Protonation and Tautomerism of 6-Benzylaminopurine Derivatives

Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F02%3A00005629" target="_blank" >RIV/00216224:14310/02:00005629 - isvavai.cz</a>
Výsledek na webu
—
DOI - Digital Object Identifier
—

Jazyk výsledku
angličtina
Název v původním jazyce
Protonation and Tautomerism of 6-Benzylaminopurine Derivatives
Popis výsledku v původním jazyce
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 nitrogenchemical 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.
Název v anglickém jazyce
Protonation and Tautomerism of 6-Benzylaminopurine Derivatives
Popis výsledku anglicky
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 nitrogenchemical 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.

Projekt
<a href="/cs/project/LN00A016" target="_blank" >LN00A016: BIOMOLEKULÁRNÍ CENTRUM</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění
2002
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Podobné výsledky(10)