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MoRuCo(CO)8(μ3-S)(η(5)-C5H4C(O)CH3) | 218283-84-2

中文名称
——
中文别名
——
英文名称
MoRuCo(CO)8(μ3-S)(η(5)-C5H4C(O)CH3)
英文别名
[η5-C5H4C(O)CH3]RuCoMo(CO)8(μ3-S);[η5-C5H4COCH3]RuCoMo(CO)8(μ3-S);(μ3-S)RuCoMo(CO)8(CpC(O)CH3);SRuCoMo(CO)8[η5-C5H4C(O)Me]
MoRuCo(CO)8(μ3-S)(η(5)-C5H4C(O)CH3)化学式
CAS
218283-84-2;191278-49-6;218283-85-3
化学式
C15H7CoMoO9RuS
mdl
——
分子量
619.284
InChiKey
HNICPOGMWMFJCW-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:
    MoRuCo(CO)8(μ3-S)(η(5)-C5H4C(O)CH3) 、 nickelocene 以 四氢呋喃 为溶剂, 以25%的产率得到[η5-C5H4COCH3]RuNi(η5-C5H5)Mo(CO)5(μ3-S)
    参考文献:
    名称:
    含SRuNiM(M = Mo,W)核的手性簇的合成,反应和对映体拆分
    摘要:
    的治疗[(η 5 -C 5 H ^ 4 R)乔鲁姆(CO)8(μ 3 -S)]与NICP 2在THF中在回流温度下使含有官能取代的环戊二烯基6个新颖簇配体[(η 5 -C 5 ħ 5)(η 5 -C 5 H ^ 4 COR)NiRuM(CO)5(μ 3 -S)](1,M =钼,R = CH 3 ; 2,M = W,R = CH 3 ; 3, M = Mo,R = OC 2 H 5;4M = W,R = OC 2 H 5;m =1。5,M = Mo,R = COC 6 H 4 COOCH 3;6 M = W,R = COC 6 H 4 COOCH 3)。群集(的反应1 - 6)与2,4-二硝基苯肼进行了调查。酯基很难水解(簇3 – 6)。酰肼可以很容易地冷凝与酮羰基(簇1和2的环戊二烯基环,以形成复合物上)[(η 5 -C 5 H ^ 5)(η 5-C 5 ħ 4 C(NR)CH 3)NiRuM(CO)5(μ
    DOI:
    10.1016/s0022-328x(02)01989-7
  • 作为产物:
    描述:
    nonacarbonyl(μ3-sulfido)dicobaltruthenium(Co-Co,2Ru-Co)sodium acetylcyclopentadienemolybdenum hexacarbonyl四氢呋喃 为溶剂, 以42%的产率得到MoRuCo(CO)8(μ3-S)(η(5)-C5H4C(O)CH3)
    参考文献:
    名称:
    研究的RuCo的反应性2(μ 3 -S)(CO)9:包含四面体芯MRuCoS(MMo,W)和两个四面体芯MRuCoS集群上的集群配合物的合成和表征
    摘要:
    新集群MRuCo(CO)8(μ 3 -S)[ η 5 -C 5 H ^ 4 C(O)CH 3 ](MMo 2,W 3)和[MRuCo(CO)8(μ 3 -S) ] 2 [ η 5 -C 5 H ^ 4 C(O)C 6 H ^ 4 C(O)C 5 H ^ 4 - η 5 ] [MMo 4,W 5 ]已从的RuCo的反应中分离2(μ 3-S)(CO)9 1与[ η 5 -C 5 H ^ 4 C(O)CH 3(CO)3 M] -(MMo,W)和- [M(CO)3 { η 5 -C 5 ħ 4 C(O)C 6 H ^ 4 C(O)C 5 H ^ 4 - η 5 }(CO)3 M] - [MMo,W],分别。已经通过单晶X射线衍射方法建立了簇2和5。簇2的晶体是斜方晶系,空间群PBCA,一个= 26.229(7),b = 18.200(3),C ^ = 15.929(4),V = 7604(6)3和Ž
    DOI:
    10.1016/s0022-328x(98)00757-8
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文献信息

  • Synthesis and reduction of [RuCoMo (μ3-S)(CO)8(RC5H4)] [R  HC(O) (2), CH3C(O) (3), C6H5(O) (4), CH3OC(O)C6H4C(O) (5)] heterometal clusters and structure of [RuCoMo (μ3-S)(CO)8C5H4C(O)C6H4C(O)OCH3]
    作者:Er-Run Ding、Sheng-Min Liu、Zhuan-Yun Zhao、Yuan-Qi Yin、Jie Shun
    DOI:10.1016/s0277-5387(96)00579-7
    日期:1997.1
  • Attempts to resolve metal clusters with chiral framework by optically active hydrazides
    作者:Yu-Hua Zhang、Chun-Gu Xia、Yuan-Qi Yin
    DOI:10.1016/s0020-1693(01)00650-8
    日期:2001.12
    Two kinds of optically active hydrazides reacted with three tetrahedron-type clusters, respectively, to form hydrazone cluster diastereoisomers, intending to separate racemic clusters. However, the mixture of diastereoisomers cannot be separated into single diastereoisomer by silica gel chromatography. The H-1 and C-13 NMR spectra established their presence. (C) 2001 Elsevier Science B.V. All rights reserved.
  • Synthesis and Characterization of New Mixed‐Metal Tetrahedral Carbonyl Clusters Containing (<i>μ</i> <sub>3</sub>‐E)RuCoM (M=Co, Mo) Core and (−)‐DIOP Diphosphine Ligand
    作者:Bao‐Hua Zhu、Yuan‐Qi Yin
    DOI:10.1080/15533170600651421
    日期:2006.5.1
    Four new mixed-metal tetrahedral clusters [(mu(3)-E)RuCo2(CO)(7) ]((-)-DIOP) (E=Se, 1; S, 2) and [(mu(3)-E)RuCoMo(CO)(7)(CpC(O)CH3)]((-)-DIOP) (E=Se, 3; E=S, 4) were obtained by the reactions of [(mu(3)-E)RuCo2(CO)(9)] (E=Se, S) and [(mu(3)-E)RuCoMo(CO)(8)(CpC(O)CH3)] (E = Se, S) with the diphosphine compound (-)-DIOP [(2,2-dimethyl-1,3-dioxolane-4,5-diylbis-methylene)bisdiphenylphosphine] in n -hexane or THF at room temperature, respectively. All clusters were characterized by C, H element analysis, IR and H-1-NMR spectroscopy. The clusters 1 and 3 also were characterized by P-31-NMR spectroscopy.
  • Synthesis and characterization of new RuCoM (M=Co, Mo) mixed-metal linked tetrahedral clusters containing (−)-DIOP and reaction of [(μ3-Se)RuCo2(CO)8]2((−)-DIOP) with Na[Mo(CO)3(η5-C5H4COCH3)]
    作者:Bao-Hua Zhu、Bin Hu、Yuan-Qi Yin、Jie Sun
    DOI:10.1016/j.poly.2005.06.008
    日期:2005.10
    The reactions of diphosphine compound (-)-DIOP [(2,2-dimethyl-1,3-dioxolane-4,5-diylbis-methylene)bisdiphenylphosphine] with [(mu(3)-E)RuCo2(CO)(9)] (E = Se, S) and [(mu(3)-E)RuCoMo(CO)(8)(CpC(O)CH3)] (E = Se, S) in n-hexane and THF at r.t. afford four mixed-metal linked tetrahedral clusters [(mu(3)-E)RuCo2(CO)(8)](2)(-)-DIOP) (E = Se, 1; S, 2) and [(mu(3)-E)RuCoMo(CO)(7)(CPC(O)-CH3)](2)((-)-DIOP) (E = Se, 3; S, 4), respectively. The treatment of 1 with Na[Mo(Co)(3)(eta(5)-C5H4COCH3)] in THF at 60 degrees C produces a known cluster (mu(3)-Se)RuCoMo(CO)(8)(CpC(O)CH3) and a new (-)-DIOP substituted tetrahedral cluster [(mu(3)-Se)RuCoMo(CO)(6)-(CpC(O)CH3)((-)-DIOP)] (5). The structure of cluster I has been determined by single-crystal X-ray diffraction. All clusters were characterized by C, H elemental analysis, IR and H-1 NMR spectroscopy. The clusters 1, 2, 4, 5 also were characterized by P-31 NMR spectroscopy. (c) 2005 Elsevier Ltd. All rights reserved.
  • Zhang, Yu-hua; Yuan, Jian-chao; Yin, Yuan-qi, New Journal of Chemistry, 2001, vol. 25, p. 939 - 944
    作者:Zhang, Yu-hua、Yuan, Jian-chao、Yin, Yuan-qi、Zhou, Zhong-yuan、Chan, Albert S. C.
    DOI:——
    日期:——
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