Related Products of 88150-62-3, The transformation of simple hydrocarbons into more complex and valuable products via catalytic C–H bond functionalisation has revolutionised modern synthetic chemistry. 88150-62-3, Name is Phthaloylamlodipine, SMILES is O=C(C1=C(COCCN(C(C2=C3C=CC=C2)=O)C3=O)NC(C)=C(C(OC)=O)C1C4=CC=CC=C4Cl)OCC, belongs to pyridine-derivatives compound. In a article, author is Chen, Hongyun, introduce new discover of the category.
Synthesis, spectroscopic and DFT studies of copper(I) complexes inserting the electron-donating groups into pyridine-imidazole ligands vis an acetylide linker
The three Cu(I) complexes [Cu(POP)(N<^>N)]PF6, N<^>N = 2-(1H-imidazol-2-yl)-5-(p-tolylethynyl)pyridine (P1), 2-(1H-imidazol-2-yl)-5-((4-methoxyphenyl)ethynyl)pyridine (P2), 4-((6-(1H-imidazol-2-yl)pyridin-3-yl)ethynyl)-N,N-diphenylaniline (P3), were prepared and characterized. The different electron-donating groups such as methylphenyl, methoxyphenyl, and diphenylamine substituents were functionalized onto the pyridine ring part of the diimine ligands through an acetylide linker to enhance the light-absorption abilities, giving the larger light-absorption ability and red-shifted absorption bands for the investigated Cu(I) complexes. Yellow emissions in the range of 579-590 nm with quantum yields of 8.40-15.1% can be observed for all complexes at room temperature. The photophysical properties were further explained by DFT and TDDFT methods.
Related Products of 88150-62-3, The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 88150-62-3 is helpful to your research.
Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem