2012
Tris(phosphonomethyl) Cyclen Derivatives: Synthesis, Acid-Base Properties and Complexation Studies with Cu2+ and Zn2+ Ions
LIMA, Luis M.P., Catarina V. ESTEVES, Rita DELGADO, Petr HERMANN, Jan KOTEK et. al.Základní údaje
Originální název
Tris(phosphonomethyl) Cyclen Derivatives: Synthesis, Acid-Base Properties and Complexation Studies with Cu2+ and Zn2+ Ions
Autoři
LIMA, Luis M.P. (620 Portugalsko), Catarina V. ESTEVES (620 Portugalsko), Rita DELGADO (620 Portugalsko), Petr HERMANN (203 Česká republika, garant), Jan KOTEK (203 Česká republika), Romana ŠEVČÍKOVÁ (203 Česká republika, domácí) a Přemysl LUBAL (203 Česká republika, domácí)
Vydání
Eur. J. Inorg. Chem. WEINHEIM, Wiley-VCH Verlag GMBH, 2012, 1434-1948
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10402 Inorganic and nuclear chemistry
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 3.120
Kód RIV
RIV/00216224:14740/12:00060067
Organizační jednotka
Středoevropský technologický institut
UT WoS
000303987800008
Klíčová slova anglicky
macrocyclic ligands; copper; thermodynamics; kinetics; phosphonate complexes
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 7. 4. 2013 07:54, Olga Křížová
Anotace
V originále
Three compounds that are based on cyclen and contain three methylphosphonate pendant arms ? (1,4,7,10-tetraazacyclododecane-1,4,7-triyl)tris(methylene)triphosphonic acid (H6do3p), 3-{4,7,10-tris[(dihydroxyphosphoryl)methyl]-1,4,7,10-tetraazacyclododecan-1-yl}propanoic acid (H7do3p1pr) and [10-(3-hydroxypropyl)-1,4,7,10-tetraazacyclododecane-1,4,7-triyl]tris(methylene)triphosphonic acid (H6do3p1ol) ? were synthesized and characterized. X-ray crystal structures were determined for H6do3p and for the complex [Cu(H2O)6]2+[Cu(H2O)(H4dotp)]2 of a related ligand H8dotp [H8dotp = (1,4,7,10-tetraazacyclododecane-1,4,7,10-tetrayl)tetrakis(methylene)tetraphosphonic acid]. They show the copper(II) centre coordinated only to the four amines of the macrocycle and one water molecule in the apical position. The acidbase properties of the three compounds were studied in aqueous solution by potentiometry and 31P NMR spectroscopy. All ligands exhibit very high basicity and their protonation schemes are dominated by proton relocations between the basic sites and intramolecular hydrogen bonding. The thermodynamic stability constants for complexes of the three ligands with Cu2+ and Zn2+ metal ions were determined by potentiometry and exhibit very high values for the complexes of Cu2+. UV/Vis spectroscopy was used to assess the acid-assisted dissociation of the Cu2+ complexes and showed that the dissociation rates are faster than for the corresponding complex of H8dotp, whereas the [Cu(do3p1ol)]4 complex is the most inert one in this series.
Návaznosti
ED1.1.00/02.0068, projekt VaV |
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LC06035, projekt VaV |
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ME09065, projekt VaV |
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