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[Ni(1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane)(NCO)]ClO4 | 194303-53-2

中文名称
——
中文别名
——
英文名称
[Ni(1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane)(NCO)]ClO4
英文别名
——
[Ni(1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane)(NCO)]ClO4化学式
CAS
194303-53-2
化学式
C15H32N5NiO*ClO4
mdl
——
分子量
456.593
InChiKey
GWXFULRNHQRALH-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:
    参考文献:
    名称:
    Three new mononuclear nickel(II) cyanate and isocyanate compounds derived from macrocyclic ligands: [Ni(TMCY) (NCO)](ClO4), [Ni(m-CTH)(OCN)1.5(ClO4)0.5]
    摘要:
    The compounds [Ni(TMCY)(NCO)](ClO4) (1), [Ni(Cyclam)(NCO)(H2O)](ClO4) (2) and [Ni(m-CTH)(OCN)(1.5)(ClO4)(0.5)] (3) in which TMCY is 1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane, Cyclam is 1,4,8,11-tetraazacyclotetradecane and m-CTH is meso-5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane have been synthesized and structurally characterized. 1 crystallizes in the orthorhombic system, space group Pbca, with FW=456.62, a=15.296(3), b=15.772(3), c=17.521(3) Angstrom, V=4227(2) Angstrom(3), Z=8, R=0.027, R-w=0.033. The nickel atom is pentacoordinated. 2 crystallizes in the monoclinic system, space group P2(1)/a, with FW=418.52,a=11.277(5), b=16.070(6), c=9.873(4) Angstrom, beta=90.68(3)degrees, V=1789(2) Angstrom(3), Z=4, R=0.062, R-w=0.069. The nickel atom is placed in an octahedral environment. 3 crystallizes in the triclinic system, space group P-l, with FW=911.89, a=8.752(2), b=8.718(2), c=15.671(3) Angstrom, alpha=104.01(2), beta=105.25(2), gamma=95.96(2)degrees, V=1101.2(4) Angstrom 3, Z=1, R=0.0553, R-w=0.1624. The nickel atom is placed in an octahedral environment with the oxygen atom of the cyanato ligand occupyng one of the coordination sites.
    DOI:
    10.1016/s0020-1693(97)05481-9
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