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2,6-Me2C6H3SCo(dimethylglyoximate(1-))2(pyridine) | 185690-76-0

中文名称
——
中文别名
——
英文名称
2,6-Me2C6H3SCo(dimethylglyoximate(1-))2(pyridine)
英文别名
——
2,6-Me2C6H3SCo(dimethylglyoximate(1-))2(pyridine)化学式
CAS
185690-76-0
化学式
C21H28CoN5O4S
mdl
——
分子量
505.544
InChiKey
PVSYLVVUDDAGID-NMBSQECASA-K
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:
    2,6-二甲基巯基苯酚 、 bis(dimethylglyoximato)(pyridine)cobalt(II) dimer 以 甲醇 为溶剂, 以53%的产率得到2,6-Me2C6H3SCo(dimethylglyoximate(1-))2(pyridine)
    参考文献:
    名称:
    The First X-ray Structural Evidence Demonstrating Thiolate Coordination in an Organocobalt B12 Model Complex:  Implications for Methionine Synthase
    摘要:
    Enzyme-bound methyl-B-12 transfers its methyl group to homocysteine during methionine synthesis. However, treatment of several types of organocobalt B-12 models with arene- and alkanethiolates under ambient conditions leads only to thiolate ligation. The structure of [AsPh(4)][EtSCo(DH)(2)CH3] (DH = monoanion of dimethylglyoxime), the first characterization by X-ray crystallography of an organocobalt complex containing a unidentate coordinated thiolate, demonstrates unambiguously the S-ligation of ethanethiolate to Co, trans to the CH3 ligand. This compound contains a very long Co-S bond (2.342(2) Angstrom). However, the length of the Co-C bond (2.005(7) Angstrom) is typical; this result strongly supports reported FT-Raman spectroscopic data indicating that the thiolate-type ligand does not have a strong trans influence and does not significantly weaken the Co-C bond in the ground state. Since a strong trans influence alkyl ligand weakens the trans Co-C bond, we examined the effect of EtS(-) on Co((DO)(DOH)pn)(CH3)(2) ((DO)(DOH)pn = N-2,N-2'-propanediylbis(2,3-butanedione 2-imine 3-oxime) is an imine/oxime quadridentate ligand]. Even for this compound, no attack on the Co-C bond was observed, although independently synthesized EtSCo((DO)DOH)pn)CH3 was stable. Furthermore, thiolate did not cleave the Co-C bond of an organocobalt complex with a highly distorted Co-C group. Several new spectroscopic and ligand-exchange reactions were observed in this study. Ligand-responsive NMR shift trends in these other new complexes also indicate that thiolate ligands have a weak trans influence.
    DOI:
    10.1021/ic961019z
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