The novel non-covalent interactions between the charged and neutral aromatic rings and with anions are utilized to design the solid-state assembly of triply protonated PTPH 3 (PTP = 4'-(4-pyridyl)-3,2':6',3''-terpyridine) with H 2 O and three ClO 4 -, which is synthesized and characterized by single crystal X-ray diffraction analysis. Crystallography reveals that the π + -π + , π + -π and various anion···π interactions are the major driving forces in the stabilization of the selfassembled structure. In the title complex, a layered assembly is formed through the mutual influence of π + -π + and π + -π interactions. The anions are interacting with the charged π-acceptors which are again stabilized through π + -π interactions. So, the overall stabilization is governed through π + -π/π-π + , (π + -π + ) n and anion···π + /π + -π/π-π + networks in the solid state. The interaction energies of the main driving forces observed in the crystal structure have been calculated using density functional theory. In addition, the short O···O contact between ClO 4 -, anions has been analyzed in detail both computationally and exploring the Cambridge Structural Database.