Selected dechlorination of triclosan by high-performance g-C3N4/Bi2MoO6 composites: Mechanisms and pathways

Yu, Bingzhi; Ye, Wen; Meng, Yunjuan; Zhang, Yinan; Li, Xizi; Li, Yan; Zhong, Yuchi; Ding, Jiafeng; Zhang, Hangjun

doi:10.1016/j.chemosphere.2022.137247

Cited by 9 publications

(5 citation statements)

References 58 publications

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“…Dechlorination, hydroxylation, and cyclization along with other bond-breaking mechanisms were attributed to the triclosan degradation purpose. In one of the recent articles, Yu et al [114] described the highly efficient degradation performance of a novel catalyst g-C 3 N 4 /Bi 2 MoO 6 towards TCS drug. TCS was converted to 2-phenoxyphenol under visible light irradiation.…”

Section: Other Drugsmentioning

confidence: 99%

A Brief Review on the Latest Developments on Pharmaceutical Compound Degradation Using g-C3N4-Based Composite Catalysts

Biswas¹,

Pal

2023

Catalysts

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Pharmaceutical compounds (PCs) are one of the most notable water pollutants of the current age with severe impacts on the ecosystem. Hence, scientists and engineers are continuously working on developing different materials and technologies to eradicate PCs from aqueous media. Among various new-age materials, graphitic carbon nitride (g-C3N4) is one of the wonder substances with excellent catalytic property. The current review article describes the latest trend in the application of g-C3N4-based catalyst materials towards the degradation of various kinds of drugs and pharmaceutical products present in wastewater. The synthesis procedure of different g-C3N4-based catalysts is covered in brief, and this is followed by different PCs degraded as described by different workers. The applicability of these novel catalysts in the real field has been highlighted along with different optimization techniques in practice. Different techniques often explored to characterize the g-C3N4-based materials are also described. Finally, existing challenges in this field along with future perspectives are presented before concluding the article.

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Section: Other Drugsmentioning

confidence: 99%

A Brief Review on the Latest Developments on Pharmaceutical Compound Degradation Using g-C3N4-Based Composite Catalysts

Biswas¹,

Pal

2023

Catalysts

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“…Finally, protonation of IV delivers the product 11 and regenerates the catalytically active Ru(II) species I (Scheme 11 B). 12…”

Section: Alkenyl C–h Alkenylationmentioning

confidence: 99%

“…A wide range of functionalities such as amide, hydroxy, carbamate, tosylamine, carboxylic acid, ester, ketone, imine, enamide, 8-aminoquinoline and picolinamide, as well as aldehyde-derived transient directing groups, are used as mono- or bidentate directing groups. 3d , 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60…”

Section: Introductionmentioning

confidence: 99%

“…The development of efficient and environmentally benign synthetic methods is in high demand. In previous work, we were interested in the development of metal-oxidant-free cross-coupling reactions, 11 12 18 43 44 directing-group-mediated simple chemical derivations, 13,15 cross-coupling using inexpensive and fairly environmentally benign cobalt catalysis, 19 and cross-coupling by exo -cyclopalladation 23 26 31 36 and tandem cyclization. 57…”

Section: Introductionmentioning

confidence: 99%

“…In this account, we summarize transition-metal-catalyzed cross-coupling reactions between alkenes to generate 1,3-dienes by C–H alkenylation, 3d , 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 1,4-dienes via C–H allylation, 37–44 multisubstituted alkenes through hydroalkenylation, 45–50 and heterocycles via tandem alkenyl C–H functionalization and annulation. 51 52 53 54 55 56 57 58 59 60 Asymmetric alkenyl C–H alkenylation to prepare axially chiral aryl 1,3-dienes is also discussed.…”

Section: Introductionmentioning

confidence: 99%

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Cross-Coupling Reactions between Alkenes by C–H Cyclometalation

Wang

Xie

et al. 2023

Synlett

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Alkenes are one of the most abundant raw feedstocks to construct complex chemicals, cross-coupling reactions using alkenes provides powerful methods toward valuable chemicals. In the past decade, cross-coupling reaction of simple alkenes by chelation-assisted alkenyl C−H functionalization has attracted many attentions due to its atom- and step efficiency, as well as excellent Z/E selectivity, proceeding by C−H exo-cyclometallation and endo-cyclometallation. In this Account, we would like to summarize transition-metal-catalyzed cross-coupling reactions between alkenes to generate 1,3-dienes by C−H alkenylation,1,4-dienes by C−H allylation, multi-substituted alkenes by hydroalkenylation, and heterocycles by tandem alkenyl C-H functionalization/annulation. Asymmetric alkenyl C−H alkenylation to prepare axially chiral aryl 1,3-dienes was also included.

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Elemental imprinting-induced interfacial growth strategy to bridge g-C3N4 and Bi2MoO6 with engineering rapid electron transfer pathway for efficient visible light-driven photocatalysis

Liu,

Yu,

Liang

et al. 2024

Chemical Engineering Journal

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Selected dechlorination of triclosan by high-performance g-C3N4/Bi2MoO6 composites: Mechanisms and pathways

Cited by 9 publications

References 58 publications

A Brief Review on the Latest Developments on Pharmaceutical Compound Degradation Using g-C3N4-Based Composite Catalysts

A Brief Review on the Latest Developments on Pharmaceutical Compound Degradation Using g-C3N4-Based Composite Catalysts

Cross-Coupling Reactions between Alkenes by C–H Cyclometalation

Elemental imprinting-induced interfacial growth strategy to bridge g-C3N4 and Bi2MoO6 with engineering rapid electron transfer pathway for efficient visible light-driven photocatalysis

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