Application In Synthesis of 1H-1,2,3-TriazoleIn 2020 ,《Identification of the Electronic and Structural Dynamics of Catalytic Centers in Single-Fe-Atom Material》 was published in Chem. The article was written by Li, Xuning; Cao, Chang-Su; Hung, Sung-Fu; Lu, Ying-Rui; Cai, Weizheng; Rykov, Alexandre I.; Miao, Shu; Xi, Shibo; Yang, Hongbin; Hu, Zehua; Wang, Junhu; Zhao, Jiyong; Alp, Esen Ercan; Xu, Wei; Chan, Ting-Shan; Chen, Haoming; Xiong, Qihua; Xiao, Hai; Huang, Yanqiang; Li, Jun; Zhang, Tao; Liu, Bin. The article contains the following contents:
The lack of model single-atom catalysts (SACs) and at.-resolution operando spectroscopic techniques greatly limits our comprehension of the nature of catalysis. Herein, based on the designed model single-Fe-atom catalysts with well-controlled microenvironments, we have explored the exact structure of catalytic centers and provided insights into a spin-crossover-involved mechanism for oxygen reduction reaction (ORR) using operando Raman, X-ray absorption spectroscopies, and the developed operando57Fe Mossbauer spectroscopy. In combination with theor. studies, the N-FeN4C10 moiety is evidenced as a more active site for ORR. Moreover, the potential-relevant dynamic cycles of both geometric structure and electronic configuration of reactive single-Fe-atom moieties are evidenced via capturing the peroxido (*O-2) and hydroxyl (*OH-) intermediates under in situ ORR conditions. We anticipate that the integration of operando techniques and SACs in this work shall shed some light on the electronic-level insight into the catalytic centers and underlying reaction mechanism. In the experimental materials used by the author, we found 1H-1,2,3-Triazole(cas: 288-36-8Application In Synthesis of 1H-1,2,3-Triazole)
1H-1,2,3-Triazole(cas: 288-36-8) belongs to triazoles. Triazoles are an important group of nitrogen-containing five-membered heterocyclic scaffolds. Triazoles are core structures of several drugs and pharmaceutical agents. Triazole derivatives possess antimicrobial, antiparasitic, antidiabetic, analgesic, and anti-inflammatory properties Application In Synthesis of 1H-1,2,3-Triazole
Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics