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tris(triethylphosphine)nickel(0) | 51340-83-1

中文名称
——
中文别名
——
英文名称
tris(triethylphosphine)nickel(0)
英文别名
tris(triethylphosphine)nickel;Nickel--triethylphosphane (1/3);nickel;triethylphosphane
tris(triethylphosphine)nickel(0)化学式
CAS
51340-83-1
化学式
C18H45NiP3
mdl
——
分子量
413.167
InChiKey
DRJOTQNPAMOTML-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):
    7.58
  • 重原子数:
    22
  • 可旋转键数:
    9
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

SDS

SDS:2d78294a715dc4eb84a2025dc4d48a62
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反应信息

  • 作为反应物:
    描述:
    吲哚tris(triethylphosphine)nickel(0)甲苯 为溶剂, 以43%的产率得到trans-[HNi(C8H6N)(PEt3)2]
    参考文献:
    名称:
    Oxidative insertion into the N–H bond of carbazole, indole and pyrrole with zerovalent metals
    摘要:
    The reactions of carbazole (C12H8NH), indole (C8H6NH) and pyrrole (C4H4NH) with the zerovalent [Pt(PEt3)(3)], [Pd(PEt3)(3)] and [Ni(PEt3)(3)] gave oxidative insertion into the N-H bond, affording the corresponding hydrides of the type trans-[HM(LN)(PEt3)(2)], LN = de-protonated heterocyclic ligand; the isolated compounds for platinum were trans-[HPt(C8H6N)(PEt3)(2)] (1), trans-[HPt(C4H4N)(PEt3)(2)] (2), and for nickel trans-[HNi(C12H8N)(PEt3)(2)] (3), trans-[HNi(C8H6N)(PEt3)(2)] (4) and trans-[HNi(C4H4N)(PEt3)(2)] (5); on using palladium the corresponding hydrides were also detected in solution, however, after longer reaction time the double substituted compounds: trans-[Pd(C12H8N)(2)(PEt3)(2)] (6), trans-[Pd(C8H6N)(2)(PEt3)(2)] (7) and trans-[Pd(C4H4N)(2)(PEt3)(2)] (8) were obtained. A crystal structure is reported for 6. (C) 2002 Elsevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0022-328x(02)01979-4
  • 作为产物:
    描述:
    三乙基膦 、 bis(triethylphosphine)nickel(II) bromide 在 作用下, 以 not given 为溶剂, 生成 tris(triethylphosphine)nickel(0)
    参考文献:
    名称:
    Pasto, Daniel J.; Huang, Nai-Zhong, Organometallics, 1985, vol. 4, # 8, p. 1386 - 1395
    摘要:
    DOI:
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文献信息

