Category: pyrazoles-derivatives. In 2021.0 J MOL STRUCT published article about BIOORGANOMETALLIC CHEMISTRY; CRYSTAL-STRUCTURE; METAL-COMPLEXES; AMINO-ACIDS; DERIVATIVES; PYRAZOLE in [Champaka, Gurudevaru; Senthilkumar, Kabali; David, Ezhumalai; Palanisami, Nallasamy] Vellore Inst Technol, Ctr Funct Mat, Dept Chem, Sch Adv Sci, Vellore 632014, Tamil Nadu, India; [Shanmugan, Swaminathan] SRM Inst Sci & Technol, Dept Chem, Fac Engn & Technol, Kancheepuram 603203, Tamil Nadu, India in 2021.0, Cited 40.0. The Name is 3,5-Dimethyl-1H-pyrazole. Through research, I have a further understanding and discovery of 67-51-6.
Monomeric zinc ferrocene carboxylate [Zn(FcCOO)(3,5-dmp)(2)Cl] (1) has been synthesized from a reaction between the zinc chloride, sodium salt of ferrocene carboxylic acid (FcCOONa) and 3,5-dimethylpyrazole (3,5-dmp) at room temperature. Compound 1 was further characterized by elemental analysis, H-1 NMR, FT-IR, absorption, emission spectroscopic techniques, and molecular structure was confirmed by single-crystal X-ray diffraction studies. The molecular structure of compound 1 crystallized in triclinic system with P (1) over bar space group and the central Zn2+ ion is in a distorted tetrahedral geometry with -FeN2OCl coordination environment. Compound 1 was further stabilized with the aid of inter and intramolecular hydrogen bonding and pi-pi interaction between cyclopentadienyl ring of ferrocene and aromatic heterocyclic five membered 3,5-dimethylpyrazole. Compound 1 exhibits broad emission band, indicating ligandto-metal charger transfer (LMCT) or metal-to-ligand charger transfer (MLCT) nature. The electrochemical property of compound 1 revealed that one-electron anodic and cathodic peaks corresponding to the redox responsible of ferrocene/ferrocenium (FeII <-> Fe-III) moiety. Among the different strains of bacteria, the antibacterial activity of compound 1 showed comparatively a significant activity against gram negative bacterium Proteus vulgaris. (C) 2020 Elsevier B.V. All rights reserved.
Welcome to talk about 67-51-6, If you have any questions, you can contact Champaka, G; Senthilkumar, K; David, E; Shanmugan, S; Palanisami, N or send Email.. Category: pyrazoles-derivatives
Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics