Fluorescence Sensing of Anions by Silanediols Bearing Substituted Naphthyl Groups.
Chempluschem
; 88(2): e202300006, 2023 Feb.
Article
em En
| MEDLINE
| ID: mdl-36740567
ABSTRACT
Silanediols bearing naphthyl moieties substituted at 5-position with an electron-withdrawing cyano group and an electron-donating N,N-dimethylamino group, respectively, have been prepared and characterized. The substituents on the naphthyl moieties strongly influence the reactivity, photophysical properties, and sensing abilities for anions. The silanediol bearing 1-(5-N,N-dimethylaminonaphthyl) groups exhibited large Stokes shifts based on intramolecular charge transfer and large quantum yields in organic solvents. The silanediol showed favorable ratiometric fluorescence responses of upon the addition of biologically important anions, AcO- and H2 PO4 - with the association constants of 4.08×104 and 8.76×103 â
mol-1 dm3 , respectively.
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Idioma:
En
Revista:
Chempluschem
Ano de publicação:
2023
Tipo de documento:
Article
País de afiliação:
Japão