Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Quantitative 13C Analysis

Quantitative 13C NMR is desirable in two situations. First in structure determinations, it is clearly useful to know whether a signal results from more than one shift-equivalent carbon. Second, quantitative analysis of a mixture of two or more components requires that the area of the peaks be proportional to the number of carbons atoms causing that signal. [Pg.213]

There are two reasons that broadband-decoupled l3C spectra are usually not susceptible to quantitative analysis  [Pg.213]

FIGURE 4.7 Inverse gated proton decoupling pulse sequence. Rd is relaxation delay, 0 is a variable pulse angle, t2 is the acquisition time. [Pg.213]

FIGURE 4.8 (a) Standard ll decoupled 13C spectrum of diethyl phthalate with relaxation delay (/ ,/) 7), [Pg.214]

The definition of chemical shift equivalence given for protons also applies to carbon atoms interchangeability by a symmetry operation or by a rapid mechanism. The presence of equivalent carbon atoms (or coincidence of shift) in a molecule results in a discrepancy [Pg.214]


See other pages where Quantitative 13C Analysis is mentioned: [Pg.213]    [Pg.213]   


SEARCH



13C analysis

© 2024 chempedia.info