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Formation of layered proton-conducting zirconium and titanium organophosphonates by topotactic reaction: physicochemical properties, proton dynamics, and atomic-resolution structure

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61389013%3A_____%2F20%3A00519074" target="_blank" >RIV/61389013:_____/20:00519074 - isvavai.cz</a>

  • Nalezeny alternativní kódy

    RIV/00216275:25310/20:39916165

  • Výsledek na webu

    <a href="https://pubs.acs.org/doi/abs/10.1021/acs.inorgchem.9b02755" target="_blank" >https://pubs.acs.org/doi/abs/10.1021/acs.inorgchem.9b02755</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/acs.inorgchem.9b02755" target="_blank" >10.1021/acs.inorgchem.9b02755</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Formation of layered proton-conducting zirconium and titanium organophosphonates by topotactic reaction: physicochemical properties, proton dynamics, and atomic-resolution structure

  • Popis výsledku v původním jazyce

    A series of new zirconium and titanium phosphates-organophosphonates, in which the organophosphonate moiety is functionalized with a sulfo group, was prepared by a topotactic reaction involving the gamma modification of zirconium or titanium hydrogen phosphate with 2-bis(phosphonomethyl)amino-ethan-1-sulfonic acid (H4TDP). H4TDP represents a new type of functionalizing agent, which can be easily prepared by a Moedritzer–Irani reaction from taurine (2-aminoethanesulfonic acid). The gamma modification of zirconium hydrogen phosphate (γ-ZrP) with H4TDP provides mixed phosphate-organophosphonate compounds with the formula Zr(PO4)(H2PO4)1–2x(H2TDP)x·yH2O, where x = 0.15, 0.34, 0.45, and is controlled by the γ-ZrP/H4TDP ratio in the starting mixture. On the contrary, by the topotactic gamma modification of titanium hydrogen phosphate (γ-TiP) with H4TDP, only one product with the formula Ti(PO4)(H2PO4)1–2z(H2TDP)z·yH2O, where z = 0.41 ± 0.01, was obtained regardless of the composition of the starting mixture. The synthesized compounds were characterized by elemental analysis, thermogravimetric analysis, energy-dispersive X-ray analysis, and infrared spectroscopy. The way the topotactic reaction proceeds and how the grafted organophosphonate groups are bonded to the layers of the host structure were suggested on the basis of the solid-state NMR data. It was found that the grafted moieties are spread evenly in the host layers among the hydrogen phosphate groups. The obtained solids are able to intercalate basic molecules, as was proved by the intercalation reactions of the zirconium series with butylamine. The amount of intercalated butylamine increases with increasing x. It is known that both host compounds, γ-ZrP and γ-TiP, are protonic conductors. It was found that the incorporation of H2TDP increases conductivity of the zirconium compound when x = 0.15, but further incorporation of H2TDP into the γ-ZrP host structure leads to a decrease of conductivity. This behavior is explained on the basis of the 1H MAS and the 1H–1H EXSY NMR data.

  • Název v anglickém jazyce

    Formation of layered proton-conducting zirconium and titanium organophosphonates by topotactic reaction: physicochemical properties, proton dynamics, and atomic-resolution structure

  • Popis výsledku anglicky

    A series of new zirconium and titanium phosphates-organophosphonates, in which the organophosphonate moiety is functionalized with a sulfo group, was prepared by a topotactic reaction involving the gamma modification of zirconium or titanium hydrogen phosphate with 2-bis(phosphonomethyl)amino-ethan-1-sulfonic acid (H4TDP). H4TDP represents a new type of functionalizing agent, which can be easily prepared by a Moedritzer–Irani reaction from taurine (2-aminoethanesulfonic acid). The gamma modification of zirconium hydrogen phosphate (γ-ZrP) with H4TDP provides mixed phosphate-organophosphonate compounds with the formula Zr(PO4)(H2PO4)1–2x(H2TDP)x·yH2O, where x = 0.15, 0.34, 0.45, and is controlled by the γ-ZrP/H4TDP ratio in the starting mixture. On the contrary, by the topotactic gamma modification of titanium hydrogen phosphate (γ-TiP) with H4TDP, only one product with the formula Ti(PO4)(H2PO4)1–2z(H2TDP)z·yH2O, where z = 0.41 ± 0.01, was obtained regardless of the composition of the starting mixture. The synthesized compounds were characterized by elemental analysis, thermogravimetric analysis, energy-dispersive X-ray analysis, and infrared spectroscopy. The way the topotactic reaction proceeds and how the grafted organophosphonate groups are bonded to the layers of the host structure were suggested on the basis of the solid-state NMR data. It was found that the grafted moieties are spread evenly in the host layers among the hydrogen phosphate groups. The obtained solids are able to intercalate basic molecules, as was proved by the intercalation reactions of the zirconium series with butylamine. The amount of intercalated butylamine increases with increasing x. It is known that both host compounds, γ-ZrP and γ-TiP, are protonic conductors. It was found that the incorporation of H2TDP increases conductivity of the zirconium compound when x = 0.15, but further incorporation of H2TDP into the γ-ZrP host structure leads to a decrease of conductivity. This behavior is explained on the basis of the 1H MAS and the 1H–1H EXSY NMR data.

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

    Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2020

  • 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

    59

  • Číslo periodika v rámci svazku

    1

  • Stát vydavatele periodika

    US - Spojené státy americké

  • Počet stran výsledku

    9

  • Strana od-do

    505-513

  • Kód UT WoS článku

    000506719300053

  • EID výsledku v databázi Scopus

    2-s2.0-85076720577