Formation of metal carbonyl derivatives of monothiocarbamates and dithio-carbamates from CS2 and COS
作者:Luigi Busetto、Antonio Palazzi、Vassilios Foliadis
DOI:10.1016/s0020-1693(00)91995-9
日期:1980.1
variable quantities of (C5H5)Fe(CO)S2CNHCH3 are obtained depending on reaction conditions. The carbamoyl derivatives (C5H5Re(CO)(NO)CONHCH3, cis-(CO)4M(NH2CH3)CONHCH3 (M = Mn, Re) react with CS2 to give (C5H5)Re(CO)(NO)S2CNHCH3 and (CO)4MS2CNHCH3 respectively. The mechanism of thiocarbamate formation is discussed on the basis of chemical evidence which indicates nucleophilic attack of the N-carbamoylic
(C5H5)Fe(CO)2CONHCH3与CSX的反应(X = O,S)得到(C5H5)Fe(CO)2SC(X)NHCH3,其中一硫代或二硫代氨基甲酸酯起单齿配体的作用。在二硫化碳的情况下,取决于反应条件,会获得少量可变的(C5H5)Fe(CO)S2CNHCH3。氨基甲酰基衍生物(C5H5Re(CO)(NO)CONHCH3,顺式(CO)4M(NH2CH3)CONHCH3(M = Mn,Re)与CS2反应生成(C5H5)Re(CO)(NO)S2CNHCH3和(CO) 4MS2CNHCH3分别根据化学证据讨论了硫代氨基甲酸酯的形成机理,化学证据表明N-氨基甲酸酯原子对CSX试剂碳的亲核攻击。