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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Cyclobis(paraquat-p-phenylene) : a novel synthetic receptor for amino acids with electron-rich aromatic moieties
TL;DR: In this article, the remarkable ability of cyclobis (paraquat-p-phenylene) exhibits to form very stable inclusion charge-transfer complexes with amino acids possessing electron-rich aromatic subunits was reported.
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Mechanically Interlocked Molecules Assembled by π–π Recognition
Gokhan Barin,Gokhan Barin,Ali Coskun,Ali Coskun,Moustafa M.G. Fouda,J. Fraser Stoddart,J. Fraser Stoddart +6 more
TL;DR: This review focuses on the progress which has been accomplished during the past decade involving MIMs comprising aromatic π–π stacking interactions and the few integrated systems that have so far emerged based on this class of MIM's demonstrate their ability to act as active components in many potential applications.
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Quantitative emergence of hetero[4]rotaxanes by template-directed click chemistry
Chenfeng Ke,Ronald A. Smaldone,Takashi Kikuchi,Hao Li,Anthony P. Davis,J. Fraser Stoddart,J. Fraser Stoddart +6 more
TL;DR: In one fell swoop, polyrotaxanes comprising up to 64 rings can be synthesized as a result of cucurbit[6]uril-templated 1,3-dipolar azide-alkyne cycloadditions accelerated in the presence of cyclodextrins as a consequence of self-sorting and positive cooperativity, brought about by hydrogen bonding.
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Toward Daisy Chain Polymers: “Wittig Exchange” of Stoppers in [2]Rotaxane Monomers
TL;DR: Two ammonium ion/crown ether-based [2]rotaxane monomers-each incorporating a dumbbell-shaped component, possessing an exchangeable benzylic triphenylphosphonium stopper, and a ring component bearing an aldehyde function-undergo a sequence of Wittig reactions.