. . "39" . "Kotek, Jan" . . . "GB - Spojen\u00E9 kr\u00E1lovstv\u00ED Velk\u00E9 Brit\u00E1nie a Severn\u00EDho Irska" . . "10.1039/c1dt10543d" . "C\u00EDsa\u0159ov\u00E1, Ivana" . "Havl\u00ED\u010Dkov\u00E1, Jana" . "7"^^ . . . . "40" . "T\u00F3th, Eva" . . "Mn(2+) complexes of 1-oxa-4,7-diazacyclononane based ligands with acetic, phosphonic and phosphinic acid pendant arms: Stability and relaxation studies"@en . "8"^^ . "Pniok, Miroslav" . . "16"^^ . . . "Mn(2+) complexes of 1-oxa-4,7-diazacyclononane based ligands with acetic, phosphonic and phosphinic acid pendant arms: Stability and relaxation studies" . . "[4D125CB6AF87]" . "Hermann, Petr" . . . . . "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, but they induce their slow decomposition. All Mn2+ complexes are stable toward air-oxidation." . . "11310" . . "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, but they induce their slow decomposition. All Mn2+ complexes are stable toward air-oxidation."@en . . "Mn(2+) complexes of 1-oxa-4,7-diazacyclononane based ligands with acetic, phosphonic and phosphinic acid pendant arms: Stability and relaxation studies" . "Mn(2+) complexes of 1-oxa-4,7-diazacyclononane based ligands with acetic, phosphonic and phosphinic acid pendant arms: Stability and relaxation studies"@en . . "Luke\u0161, Ivan" . . . . . . "Draho\u0161, Bohuslav" . . "RIV/00216208:11310/11:10104182!RIV12-GA0-11310___" . "212778" . "Dalton Transactions" . . "P(GA203/09/1056), P(GAP207/11/1437), P(OC 179), S, Z(MSM0021620857)" . "RIV/00216208:11310/11:10104182" . . "000295843100023" . . "field dependence; crystal-structures; manganese(II) complexes; lanthanide(III) complexes; structural-characterization; macrocyclic ligands; water-exchange; pressure NMR kinetics; nuclear-magnetic-resonance; MRI contrast agents"@en . . "http://dx.doi.org/10.1039/c1dt10543d" . . . "1477-9226" . .