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The most reasonable fit to this spectrum corresponds to the pseudomolecular m/z signal expected for the 1,3 cyclohexanedione derivate [ 20] of 4-hydroxy 2-nonenal).
This spectrum corresponds to the spectra of [FeIII(OH)(MeN4Py)]2+.[ 11c] Addition of a further 0.5 equiv of NaOCl resulted in an initial increase in absorbance at λ=480 nm (ε>500 m−1 cm−1).[ 14] After it had reached a maximum, the absorbance at λ=480 nm then decreased concomitant with an increase in absorbance at λ=670 nm.
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At the end of this rapid phase, the spectrum corresponds to a mixture of ferric rTHB1 and rTHB1-O2 (66 and 34%, respectively, in this particular experiment).
The two steep peaks shown in the both sides of the spectrum corresponds the vibrational frequency of DNA molecule.
The increased attenuation occurring at a specific energy level of the spectrum corresponds to the binding energy of the k-shell electrons above which photoelectric absorption occurs.
In the limit of infinite wavenumber times width, the miniband widths vanish and the spectrum corresponds to that of an isolated quantum well (QW).
Since the measurement was at pH 3, then the spectrum corresponds to H2Ox (pKa = 1.27) and HOx- (pKa = 4.28) in rapid exchange equilibrium (time-average).
The LSPR peak in the spectrum corresponds to a position where the ratio of reflection amplitude between p- to s-polarization is a maximum whereas the SPR dip in the spectrum corresponds to a position where the ratio of reflection amplitude between p- to s-polarization is a minimum [see Eq. (1)].
All of the peaks in the spectrum correspond to fragments of this peptide.
The major peaks in the spectrum correspond to the Cd(Kα) lines suggesting the component corresponds to cadmium red and cadmium yellow in under-layers.
Most lines in the spectrum correspond to the emission from neutral Fe atoms, a situation which is common in meteor spectra (Borovička 1993, 1994).
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