高等学校化学研究 ›› 1988, Vol. 4 ›› Issue (2): 61-66.
Geng Bolin1, Xu Shansheng1, Huang Changhua1, Zhou Xiuzhong1, Wang yongtai2, Lin Chui2
Geng Bolin1, Xu Shansheng1, Huang Changhua1, Zhou Xiuzhong1, Wang yongtai2, Lin Chui2
摘要: The dependence of reactivity on molecular structure in hydro-silation of aromatic aldehydes catalyzed by (PPh3)3 RhCl was studied by "IN SITU" FT-IR technique and a plausible mechanism was proposed.The results show that: (1) Model reaction Ⅰ, Ⅱ and Ⅲ are all characterized by an induction period; (2) The reaction constant of model reaction Ⅰ is +1.57, so the rare of reaction Ⅰ is increased by the electron-withdrawing groups; (3) The rate of model reaction Ⅲ decreases when the size of R1 becomes larger; (4) The reaction constant of model reaction Ⅲ is -0. 50, so the rate of it is increased by electron-donating groups.