tetraphenylcyclobutadienepentakis(methylthiomercurio)cyclopentadienylcobalt | 218131-44-3

• 英文名称: tetraphenylcyclobutadienepentakis(methylthiomercurio)cyclopentadienylcobalt
• CAS: 218131-44-3
• 化学式: C₃₈H₃₅CoHg₅S₅
• 分子量: 1713.97
• InChiKey: OCYMNDOSJHNDLN-UHFFFAOYSA-I

反应信息

• 作为产物：
  描述：

  (tetraphenylcyclobutadiene)[pentakis((trifluoroacetoxy)mercurio)cyclopentadienyl]cobalt 、 sodium thiomethoxide 以 四氢呋喃 、 水 为溶剂， 以66%的产率得到tetraphenylcyclobutadienepentakis(methylthiomercurio)cyclopentadienylcobalt
  参考文献：
  名称：

  Toward a Square Grid Polymer:  Electrochemistry of Tentacled Tetragonal Star Connectors, C₄R₄−Co−C₅(HgY)₅, on Mercury

  摘要：

  Electrochemical reduction of cyclobutadienecyclopentadienylcobalt derivatives, C4Ra4-Co-C-5(HgY)(5) [R = C6H5- Y = -SMe (3), -SCOMe (4), -SCH2CH2SCH3 (5), -SCH2CH2SCOCH3 (6); R = p-EtOCOC6H4-, Y = -SEt (7), -SCOMe (8), -SCH2CH2SCH3 (9), -SCH2CH2SCOCH3 (10)3] and the parent C4R4-Co-C5H5 [R = C6H5- (11) and R = p-EtOCOC6H4- (12)] has been examined. Reversible one-electron "metal-centered" reduction of 11 (-2.24 V vs Ag/AgCl) yields a stable radical anion. In 12, it takes place at -1.70 V. In 3-10, similar metal-centered reduction occurs irreversibly, accompanied by an adsorption pre-wave at -0.7 to -1.15 V. We propose that the radical anion loses a -HgSX substituent soon after it is formed. Electrochemical cleavage of the substituents occurs before the metal-centered reduction in 4 and 8 and afterward in the others. The cleaved thiolate fragments yield an anodic peak. In all compounds with ester groups, ester reduction is observed at -2.1 to -2,5 V.

  DOI：

  10.1021/jp983242i