One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, such as the rate of change in the concentration of reactants or products with time. 99368-66-8, Name is 5-Nitro-3-(trifluoromethyl)pyridin-2-ol, formurla is C6H3F3N2O3. In a document, author is Qian, Bing-Feng, introducing its new discovery. SDS of cas: 99368-66-8.
Syntheses, reactivity, structures and photocatalytic properties of mononuclear ruthenium(II) complexes supported by 1,4,7-trime- thyl-1,4,7-triazacyclononane (Me(3)tacn) ligands
Treatment of ruthenium(II) precursor [(Me(3)tacn)Ru(dmso)Cl-2] (Me(3)tacn = 1,4,7-trimethyl-1,4,7-triazacyclononane, dmso = dimethylsulfoxide) (1) with concentrated HCl in the presence of air afforded a ruthenium(III) complex 1(Me(3)tacn)RuCl3 center dot H2O] (2). Reaction of 2, 2,2′-bipyridine or substituted 2,2′-bipyridine, and zinc metal powder in the presence of sodium perchlorate gave the corresponding cationic aquaruthenium(II) complex [(Me(3)tacn)Ru(R-bpy)(H2O)](ClO4)(2) (bpy = 2,2′-bipyridine, R = H, 3; 4,4′-Me-2, 4; 5,5′-Me-2, 5; 4,4′-di-Bu-t, 6). The hydrate ligand in complexes 3 and 5 could be substituted by acetonitrile or pyridine forming complexes [(Me(3)tacn)Ru(5,5′-Me-2-bpy)(CH3CN)](ClO4)(2) (7) and [(Me(3)tacn)Ru(R-bpy)(py)(ClO4)(2) (py = pyridine, R = H (8), R = 5,5′-Me-2 (9), respectively. Interaction of [(Me(3)tacn)Ru(bpy)(H2O)](PF6)(2) with phenylacetylene in methanol afforded a ruthenium-carbene complex [(Me(3)tacn)(bpy)Ru=C(OMe)CH2Ph](PF6)(2) (10). All complexes are well characterized by infrared, UV/Vis, and NMR spectroscopies. The molecular structures of 1, 1 center dot 2H(2)O, 4 center dot 2H(2)O, 7, 8, 9, and 10 have been also established by single-crystal X-ray diffraction. The photocatalysis properties of complexes 3, 5, and 6 for H-2 evolution by water splitting were also investigated in the paper.
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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem