{"id":787,"date":"2022-01-17T16:29:16","date_gmt":"2022-01-17T16:29:16","guid":{"rendered":"http:\/\/ptnmr.dq.ua.pt\/wp\/?page_id=787"},"modified":"2022-02-15T15:57:31","modified_gmt":"2022-02-15T15:57:31","slug":"universidade-do-minho-cq","status":"publish","type":"page","link":"https:\/\/ptnmr.web.ua.pt\/index.php\/universidade-do-minho-cq\/","title":{"rendered":"Universidade do Minho – CQ"},"content":{"rendered":"

 <\/p>\n\n\n\n\n
\"\"<\/td>\n\n
Centro de Qu\u00edmica<\/div>\n
Universidade do Minho<\/div>\n
Campus de Gualtar<\/div>\n
4710-057 Braga<\/div>\n
Portugal<\/div>\n<\/td>\n
\n
Tel: + 351 253 604\u00a0378 \/ 80<\/div>\n<\/td>\n<\/tr>\n
\"\"<\/td>\n\n
NMR Equipment<\/h5>\n
    \n
  • Bruker Avance 400 III<\/li>\n<\/ul>\n<\/td>\n
\n
Unit Homepage<\/h5>\n

UMinho – CQ<\/a><\/p>\n

Booking | Scheduling<\/h5>\n

emp@quimica.uminho.pt<\/a><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

 <\/p>\n

Main Research Topics<\/h4>\n

Structural characterization of different compounds (heterocyclic compounds with biological activity and for materials, amino acids and peptides with biological activity and as sensors and probes, functionalized Carbon-Based Materials) using 1D- 1<\/sup>H, 13<\/sup>C, 19<\/sup>F and 31<\/sup>P spectra, and 2D NMR techniques including homonuclear 1<\/sup>H-1<\/sup>H and heteronuclear correlations 1<\/sup>H-13<\/sup>C and 1<\/sup>H-15<\/sup>N. Characterization of quadrupolar metallic (27<\/sup>Al, 71<\/sup>Ga) complexes, with relevance for medical imaging diagnostic.<\/p>\n

 <\/p>\n

Selected Publications<\/strong><\/p>\n

    \n
  1. Sousa, R. P. C. L.; Figueira, R. B.; Gomes, B. R.; Ferreira, R. C.; Costa, S. P. G.; Raposo, M. M. M. Hybrid sol-gel matrices doped with colorimetric\/fluorimetric imidazole derivatives. Nanomaterials<\/em> 2021, 11<\/em>(12), 3401. https:\/\/doi.org\/10.3390\/nano11123401<\/a>.<\/li>\n
  2. Gon\u00e7alves, R.; Pina, J.; Costa, S. P. G.; Raposo, M. M. M.; Synthesis and characterization of aryl-substituted BODIPY dyes displaying distinct solvatochromic singlet oxygen photosensitization efficiencies. Dyes Pigments <\/em>2021, 196<\/em>, 109784. https:\/\/doi.org\/10.1016\/j.dyepig.2021.109784<\/a><\/li>\n
  3. Moreira, ; Santos, P.; Faustino, M. A. F.; Raposo, M. M. M.; Costa, S. P. G.; Moura, N. M. M.; Gomes, A. T. P. C.; Almeida, A.; Neves, M. G. P. M. S. An insight into the synthesis of cationic porphyrin-imidazole derivatives and their photodynamic inactivation efficiency against Escherichia coli<\/em>. Dyes Pigments <\/em>2020, 178<\/em>, 108330. https:\/\/doi.org\/10.1016\/j.dyepig.2020.108330<\/a><\/li>\n
  4. Okda, H. E.; Sayed, S. E.; Ferreira, R. C. M.; Otri, I.; Costa, S. P. G.; Raposo, M. M. M., Mart\u00ednez-M\u00e1\u00f1ez, R. Sancen\u00f3n, A simple and easy-to-prepare imidazole-based probe for the selective chromofluorogenic recognition of biothiols and Cu(II) in aqueous environments. Dyes Pigments <\/em>2019, 162<\/em>, 303-308. https:\/\/doi.org\/10.1016\/j.dyepig.2018.10.017<\/a><\/li>\n
  5. Batista, R. M. F.; de Matos Gomes, E.; Raposo, M. M. M.; Costa, S. P. G.; Lopes, P. E.; Almeida, B.; Belsley, M. S. Self-assembling of dipeptide Boc-diphenylalanine nanotubes inside electrospun polymeric fibers with strong piezoelectric response. Nanoscale Adv. <\/em>2019,1<\/em>, 4339-4346. https:\/\/doi.org\/10.1039\/C9NA00464E<\/a><\/li>\n
  6. Garcia-Amor\u00f3s, ; Reig. M.; Castro, M. C. R.; Nonell, S.; Vilchez, S.; Esquena, J.; Raposo, M. M. M.; Velasco, D. Adaptable photochromic switches with self-aggregating heterocyclic azo dyes. J.<\/em> Phys.<\/em> Chem. C <\/em>2019, 123<\/em>(37), 23140\u221223144. <\/em>https:\/\/doi.org\/10.1021\/acs.jpcc.9b07527<\/a><\/li>\n
  7. Veloso, S.R.S.; Jervis, P.J.; Silva, J.F.G.; Hilliou, L.; Moura, C.; Pereira, D.M.; Coutinho, P.J.G.; Martins, J.A.; Castanheira, E.M.S.; Ferreira, P.M.T. Supramolecular ultra-short carboxybenzyl-protected dehydropeptide-based hydrogels for drug delivery”, Materials Science & Enginneering C, 2021, 122<\/em>, 111869, https:\/\/doi.org\/10.1016\/j.msec.2021.111869<\/a><\/li>\n
  8. Veloso, S.R.S.; Martins, J.A.; Hilliou, L.; Amorim, C.O.; Amaral, V.S.; Almeida, B.G.; Jervis, P.J.; Moreira, R.M.; Pereira, D.M.; Coutinho, P.J.G.; Ferreira, P.M.T.; Castanheira, E.M.S. Dehydropeptide-based plasmonic magnetogels: a supramolecular composite nanosystem for multimodal cancer therapy Mater. <\/em>Chem. B<\/em>, 2020, 8<\/em>, 45-64. https:\/\/doi.org\/10.1039\/C9TB01900F<\/a><\/li>\n
  9. Moreira, R.; Jervis, P. J.; Carvalho, A.; Ferreira, P.M.T.; Martins, J.A.; Valentao, P.; Andrade, P.B.; Pereira, D.M. Biological Evaluation of Naproxen-Dehydrodipeptide Conjugates with Self-Hydrogelation Capacity as Dual LOX\/COX Inhibitors\u201d Pharmaceutics, 2020, 12, 122. https:\/\/doi.org\/10.3390\/pharmaceutics12020122<\/a><\/li>\n
  10. Carvalho, A.; Gallo, J.; Pereira, D.M.; Valent\u00e3o, P.; Andrade, P.B.; Hilliou, L.; Ferreira, P.M.T. Ba\u00f1obre-L\u00f3pez, M.; Martins, J.A. Magnetic Dehydrodipeptide-Based Self-Assembled Hydrogels for Theragnostic Applications Nanomaterials<\/em>, 2019, 9<\/em>, 541. http:\/\/www.dx.doi.org\/10.3390\/nano9040541<\/a><\/li>\n
  11. Jervis, P.J.; Hilliou, L.; Pereira, R.B.; Pereira, D.M.; Martins, J.A.; Ferreira, P.M.T. Evaluation of a Model Photo-Caged Dehydropeptide as a Stimuli-Responsive Supramolecular Hydrogel Nanomaterials<\/em>, 2021, 11<\/em>, 3, 704. http:\/\/dx.doi.org\/10.3390\/nano11030704<\/a><\/li>\n
  12. Amorim, C.; Veloso, S.R.S.; Castanheira, E.M.S.; Hilliou, L.; Pereira, R.B.; Pereira, D.M. Martins, J.A.; Jervis, P.J.; Ferreira, P.M.T. Bolaamphiphilic Bis-Dehydropeptide Hydrogels as Potential Drug Release Systems Gels<\/em>, 2021, 7, 52. http:\/\/dx.doi.org\/10.3390\/gels7020052<\/a><\/li>\n
  13. 13-Leit\u00e3o, M. I. P.S., Raju, B. R., Cerqueira, N. M. F. S. A., Sousa, M. J., Gon\u00e7alves, M. S. T., Benzo[a<\/em>]phenoxazinium chlorides: synthesis, antiproliferative activity, in silico studies and evaluation as fluorescent probes, Bioorganic Chemistry<\/em> 2020, 98, 103730. https:\/\/doi.org\/10.1016\/j.bioorg.2020.103730<\/a><\/li>\n
  14. Fernandes, M. J. G., Pereira, R. B., Pereira, D. M., Fortes, A. G., Castanheira, E. M. S., Gon\u00e7alves, M. S. T., New eugenol derivatives with enhanced insecticidal activity, International Journal of Molecular Sciences<\/em> 2020, 21, 9257. https:\/\/doi.org\/10.3390\/ijms21239257<\/a><\/li>\n
  15. Pinto, N. F. S., Fernandes, M. J. G., Pereira, B., Vieira, T. F., Rodrigues, A. R. O., Pereira, D. M., Sousa, S. F., Castanheira, E. M. S., Fortes, A. G., Gon\u00e7alves, M. S.T.,\u00a0<\/sup>Amino alcohols from eugenol as potential semisynthetic insecticides: chemical, biological and computational insights, Molecules <\/em>2021, 26, 6616. https:\/\/doi.org\/10.3390\/molecules26216616<\/a><\/li>\n
  16. Rodrigues, J. M.; Cend\u00f3n, B.; Gul\u00edas, M.; Mascare\u00f1as, J. L.; Queiroz, M.-J.R.P. Rhodium(III)\u2010catalyzed formal cycloaddition between thienopyridine\/thienopyrazine carboxylic acids and alkynes, triggered by C\u2010H activation J. Org. Chem. <\/em>2021, 3234-3240. https:\/\/doi.org\/10.1002\/ejoc.202100439<\/a><\/li>\n
  17. Silva, B.R.; Rebelo, R.; Rodrigues, J. M., Xavier, C.P.R.; Vasconcelos, M. H.; Queiroz, M.-J.R.P. Synthesis of Novel Methyl 3-(hetero)arylthieno[3,2-b<\/em>]pyridine-2-carboxylates and Antitumor Activity Evaluation: Studies In Vitro and In Ovo Grafts of Chick Chorioallantoic Membrane (CAM) with a Triple Negative Breast Cancer Cell Lines, Molecules<\/em> 2021, 26<\/em>, 1594 (15pp). https:\/\/doi.org\/10.3390\/molecules26061594<\/a><\/li>\n
  18. Rodrigues, J. M.; Calhelha, R. C; Nogueira, A.; Ferreira, I. C.F.R.; Barros, L.; Queiroz, M.-J.R.P. Synthesis of Novel Methyl 7-[(Hetero)arylamino]thieno[2,3-b]pyrazine-6-carboxylates and Antitumor Activity Evaluation: Effects in Human Tumor Cells Growth, Cell Cycle Analysis, Apoptosis and Toxicity in Non-Tumor Cells Molecules <\/em>2021, 26, 4823 (14pp). https:\/\/doi.org\/10.3390\/molecules26164823<\/a><\/li>\n
  19. Sousa, C.E.A.; Alves, M. J.; Synthesis of novel sugar derived aziridines, as starting materials giving access to sugar amino acid derivatives\u201d Amino Acids<\/em>, 2021, 53<\/em>(7), 1123-1134. https:\/\/doi.org\/1007\/s00726-021-03017-4<\/a><\/li>\n
  20. Freitas, D. S.; Sousa, C. E. A.; Parente, J.; Drogalin, A.; Gil Fortes, A.; Cerqueira, N. M. F. S. A.; Alves, M. J. \u201c(3S,4R)-3,4-Dihydroxy-N-alkyl-L-homoprolines: Synthesis and Computational Mechanistic Studies\u201d & Biomol. Chem.<\/em>, 2019, 17<\/em>, 10052\u201310064. https:\/\/doi.org\/10.1039\/C9OB02141H<\/a><\/li>\n
  21. Oliveira-Pinto, ; Pontes, O., Lopes, D.; Sampaio-Marques, B.; Costa, M. D.; Carvalho, L.; Gon\u00e7alves, C.S.; Costa, B. M.; Maciel, P.; Ludovico, P.;<\/a> Baltazar, F.;<\/a> Proen\u00e7a F.; Costa, M. Unravelling the anticancer potential of functionalized chromeno[2,3-b<\/em>]pyridines for breast cancer treatment Bioorg. Chem.<\/em>, 2020, 100<\/em>, 103942. https:\/\/doi.org\/10.1016\/j.bioorg.2020.103942<\/a><\/li>\n
  22. Lopes, D.; Costa, M.; Lou\u00e7ano, J.; Proen\u00e7a, Fernanda \u201cA Convenient One-pot Synthesis of Chromenyl Acrylates and Acrylonitriles\u201d Synlett<\/em>, 2020, 31<\/em>(13), 1298-1302. https:\/\/doi.org\/10.1055\/s-0039-1690880<\/a><\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"

      Centro de Qu\u00edmica Universidade do Minho Campus de Gualtar 4710-057 Braga Portugal Tel: + 351 253 604\u00a0378 \/ 80 NMR Equipment Bruker Avance 400 III Unit Homepage UMinho – CQ Booking | Scheduling emp@quimica.uminho.pt   Main Research Topics Structural characterization of different compounds (heterocyclic compounds with biological activity and for materials, amino acids and… Read More »Universidade do Minho – CQ<\/span><\/a><\/p>\n","protected":false},"author":4,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"neve_meta_sidebar":"","neve_meta_container":"","neve_meta_enable_content_width":"off","neve_meta_content_width":100,"neve_meta_title_alignment":"","neve_meta_author_avatar":"","neve_post_elements_order":"","neve_meta_disable_header":"","neve_meta_disable_footer":"","neve_meta_disable_title":""},"_links":{"self":[{"href":"https:\/\/ptnmr.web.ua.pt\/index.php\/wp-json\/wp\/v2\/pages\/787"}],"collection":[{"href":"https:\/\/ptnmr.web.ua.pt\/index.php\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/ptnmr.web.ua.pt\/index.php\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/ptnmr.web.ua.pt\/index.php\/wp-json\/wp\/v2\/users\/4"}],"replies":[{"embeddable":true,"href":"https:\/\/ptnmr.web.ua.pt\/index.php\/wp-json\/wp\/v2\/comments?post=787"}],"version-history":[{"count":14,"href":"https:\/\/ptnmr.web.ua.pt\/index.php\/wp-json\/wp\/v2\/pages\/787\/revisions"}],"predecessor-version":[{"id":3274,"href":"https:\/\/ptnmr.web.ua.pt\/index.php\/wp-json\/wp\/v2\/pages\/787\/revisions\/3274"}],"wp:attachment":[{"href":"https:\/\/ptnmr.web.ua.pt\/index.php\/wp-json\/wp\/v2\/media?parent=787"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}