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| 874197-36-1

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
874197-36-1
化学式
C43H67FeKN4O2
mdl
——
分子量
766.976
InChiKey
GOGZRBMLDOBDIT-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

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Bis(imino)pyridine Ligand Deprotonation Promoted by a Transient Iron Amide
    摘要:
    Addition of 2 equiv of LiNMe2 to the bis(imino)pyridine ferrous dichloride, ((PDI)-P-iPr)FeCl2 ((PDI)-P-iPr = (2,6-Pr-i(2)-C6H3N=CMe)(2)C5H3N), resulted in deprotonation of the chelate methyl groups, yielding the bis(enamide)pyridine iron dimethylamine adduct, ((iPr)PDEA)Fe-(NHMe2) ((iPr)PDEA = (2,6-Pr-i(2)-C6H3NC=CH2)(2)C5H3N). Performing a similar procedure with KN(SiMe3)(2) in THF solution afforded the corresponding bis(THF) adduct, ((iPr)PDEA)Fe(THF)(2). ((iPr)PDEA)Fe-(NHMe2) has also been prepared by addition of the free amine to the iron dialkyl complex, ((PDI)-P-iPr)Fe(CH2SiMe3)(2), implicating formation of a transient iron amide that is sufficiently basic to deprotonate the bis(imino)pyridine methyl groups. Deprotonation of the amine ligand in ((iPr)PDEA)Fe(NHMe2) has been accomplished by addition of amide bases to afford the ferrous amide-ate complexes, [((iPr)PDEA)Fe(mu-NMe2)M] (M = Li, K).
    DOI:
    10.1021/ic051839o
  • 作为产物:
    参考文献:
    名称:
    Bis(imino)pyridine Ligand Deprotonation Promoted by a Transient Iron Amide
    摘要:
    Addition of 2 equiv of LiNMe2 to the bis(imino)pyridine ferrous dichloride, ((PDI)-P-iPr)FeCl2 ((PDI)-P-iPr = (2,6-Pr-i(2)-C6H3N=CMe)(2)C5H3N), resulted in deprotonation of the chelate methyl groups, yielding the bis(enamide)pyridine iron dimethylamine adduct, ((iPr)PDEA)Fe-(NHMe2) ((iPr)PDEA = (2,6-Pr-i(2)-C6H3NC=CH2)(2)C5H3N). Performing a similar procedure with KN(SiMe3)(2) in THF solution afforded the corresponding bis(THF) adduct, ((iPr)PDEA)Fe(THF)(2). ((iPr)PDEA)Fe-(NHMe2) has also been prepared by addition of the free amine to the iron dialkyl complex, ((PDI)-P-iPr)Fe(CH2SiMe3)(2), implicating formation of a transient iron amide that is sufficiently basic to deprotonate the bis(imino)pyridine methyl groups. Deprotonation of the amine ligand in ((iPr)PDEA)Fe(NHMe2) has been accomplished by addition of amide bases to afford the ferrous amide-ate complexes, [((iPr)PDEA)Fe(mu-NMe2)M] (M = Li, K).
    DOI:
    10.1021/ic051839o
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