Synthesis and chiral self-sorting of spirobifluorene-containing boronate ester cages†‡

Abstract

2,2′-Functionalization induces axial chirality within the orthogonal aromatic scaffold of 9,9′-bispirofluorene. By implementing boronic acids at these positions, well-suited precursors for chiral boronate ester cages are generated. As a key intermediate, (P)-9,9′-bispirofluorene-2,2′-bistriflate (P)- was synthesized via a four-step sequence of twofold Friedel–Crafts acylation, Baeyer–Villiger oxidation, hydrolysis, and triflate formation. Chiral resolution was achieved via chiral HPLC for the dihydroxy intermediate. In a modular manner, Pd-catalyzed borylation or cross-coupling afforded either diboronic acid (P)- or elongated derivative (P)- possessing additional phenylene spacers. For both enantiomerically pure linkers, reaction with hexahydroxy tribenzotriquinacene in THF under water-removing conditions afforded isoreticular chiral organic cages (P,P,P)- and (P,P,P)-. Both cages possess a chiral trigonal–bipyramidal geometry and were characterized by ¹H, ¹³C and DOSY NMR spectroscopy and MALDI-TOF mass spectrometry. Chiral self-sorting of the bispirofluorene precursors was investigated by reactions of with racemic linkers rac- and rac-. For shorter linker rac-, quantitative self-sorting into a racemic mixture of (P,P,P)- and (M,M,M)- occurred. For elongated derivative rac- however, the increased flexibility introduced by the phenylene extension resulted in much lower selectivity and self-recognition. Instead a more complex product mixture was obtained and the racemic mixture of was isolated in much lower yield of around 20%. Semiempirical PM6 calculations for both homo- and heterochiral cages and macrocyclic intermediates allowed for an estimation of macrocyclic strain energies and provided in-depth insight into cage formation pathways and self-sorting properties.