  • Reactivity of Substituted Thiophenes toward Tris(triethylphosphine)platinum(0), -palladium(0), and -nickel(0)
    作者:Maira Hernández、Georgina Miralrio、Alma Arévalo、Sylvain Bernès、Juventino J. García、Carolina López、Peter M. Maitlis、Federico del Rio
    DOI:10.1021/om0103512
    日期:2001.9.1
    The reactions of [M(PEt3)3] (M = Pt (1), Pd (2), Ni (3)) with 3-chlorothiophene, 2-chlorothiophene, 3-nitrothiophene, 2-nitrothiophene, 2-methoxythiophene, 3-methoxythiophene, 2-acetylthiophene, and 3-acetylthiophene afforded thiaplatinacycles of the type [(Et3P)2M(C,S-C4H3RS)], (for M = Pt, R = Cl (4 and 5), NO2 (6 and 7), MeO (8 and 9), Ac (10 and 11); for M = Pd, R = Cl (12 and 13), NO2 (14), MeO
    [M(PEt 3)3 ](M = Pt(1),Pd(2),Ni(3))与3-氯噻吩,2-氯噻吩,3-硝基噻吩,2-硝基噻吩,2-甲氧基噻吩的反应, 3-甲氧基噻吩,2-乙酰基噻吩和3-乙酰基噻吩提供了[(Et 3 P)2 M(C,S- C 4 H 3 RS)]类型的硫氨铂环(对于M = Pt,R = Cl(4和5),NO 2(6和7),MeO(8和9),Ac(10和11)); 对于M = Pd,R = Cl(12和13),NO 2(14),MeO(15和16),Ac(17和18),对于M = Ni,R = Cl(19))。当3和2-氯噻吩进行反应,从氧化加成的C-Cl键的所得的另一种化合物可被分离,与制剂[(ET 3 P)2的Ni(CL)(η 1 -T)](20) 。此外,3与2-硝基噻吩的反应还产生了一种由CH活化反应衍生的化合物[[Et 3 P)2的Ni(H)(η 1 -NO 2 T)
  • Reactions of halogen(2,4,6-tri-tert-butylphenylimino)phosphine complexes with electrophiles and nucleophiies: abstraction or substitution of the halogen
    作者:E. Niecke、J. F. Nixon、P. Wenderoth、B. F. Trigo Passos、M. Nieger
    DOI:10.1039/c39930000846
    日期:——
    The structure of the first nickel halogeniminophosphine complex, i.e.(PEt3)2Ni(X–PNAr)2(Ar = 2,4,6-tri-tert-butylphenyl); X = Cl is reported; reactions of this and related compounds with AlCl3 afford the cationic complexes 7–10; the alkyliminophosphine complexes 12 and 13 are obtained by treatment of the chloroiminophosphine complexes 1a and 4a with Grignard reagent.
    第一镍halogeniminophosphine复合物的结构,即(PET 3)2的Ni(X-P NAR)2(AR = 2,4,6-三-叔丁基苯基); X =报道氯;这种反应和相关的化合物与氯化铝3得到阳离子络合物7 - 10 ; 烷基亚氨基膦配合物12和13是通过用格氏试剂处理氯亚氨基膦配合物1a和4a而获得的。
  • Reaktionen vontBu2P-P=P(Me)tBu2 mit (Et3P)2NiCl2 und [{η2-C2H4}Ni(PEt3)2]
    作者:Helmut Goesmann、Eberhard Matern、Jolanta Olkowska-Oetzel、Jerzy Pikies、Gerhard Fritz
    DOI:10.1002/1521-3749(200106)627:6<1181::aid-zaac1181>3.0.co;2-2
    日期:2001.6
    (Bu2P)-Bu-t-P=P(Me)Bu-t(2) (1) forms with (Et3P)(2)NiCl2 (2) and Na(Nph) the [mu-(1,3: 2,3-eta-(Bu2P4Bu2)-Bu-t-Bu-t)Ni(PEt3)Cl}(2)] (3) as main product. Using Na/Hg instead as reducing agent the Ni-0 compounds [eta (2)-(Bu2P)-Bu-t-P}Ni(PEt3)(2)] (4), [eta (2)-(Bu2P)-Bu-t-P=P-(PBu2)-Bu-t}Ni(PEt3)(2)] (5) and [(Et3P)Ni(mu -(PBu2)-Bu-t)](2) (6) with four-membered Ni2P2 ring result. [eta (2)-C2H4}Ni(PEt3)(2)] yields with 1 also 4. The compounds were characterized by H-1 and P-31H-1} NMR investigations and 3 also by a single crystal X-ray analysis. It crystallizes triclinic in the space group P (1) over bar with a = 1129.4(2), b = 1256.8(3), c = 1569.5(3) pm, alpha = 72.44(3)degrees, beta = 70.52(3)degrees and gamma = 74.20(3)degrees.
    (Bu2P)-Bu-t-P=P(Me)Bu-t(2) (1) 与 (Et3P)(2)NiCl2 (2) 和 Na(Nph) 反应,生成主产物 [μ-(1,3:2,3-η(Bu2P4Bu2)-Bu-t-Bu-t)Ni(PEt3)Cl}(2)] (3)。使用 Na/Hg 作为还原剂时,生成 Ni-0 化合物 [η(2)-(Bu2P)-Bu-t-P}Ni(PEt3)(2)] (4)、[η(2)-(Bu2P)-Bu-t-P=P-(PBu2)-Bu-t}Ni(PEt3)(2)] (5) 以及含有四元 Ni2P2 环的 [(Et3P)Ni(μ-(PBu2)-Bu-t)](2) (6)。[η(2)-C2H4}Ni(PEt3)(2)] 与 1 反应生成 4。这些化合物通过 H-1 和 P-31H-1} NMR 实验表征,3 还通过单晶 X 射线分析表征。该化合物为三斜晶系,空间群为 P (1) over bar,晶格参数为 a = 1129.4(2) pm,b = 1256.8(3) pm,c = 1569.5(3) pm,α = 72.44(3)°,β = 70.52(3)°,γ = 74.20(3)°。
  • Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: Ni: Org.Verb.1, 1.1.1.1.3, page 31 - 47
    作者:
    DOI:——
    日期:——
  • Breil,H.; Wilke,G., Angewandte Chemie, 1970, vol. 82, p. 355 - 356
    作者:Breil,H.、Wilke,G.
    DOI:——
    日期:——
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