摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1-nitropyridinium tetrafluoroborate | 2375-72-6

中文名称
——
中文别名
——
英文名称
1-nitropyridinium tetrafluoroborate
英文别名
N-nitropyridinium tetrafluoroborate
1-nitropyridinium tetrafluoroborate化学式
CAS
2375-72-6
化学式
BF4*C5H5N2O2
mdl
——
分子量
211.912
InChiKey
QUSMALDKLXBOPY-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):
    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

SDS

SDS:21cf906c4ca14ca362caba54500cb5b0
查看

反应信息

  • 作为反应物:
    描述:
    1-nitropyridinium tetrafluoroborate 在 KN3O4 作用下, 以 乙腈 为溶剂, 以18%的产率得到N-nitropyridinium dinitramidate
    参考文献:
    名称:
    Dinitramide and its salts
    摘要:
    The methods for preparation and the properties of dinitramide salts with ammonia, hydrazine, hydroxylamine, formamidine, their alkylated and aminated derivatives, etc. are described.
    DOI:
    10.1007/bf00696969
  • 作为试剂:
    描述:
    1-nitropyridinium tetrafluoroborate 作用下, 以 乙腈 为溶剂, 反应 10.0h, 生成 硝基萘2-硝基萘
    参考文献:
    名称:
    Kim, Eun K.; Bockman, T. Michael; Kochi, Jay K., Journal of the Chemical Society. Perkin transactions II, 1992, # 11, p. 1879 - 1891
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • Sankararaman, S.; Kochi, J. K., Journal of the Chemical Society. Perkin transactions II, 1991, # 1, p. 1 - 12
    作者:Sankararaman, S.、Kochi, J. K.
    DOI:——
    日期:——
  • Bimetallic Reactivity. One-site Addition Two-metal Oxidation Reactions Using a Di-Co(II) Complex of a Binucleating Ligand with 5- and 6-Coordinate Sites
    作者:Christopher Incarvito、Arnold L. Rheingold、Anna L. Gavrilova、C. Jin Qin、B. Bosnich
    DOI:10.1021/ic010235r
    日期:2001.8.1
    The preparation of an unsymmetrical binucleating ligand bearing a bridging oxadiazole ring flanked on one side by three ligands and on the other by four ligands is described. When bound to two metals, the ligand forms complexes where the metals are in 5- and 6-coordinate sites after the incorporation of an exogenous bridging ligand. A di-Co2+ complex of th is ligand has been prepared containing a hydroxide bridge. The complex is readily oxidized to the di-Co3+ state by outer sphere electron transfer with ferrocenium ions. Addition of Br-2 or NO2+ to the di-Co2+ complex leads to the rapid formation of the di-Co3+ bromo or nitro complexes, respectively. The ligand characteristics which allow for double oxidation with ferrocenium ions and for the one-site addition two-metal oxidations with Br-2 and NO2+ are discussed in terms of mechanical coupling between the two metal sites.
  • Bockman, T. M.; Kim, E. K.; Kochi, J. K., Bulletin de la Societe Chimique de France, 1993, vol. 130, # 3, p. 323 - 335
    作者:Bockman, T. M.、Kim, E. K.、Kochi, J. K.
    DOI:——
    日期:——
查看更多