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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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (9/9 displayed)

  • 2021Natural Benzo/Acetophenones as Leads for New Synthetic Acetophenone Hybrids Containing a 1,2,3-Triazole Ring as Potential Antifouling Agents11citations
  • 2021Fabrication of biocompatible porous SAIB/silk fibroin scaffolds using ionic liquids12citations
  • 2016Preparation and characterization of electrical conductive PVA based materials for peripheral nerve tube-guides13citations
  • 2015Wetting behaviour of SAC305 solder on different substrates in high vacuum and inert atmosphere18citations
  • 2015Evaluation of biodegradable electric conductive tube-guides and mesenchymal stem cells21citations
  • 2014In vitro anticoagulant and antioxidant performance of a marine sulfated polysaccharidecitations
  • 2014Unveiling the physicochemical properties of a sulfated polysaccharide based on Ulvan with high biomedical potentialcitations
  • 2013TiAgx thin films for lower limb prosthesis pressure sensors: Effect of composition and structural changes on the electrical and thermal response of the films34citations
  • 2005Low-temperature deposition of weakly-stressed nanocrystalline silicon films by reactive magnetron sputtering3citations

Places of action

Chart of shared publication
Correia Da Silva, M.
1 / 3 shared
Pereira, D.
1 / 5 shared
Pinto, M.
1 / 6 shared
Cidade, H.
1 / 2 shared
Cardoso, J.
1 / 3 shared
Neves, Ar
1 / 2 shared
Vasconcelos, V.
1 / 8 shared
Almeida, Jr
1 / 2 shared
Sousa, E.
1 / 3 shared
Radhouani, H.
3 / 4 shared
Silva, S. S.
1 / 48 shared
Gomes, J. M.
1 / 2 shared
Maia, F. R.
1 / 7 shared
Reis, Rui Luís
3 / 1359 shared
Oliveira, J. M.
3 / 157 shared
Pereira, T.
2 / 6 shared
Mauricio, Ac
2 / 5 shared
Luis, Al
2 / 4 shared
Ribeiro, J.
2 / 4 shared
Santos, Jd
2 / 37 shared
Lopes, Ma
2 / 37 shared
Teixeira, S.
1 / 13 shared
Soares, D.
1 / 20 shared
Cerqueira, Mf
1 / 6 shared
Teixeira, Jc
1 / 9 shared
Macedo, F.
2 / 10 shared
Ribas, L.
1 / 6 shared
Lau, Cs
1 / 2 shared
Leitao, H.
1 / 2 shared
Caseiro, Ar
1 / 2 shared
Franca, M.
1 / 1 shared
Armada Da Silva, P.
1 / 1 shared
Amorim, I.
1 / 2 shared
Prada, J.
1 / 1 shared
Silva, Dm
1 / 4 shared
Amado, S.
1 / 3 shared
Geuna, S.
1 / 3 shared
Pires, I.
1 / 3 shared
Sousa, R. A.
2 / 104 shared
Gertrudes, A.
2 / 4 shared
Bacelar, A. H.
1 / 2 shared
Correia, C.
1 / 18 shared
Martin, N.
1 / 47 shared
Lopes, C.
1 / 27 shared
Fonseca, Carlos
1 / 27 shared
Alves, E.
1 / 129 shared
Vaz, F.
1 / 127 shared
Pedrosa, P.
1 / 20 shared
Barradas, Np
1 / 7 shared
Leconte, Y.
1 / 21 shared
Zellama, K.
1 / 10 shared
Bouchriha, H.
1 / 10 shared
Portier, X.
1 / 14 shared
Marie, P.
1 / 8 shared
Rizk, R.
1 / 4 shared
Ben Othman, Afef
1 / 1 shared
Daouahi, M.
1 / 1 shared
Chart of publication period
2021
2016
2015
2014
2013
2005

Co-Authors (by relevance)

  • Correia Da Silva, M.
  • Pereira, D.
  • Pinto, M.
  • Cidade, H.
  • Cardoso, J.
  • Neves, Ar
  • Vasconcelos, V.
  • Almeida, Jr
  • Sousa, E.
  • Radhouani, H.
  • Silva, S. S.
  • Gomes, J. M.
  • Maia, F. R.
  • Reis, Rui Luís
  • Oliveira, J. M.
  • Pereira, T.
  • Mauricio, Ac
  • Luis, Al
  • Ribeiro, J.
  • Santos, Jd
  • Lopes, Ma
  • Teixeira, S.
  • Soares, D.
  • Cerqueira, Mf
  • Teixeira, Jc
  • Macedo, F.
  • Ribas, L.
  • Lau, Cs
  • Leitao, H.
  • Caseiro, Ar
  • Franca, M.
  • Armada Da Silva, P.
  • Amorim, I.
  • Prada, J.
  • Silva, Dm
  • Amado, S.
  • Geuna, S.
  • Pires, I.
  • Sousa, R. A.
  • Gertrudes, A.
  • Bacelar, A. H.
  • Correia, C.
  • Martin, N.
  • Lopes, C.
  • Fonseca, Carlos
  • Alves, E.
  • Vaz, F.
  • Pedrosa, P.
  • Barradas, Np
  • Leconte, Y.
  • Zellama, K.
  • Bouchriha, H.
  • Portier, X.
  • Marie, P.
  • Rizk, R.
  • Ben Othman, Afef
  • Daouahi, M.
OrganizationsLocationPeople

article

Natural Benzo/Acetophenones as Leads for New Synthetic Acetophenone Hybrids Containing a 1,2,3-Triazole Ring as Potential Antifouling Agents

  • Correia Da Silva, M.
  • Pereira, D.
  • Pinto, M.
  • Cidade, H.
  • Cardoso, J.
  • Neves, Ar
  • Vasconcelos, V.
  • Almeida, Jr
  • Sousa, E.
  • Goncalves, C.
Abstract

Marine biofouling is a natural process that represents major economic, environmental, and health concerns. Some booster biocides have been used in biofouling control, however, they were found to accumulate in environmental compartments, showing negative effects on marine organisms. Therefore, it is urgent to develop new eco-friendly alternatives. Phenyl ketones, such as benzophenones and acetophenones, have been described as modulators of several biological activities, including antifouling activity (AF). In this work, acetophenones were combined with other chemical substrates through a 1,2,3-triazole ring, a strategy commonly used in Medicinal Chemistry. In our approach, a library of 14 new acetophenone-triazole hybrids was obtained through the copper(I)-catalyzed alkyne-azide cycloaddition "click" reaction. All of the synthesized compounds were evaluated against the settlement of a representative macrofouling species, Mytilus galloprovincialis, as well as on biofilm-forming marine microorganisms, including bacteria and fungi. The growth of the microalgae Navicula sp. was also evaluated after exposure to the most promising compounds. While compounds 6a, 7a, and 9a caused significant inhibition of the settlement of mussel larvae, compounds 3b, 4b, and 7b were able to inhibit Roseobacter litoralis bacterial biofilm growth. Interestingly, acetophenone 7a displayed activity against both mussel larvae and the microalgae Navicula sp., suggesting a complementary action of this compound against macro- and microfouling species. The most potent compounds (6a, 7a, and 9a) also showed to be less toxic to the non-target species Artemia salina than the biocide Econea(R). Regarding both AF potency and ecotoxicity activity evaluation, acetophenones 7a and 9a were put forward in this work as promising eco-friendly AF agents.

Topics
  • impedance spectroscopy
  • compound
  • laser emission spectroscopy
  • copper
  • forming
  • ketone
  • alkyne