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trans-carbonylchlorobis(triphenylarsine)iridium(I) | 15682-62-9

中文名称
——
中文别名
——
英文名称
trans-carbonylchlorobis(triphenylarsine)iridium(I)
英文别名
——
trans-carbonylchlorobis(triphenylarsine)iridium(I)化学式
CAS
15682-62-9;23954-42-9
化学式
C37H30As2ClIrO
mdl
——
分子量
868.161
InChiKey
CILFPAHRHDXIBS-UHFFFAOYSA-M
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:
    trans-carbonylchlorobis(triphenylarsine)iridium(I)氧代[二(三氟甲基)]铵 为溶剂, 以44%的产率得到bis{bis(trifluoromethyl)amino-oxy}carbonylchlorobis(triphenylarsine)iridium(III)
    参考文献:
    名称:
    Booth, Brian L.; Haszeldine, Robert N.; Holmes, Robert G.G., Journal of the Chemical Society, Dalton Transactions, 1982, p. 523 - 530
    摘要:
    DOI:
  • 作为产物:
    描述:
    (tetrabutylammonium)[IrCl2(CO)2]三苯胂四氢呋喃 为溶剂, 以69%的产率得到trans-carbonylchlorobis(triphenylarsine)iridium(I)
    参考文献:
    名称:
    一种高收率的合成方法,以反式-的[Ir(ER 3)2(CO)X](ER 3 = PME 3,PET 3,PPhMe 2,PPH 2我,P(OME)3,ASME 3,ASET 3, AsPh 3,SbPh 3; X = Cl,Br)
    摘要:
    当用两个当量的芳基处理时,配合物[Ir(CO)2 X 2 ] [NBu 4 ](X = Cl,Br)形成Vaska型配合物,反式-[Ir(ER 3)2(CO)X]。 -或在CO气氛下的烷基膦,rs或啶。不论锥角如何,合成都是针对广泛的膦,rs或stibines进行的。对于小锥角配体,在低温下将配体初始添加到[Ir(CO)2 X 2 ] [NBu 4 ]中。三种新型Vaska型配合物反式-[Ir(P(OMe)3)2(CO)Cl]的合成与表征还报道了反式-[Ir(AsMe 3)2(CO)Cl]和反式-[Ir(AsEt 3)2(CO)Cl]。
    DOI:
    10.1016/s0277-5387(99)00225-9
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文献信息

  • Trimethylenemethane metal complexes. Part 1. Synthesis of ruthenium, osmium, rhodium, and iridium complexes
    作者:Michael D. Jones、Raymond D. W. Kemmitt、Andrew W. G. Platt
    DOI:10.1039/dt9860001411
    日期:——
    methyl]-3-trimethylsilylprop-1-ene, available from 2-methylprop-2-en-1-ol, serves as a new entry into trimethylenemethane (tmm) metal complexes. Reaction with low-valent metal complexes affords the first tmm metal complexes of ruthenium, osmium, rhodium, and iridium: [MCl(NO)(PPh3)(η4-tmm)](M = Ru or Os), [Os(CO)2(PPh3)(η4-tmm)], [MCI(PPh3)2(η4-tmm)](M = Rh or Ir), and [IrX(CO)(L)(η4-tmm)](X = CI,
    可从2-甲基丙-2-烯-1-醇获得的2-[(甲基磺酰氧基)甲基] -3-三甲基甲硅烷基丙-1-烯作为三甲甲烷(TMm)属络合物的新入口。具有低原子价的属配合物反应,得到的第一TMM属配合物:[的MC1(NO)(PPH 3)(η 4 -TMm)](M = Ru或OS),[OS( CO)2(PPH 3)(η 4 -TMm)],[MCI(PPH 3)2(η 4 -TMm)](M =)和[IRX(CO)(L)(η 4 - TMm)](X = CI,L = PPh 3或AsPh 3; X = Br,L = PPh 3)。一个η的脱甲硅烷基3-烯丙基中间更趋合理的结果,并通过与的[Rh η反应已经被核实3 -CH 2 C(CH 2森达3)CH 2 }(CO)(PME 2 PH)2 ] BPH 4在含这给了复杂甲基化物的[Rh(CO)(PME 2 PH)2(η 4
  • Developing Reagents To Orient Fullerene Derivatives. Formation and Structural Characterization of <b>(</b>η<sup>2</sup>-C<sub>60</sub>O)Ir(CO)Cl(As(C<sub>6</sub>H<sub>5</sub>)<sub>3</sub>)<sub>2</sub>
    作者:Alan L. Balch、David A. Costa、Bruce C. Noll、Marilyn M. Olmstead
    DOI:10.1021/ic950484d
    日期:1996.1.1
    fullerene oxides that are suitable for single-crystal X-ray diffraction, the reactions between C(60)O and Vaska type iridium complexes have been examined. While reaction with Ir(CO)Cl(P(C(6)H(5))(3))(2)(and with triphenylphosphine but not triphenylarsine) results in partial deoxygenation of the fullerene epoxide, reaction with Ir(CO)Cl(As(C(6)H(5))(3))(2)()()produces crystalline (eta(2)-C(60)O)Ir(CO)Cl(AsPh(3))(2)
