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All compounds were characterized by mass, IR and 1H NMR spectra (Table 2).
Results were compared with literature data of FTIR spectra (Table 1).
The 13C-NMR spectra (Table 1) showed two ketonic carbonyl signals at δ 186.3 and 220.1 (Additional file 4).
The radial breathing mode (RBM) peak of Raman spectra (Table 1) was used to study the SWCNT diameter.
The 1H and 13C NMR spectra (Table 1) of 3 were similar to those of 2 except that there was one more methoxy group in compound 3.
The spectroelectrochemical oxidation of PTD on a platinum electrode at neutral pH resulted in the formation of a dimer proven by UV/VIS and EPR spectra (Table 3).
Similar(6)
The 1H NMR and 13C NMR spectra (Tables 3, 4) displayed signals very similar to those of 7 [ 2].
at m/z 568.3025 (calcd for C31H42N3O7, 568.3022), in combination with NMR spectra (Tables 1 and 3), requiring 13 degrees of unsaturation.
Additionally, an N-methyl group [δ H 2.69 (3H, s), δ C 38.0] was also displayed in the 1H, 13C NMR, and DEPT spectra (Tables 1, 2).
Typical γ-ray spectra, tables for the most suitable γ-ray lines for elemental analysis and a complete series of absolute thick-target yields for the most characteristic γ-rays of elements with Z=3 20 (except for Be, Ne, P and Ar) in the deuteron energy range of 0.7 3.4 MeV are presented.
The interpretation spectra were made based on infrared (IR) spectra tables and general information available in the literature as well [ 34].
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