Interaction of the Zn(II)-cyclen complex with aminomethylphosphonic acid: Original simultaneous potentiometric and P-31 NMR data treatment
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F17%3A10366408" target="_blank" >RIV/00216208:11310/17:10366408 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1039/c7nj00254h" target="_blank" >http://dx.doi.org/10.1039/c7nj00254h</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1039/c7nj00254h" target="_blank" >10.1039/c7nj00254h</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Interaction of the Zn(II)-cyclen complex with aminomethylphosphonic acid: Original simultaneous potentiometric and P-31 NMR data treatment
Popis výsledku v původním jazyce
The interaction of aminomethylphosphonic acid (H(2)amp) with the Zn(II)-cyclen complex and the formation of ternary complexes was studied by potentiometry and P-31 NMR titrations. Data evaluation of each of the methods separately was found to be insufficient. Thus, data obtained from the both methods were simultaneously treated with the computer program OPIUM. The determined stability constants indicated only weak (logK similar to 3) coordination of aminomethylphosphonic acid through the phosphonate group. The chelating coordination mode with the participation of the amine group was not confirmed. In excess of Zn(II)-cyclen, the formation of dinuclear complexes, in which two Zn(II)-cyclen units are bridged by a phosphonate group, was observed and their presence was confirmed by mass spectrometry. Such a coordination motif is typical for phosphonates in the solid state and also for phosphatases.
Název v anglickém jazyce
Interaction of the Zn(II)-cyclen complex with aminomethylphosphonic acid: Original simultaneous potentiometric and P-31 NMR data treatment
Popis výsledku anglicky
The interaction of aminomethylphosphonic acid (H(2)amp) with the Zn(II)-cyclen complex and the formation of ternary complexes was studied by potentiometry and P-31 NMR titrations. Data evaluation of each of the methods separately was found to be insufficient. Thus, data obtained from the both methods were simultaneously treated with the computer program OPIUM. The determined stability constants indicated only weak (logK similar to 3) coordination of aminomethylphosphonic acid through the phosphonate group. The chelating coordination mode with the participation of the amine group was not confirmed. In excess of Zn(II)-cyclen, the formation of dinuclear complexes, in which two Zn(II)-cyclen units are bridged by a phosphonate group, was observed and their presence was confirmed by mass spectrometry. Such a coordination motif is typical for phosphonates in the solid state and also for phosphatases.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10402 - Inorganic and nuclear chemistry
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2017
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
New Journal of Chemistry
ISSN
1144-0546
e-ISSN
—
Svazek periodika
41
Číslo periodika v rámci svazku
15
Stát vydavatele periodika
GB - Spojené království Velké Británie a Severního Irska
Počet stran výsledku
7
Strana od-do
7253-7259
Kód UT WoS článku
000406192800037
EID výsledku v databázi Scopus
2-s2.0-85026219871