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Statements

Subject Item
n2:RIV%2F00216224%3A14310%2F02%3A00005629%21RIV08-MSM-14310___
rdf:type
skos:Concept n13:Vysledek
dcterms:description
The 15N NMR parameters were measured by inverse and direct methods in solution at various temperatures. 15N CP/MAS data of selected compounds were recorded in order to study the principal values of 15N chemical shifts. Ab initio calculations of nitrogen chemical shifts were used for assigning the nitrogen resonances observed in the solid-state spectra and for determining the orientation of principal components of the chemical shift tensors. The partial results of this project including solution-state temperature measurements are discussed. The 15N NMR parameters were measured by inverse and direct methods in solution at various temperatures. 15N CP/MAS data of selected compounds were recorded in order to study the principal values of 15N chemical shifts. Ab initio calculations of nitrogen chemical shifts were used for assigning the nitrogen resonances observed in the solid-state spectra and for determining the orientation of principal components of the chemical shift tensors. The partial results of this project including solution-state temperature measurements are discussed. The 15N NMR parameters were measured by inverse and direct methods in solution at various temperatures. 15N CP/MAS data of selected compounds were recorded in order to study the principal values of 15N chemical shifts. Ab initio calculations of nitrogen chemical shifts were used for assigning the nitrogen resonances observed in the solid-state spectra and for determining the orientation of principal components of the chemical shift tensors. The partial results of this project including solution-state temperature measurements are discussed.
dcterms:title
Protonation and Tautomerism of 6-Benzylaminopurine Derivatives Protonation and Tautomerism of 6-Benzylaminopurine Derivatives Protonation and Tautomerism of 6-Benzylaminopurine Derivatives
skos:prefLabel
Protonation and Tautomerism of 6-Benzylaminopurine Derivatives Protonation and Tautomerism of 6-Benzylaminopurine Derivatives Protonation and Tautomerism of 6-Benzylaminopurine Derivatives
skos:notation
RIV/00216224:14310/02:00005629!RIV08-MSM-14310___
n4:strany
27
n4:aktivita
n8:P
n4:aktivity
P(LN00A016)
n4:dodaniDat
n15:2008
n4:domaciTvurceVysledku
n7:2050285 n7:8533113 n7:5834368
n4:druhVysledku
n16:D
n4:duvernostUdaju
n20:S
n4:entitaPredkladatele
n14:predkladatel
n4:idSjednocenehoVysledku
660952
n4:idVysledku
RIV/00216224:14310/02:00005629
n4:jazykVysledku
n10:eng
n4:klicovaSlova
NMR; spectroscopy; purine
n4:klicoveSlovo
n11:NMR n11:spectroscopy n11:purine
n4:kontrolniKodProRIV
[121258E8A2E9]
n4:mistoKonaniAkce
8.-10.4. Valtice
n4:mistoVydani
Brno
n4:nazevZdroje
17th NMR Valtice
n4:obor
n18:CF
n4:pocetDomacichTvurcuVysledku
3
n4:pocetTvurcuVysledku
5
n4:projekt
n6:LN00A016
n4:rokUplatneniVysledku
n15:2002
n4:tvurceVysledku
Toušek, Jaromír Trávníček, Zdeněk Brus, Jiří Marek, Radek Lukášková, Marcela
n4:typAkce
n12:EUR
n4:zahajeniAkce
2002-01-01+01:00
s:numberOfPages
1
n21:hasPublisher
Masaryk University
n5:isbn
80-210-2808-4
n17:organizacniJednotka
14310