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zinc glycolate | 6669-35-8

分子结构分类

中文名称
——
中文别名
——
英文名称
zinc glycolate
英文别名
zinc glycoxide;zinc(II) glycolate;zinc;ethane-1,2-diolate
zinc glycolate化学式
CAS
6669-35-8
化学式
C2H4O2*Zn
mdl
——
分子量
125.443
InChiKey
WFOVFKBDGXAYIO-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):
    -2.3
  • 重原子数:
    5.0
  • 可旋转键数:
    1.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    46.12
  • 氢给体数:
    0.0
  • 氢受体数:
    2.0

反应信息

  • 作为反应物:
    描述:
    zinc glycolate乙基氯化镁乙醚 为溶剂, 生成 diethylzinc
    参考文献:
    名称:
    WO2008/134890
    摘要:
    公开号:
  • 作为产物:
    描述:
    zinc(II) formate dihydrate 、 乙二醇 生成 zinc glycolate
    参考文献:
    名称:
    乙醇酸锌 Zn(OCH2CH2O):合成和结构、光谱和光学性质、电子结构和化学键合
    摘要:
    本文介绍了研究乙醇酸锌 Zn(OCH 2 CH 2 O) 的形成条件、晶体结构、热学、光谱学、光学性质和电子能带结构的新发现。该化合物是通过加热甲酸锌 Zn(HCOO) 2 ·2H 2 O 在乙二醇 (A) 或乙二醇和蒸馏水的混合物 (B) 中的溶液来合成的。已经使用X射线粉末衍射法研究了Zn(OCH 2 CH 2 O)的晶体结构。结果表明,晶体结构是通过[Zn 4 O 12 C 8 H 16的锯齿形连接建立的。] 四环与四面体配位的锌 (ZnO 4 )。四环内的锌原子和四环本身与氧桥相互连接。复合阴离子OCH 2 CH 2 O 2-通过螯合与锌原子键合。Zn(OCH 2 CH 2 O)的晶胞参数如下:四方结构,空间群I4 1 /a (88-2),Z = 16,a = b = 11.08673(9) Å,c = 11.5902 (1) Å, V = 1424.62(2) Å 3。Zn(OCH
    DOI:
    10.1016/j.jallcom.2022.166320
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文献信息

  • Synthesis of Novel Layered Zinc Glycolate and Exchange of Ethylene Glycol with Manganese Acetate Complex
    作者:Kaori Takase、Hitoshi Nishizawa、Kazuya Imamura、Ayumu Onda、Kazumichi Yanagisawa、Shu Yin
    DOI:10.1246/bcsj.20180132
    日期:2018.10.15
    The novel layered zinc glycolate (LZG) with a lamella structure was successfully synthesized from zinc acetate by solvothermal reactions in ethylene glycol (EG) without water. The octahedral-shaped zinc glycolate (OZG) particles were formed in EG containing 1% water. LZG and OZG are crystal polymorphs with the same composition, Zn(OCH2CH2O). At 5% water content, the uniform and spherical particles of ZnO were formed. EG moieties in LZG were partially exchanged with Mn acetate complex in Mn acetate solution and the interlayer spacing of LZG was increased from 1.09 nm to 1.42 nm. ZnO and ZnMn2O4 were formed by heating the exchanged LZG at 600 °C. Acetate ions in the exchanged LGZ were exchanged with salicylic ions. EG moieties in OZG were mainly exchanged with OH in Mn acetate solution to form an amorphous phase.
    在不含乙二醇EG)中,通过溶热反应成功合成了具有薄片结构的新型层状羟基乙酸(LZG)。在含量为 1%的乙二醇中形成了八面体形的羟基乙酸(OZG)颗粒。LZG 和 OZG 是具有相同成分 Zn(OCH2CH2O) 的晶体多晶型。含量为 5%时,形成了均匀的球形氧化锌颗粒。在醋酸溶液中,LZG 中的 EG 分子与醋酸络合物发生了部分交换,LZG 的层间距从 1.09 nm 增加到 1.42 nm。将交换后的 LZG 在 600 °C 下加热可形成 ZnO 和 ZnMn2O4。交换 LGZ 中的醋酸根离子被水杨酸根离子交换。OZG 中的 EG 分子主要与醋酸溶液中的 OH 交换,形成无定形相。
  • Synthesis and photocatalytic properties of low-dimensional cobalt-doped zinc oxide with different crystal shapes
    作者:V. N. Krasil’nikov、O. I. Gyrdasova、L. Yu. Buldakova、M. Yu. Yanchenko
    DOI:10.1134/s0036023611020136
    日期:2011.2
    The glycoxide complexes Zn(1-x) Co (x) (HCOO)(HOCH(2)CH(2)O)(1/2) and Zn(1-x) Co (x) (OCH(2)CH(2)O) (0 a parts per thousand currency sign x a parts per thousand currency sign 0.3) have been synthesized by heating ethylene glycol solutions of zinc formate Zn(HCOO)(2) center dot 2H(2)O or its mixtures with cobalt formate Co(HCOO)(2) center dot 2H(2)O. The crystals of these complexes have the shape of filaments (needles, bars) and distorted octahedra, respectively. A new method in which these complexes are used as the precursor is suggested for the synthesis of low-dimensional wurtzite-like Zn(1-x) Co (x) O. The shape of the precursor crystals is fully inherited by Zn(1-x) Co (x) O resulting from their heat treatment. The Zn(1-x) Co (x) O solid solutions show high photocatalytic activity in hydroquinone oxidation in aqueous solution under UV or blue light irradiation, and their activity increases as their cobalt content is increased.
  • Synthesis and structure of quasi-one-dimensional zinc oxide doped with manganese
    作者:O. I. Gyrdasova、V. N. Krasil’nikov、E. V. Shalaeva、M. V. Kuznetsov、A. P. Tyutyunnik
    DOI:10.1134/s0036023612010111
    日期:2012.1
    Nanotubes of manganese-doped zinc oxide Zn1-xMnxO (0 <= x <= 0.2) were synthesized by heating the Zn1-xMnx(HCOO)(OCH2CH2O)(1/2) precursor in air at 500 degrees C. The precursor with extended crystals was synthesized by a solvothermal method based on heat treatment of a mixture of Zn1-xMnx(HCOO)(2) center dot 2H(2)O with an ethylene glycol excess at 100-130 degrees C. The tubular morphology of Zn1-xMnxO particles was identified by transmission electron microscopy. Tubular quasi-one-dimensional particles were shown to have a nanodispersed polycrystalline structure, the size of separate crystallites being from 5 to 20 nm. X-ray photo-electron spectroscopy suggested that the manganese distribution on the outer surface layer of Zn1-xMnxO nanotubes is nonuniform.
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