Počet záznamů: 1  

Efficient strategy for determining the atomic-resolution structure of micro- and nanocrystalline solids within polymeric microbeads: domain-edited NMR crystallography

  1. 1.
    SYSNO ASEP0491936
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevEfficient strategy for determining the atomic-resolution structure of micro- and nanocrystalline solids within polymeric microbeads: domain-edited NMR crystallography
    Tvůrce(i) Brus, Jiří (UMCH-V) RID, ORCID
    Czernek, Jiří (UMCH-V) RID
    Hrubý, Martin (UMCH-V) RID, ORCID
    Švec, Pavel (UMCH-V) RID, ORCID
    Kobera, Libor (UMCH-V) RID, ORCID
    Abbrent, Sabina (UMCH-V) RID, ORCID
    Urbanová, Martina (UMCH-V) RID, ORCID
    Zdroj.dok.Macromolecules. - : American Chemical Society - ISSN 0024-9297
    Roč. 51, č. 14 (2018), s. 5364-5374
    Poč.str.11 s.
    Jazyk dok.eng - angličtina
    Země vyd.US - Spojené státy americké
    Klíč. slovaNMR crystalography ; polymer microbeads ; solid-state self-assembly
    Vědní obor RIVCF - Fyzikální chemie a teoretická chemie
    Obor OECDPhysical chemistry
    CEPGA16-04109S GA ČR - Grantová agentura ČR
    LO1507 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    LM2015064 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    Institucionální podporaUMCH-V - RVO:61389013
    UT WOS000440105200035
    EID SCOPUS85050672452
    DOI10.1021/acs.macromol.8b00392
    AnotacePrecise structural analysis of multiphase polymeric nanocomposites remains a challenge even in the presence of high-quality X-ray diffraction data. This contribution thus addresses our attempt to formulate a combined analytical strategy for obtaining the atomic-resolution structure of multicomponent polymeric solids with complex nanodomain architecture. In this strategy, through the application of T1-filtered solid-state NMR spectroscopy, the individual components are successively distinguished and selected, and the corresponding 1H, 13C, and 15N isotropic chemical shifts are explicitly assigned. Thereafter, using an automated protocol allowing for processing and statistical analysis of large data sets, the experimentally determined NMR parameters are systematically compared with those DFT-calculated for the representative set of crystal structure predictions. Particular attention is devoted to the analysis of NMR parameters of hydrogen-bonded protons which are responsible for molecular packing. As a result of this search, the structures of micro- and nanosized crystallites dispersed in the polymeric matrix are determined and independently verified by the measurements of through-space dipolar couplings. The potential of this strategy is demonstrated on injectable polyanhydride microbeads consisting of a mixture of microcrystalline decitabine and nanocrystalline sebacic acid, both incorporated in the semicrystalline polymeric matrix of poly(sebacic acid). Through the synergistic interplay between the measurements, calculations, and the statistical analysis, we have developed an integrated approach providing structural information that is challenging to elucidate using conventional diffraction approaches. This combination of experimental and theoretical approaches enables one to determine the structural arrangements of molecules in situations which are not tractable by conventional spectroscopic techniques.
    PracovištěÚstav makromolekulární chemie
    KontaktEva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358
    Rok sběru2019
Počet záznamů: 1  

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