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[(Bu2Sn(6-nitropiperonylate))2O]2*CHCl3 | 1210038-92-8

中文名称
——
中文别名
——
英文名称
[(Bu2Sn(6-nitropiperonylate))2O]2*CHCl3
英文别名
——
[(Bu2Sn(6-nitropiperonylate))2O]2*CHCl3化学式
CAS
1210038-92-8
化学式
CHCl3*C64H88N4O26Sn4
mdl
——
分子量
1923.63
InChiKey
JNUXBINTAKRBFI-UHFFFAOYSA-J
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:
    氯仿6-硝基-1,3-苯并二氧代-5-羧酸二正丁基氧化锡甲苯 为溶剂, 以65%的产率得到[(Bu2Sn(6-nitropiperonylate))2O]2*CHCl3
    参考文献:
    名称:
    In vitro biological studies and structural elucidation of organotin(IV) derivatives of 6-nitropiperonylic acid: Crystal structure of {[(CH2O2C6H2(o-NO2)COO)SnBu2]2O}2
    摘要:
    Six organotin(IV) compounds with general formulae R3SnL, R = Me (2), Ph (6), R2SnL2, R = Me (1), Et (3), n-Oct (5), [((R2SnL)(2)O)(2)], R = Bu (4). L = 6-nitropiperonylate, have been prepared. The newly synthesized compounds have been characterized by elemental analysis, FT-IR and multinuclear NMR (H-1, C-13 and Sn-119). The structure of 4 has been determined by single crystal X-ray crystallography which is triclinic with the space group P (1) over bar The crystal Structure contains centrosymmetric dimer distannoxane with planar central four-membered Sn2O2 core. The 6-nitropiperonylate ligand shows different modes of coordination with Sn, as a result the central Sn2O2 core is fused with two four-membered (Sn(1)-O(1)-Sn(2)-O(13)) and two six-membered (Sn(1)-O(13)-Sn(2)-O(8)-C(9)-O(7)) rings. The endocyclic Sn(2) is six coordinated in a skew trapezoidal bipyramidal environment while exocyclic Sn(1) is five coordinated with distorted trigonal bipyramidal geometry. The ligand acid and synthesized organotin compounds were also screened for antibacterial, antifungal, brine-shrimp lethality and potato disc antitumor activities. Results of bioassay demonstrate that organotin derivatives are in general more active than the ligand acid. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2009.07.039
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