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Updated: Apr 30, 2026

Facile Preparation of 4-Substituted Quinazoline Derivatives
Published on: February 15, 2016
Self-assembly of five 8-hydroxyquinolinate-based complexes: tunable core, supramolecular structure, and
Guozan Yuan1, Weilong Shan, Xuelong Qiao
1School of Chemistry and Chemical Engineering, Anhui University of Technology, Maanshan 243002 (P. R. China), Fax: (+86) 555-2311552; State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter Institution, Chinese Academy of Sciences, Fuzhou, Fujian 350002 (P. R. China). yuanguozan@163.com.
Abstract:
Five new Zn(II) complexes, namely [Zn(3)(L)(6)] (1), [Zn(2)(Cl)(2)(L)(2) (py)(2)] (2), [Zn(2)(Br)(2) (L)(2)(py)(2)] (3), [Zn(L)(2)(py)] (4), and [Zn(2)(OAc)(2)(L)(2)(py)(2)] (5), were prepared by the solvothermal reaction of ZnX(2) (X(-) =Cl(-), Br(-), F(-), and OAc(-)) salts with a 8-hydroxyquinolinate ligand (HL) that contained a trifluorophenyl group. All of the complexes were characterized by elemental analysis, IR spectroscopy, and powder and single-crystal X-ray crystallography. The building blocks exhibited unprecedented structural diversification and their self-assembly afforded one mononuclear, three binuclear, and one trinuclear Zn(II) structures in response to different anions and solvent systems. Complexes 1-5 featured four types of supramolecular network controlled by non-covalent interactions, such as π⋅⋅⋅π-stacking, C-H⋅⋅⋅π, hydrogen-bonding, and halogen-related interactions. Investigation of their photoluminescence properties exhibited disparate emission wavelengths, lifetimes, and quantum yields in the solid state.
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