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John C. Jeffery

Researcher at University of Florence

Publications -  225
Citations -  3777

John C. Jeffery is an academic researcher from University of Florence. The author has contributed to research in topics: Carbyne & Carbene. The author has an hindex of 34, co-authored 225 publications receiving 3701 citations. Previous affiliations of John C. Jeffery include École Polytechnique Fédérale de Lausanne & Australian National University.

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Anion-templated self-assembly of tetrahedral cage complexes of cobalt(II) with bridging ligands containing two bidentate pyrazolyl-pyridine binding sites

TL;DR: Solution NMR experiments show that the central anion acts as a template for cage formation, with a mixture of Co(II) and the appropriate bridging ligand alone giving no assembly into a cage until the tetrahedral anion is added, at which point cage assembly is fast and quantitative.
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Coordination chemistry of tetradentate N-donor ligands containing two pyrazolyl-pyridine units separated by a 1,8-naphthyl spacer: dodecanuclear and tetranuclear coordination cages and cyclic helicates.

TL;DR: The tetradentate ligand L(naph) contains two N-donor bidentate pyrazolyl-pyridine units connected to a 1,8-naphthyl core via methylene spacers; L45 and L56 are chiral ligands with a structure similar to that of L( naph) but bearing pinene groups fused to either C4 and C5 or C5 and C6 of the terminal pyridyl rings.
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Synthesis of the new tripodal ligand tris-[3-(2′-pyridyl)pyrazol-1-yl]hydroborate, and the crystal structure of its europium(III) complex

TL;DR: The new tripodal ligand tris-[3-(2′-pyridyl)pyrazol-1-yl]hydroborate, comprising three N,N-bidentate chelating arms linked by the apical boron atom, has been synthesized as mentioned in this paper.
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Roles of Bridging Ligand Topology and Conformation in Controlling Exchange Interactions between Paramagnetic Molybdenum Fragments in Dinuclear and Trinuclear Complexes.

TL;DR: The magnetic properties of two series of dinuclear complexes, and one trinuclear complex, have been examined as a function of the bridging pathway between the metal centers, and the sign and magnitude of the exchange coupling constant J is clearly related to both the topology and the conformation of the bridge ligand.
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A cyclic supramolecular complex containing eight metal ions, twelve bridging ligands, and an anion encapsulated in the central cavity

TL;DR: The reaction of the bis-bidentate ligand with cobalt (II) or nickel(II) supplements results in formation of complexes, which have a cyclic structure with one ion encapsulated in the central cavity as mentioned in this paper.