scholarly journals A multi-nuclear magnetic resonance and density functional theory investigation of epitaxially grown InGaP2

2016 ◽  
Vol 18 (31) ◽  
pp. 21296-21304 ◽  
Author(s):  
P. J. Knijn ◽  
P. J. M. van Bentum ◽  
C. M. Fang ◽  
G. J. Bauhuis ◽  
G. A. de Wijs ◽  
...  
Keyword(s):  
Density Functional Theory ◽  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Density Functional ◽  
Nmr Spectra ◽  
Functional Theory ◽  
Dft Modelling ◽  
Nuclear Magnetic

NMR spectra of InGaP2, dependent on coordination and disorder. Experimental (left) and DFT modelling (right).

Density Functional Theory Calculations of the Nuclear Magnetic Resonance Parameters for Two Dihydrochalcones

2012 ◽  
Vol 9 (7) ◽  
pp. 953-956 ◽  
Author(s):  
Silvana deO. Silva ◽  
MarivaldoJ. C. Corrêa ◽  
HeribertoR. Bitencourt ◽  
Waldinei Rosa Monteiro ◽  
Jerônimo Lameira ◽  
...  
Keyword(s):  
Density Functional Theory ◽  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Density Functional ◽  
Density Functional Theory Calculations ◽  
Functional Theory ◽  
Resonance Parameters ◽  
Magnetic Resonance Parameters ◽  
Nuclear Magnetic

Systematic Gauge-Including Atomic Orbital-Hybrid Density Functional Theory Linear Regressions for 13C NMR Chemical Shifts Calculation

2020 ◽  
Vol 12 (3) ◽  
pp. 364-370
Author(s):  
Sara Sâmitha Souza ◽  
Mariana Aparecida de Souza Martins ◽  
Antonio Maia de Jesus Chaves Neto ◽  
Gunar Vingre Da Silva Mota ◽  
Fabio Luiz Paranhos Costa
Keyword(s):  
Density Functional Theory ◽  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Density Functional ◽  
Chemical Shifts ◽  
Atomic Orbital ◽  
Basis Set ◽  
Functional Theory ◽  
Linear Regressions ◽  
Nuclear Magnetic

Density-functional theory calculations of the magnetic shielding for nuclear magnetic resonance provide an important contribution to understand the experimental values obtained in laboratory for chemical shifts present in the samples. From of a comparative of the performance of ten hybrid functional within of the framework of the density-functional theory using 10 different hybrid functionals with 3-21G (B1), 6-31G(d) (B2) and 6-31+ G(d, p) (B3) basis set, with intuit of evaluating of performance of the 13 C nuclear magnetic resonance from a representative of the terpene class and a heterocyclic compound, (–)-loliolide ((7aR)-6-hydroxy-4,4,7a-trimethyl-6,7-dihydro-5H1-benzofuran-2-one). This molecule, satisfactorily, represents the main structure of this class, with conformational freedom, optical activity and a benzofuran nucleus. The ωB97X-D, MPW1K and HSEH1PBE functionals presented the best calculation performance. It is interesting to note that after the use of linear regressions all root mean square error values for ωB97X-D were lower than 3 ppm. These are 2.91 ppm (B1), 2.46 (B2) ppm and 2.62 ppm (B3). The information contained in this work can be used for the assignment of experimental nuclear magnetic resonance spectra and will motivate further studies involving the theoretical calculation of the chemical shift of 13C.

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