Pd-KIT-6: synthesis of a novel three-dimensional mesoporous catalyst and studies on its enhanced catalytic applications

被引:29
|
作者
Chirra, Suman [1 ]
Siliveri, Suresh [1 ]
Adepu, Ajay Kumar [1 ]
Goskula, Srinath [1 ]
Gujjula, Sripal Reddy [1 ]
Narayanan, Venkatathri [1 ]
机构
[1] Natl Inst Technol Warangal, Dept Chem, Warangal 506004, Telangana, India
关键词
Three-dimensional; Mesoporous; Pd-KIT-6; Catalytic activity; CROSS-COUPLING REACTION; SUZUKI-MIYAURA; PALLADIUM NANOPARTICLES; MOLECULAR-SIEVE; PORE STRUCTURE; EFFICIENT; HECK; STILLE; KIT-6; FABRICATION;
D O I
10.1007/s10934-019-00763-5
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Synthesis of a novel three-dimensional mesoporous Pd-KIT-6 is carried out by a room temperature sol-gel method. The synthesised material is well crystalline observed from the Small angle powder X-ray diffraction. Calcination at 550 degrees C for 8 h retains the structure. The particle sizes are in the micron range. Si/Pd ratio of the as-synthesized material is found to be 45 against the input ratio 100. Transmission electron micrograph reveals the presence of the porous hexagonal structure. Thermogravimetric studies reveal that the KIT-6 (Korea Advanced Institute of Science and Technology number 6) undergo less weight-loss compared to Pd-KIT-6, which indicates the material is more crystalline than its metal-free counterpart due to the enhanced crystallisation rate. These results also supported by BET-surface area and Transmission electron microscopic picture. The 960 cm(-1) band at Fourier transform Infrared spectroscopic analysis shows that the incorporation of Pd in the framework. These FT-IR results also supported by Raman Spectroscopic analysis. Electron spin resonance spectroscopic analysis shows that the Palladium is present in the +2 oxidation state in as-synthesized samples. Diffused reflectance Ultraviolet-Visible spectroscopic results show that Palladium is in tetrahedral coordination. Microwave irradiated Suzuki-Miyaura (SM) cross-coupling reactions studied by using the Pd-KIT-6 catalyst in detail without any organic solvent at 100 degrees C for 10 min. The reaction carried out in the presence of phenyl iodide, phenylboronic (PhB(OH)(2)), and K2CO3 produce biphenyl, with 98% yield. Change of halide to Phenyl bromide gave similar results, but Phenyl chloride gave lesser conversion (20%). It is due to the electronegativity difference between the halides. A plausible reaction mechanism is also proposed.
引用
收藏
页码:1667 / 1677
页数:11
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