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M

M. Manuela M. Raposo

Researcher at University of Minho

Publications -  304
Citations -  6066

M. Manuela M. Raposo is an academic researcher from University of Minho. The author has contributed to research in topics: Thiophene & Adsorption. The author has an hindex of 40, co-authored 288 publications receiving 5365 citations. Previous affiliations of M. Manuela M. Raposo include University of São Paulo & Faculdade de Ciências e Tecnologia da Universidade Nova de Lisboa.

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Water VUV electronic state spectroscopy by synchrotron radiation

TL;DR: In this article, the authors presented the highest resolution (∼0.075nm) measurements in the energy range 6.0-11.0 eV and allowed a detailed analysis of several new vibrational progressions to be observed in the 8.5-10 eV region and enabled them to assign the Rydberg series in the 9.9-10.8 eV energy absorption for the first time.
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Kinetics of Adsorption of Poly(o-methoxyaniline) Self-Assembled Films

TL;DR: In this article, the kinetics of adsorption of poly(o-methoxyaniline) (POMA) via self-assembly was investigated using UV-vis spectroscopy.
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Synthesis and ion sensing properties of new colorimetric and fluorimetric chemosensors based on bithienyl-imidazo-anthraquinone chromophores.

TL;DR: Novel colorimetric receptors for fluoride ion sensing containing anthraquinone as a chromogenic signaling unit and imidazo-2,2'-bithiophene binding sites are reported.

A Guide for Atomic Force Microscopy Analysis of Soft- Condensed Matter

TL;DR: In this paper, the most common causes of image artifacts are reviewed, solutions to avoid them proposed and good practices suggested, and quantities used to evaluate surface topographic features and its dynamics as result image processing data are also described.
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Synthesis and characterization of novel diazenes bearing pyrrole, thiophene and thiazole heterocycles as efficient photochromic and nonlinear optical (NLO) materials

TL;DR: In this paper, two series of novel thermally stable second-order nonlinear optical and photochromic chromophores have been designed and synthesized, which act simultaneously as π-conjugated bridges, together with diazoaryl or diazothiazolyl as acceptor moieties.