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Neil R. Champness

Researcher at University of Nottingham

Publications -  318
Citations -  25201

Neil R. Champness is an academic researcher from University of Nottingham. The author has contributed to research in topics: Supramolecular chemistry & Adsorption. The author has an hindex of 78, co-authored 311 publications receiving 23591 citations. Previous affiliations of Neil R. Champness include National Institute of Standards and Technology & University of Southampton.

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Inorganic crystal engineering using self-assembly of tailored building-blocks

TL;DR: The use of transition metal complexes of bridging bidentate ligands to construct predictable, multi-dimensional infinite networks is an area of chemistry which has received everincreasing attention over recent years as discussed by the authors.
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Supramolecular design of one-dimensional coordination polymers based on silver(I) complexes of aromatic nitrogen-donor ligands

TL;DR: In this article, the design and structure of coordination polymers derived from Ag(I) with N-donor ligands and their role in the investigation of weak non-covalent interactions in the solid state are discussed.
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Controlling molecular deposition and layer structure with supramolecular surface assemblies

TL;DR: This work uses hydrogen bonding to guide the assembly of two types of molecules into a two-dimensional open honeycomb network that then controls and templates new surface phases formed by subsequently deposited fullerene molecules, and finds that the open network acts as aTwo-dimensional array of large pores of sufficient capacity to accommodate several large guest molecules.
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High capacity hydrogen adsorption in Cu(II) tetracarboxylate framework materials: the role of pore size, ligand functionalization, and exposed metal sites

TL;DR: A series of isostructural metal-organic framework polymers of composition [Cu2(L)(H2O)2] (L= tetracarboxylate ligands), denoted NOTT-nnn, has been synthesized and characterized and it is suggested that introducing methyl groups or using kinked ligands to create smaller pores can enhance the isosteric heat of adsorption and improve H2 adsorptive capacity.