FÖRSTEROVÁ, Michaela, Ivona SVOBODOVÁ, Přemysl LUBAL, Petr TÁBORSKÝ, Jan KOTEK, Petr HERMANN and Ivan LUKEŠ. Thermodynamic study of lanthanide(III) complexes with bifunctional monophosphinic acid analogues of H4dota and comparative kinetic study of yttrium(III) complexes. Dalton transactions : an international journal of inorganic chemistry. Cambridge: The Royal Society of Chemistry, 2007, xxx, No 2, p. 535-549, 16 pp. ISSN 1477-9226.
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Basic information
Original name Thermodynamic study of lanthanide(III) complexes with bifunctional monophosphinic acid analogues of H4dota and comparative kinetic study of yttrium(III) complexes
Name in Czech Termodynamické studium Ln(III) komplexů s bifunkčními monofosfinovými analogy H4dota a komparativní kinetické studium yttritých komplexů
Authors FÖRSTEROVÁ, Michaela (203 Czech Republic), Ivona SVOBODOVÁ (203 Czech Republic), Přemysl LUBAL (203 Czech Republic, guarantor), Petr TÁBORSKÝ (203 Czech Republic), Jan KOTEK (203 Czech Republic), Petr HERMANN (203 Czech Republic) and Ivan LUKEŠ (203 Czech Republic).
Edition Dalton transactions : an international journal of inorganic chemistry, Cambridge, The Royal Society of Chemistry, 2007, 1477-9226.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10402 Inorganic and nuclear chemistry
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 3.212
RIV identification code RIV/00216224:14310/07:00020139
Organization unit Faculty of Science
UT WoS 000243536100004
Keywords in English azacrown compounds; phosphonate/phosphinate complexes; macrocyclic ligand; cyclen derivative; tetraazacyclododecane; DOTA; thermodynamics; kinetics; crystal structure determination; potentiometry; yttrium(III); lanthanide(III) cations
Tags Azacrown compounds, Crystal structure determination, Cyclen derivative, DOTA, kinetics, lanthanide(III) cations, macrocyclic ligand, phosphonate/phosphinate complexes, potentiometry, Tetraazacyclododecane, Thermodynamics, yttrium(III)
Tags International impact, Reviewed
Changed by Changed by: prof. RNDr. Přemysl Lubal, Ph.D., učo 1271. Changed: 8/4/2010 19:42.
Abstract
New bifunctional H4dota-like ligands with three acetic acid and one phosphinic acid pendant arms and propionate (H5do3apPrA) or 4-aminobenzyl (H4do3apABn) reactive groups bound to the phosphorus atom were investigated. Potentiometric studies showed that the ligands have a similar basicity to the parent H4dota and the stability constants of their complexes with sodium(I) and selected lanthanide(III) ions are also similar. Formation and acid-assisted decomplexation kinetics of yttrium(III) complexes with a series of H4dota-like ligands (H4dota and its phosphinic/phosphonic acid analogues) were studied and the reactions are sensitive to a slight modification of the ligand structure. The (2-carboxyethyl)phosphinic acid derivative H5do3apPrA and the phosphonic acid ligand H5do3ap form complexes faster than H4dota. The most kinetically inert complex is that with H4do3apABn. Rates of complexation and decomplexation can depend on the ability to transfer proton(s) outside/inside the complex cavity.
Abstract (in Czech)
Nové bifunkční ligandy typu H4dota s 3 octanovými a 1 fosfinovým pendantním ramenem nebo 1 propionátými (H5do3apPrA) nebo 4-aminobenzylovými (H4do3apABn) reaktivními skupinami vázanými na fosforový atom byly studovány. Potenciometrická studia ukázaly, že ligandy mají podobnou bazicitu ve srovnání s H4dota and konstanty stability jejich komplexů se sodnými a vybranými Ln(III) ionty jsou podobné. Formační a kysele katalyzovaná disociační kinetika Y(III) komplexů se sérií ligandů typu H4dota (H4dota a jeho fosfinové/fosfonové analogy) byly studovány, kdy reakce jsou citlivé k modifikaci struktury ligandu. (2-karboxyethyl)fosfinový derivát H5do3apPrA a fosfonový derivát H5do3ap tvoří komplexy rychleji než H4dota. Kineticky nejinertněnjší komplex je ten s H4do3apABn. Rychlostni komplexace a dekomplexace mohou záviset na schopnosti přenášet proton(y) vně/uvnitř dutiny komplexu.
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