|کد مقاله||کد نشریه||سال انتشار||مقاله انگلیسی||ترجمه فارسی||نسخه تمام متن|
|1192357||1492324||2010||5 صفحه PDF||سفارش دهید||دانلود رایگان|
The dissociation of energy-selected acetic acid ions (CH3COOH+) has been investigated by Threshold Photoelectron–photoion Coincidence (TPEPICO) spectroscopy. The lowest energy dissociation pathway for CH3COOH+ is OH loss, and the 0 K onset (E0) of this process is measured to be 11.641 ± 0.008 eV. The reaction rate for this step is instantaneous on the time-scale of the experiment so that no rate theory is required to extract its onset. Because the heats of formation of acetic acid and the OH radical are known to an accuracy of ±0.5 kJ/mol, we can use the OH loss onset to obtain an accurate heat of formation of the acetyl ion, ΔfH°298 K[CH3CO+] = 658.5 ± 1.0 kJ/mol, which agrees to within 0.9 kJ/mol with an earlier determination based on CH3 loss from the acetone ion. At higher energies, the acetic acid ion loses CH3 to form the HOCO+ ion in competition with the lower energy OH-loss. Two versions of the statistical reaction rate theory failed to reproduce the branching ratios for these higher energy parallel reactions. Because of the magnitude of this disagreement, we conclude that the acetic ion may dissociate non-statistically at these higher energies.
Threshold photoelectron photoion coincidence study of the dissociation dynamics of the acetic acid ion. Acetyl ion onset is 11.641 eV, but the reaction turns non-statistical at higher energies.Figure optionsDownload high-quality image (125 K)Download as PowerPoint slide
Journal: International Journal of Mass Spectrometry - Volume 294, Issues 2–3, 1 July 2010, Pages 88–92