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Salvatore Failla

Researcher at University of Catania

Publications -  112
Citations -  1596

Salvatore Failla is an academic researcher from University of Catania. The author has contributed to research in topics: Schiff base & Phosphonate. The author has an hindex of 20, co-authored 109 publications receiving 1450 citations. Previous affiliations of Salvatore Failla include Sapienza University of Rome & University of Düsseldorf.

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Conformational investigation of N-aralkylpyridinium ions by Cotton-Mouten effect method

TL;DR: In this article, the same authors reported the molar Cotton-Mouton constants and refractions for N -aralkylpyridinium cations as solutes in water or acetonitrile.
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Supramolecular Aggregation/Deaggregation in Amphiphilic Dipolar Schiff-Base Zinc(II) Complexes

TL;DR: The synthesis, characterization, optical, and fluorescent properties of an amphiphilic Schiff-base bis(salicylaldiminato)zinc(II) complex are reported and these complexes are promising systems for the development of new supramolecular architectures and supramolescular fluorescent probes.
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Aggregation properties of bis(salicylaldiminato)zinc(II) Schiff-base complexes and their Lewis acidic character

TL;DR: The synthesis, characterization, (1)H NMR, optical absorption and fluorescent properties of a series of amphiphilic Schiff-base bis(salicylaldiminato)zinc(II) complexes are reported and the existence of aggregate species in solutions of non-coordinating solvents is indicated.
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Controlling the molecular aggregation. An amphiphilic Schiff-base zinc(II) complex as supramolecular fluorescent probe.

TL;DR: A designed amphiphilic Schiff-base bis(salicylaldiminato)zinc(II) complex, 1, forms defined aggregates in dilute solutions of non-coordinating solvents and can be driven by addition of a coordinating species and involves a dramatic enhancement of the fluorescence emission.
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An unprecedented structural interconversion in solution of aggregate zinc(II) salen Schiff-base complexes.

TL;DR: The aggregation properties in solution of noncoordinating solvents of a series of amphiphilic Zn(salen) derivatives are explored, finding that these aggregate species are involved in a unique structural interconversion between two defined dimers, A and B, driven by the concentration of water dissolved in chloroform.