High resolution in heteronuclear1H-13C NMR experiments by optimizing spectral aliasing with one-dimensional carbon data

2002 ◽  
Vol 41 (1) ◽  
pp. 3-17 ◽  
Author(s):  
Damien Jeannerat

Author(s):  
Francesco Panattoni ◽  
Jonathan Mitchell ◽  
Edmund J. Fordham ◽  
Ravinath Kausik ◽  
Clare P. Grey ◽  
...  


1994 ◽  
Vol 26 (3) ◽  
pp. 267-271 ◽  
Author(s):  
Koichi Hatada ◽  
Koichi Ute ◽  
Hiroshi Okuda ◽  
F W Hein Kruger ◽  
Otto Vogl


1995 ◽  
Vol 28 (19) ◽  
pp. 6677-6679 ◽  
Author(s):  
Masatoshi Kobayashi ◽  
Isao Ando ◽  
Takahiro Ishii ◽  
Shigetoshi Amiya


1999 ◽  
Vol 72 (5) ◽  
pp. 844-853 ◽  
Author(s):  
Seiichi Kawahara ◽  
Saori Bushimata ◽  
Takashi Sugiyama ◽  
Chihiro Hashimoto ◽  
Yasuyuki Tanaka

Abstract A novel analytical method using high resolution 13C-NMR spectroscopy to study polymer latex, which is a heterogeneous system comprising polymer dispersoid and water, is described. The appropriate concentrations of surfactant and dried rubber content of a polybutadiene latex, which give the best spectrum, were found to be 1 w/v % and 10%, respectively. The half-widths of resonance peaks for the latex sample were almost identical to the half-widths obtained in solution, which were about one-third the width of those obtained using a solid sample of either a crosslinked or soluble polybutadiene. Nevertheless, the signal to noise ratio for the latex sample was slightly smaller than that for the solution sample. The values of spin-lattice relaxation time, T1, for the latex sample were similar to those for the solid sample. These demonstrate that the latex state C-NMR spectroscopy will be a powerful technique for structural characterization of crosslinked gels in the dispersoid because it gives a high resolution spectrum comparable to solution state spectroscopy, showing short T1 values corresponding to those for solid state C-NMR spectroscopy. High resolution latex state 13C-NMR spectroscopy was used to determine the concentrations of the various isomers of the polybutadiene in the dispersoid.





2021 ◽  
Author(s):  
Munkh-Uchral Erdenebat ◽  
Ki-Chul Kwon ◽  
Nyamsuren Darkhanbaatar ◽  
Jin Kyu Jung ◽  
Sang-Keun Gil ◽  
...  


Molecules ◽  
2018 ◽  
Vol 23 (7) ◽  
pp. 1785 ◽  
Author(s):  
Peter Lankhorst ◽  
Jozef van Rijn ◽  
Alexander Duchateau

The discrimination of enantiomers of mandelonitrile by means of 1D 13C NMR and with the aid of the chiral solvating agent (S)-(+)-1-(9-anthryl)-2,2,2-trifluoroethanol (TFAE) is presented. 1H NMR fails for this specific compound because proton signals either overlap with the signals of the chiral solvating agent or do not show separation between the (S)-enantiomer and the (R)-enantiomer. The 13C NMR method is validated by preparing artificial mixtures of the (R)-enantiomer and the racemate, and it is shown that with only 4 mg of mandelonitrile a detection limit of the minor enantiomer of 0.5% is obtained, corresponding to an enantiomeric excess value of 99%. Furthermore, the method shows high linearity, and has a small relative standard deviation of only 0.3% for the minor enantiomer when the relative abundance of this enantiomer is 20%. Therefore, the 13C NMR method is highly suitable for quantitative enantiodiscrimination. It is discussed that 13C NMR is preferred over 1H NMR in many situations, not only in molecules with more than one chiral center, resulting in complex mixtures of many stereoisomers, but also in the case of molecules with overlapping multiplets in the 1H NMR spectrum, and in the case of molecules with many quaternary carbon atoms, and therefore less abundant protons.



Polymer ◽  
2000 ◽  
Vol 41 (7) ◽  
pp. 2391-2404 ◽  
Author(s):  
M. Kanekiyo ◽  
M. Kobayashi ◽  
I. Ando ◽  
H. Kurosu ◽  
S. Amiya


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