Papers published in 2012

  1. T. Lu, M. A. Porterfield, and S. E. Wheeler, "Explaining the Disparate Stereoselectivities of N-Oxide Catalyzed Allylations and Propargylations of Aromatic Aldehydes", Org. Lett. 14, 5310 (2012).
  2. M. D. Wodrich, J. Gonthier, C. Corminboeuf, and S. E. Wheeler, "Reply to "Comment on 'Accurate Thermochemistry of Hydrocarbon Radicals via an Extended Generalized Bond Separation Scheme'"", J. Phys. Chem. A 116, 8794 (2012).
  3. J. W. G. Bloom, R. K. Raju, and S. E. Wheeler, "Physical Nature of Substituent Effects in XH/π Interactions ", J. Chem. Theory Comput. 8, 3167 (2012).
  4. D. V. Voronine, A. M. Sinyukov, X. Hua, K. Wang, P. K. Jha, E. Munusamy, S. E. Wheeler, G. Welch, A. V. Sokolov, and M. O. Scully, "Time-resolved surface-enhanced coherent sensing of nanoscale molecular complexes", Sci. Rep. 2, 891 (2012).
  5. B. Bandyopadhyay, T. C. Cheng, S. E. Wheeler, and M. A. Duncan, "Vibrational spectroscopy and theory of the protonated benzene dimer and trimer", J. Phys. Chem. A 116, 7065 (2012).
  6. S. E. Wheeler, "Controlling the Local Arrangements of π-Stacked Polycyclic Aromatic Hydrocarbons through Substituent Effects", CrystEngComm 14, 6140 (2012).
  7. O. Khakshoor, S. E. Wheeler, K. N. Houk, and E. T. Kool, "Measurement and Theory of Hydrogen Bonding Contribution to Isosteric DNA Base Pairs", J. Am. Chem. Soc. 134, 3154 (2012).
  8. E. C. Vujanovich, J. W. G. Bloom, and S. E. Wheeler, "Impact of Neighboring Chains on Torsional Defects in Oligothiophenes", J. Phys. Chem. A 116, 2997 (2012).
  9. M. D. Wodrich, C. Corminboeuf, and S. E. Wheeler, "Accurate Thermochemistry of Hydrocarbon Radicals via an Extended Generalized Bond Separation Reaction Scheme", J. Phys. Chem. A 116, 3436 (2012).
  10. T. Lu, R. Zhu, Y. An, and S. E. Wheeler, "Origin of Enantioselectivity in the Propargylation of Aromatic Aldehydes Catalyzed by Helical N-Oxides", J. Am. Chem. Soc. 134, 3095 (2012).
  11. S. E. Wheeler, "Homodesmotic Reactions for Thermochemistry", WIREs Comput. Mol. Sci. 2, 204 (2012).