Abstract
In this work we report the first small and wide-angle X-Ray diffraction study (S-WAXS) of L-proline ester based ionic liquids, a family of chiral ionic liquids (CILs) with several potential useful applications. Along the synthetic pathway that was followed to obtain the already described systems in ultra-pure form, some new compounds were synthesized. Noteworthy differences were observed in the SAXS low Q peak positions trends between chloride and nitrate salts.
Keywords: Chiral ionic liquids, L-Proline esters, small and wide angle X-ray scattering, synthesis.
Graphical Abstract
Call for Papers in Thematic Issues
Catalytic C-H bond activation as a tool for functionalization of heterocycles
The major topic is the functionalization of heterocycles through catalyzed C-H bond activation. The strategies based on C-H activation not only provide straightforward formation of C-C or C-X bonds but, more importantly, allow for the avoidance of pre-functionalization of one or two of the cross-coupling partners. The beneficial impact of ...read more
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