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Christoph Kuhlmann

Researcher at Bielefeld University

Publications -  14
Citations -  555

Christoph Kuhlmann is an academic researcher from Bielefeld University. The author has contributed to research in topics: Nucleophile & Type (model theory). The author has an hindex of 7, co-authored 14 publications receiving 533 citations.

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A variety of combinatorially linkable units as disposition:† from a giant icosahedral Keplerate to multi-functional metal–oxide based network structures

TL;DR: In polyoxometalate chemistry, a large variety of compounds, clusters and solid-state structures can be formed by linking together metal-oxygen building blocks as discussed by the authors, resulting for instance in the high-yield synthesis of inorganic superfullerenes and giant ring-shaped, electron-rich, mixed-valence polyoxomolybdates with nanosized cavities.
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Hierarchic patterning: architectures beyond‘giant molecular wheels’

TL;DR: Based on symmetry breaking steps under one-pot conditions, simple molybdenum oxide-based building blocks initially assemble to 'giant molecular wheels' in a fast process followed by further slower assembly processes leading stepwise to more complex mesoscopic architectures including spherical ones and finally to those with a size larger than 500 nm.
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A hydrogen-bonded cluster with ‘onion-type’ structure, encapsulated and induced by a spherical cluster shell: [(H2O)n⊂ MoVI72MoV60O372(HCO2)30(H2O)72]42–

TL;DR: In this paper, an ion-type stable cluster anion with spherically shaped stable shell was obtained, and the anion 1a exhibited a remarkable overall "onion-type" structure, thereby revealing also a novel type of inclusion: a hydrogen-bonded cluster with 'onion type' structure.
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On the option of generating novel type surfaces with multiphilic ligands within the cavity of a giant metal–oxide based wheel type cluster: chemical reactions with well-defined nanoobjects

TL;DR: The reaction of an aqueous solution of sodium molybdate with cystine hydrochloride acting as educt and reducing agent at rather low pH values (≈ 1.5) results in the formation of ring-shaped clusters which capture the oxidation product of ======COO−, i.e., the diprotonated cystines at the inner wall of their cavities as mentioned in this paper.
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‘Adding’ stable functional complementary, nucleophilic and electrophilic clusters: a synthetic route to [{(SiW11O39)Mo3S4(H2O)3(µ-OH)}2]10– and [{(P2W17O61)Mo3S4(H2O)3(µ-OH)}2]14– as examples

TL;DR: In this paper, stable functional complementary clusters, i.e. of the electrophilic and nucleophilic type, can be added, resulting in the planned formation of the related reaction products: the high-yield synthesis of the crystalline compounds [Me2NH2]10- [{(SiW11O39)Mo3S4(H2O)3(µ-OH)}2]