Detailed Information on Publication Record
2018
The time-resolved fluorescence study of kinetics and thermodynamics of Eu(III) and Tb(III) complexes with the DO2A macrocyclic ligand
SMRČKA, Filip and Přemysl LUBALBasic information
Original name
The time-resolved fluorescence study of kinetics and thermodynamics of Eu(III) and Tb(III) complexes with the DO2A macrocyclic ligand
Authors
SMRČKA, Filip (203 Czech Republic, belonging to the institution) and Přemysl LUBAL (203 Czech Republic, guarantor, belonging to the institution)
Edition
New Journal of Chemistry, Cambridge, ROYAL SOC. CHEMISTRY, 2018, 1144-0546
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10402 Inorganic and nuclear chemistry
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 3.069
RIV identification code
RIV/00216224:14310/18:00101195
Organization unit
Faculty of Science
UT WoS
000434245500053
Keywords in English
LANTHANIDE(III) COMPLEXES; METAL COMPLEXES; LUMINESCENCE; DISSOCIATION; EQUILIBRIA; STABILITY; PROBES; SENSOR
Tags
Tags
International impact, Reviewed
Změněno: 23/4/2024 12:30, Mgr. Michal Petr
Abstract
V originále
The thermodynamics of the interaction of the H(2)DO2A (= 1,4,7,10-tetraazacyclododecane-1,7-diacetic acid) macrocyclic ligand with both Eu(III) and Tb(III) ions was studied by means of luminescence spectroscopy in steady-state and time-resolved modes. It was shown that it is possible to calculate stability constants for both complexes that agree with values determined by other experimental techniques. The study of the formation and dissociation of both Ln(III) complexes shows that there is no significant difference in their reactivity if they contain three (Eu) or two (Tb) water molecules in their coordination shell. The two species of ligands present in the formation reaction, HL- and L2-, differ in their reactivity, which can be explained by the difference in charge and the presence of a proton in the macrocyclic cavity. A detailed study of the dissociation reaction proved that the reaction mechanism consists of several pathways of intermediates, which differ in their structure and rate of decomposition.
Links
GA13-08336S, research and development project |
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LQ1601, research and development project |
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MUNI/A/1237/2016, interní kód MU |
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