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Pregled bibliografske jedinice broj: 945894

2 H magic-angle spinning NMR and powder diffraction study of deuterated paramagnetic copper(II) glycinato complexes. Information on crystallographic symmetries, stereo-isomerism, and molecular mobility available from ssNMR spectra


Szalontai, Gábor; Csonka, Róbert; Kaizer, József; Bombicz, Petra; Sabolović, Jasmina
2 H magic-angle spinning NMR and powder diffraction study of deuterated paramagnetic copper(II) glycinato complexes. Information on crystallographic symmetries, stereo-isomerism, and molecular mobility available from ssNMR spectra // Inorganica chimica acta, 472 (2018), 320-329 doi:10.1016/j.ica.2017.05.071 (međunarodna recenzija, članak, znanstveni)


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Naslov
2 H magic-angle spinning NMR and powder diffraction study of deuterated paramagnetic copper(II) glycinato complexes. Information on crystallographic symmetries, stereo-isomerism, and molecular mobility available from ssNMR spectra

Autori
Szalontai, Gábor ; Csonka, Róbert ; Kaizer, József ; Bombicz, Petra ; Sabolović, Jasmina

Izvornik
Inorganica chimica acta (0020-1693) 472 (2018); 320-329

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
2H MAS NMR Paramagnetic bis(glycinato-d4)copper(II) complexes ; Effects of crystallographic symmetry and molecular mobility ; Conformational dependence ; Karplus-like correlations

Sažetak
Effects of stereochemistry, polymorphism, crystal packing, and solid phase mobility on the 2H magic-angle spinning (MAS) NMR spectra of the paramagnetic Cu(II) glycinato complexes have been investigated. The reliability of information obtained from the spectra, such as symmetry relations within a molecule, number of chemical sites or molecules found in the asymmetric units, was confirmed by previously published X-ray crystal and molecular structures. From the 2H MAS spectra, complemented with powder diffractograms of the synthetized bis(glycinato-d4)copper(II) complexes, we could identify three solid phases, namely the cis aqua and non-aqua forms and the trans non-aqua crystals. A fourth sample was identified as octahedral copper(II) complex chain with bidentate glycine and NO3 ligands in the octahedral building units. Correlations between the sign and magnitude of the observed paramagnetic shifts and the number of bonds and/or the dihedral angles connecting the actual 2H nucleus and the paramagnetic center, useful in structural assignments, were revealed. The agreement of the 2H MAS NMR spectral information with the available crystal diffraction data forecast their applicability in NMR crystallographic works too.

Izvorni jezik
Engleski

Znanstvena područja
Fizika, Kemija



POVEZANOST RADA


Projekti:
022-0222148-2822 - Modeliranje i međudjelovanje kompleksa prijelaznih metala i bioliganada (Sabolović, Jasmina, MZOS ) ( CroRIS)

Ustanove:
Institut za medicinska istraživanja i medicinu rada, Zagreb

Profili:

Avatar Url Jasmina Sabolović (autor)

Poveznice na cjeloviti tekst rada:

doi www.sciencedirect.com doi.org

Citiraj ovu publikaciju:

Szalontai, Gábor; Csonka, Róbert; Kaizer, József; Bombicz, Petra; Sabolović, Jasmina
2 H magic-angle spinning NMR and powder diffraction study of deuterated paramagnetic copper(II) glycinato complexes. Information on crystallographic symmetries, stereo-isomerism, and molecular mobility available from ssNMR spectra // Inorganica chimica acta, 472 (2018), 320-329 doi:10.1016/j.ica.2017.05.071 (međunarodna recenzija, članak, znanstveni)
Szalontai, G., Csonka, R., Kaizer, J., Bombicz, P. & Sabolović, J. (2018) 2 H magic-angle spinning NMR and powder diffraction study of deuterated paramagnetic copper(II) glycinato complexes. Information on crystallographic symmetries, stereo-isomerism, and molecular mobility available from ssNMR spectra. Inorganica chimica acta, 472, 320-329 doi:10.1016/j.ica.2017.05.071.
@article{article, author = {Szalontai, G\'{a}bor and Csonka, R\'{o}bert and Kaizer, J\'{o}zsef and Bombicz, Petra and Sabolovi\'{c}, Jasmina}, year = {2018}, pages = {320-329}, DOI = {10.1016/j.ica.2017.05.071}, keywords = {2H MAS NMR Paramagnetic bis(glycinato-d4)copper(II) complexes, Effects of crystallographic symmetry and molecular mobility, Conformational dependence, Karplus-like correlations}, journal = {Inorganica chimica acta}, doi = {10.1016/j.ica.2017.05.071}, volume = {472}, issn = {0020-1693}, title = {2 H magic-angle spinning NMR and powder diffraction study of deuterated paramagnetic copper(II) glycinato complexes. Information on crystallographic symmetries, stereo-isomerism, and molecular mobility available from ssNMR spectra}, keyword = {2H MAS NMR Paramagnetic bis(glycinato-d4)copper(II) complexes, Effects of crystallographic symmetry and molecular mobility, Conformational dependence, Karplus-like correlations} }
@article{article, author = {Szalontai, G\'{a}bor and Csonka, R\'{o}bert and Kaizer, J\'{o}zsef and Bombicz, Petra and Sabolovi\'{c}, Jasmina}, year = {2018}, pages = {320-329}, DOI = {10.1016/j.ica.2017.05.071}, keywords = {2H MAS NMR Paramagnetic bis(glycinato-d4)copper(II) complexes, Effects of crystallographic symmetry and molecular mobility, Conformational dependence, Karplus-like correlations}, journal = {Inorganica chimica acta}, doi = {10.1016/j.ica.2017.05.071}, volume = {472}, issn = {0020-1693}, title = {2 H magic-angle spinning NMR and powder diffraction study of deuterated paramagnetic copper(II) glycinato complexes. Information on crystallographic symmetries, stereo-isomerism, and molecular mobility available from ssNMR spectra}, keyword = {2H MAS NMR Paramagnetic bis(glycinato-d4)copper(II) complexes, Effects of crystallographic symmetry and molecular mobility, Conformational dependence, Karplus-like correlations} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus


Uključenost u ostale bibliografske baze podataka::


  • CA Search (Chemical Abstracts)
  • Cahiers Bibliographiques de Chimie
  • FIZ Karlsruhe
  • PASCAL/CNRS
  • Physikalische Berichte


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