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[Cd2(4'-(2-pyridyl)-2,2':6',2''-terpyridine)2(azido)4] | 1024599-13-0

中文名称
——
中文别名
——
英文名称
[Cd2(4'-(2-pyridyl)-2,2':6',2''-terpyridine)2(azido)4]
英文别名
——
[Cd2(4'-(2-pyridyl)-2,2':6',2''-terpyridine)2(azido)4]化学式
CAS
1024599-13-0
化学式
C40H28Cd2N20
mdl
——
分子量
1013.62
InChiKey
UDWQLGDJRXGVJO-UHFFFAOYSA-N
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:
    cadmium(II) nitrate tetrhydrate4'-(pyridin-2-yl)-2,2':6',2''-terpyridine 、 sodium azide 以 四氢呋喃甲醇 为溶剂, 以73%的产率得到[Cd2(4'-(2-pyridyl)-2,2':6',2''-terpyridine)2(azido)4]
    参考文献:
    名称:
    An investigation of the positional isomeric effect of terpyridine derivatives: Self-assembly of novel cadmium coordination architectures driven by N-donor covalence and π⋯π non-covalent interactions
    摘要:
    Four cadmium compounds based on two pyridyl substituted terpyridine isomers, namely {[Cd-3(L1)(2)(SCN)(6)](THF)(2)}(n) (1), [Cd-2(L1)(CH3OH)Cl-4](n) (2), [Cd-2(L-2)(2)(N-3)(4)] (3) and [Cd-2(L-2)(2)(SCN)(4)] (4) (L1 = 4'-(3-pyridyl)-2,2':6',2 ''-terpyfidine, L2 = 4'-(2-pyridyl)-2,2':6',2 ''-terpyridine) have been synthesized and characterized by IR, elemental analyses, and luminescent spectroscopy with the purpose of investigating the influence of isomeric effect on network assembly. In compounds 1 and 2, L1 as a mono-tridentate bridging ligand links Cd-11 atoms into ID grid-like and 2D wave-like polymers. In contrast, in compounds 3 and 4, L2 as a chelating ligand forms Cd-II dimeric structures. The different coordination behaviors and the positional isomer effect were discussed under the same reaction conditions. In addition, three kind of pi...pi interactions in the four compounds were summarized, two of which could not be observed on tpy-based complexes. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2008.01.024
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