Electron self-exchange activation parameters of diethyl sulfide and tetrahydrothiophene

• Martin Goez and
• Martin Vogtherr

Beilstein J. Org. Chem. 2013, 9, 1448–1454, doi:10.3762/bjoc.9.164

• was done with a Lambda Physik EMG 101 excimer laser (medium, XeCl; wavelength, 308 nm; pulse width, 15 ns) triggered by the computer of the spectrometer. The probe was thermostated to ±0.3 K. Quantum mechanical calculations were carried out with the Gaussian 09 package [53] using the AM1 Hamiltonian

Synthesis and spectroscopic properties of 4-amino-1,8-naphthalimide derivatives involving the carboxylic group: a new molecular probe for ZnO nanoparticles with unusual fluorescence features

• Laura Bekere,
• David Gachet,
• Vladimir Lokshin,
• Wladimir Marine and
• Vladimir Khodorkovsky

Beilstein J. Org. Chem. 2013, 9, 1311–1318, doi:10.3762/bjoc.9.147

• square of the laser power shown in the inset (Figure 5) clearly demonstrates the two-photon excitation nature. Quantum mechanical calculations Quantum mechanical calculations were performed for derivative 4 to gain deeper insight into the nature of the longest wavelength transition and to estimate the

The β-cyclodextrin/benzene complex and its hydrogen bonds – a theoretical study using molecular dynamics, quantum mechanics and COSMO-RS

• Jutta Erika Helga Köhler and
• Nicole Grczelschak-Mick

Beilstein J. Org. Chem. 2013, 9, 118–134, doi:10.3762/bjoc.9.15

• . Since quantum-mechanical calculations lead to these highly ordered optimised structures, they represent the lowest energy conformers in vacuo at 0 K. Nevertheless, they will be the basis for the assumptions of the COSMO-RS method and its thermodynamic formulas and calculations/extrapolations based on

A new family of four-ring bent-core nematic liquid crystals with highly polar transverse and end groups

• Kalpana Upadhyaya,
• Venkatesh Gude,
• Golam Mohiuddin and
• Rao V. S. Nandiraju

Beilstein J. Org. Chem. 2013, 9, 26–35, doi:10.3762/bjoc.9.4

• to possibly weakened lateral interactions and increased intermolecular spacing between molecules. Density functional theory calculations The quantum mechanical calculations of molecular properties in the gas phase were performed by using density functional theory (DFT) [58] employing the combination

Theoretical study on β-cyclodextrin inclusion complexes with propiconazole and protonated propiconazole

• Adrian Fifere,
• Narcisa Marangoci,
• Stelian Maier,
• Adina Coroaba,
• Dan Maftei and
• Mariana Pinteala

Beilstein J. Org. Chem. 2012, 8, 2191–2201, doi:10.3762/bjoc.8.247

• theoretically investigates the interaction between PP, PPH+ and β-CD molecules by means of AM1 and PM3 semi-empirical quantum-mechanical calculations, to examine in detail the insertion pathways and to determine the intimate configurations of the β-CD/propiconazole (β-CD/PP and β-CD/PPH+) inclusion complexes

• parameter and the complex stability by means of quantum-mechanical calculations has been previously reported [19][20]. The PP molecule has a permanent electric dipole, and the dipole–dipole interaction can make the difference between the A and B configurations. The decrease of the global dipole moment

The crystal structure of the Dess–Martin periodinane

• Albert Schröckeneder,
• Desiree Stichnoth,
• Peter Mayer and
• Dirk Trauner

Beilstein J. Org. Chem. 2012, 8, 1523–1527, doi:10.3762/bjoc.8.172

• respect to the mechanism of the Dess–Martin oxidation. Our X-ray structure will serve as a starting point for detailed quantum mechanical calculations to address this topic. Experimental Crystallographic data for 1: Data collected by means of an Oxford Diffraction Xcalibur 3 diffractometer, Mo Kα

NMR studies of anion-induced conformational changes in diindolylureas and diindolylthioureas

• Damjan Makuc,
• Jennifer R. Hiscock,
• Mark E. Light,
• Philip A. Gale and
• Janez Plavec

Beilstein J. Org. Chem. 2011, 7, 1205–1214, doi:10.3762/bjoc.7.140

• complexes by quantum mechanics calculations The observations on the conformational equilibria in the absence and in the presence of anions were corroborated by quantum mechanical calculations at the B3LYP/6-311+G(d,p) level of theory by means of the Gaussian 03 [40] and Gaussian 09 [41] programs. Indole

• H1 and H7α NMR resonances prevented conformational analysis of 2 upon addition of other anions used in the study. The conformational preferences of 2 were evaluated by quantum mechanical calculations at the B3LYP/6-311+G(d,p) level of theory. The freely optimized anti–anti conformer of 2 exhibited

Synthesis of some novel hydrazono acyclic nucleoside analogues

• Mohammad N. Soltani Rad,
• Ali Khalafi-Nezhad and
• Somayeh Behrouz

Beilstein J. Org. Chem. 2010, 6, No. 49, doi:10.3762/bjoc.6.49

• quantum mechanical calculations were carried out using MOPAC in CS Chem 3D Ultra 8 (Cambridge Soft, 2004) or Hyperchem (Hypercube Inc., Version 7). The results are summarized in Table 2; ΔE refers to the energy difference between the (Z)- and (E)-isomer (ΔE = EZ − EE (kcal/mol)). As can be seen in Table 2

• the (E)-hydrazone derivatives rather than the (Z)-isomers, PM3 semiempirical quantum mechanical calculations were carried out which showed that the heats of formation of the (E)-isomers were lower. The biological studies of compounds 2a–2o are currently under investigation and will be reported in due