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Andreia Leite

Researcher at University of Porto

Publications -  60
Citations -  739

Andreia Leite is an academic researcher from University of Porto. The author has contributed to research in topics: Chemistry & Interferometry. The author has an hindex of 16, co-authored 53 publications receiving 651 citations.

Papers
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Hybrid sol-gel channel waveguide patterning using photoinitiator-free materials

TL;DR: In this paper, an organic-inorganic sol-gel glass channel waveguide was constructed by ultraviolet photopolymerization of material synthesized from the precursor methacryloxypropyltrimethoxysilane using a pulsed 248nm excimer laser.
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Novel tetradentate chelators derived from 3-hydroxy-4-pyridinone units: synthesis, characterization and aqueous solution properties

TL;DR: In this article, the synthesis and characterization of three novel tetradentate ligands (T1, T2 and T3) based on 3-hydroxy-4-pyridinone chelating units are described.
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Antibacterial activity of naphthyl derived bis-(3-hydroxy-4-pyridinonate) copper(II) complexes against multidrug-resistant bacteria.

TL;DR: The complex Cu(naph1pp)2 shows the highest antibacterial activity, including against multidrug-resistant isolates, nonetheless, being more active against Gram-positive than Gram-negative bacteria.
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Synthesis and coordination studies of 5-(4′-carboxyphenyl)-10,15,20-tris(pentafluorophenyl)porphyrin and its pyrrolidine-fused chlorin derivative

TL;DR: In this paper, a synthetic strategy to obtain 5-(4′-carboxyphenyl)-10,15,20-tris(pentafluorophenyl)porphyrin and its pyrrolidine-fused chlorin derivative was developed by the 1,3-dipolar cycloaddition of a carbomethoxyphensyl substituted porphyrin with an azomethine ylide, followed by hydrolysis under thermal acidic conditions.
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Distinctive EPR signals provide an understanding of the affinity of bis-(3-hydroxy-4-pyridinonato) copper(II) complexes for hydrophobic environments.

TL;DR: The use of EPR spectroscopy is put forward to assess the affinity of copper(ii) complexes for a hydrophobic environment and also to obtain indirect information about the lipophilicity of the ligands and similar EPR silent complexes.