R - Lorentz JÄNTSCHI
R - Lorentz JÄNTSCHI
R - Lorentz JÄNTSCHI
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Conclusion<br />
- 107 -<br />
Thin-layer chromatography was used to study the retention behavior of 14<br />
newly synthesized s-triazines. The stationary phase used was silica gel with<br />
covalently bonded C-18 phase (HPTLC) or silica gel impregnated with paraffin oil<br />
(TLC), whith two-component mixtures of water and different organic solvents as<br />
mobile phases.<br />
On the basis of the obtained results the following conclusions can be drawn:<br />
1. The retention behavior of the invesigated newly synthesized s-triazines is generaly<br />
influenced by their molecular structure.<br />
2. The retention is influenced by the polarity of the nature of the organic solvent<br />
used as a mobile phase modifier in the case of the protic solvents, whereas the<br />
retention is more or less the same with aprotic solvents.<br />
3. Linear change of the retention with the change of volume ratio of the modifier in<br />
the reverse phase was confirmed for the majority of tested chromatographic<br />
systems. The exceptions were methanol on RP C-18 and acetonitrile on silica gel<br />
impreganted with paraffin oil, for which a quadratic dependence was found.<br />
4. High degree of mutual correlation between the retention parameters obtained for<br />
the different mobile phases indicates the existence of compatibility of the<br />
modifiers, and by the same token, it offers the posibility of optimization of the<br />
retention of studied compounds.<br />
5. Retention parameters obtained by the extrapolation to 0% of organic modifier,<br />
RM 0 , represent a real measure of the lipohilicity of molecules, in contrast to the<br />
programs for calculating logP values, which are not always equally valid and<br />
reliable for expressing the partition coefficient.<br />
Doktorska disertacija Lidija Jevrić