@article{BalciYaparAkkayaetal.2012,
  author    = {Balci, Kubilay and Yapar, G. and Akkaya, Y. and Akyuz, S. and Koch, Andreas and Kleinpeter, Erich},
  title     = {A conformational analysis and vibrational spectroscopic investigation on 1,2-bis(o-carboxyphenoxy) ethane molecule},
  series = {Vibrational spectroscopy : an international journal devoted to applications of infrared and raman spectroscopy},
  volume    = {58},
  journal   = {Vibrational spectroscopy : an international journal devoted to applications of infrared and raman spectroscopy},
  number    = {1-2},
  publisher = {Elsevier},
  address   = {Amsterdam},
  issn      = {0924-2031},
  doi       = {10.1016/j.vibspec.2011.11.011},
  pages     = {27 -- 43},
  year      = {2012},
  abstract  = {The minima on the potential energy surface of 1,2-bis(o-carboxyphenoxy)ethane (CPE) molecule in its electronic ground state were searched by a molecular dynamics simulation performed with MM2 force field. For each of the found minimum-energy conformers, the corresponding equilibrium geometry, charge distribution, HOMO-LUMO energy gap, force field, vibrational normal modes and associated IR and Raman spectral data were determined by means of the density functional theory (DFT) based electronic structure calculations carried out by using B3LYP method and various Pople-style basis sets. The obtained theoretical data confirmed the significant effects of the intra- and inter-molecular hydrogen bonding interactions on the conformational structure, force field, and group vibrations of the molecule. The same data have also revealed that two of the determined stable conformers, both of which exhibit pseudo-crown structure, are considerably more favorable in energy to the others and accordingly provide the major contribution to the experimental spectra of CPE. In the light of the improved vibrational spectral data obtained within the "SQM FF" methodology and "Dual Scale Factors" approach for the monomer and dimer forms of these two conformers, a reliable assignment of the fundamental bands observed in the experimental room-temperature IR and Raman spectra of the molecule was given, and the sensitivities of its group vibrations to conformation, substitution and dimerization were discussed.},
  language  = {en}
}
@article{ShainyanSuslovaKleinpeter2012,
  author    = {Shainyan, Bagrat A. and Suslova, Elena N. and Kleinpeter, Erich},
  title     = {Conformational analysis of 4,4-dimethyl-1-(trifluoromethylsulfonyl)-1,4-azasilinane and 2,2,6,6-tetramethyl-4-(trifluoromethylsulfonyl)-1,4,2,6-oxazadisilinane},
  series = {Journal of physical organic chemistry},
  volume    = {25},
  journal   = {Journal of physical organic chemistry},
  number    = {1},
  publisher = {Wiley-Blackwell},
  address   = {Hoboken},
  issn      = {0894-3230},
  doi       = {10.1002/poc.1882},
  pages     = {83 -- 90},
  year      = {2012},
  abstract  = {4,4-Dimethyl-1-(trifluoromethylsulfonyl)-1,4-azasilinane 1 and 2,2,6,6-tetramethyl-4-(trifluoromethylsulfonyl)-1,4,2,6-oxazadisilinane 2 were studied by variable temperature dynamic 1H, 13C, 19F NMR spectroscopy and theoretical calculations at the DFT (density functional theory) and MP2 (Moller-Plesset 2) levels of theory. Both kinetic (barriers to ring inversion) and thermodynamic data (frozen conformational equilibria) could be obtained for the two compounds. The computations revealed two minima on the potential energy surface for molecules 1 and 2 corresponding to the rotamers with the CF3SO2 group directed inward and outward the ring, the latter being 0.20.4 kcal/mol (for 1) and 1.1 kcal/mol (for 2) more stable than the former. The vibrational calculations at the DFT and MP2 levels of theory give the values of the free energy difference Delta G degrees for the 'inward' reversible arrow 'outward' equilibrium consistent with those determined from the experimentally measured ratio of the rotamers. The structure of crystalline compound 2 was ascertained by X-ray diffraction analysis.},
