Dynamic and Persistent Cyclochirality in Hydrogen-Bonded Derivatives of Medium-Ring Triamines

• Published in: Journal of the American Chemical Society Vol. 145; no. 34; pp. 19030 - 19041
• Main Authors: Morris, David T. J., Wales, Steven M., Echavarren, Javier, Žabka, Matej, Marsico, Giulia, Ward, John W., Pridmore, Natalie E., Clayden, Jonathan
• Format: Journal Article
• Language: English
• Published: American Chemical Society 30.08.2023
• Subjects: enantiomerism; enantiomers; ethylene; hydrogen; hydrogen bonding; spectroscopy; stereochemistry; urea; X-ray diffraction
• ISSN: 0002-7863; 1520-5126; 1520-5126
• DOI: 10.1021/jacs.3c06570

Cyclic triureas derived from 1,4,7-triazacyclononane (TACN) were synthesized; X-ray crystallography showed a chiral bowl-like conformation with each urea hydrogen-bonded to its neighbor with uniform directionality, forming a “cyclochiral” closed loop of hydrogen bonds. Variable-temperature 1H NMR, 1H-1H exchange spectroscopy, Eyring analysis, computational modeling, and studies in various solvents revealed that cyclochirality is dynamic (ΔG ‡ 25°C = 63–71 kJ mol–1 in noncoordinating solvents), exchanging between enantiomers by two mechanisms: bowl inversion and directionality reversal, with the former subject to a slightly smaller enantiomerization barrier. The enantiomerization rate substantially increased in the presence of hydrogen-bonding solvents. Population of only one of the two cyclochiral hydrogen-bond directionalities could be induced by annulating one ethylene bridge with a trans-cyclohexane. Alternatively, enantiomerization could be inhibited by annulating one ethylene bridge with a cis-cyclohexane (preventing bowl inversion) and replacing one urea function with a formamide (preventing directionality reversal). Combining these structural modifications resulted in an enantiomerization barrier of ΔG ‡ 25°C = 93 kJ mol–1, furnishing a planar-chiral, atropisomeric bowl-shaped structure whose stereochemical stability arises solely from its hydrogen-bonding network.