82419-52-1Relevant articles and documents
Facile synthesis of carbon quantum dots loaded with mesoporous g-C3N4 for synergistic absorption and visible light photodegradation of fluoroquinolone antibiotics
Wang, Yingfei,Wang, Fengliang,Feng, Yiping,Xie, Zhijie,Zhang, Qianxin,Jin, Xiaoyu,Liu, Haijin,Liu, Yang,Lv, Wenying,Liu, Guoguang
supporting information, p. 1284 - 1293 (2018/02/07)
The development of facile and efficient synthetic approaches of carbon quantum dots loaded with mesoporous g-C3N4 (mpg-C3N4/CQDs) is of critical urgency. Here, a facile strategy was developed to synthesize the mpg-C3N4/CQDs by using calcinations of the mixture of CQDs, cyanamide, and silica colloid. The obtained composite still retained a considerable total surface area, which could offer a larger population of adsorption sites; therefore enhance the capacity for the adsorption of fluoroquinolones antibiotics (FQs). Under visible light irradiation, mpg-C3N4/CQDs demonstrated a higher photocatalytic activity for FQs degradation than did bulk g-C3N4 or mpg-C3N4. This enhancement might have been ascribed to the high surface area of the mpg-C3N4, unique up-converted photoluminescence (PL) properties, and the efficient charge separation of the CQDs. The eradication of FQs followed the Langmuir-Hinshelwood (L-H) kinetic degradation model and absorption pseudo-second-order kinetic model, indicating that surface reactions and chemical sorption played significant roles during the photocatalysis process. The results of electron spin resonance (ESR) technology and reactive species (RSs) scavenging experiments revealed that the superoxide anion radical (O2-) and photo-hole (h+) were the primarily active species that initiated the degradation of FQs. Based on the identification of intermediates and the prediction of reactive sites, the degradation pathways of ofloxacin (OFX) were proposed. A residual antibiotic activity experiment revealed that mpg-C3N4/CQDs provided very desirable performance for the reduction of antibiotic activity.
Conventional and microwave-assisted synthesis of quinolone carboxylic acid derivatives
Mirzaie,Lari,Vahedi,Hakimi
, p. 2865 - 2869 (2017/03/22)
Various antibacterial fluoroquinolone compounds are synthesized by the direct amination of 7-halo-6-fluoroquinolone-3-carboxylic acids with a variety of piperazine derivatives and (4aR,7aR)-octahydro-1H-pyrrolo[3,4-b]pyridine using microwave under different reaction conditions. Solvent free high yield microwave synthesis of antibacterial fluoroquinolone compounds is convenient, rapid and environmentally friendly method.
Microwave assisted amination of quinolone carboxylic acids: An expeditious synthesis of fluoroquinolone antibacterials
Reddy,Baskaran
, p. 6775 - 6777 (2007/10/03)
A facile amination of quinolone carboxylic acids to fluoroquinolone antibacterials under microwave irradiation is described.
