2004
Synthesis of 3,3'-substituted[2]staffane derivatives and NMR study of their inclusion complexes with beta-cyclodextrin in water
BARTOŠ, Petr a Ctibor MAZALZákladní údaje
Originální název
Synthesis of 3,3'-substituted[2]staffane derivatives and NMR study of their inclusion complexes with beta-cyclodextrin in water
Název česky
Synthesis of 3,3'-substituted[2]staffane derivatives and NMR study of their inclusion complexes with beta-cyclodextrin in water
Autoři
BARTOŠ, Petr (203 Česká republika) a Ctibor MAZAL (203 Česká republika, garant)
Vydání
Praha, Chemické listy, IV. Mezioborové setkání mladých biologů, s. 274-274, 2004
Nakladatel
Česká společnost chemická
Další údaje
Jazyk
angličtina
Typ výsledku
Stať ve sborníku
Obor
10401 Organic chemistry
Stát vydavatele
Česká republika
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 0.348
Kód RIV
RIV/00216224:14310/04:00010131
Organizační jednotka
Přírodovědecká fakulta
ISSN
Klíčová slova anglicky
bicyclopentanes; staffanes; cyclodextrin; pseudorotaxanes; NMR
Štítky
Změněno: 21. 5. 2009 17:31, doc. RNDr. Ctibor Mazal, CSc.
V originále
Derivatives of bicyclo[1.1.1]pentante (BCP) I were recognized as very interesting class of compounds due to their structural features. For example, BCP cage represents a basic construction module for rigid rod like molecules . [n]staffanes II, the fundamental part of suggested molecular size construction set1. Having the set of predefined properties with appropriate tools of supramolecular chemistry in hand, one might be able to construct novel molecular materials. Since practically useful synthesis of [1.1.1]propellane had been found, synthetic aspects of BCP chemistry became relatively developed recently2. On the other hand, there is little known about supramolecular chemistry of BCP derivatives so far. Inspired with Berg et al. (cf.3) describing complexation of bicyclo[2.2.2]octane derivatives with cyclodextrins (CD) and with CD-based pseudo-rotaxane model4 in our minds, we focused our interest to the host-guest chemistry of BCPs.
Česky
Derivatives of bicyclo[1.1.1]pentante (BCP) I were recognized as very interesting class of compounds due to their structural features. For example, BCP cage represents a basic construction module for rigid rod like molecules . [n]staffanes II, the fundamental part of suggested molecular size construction set1. Having the set of predefined properties with appropriate tools of supramolecular chemistry in hand, one might be able to construct novel molecular materials. Since practically useful synthesis of [1.1.1]propellane had been found, synthetic aspects of BCP chemistry became relatively developed recently2. On the other hand, there is little known about supramolecular chemistry of BCP derivatives so far. Inspired with Berg et al. (cf.3) describing complexation of bicyclo[2.2.2]octane derivatives with cyclodextrins (CD) and with CD-based pseudo-rotaxane model4 in our minds, we focused our interest to the host-guest chemistry of BCPs.
Návaznosti
| ME 571, projekt VaV |
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| MSM 143100011, záměr |
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