Heavy‐Atom Tunneling in the Ring Opening of a Strained Cyclopropene at Very Low Temperatures |
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Authors: | Melanie Ertelt Dr. David A. Hrovat Prof. Dr. Weston Thatcher Borden Prof. Dr. Wolfram Sander |
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Affiliation: | 1. Lehrstuhl für Organische Chemie II, Ruhr‐Universit?t Bochum, 44781 Bochum (Germany);2. Department of Chemistry and the Center for Advanced, Scientific Computing and Modeling, University of North Texas, 1155 Union Circle, #305070, Denton, Texas 76203‐5070 (USA) |
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Abstract: | The highly strained 1H‐bicyclo[3.1.0]‐hexa‐3,5‐dien‐2‐one 1 is metastable, and rearranges to 4‐oxacyclohexa‐2,5‐dienylidene 2 in inert gas matrices (neon, argon, krypton, xenon, and nitrogen) at temperatures as low as 3 K. The kinetics for this rearrangement show pronounced matrix effects, but in a given matrix, the reaction rate is independent of temperature between 3 and 20 K. This temperature independence means that the activation energy is zero in this temperature range, indicating that the reaction proceeds through quantum mechanical tunneling from the lowest vibrational level of the reactant. At temperatures above 20 K, the rate increases, resulting in curved Arrhenius plots that are also indicative of thermally activated tunneling. These experimental findings are supported by calculations performed at the CASSCF and CASPT2 levels by using the small‐curvature tunneling (SCT) approximation. |
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Keywords: | calculations carbene matrix isolation rearrangement tunneling |
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