Organosilicon compounds containing carbofunctional biguanidine group
摘要:
The reaction of triethoxysilylpropylamine (AGM-9) with dicyanodiamide was studied. ne condensation of AGM-9 with dicyanodiamide occurs in the presence of a catalytic amount of CuCl2 at 125-145 degrees C within 5-24 h; it involves both the amino group of AGM-9 and ethoxy substituents at the Si atoms, with an unusual exchange of a Si-O bond for a Si-N bond. The final reaction product is 1-N-(3-triethoxysilylpropyl)-2-N-[3-aminopropylsilyl(diethoxy)]biguanidine. Its hydrolytic polycondensation yields an organo-silicon polymer, a polycondensate of AGM-9 with 1-N-(3-triethoxysilylpropyl)biguanidine, which is a highly efficient sorbent for Ag(I) (static sorption capacity 544 mg g(-1)).