J
J. Fraser Stoddart
Researcher at Northwestern University
Publications - 1277
Citations - 106134
J. Fraser Stoddart is an academic researcher from Northwestern University. The author has contributed to research in topics: Catenane & Supramolecular chemistry. The author has an hindex of 147, co-authored 1239 publications receiving 96083 citations. Previous affiliations of J. Fraser Stoddart include Zhejiang University & Northwest University (United States).
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Growing community of artificial molecular machinists
TL;DR: A better way to design AMMs with unprecedented functions would be to construct molecularly precise architectures based on recent advances in supramolecular chemistry: explore what has not been built by Nature.
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Conformational behaviour of medium-sized rings. Part 11. Dianthranilides and trianthranilides
Alireza Hoorfar,W. David Ollis,Jennifer A. Price,Julia Stephanidou Stephanatou,J. Fraser Stoddart +4 more
TL;DR: In this article, two approaches to the stepwise synthesis of N,N′-di and N, N′,N″-tri-substituted trianthranilide derivatives are described.
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Photochemistry of a Dumbbell-Shaped Multicomponent System Hosted Inside the Mesopores of AL/MCM-41 Aluminosilicate. Generation of Long-Lived Viologen Radicals
Mercedes Alvaro,Belén Ferrer,Hermenegildo García,Emilio Palomares,Vincenzo Balzani,Alberto Credi,Margherita Venturi,J. Fraser Stoddart,Sabine Wenger +8 more
TL;DR: In this article, a dumbbell-shaped compound, 26+, comprising a Ru(II) polypyridine complex, a p-terphenyl, a 4,4‘-bipyridinium unit, a 3,3'dimethyl-4,4'biprithm unit, and a tetraarylmethane unit, has been enclosed in the channels (3.2 nm diameter) of an Al/MCM-41 aluminosilicate.
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Self-assembly of a water-soluble [2]rotaxane with carbohydrate stoppers
Peter R. Ashton,Simon R. L. Everitt,Marcos Gómez-López,Narayanaswamy Jayaraman,J. Fraser Stoddart +4 more
TL;DR: In this article, a dumbbell-shaped compound, containing a hydroquinone ring recognition site and terminated by β-D-glucopyranose units, is mixed with cyclobis(paraquat-p -phenylene) tetrachloride.
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Formation of a hetero[3]rotaxane by a dynamic component-swapping strategy.
Eleanor A. Wilson,Nicolaas A. Vermeulen,Paul R. McGonigal,Alyssa-Jennifer Avestro,Amy A. Sarjeant,Charlotte L. Stern,J. Fraser Stoddart +6 more
TL;DR: Acid-catalysed scrambling of the mechanically interlocked components between two different homo[3]rotaxanes affords a statistical mixture of a hetero-rotaxane along with the two homo-3] rotaxanes, indicating that neither selectivity nor cooperativity is operating during the assembly process.