Amino-cobalt(II)phthalocyanine supported on silica chloride as an efficient and reusable heterogeneous photocatalyst for oxidation of alcohols

被引:9
作者
Farahmand, Shohreh [1 ]
Ayazi-Nasrabadi, Roya [1 ]
Zolfigol, Mohammad Ali [1 ]
机构
[1] Bu Ali Sina Univ, Fac Chem, Dept Organ Chem, Hamadan 6517838683, Iran
关键词
Heterogeneous; Photocatalyst; Cobalt (II) phthalocyanine (CoPc); TACoPc; Si-Cl; Eco-friendly; Oxidant; Visible light irradiation; SELECTIVE OXIDATION; AEROBIC OXIDATION; COBALT(II) PHTHALOCYANINE; COMPOSITE-MATERIAL; BENZYL ALCOHOL; COPPER(II) DETECTION; AROMATIC ALCOHOLS; ALKYL ARENES; CATALYST; REMOVAL;
D O I
10.1016/j.tetlet.2023.154403
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The selective photocatalytic oxidation of alcohols is considered as a valuable process in order to produce aldehydes and ketones. In the present study, novel heterogeneous and recoverable cobalt (II) phthalocya-nine (CoPc) was designed and synthesized through a covalent binding between an amino-cobalt (II) phthalocyanine on the surface of silica, and named as TACoPc/Si-Cl. This catalyst was fully characterized using IR, X-ray diffraction patterns (XRD), Scanning electron microscope (SEM), Transmission electron microscopy (TEM), Brunauer-Emmett-Teller (BET), element analysis (CHN), and ultraviolet-visible spec-troscopy (UV/Vis). Various reaction parameters such as catalyst amount, temperature, time, solvent and amount of oxidant were investigated in the oxidation of primary and secondary alcohols to the corre-sponding carbonyl compounds. The desired products were obtained with acceptable efficiency and selec-tivity of over 98%, under visible light irradiation conditions. The supported catalyst exhibited a higher reactivity than the unsupported and after the reaction comes off easily and reusable. The recovered cat-alyst was reused six times. The obtained results show that the stability, efficiency and selectivity of described catalyst have not changed much compared to the fresh catalyst. (c) 2023 Elsevier Ltd. All rights reserved.
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页数:10
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