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Description
| - A series of tri- and diorganotin(IV) compounds containing potentially chelating S,N-ligand(s) (L(SN), where L(SN) is 6-phenylpyridazine-3-thiolate) were prepared and structurally characterized by multinuclear NMR spectroscopy. X-ray diffraction techniques were used for determination of the structure of compounds containing one [(L(SN))Ph(2)SnCl], two [(n-Bu)(2)Sn(L(SN))(2)] and the combination of two L(SN) and one L(CN) [(L(CN))(n-Bu)Sn(L(SN))(2)] (where L(CN) is {2-[(CH(3))(2)NCH(2)]C(6)H(4)}-) ligands. The coordination number of the tin atom varies from five to seven and is dependent on the number of chelating ligands present. The formation of the five-membered azastanna heterocycle is favored over the formation of four-membered azastannathia heterocycle in compounds containing both types of ligands. The di-n-butyl-substituted compounds are the most efficient ones in inhibition of growth of yeasts, molds and G(+) bacteria strains.
- A series of tri- and diorganotin(IV) compounds containing potentially chelating S,N-ligand(s) (L(SN), where L(SN) is 6-phenylpyridazine-3-thiolate) were prepared and structurally characterized by multinuclear NMR spectroscopy. X-ray diffraction techniques were used for determination of the structure of compounds containing one [(L(SN))Ph(2)SnCl], two [(n-Bu)(2)Sn(L(SN))(2)] and the combination of two L(SN) and one L(CN) [(L(CN))(n-Bu)Sn(L(SN))(2)] (where L(CN) is {2-[(CH(3))(2)NCH(2)]C(6)H(4)}-) ligands. The coordination number of the tin atom varies from five to seven and is dependent on the number of chelating ligands present. The formation of the five-membered azastanna heterocycle is favored over the formation of four-membered azastannathia heterocycle in compounds containing both types of ligands. The di-n-butyl-substituted compounds are the most efficient ones in inhibition of growth of yeasts, molds and G(+) bacteria strains. (en)
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Title
| - S,N-Chelated organotin(IV) compounds containing 6-phenylpyridazine-3-thiolate ligand - structural, antibacterial and antifungal study
- S,N-Chelated organotin(IV) compounds containing 6-phenylpyridazine-3-thiolate ligand - structural, antibacterial and antifungal study (en)
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skos:prefLabel
| - S,N-Chelated organotin(IV) compounds containing 6-phenylpyridazine-3-thiolate ligand - structural, antibacterial and antifungal study
- S,N-Chelated organotin(IV) compounds containing 6-phenylpyridazine-3-thiolate ligand - structural, antibacterial and antifungal study (en)
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skos:notation
| - RIV/00216208:11160/11:10118896!RIV12-MSM-11160___
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http://linked.open...avai/riv/aktivita
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http://linked.open...avai/riv/aktivity
| - I, P(GAP207/10/0215), S, Z(MSM0021627501)
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http://linked.open...iv/cisloPeriodika
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http://linked.open...vai/riv/dodaniDat
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http://linked.open...aciTvurceVysledku
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http://linked.open.../riv/druhVysledku
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http://linked.open...iv/duvernostUdaju
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http://linked.open...titaPredkladatele
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http://linked.open...dnocenehoVysledku
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http://linked.open...ai/riv/idVysledku
| - RIV/00216208:11160/11:10118896
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http://linked.open...riv/jazykVysledku
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http://linked.open.../riv/klicovaSlova
| - antibacterial and fungicidal study; X-ray diffraction analyses; NMR spectroscopy; organotin(IV) compounds (en)
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http://linked.open.../riv/klicoveSlovo
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http://linked.open...odStatuVydavatele
| - US - Spojené státy americké
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http://linked.open...ontrolniKodProRIV
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http://linked.open...i/riv/nazevZdroje
| - Applied Organometallic Chemistry
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http://linked.open...in/vavai/riv/obor
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http://linked.open...ichTvurcuVysledku
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http://linked.open...cetTvurcuVysledku
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http://linked.open...vavai/riv/projekt
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http://linked.open...UplatneniVysledku
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http://linked.open...v/svazekPeriodika
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http://linked.open...iv/tvurceVysledku
| - Padělková, Zdeňka
- Růžička, Aleš
- Švec, Petr
- Vejsová, Marcela
- Holeček, Jaroslav
- Česlová, Lenka
- Ozerianskyi, Andrii
- Vaňkátová, Hana
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http://linked.open...ain/vavai/riv/wos
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http://linked.open...n/vavai/riv/zamer
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issn
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number of pages
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http://bibframe.org/vocab/doi
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http://localhost/t...ganizacniJednotka
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