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Pd-xanthate | 29649-61-4

中文名称
——
中文别名
——
英文名称
Pd-xanthate
英文别名
bis(O-ethyl dithiocarbonato-κ2S,S')palladium(II);ethoxymethanedithioate;palladium(2+)
Pd-xanthate化学式
CAS
29649-61-4
化学式
C6H10O2PdS4
mdl
——
分子量
348.828
InChiKey
SDSWFUWLOVEKTG-UHFFFAOYSA-L
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):
    1.71
  • 重原子数:
    13
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    84.6
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    Pd-xanthate 、 PhHgS(S)CNEt2氯仿 为溶剂, 生成 PhHgdtcPd(xant)2
    参考文献:
    名称:
    Singh, Nanhai; Singh, Nand Kishore; Kaw, Chetna, Bulletin of the Chemical Society of Japan, 1990, vol. 63, p. 1801 - 1806
    摘要:
    DOI:
  • 作为产物:
    描述:
    trans-[PdCl2(THT)2] 、 zinc ethylxanthate 以82%的产率得到Pd-xanthate
    参考文献:
    名称:
    Bis(O-ethyl dithiocarbonato-κ2S,S′)palladium(II)
    摘要:
    The Pd atom in the title compound, [Pd(C3H5OS2)(2)], lies on an inversion center and adopts a square-planar coordination geometry defined by the four S atoms of the two dithiocarbonate (xanthate) ligands. In the solid state, the molecules aggregate into layers in which the rows of molecules alternate their orientation to allow each Pd atom to interact with two symmetry-equivalent S atoms of the xanthate ligands of adjacent molecules, generating a pseudo-octahedral environment around each Pd atom. This weak interaction of 3.3579 (7) Angstrom can be classified as a closed-shell electrostatic intermolecular interaction.
    DOI:
    10.1107/s0108270103007406
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文献信息

  • Dithiocarbonato nickel, palladium and platinum complexes bearing bis(diphenylphosphino)ferrocene: synthesis and X-ray structure determination
    作者:MOHAMMAD EL-KHATEEB、QUSAY TANASH、HASSAN ABUL-FUTOUH、HELMAR GÖRLS、WOLFGANG WEIGAND
    DOI:10.1007/s12039-019-1680-z
    日期:2019.10
    AbstractThe dithiocarbonato metal complexes M(κ2S,S-S2CO)(κ2P,P-dppf) M= Ni, Pd, Pt; dppf= bis(diphenylphosphino)ferrocene} are obtained from the reaction of the metal(II) complexes [M(κ2S,S-S2COEt)2] with the dppf ligand or from the chloride substitution of M(κ2P,P-dppf)Cl2 by the O-ethyldithiocabonato anion. These complexes are produced by C-O bond cleavage by the O-ethyldithiocarbonato anion present
    摘要所述dithiocarbonato金属络合物M(κ 2小号,小号-S 2 CO)(κ 2 P,P -dppf)M =镍,钯,铂; DPPF =双(二苯基膦基)二茂铁}从金属的反应(II)配合物[M(得到κ 2小号,小号-S 2 COET)2 ]与DPPF配体或从M(氯化物替代κ 2 P,P -dppf)Cl 2由O-乙基二硫代羰基阴离子形成。这些复合物是由O裂解CO键产生的-乙基二硫代碳酸根阴离子存在于溶液中。这些新的配合物已通过UV-Vis,NMR,IR光谱和元素分析进行​​了表征。通过单晶X射线衍射分析进一步证实了三种配合物的结构。 图形概要所述dithiocarbonato金属络合物M(κ 2小号,小号-S 2 CO)(κ 2 P,P -dppf)M =镍,钯,铂,DPPF =双(二苯基膦基)二茂铁}从金属的反应得到的(II)配合物[M(κ 2小号,小号-S 2 COET)2
  • Metal complexes of sulphur ligands. Part 11. Reactions of platinum(II) and palladium(II) dithiocarbonates with dithiocarbonate ions
    作者:Margaret C. Cornock、Robert O. Gould、C. Lynn Jones、John D. Owen、David F. Steele、T. Anthony Stephenson
    DOI:10.1039/dt9770000496
    日期:——
    Reaction of the complexes [Pt(S2COR)2] with K[S2COR](R = Et or Pri) followed by addition of [AsPh4]Cl generates [AsPh4][Pt(S2COR)3]. Variable-temperature 1H n.m.r. studies indicate rapid unidentate–bidentate exchange at ambient temperature. Attempted recrystallisation from CH2Cl2 or CDCl3, results in an intramolecular rearrangement to give [AsPh4][Pt(S2CO)(S2COR)]. Reaction of [Pd(S2COEt)2] with K[S2COEt]
    配合物[Pt(S 2 COR)2 ]与K [S 2 COR](R = Et或Pr i)反应,然后添加[AsPh 4 ] Cl生成[AsPh 4 ] [Pt(S 2 COR)3 ]。可变温度1 H nmr研究表明,在环境温度下快速不对称交换。尝试从CH 2 Cl 2或CDCl 3重结晶,导致分子内重排得到[AsPh 4 ] [Pt(S 2 CO)(S 2 COR)]。[Pd(S 2 COEt)2 ]与K [S]的反应2 COEt]和[AsPh 4 ] Cl给出了[AsPh 4 4] [Pd(S 2 CO)(S 2 COEt)]作为主要产物。[Pt(S 2 COR) 2 ]与K [S 2 COR](R = Me或CH 2 Ph)和[AsPh 4 ] Cl的反应生成[AsPh 4 ] [Pt(S 2 CO)(S 2 COMe )]或[AsPh 4 ] 2 [Pt(S 2 CO) 2 ],在添加各种Lewis碱L(L
  • Ansari, Mohammad A.; Mahler, Charles H.; Chorghade, Gayatri S., Inorganic Chemistry, 1990, vol. 29, # 19, p. 3832 - 3839
    作者:Ansari, Mohammad A.、Mahler, Charles H.、Chorghade, Gayatri S.、Lu, Ying-Jie、Ibers, James A.
    DOI:——
    日期:——
  • McConnachie, Jonathan M.; Ansari, Mohammad A.; Ibers, James A., Inorganic Chemistry, 1993, vol. 32, # 15, p. 3250 - 3255
    作者:McConnachie, Jonathan M.、Ansari, Mohammad A.、Ibers, James A.
    DOI:——
    日期:——
  • Piotraschke, J.; Strauch, P.; Abram, S., Zeitschrift fur Anorganische und Allgemeine Chemie
    作者:Piotraschke, J.、Strauch, P.、Abram, S.、Abram, U.
    DOI:——
    日期:——
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