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)(2)Cl-2 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.