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Published on WebAre 1,5-Disubstituted Semibullvalenes that Have C2v Equilibrium Geometries Necessarily Bishomoaromatic? Eric C. Brown,* Daven K. Henze, and Weston Thatcher Borden Contribution from the Depart
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Document Date: 2004-10-13 15:35:33


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Lund / Pittsburgh / Rappoport / Kelly / Deerfield Beach / /

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Cyclopropyl Group / J. Wiley & Sons / Gaussian Inc. / /

Country

Sweden / /

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UniVersity of Washington / University of Lund / University of Washington Student Technology Fund / /

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bond dissociation energy / kcal/mol lower energy / energy minimum / hydrogenation energy / singlet-triplet energy splittings / energy/enthalpy / stabilization energy / strain energy / adiabatic singlet-triplet energy difference / energy difference / energy differences / energy / /

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A. D. / /

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American Chemical Society / University of Washington Student Technology Fund / National Science Foundation / University of Lund / Mary M. Gates Foundation / UniVersity of Washington / Seattle / SEsc / Department of Theoretical Chemistry / Chemical Centre / Department of Chemistry / /

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Fox / Eric C. Brown / Weston Thatcher Borden / Tantillo / /

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D. J. / A. D. J. / W. D. J. / /

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CASPT2 / UB3LYP / /

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Missouri / Pennsylvania / South Carolina / Florida / Washington / /

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14982 J. AM / 14978 J. AM / J. AM / 14980 J. AM / /

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