alkynylation of ClMe2SiC5H4Mn(CO)3 (6) with PhC≡CMgBr was also successful. In contrast, the direct complexation of (alkynylsilyl)cyclopentadiene or the direct alkynylsilylation of cymantrene were not feasible. Redox reactions and the desilylation of the cyclopentadienyl ring were hampering side reactions in all routes but to varying extent. All three complexes were characterized by NMR spectroscopy. 1 and
                                    研究了(炔基甲
硅烷基)
环戊二烯基
钛锰配合物的合成。通过用合适的卤化
钛 (IV) 处理 LiC5H4SiMe2C≡CPh 制备
钛化合物 PhC≡CMe2SiC5H4CPTiCl2 (1) 和 (PhC≡CMe2SiC5H4)2TiCl2 (2)。
锰化合物PhC≡CMe2SiC5H4Mn(CO)3(3)可以通过用TlC5H4SiMe2C≡CPh或LiC5H4SiMe2C≡CPh处理Mn(CO)5Cl来合成。或者,ClMe2SiC5H4Mn(CO)3 (6) 与 PhC≡CMgBr 的炔化反应也成功。相比之下,(炔基甲
硅烷基)
环戊二烯的直接络合或花桂烯的直接炔基甲
硅烷基化是不可行的。氧化还原反应和
环戊二烯基环的脱甲
硅烷基化在所有途径中都阻碍了副反应,但程度不同。所有三种配合物均通过核磁共振光谱表征。还通过红外和紫外/可见光谱研究了 1 和 3。通过X射线衍射分析确定了化合物1的分子和晶体结构。