Toxic metal complexes of macrocyclic cyclen molecule - synthesis, structure and complexing properties
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F17%3A10360085" target="_blank" >RIV/00216208:11310/17:10360085 - isvavai.cz</a>
Výsledek na webu
<a href="https://doi.org/10.1080/00958972.2017.1305493" target="_blank" >https://doi.org/10.1080/00958972.2017.1305493</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1080/00958972.2017.1305493" target="_blank" >10.1080/00958972.2017.1305493</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Toxic metal complexes of macrocyclic cyclen molecule - synthesis, structure and complexing properties
Popis výsledku v původním jazyce
Toxic metal (Cd2+, Hg2+, Pb2+, and Ag+) complexes with the tetradentate macrocyclic ligand - cyclen (1,4,7,10-tetraazacyclododecane, [12]aneN(4), L) were prepared and studied in the solid state by IR, X-ray diffraction, elemental and thermal analysis. Diffraction results have yielded three molecular structures, [Cd([12]ane-N-4(1,4,7,10))(NO3)(2))] (1), [Hg([12]ane-N-4(1,4,7,10))(NO3-O-2,O')]NO3 (2), [Pb-2([12]ane-N-4(1,4,7,10))(2)][Pb(NO3)(6)] (3) and one polymeric structure {[Ag-2([12]ane-N-3(1,4,7))((2)-[12]aneN(10))](NO3)(2).2H(2)O)}(n) (4) featuring a unique coordination mode not observed before with cyclen as a ligand. The monodentate (1) and chelate (with small bite angle 50.3(3)degrees, (2) coordination modes of nitrate ligands were confirmed. Stereochemically active 6s(2) lone pair was suggested in 3 and DFT results confirmed no significant metal-metal covalent bond. The stability constants of the complexes with Cd2+ and Pb2+ ions were determined by potentiometric methods in aqueous solutions. Additionally, the structures of complexes in solution were observed by H-1 NMR. Both methods confirm similar cyclen complexing properties toward Zn2+ biometal and Cd2+, Pb2+ toxic metals.
Název v anglickém jazyce
Toxic metal complexes of macrocyclic cyclen molecule - synthesis, structure and complexing properties
Popis výsledku anglicky
Toxic metal (Cd2+, Hg2+, Pb2+, and Ag+) complexes with the tetradentate macrocyclic ligand - cyclen (1,4,7,10-tetraazacyclododecane, [12]aneN(4), L) were prepared and studied in the solid state by IR, X-ray diffraction, elemental and thermal analysis. Diffraction results have yielded three molecular structures, [Cd([12]ane-N-4(1,4,7,10))(NO3)(2))] (1), [Hg([12]ane-N-4(1,4,7,10))(NO3-O-2,O')]NO3 (2), [Pb-2([12]ane-N-4(1,4,7,10))(2)][Pb(NO3)(6)] (3) and one polymeric structure {[Ag-2([12]ane-N-3(1,4,7))((2)-[12]aneN(10))](NO3)(2).2H(2)O)}(n) (4) featuring a unique coordination mode not observed before with cyclen as a ligand. The monodentate (1) and chelate (with small bite angle 50.3(3)degrees, (2) coordination modes of nitrate ligands were confirmed. Stereochemically active 6s(2) lone pair was suggested in 3 and DFT results confirmed no significant metal-metal covalent bond. The stability constants of the complexes with Cd2+ and Pb2+ ions were determined by potentiometric methods in aqueous solutions. Additionally, the structures of complexes in solution were observed by H-1 NMR. Both methods confirm similar cyclen complexing properties toward Zn2+ biometal and Cd2+, Pb2+ toxic metals.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10402 - Inorganic and nuclear chemistry
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2017
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal of Coordination Chemistry
ISSN
0095-8972
e-ISSN
—
Svazek periodika
70
Číslo periodika v rámci svazku
10
Stát vydavatele periodika
GB - Spojené království Velké Británie a Severního Irska
Počet stran výsledku
15
Strana od-do
1698-1712
Kód UT WoS článku
000401250400006
EID výsledku v databázi Scopus
2-s2.0-85016116716