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chloro(chlorodimethylaminomethylene)(4,4'-di-tert-butyl-2,2'-bipyridine)dimethylplatinum(IV) chloride | 162477-72-7

中文名称
——
中文别名
——
英文名称
chloro(chlorodimethylaminomethylene)(4,4'-di-tert-butyl-2,2'-bipyridine)dimethylplatinum(IV) chloride
英文别名
——
chloro(chlorodimethylaminomethylene)(4,4'-di-tert-butyl-2,2'-bipyridine)dimethylplatinum(IV) chloride化学式
CAS
162477-72-7
化学式
C23H36Cl2N3Pt*Cl
mdl
——
分子量
655.998
InChiKey
GROIJWCEDLZJOR-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

  • 作为产物:
    描述:
    (4,4'-di-tert-butyl-2,2'-bipyridine)dimethylplatinum(II) 、 二氯亚甲基二甲基氯化铵四氢呋喃二氯甲烷 为溶剂, 以79%的产率得到chloro(chlorodimethylaminomethylene)(4,4'-di-tert-butyl-2,2'-bipyridine)dimethylplatinum(IV) chloride
    参考文献:
    名称:
    Cationic Carbene Complexes of Platinum(IV): Structure of a Secondary Carbene Complex
    摘要:
    Treatment of the organoplatinum(II) precursors [PtMeCl((t)bu(2)bpy)] ((t)bu(2)bpy = 4,4'-di-tert-butyl-2,2'-bipyridine) and [PtMe(2)((t)bu(2)bpy)] with chloroiminium (Vilsmeier) salts affords the novel cationic platinum(IV)-carbene complexes [PtCl(2)Me(CHNMe(2))((t)bu(2)bpy)]Cl (1), [PtCl2-Me(CClNMe(2))((t)bu(2)bpy)]Cl (2), [PtClMe(2)(CHNMe(2))((t)bu(2)bpy)]Cl (3), and [PtClM(2)(CClNMe(2))((t)bu(2)bpy)]Cl (4) in good yield. For 1 and 2, the carbene moiety is located trans to one of the chloro ligands, whereas in 3 and 4 it is found trans to the N-donor. The complexes show good stability toward air and moisture, but 1 and 2 are thermally unstable and decompose to [PtCl2((t)bu(2)bpy)] after a few days at room temperature. Complex 4 can also be prepared as a mixture of two geometrical isomers which do not interconvert; it is proposed that the isomers are formed by two independent pathways. The major (4a) and minor (4b) isomers are formed by cis- and trans-oxidative addition, respectively, of [Cl2C=NMe(2)]Cl to [PtMe(2)((t)bu(2)bpy)], and likely mechanisms are discussed. Crystals of 1 are monoclinic, space group P2(1)/c, with a = 11.064(1) Angstrom, b = 21.310(2) Angstrom, c = 12.277(3) Angstrom, beta = 91.20(2)degrees, Z = 4, and R = 0.0718. The structure of 1 consists of discrete [PtCl(2)Me(CHNMe(2))((t)bu(2)bpy)](+) cations and chloride anions, with one CH2Cl2 molecule of crystallization per complex ion. The carbene ligand occupies a position trans to one of the chloro ligands, and the Pt-(Carbene) bond length (1.99(2) Angstrom) is significantly shorter than the Pt-Me distance (2.13(2) Angstrom). The C-N bond length of 1.31(2) Angstrom is indicative of substantial p(pi)-p(pi) bonding. Reaction of nucleophiles with 3 leads to rapid reductive elimination to give an iminium salt [H(X)C = NMe(2)]Cl (X = nucleophile) and [PtMe(2)((t)bu(2)bpy)]. This work demonstrates the versatility of chloroiminium salts in the preparation of aminocarbene complexes of metals in high oxidation states.
    DOI:
    10.1021/om00002a058
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