The effect of the change of synthetic route on the product 1008-89-5

Here is just a brief introduction to this compound(1008-89-5)Electric Literature of C11H9N, more information about the compound(2-Phenylpyridine) is in the article, you can click the link below.

Electric Literature of C11H9N. The reaction of aromatic heterocyclic molecules with protons is called protonation. Aromatic heterocycles are more basic than benzene due to the participation of heteroatoms. Compound: 2-Phenylpyridine, is researched, Molecular C11H9N, CAS is 1008-89-5, about Synthesis, structures and photophysical properties of hexacoordinated organosilicon compounds with 2-(2-pyridyl)phenyl groups. Author is Furuta, Shohei; Mori, Toshiaki; Yoshigoe, Yusuke; Sekine, Kohei; Kuninobu, Yoichiro.

The authors synthesized novel hexacoordinated organosilicon compounds with two 2-(2-pyridyl)phenyl groups. Single-crystal x-ray structure analyses indicated that Lewis acid-base interactions exist between the Si atom and two N atoms of the pyridine rings, and that hexacoordinated organosilicon compounds have slightly distorted octahedral structures in the solid state. The hexacoordinated organosilicon compounds are stable in air, H2O, heat, acids, and bases. The fluorescent quantum yield increased dramatically and a significant red shift of the maximum fluorescence wavelength was observed with the introduction of amino groups on the 2-(2-pyridyl)phenyl aromatic rings. The fluorescence colors of a hexacoordinated organosilicon compound with two amino groups can be switched by protonation and deprotonation (neutralization) of the amino groups.

Here is just a brief introduction to this compound(1008-89-5)Electric Literature of C11H9N, more information about the compound(2-Phenylpyridine) is in the article, you can click the link below.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles