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(η5-cyclopentadienyl)methylbis(triphenylphosphine)ruthenium | 34692-09-6

中文名称
——
中文别名
——
英文名称
(η5-cyclopentadienyl)methylbis(triphenylphosphine)ruthenium
英文别名
[RuMe(η-C5H5)(PPh3)2];[RuMe(PPh3)2(η-C5H5)];(cyclopentadienyl)Ru(PPh3)2(Me);(η5-C5H5)Ru(PPh3)2Me;CpRu(PPh3)2(Me)
(η5-cyclopentadienyl)methylbis(triphenylphosphine)ruthenium化学式
CAS
34692-09-6
化学式
C42H38P2Ru
mdl
——
分子量
705.781
InChiKey
TXMGRYMKVZDGCY-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:
    (η5-cyclopentadienyl)methylbis(triphenylphosphine)ruthenium四丁基氯化铵 、 tetrabutylammonium tetrafluoroborate 作用下, 以 二氯甲烷 为溶剂, 以60%的产率得到二(三苯基膦)环戊二烯基氯化钌(II)
    参考文献:
    名称:
    CpRuLL'R类型的化合物的氧化裂解反应(L,L'= CO,PPh3; R = Me,PhCH2)
    摘要:
    DOI:
    10.1021/om00089a027
  • 作为产物:
    描述:
    B-methylcatecholborane四氢呋喃 为溶剂, 以0%的产率得到(η5-cyclopentadienyl)methylbis(triphenylphosphine)ruthenium
    参考文献:
    名称:
    Hartwig, John F.; Bhandari, Sonali; Rablen, Paul R., Journal of the American Chemical Society, 1994, vol. 116, # 5, p. 1839 - 1844
    摘要:
    DOI:
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文献信息

  • Cyclometallation reactions. Part 16. Some reactions of η-cyclopentadienylruthenium phosphine complexes
    作者:Michael I. Bruce、Richard C. F. Gardner、F. Gordon A. Stone
    DOI:10.1039/dt9760000081
    日期:——
    ortho-Metallation reactions of several η-cyclopentadleylruthenium complexes are described. The complex [RuMe(ηC5H5)(PPh3)2] affords [[graphic omitted]Ph2)(ηC5H5)(PPh3)], which with hexafluorobut-2-yne gives [[graphic omitted]Ph2}(ηC5H5)]. The tripheyl phosphite complex [Ru(η-C5H5)ClP(OPh)3}2] on heating yields [[graphic omitted](OPh)2}(η-C5H5)P(OPh)3}].With azobenzenes, m-RC6H4N:Nph (R = H, Me, OMe
    描述了几种η-环戊二配合物的邻位属化反应。络合物[RuMe(ηc为5 ħ 5)(PPH 3)2 ]得到[[图形省略]博士2)(ηc为5 ħ 5)(PPH 3)],其与六丁-2-炔给出[[图形省略] pH值2 }(ηc为5 ħ 5)]。的三苯基磷酸盐络合的[Ru(η-C 5 H ^ 5)P(OPH)3 } 2在加热产率] [[图形省略](OPH)2 }(η-C 5 H ^ 5)P(OPH)3。}]以偶氮苯,中号-RC 6 ħ 4 N:NPH(R = H,Me中的OME,CO 2 Et或CF 3),络合物[RuMe(ηc为5 ħ 5)(PPH 3) 2 ]得到异构体[[图形省略]℃的混合物6 ħ 4)Z-(η-C 5 H ^ 5)(PPH 3)](Y = H,Z = R:或Y = R,Z = H)。使用m -RC 6 H 4 N:NC 6 F 5(R = H,Me或CF 3),络合物[[未显示图形]
  • Cyclopentadienyl-ruthenium and -osmium chemistry. Part 6. Reactions of alkylruthenium complexes with disubstituted acetylenes
    作者:Michael I. Bruce、Richard C. F. Gardner、F. Gordon A. Stone
    DOI:10.1039/dt9790000906
    日期:——
    and [[graphic omitted]OMe}(PPh3)(η-C5H5)]; an analogous product to the latter is obtained from C2(CO2Me)2 and [Ru(CH2Ph)(PPh3)2(η-C5H5)]. The hydrido-complex [RuH(CO)(PPh3)(η-C5H5)] reacts with the acetylenic diester to give [RuC(CO2Me):C(CO2Me)H}(PPh3)2(η-C5H5)], which reacts further with C2(CF3)2 to give a ruthenocene derivative [Ruη5-C5(CO2Me)2(CF3)2(OMe)}(η-C5H5)]. 4-Phenylbut-3-yn-2-one and [RuMe(PPh3)2(η-C5H5)]
    丁-2-炔与[RuMe(PPH发生反应3)2(η-C 5 H ^ 5)]苯,得到丁二烯复杂[[图形省略] CME(CF 3)}(PPH 3)(η-C 5 H 5)]。使用1,2-二甲氧基乙烷作为溶剂,所述乙烯基复杂的[Ru C(CF 3):CME(CF 3)}(CO)(PPH 3)(η-C 5 H ^ 5)]已被分离。用C 2(CF 3)2,羰基配合物[RuMe(CO)(PPH 3)(η-C 5 H ^ 5)],得到一个二复合物配制为[(η-C 5 H ^ 5)(OC)(PH 3 P)的Ru C(CF 3)C(CF 3)} [图形省略]博士2)],并且苄基配合物的[Ru(CH 2 PH)(PPH 3)2(η-C 5 H ^ 5)]给出分配一个结构[[图形省略] C(CF产品3)H}(PPH 3)(η-C 5 H 5)]。用乙炔二反作用[RuMe(PPH 3)2(η-C 5 H ^
  • Photochemical studies of (η<sup>5</sup>-C<sub>5</sub>H<sub>5</sub>)Ru(PPh<sub>3</sub>)<sub>2</sub>Cl and (η<sup>5</sup>-C<sub>5</sub>H<sub>5</sub>)Ru(PPh<sub>3</sub>)<sub>2</sub>Me: formation of Si–H and C–H bond activation products
    作者:Johnathan L. Clark、Simon B. Duckett
    DOI:10.1039/c3dt52069b
    日期:——
    CpRu(PEt3)2Cl can be formed. Room temperature irradiation of the related complex CpRu(PPh3)2Me with L = PEt3, C2H4, and DMSO also produces CpRu(PPh3)(L)Me. However, when these reactions are followed by in situ laser irradiation (325 nm source) at low temperature, three solvent activated isomers (ortho, meta and para) of CpRu(PPh3)2(C6H4Me) are detected in toluene in addition to η1- and η3-coordinated
    研究CpRu(PPh 3)2 Cl和CpRu(PPh 3)2 Me对两个电子给体配体PEt 3,C 2 H 4,DMSO,CH键可活化试剂四氢呋喃甲苯吡啶的光化学反应性的研究,以及给出了SiH键可活化试剂HSiEt 3和HSi(Me)2 CH CH 2)。CpRu(PPh 3)2 Cl的宽带紫外线照射导致单取代产物的形成,例如CpRu(PPh 3)(PEt 3尽管可以形成热双取代的产物,如CpRu(PEt 3)2 Cl ,但对进一步的光化学反应呈惰性。在室温下辐照L = PEt 3,C 2 H 4和DMSO的相关复合物CpRu(PPh 3)2 Me也会产生CpRu(PPh 3)(L)Me。但是,在低温下进行原位激光照射(325 nm源)进行这些反应后,CpRu(PPh 3)2(C 6 H )的三种溶剂活化的异构体(邻位,间位和对位)4 Me)中的甲苯中检测除了η 1 -和η 3个配位的
