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Francesco A. Bottino

Researcher at University of Catania

Publications -  154
Citations -  2209

Francesco A. Bottino is an academic researcher from University of Catania. The author has contributed to research in topics: Polystyrene & Thermal stability. The author has an hindex of 28, co-authored 154 publications receiving 2124 citations.

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Reaction of tosylamide monosodium salt with bis(halomethyl) compounds: an easy entry to symmetrical N-tosyl aza macrocycles

TL;DR: Synthese de composes crown azote, de diaza [3.3] meta- et paracyclophanes, de pyridinophanes as mentioned in this paper.
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Polystyrene-Clay Nanocomposites Prepared with Polymerizable Imidazolium Surfactants

TL;DR: In this article, polystyrene/montmorillonite nanocomposites were prepared via in situ bulk polymerization using new imidazolium salts, which facilitate the formation of partially exfoliated structures because of the presence in their structure of a polymerizable group.
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Calix[4]arenes with pyridine pendant groups. Regioselective proximal alkylation at the "lower rim"

TL;DR: La reaction de calix[4] arenes avec le chlorhydrate de chloromethyl-2 pyridine donne des tetrakis-[pyridyl]-2 methoxy] calix.
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Chemical modifications, mechanical properties and surface photo-oxidation of films of polystyrene (PS)

TL;DR: In this paper, polystyrene (PS) was exposed to accelerated weathering in a Xenotest Alpha apparatus to mimic outdoor conditions (λ≥300 nm), and the changes of the chemical structure in the films were studied by Fourier transform infrared spectroscopy (FT-IR) and the surface photo-oxidation by X-ray-photoelectron spectrograms (XPS).
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Thermal degradation of differently substituted Cyclopentyl Polyhedral Oligomeric Silsesquioxane (CP-POSS) nanoparticles

TL;DR: In this paper, seven substituted derivatives of polyhedral oligomeric silsesquioxanes (POSSs) with general formula R7R′1 (SiO1.5)8, where R- and R′- were a cyclopentyl and a substituted phenyl group, respectively, were prepared, and their compositions were checked by elemental analysis, 1H NMR and 13C NMR spectroscopy.