Mn(2+) complexes of 1-oxa-4,7-diazacyclononane based ligands with acetic, phosphonic and phosphinic acid pendant arms: Stability and relaxation studies
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F11%3A10104182" target="_blank" >RIV/00216208:11310/11:10104182 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1039/c1dt10543d" target="_blank" >http://dx.doi.org/10.1039/c1dt10543d</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1039/c1dt10543d" target="_blank" >10.1039/c1dt10543d</a>
Alternative languages
Result language
angličtina
Original language name
Mn(2+) complexes of 1-oxa-4,7-diazacyclononane based ligands with acetic, phosphonic and phosphinic acid pendant arms: Stability and relaxation studies
Original language description
A new class of macrocyclic ligands based on 1-oxa-4,7-diazacyclononane was synthesized and their Mn2+ complexes were investigated with respect to stability and relaxation properties. Each ligand has two pendant arms involving carboxylic, phosphonic, phosphinic or phenylphosphinic acid moieties. The crystal structure of the Mn2+ complex with H2L4 confirmed a coordination number of 6 for Mn2+. The protonation constants of all ligands and the stability constants of their complexes with Mn2+ and some biologically or biomedically relevant metal ions were determined by potentiometry and NMR. Variable temperature 1HNMRD and 17O NMR measurements have been performed on MnL1 and MnL2 to provide information on water exchange and rotational dynamics. The 17O chemical shifts indicate hydration equilibrium between mono- and bishydrated species for MnL1, while MnL2 is monohydrated. Small endogenous anions (phosphate, carbonate, citrate) do not replace the coordinated water in either of the complexes,
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CA - Inorganic chemistry
OECD FORD branch
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Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)<br>S - Specificky vyzkum na vysokych skolach
Others
Publication year
2011
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Dalton Transactions
ISSN
1477-9226
e-ISSN
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Volume of the periodical
40
Issue of the periodical within the volume
39
Country of publishing house
GB - UNITED KINGDOM
Number of pages
16
Pages from-to
10131-10146
UT code for WoS article
000295843100023
EID of the result in the Scopus database
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