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 (2/2 displayed)

  • 2018New phenyl-nickel complexes of bulky 2-iminopyrrolyl chelates26citations
  • 2015Exploring the influence of steric hindrance and electronic nature of substituents in the supramolecular arrangements of 5-(substituted phenyl)-2-formylpyrroles15citations

Places of action

Chart of shared publication
Gomes, Pedro T.
2 / 5 shared
Gomes, Clara
2 / 8 shared
Gomes, Joselaine C. S.
1 / 1 shared
Lemos, Francisco
1 / 1 shared
Figueira, Cláudia A.
2 / 3 shared
Veiros, Luís F.
1 / 1 shared
Chart of publication period
2018
2015

Co-Authors (by relevance)

  • Gomes, Pedro T.
  • Gomes, Clara
  • Gomes, Joselaine C. S.
  • Lemos, Francisco
  • Figueira, Cláudia A.
  • Veiros, Luís F.
OrganizationsLocationPeople

article

New phenyl-nickel complexes of bulky 2-iminopyrrolyl chelates

  • Gomes, Pedro T.
  • Gomes, Clara
  • Lopes, Patrícia S.
  • Gomes, Joselaine C. S.
  • Lemos, Francisco
  • Figueira, Cláudia A.
Abstract

<p>A family of mono(2-iminopyrrolyl) complexes with the general formula [Ni{κ<sup>2</sup>N,N′-5-(aryl)-NC<sub>4</sub>H<sub>2</sub>-2-C(H)═N-2,6-(aryl)}(C<sub>6</sub>H<sub>5</sub>)(PPh<sub>3</sub>)] were obtained from the reaction of the sodium salts of the newly synthesised 5-aryl-2-(N-arylformimino)pyrroles with the square planar complex trans-[Ni(C<sub>6</sub>H<sub>5</sub>)(PPh<sub>3</sub>)<sub>2</sub>Cl]. These new iminopyrrole ligand precursors, designed with increasing bulkiness and different electronic properties, and their corresponding nickel(ii) complexes were characterised by NMR spectroscopy and elemental analysis, and their structural features were analysed by single crystal X-ray diffraction. The nickel complexes were tested as aluminium-free catalysts for the polymerisation of ethylene, at low to moderate pressures and different temperatures and in the absence or presence of the phosphine scavenger [Ni(COD)<sub>2</sub>], giving rise to catalytic activities in the range of 3.61-73.12 kg<sub>PE</sub> mol<sub>Ni</sub><sup>−1</sup> h<sup>−1</sup> bar<sup>−1</sup>. The polyethylene products formed in these catalytic reactions were characterised by GPC/SEC and NMR spectroscopy. Generally, low molecular weight (M<sub>n</sub> 510-1300 g mol<sup>−1</sup>) low viscosity oils were obtained, presenting high branching degrees (80-125 branches per 1000 C atoms), which are characteristic of hyperbranched polyethylene products. In particular, polymerisation reactions using catalyst 7 led to higher viscosity oils with molecular weights between 11 000 and 20 000 g mol<sup>−1</sup>, and branching degrees of 100-120 branches per 1000 C atoms.</p>

Topics
  • single crystal X-ray diffraction
  • single crystal
  • nickel
  • aluminium
  • Sodium
  • viscosity
  • molecular weight
  • size-exclusion chromatography
  • Nuclear Magnetic Resonance spectroscopy
  • elemental analysis