Synthesis of a sulfonato-salen-nickel(II) complex immobilized in LDH for tetralin oxidation

被引:31
作者
Bhattacharjee, Samiran [1 ]
Jeong, Kwang-Eun [2 ]
Jeong, Soon-Yong [2 ]
Ahn, Wha-Seung [1 ]
机构
[1] Inha Univ, Dept Chem Engn, Inchon 402751, South Korea
[2] KRICT, Appl Chem & Engn Div, Yuseong 305600, South Korea
关键词
MCM-41; MOLECULAR-SIEVES; ENANTIOSELECTIVE EPOXIDATION; UNFUNCTIONALIZED OLEFINS; ALLYLIC OXIDATION; BASE COMPLEXES; ZEOLITE-Y; CATALYSTS; OXYGEN; CHROMIUM; NICKEL(II);
D O I
10.1039/b9nj00314b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel sulfonato-salen-nickel(II) complex has been immobilized on a Zn(II)-Al(III) layered double hydroxide (LDH) host. XRD, FT-IR, TGA and UV-vis spectroscopy, as well as chemical analysis, confirmed the successful incorporation of the nickel-salen complex within the LDH structure. BET surface area measurements, SEM and TEM were also used to characterize the heterogenized catalyst. The sulfonato-salen-nickel(II) complex-immobilized material, LDH-[nickel-salen], was found to be effective in the oxidation of tetralin, where a combination of trimethylacetaldehyde and dioxygen at atmospheric pressure was employed as the oxidant. At 72.3% conversion, tetralin was converted to 1-tetralone with 72.2% selectivity at 70 degrees C after 7 h. Tetralin oxidation using tert-butyl hydroperoxide afforded a lower conversion and selectivity of 1-tetralone than with trimethylacetaldehyde and dioxygen as the oxidant. The effect of various reaction parameters on catalytic performance was also investigated. A hot filtration experiment coupled with a blank test revealed that oxidation proceeded mostly on nickel-salen sites in LDH-[nickel-salen]. A reaction mechanism is proposed based on the experimental results.
引用
收藏
页码:156 / 162
页数:7
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