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[Ag(saccharinato)(N,N-bis(pyridin-2-ylmethyl)amine)](n) | 1226813-79-1

中文名称
——
中文别名
——
英文名称
[Ag(saccharinato)(N,N-bis(pyridin-2-ylmethyl)amine)](n)
英文别名
[Ag(sac)(bpma)](n)
[Ag(saccharinato)(N,N-bis(pyridin-2-ylmethyl)amine)](n)化学式
CAS
1226813-79-1
化学式
C19H17AgN4O3S
mdl
——
分子量
489.303
InChiKey
ODXWTUYNMMELPC-UHFFFAOYSA-M
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:
    [Ag(saccharinato)(N,N-bis(pyridin-2-ylmethyl)amine)](n) 在 air 作用下, 以 neat (no solvent) 为溶剂, 生成
    参考文献:
    名称:
    Dimeric and polymeric silver(I) saccharinato complexes of two bis(pyridine) ligands: Synthesis, structural, spectroscopic, fluorescent and thermal properties
    摘要:
    The reaction of silver(I) with 1,2-bis[1-(pyridin-2-yl)ethylidene]hydrazine (bpeh) and N,N-bis(pyridin-2-ylmethyl)amine (bpma) in the presence of Na(sac) (sac = saccharinate) yielded [Ag-2(sac)(2)(bpeh)] (1) and [Ag(sac)(bpma)](n) (2) with conformational chirality. Both complexes have been characterized by elemental analysis, IR, thermal analysis and X-ray single crystal diffraction. Complex 1 displays a binuclear composition, in which each silver(I) ion is bound to one monodentate sac ligand and one of the bidentate pyridylimino groups of the bpeh ligand in a distorted trigonal coordination geometry. Complex 2 is a one-dimensional helical polymer, in which silver(I) centers are bridged by tridentate bpma ligands, and each silver(I) ion is coordinated in a distorted tetrahedral geometry by one monodentate sac ligand, a bidentate pyridylamine group of one bpma ligand, and a pyridylimino group of another bpma ligand. Weak intermolecular C-H center dot center dot center dot O hydrogen bonds and C-H center dot center dot center dot pi interactions lead to assembly of 1 and 2 into threedimensional supramolecular frameworks. Spectral and thermal analysis data for 1 and 2 are in agreement with the crystal structures. In addition, both complexes in the solid state display intraligand pi-pi* fluorescence. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2010.01.019
  • 作为产物:
    描述:
    sodium saccharinate dihydrate二甲基吡啶胺silver nitrate 以 further solvent(s) 为溶剂, 以90%的产率得到[Ag(saccharinato)(N,N-bis(pyridin-2-ylmethyl)amine)](n)
    参考文献:
    名称:
    Dimeric and polymeric silver(I) saccharinato complexes of two bis(pyridine) ligands: Synthesis, structural, spectroscopic, fluorescent and thermal properties
    摘要:
    The reaction of silver(I) with 1,2-bis[1-(pyridin-2-yl)ethylidene]hydrazine (bpeh) and N,N-bis(pyridin-2-ylmethyl)amine (bpma) in the presence of Na(sac) (sac = saccharinate) yielded [Ag-2(sac)(2)(bpeh)] (1) and [Ag(sac)(bpma)](n) (2) with conformational chirality. Both complexes have been characterized by elemental analysis, IR, thermal analysis and X-ray single crystal diffraction. Complex 1 displays a binuclear composition, in which each silver(I) ion is bound to one monodentate sac ligand and one of the bidentate pyridylimino groups of the bpeh ligand in a distorted trigonal coordination geometry. Complex 2 is a one-dimensional helical polymer, in which silver(I) centers are bridged by tridentate bpma ligands, and each silver(I) ion is coordinated in a distorted tetrahedral geometry by one monodentate sac ligand, a bidentate pyridylamine group of one bpma ligand, and a pyridylimino group of another bpma ligand. Weak intermolecular C-H center dot center dot center dot O hydrogen bonds and C-H center dot center dot center dot pi interactions lead to assembly of 1 and 2 into threedimensional supramolecular frameworks. Spectral and thermal analysis data for 1 and 2 are in agreement with the crystal structures. In addition, both complexes in the solid state display intraligand pi-pi* fluorescence. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2010.01.019
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