Dissociative ionization of the 1-propanol dimer in a supersonic expansion under tunable synchrotron VUV radiation

Photoionization and dissociation of the 1-propanol dimer and subsequent fragmentations have been investigated by synchrotron vacuum ultraviolet (VUV) photoionization mass spectrometry and theoretical calculations. Besides the protonated monomer cation (C3H7OH)center dot H+ (m/z = 61) and C-alpha-C-beta bond cleavage fragment CH2O center dot(C3H7OH)H+ (m/z = 91), the measured mass spectrum at an incident photon energy of 13 eV suggests a new dissociation channel resulting in the formation of the (C3H7OH)center dot H+center dot (C2H5OH) (m/z = 107) fragment. The appearance energies of the fragments (C3H7OH)center dot H+, CH2O center dot (C3H7OH)H+ and (C3H7OH)center dot H+center dot(C2H5OH) are measured at 10.05 +/- 0.05 eV, 9.48 +/- 0.05 eV, and 12.8 +/- 0.1 eV, respectively, by scanning photoionization efficiency (PIE) spectra. The 1-propanol ion fragments as a function of VUV photon energy were interpreted with the aid of theoretical calculations. In addition to O-H and C-alpha-C-beta bond cleavage, a new dissociation channel related to C-beta-C-gamma bond cleavage opens. In this channel, molecular rearrangement (proton transfer and hydrogen transfer after surmounting an energy barrier) gives rise to the generated complex, which then dissociates to produce the mixed propanol/ethanol proton bound cation (C3H7OH)center dot H+center dot(C2H5OH). This new dissociation channel has not been reported in previous studies of ethanol and acetic acid dimers. The photoionization and dissociation processes of the 1-propanol dimer are described in the photon energy range of 9-15 eV.