Structural determination of N6-isopentenyladenine decomposition products during acid hydrolysis
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15410%2F03%3A00001524" target="_blank" >RIV/61989592:15410/03:00001524 - isvavai.cz</a>
Výsledek na webu
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DOI - Digital Object Identifier
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Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Structural determination of N6-isopentenyladenine decomposition products during acid hydrolysis
Popis výsledku v původním jazyce
Novel products of N6-isopentenyladenine (IPA) transformation in 0.01, 0.1 and 2M HCl solutions have been characterized by single crystal X-ray analysis. IPA is converted to compounds of various structures depending on physical conditions such are temperature, pH medium and time. IPA is simply protonated in 0.01M HCl. The main structural changes arise in 0.1M HCl (L1) while the greatest ones have been observed in 2M HCl, where (H2+L2)Cl2.2H2O formed {i.e. 5-(4,4-dimethyl-1,3,5,6-hexahydropyrimidinium-2-yl)-1,3H-imidazolium-4-yl-amine dichloride dihydrate}. The coordination ability of the acid hydrolysis various organic products towards zinc(II) chloride has also been examined. The following complexes have been formed and their structures have been determided: [ZnCl3(H+IPA)], [Zn3Cl8(H+L1)2] and (H2+L2)[ZnCl4]. The results of biological activity testing (cytotoxicity for selected human tumor cell lines) of the prepared compounds will be also presented.
Název v anglickém jazyce
Structural determination of N6-isopentenyladenine decomposition products during acid hydrolysis
Popis výsledku anglicky
Novel products of N6-isopentenyladenine (IPA) transformation in 0.01, 0.1 and 2M HCl solutions have been characterized by single crystal X-ray analysis. IPA is converted to compounds of various structures depending on physical conditions such are temperature, pH medium and time. IPA is simply protonated in 0.01M HCl. The main structural changes arise in 0.1M HCl (L1) while the greatest ones have been observed in 2M HCl, where (H2+L2)Cl2.2H2O formed {i.e. 5-(4,4-dimethyl-1,3,5,6-hexahydropyrimidinium-2-yl)-1,3H-imidazolium-4-yl-amine dichloride dihydrate}. The coordination ability of the acid hydrolysis various organic products towards zinc(II) chloride has also been examined. The following complexes have been formed and their structures have been determided: [ZnCl3(H+IPA)], [Zn3Cl8(H+L1)2] and (H2+L2)[ZnCl4]. The results of biological activity testing (cytotoxicity for selected human tumor cell lines) of the prepared compounds will be also presented.
Klasifikace
Druh
D - Stať ve sborníku
CEP obor
CC - Organická chemie
OECD FORD obor
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Návaznosti výsledku
Projekt
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Návaznosti
Z - Vyzkumny zamer (s odkazem do CEZ)
Ostatní
Rok uplatnění
2003
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název statě ve sborníku
21st European Crystallographic Meeting, Durban, South Africa, 24-29 August 2003
ISBN
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ISSN
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e-ISSN
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Počet stran výsledku
400
Strana od-do
229
Název nakladatele
South African Crystallographic Society
Místo vydání
Durban, South Africa
Místo konání akce
Durban, South Africa
Datum konání akce
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Typ akce podle státní příslušnosti
WRD - Celosvětová akce
Kód UT WoS článku
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