DABCO-functionalized silica-copper(I) complex: a novel and recyclable heterogeneous nanocatalyst for palladium-free Sonogashira cross-coupling reactions

被引:34
作者
Hajipour, Abdol Reza [1 ,2 ]
Hosseini, Seyed Mostafa [1 ]
Mohammadsaleh, Fatemeh [1 ]
机构
[1] Isfahan Univ Technol, Dept Chem, Pharmaceut Res Lab, Esfahan 84156, Iran
[2] Univ Wisconsin, Dept Neurosci, Sch Med, 1300 Univ Ave, Madison, WI 53706 USA
关键词
SUZUKI-MIYAURA; CATALYTIC-ACTIVITY; TERMINAL ALKYNES; ARYL IODIDES; NANO-SILICA; NANOPARTICLES; EFFICIENT; LIGAND; HECK; WATER;
D O I
10.1039/c6nj00612d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A DABCO-functionalized silica supported copper(I)-based nanocatalyst was successfully prepared using a novel and simple route, in which the DABCO as an important functional entity acts as both a stable linker and an excellent chelator. Initially, Cu(II) ions were fixed in the DABCO-functionalized SiO2 matrix via complex formation with N-groups of DABCO, and subsequently this Cu(II)-DABCO@SiO2 composite as a precursor reacted with NaI in methanol solvent at room temperature under aerobic conditions to produce the DABCO-functionalized silica-copper(i) complex (catalyst A). This catalyst was well characterized by FT-IR, CHN, XRD, FE-SEM, TEM, EDX, ICP-AES and TG analysis, and was found to be efficient and recyclable for the C-C bond formation reaction in the palladium-free copper-catalyzed Sonogashira coupling of aryl halides with phenylacetylene. The grafted DABCO, having a synergistic effect of coordination and electrostatic interactions, plays an important role in this catalytic system, and as an effective ligand and a quaternary ammonium salt, demonstrates an efficient stabilizing effect on the Cu(I) species.
引用
收藏
页码:6939 / 6945
页数:7
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