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catena-(1H-1,2,4-triazole-3-carboxyliate)(μ2-iodo)lead(II) | 1429689-06-4

中文名称
——
中文别名
——
英文名称
catena-(1H-1,2,4-triazole-3-carboxyliate)(μ2-iodo)lead(II)
英文别名
——
catena-(1H-1,2,4-triazole-3-carboxyliate)(μ<sub>2</sub>-iodo)lead(II)化学式
CAS
1429689-06-4
化学式
C3H2N3O2*I*Pb
mdl
——
分子量
446.172
InChiKey
BDJFVRYSRYEURS-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):
    -5.21
  • 重原子数:
    10.0
  • 可旋转键数:
    1.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    81.7
  • 氢给体数:
    1.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Sonochemical syntheses of nano lead(II) iodide triazole carboxylate coordination polymer: Precursor for facile fabrication of lead(II) oxide/iodide nano-structures
    摘要:
    Nanoparticles of a one-dimensional coordination polymer [Pb(L)(mu(2)-I)](n) (1), (L = 1H-1,2,4-triazole3- carboxylate), have been synthesized by a sonochemical process and characterized by field emission scanning electron microscopy (FESEM), X-ray powder diffraction (XRPD), FT-IR spectroscopy and elemental analyses. The thermal stability of compound 1 both its bulk and nano-size has been studied by thermal gravimetric (TG) and compared each other. Concentration of initial reagents effects and the role of power ultrasound irradiation on size and morphology of nano-structured compound 1 have been studied and show that low concentrations of initial reagents and also high power of ultrasound irradiation decreased particles size and leaded to uniform nanoparticles morphology. PbO nano-structures were simply synthesized by solid-state transformation of compound 1 at 630 degrees C under air atmosphere whereas thermal decomposition of compound 1 in oleic acid as surfactant at 200 degrees C yield PbI2 nanoparticles. (C) 2012 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2012.12.029
  • 作为产物:
    描述:
    1H-1,2,4-三氮唑-3-羧酸lead(II) nitrate 、 potassium iodide 以 为溶剂, 反应 240.0h, 以63%的产率得到catena-(1H-1,2,4-triazole-3-carboxyliate)(μ2-iodo)lead(II)
    参考文献:
    名称:
    Sonochemical syntheses of nano lead(II) iodide triazole carboxylate coordination polymer: Precursor for facile fabrication of lead(II) oxide/iodide nano-structures
    摘要:
    Nanoparticles of a one-dimensional coordination polymer [Pb(L)(mu(2)-I)](n) (1), (L = 1H-1,2,4-triazole3- carboxylate), have been synthesized by a sonochemical process and characterized by field emission scanning electron microscopy (FESEM), X-ray powder diffraction (XRPD), FT-IR spectroscopy and elemental analyses. The thermal stability of compound 1 both its bulk and nano-size has been studied by thermal gravimetric (TG) and compared each other. Concentration of initial reagents effects and the role of power ultrasound irradiation on size and morphology of nano-structured compound 1 have been studied and show that low concentrations of initial reagents and also high power of ultrasound irradiation decreased particles size and leaded to uniform nanoparticles morphology. PbO nano-structures were simply synthesized by solid-state transformation of compound 1 at 630 degrees C under air atmosphere whereas thermal decomposition of compound 1 in oleic acid as surfactant at 200 degrees C yield PbI2 nanoparticles. (C) 2012 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2012.12.029
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文献信息

  • Solid state syntheses of nano lead(II) iodide triazole carboxylate coordination polymer from its bromide/thiocyanate/chloride analogs via mechanochemical crystal to crystal transformations
    作者:Vahid Safarifard、Ali Morsali
    DOI:10.1016/j.ica.2013.05.008
    日期:2013.8
    Irreversible crystal-to-crystal transformations of 3D lead(II) coordination polymers with the ligand 1H-1,2,4-triazole-3-carboxylic acid (HL), [Pb(L)(mu(2)-Br)(H2O)](n) (1), [Pb(L)(mu(1,1)-NCS)(H2O)](n) (2) and [Pb(L)(mu(2)-Cl)(H2O)](n) (3) to 3D supramolecular compound [Pb(L)(mu(2)-I)](n) (4) by solid state anion-replacement processes under mechanochemical reactions, have been studied. The thermal stabilities of compounds 1-4 were studied by thermogravimetric and differential thermal analyses. The irreversible solid state structural transformations of compounds 1-4, by anion-replacement processes under mechanochemical reaction, have been verified by PXRD measurements. Nanoparticles of compounds 1 and 2 were synthesized by sonochemical process and characterized by scanning electron microscopy (SEM), powder X-ray diffraction, IR spectroscopy, elemental analyses, thermogravimetric and differential thermal analyses. The SEM images showed that no morphology change occurs during solid state anion-replacements of nanocrystals. (C) 2013 Elsevier B.V. All rights reserved.
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