J-aggregation of a sulfur-substituted naphthalenediimide (NDI) with remarkably bright fluorescence

This communication reveals the H-bonding driven supramolecular assembly of a sulfur-substituted naphthalenediimide leading to the formation of very strong (T-g > 90 degrees C) organogel in aliphatic hydrocarbons. Mechanistic investigation reveals nucleation-elongation pathway for self-assembly. Photophysical studies show explicit features of classical J-aggregation which reduces the non-radiative fluorescence rate constant considerably and thus results in a remarkable fluorescence enhancement (UPL increases from 1% to 30%) which is unprecedented in the entire NDI literature.