Reaction of Thin Films of Solid-State Benzene and Pyridine with Calcium

• Published in: Journal of the American Chemical Society Vol. 134; no. 31; pp. 12989 - 12997
• Main Authors: Matz, Dallas L, Schalnat, Matthew C, Pemberton, Jeanne E
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 08-08-2012
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/ja3016186

The reaction between small organic molecules and low work function metals is of interest in organometallic, astronomical, and optoelectronic device chemistry. Here, thin, solid-state, amorphous benzene and pyridine films are reacted with Ca at 30 K under ultrahigh vacuum with the reaction progress monitored by Raman spectroscopy. Although both films react with Ca to produce product species identifiable by their vibrational spectroscopic signatures, benzene is less reactive with Ca than pyridine. Benzene reacts by electron transfer from Ca to benzene producing multiple species including the phenyl radical anion, the phenyl radical, and the benzyne diradical. Pyridine initially reacts along a similar electron transfer pathway as indicated by the presence of the corresponding pyridyl radical and pyridyne diradical species, but these pyridyl radicals are less stable and subject to further ring-opening reactions that lead to a complex array of smaller molecule reaction products and ultimately amorphous carbon. The elucidation of this reaction pathway provides insight into the reactions of aromatics with Ca that are relevant in the areas of catalysis, astrochemistry, and organic optoelectronics.