摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

(2,6-bis(3,5-dimethylpyrazolyl-1-carbonyl)pyridine)palladium(II) dichloride | 884870-73-9

中文名称
——
中文别名
——
英文名称
(2,6-bis(3,5-dimethylpyrazolyl-1-carbonyl)pyridine)palladium(II) dichloride
英文别名
Pd(2,6-(3,5-Me2pzCO)2py)Cl2;Pd(2,6-bis(3,5-dimethylpyrazol-1-ylcarbonyl)pyridine)Cl2;(2,6-(3,5-MepzCO)2C5H3N)PdCl2;(2,6-di(3,5-dimethylpyrazolyl-1-carbonyl)pyridine)PdCl2
(2,6-bis(3,5-dimethylpyrazolyl-1-carbonyl)pyridine)palladium(II) dichloride化学式
CAS
884870-73-9
化学式
C17H17Cl2N5O2Pd
mdl
——
分子量
500.68
InChiKey
QOYLNSNHGUQTCO-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:
    (2,6-bis(3,5-dimethylpyrazolyl-1-carbonyl)pyridine)palladium(II) dichloride四(3,5-二(三氟甲基)苯基)硼酸钠氘代氯仿 为溶剂, 生成 [Pd(2,6-bis(3,5-dimethylpyrazol-1-ylcarbonyl)pyridine)Cl]B(C6H3(CF3)2-3,5)4
    参考文献:
    名称:
    Palladium complexes of multidentate pyrazolylmethyl pyridine ligands: Synthesis, structures and phenylacetylene polymerization
    摘要:
    The compounds, 2,6-bis(3,5-dimethylpyrazol-1-ylmethyl)pyridine (MeNNN) (L1) and 2,6-bis(3,5-ditertbutylpyrazol-1-ylmethyl)pyridine (tBuNNN) (L2), react with either [Pd(NCMe)(2)Cl-2] or [Pd(COD)ClMe] to form the mononuclear palladium complexes [Pd(MeNNN)Cl-2] (1), [Pd(MeNNN)ClMe] (2), [Pd((tBu)(N) over cap(N) over capN)Cl-2](3) and [Pd((tBu)(N) over cap(N) over capN)ClMe] (4). Reactions of 1, 2 and 4 with the halide abstractor, NaBAr4 (Ar = 3,5-(CF3)(2)C6H3), led to the formation of stable tridentate cationic species [Pd((Me)(N) over cap(N) over capN)Cl](+)(5), [Pd((Me)(N) over cap(N) over capN)Me](+) (6) and [Pd((tBu)(N) over cap(N) over capN)Cl](+) (7) respectively. The analogous carbonyl linker cationic species [Pd{(3,5-Me(2)pz-CO)(2)py}Cl](+) (9) and [Pd{(3,5-(t)Bu(2)pz-CO)(2-py)}Cl](+) (10), prepared by halide abstraction of the neutral complexes [Pd{(3,5-Me(2)pz-CO)(2)py}Cl-2] and [Pd{(3,5-(t)Bu(2)pz-CO)(2)-py}Cl-2] by NaBAr4, were however less stable with t(1/2) of 14 and 2 days respectively. Attempts to crystallize 1 and 3 from the mother liquor resulted in the isolation of the salts [Pd((Me)(N) over cap(N) over capN)Cl](2)[Pd2Cl6] (11) and [Pd((tBu)(N) over cap(N) over capN)Cl](2)[Pd2Cl6] (12). Although when complexes 1-4 were reacted with modified methylaluminoxane (MMAO) or NaBAr4, no active catalysts for ethylene oligomerization or polymerization were formed, activation with silver triflate (AgOTf) produced active catalysts that oligomerized and polymerized phenylacetylene to a mixture of cis-transoidal and trans-cisoidal polyphenylacetylene. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2006.09.007
  • 作为产物:
    描述:
    双(乙腈)氯化钯(II)2,6-bis(3,5-dimethyl-1-pyrazolylcarbonyl)pyridine二氯甲烷 为溶剂, 以51%的产率得到(2,6-bis(3,5-dimethylpyrazolyl-1-carbonyl)pyridine)palladium(II) dichloride
    参考文献:
    名称:
    吡啶连接基吡唑基钯配合物:合成,表征和乙烯聚合活性
    摘要:
    具有2,6-吡啶二羰基连接基,{RR'pz(CO)} 2 py,R = R'=  t Bu(L1)的一系列吡唑基化合物;R = R'= Me(L2); R = R'= H(L3)中,R = H,R'=我(L4)已经从2,6- pyridinedicarbonyl酰氯与适当的吡唑和弱碱的反应来制备。配体L1 – L3与Pd(NCMe)2 Cl 2反应形成单核络合物,而与L4的反应产生难以处理的产物。配合物1和2在用甲基铝氧烷(MAO)活化后,测试了它们对乙烯聚合的催化活性。用MAO原位形成活性聚合催化​​剂,该催化剂催化乙烯聚合成高密度线性聚乙烯。报告了助催化剂浓度和温度的影响。助催化剂与催化剂的最佳比例为3000:1,且由于催化剂失活,催化剂活性在40°C以上下降。
    DOI:
    10.1016/j.molcata.2005.06.040
点击查看最新优质反应信息