“Choose-a-Size” Approach in Dynamic Combinatorial Chemistry: A Single Substrate Dynamic Combinatorial Library of Oligomacrocycles That Adapts to the Size and Shape of Carboxylates
journal contributionposted on 2014-10-17, 00:00 authored by Filip Ulatowski, Agnieszka Sadowska-Kuziol̷a, Janusz Jurczak
A neutral anion binding receptor based on dipicolinic acid diamide was equipped with thiol groups in the amidic side arms. After the thiol was oxidized to disulfide groups with I2, a mixture of cyclic oligomers (a library) was obtained. The distribution of macrocycles can be controlled kinetically during the oxidation process or thermodynamically at basic conditions via disulfide bond exchange. The library proved to be very sensitive to templation with various carboxylates in DMSO. The amplification pattern reflects the structural features of the anionic template and is sensitive to changes in the template’s geometry. The application of carboxylates with multiple functional groups resulted in very strong amplification of the large penta- and hexameric macrocycles. The thermodynamic parameters of some templation effects were rationalized using a simple model and confirmed using competitive NMR titration.
NMR titrationamidic side armsanion binding receptordipicolinic acid diamidecarboxylatetemplatehexameric macrocyclesamplification patterncyclic oligomersdisulfide bond exchangeDynamic Combinatorial ChemistrySingle Substrate Dynamic Combinatorial Librarydisulfide groupsoxidation processtemplation effectsthiol groupsDMSO