Symmetry‐Breaking Charge Transfer and Hydrogen Bonding: Toward Asymmetrical Photochemistry

Symmetry‐breaking charge transfer upon photoexcitation of a linear A‐π‐D‐π‐A molecule (D and A being electron donating and accepting groups) could be visualized using ultrafast time‐resolved infrared spectroscopy by monitoring the CN stretching modes on the A units. Whereas in apolar solvents, the S₁ state remains symmetric and quadrupolar, symmetry breaking occurs within ca. 100 fs in polar solvents as shown by the presence of two CN bands, instead of one in apolar solvents, with a splitting that increases with polarity. In protic solvents, symmetry breaking is significantly amplified by H‐bonding interactions, which are the strongest at the CN group with the highest basicity. In strongly protic solvents, the two CN bands transform in about 20 ps into new bands with a larger splitting, and the lifetime of the S₁ state is substantially reduced. This is attributed to the formation of an excited asymmetric tight H‐bond complex.