Author
Mauro Micheloni
Other affiliations: University of Florence
Bio: Mauro Micheloni is an academic researcher from University of Urbino. The author has contributed to research in topics: Protonation & Crystal structure. The author has an hindex of 35, co-authored 203 publications receiving 4431 citations. Previous affiliations of Mauro Micheloni include University of Florence.
Topics: Protonation, Crystal structure, Ligand, Nonadecane, Aqueous solution
Papers published on a yearly basis
Papers
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TL;DR: In this paper, a review of ligand molecules containing fluorophores synthesized and employed in metal ion detection in solution in the last few years is presented, with the aim of making more readable the paper has organized it by dividing the subject first for type of fluorophore, then type of metal ion.
590 citations
261 citations
TL;DR: In this article, the main purpose of this review is to collect some significant examples of proton transfer processes in order to show how the electronic properties and molecular topology of polyamines affect the thermodynamic parameters of their protonation equilibria.
230 citations
TL;DR: In this paper, the main recent advances in the design and synthesis of platinum-and palladium-based drugs, their structural features and biological studies of them are reviewed, and an overview of the main biological techniques and approaches for testing the interaction of these molecules with the biological environment, mainly DNA, to validate the effect is also provided.
187 citations
TL;DR: In this article, a cyclotridecane is described as a cycle with constant basicite, stabilisation, and basicite de the complexes of the macrocyclic cycle.
Abstract: Synthese du macrocycle: constantes de basicite et de stabilite des complexes [ML] 2+ et [MHL] 3+ ou M=Cu, Ni. Enthalpies de formation des complexes. Etude RX de [CuL'](ClO 4 ) 2 L'=tetraaza-1,4,7,10 cyclotridecane
109 citations
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1,659 citations
TL;DR: This review highlights the advances in the development of far-red to NIR fluorescent probes since 2000, and the probes are classified according to their organic dye platforms into various categories, including cyanines, rhodamine analogues, BODIPYs, squaraines, and other types.
Abstract: The long wavelength (far-red to NIR) analyte-responsive fluorescent probes are advantageous for in vivo bioimaging because of minimum photo-damage to biological samples, deep tissue penetration, and minimum interference from background auto-fluorescence by biomolecules in the living systems. Thus, great interest in the development of new long wavelength analyte-responsive fluorescent probes has emerged in recent years. This review highlights the advances in the development of far-red to NIR fluorescent probes since 2000, and the probes are classified according to their organic dye platforms into various categories, including cyanines, rhodamine analogues, BODIPYs, squaraines, and other types (240 references).
1,561 citations
1,497 citations
1,128 citations
959 citations