  language  = {en}
}
@article{BaranacStojanovicKochKleinpeter2012,
  author    = {Baranac-Stojanovic, Marija and Koch, Andreas and Kleinpeter, Erich},
  title     = {Is the conventional interpretation of the anisotropic effects of C=C double bonds and aromatic rings in NMR spectra in terms of the p-electron shielding/deshielding contributions correct?},
  series = {Chemistry - a European journal},
  volume    = {18},
  journal   = {Chemistry - a European journal},
  number    = {1},
  publisher = {Wiley-Blackwell},
  address   = {Malden},
  issn      = {0947-6539},
  doi       = {10.1002/chem.201101882},
  pages     = {370 -- 376},
  year      = {2012},
  abstract  = {Based on the nucleus-independent chemical shift (NICS) concept, isotropic magnetic shielding values have been computed along the three Cartesian axes for ethene, cyclobutadiene, benzene, naphthalene, and benzocyclobutadiene, starting from the molecular/ring center up to 10 angstrom away. These through-space NMR spectroscopic shielding (TSNMRS) values, which reflect the anisotropic effects, have been broken down into contributions from localized- and canonical molecular orbitals (LMOs and CMOs); these contributions revealed that the proton NMR spectroscopic chemical shifts of nuclei that are spatially close to the C?C double bond or the aromatic ring should not be explained in terms of the conventionally accepted p-electron shielding/deshielding effects. In fact, these effects followed the predictions only for the antiaromatic cyclobutadiene ring.},
  language  = {en}
}
@article{ShainyanKirpichenkoKleinpeter2012,
  author    = {Shainyan, Bagrat A. and Kirpichenko, Svetlana V. and Kleinpeter, Erich},
  title     = {Synthesis and conformational properties of 1,3-dimethyl-3-phenyl-1,3-azasilinane low temperature dynamic NMR and computational study},
  series = {Arkivoc : free online journal of organic chemistry},
  journal   = {Arkivoc : free online journal of organic chemistry},
  number    = {24},
  publisher = {ARKAT},
  address   = {Gainesville},
  issn      = {1551-7004},
  pages     = {175 -- 185},
  year      = {2012},
  abstract  = {1,3-Dimethyl-3-phenyl-1,3-azasilinane was synthesized and its conformational behavior was studied by the low temperature NMR spectroscopy and quantum chemical calculations. The compound was shown to exist as an equilibrium mixture of the PhaxMeeq and PheqMeax chair conformers with the N-methyl substituent in equatorial position. The barrier to ring inversion was also determined.},
  language  = {en}
}
@article{KleinpeterKoch2012,
  author    = {Kleinpeter, Erich and Koch, Andreas},
  title     = {Are lithium and sodium salts of N-(2-hydroxyphenyl)-salicylaldimine aromatic metalla-hetero[10]annulenes? An answer given by spatial magnetic properties (through space NMR shieldings-TSNMRS)},
  series = {Physical chemistry, chemical physics : a journal of European Chemical Societies},
  volume    = {14},
  journal   = {Physical chemistry, chemical physics : a journal of European Chemical Societies},
  number    = {24},
  publisher = {Royal Society of Chemistry},
  address   = {Cambridge},
  issn      = {1463-9076},
  doi       = {10.1039/c2cp40501f},
  pages     = {8742 -- 8746},
  year      = {2012},
  abstract  = {The spatial magnetic properties (through space NMR shieldings-TSNMRS) of the enol tautomer of N-(2-hydroxyphenyl)-salicylaldimine, the lithium and sodium salts in comparison with cyclodecapentaene and pyrano[2,3-b] pyrrole were studied to answer this question.},
  language  = {en}
}
@misc{PihlajaKleinpeter2012,
  author    = {Pihlaja, Kalevi and Kleinpeter, Erich},
  title     = {Professor Ferenc Fulop a tribute},
  series = {Arkivoc : free online journal of organic chemistry},
  journal   = {Arkivoc : free online journal of organic chemistry},
  publisher = {ARKAT},
  address   = {Gainesville},
  issn      = {1551-7004},
  pages     = {1 -- 5},
  year      = {2012},
  language  = {en}
}