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trans-[PdCl2(2-aminothiazole)2] | 61136-28-5

中文名称
——
中文别名
——
英文名称
trans-[PdCl2(2-aminothiazole)2]
英文别名
trans-[PdCl2(2-aminothiazole)2];trans-[PdCl2(atz)2]
trans-[PdCl2(2-aminothiazole)2]化学式
CAS
61136-28-5
化学式
C6H8Cl2N4PdS2
mdl
——
分子量
377.614
InChiKey
FZQXAVHWTJXKJT-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):
    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:
    1,2-苯异噻唑-3-(2H)-硫酮-1,1-二氧化物trans-[PdCl2(2-aminothiazole)2]甲醇氯仿 为溶剂, 反应 0.5h, 以73%的产率得到trans-[Pd(thiosaccharinate)2(2-aminothiazole)2]
    参考文献:
    名称:
    Palladium(II) saccharinate (sac) and thiosaccharinate (tsac) complexes with supporting amino- and acetylamino-thiazole ligands: Crystal structures of trans-[PdCl2(abzt)2]·dmf (abzt=2-aminobenzothiazole), trans-[PdCl2(bzta)2].dmf (bzta=2-acetylaminobenzothiazole) and trans-[Pd(sac)2(abzt)2]·2dmf
    摘要:
    Treatment of Na2PdCl4 with two equivalents of amino- or acetylamino-thiazoles [L = 2-aminobenzothiazole (abzt), 2-aminothiazole (atz), 2-acetylaminobenzothiazole (bzta) and 2-acetylaminothiazole (tza)] or 2-aminobenzimidazole (abzim)] affords trans-[PdCl2L2] complexes in which the introduced ligands are coordinated to palladium through the endocyclic nitrogen as shown by X-ray crystal structures of trans-[PdCl2(abzt)(2)]center dot dmf and trans-[PdCl2(bzta)(2)]center dot dmf. Addition of two equivalents of sodium saccharinate (Nasac) yields trans-[Pd(sac)(2)L-2] complexes whereby the saccharinate anions are coordinated through nitrogen as shown by the X-ray crystal structure of trans-[Pd(sac)(2)(abtz)(2)]center dot 2dmf. With thiosac-charin (I-Itsac) trans-[Pd(tsac)(2)L-2] result but now the thiosaccharinate ligands coordinate through the sulfur of the thiolate group as evidenced by spectroscopic studies. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2013.09.007
  • 作为产物:
    描述:
    2-氨基噻唑sodium tetrachloropalladate(II)丙酮 为溶剂, 反应 3.0h, 以98%的产率得到trans-[PdCl2(2-aminothiazole)2]
    参考文献:
    名称:
    Palladium(II) saccharinate (sac) and thiosaccharinate (tsac) complexes with supporting amino- and acetylamino-thiazole ligands: Crystal structures of trans-[PdCl2(abzt)2]·dmf (abzt=2-aminobenzothiazole), trans-[PdCl2(bzta)2].dmf (bzta=2-acetylaminobenzothiazole) and trans-[Pd(sac)2(abzt)2]·2dmf
    摘要:
    Treatment of Na2PdCl4 with two equivalents of amino- or acetylamino-thiazoles [L = 2-aminobenzothiazole (abzt), 2-aminothiazole (atz), 2-acetylaminobenzothiazole (bzta) and 2-acetylaminothiazole (tza)] or 2-aminobenzimidazole (abzim)] affords trans-[PdCl2L2] complexes in which the introduced ligands are coordinated to palladium through the endocyclic nitrogen as shown by X-ray crystal structures of trans-[PdCl2(abzt)(2)]center dot dmf and trans-[PdCl2(bzta)(2)]center dot dmf. Addition of two equivalents of sodium saccharinate (Nasac) yields trans-[Pd(sac)(2)L-2] complexes whereby the saccharinate anions are coordinated through nitrogen as shown by the X-ray crystal structure of trans-[Pd(sac)(2)(abtz)(2)]center dot 2dmf. With thiosac-charin (I-Itsac) trans-[Pd(tsac)(2)L-2] result but now the thiosaccharinate ligands coordinate through the sulfur of the thiolate group as evidenced by spectroscopic studies. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2013.09.007
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文献信息

  • Reactivity of primary amines co-ordinated to palladium and platinum. Part II. Cyclometallation and rearrangement of the co-ordinated ligands
    作者:Jean Dehand、Jeanne Jordanov、Michel Pfeffet
    DOI:10.1039/dt9760001553
    日期:——
    [MCl2L′}2] species are obtained [M = PtII or PdII; L′= HS·CH2·CH2·NH·C⋮N and HS·CH:CH·NH⋮N. The combined presence of the metal and hydroxide ions appears to induce the ring opening and rearrangement of the amine ligands.
    的反应的反式- [的PdCl 2(NH 2 X)2 ](X = NPhR或物理信道2 ; R =苯基,Me或2H)与苯乙酮给人的环palladated二聚体[的PdCl(C 6 H ^ 4 CME NX) } 2 ],苯乙酮苯环被正属化。[PtCl 4 ] 2–和[Pd 2 Cl 6 ] 2–与2-氨基噻唑啉和2-氨基噻唑(L)的反应在酸性介质中提供了环状N-配位单取代[NBu 4 ] [PdCl 3 L]和双取代顺式-[PtCl 2 L2 ]和反式-[PdCl 2 L 2 ]配合物。在碱性溶液中,获得了单体[PdCl 2 L' 2 ]和二聚体[MCl 2 L'} 2 ]物种[M = Pt II或Pd II ; L′= HS·CH 2 ·CH 2 ·NH·C⋮N和HS·CH:CH·NH⋮N。属和氢氧根离子的结合存在似乎引起胺配体的开环和重排。
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