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Relations between Structural and Luminescence Properties of Novel Lanthanide Nitrate Complexes with Bis-phosphoramidate Ligands

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F19%3A10405392" target="_blank" >RIV/00216208:11320/19:10405392 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=3Otcv5uiI2" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=3Otcv5uiI2</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/acs.inorgchem.8b03611" target="_blank" >10.1021/acs.inorgchem.8b03611</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Relations between Structural and Luminescence Properties of Novel Lanthanide Nitrate Complexes with Bis-phosphoramidate Ligands

  • Popis výsledku v původním jazyce

    Five new bisphosphoramide-based Ln(III) nitrate complexes [La-2(NO3)(6)L-3(I)](n) (1), [Ce-2(NO3)(6)L-3(I)](n) (2), [Sm-2(NO3)(6)L-3(II)](n), (3), Sm-2(NO3)(6)L-3(III) (4), and Er(NO3)(3)L-2(III) (5) [L-I = piperazine-1,4-diylbis(diphenyl phosphine oxide), L-II = N,N&apos;-(ethane-1,2-diyl)bis(N-methyl-P,P-diphenylphosphinic amide, and L-II = N,N&apos;-(ethane-1,2-diyl)bis(P,P-diphenylphosphinic amide)] have been synthesized and characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis (TGA), and single crystal X-ray and powder diffractions. The results of the X-ray diffraction analysis revealed the new polymorph of L-III, and the structural diversity of the synthesized complexes in the solid state. Complexes 1-3 display two-dimensional coordination polymers (2D-CP), containing layers with honeycomb (6, 3) topology. In these 2D-CPs, each Ln center (La, Ce, and Sm in 1, 2, and 3, respectively) could be considered as a triconnected node, linked by three bridging bisphosphoramide ligands as two-connecting linkers. In contrast, 4 is a discrete binuclear complex, in which bidentate L ill ligand has two entirely different conformations: the syn-chelating and the anti bridging. Cationic complex 5 shows the monomeric structure, where bidentate L-III adopts the syn-chelating conformation. A comprehensive luminescence investigation has been performed on free ligands and their corresponding complexes as well. The synthesized compounds display a variety of luminescence behavior, including the ligand-centered fluorescence in 1, 2, and 5, two distinct emission peaks in 1 and 2, characteristic Sm-centered f-f emission in 3 and 4, and excitation-dependent emission in L-III, 1, and 2. Furthermore, the time dependent density functional theory (TD-DFT) study was carried out on the reported compounds to understand the nature of the emission peaks and the observed luminescence properties. The solid-state emission quantum yields of lanthanide complexes were also determined at different excitation wavelengths.

  • Název v anglickém jazyce

    Relations between Structural and Luminescence Properties of Novel Lanthanide Nitrate Complexes with Bis-phosphoramidate Ligands

  • Popis výsledku anglicky

    Five new bisphosphoramide-based Ln(III) nitrate complexes [La-2(NO3)(6)L-3(I)](n) (1), [Ce-2(NO3)(6)L-3(I)](n) (2), [Sm-2(NO3)(6)L-3(II)](n), (3), Sm-2(NO3)(6)L-3(III) (4), and Er(NO3)(3)L-2(III) (5) [L-I = piperazine-1,4-diylbis(diphenyl phosphine oxide), L-II = N,N&apos;-(ethane-1,2-diyl)bis(N-methyl-P,P-diphenylphosphinic amide, and L-II = N,N&apos;-(ethane-1,2-diyl)bis(P,P-diphenylphosphinic amide)] have been synthesized and characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis (TGA), and single crystal X-ray and powder diffractions. The results of the X-ray diffraction analysis revealed the new polymorph of L-III, and the structural diversity of the synthesized complexes in the solid state. Complexes 1-3 display two-dimensional coordination polymers (2D-CP), containing layers with honeycomb (6, 3) topology. In these 2D-CPs, each Ln center (La, Ce, and Sm in 1, 2, and 3, respectively) could be considered as a triconnected node, linked by three bridging bisphosphoramide ligands as two-connecting linkers. In contrast, 4 is a discrete binuclear complex, in which bidentate L ill ligand has two entirely different conformations: the syn-chelating and the anti bridging. Cationic complex 5 shows the monomeric structure, where bidentate L-III adopts the syn-chelating conformation. A comprehensive luminescence investigation has been performed on free ligands and their corresponding complexes as well. The synthesized compounds display a variety of luminescence behavior, including the ligand-centered fluorescence in 1, 2, and 5, two distinct emission peaks in 1 and 2, characteristic Sm-centered f-f emission in 3 and 4, and excitation-dependent emission in L-III, 1, and 2. Furthermore, the time dependent density functional theory (TD-DFT) study was carried out on the reported compounds to understand the nature of the emission peaks and the observed luminescence properties. The solid-state emission quantum yields of lanthanide complexes were also determined at different excitation wavelengths.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    10301 - Atomic, molecular and chemical physics (physics of atoms and molecules including collision, interaction with radiation, magnetic resonances, Mössbauer effect)

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2019

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Inorganic Chemistry

  • ISSN

    0020-1669

  • e-ISSN

  • Svazek periodika

    58

  • Číslo periodika v rámci svazku

    9

  • Stát vydavatele periodika

    US - Spojené státy americké

  • Počet stran výsledku

    16

  • Strana od-do

    5630-5645

  • Kód UT WoS článku

    000467351100035

  • EID výsledku v databázi Scopus

    2-s2.0-85064344018