Wang Xiuli, Liu Xiaodong, Xu Na, Liu Xiaohui, Guo Yanyan, Zhang Xiaoyan, Li Xiaohui
College of Chemistry and Materials Engineering, Bohai University, Professional Technology Innovation Center of Liaoning Province for Conversion Materials of Solar Cell, Jinzhou 121013, People's Republic of China.
Inorg Chem. 2023 Aug 7;62(31):12181-12186. doi: 10.1021/acs.inorgchem.3c01907. Epub 2023 Jul 25.
Selective oxidation of aniline to azobenzene with a higher economic value is significant for modern industrial production. However, the high reaction temperature and undefined catalytic reaction center always limit the promotion of this reaction. Here, we designed and synthesized a new [PMoO]-based cobalt-containing complex (Hbiz){Co(HO)[Co(HO)]}{Co[MoO(OH)(PO)(HPO)][MoO(OH)(PO)(HPO)]}·3HO (; biz = benzimidazole) under solvothermal conditions. Using as the photocatalyst, the visible-light-driven conversion of aniline to azobenzene at room temperature was realized for the first time (conversion rate 97%, selectivity 96% of azobenzene, reaction time of 12 h). Additionally, real sunlight irradiation can produce a comparable outcome in 48 h. The mechanism investigation manifested that the Mo and Co centers in acted as Brönsted and Lewis acid centers, synergistically promoting the aniline oxidation reaction. This research advances the application of polyoxometalate-based photocatalysts while also offering a sustainable and effective method for producing azobenzene.
将苯胺选择性氧化为具有更高经济价值的偶氮苯对现代工业生产具有重要意义。然而,高反应温度和不明确的催化反应中心一直限制着该反应的推广。在此,我们在溶剂热条件下设计并合成了一种新型的基于[PMoO]的含钴配合物(Hbiz){Co(HO)[Co(HO)]}{Co[MoO(OH)(PO)(HPO)][MoO(OH)(PO)(HPO)]}·3HO(;biz = 苯并咪唑)。以该配合物作为光催化剂,首次实现了室温下可见光驱动的苯胺向偶氮苯的转化(转化率97%,偶氮苯选择性96%,反应时间12小时)。此外,实际阳光照射在48小时内可产生相当的结果。机理研究表明,该配合物中的Mo和Co中心作为布朗斯特和路易斯酸中心,协同促进苯胺氧化反应。本研究推动了基于多金属氧酸盐的光催化剂的应用,同时也为偶氮苯的生产提供了一种可持续且有效的方法。