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Solar-driven aromatic aldehydes: green production from mandelic acid derivatives by a Co(ii)/C(3)N(4) combined catalyst in aqueous media

According to the requirements for sustainable development, reclaiming fine chemicals from wastewater under mild conditions is an extremely significant line of research. A low-cost and high-efficiency polydentate chelate- and polymeric Co(ii)-based complex (Co-L)-loaded C(3)N(4) photocatalyst (Co-L/C...

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Detalles Bibliográficos
Autores principales: Wu, Mi, Wang, Hongzhao, Mao, Haifang, Wang, Chaoyang, Dong, Zhenbiao, Tang, Ting, Zheng, Wei, Jin, Lehong, Liu, Jibo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981277/
https://www.ncbi.nlm.nih.gov/pubmed/35425574
http://dx.doi.org/10.1039/d1ra08256f
Descripción
Sumario:According to the requirements for sustainable development, reclaiming fine chemicals from wastewater under mild conditions is an extremely significant line of research. A low-cost and high-efficiency polydentate chelate- and polymeric Co(ii)-based complex (Co-L)-loaded C(3)N(4) photocatalyst (Co-L/C(3)N(4)) was constructed and used to convert aromatic mandelic acids in wastewater at room temperature. The BET specific surface area increased from 28 m(2) g(−1) to 68 m(2) g(−1), indicating its excellent absorptive character. The light absorption range of Co-L/C(3)N(4) reached 650 nm, while the band energy reduced to 2.30 eV, which caused a significant enhancement in photocatalytic activity. The conversion of substituted mandelic acids was more than 90% due to the photoactivity of Co-L/C(3)N(4). Time-resolved PL spectra indicated the remarkable separation of the photogenerated electron–hole pairs in Co-L/C(3)N(4). Furthermore, the UV-vis and in situ FTIR spectra indicated the formation of aldehyde groups in the selective oxidation process, which provided support for the plausible catalytic mechanism.