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
Ultrahigh Surface Area Zirconium MOFs and Insights into the Applicability of the BET Theory
Timothy C. Wang,Wojciech Bury,Diego A. Gómez-Gualdrón,Nicolaas A. Vermeulen,Joseph E. Mondloch,Pravas Deria,Kainan Zhang,Peyman Z. Moghadam,Amy A. Sarjeant,Randall Q. Snurr,J. Fraser Stoddart,Joseph T. Hupp,Omar K. Farha +12 more
TL;DR: Critical for practical applications, NU-1103 combines for the first time ultrahigh surface area and water stability, where this material retained complete structural integrity after soaking in water.
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Dual-controlled nanoparticles exhibiting AND logic.
TL;DR: Dual-controlled nanoparticles (DCNPs) are synthesized by attaching two different types of molecular machines, light-responsive nanoimpellers and pH-responsive nanovalves, to different regions of mesoporous silica nanoparticles.
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pH-operated nanopistons on the surfaces of mesoporous silica nanoparticles.
TL;DR: The results described here present a significant step toward the development of pH-responsive nanoparticle-based dual drug delivery vehicles that are potentially capable of being interfaced with biological systems.
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Noncovalent Side-Wall Functionalization of Single-Walled Carbon Nanotubes
Alexander Star,Yi Liu,Kevin Grant,Ludek Ridvan,J. Fraser Stoddart,David W. Steuerman,Michael R. Diehl,and Akram Boukai,James R. Heath +8 more
TL;DR: A family of poly[m-phenylenevinylene)-co-(p-phenylonvinylene)]s, functionalized in the synthetically accessible C-5 position of the meta-disubstituted phenylene rings have been designed and synthesized as mentioned in this paper.
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A Chemically and Electrochemically Switchable [2]Catenane Incorporating a Tetrathiafulvalene Unit.
Masumi Asakawa,Peter R. Ashton,Vincenzo Balzani,Alberto Credi,Christoph Hamers,Gunter Mattersteig,Marco Montalti,Andrew N. Shipway,Neil Spencer,J. Fraser Stoddart,Malcolm S. Tolley,Margherita Venturi,Andrew J. P. White,David J. Williams +13 more
TL;DR: A mechanical switch in a catenane, made up of a cyclobis(paraquat-p-phenylene) tetracation interlocked with a macrocyclic polyether containing a redox-active tetrathiafulvalene (TTF) unit and a 1,5-dioxynaphthalene ring system, can be thrown either chemically or electrochemically.