Switching of photoinduced proton transfer from one six-membered hydrogen-bonded ring to other: a molecule of hydrazine and pH sensor.

The present study describes photophysical properties of 3-(benzo[ d ]oxazol-2-yl)-5-bromo-2-hydroxybenzaldehyde (HBOB) and ( E )-2-(benzo[ d ]oxazol-2-yl)-4-bromo-6-(hydrazonomethyl)phenol (HBON) molecules with asymmetric two-way proton transfer sites. The purpose of this study is to know the direction of ESIPT out of the two-way proton transfer pathways in these molecules in both the solid and solution state. The steady state and time-resolved spectral behaviour of HBOB and HBON and a comparison of the spectral features with the two distinct control compounds 2-(benzo[ d ]oxazol-2-yl)-4-bromophenol (HBO) and ( E )-4-bromo-2-(hydrazonomethyl)phenol (HBN) having single 6-membered hydrogen bonded network reveal that HBOB undergoes imine-amine photoisomerisation by proton transfer towards the oxazole side and HBON undergoes towards the hydrazone side with characteristic Stokes' shifted emission. Proton transfer forms with the red shifted emission of these molecules shows fast decay than the locally excited state. In the solid state, extremely high fluorescence intensity was observed, following a similar type of ESIPT pattern. Calculated ground (S 0 ) and excited state (S 1 ) energy barriers for the PT process obtained using density functional theory (DFT) and time-dependent density functional theory (TD-DFT) corroborate the unidirectional excited state intramolecular proton transfer (ESIPT) process for HBOB and HBON, and the theoretical spectral features validate our experimental absorption and emission spectra well. Interestingly, the unique unidirectional ESIPT behaviour of HBOB was utilised to detect hydrazine both in solution and solid phases. On the other hand, HBON was found to be a good fluorescence pH sensor with a ratiometric color change from yellow to green in acidic and basic media.