(CO)2 ]示出了一个更折叠的NiS 2的Fe菱形,短镍-铁距离,反2CN -配体,和一个semibridging CN - Ni和Fe之间。
    DOI:
    10.1021/ic900929u
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