Detailed Information on Publication Record
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.Basic information
Original name
Tris(phosphonomethyl) Cyclen Derivatives: Synthesis, Acid-Base Properties and Complexation Studies with Cu2+ and Zn2+ Ions
Authors
LIMA, Luis M.P. (620 Portugal), Catarina V. ESTEVES (620 Portugal), Rita DELGADO (620 Portugal), Petr HERMANN (203 Czech Republic, guarantor), Jan KOTEK (203 Czech Republic), Romana ŠEVČÍKOVÁ (203 Czech Republic, belonging to the institution) and Přemysl LUBAL (203 Czech Republic, belonging to the institution)
Edition
Eur. J. Inorg. Chem. WEINHEIM, Wiley-VCH Verlag GMBH, 2012, 1434-1948
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: 3.120
RIV identification code
RIV/00216224:14740/12:00060067
Organization unit
Central European Institute of Technology
UT WoS
000303987800008
Keywords in English
macrocyclic ligands; copper; thermodynamics; kinetics; phosphonate complexes
Tags
International impact, Reviewed
Změněno: 7/4/2013 07:54, Olga Křížová
Abstract
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.
Links
ED1.1.00/02.0068, research and development project |
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LC06035, research and development project |
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ME09065, research and development project |
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