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[Ag(trifuoroacetate)(5,5'-dimethyl-2,2'-pyridine)]2 | 1132664-00-6

中文名称
——
中文别名
——
英文名称
[Ag(trifuoroacetate)(5,5'-dimethyl-2,2'-pyridine)]2
英文别名
[Ag(trifluoroacetate)(5,5'-dimethyl-2,2'-pyridine)]2
[Ag(trifuoroacetate)(5,5'-dimethyl-2,2'-pyridine)]2化学式
CAS
1132664-00-6;1132664-09-5
化学式
C28H24Ag2F6N4O4
mdl
——
分子量
810.25
InChiKey
FRKXJWNXBKXFBG-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:
    参考文献:
    名称:
    An X-ray diffraction study of anion and ratio dependence in the formation of discrete molecules versus polymeric arrays involving silver salts and bipyridine ligands
    摘要:
    Described are the reaction of the silver(1) salts of trifluoroacetate (tfa(-)) and trifluoromethanesulfonate (Otf(-)) with the bidentate ligands 4,4'-dimethyl-2,2'-bipyridine (L1), 5,5'-dimethyl-2,2'-bipyridirie (L2) and 2,2'-bipyridine (13), to afford the formation of five structures. A systematic study was conducted to obtain the different coordination moieties possible by changing the ligand to metal ratio and the solvent of crystallization. In total, six discrete molecules (Agtfa)(L1), 1, (Agtfa)(L2), 2A and 2B, (AgOtf)(2)(L2)(3), 3A and 3B, (AgOtf)(2)(L3)(3), 5, and one polymeric structure (AgOtf)(L3)(n), 4 were obtained. Compounds 2 and 3 form two crystal structures each, where differences in connectivity of the corresponding anion to the metal center are observed, as directed by solvent of crystallization. The varying degree of interaction of the two anions, combined with the functionality of the ligand used in the reaction, gave rise to coordination numbers from 4 to 6, representing capped-trigonal, distorted tetrahedral, trigonal bipyramidal and distorted octahedral environments, which illustrate the range of coordination moieties that can be adopted in silver([) complexes, and the possibility of systematic control of the coordination framework topology of a compound. This study complements the already reported silver coordinated structures associated with the bipyridine ligands mentioned herein. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2008.11.040
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