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Pregled bibliografske jedinice broj: 862841

Unraveling the Structure-Affinity Relationship Between Cucurbit[n]urils (n = 7, 8) and Cationic Diamondoids


Sigwalt, David; Šekutor, Marina; Cao, Liping; Zavalij, Peter Y.; Hostaš, Jirí; Ajani, Haresh; Hobza, Pavel; Mlinarić-Majerski, Kata; Glaser, Robrt; Isaacs, Lyle
Unraveling the Structure-Affinity Relationship Between Cucurbit[n]urils (n = 7, 8) and Cationic Diamondoids // Journal of the American Chemical Society, 139 (2017), 8; 3249-3258 doi:10.1021/jacs.7b00056 (međunarodna recenzija, članak, znanstveni)


Naslov
Unraveling the Structure-Affinity Relationship Between Cucurbit[n]urils (n = 7, 8) and Cationic Diamondoids

Autori
Sigwalt, David ; Šekutor, Marina ; Cao, Liping ; Zavalij, Peter Y. ; Hostaš, Jirí ; Ajani, Haresh ; Hobza, Pavel ; Mlinarić-Majerski, Kata ; Glaser, Robrt ; Isaacs, Lyle

Izvornik
Journal of the American Chemical Society (0002-7863) 139 (2017), 8; 3249-3258

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Diamondoids ; ammonium salts ; cucurbit[n]urils ; high affinity host-guest pairs ; X-ray diffraction

Sažetak
We report measurement of the binding constants (Ka) 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 1H NMR spectroscopy. Compared to B[7]•Diam(NMe3)2, the adamantane diammonium ion complexes (e.g. CB[7]•2, 6-Ad(NH3)2 and CB[7]•2, 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 CB[7]•Diam(NMe3)2, B[7]•DiamNMe3, and CB[7]•1-AdNMe3 reveals that the preferred geometry positions the +NMe3-groups ≈ 0.32 Å above the C=O portal ; the observed 0.80Å spacing observed for CB[7]•Diam(NMe3)2 reflects the simultaneous geometrical constraints of CH2•••O=C close contacts at both portals. Remarkably, the CB[8]•IsoDiam(NHMe2)2 complex displays femtomolar binding affinity placing it firmly alongside the CB[7]•Diam(NMe3)2 complex. Primary or quaternary ammonium ion looping strategies lead to larger increases in binding affinity for CB[8] than for CB[7] which we attribute to the larger size of the carbonyl portals of CB[8] which suggests routes to develop CB[8] as the tightest binding host in the CB[n] family. We report that alkyl group fluorination (e.g. CB[7]•1-AdNH2Et versus CB[7]•1-AdNH2CH2CF3) does not result in the expected increase in Ka value. Finally, we have discussed the role of solvation in non-empirical quantum mechanical computational methodology which is used to estimate the relative changes in Gibbs binding free energies.

Izvorni jezik
Engleski

Znanstvena područja
Kemija

Napomena
Znanstveni projekt HAZU - Diamantoidni amini – novi ligandi u supramolekulskim sustavima ; voditelj: Marina Šekutor



POVEZANOST RADA


Projekt / tema
098-0982933-2911 - Kavezasti spojevi: ugradbene jedinice u molekularnim sustavima (Kata Majerski, )
HAZU

Ustanove
Institut "Ruđer Bošković", Zagreb,
Hrvatska akademija znanosti i umjetnosti

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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