    为了获得适用于单晶X射线衍射的富勒烯氧化物晶体,已经研究了C(60)O和Vaska型配合物之间的反应。与Ir(CO)Cl(P(C(6)H(5))(3))(2)(与三苯基膦而不是三苯基ar)反应会导致富勒烯环氧化物部分脱氧,而与Ir(CO)反应Cl(As(C(6)H(5))(3))(2)()()产生晶体(eta(2)-C(60)O)Ir(CO)Cl(AsPh(3))( 2).4.82C(6)H(6).0.18CHCl(3)。(eta(2)-C(60)O)Ir(CO)Cl(AsPh(3))(2).4.82C(6)H(6).0.18CHCl(3)形式的黑色三角棱镜空间组P2(1)/ n,其中a = 14.662(2)Å,b = 19.836(2)Å,c = 28.462(5)Å,并且在123(2)K时beta = 100.318(12)度,其中Z = 4.对10 472个反射和1095个参数(
  • Reactions of 3-trimethylsilyl-2-(methylsulphonyloxymethyl)prop-1-ene with low-valent complexes of molybdenum, ruthenium, osmium, rhodium, iridium, palladium, and platinum. New syntheses of η<sup>4</sup>-trimethylenemethane complexes of ruthenium, osmium, and iridium
    作者:Michael D. Jones、Raymond D. W. Kemmitt
    DOI:10.1039/c39850000811
    日期:——
    The η4-trimethylenemethane (tmm) metal complexes [MCl(NO)(PPh3)(tmm)](M = Ru or Os), [Os(CO)2(PPh3)(tmm)], [IrX(CO)(L)(tmm)](X = Cl, L = PPh3 or AsPh3; X = Br, L = PPh3), [IrCl(PPh3)2(tmm)], and [Ir(CO)(PPh3)2(tmm)][OS(O)2Me] have been prepared in good yields by the action of Me3SiCH2C(CH2)-CH2OS(O)2Me} upon [MCl(NO)(PPh3)n](M = Ru, n= 2; M = Os, n= 3), [IrX(CO)L2], [Ir2Cl2(C8H14)4]+ 4PPh3, and [IrH(CO)(PPh3)3]
    的η 4 -trimethylenemethane(TMM)属配合物[的MC1(NO)(PPH 3)(TMM)](M = Ru或OS),[OS(CO)2(PPH 3)(TMM)],[IRX(CO )(L)(TMm)](X = Cl,L = PPh 3或AsPh 3; X = Br,L = PPh 3),[IrCl(PPh 3)2(TMm)]和[Ir(CO)( PPh 3)2(TMm)] [OS(O)2 Me]是通过Me 3 SiCH 2 C(CH 2)-CH 2 OS(O)2 Me}对[MCl( NO)(PPh 3)n ](M = Ru,n = 2;M = OS,n= 3),[IrX(CO)L 2 ],[Ir 2 Cl 2(C 8 H 14)4 ] + 4PPh 3和[IrH(CO)(PPh 3)3 ]。
  • New products in an old reaction: isomeric products from H2 addition to Vaska’s complex and its analogues
    作者:Sarah K. Hasnip、Simon B. Duckett、Christopher J. Sleigh、Diana R. Taylor、Graham K. Barlow、Mike J. Taylor
    DOI:10.1039/a905590h
    日期:——
    para-Hydrogen enhanced NMR signals aid detection of minor isomers of complexes IrH2(L)2(CO)Cl (L = PPh3, PMe3, PPh2Cl and AsPh3) containing magnetically inequivalent hydride ligands that are produced via addition across the L–Ir–L axis of Ir(L)2(CO)Cl: in the case of L = PPh3, reaction with CO and H2 is shown to yield the substitution product IrH2(CO)2(PPh3)Cl which reacts further via HCl transfer to form IrH(CO)(PPh3)2Cl2 and thereby enables the detection of IrH3(CO)2(PPh3).
    对氢增强的核磁共振信号有助于检测IrH2(L)2(CO)Cl(L = PPh3、PMe3、PPh2Cl和AsPh3)的次要异构体,这些化合物含有磁不等的氢化物配体,通过Ir(L)2(CO)Cl的L-Ir-L轴上的加成反应生成:在L = PPh3的情况下,与CO和H2的反应生成取代产物IrH2(CO)2(PPh3)Cl,该产物通过HCl转移进一步反应生成IrH(CO)(PPh3)2Cl2,从而能够检测IrH3(CO)2(PPh3)。
  • Some oxidative-addition reactions of the diradical, perfluoro-NN′-dimethylethane-1,2-bis(amino-oxyl), CF<sub>3</sub>N(O)CF<sub>2</sub>CF<sub>2</sub>N(O)CF<sub>3</sub>, with iridium(<scp>I</scp>) and platinum(<scp>0</scp>) complexes
    作者:Brian L. Booth、Robert N. Haszeldine、Robert G. G. Holmes
    DOI:10.1039/dt9820000671
    日期:——
    The stable diradical CF3N(O)CF2CF2N(O)CF3 reacts with trans-[IrCl(CO)L2](L = PPh3, AsPh3, or PMePh2), trans-[IrON(CF3)2}(CO)(PPh3)2], and [Pt(PPh3)4] to form the seven-membered ring metallacyclic complexes [[graphic omitted]Cl(CO)L2], [[graphic omitted]ON(CF3)2}(CO)(PPh3)2], and [[graphic omitted](PPh3)2] respectively.
    稳定的双自由基CF 3 N(O)CF 2 CF 2 N(O)CF 3与反式-[IrCl(CO)L 2 ](L = PPh 3,AsPh 3或PMePh 2),反式-[Ir ON(CF 3)2 }(CO)(PPh 3)2 ]和[Pt(PPh 3)4 ]形成七元环属环配合物[[图略] Cl(CO)L 2 ],[[图片省略] ON(CF 3)2 }(CO)(PPh 3)2]和[[省略图示](PPh 3)2 ]。
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