Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2013Benzoxaborolate ligands in group 13 metal complexes14citations

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Chart of shared publication
Ziemkowska, Wanda
1 / 18 shared
Zygadło-Monikowska, Ewa
1 / 11 shared
Sporzyński, Andrzej
1 / 2 shared
Justyniak, Iwona
1 / 9 shared
Adamczyk-Woźniak, Agnieszka
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Cyrański, Michał K.
1 / 2 shared
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2013

Co-Authors (by relevance)

  • Ziemkowska, Wanda
  • Zygadło-Monikowska, Ewa
  • Sporzyński, Andrzej
  • Justyniak, Iwona
  • Adamczyk-Woźniak, Agnieszka
  • Cyrański, Michał K.
OrganizationsLocationPeople

article

Benzoxaborolate ligands in group 13 metal complexes

  • Ziemkowska, Wanda
  • Zygadło-Monikowska, Ewa
  • Sporzyński, Andrzej
  • Justyniak, Iwona
  • Adamczyk-Woźniak, Agnieszka
  • Jaśkowska, Eliza
  • Cyrański, Michał K.
Abstract

A series of group 13 metal benzoxaborolates [R2MOB(o-CH2O)(C6H4)]2 [R = tBu, M = Al (2), R = Me, M = Ga (3), R = tBu, M = Ga (4), R = tBu, M = In (5)] were synthesized in reactions of 1,3-dihydro-1-hydroxy-2,1-benzoxaborole (1) with group 13 metal trialkyls. The compounds were characterized by elemental analysis, melting point measurements, 1H, 13C NMR, and IR spectroscopy. The molecular structure of 2–5 was determined by single-crystal X-ray diffraction. The structure of the compounds depends on the kind of metallic center. Reaction of tBu3Al with the benzoxaborole 1 leads to the aluminum derivative 2, similar to typical dialkylaluminum carboxylates, with a central eight-membered B2Al2O4 ring, in which two oxygen atoms of the benzoxaborolate unit are bonded to aluminum atoms. In the presence of gallium and indium trialkyls, the benzoxaborole 1 acts as an alcohol yielding complexes 3–5, similar to dialkylmetal alkoxides, with a central M2O2 (where M = Ga, In) ring. Thermal decomposition of compounds 2 and 4 revealed the liberation of a mixture of organoboron compounds.

Topics
  • compound
  • x-ray diffraction
  • Oxygen
  • aluminium
  • Nuclear Magnetic Resonance spectroscopy
  • thermal decomposition
  • alcohol
  • molecular structure
  • infrared spectroscopy
  • elemental analysis
  • Gallium
  • Indium