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Molecular Quadripod as a Noncovalent Interfacial Coupling Reagent for Forming Immobilized Coordination Assemblies.
J Am Chem Soc ; 140(39): 12337-12340, 2018 10 03.
Artigo em Inglês | MEDLINE | ID: mdl-30220199
A pyrene-cored molecular quadripod 1,3,6,8-tetra(di( p-pyrid-4-ylphenyl)amino)pyrene (TAPyr) is presented as a noncovalent interfacial coupling reagent for the immobilization of coordination assemblies. This bench-stable molecule is readily available and has a quadripod shape with four pyridine legs and four pyridine handles on the top exterior. By a simple and short dipping procedure under ambient conditions, TAPyr is firmly immobilized on electrode surfaces in an upright fashion as probed by electrochemical, absorption spectral, atomic force microscopy, and scanning tunneling microscopy analysis. Using Pd(PhCN)2Cl2 as a metallolinker, 4-ferrocenylpyridine, a pyridine-terminated monoruthenium complex 1, and a diruthenium complex 2 with two pyridine ends have been grafted onto the ITO/TAPyr surface. The obtained thin films exhibit good electrochemical stability that is comparable or superior to those prepared by the state-of-the-art Si-O-Sn covalent functionalization. Appealing electrochromism is demonstrated with the thin films of ruthenium complexes on ITO.





Texto completo: Disponível Coleções: Bases de dados internacionais Base de dados: MEDLINE Idioma: Inglês Revista: J Am Chem Soc Ano de publicação: 2018 Tipo de documento: Artigo País de afiliação: China