摘要
在温和的条件下实现对芳香醇选择性氧化是一个重大挑战。以中-四(4-羧基苯基)卟吩或中-四(4-羧基苯基)钴卟吩为有机配体、Zn_(2)^(4+)为无机金属节点、4,4’-联吡啶为连接体,通过分步方式制备自组装膜(分别命名为TCPP和TCPP-CoTCPP)。利用紫外可见吸收光谱和原子力显微镜对上述自组装膜的制备过程及组装结果进行表征。结果表明:TCPP-CoTCPP中光生电子-空穴对的分离效率和界面电荷迁移率较TCPP高,室温有氧条件下该自组装膜表现出良好的同步光催化芳香醇选择性氧化和过氧化氢生成性能;在优化的反应条件下,TCPP的过氧化氢产量为47.23 mmol,芳香醇氧化为芳香醛的选择性为48.4%;通过对自组装膜的有机配体调控,TCPP-CoTCPP过氧化氢产量提高到68.73 mmol,芳香醇氧化为芳香醛的选择性提升到84.2%。
Achieving selective oxidation of aromatic alcohols under mild conditions is a major challenge.In this work,selfassembled films were prepared by a step-by-step approach,using meso-tetra(4-carboxyphenyl)porphine or meso-tetra(4-carboxyphenyl)porphine cobalt(II)ligands,zinc inorganic metal node,and 4,4’-bipyridine linker,named TCPP and TCPP-CoTCPP,respectively.The preparation process and assembly results of the above self-assembled films were characterized using UV-vis spectroscopy and atomic force microscopy.The results reveal that TCPP-CoTCPP demonstrated higher photogenerated electron-hole(e-h)separation and charge transfer efficiency than TCPP.Under aerobic conditions at room temperature,the TCPP-CoTCPP exhibited excellent simultaneous photocatalytic selective oxidation of aromatic alcohol and H2O2 generation.Under the optimized reaction conditions,the H2O2 evolution of TCPP was 47.23 mmol,and the selectivity of oxidation of aromatic alcohols to aromatic aldehydes was 48.4%.By regulating the organic ligand of the self-assembled membrane,the H_(2)O_(2) evolution of TCPP-CoTCPP was increased to 68.73 mmol,and the selectivity of oxidation of aromatic alcohol to aromatic aldehyde was improved to 84.2%.
作者
黄昌庚
卜冬蕾
HUANG Changgeng;BU Donglei(School of Materials and Energy/Guangzhou Key Laboratory of Low-Dimensional Materials and Energy Storage Devices,Guangdong University of Technology,Guangzhou 510006,China)
出处
《材料研究与应用》
CAS
2023年第2期213-219,共7页
Materials Research and Application
关键词
自组装膜
芳香醇
卟啉
光催化
选择性氧化
self-assembled film
aromatic alcohol
porphyrin
photocatalysis
selective oxidation