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Mercury-199, chemical shift determination

The degree of deacetylation (DD) of chitin/chitosan samples was successfully determined using NMR spectroscopy. Chitin/chitosan samples were dissolved in a mixture of 25% DCl in D2O and chitosan samples in a mixture of 0.25% DCl in D2O. The concentration of chitosan in the solution was about 0.5% (w/v). The NMR spectra were recorded using a Varian Mercury 400 MHz spectrometer (Fig. 2.35). Table 2.20 shows the chemical shifts of chitin/chitosan protons in D2O/DCI at 70 °C. The DD values were calculated using integrals of the peak of proton HI of... [Pg.81]

Chemical shifts and coupling constants have been determined in for example cyclopropyl magnesium bromide and the compounds formed with gallium, silicon, mercury, tin and lead. A complete analysis of the metal satellite spectra of tetracyclop-ropyl lead and tin and dicyclopropyl mercury has been presented ... [Pg.148]

Dean et al. (65) have prepared organometallic mercury (2+) compounds of the type Hg2(AsF6)a Arene. The NMR spectra of these complexes exhibit averaged arene carbon signals due to rapid free-complexed arene exchange at NMR probe temperatures. On the basis of the variation of the aryl carbon chemical shift with the arene/Hg22 ratio for the system Hg2(AsFe)2-hexa-methylbenzene (HMB) the existence of the following two equilibria was determined ... [Pg.322]


See other pages where Mercury-199, chemical shift determination is mentioned: [Pg.2595]    [Pg.272]    [Pg.122]    [Pg.154]    [Pg.379]    [Pg.2594]    [Pg.254]    [Pg.21]    [Pg.120]    [Pg.574]    [Pg.369]    [Pg.115]    [Pg.311]    [Pg.527]    [Pg.108]    [Pg.29]    [Pg.57]    [Pg.515]    [Pg.47]    [Pg.420]    [Pg.214]    [Pg.411]    [Pg.6298]    [Pg.515]    [Pg.57]   


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Mercury determination

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