tricarbonyl-bis(triethylphosphite)rhenium(H) | 209606-17-7

• 英文名称: tricarbonyl-bis(triethylphosphite)rhenium(H)
• 英文别名: ReH(CO)3(triethylphosphite)2
• CAS: 209606-17-7
• 化学式: C₁₅H₃₁O₉P₂Re
• 分子量: 603.56
• InChiKey: KCECCKZWPCRBSJ-UHFFFAOYSA-N

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：

  tricarbonyl-bis(triethylphosphite)rhenium(H) 、 benzenediazonium tetrafluoroborate 以 丙酮 为溶剂， 生成
  参考文献：
  名称：

  of的芳基二氮杂配合物的制备，结构和电化学研究：带有双（二氮烯）或双（二重氮基）桥联配体的第一个杂双核和杂三核衍生物的合成。

  摘要：

  单核和双核芳基二氮杂配合物[Re（C6H5N = NH）（CO）5-nPn] BY4（1-5）和[（Re（CO）5-nPn）2-（mu-HN = NAr-ArN = NH ）]（BY4）2（6-12）[P = P（OEt）3，PPh（OEt）2，PPh2OEt; n = 1-4；Ar-Ar = 4,4'-C6H4-C6H4，4,4'-（2-CH3）C6H3-C6H3（2-CH3），4,4'-C6H4-CH2-C6H4; 通过使氢化物种类ReH（CO）5-nPn与适当的单和双（芳基重氮）阳离子反应来制备Y = F，Ph）。对这些化合物以及其他制备的化合物进行光谱表征（IR； 1H，31P，13C和15N NMR数据），并通过X射线晶体结构测定表征1a。[Re（C6H5N = NH）（CO）（P（OEt）3）4] BPh4（1a）在空间组P1中结晶，其中a = 15.380（5）A，b = 13

  DOI：

  10.1021/ic991393+

文献信息

• Preparation and Reactivity of Hydrazine Complexes of Rhenium: Synthesis of 1,2‐Diazene (NH=NH) and Methyleneimine (CH ₂ =NH) Derivatives
  作者：Gabriele Albertin、Stefano Antoniutti、Maria Teresa Giorgi

  DOI：10.1002/ejic.200300155

  日期：2003.8

  The hydrazine complexes [Re(RNHNH2)(CO)nP5−n]BPh4 [R = H, CH3, Ar; n = 1−4; P = P(OEt)3, PPh(OEt)2, PPh2OEt] were prepared by allowing the hydride species [ReH(CO)nP5−n] to react first with a Bronsted acid and then with hydrazine. The reaction of either [Re(NH2NH2)(CO)nP5−n]BPh4 or [Re(ArNHNH2)(CO)nP5−n]BPh4 with Pb(OAc)4 at −40 °C proceeds with the selective oxidation of the hydrazine ligand to yield

  肼配合物 [Re(RNHNH2)(CO)nP5−n]BPh4 [R = H, CH3, Ar; n = 1−4; P = P(OEt)3, PPh(OEt)2, PPh2OEt] 通过使氢化物 [ReH(CO)nP5-n] 首先与布朗斯台德酸反应，然后与肼反应来制备。[Re(NH2NH2)(CO)nP5−n]BPh4 或 [Re(ArNHNH2)(CO)nP5−n]BPh4 与 Pb(OAc)4 在 -40 °C 的反应伴随着肼的选择性氧化配体产生 [Re(NH=NH)(CO)nP5−n]BPh4 或 [Re(ArN=NH)(CO)nP5−n]BPh4。[Re( NHNH2)(CO)nP5−n]BPh4 (n = 1, 2) 与 Pb(OAc)4 在 -40 °C 下氧化得到 [Re( N=NH)(CO)nP5−n] BPh4 和 [Re(η1-NH=CH2)(CO)nP5−n]B
• Albertin, Gabriele; Antoniutti, Stefano; Garcia-Fontan, Soledad, Journal of the Chemical Society, Dalton Transactions, 1998, # 12, p. 2071 - 2081
  作者：Albertin, Gabriele、Antoniutti, Stefano、Garcia-Fontan, Soledad、Carballo, Rosa、Padoan, Fabio

  DOI：——

  日期：——
• Preparation of benzophenone imine complexes of transition metals
  作者：Gabriele Albertin、Stefano Antoniutti、Alberto Magaton

  DOI：10.1016/j.ica.2006.12.001

  日期：2008.5

  Benzophenone imine [M(eta(1)-NH=CPh2)(CO)(n)P5-n] BPh4 [M = Mn, Re; n = 2, 3; P = P(OEt)(3), PPh(OEt)(2), PPh2OEt, PPh3] complexes were prepared by allowing triflate M(K-1-OTf)(CO)(n)P5-n compounds to react with an excess of the imine. Hydride-imine [MH(eta(1)-NH=CPh2)P-4]BPh4 (M = Ru, Os), triflate-imine [Os(k(1)-OTf)(eta(1)-NH=CPh2)P-4]BPh4 and bis(imine) [Ru(eta(1)-NH= CPh2)(2) P-4](BPh4)(2) [P = P(OEt)(3)] derivatives were also prepared. The complexes were characterized spectroscopically (IR, H-1, P-31, C-13 NMR) and a geometry in solution was also established. Hydride-benzophenone imine [IrHCl(eta(1)-NH=CPh2)LdPPh(3))(2)]BPh4 and [IrHCl(eta(NH)-N-1= CPh2)LdAsPh(3))(2)] BPh4 [L = P(OEt)(3) and PPh(OEt)(2)] complexes were prepared by reacting hydride IrHCl2L(PPh3)(2) and IrHCl2L(AsPh3)(2) precursors with an excess of imine. Dihydride IrH2(eta(1)-NH=CPh2)(PPh3)(3) complex was also obtained and a geometry in solution was proposed. (C) 2006 Elsevier B. V. All rights reserved.
• Albertin, Gabriele; Antoniutti, Stefano; Castro, Jesus, Journal of Organometallic Chemistry, 2006, vol. 691, p. 5592 - 5601
  作者：Albertin, Gabriele、Antoniutti, Stefano、Castro, Jesus、Carniato, Stefano、Garcia-Fontan, Soledad

  DOI：——

  日期：——