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[Ni(N3)(H2O)(phen)2]ClO4 | 1432625-70-1

中文名称
——
中文别名
——
英文名称
[Ni(N3)(H2O)(phen)2]ClO4
英文别名
——
[Ni(N<sub>3</sub>)(H<sub>2</sub>O)(phen)<sub>2</sub>]ClO<sub>4</sub>化学式
CAS
1432625-70-1
化学式
C24H18N7NiO*ClO4
mdl
——
分子量
578.594
InChiKey
QKRYBFNBDHWFCA-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

  • 作为产物:
    描述:
    1,10-菲罗啉 、 nickel(II) perchlorate hexahydrate 、 sodium azide 以 乙醇 为溶剂, 反应 10.0h, 以10%的产率得到[Ni(N3)(H2O)(phen)2]ClO4
    参考文献:
    名称:
    Microwave synthesis of mono- and bis-tetrazolato complexes via 1,3-dipolar cycloaddition of organonitriles with nickel(II)-bound azides: Isolation of 5-substituted tetrazoles from parent complex
    摘要:
    [2 + 3] Cycloaddition reaction of diazidonickel(II) complexes cis-[Ni(N-3)(2)(phen)(2)] I with organonitriles NCR 2 under microwave irradiation give the bis(tetrazolato) complexes cis-[Ni(N4CR)(2)(pben)(2)] [R = Ph (3a), 4-NC5H4 (3b), 3-NC5H4 (3c), 4-CNPh (3d)]. Treatment of the tetrazolato complexes with excess of NaN3 liberates the free tetrazoles from the parent metal complexes. Reaction of 2-cyanopyridine with cis-[Ni(N-3)(2)(phen)(2)] 1 in presence of NaClO4 gives a mono(tetrazolato) complex [Ni(5-(2-pyridyl)-tetrazolato)(phen)(2)](ClO4) 3e along with formation of pure 2-(1H-tetrazol-5-yl)-pyridine. Reaction of tetracyanoethylene with cis-[Ni(N-3)(2)(biPy)(2)](4) at room temperature produced a bis(tetrazolato) complex [Ni{2-cyano-3-(tetrazolato-5-y1)-but-2-enedintrile}(2)(biPy)(2)] 5. A monoazidonickel complex [Ni(N-3)(H2O)-(Pben)(2)]ClO4 6 was isolated as a minor product during the synthesis of cis-[Ni(N-3)(2)(phen)(2)] I. All the complexes obtained were characterized by IR, elemental analyses and ESI-MS apart from single crystal X-ray crystallography. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2013.02.069
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