Application of 7048-04-6, The transformation of simple hydrocarbons into more complex and valuable products via catalytic C–H bond functionalisation has revolutionised modern synthetic chemistry. 7048-04-6, Name is H-Cys-OH.HCl.H2O, SMILES is O=C(O)[C@@H](N)CS.[H]Cl.[H]O[H], belongs to amides-buliding-blocks compound. In a article, author is Chicca, Andrea, introduce new discover of the category.
We prepared amide-heterocycle (HC) compounds having various aromatic pi-electron systems (Ar), such as phenyl, naphthyl, furyl, thienyl and phenanthryl moieties, and converted them as ligands to difluoroboronated complexes, Ar@HCs. Blue fluorescence from Ar@HCs was observed in solution and the solid state, and the fluorescence quantum yields (phi(f)) and lifetimes (tau(f)) were determined. The phi(f) values in CHCl3 were as small as 0.1 except for the phenanthrene derivatives (0.4-0.6). Observation of the triplet-triplet absorption upon laser flash photolysis of Ar@HCs in solution indicated that the fluorescence process competes with intersystem crossing to the triplet state. Blue fluorescence in the solid state was observed with the phi(f) values of 0.3-0.7. Based on the crystallographic data, the relationship between the crystal structures and emission features of Ar@HCs in the solid state is discussed.
Application of 7048-04-6, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 7048-04-6.
Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics