Susana P. G. Costa

ORCID: 0000-0001-7915-4720
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Molecular Sensors and Ion Detection
  • Photochromic and Fluorescence Chemistry
  • Luminescence and Fluorescent Materials
  • Analytical Chemistry and Sensors
  • Radical Photochemical Reactions
  • Chemical Synthesis and Analysis
  • Multicomponent Synthesis of Heterocycles
  • Synthesis and biological activity
  • Porphyrin and Phthalocyanine Chemistry
  • Click Chemistry and Applications
  • Nonlinear Optical Materials Research
  • Inorganic and Organometallic Chemistry
  • Photochemistry and Electron Transfer Studies
  • Advanced Chemical Sensor Technologies
  • Synthesis of Organic Compounds
  • Analytical Chemistry and Chromatography
  • Carbohydrate Chemistry and Synthesis
  • Synthesis of Indole Derivatives
  • Photoreceptor and optogenetics research
  • Synthesis and Characterization of Heterocyclic Compounds
  • Nonlinear Optical Materials Studies
  • Nanoplatforms for cancer theranostics
  • Advanced biosensing and bioanalysis techniques
  • Conducting polymers and applications
  • bioluminescence and chemiluminescence research

University of Minho
2016-2025

University of Coimbra
2007-2022

Instituto Superior da Maia
2022

Clinical Academic Center of Braga
2015-2021

Rede de Química e Tecnologia
2003-2015

University of Aveiro
2013-2015

Universidade Nova de Lisboa
2007

Universidade do Porto
2003

Novel colorimetric receptors for fluoride ion sensing containing anthraquinone as a chromogenic signaling unit and imidazo-2,2'-bithiophene binding sites are reported. Well-defined color change was observed upon addition of ions to acetonitrile solutions 2. Compounds 2a−c, deprotonated after addition, were studied metal chemosensors in the presence Zn(II), Hg(II), Cu(II) solutions, especially compound 2a which displayed marked from pink yellow-gold colors complexation.

10.1021/ol071029b article EN Organic Letters 2007-07-24

Four imidazoanthraquinone derivatives (2a-d) were synthesized and characterized their coordination behavior against selected anions cations tested. Acetonitrile solutions of probes showed charge-transfer absorptions in the 407-465 nm range. The four emitted 533-571 interval. recognition ability 2a-d was evaluated presence F(-), Cl(-), Br(-), I(-), OCN(-), BzO(-), ClO4(-), AcO(-), HSO4(-), H2PO4(-), CN(-). Only H2PO4(-) induced a new red-shifted absorption band that attributed to...

10.1021/jo501515e article EN The Journal of Organic Chemistry 2014-11-03

In chronic wound (CW) scenarios, Staphylococcus aureus-induced infections are very prevalent. This leads to abnormal inflammatory processes, in which proteolytic enzymes, such as human neutrophil elastase (HNE), become highly expressed. Alanine-Alanine-Proline-Valine (AAPV) is an antimicrobial tetrapeptide capable of suppressing the HNE activity, restoring its expression standard rates. Here, we proposed incorporation peptide AAPV within innovative co-axial drug delivery system, liberation...

10.1016/j.bioadv.2023.213488 article EN cc-by-nc-nd Biomaterials Advances 2023-06-01

Chronic wounds represent a serious worldwide concern, being often associated with bacterial infections. As the prevalence of infections increase, it is crucial to search for alternatives. Essential oils (EOs) constitute promising option antibiotics due their strong anti-inflammatory, analgesic, antioxidant and antibacterial properties. However, such compounds present high volatility. To address this issue, drug delivery system composed coaxial wet-spun fibers was engineered different EOs,...

10.1016/j.ijbiomac.2024.134565 article EN cc-by International Journal of Biological Macromolecules 2024-08-06

Fluorescent labelling is a versatile tool to visualize biomolecules containing primary amines in their cellular environment, allowing the study of function or interactions. Here, three organic fluorophores that can irreversibly bind amine group on target biomolecule are reported. They consist push–pull heterocyclic dyes based bithiophene and incorporating terminal N -hydroxysuccinimidyl ester as reactive for groups from (poly)amines, peptides proteins. Their potential chemosensors amines,...

10.1098/rsos.241816 article EN cc-by Royal Society Open Science 2025-02-01

Abstract A series of nonlinear optical chromophores 6 containing a substituted benzothiazole ring have been synthesized and characterized. 1,3‐Benzothiazoles were prepared by treating various formyl derivatives thienyl compounds with ortho ‐aminobenzenethiol in fair to excellent yields. These turn Suzuki coupling between aryl precursors. The electronic interactions donor acceptor end groups the conjugated 1,3‐benzothiazoles are revealed intense markedly solvatochromic CT transitions....

10.1002/ejoc.200600059 article EN European Journal of Organic Chemistry 2006-07-05

A family of heterocyclic thiosemicarbazone dyes (3a-f and 4) containing furyl groups was synthesized in good yields, characterized their response acetonitrile the presence selected anions studied. Acetonitrile solutions 3a-f 4 showed absorption bands 335-396 nm range which are modulated by electron donor or acceptor strength systems appended to moiety. Fluoride, chloride, bromide, iodide, dihydrogen phosphate, hydrogen sulphate, nitrate, acetate cyanide were used recognition studies. From...

10.1039/c2ob26200b article EN Organic & Biomolecular Chemistry 2012-01-01

The synthesis and comprehensive characterization of the excited states four novel triphenylamine-benzimidazole derivatives has been undertaken in solution (ethanol methylcyclohexane) at room temperature. This includes determination absorption, fluorescence, triplet-triplet absorption spectra, together with quantum yields internal conversion, intersystem crossing, singlet oxygen. From overall data radiative radiationless rate constants could be obtained, it is shown that compounds are highly...

10.1021/jo401803u article EN The Journal of Organic Chemistry 2013-10-11

Seven new bioinspired chemosensors (2–4 and 7–10) based on fluorescent peptides were synthesized characterized by elemental analysis, 1H 13C NMR, melting point, matrix-assisted laser desorption–ionization time-of-flight mass spectrometry (MALDI-TOF-MS), IR UV–vis absorption emission spectroscopy. The interaction with transition- post-transition-metal ions (Cu2+, Ni2+, Ag+, Zn2+, Cd2+, Hg2+, Pb2+, Fe3+) has been explored fluorescence spectroscopy MALDI-TOF-MS. reported peptide systems,...

10.1021/ic200792t article EN Inorganic Chemistry 2011-08-17

Dipeptide biomaterials are strong piezoelectric materials that can convert applied mechanical forces into electricity. We have developed large-scale hybrid electrospun arrays containing N-tert-butoxycarbonyl (Boc) diphenylalanine in the form of nanotubes embedded biocompatible polymers. These nanofibers exhibit properties when a periodic force is applied. The nanostructured were produced by electrospinning technique. Optical absorption measurements show four bands spectral region 240-280 nm...

10.1039/c9na00464e article EN cc-by-nc Nanoscale Advances 2019-01-01

Novel imidazo-anthraquinones functionalised with indole and carbazole have been synthesised characterised their evaluation as colorimetric chemosensors was carried out in acetonitrile well acetonitrile/H2O (97:3) the presence of several anions such F− , Cl− Br− I− CN− AcO− BzO− . In addition, behaviour H+ OH− also studied. Upon addition to solutions compounds 1–3, a marked colour change from yellow orange observed fluorescence emission 1 2 switched 'on'. The recognition organic aqueous...

10.1080/10610278.2013.824082 article EN Supramolecular chemistry 2013-08-22

Unnatural amino acids with enhanced properties, such as increased complexing ability and luminescence, are considered to be highly attractive building blocks for bioinspired frameworks, probes biomolecule dynamics, sensitive fluorescent chemosensors, peptides molecular imaging, among others. Therefore, a novel series of emissive heterocyclic alanines bearing benzo[d]oxazolyl unit functionalized different π-spacers (aza)crown ether moieties was synthesized. The new compounds were completely...

10.3390/molecules28083326 article EN cc-by Molecules 2023-04-09

The synthesis of new fluorescent probes containing the thiophene andbenzoxazole moieties combined with an alanine residue is described. resulting highlyfluorescent heterocyclic derivatives respond via a quenching effect, withparamagnetic Cu(II) and Ni(II) metal ions diamagnetic Hg(II), as shown by theabsorption steady-state fluorescence spectroscopy studies. formation ofmononuclear or dinuclear complexes was postulated based on presence thefree carboxylic acid binding site also interaction...

10.3390/s7102096 article EN cc-by Sensors 2007-10-03
Coming Soon ...