KOLMAN, Viktor, Radek MAREK, Zora STŘELCOVÁ, Petr KULHÁNEK, Marek NEČAS, Jan ŠVEC and Vladimír ŠINDELÁŘ. Electron Density Shift in Imidazolium Derivatives upon Complexation with Cucurbit[6]uril. Chemistry - A European Journal. WILEY-VCH, 2009, vol. 15, No 28, p. 6926-6931. ISSN 0947-6539. Available from: https://dx.doi.org/10.1002/chem.200900570.
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Basic information
Original name Electron Density Shift in Imidazolium Derivatives upon Complexation with Cucurbit[6]uril
Name in Czech Posun elektronové hustoty u derivátů imidazolia indukovaný komplexací s cucurbit[6]urilem
Authors KOLMAN, Viktor (203 Czech Republic, belonging to the institution), Radek MAREK (203 Czech Republic, belonging to the institution), Zora STŘELCOVÁ (203 Czech Republic, belonging to the institution), Petr KULHÁNEK (203 Czech Republic, belonging to the institution), Marek NEČAS (203 Czech Republic, belonging to the institution), Jan ŠVEC (203 Czech Republic, belonging to the institution) and Vladimír ŠINDELÁŘ (203 Czech Republic, guarantor, belonging to the institution).
Edition Chemistry - A European Journal, WILEY-VCH, 2009, 0947-6539.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10401 Organic chemistry
Country of publisher Germany
Confidentiality degree is not subject to a state or trade secret
WWW DOI: 10.1002/chem.200900570
Impact factor Impact factor: 5.382
RIV identification code RIV/00216224:14310/09:00029441
Organization unit Faculty of Science
Doi http://dx.doi.org/10.1002/chem.200900570
UT WoS 000268286200020
Keywords in English cucurbiturils;host-guest systems;ionic liquids;supramolecular chemistry
Tags International impact, Reviewed
Changed by Changed by: prof. RNDr. Radek Marek, Ph.D., učo 381. Changed: 17/6/2013 14:38.
Abstract
In this study, we have investigated the supramolecular interaction between series of 1-alkyl-3-methylimidazolium guests with variable alkyl substituent lengths and cucurbit[6]uril (CB6) in the solution and the solid state. Correct interpretation of 1H NMR spectra was a key issue for determining the binding modes of the complexes in solution. Unusual chemical shifts of some protons in the 1H NMR spectra were explained by the polarization of the imidazolium aromatic ring upon the complexation with the host. The formation of 1:1 complex between 1-ethyl-3-methylimidazolium and CB6 is in disagreement with previously reported findings describing an inclusion of two guest molecules in the CB6 cavity.
Abstract (in Czech)
Supramolekulární interakce 1-alkyl-3-methylimidazoliových hostů s cucurbit[6]urilem byla studována v roztoku a v pevném stavu.
Links
GP203/07/P382, research and development projectName: Nové deriváty cucurbit[n]urilu
Investor: Czech Science Foundation, New cucurbit[n]uril derivates
LC06030, research and development projectName: Biomolekulární centrum
Investor: Ministry of Education, Youth and Sports of the CR, Biomolecular centre
MSM0021622413, plan (intention)Name: Proteiny v metabolismu a při interakci organismů s prostředím
Investor: Ministry of Education, Youth and Sports of the CR, Proteins in metabolism and interaction of organisms with the environment
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