The structure of p-chlorophenol and barrier to internal OH rotation in the S1-state

The structure and barrier to internal rotation of 4-chlorophenol in the ground state and the electronically excited S1-state has been examined by rotationally resolved laser induced fluorescence spectroscopy of 4-35Cl-phenol, 4-37Cl-phenol, 4-35Cl-phenol-d1, and 4-37Cl-phenol-d1. The overlapping spectra have been assigned simultaneously using a genetic algorithm approach. The rotationally resolved spectrum of the electronic origin of 4-chlorophenol is comprised of two subbands, which are split by 60 MHz due to the internal rotation of the hydroxy group. The torsional barrier in the electronically excited state could be estimated to be 1400 cm−1, only about 250 cm−1 higher than in the ground state. The CCl bond lengths decreases by approximately 6 pm upon electronic excitation and the aromatic ring is distorted quinoidally.