Abstract
Fourier transform mass spectrometry is used with chemical ionization to observe iron pentacarbonyl molecules in an ultra-high vacuum system. Mass spectra are obtained from molecules desorbed from a cold Pd(111) surface using laser-induced thermal desorption (LITD) and directly from Fe(CO) 5 vapors. A variety of ions are formed when using 70 eV electrons, including some molecular ion. Charge exchange using Ar + and Xe + produces fewer fragment peaks but no molecular ion. Very little fragmentation occurs to the organometallic when using CH 5 + for proton-transfer reactions. The proton transfer-LITD spectrum does, however, show an unexpected, nonprotonated iron tricarbonyl cation, presumably due to desorption of a surface-activated species.
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