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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Materials Map under construction

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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693.932 PEOPLE
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Naji, M.
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Gomes, Clara

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (8/8 displayed)

  • 2023A Polymorph of Dipeptide Halide Glycyl-L-Alanine Hydroiodide Monohydrate: Crystal Structure, Optical Second Harmonic Generation, Piezoelectricity and Pyroelectricity4citations
  • 2023Reversible Single-Crystal-to-Single-Crystal Transformations in a salEen Fe(III) Spin Crossover Sponge10citations
  • 2019Cu(II) complexes derived from N-carboxymethyl and N-carboxyethyl amino acids as catalysts for asymmetric oxidative coupling of 2-naphthol6citations
  • 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
  • 2014Copper(ii) complexes of bis(aryl-imino)acenaphthene ligands25citations
  • 2011New tetradentate N,N,N,N-chelating α-diimine ligands and their corresponding zinc and nickel complexes46citations
  • 2009Trans-Chlorido(phen-yl)bis-(triphenyl-phosphine)nickel(II) and its 1:1 cocrystal with chloridobis(triphenyl-phosphine)nickel(I)5citations

Places of action

Chart of shared publication
Castro, M. Cidália R.
1 / 5 shared
Almeida, Bernardo
1 / 7 shared
Rodrigues, Manuel J. L. F.
1 / 2 shared
Gomes, Etelvina De Matos
1 / 6 shared
Belsley, Michael
1 / 7 shared
Freitas, R. B.
1 / 1 shared
Peixoto Oliveira, João Miguel
1 / 2 shared
Machado Da Silva, Bruna
1 / 4 shared
Veiga Rodrigues, Pedro
1 / 5 shared
Batista, Rosa M. F.
1 / 5 shared
Machado, Ana
1 / 8 shared
Keyes, Tia E.
1 / 1 shared
Sarangi, Nirod Kumar
1 / 1 shared
Lopes, Cátia S. D.
1 / 1 shared
Ferreira, Liliana P.
1 / 1 shared
Marques, Rafaela T.
1 / 1 shared
Bernardes, Carlos E. S.
1 / 2 shared
Martinho, Paulo N.
1 / 1 shared
Carvalho, M. Fernanda N. N.
1 / 2 shared
Teixeira, Carlos M.
1 / 1 shared
Adão, P.
1 / 1 shared
Pessoa, João Costa
1 / 3 shared
Kuznetsov, Maxim L.
1 / 1 shared
Gomes, Pedro T.
5 / 5 shared
Lopes, Patrícia S.
2 / 2 shared
Gomes, Joselaine C. S.
1 / 1 shared
Lemos, Francisco
1 / 1 shared
Figueira, Cláudia A.
3 / 3 shared
Veiros, Luís F.
1 / 1 shared
Lemos, M. Amélia N. D. A.
1 / 1 shared
Aullón, Gabriel
1 / 1 shared
Avilés, Teresa
1 / 4 shared
Santos, Carla I. M.
1 / 1 shared
Almeida, Rui M.
1 / 3 shared
Gonzalez, Pablo Javier
1 / 1 shared
Welter, Richard
1 / 2 shared
Rosa, V.
1 / 5 shared
Li, Lidong
2 / 2 shared
Fan, Zhiqiang
1 / 1 shared
Duarte, M. Teresa
2 / 3 shared
Chart of publication period
2023
2019
2018
2015
2014
2011
2009

Co-Authors (by relevance)

  • Castro, M. Cidália R.
  • Almeida, Bernardo
  • Rodrigues, Manuel J. L. F.
  • Gomes, Etelvina De Matos
  • Belsley, Michael
  • Freitas, R. B.
  • Peixoto Oliveira, João Miguel
  • Machado Da Silva, Bruna
  • Veiga Rodrigues, Pedro
  • Batista, Rosa M. F.
  • Machado, Ana
  • Keyes, Tia E.
  • Sarangi, Nirod Kumar
  • Lopes, Cátia S. D.
  • Ferreira, Liliana P.
  • Marques, Rafaela T.
  • Bernardes, Carlos E. S.
  • Martinho, Paulo N.
  • Carvalho, M. Fernanda N. N.
  • Teixeira, Carlos M.
  • Adão, P.
  • Pessoa, João Costa
  • Kuznetsov, Maxim L.
  • Gomes, Pedro T.
  • Lopes, Patrícia S.
  • Gomes, Joselaine C. S.
  • Lemos, Francisco
  • Figueira, Cláudia A.
  • Veiros, Luís F.
  • Lemos, M. Amélia N. D. A.
  • Aullón, Gabriel
  • Avilés, Teresa
  • Santos, Carla I. M.
  • Almeida, Rui M.
  • Gonzalez, Pablo Javier
  • Welter, Richard
  • Rosa, V.
  • Li, Lidong
  • Fan, Zhiqiang
  • Duarte, M. Teresa
OrganizationsLocationPeople

article

Cu(II) complexes derived from N-carboxymethyl and N-carboxyethyl amino acids as catalysts for asymmetric oxidative coupling of 2-naphthol

  • Gomes, Clara
  • Carvalho, M. Fernanda N. N.
  • Teixeira, Carlos M.
  • Adão, P.
  • Pessoa, João Costa
  • Kuznetsov, Maxim L.
Abstract

<p>The synthesis, characterization and catalytic performance of chiral Cu(II) complexes derived from N-carboxymethylated and N-carboxyethylated amino acids is reported. The ligand precursors are prepared by single step N-alkylation of the sodium salts of the appropriate chiral amino acid with either sodium chloroacetate or sodium 3-chloropropionate in water. The Cu(II) complexes are obtained upon reaction of Cu(CH<sub>3</sub>COO)<sub>2</sub> with the aqueous or alcoholic suspension of the suitable ligand under vigorous stirring or ultrasound irradiation at room temperature. The Cu(II) compounds are characterised by EPR, UV–vis, circular dichroism and ESI-MS. The molecular structures of two of the prepared complexes are also obtained by single-crystal X-ray diffraction analysis. The catalytic activity of the complexes in the asymmetric oxidative coupling of 2-naphthol is described. All compounds exhibit moderate activity, selectivity and enantioselectivity in ethanol/water mixtures, under aerobic conditions and using potassium iodide as additive. The yields of 1,1′-bi-2-naphthol (BINOL) reached 50% under the optimal conditions, while enantiomeric excesses reached ca. 48%. The effect of variables such as ligand substituents, solvent, temperature and additives on the catalytic activity is also described. In the absence of a base, the complexes only show catalytic activity in the presence of alkali metal iodide such as KI. Details of the oxidative coupling mechanism are studied using spectroscopic and electrochemical methodologies.</p>

Topics
  • impedance spectroscopy
  • compound
  • x-ray diffraction
  • Sodium
  • Potassium
  • electron spin resonance spectroscopy
  • molecular structure
  • electrospray ionisation
  • electrospray ionisation mass spectrometry