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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Molecular Mosaics Formed by a Square Cyclophane and Its Inclusion Complex with Ferrocene
Peter R. Ashton,Christian G. Claessens,Wayne Hayes,J. Fraser Stoddart,Stephan Menzer,Andrew J. P. White,David J. Williams +6 more
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Template‐Directed Syntheses of Rigid Oligorotaxanes under Thermodynamic Control
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Dynamic chirality: keen selection in the face of stereochemical diversity in mechanically bonded compounds.
Hsian-Rong Tseng,Scott A. Vignon,Paul C. Celestre,J. Fraser Stoddart,Andrew J. P. White,David J. Williams +5 more
TL;DR: The template-directed syntheses, employing bisparaphenylene-[34]crown-10 (BPP34C10), 1,5-dinaphthoparaphenane (1/5NPPP36C10, and 1/5DNP38C10) as templates, result in a rich reserve of new stereochemical types that might be tapped for their switching and mechanical properties.
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Pseudorotaxanes and Catenanes Containing a Redox‐Active Unit Derived from Tetrathiafulvalene
Masumi Asakawa,Peter R. Ashton,Vincenzo Balzani,Sue E. Boyd,Alberto Credi,Gunter Mattersteig,Stephan Menzer,Marco Montalti,Françisco M. Raymo,Cristina Ruffilli,J. Fraser Stoddart,J. Fraser Stoddart,Margherita Venturi,David J. Williams +13 more
TL;DR: In this article, two bis(2-oxy-1,3-propylenedithio)tetrathiafulvalene-containing acyclic polyethers and two macrocyclic poly-ethers, each incorporating one bis( 2-oxy 1,3,propylenithio)-tetracationic cyclophane unit and one p-phenylene ring, have been synthesized and the results obtained from electrochemical experiments are consistent with the reversible, redox-driven dethreading/rethreading process observed by 1
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Supramolecular Tessellations by a Rigid Naphthalene Diimide Triangle.
Yassine Beldjoudi,Ashwin Narayanan,Indranil Roy,Tyler J. Pearson,M. Mustafa Cetin,Minh T. Nguyen,Matthew D. Krzyaniak,Fehaid Alsubaie,Michael R. Wasielewski,Samuel I. Stupp,J. Fraser Stoddart,J. Fraser Stoddart +11 more
TL;DR: The approach of exploring the 3D topology of 2D tessellations of a naphthalene diimide-based molecular triangle (NDI-Δ) reveals that the 2D molecular arrangement is sensitive to the identity of the solvent and solute concentrations.