Solvent effects in the GIAO-DFT calculations of the 15N NMR chemical shifts of azoles and azines

Copyright © 2014 John Wiley & Sons, Ltd.

Bibliographische Detailangaben
Veröffentlicht in:Magnetic resonance in chemistry : MRC. - 1985. - 52(2014), 11 vom: 15. Nov., Seite 686-93
1. Verfasser: Semenov, Valentin A (VerfasserIn)
Weitere Verfasser: Samultsev, Dmitry O, Krivdin, Leonid B
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2014
Zugriff auf das übergeordnete Werk:Magnetic resonance in chemistry : MRC
Schlagworte:Journal Article 15N NMR GIAO-DFT azines azoles chemical shift shielding constant solvent effects
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520 |a The calculation of (15)N NMR chemical shifts of 27 azoles and azines in 10 different solvents each has been carried out at the gauge including atomic orbitals density functional theory level in gas phase and applying the integral equation formalism polarizable continuum model (IEF-PCM) and supermolecule solvation models to account for solvent effects. In the calculation of (15)N NMR, chemical shifts of the nitrogen-containing heterocycles dissolved in nonpolar and polar aprotic solvents, taking into account solvent effect is sufficient within the IEF-PCM scheme, whereas for polar protic solvents with large dielectric constants, the use of supermolecule solvation model is recommended. A good agreement between calculated 460 values of (15)N NMR chemical shifts and experiment is found with the IEF-PCM scheme characterized by MAE of 7.1 ppm in the range of more than 300 ppm (about 2%). The best result is achieved with the supermolecule solvation model performing slightly better (MAE 6.5 ppm) 
650 4 |a Journal Article 
650 4 |a 15N NMR 
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650 4 |a azines 
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650 4 |a shielding constant 
650 4 |a solvent effects 
700 1 |a Samultsev, Dmitry O  |e verfasserin  |4 aut 
700 1 |a Krivdin, Leonid B  |e verfasserin  |4 aut 
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