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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Journal ArticleDOI
Molecular Meccano. 3. Constitutional and Translational Isomerism in [2]Catenanes and [n]Pseudorotaxanes
J. Fraser Stoddart,David J. Williams,David B. Amabilino,Pier-Lucio Anelli,Peter R. Ashton,Brown George Robert,Emilio J. Cordova,Luis A. Godínez,Wayne Hayes +8 more
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A Polymolecular Donor–Acceptor Stack Made of Paraquat and a 1, 5‐Dihydroxynaphthalene‐ Derived Crown Ether
Jean‐Yves ‐Y Ortholand,Alexandra M. Z. Slawin,Neil Spencer,J. Fraser Stoddart,David J. Williams +4 more
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Complexation of Paraquat and Diquat by a bismetaphenylene-32-crown-10 derivative
TL;DR: In this paper, X-ray crystal structures on the free bismetaphenylene-32-crown-10 derivative (BMP32C10) were analyzed in solution on the 1:1 complexes.
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Molecular Pumps and Motors
Yuanning Feng,Marco Ovalle,James S. W. Seale,Christopher K Lee,Dong Jun Kim,R. Dean Astumian,J. Fraser Stoddart +6 more
TL;DR: In this article, the authors outline the history of pumps and motors, focusing specifically on the innovations that enable the design and synthesis of the artificial molecular machines central to this Perspective, connecting biomolecular and artificial molecular machine is that the physical motions by which these machines carry out their function are unambiguously in mechanical equilibrium.
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Molecular belts. 2. Substrate-directed syntheses of belt-type and cage-type structures
Peter R. Ashton,Ulrich Girreser,Daniele Giuffrida,J. Fraser Stoddart,F. H. Kohnke,John P. Mathias,Françisco M. Raymo,Alexandra M. Z. Slawin,David J. Williams +8 more
TL;DR: In this paper, the angular syn bisdienophile 3 has been used as a Diels-Alder building block with the bisdiene 12 in a trebly-diastereoselective synthesis of the angular macropolycyclic derivative 5.