  • Heterobimetallic complexes with dppm-bridged Ru/Pd, Ru/Pt, Ru/Au and Ru/Cu centers
    作者:Ying Yang、Khalil A. Abboud、Lisa McElwee-White
    DOI:10.1039/b307990b
    日期:——
    heterobimetallic Ru/Pd, Ru/Pt, Ru/Au and Ru/Cu complexes Cp(PPh3)Ru(μ-I)(μ-dppm)PdCl2 (4), Cp(PPh3)Ru(μ-Cl)(μ-dppm)Pd(CH3)Cl (5), Cp(PPh3)Ru(μ-I)(μ-dppm)PtCl2 (6), Cp(PPh3)Ru(μ-I)(μ-dppm)PtI2 (7), Cp(PPh3)RuI(μ-dppm)AuI (8), Cp(PPh3)RuBr(μ-dppm)AuCl (9), Cp(PPh3)RuCl[μ-PPh2(CH2)4PPh2]AuCl (10), Cp(PPh3)RuCl(μ-Ph2PNHPPh2)AuCl (11) and Cp(PPh3)Ru(μ-I)(μ-dppm)CuI (12) were prepared by the reactions of CpRu(PPh3)(η1-Ph2PQPPh2)X
    异双属Ru / Pd,Ru / Pt,Ru / Au和Ru / Cu络合物CP(PPh 3)Ru(μ-I)(μ-DPPM)PdCl 2 (4),CP(PPh 3)Ru(μ-Cl )(μ-DPPM)Pd(CH 3)Cl(5),CP(PPh 3)Ru(μ-I)(μ-DPPM)PtCl 2 (6),CP(PPh 3)Ru(μ-I)( μ-DPPM)PtI 2 (7),CP(PPh 3)RuI(μ-DPPM)AuI(8),CP(PPh 3)RuBr(μ-DPPM)AuCl(9),CP(PPh 3)RuCl [μ -PPh 2(CH 2)4 PPh 2 ] AuCl(10)中,CP(PPH 3)的RuCl(μ-PH 2 PNHPPh 2)AUCL(11)和CP(PPH 3)的Ru(μ-I)(μ-DPPM)的CuI(12)通过CPRU的反应(制备PPH 3)(η 1 -Ph 2 PQPPh 2)X [Q
  • Silyl and bis(silyl)hydride complexes of ruthenium: Effect of ancillary groups on the oxidative addition of Si-H bonds
    作者:Frederick R. Lemke、Chanpen Chaitheerapapkul
    DOI:10.1016/0277-5387(95)00539-0
    日期:1996.8
    mixture of the silyl Cp(PMe 3 ) 2 RuSiEt 3 ( 7 ) and the bis(silyl)hydride Cp(PMe 3 )Ru(SiEt 3 ) 2 H ( 8 ); this mixture can be converted solely to 7 upon reaction with PMe 3 . Complex 3 reacted with HSiEt 3 at 100°C forming Cp(PPh 3 ) 2 RuSiEt 3 ( 9 ). The reaction of 3 with neat HSiCl 3 at 100°C forms a mixture of Cp(PPh 3 )Ru(SiCl 3 ) 2 H ( 10 ) and Cp(PPh 3 ) 2 RuSiCl 3 ( 11 ), with 10 being the major
    摘要烷基络合物Cp(PMe 3)2 RuCH 2 SiMe 3(2)和Cp(PPh 3)2 RuMe(3)与氢化硅烷反应形成硅烷基和/或双(甲硅烷基)氢化物。络合物2与HSiR 3在100°C下反应,以高收率形成相应的甲硅烷基络合物Cp(PMe 3)2 RuSiR 3 [SiR 3 = SiCl 3(4),SiMeCl 2(5),SiMe 2 Cl(6)]。在125–150°C下,2与HSiEt 3反应,得到甲硅烷基Cp(PMe 3)2 RuSiEt 3(7)和双(甲硅烷基)氢化物Cp(PMe 3)Ru(SiEt 3)2 H(8)的混合物); 与PMe 3反应后,该混合物可以单独转化为7。配合物3在100℃下与HSiEt 3反应,形成Cp(PPh 3)2 RuSiEt 3(9)。3与纯HSiCl 3在100°C下的反应形成Cp(PPh 3)Ru(SiCl 3)2 H(10)和Cp(PPh
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