Knock-on synthesis of tritopic calix[4]pyrrole host for enhanced anion interactions

Chahal, Mandeep K.; Labuta, Jan; Březina, Václav; Karr, Paul A.; Matsushita, Yoshitaka; Webre, Whitney A.; Payne, Daniel T.; Ariga, Katsuhiko; D'Souza, Francis and Hill, Jonathan P. (2019). Knock-on synthesis of tritopic calix[4]pyrrole host for enhanced anion interactions. Dalton Transactions, 48(41) pp. 15583–15596.

DOI: https://doi.org/10.1039/c9dt02365h

Abstract

Interactions of anionic guests with a tritopic peripherally functionalized conjugated calix[4]pyrrole host (1) prepared using a regioselective synthetic method is reported. The regioselectivity of synthesis relies on selective N-alkylation of the calix[4]pyrrole caused by peripheral substitution of one pyrrole group with subsequent N-alkylation at the opposing pyrrole group termed by us ‘knock-on’ regioselectivity. The resulting host molecule exhibits anion interactions with common chloride and nitrate anions enhanced by an order of magnitude over the parent conjugated calix[4]pyrrole. Combined analysis of ¹H NMR and UV-vis spectroscopic titration data enabled an evaluation of binding strengths of anions with the host K_A in a binding model where the salt dissociation process is also incorporated in the form of its dissociation constant K_d. Anions could be classified as two types based on their interactions with 1: Type A anions (chloride, nitrate, perchlorate, hydrogensulphate) associate as 1 : 1 complexes through hydrogen bonding while interactions involving Type B anions (acetate, fluoride, dihydrogenphosphate) are complicated by host deprotonation and/or countercation association. Hosts based on rim-functionalized calix[4]pyrroles such as 1 represent a promising new family of chromophores for estimation of biologically relevant anions or other species.