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[(p-cymene)RuCl2(N-(pyridin-4-ylmethylene)propan-1-amine)] | 1192578-30-5

中文名称
——
中文别名
——
英文名称
[(p-cymene)RuCl2(N-(pyridin-4-ylmethylene)propan-1-amine)]
英文别名
——
[(p-cymene)RuCl2(N-(pyridin-4-ylmethylene)propan-1-amine)]化学式
CAS
1192578-30-5
化学式
C19H26Cl2N2Ru
mdl
——
分子量
454.405
InChiKey
IIPPOOHRGIDDDQ-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

反应信息

  • 作为产物:
    描述:
    [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2 、 N-(pyridin-4-ylmethylene)propan-1-amine 以 二氯甲烷 为溶剂, 以91.1%的产率得到[(p-cymene)RuCl2(N-(pyridin-4-ylmethylene)propan-1-amine)]
    参考文献:
    名称:
    Anticancer activity of multinuclear arene ruthenium complexes coordinated to dendritic polypyridyl scaffolds
    摘要:
    The rational development of multinuclear arene ruthenium complexes (arene = p-cymene, hexamethylbenzene) from generation 1 (G(1)) and generation 2 (G(2)) of 4-iminopyridyl based poly( propyleneimine) dendrimer scaffolds of the type, DAB-(NH2)(n) (n = 4 or 8, DAB = diaminobutane) has been accomplished in order to exploit the 'enhanced permeability and retention' (EPR) effect that allows large molecules to selectively enter cancer cells. Four compounds were synthesised, i.e. [{(p-cymene)RuCl2}(4)G(1)] (1), [{(hexamethylbenzene)RuCl2}(4)G(1)] (2), [{(p-cymene)RuCl2}(8)G(2)] (3), and [{(hexamethylbenzene)RuCl2}(8)G(2)] ( 4), by first reacting DAB-( NH2) n with 4-pyridinecarboxaldehyde and subsequently metallating the iminopyridyl dendrimers with [(p-cymene)RuCl2](2) or [(hexamethylbenzene)RuCl2](2). The related mononuclear complexes [(p-cymene) RuCl2(L)] (5) and [(hexamethylbenzene)RuCl2(L)] (6) were obtained in a similar manner from N-(pyridin-4-ylmethylene)propan-1-amine (L). The molecular structure of 5 has been determined by X-ray diffraction analysis and the in vitro anticancer activities of the mono-, tetra- and octanuclear complexes 1-6 studied on the A2780 human ovarian carcinoma cell line showing a close correlation between the size of the compound and cytotoxicity. (C) 2009 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2009.06.028
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