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Vieri Fusi

Researcher at University of Urbino

Publications -  166
Citations -  4113

Vieri Fusi is an academic researcher from University of Urbino. The author has contributed to research in topics: Ligand & Aqueous solution. The author has an hindex of 32, co-authored 155 publications receiving 3767 citations. Previous affiliations of Vieri Fusi include University of Florence & Universidade Nova de Lisboa.

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Crystal structure of bis-{μ2-2,2'-[(4,10-dimethyl-1,4,7,10-tetra-aza-cyclo-dodecane-1,7-di-yl)bis(meth-yl-ene)]bis-(4-oxo-4H-pyran-3-olato)}dicobalt-calcium bis-(perchlorate) 1.36-hydrate.

TL;DR: The title compound is a new heterotrinuclear CoII–CaII–Co II–CoII dimer of L1 that undergoes a cobalt-driven preorganization, leading to the formation of an electron-rich area able to host a hard metal ion such as CaII.
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A novel 2,6-bis(benzoxazolyl)phenol macrocyclic chemosensor with enhanced fluorophore properties by photoinduced intramolecular proton transfer.

TL;DR: Macrocyclic ligand L, in which a 2,6-bis(2-benzoxazolyl)phenol (bis-HBO) group is incorporated in triethylenetetramine, was designed and synthesized with the aim of creating a chemosensor with high selectivity and specificity for metal cations in an aqueous environment as discussed by the authors .
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Bis-maltol-polyamine family: structural modifications at strategic positions. Synthesis, coordination and antineoplastic activity of two new ligands

TL;DR: In this paper, diamino-bis-maltol-based ligands were designed by inserting a methyl or hydroxymethyl function at C6, to study the previously hypothesized involvement of that ring position in the anticancer properties and the peculiar metal coordination ability in aqueous solution.
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A New Family of Macrocyclic Polyamino Biphenolic Ligands: Acid-Base Study, Zn(II) Coordination and Glyphosate/AMPA Binding

TL;DR: In this article , the ligands 23,24-dihydroxy-3,6,9,12-tetraazatricyclo[17.3.1.1] and 26,27dihidroxy -3, 6, 9, 12, 15-pentaazaticyclosaepta-1(26), 17, 19, 21, 27, 22, 24-hexaene, L2, were synthesized: they represent a new class of molecules containing a biphenol unit inserted into a macrocyclic polyamine fragment.
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Conformational investigation of some macrobicyclic compounds and of their monoprotonated cations through a comparison between X-ray crystal structures and molecular dynamics simulations

TL;DR: In this article, it was shown that if the protonation occurs on a bridge-head nitrogen, the resulting geometry of the donors is a trigonal bipyramid, whereas it is square pyramidal when the Proton is bound to a nitrogen belonging to a macrobicyclic chain.