Ultrafast excited state intramolecular proton transfer and isomerization of long-chain linked Schiff bases.

The ultrafast proton transfer and the following dynamics for aromatic Schiff bases N,N′-bis(salicylidene)ethylenediamine (salen) and N,N′-bis(salicylidene)-1,4-butylenediamine (salbn) were investigated with experimental and theoretical methods. A dual emission property with a large Stokes shift in salen and salbn indicates that excited state intramolecular proton transfer occurs with photoexcitation. An efficient single proton transfer was confirmed within 200 fs for both molecules. Subsequently, a fast twisted motion of the keto moiety carries cis-keto to a relaxed stable geometry in the S₁ state. Following the twisted motion, the phenol ring at keto moiety further rotates to a conical intersection with the ground state and a cis–trans isomerization occurs. The isomerization rate is high, which dominates the competition with the radiative transition, resulting in weak emission intensity. It is confirmed that the length of alkyl chain affects the direction of phenol ring twisting and rotation during the whole subsequent relaxation of excited cis-keto tautomer. Compared with polar solvent acetonitrile, the barrier of isomerization is higher and the hydrogen bond on keto moiety is stronger in nonpolar solvent toluene. It makes fluorescence radiation channels competing with isomerism more likely to occur, contributing to the observed difference of enol/keto emission ratios of salen and salbn in toluene and acetonitrile. [ABSTRACT FROM AUTHOR]