About: Inclusion compounds of cystostatic active (C5H5)2 VCl2 and (CH3C5H4)2 VCl2 with a-, b- and c- cyclodextrines: Synthesis, EPR study and microbiological behavior toward Escherichia coli.

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About: Inclusion compounds of cystostatic active (C5H5)2 VCl2 and (CH3C5H4)2 VCl2 with a-, b- and c- cyclodextrines: Synthesis, EPR study and microbiological behavior toward Escherichia coli. Goto Sponge NotDistinct Permalink

An Entity of Type : http://linked.opendata.cz/ontology/domain/vavai/Vysledek, within Data Space : linked.opendata.cz associated with source document(s)

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rdf:type	skos:Concept http://linked.opendata.cz/ontology/domain/vavai/Vysledek
Description	The inclusion of vanadocene dichloride (VDC) and 1,1'-dimethyl vanadocene dichloride (MeVDC) into cyclodextrines (a-CD, b-CD and c-CD) was studied by EPR spectroscopy. It was found that VDC and MeVDC with b-CD and c-CD form true inclusion compounds, but with a-CD, VDC and MeVDC gave only fine dispersion mixtures. The inclusion was validated by anisotropic EPR spectra of solid samples. In addition, the antimicrobial behavior (against E. coli) of each of the complexes was determined. It was established that not only did VDC and MeVDC cause elongation of E. coli, but also the new vanadocene inclusion complexes were effective in this regard. The inclusion of vanadocene dichloride (VDC) and 1,1'-dimethyl vanadocene dichloride (MeVDC) into cyclodextrines (a-CD, b-CD and c-CD) was studied by EPR spectroscopy. It was found that VDC and MeVDC with b-CD and c-CD form true inclusion compounds, but with a-CD, VDC and MeVDC gave only fine dispersion mixtures. The inclusion was validated by anisotropic EPR spectra of solid samples. In addition, the antimicrobial behavior (against E. coli) of each of the complexes was determined. It was established that not only did VDC and MeVDC cause elongation of E. coli, but also the new vanadocene inclusion complexes were effective in this regard. (en) The inclusion of vanadocene dichloride (VDC) and 1,1'-dimethyl vanadocene dichloride (MeVDC) into cyclodextrines (a-CD, b-CD and cCD) was studied by EPR spectroscopy. It was found that VDC and MeVDC with b-CD and c-CD form true inclusion compounds, but with a-CD, VDC and MeVDC gave only fine dispersion mixtures. The inclusion was validated by anisotropic EPR spectra of solid samples. In addition, the antimicrobial behavior (against E. coli) of each of the complexes was determined. It was established that not only did VDC and MeVDC cause elongation of E. coli, but also the new vanadocene inclusion complexes were effective in this regard. (cs)
Title	Inclusion compounds of cystostatic active (C5H5)2 VCl2 and (CH3C5H4)2 VCl2 with a-, b- and c- cyclodextrines: Synthesis, EPR study and microbiological behavior toward Escherichia coli. Inclusion compounds of cystostatic active (C5H5)2 VCl2 and (CH3C5H4)2 VCl2 with a-, b- and c- cyclodextrines: Synthesis, EPR study and microbiological behavior toward Escherichia coli. (en) Inclusion compounds of cystostatic active (C5H5)2 VCl2 and (CH3C5H4)2 VCl2 with a-, b- and c- cyclodextrines: Synthesis, EPR study and microbiological behavior toward Escherichia coli. (cs)
skos:prefLabel	Inclusion compounds of cystostatic active (C5H5)2 VCl2 and (CH3C5H4)2 VCl2 with a-, b- and c- cyclodextrines: Synthesis, EPR study and microbiological behavior toward Escherichia coli. Inclusion compounds of cystostatic active (C5H5)2 VCl2 and (CH3C5H4)2 VCl2 with a-, b- and c- cyclodextrines: Synthesis, EPR study and microbiological behavior toward Escherichia coli. (en) Inclusion compounds of cystostatic active (C5H5)2 VCl2 and (CH3C5H4)2 VCl2 with a-, b- and c- cyclodextrines: Synthesis, EPR study and microbiological behavior toward Escherichia coli. (cs)
skos:notation	RIV/00216275:25310/05:00001636!RIV08-MSM-25310___
http://linked.open.../vavai/riv/strany	72-81
http://linked.open...avai/riv/aktivita	Z
http://linked.open...avai/riv/aktivity	Z(MSM0021627501)
http://linked.open...iv/cisloPeriodika	1
http://linked.open...vai/riv/dodaniDat	2008
http://linked.open...aciTvurceVysledku	Vinklárek, Jaromír Holubová, Jana
http://linked.open.../riv/druhVysledku	J - Článek v odborném periodiku
http://linked.open...iv/duvernostUdaju	S - Úplné a pravdivé údaje nepodléhající ochraně podle zvláštních právních předpisů
http://linked.open...titaPredkladatele	Univerzita Pardubice / Fakulta chemicko-technologická
http://linked.open...dnocenehoVysledku	524504
http://linked.open...ai/riv/idVysledku	RIV/00216275:25310/05:00001636
http://linked.open...riv/jazykVysledku	eng - angličtina
http://linked.open.../riv/klicovaSlova	cyclodextrine (en)
http://linked.open.../riv/klicoveSlovo	cyclodextrine
http://linked.open...odStatuVydavatele	PL - Polská republika
http://linked.open...ontrolniKodProRIV	[E67480C1BEEF]
http://linked.open...i/riv/nazevZdroje	Central European Journal of Chemistry
http://linked.open...in/vavai/riv/obor	CA
http://linked.open...ichTvurcuVysledku	2 (xsd:int)
http://linked.open...cetTvurcuVysledku	3 (xsd:int)
http://linked.open...UplatneniVysledku	2005
http://linked.open...v/svazekPeriodika	3
http://linked.open...iv/tvurceVysledku	Holubová, Jana Vinklárek, Jaromír Honzíček, Jan
http://linked.open...n/vavai/riv/zamer	Aimed preparation of special compounds and materials and investigation of their physical and chemical properties and supramolecular structures
issn	1644-3624
number of pages	10 (xsd:int)
http://localhost/t...ganizacniJednotka	25310

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