Novel reactions of extremely hindered plumbylenes with elemental sulfur and carbon disulfide

被引:0
作者
Tokitoh, N [1 ]
Kano, N [1 ]
Okazaki, R [1 ]
机构
[1] Univ Tokyo, Grad Sch Sci, Dept Chem, Bunkyo Ku, Tokyo 113, Japan
关键词
plumbylenes; kinetic stabilization; elemental sulfur; 1,2-aryl migration; plumbanethione; carbon disulfide;
D O I
暂无
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Synthesis, structure, and some reactivities of kinetically stabilized plumbylenes are described. The reaction of an extremely hindered plumbylene Tbt(2)Pb: (Tbt= 2,4,6-tris[bis(trimethylsilyl)methyl]pheyl with elemental sulfur gave Tbt(TbtS)Pb: via an interesting 1,2-aryl migration of the intermediary plumbanethione, Tbt(2)Pb=S. The reactions of overcrowded aryl(arylthio)plumbylenes and bis(arylthio)-plumbylenes with carbon disulfide are also described.
引用
收藏
页码:333 / 334
页数:2
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共 2 条
  • [1] Synthesis and reactions of the first lead-sulfur double-bond compounds, plumbanethiones
    Kano, N
    Tokitoh, N
    Okazaki, R
    [J]. CHEMISTRY LETTERS, 1997, (03) : 277 - 278
  • [2] A novel 1,2-aryl migration in metallanethione: Unusual formation of an aryl(arylthio)plumbylene from a plumbanethione
    Kano, N
    Tokitoh, N
    Okazaki, R
    [J]. ORGANOMETALLICS, 1997, 16 (20) : 4237 - 4239