Počet záznamů: 1
Unraveling the Structure-Affinity Relationship between Cucurbit[n]urils (n=7, 8) and Cationic Diamondoids
- 1.0475010 - UOCHB-X 2018 RIV US eng J - Článek v odborném periodiku
Sigwalt, D. - Šekutor, M. - Cao, L. - Zavalij, P. Y. - Hostaš, Jiří - Ajani, Haresh - Hobza, Pavel - Mlinaric-Majerski, K. - Glaser, R. - Isaacs, L.
Unraveling the Structure-Affinity Relationship between Cucurbit[n]urils (n=7, 8) and Cationic Diamondoids.
Journal of the American Chemical Society. Roč. 139, č. 8 (2017), s. 3249-3258. ISSN 0002-7863
Grant CEP: GA ČR(CZ) GBP208/12/G016
Institucionální podpora: RVO:61388963
Klíčová slova: host-guest complexation * high-energy water * driving force
Kód oboru RIV: CF - Fyzikální chemie a teoretická chemie
Obor OECD: Physical chemistry
Impakt faktor: 14.357, rok: 2017
We report the measurement of the binding constants (K-a) for cucurbit[n]uril (n = 7, 8) toward four series of guests based on 2,6-disubstituted adamantanes, 4,9-disubstituted diamantanes, 1,6-disubstituted diamantanes, and 1-substituted adamantane ammonium ions by direct and competitive H-1 NMR spectroscopy. Compared to the affinity of CBDiam(NMe3)(2), the adamantane diammonium ion complexes (e.g., CB2,6-Ad(NH3)(2) and CB2,6-Ad(NMe3)(2)) are less effective at realizing the potential 1000-fold enhancement in affinity due to ion-dipole interactions at the second ureidyl C=O portal. Comparative crystallographic investigation of CBDiam(NMe3)(2), CBDiamNMe(3), and CB1-AdNMe(3) revealed that the preferred geometry positions the +NMe3 groups approximate to 0.32 above the C=O portal, the observed 0.80 spacing observed for CBDiam(NMe3)(2) reflects the simultaneous geometrical constraints of CH2O=C close contacts at both portals. Remarkably, the CBIsoDiam(NHMe2)2 complex displays femtomolar binding affinity, placing it firmly alongside the CBDiam(NMe3)(2) complex. Primary or quaternary ammonium ion looping strategies lead to larger increases in binding affinity for CB than for CB, which we attribute to the larger size of the carbonyl portals of CB, this suggests routes to develop CB as the tightest binding host in the CB[n] family. We report that alkyl group fluorination (e.g., CB1-AdNH(2)Et versus CB1-AdNH(2)CH(2)CF(3)) does not result in the expected increase in Ka value. Finally, we discuss the role of solvation in nonempirical quantum mechanical computational methodology, which is used to estimate the relative changes in Gibbs binding free energies.
Trvalý link: http://hdl.handle.net/11104/0271891