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
Radical-pairing-induced molecular assembly and motion
TL;DR: Radical-pairing interactions between conjugated organic π-radicals are relative newcomers to the inventory of molecular recognition motifs explored in supramolecular chemistry as mentioned in this paper.
Journal ArticleDOI
Diastereoselective Self-Assembly of [2]Catenanes
Peter R. Ashton,Aaron M. Heiss,Dario Pasini,Françisco M. Raymo,Andrew N. Shipway,J. Fraser Stoddart,J. Fraser Stoddart,Neil Spencer +7 more
TL;DR: Two chiral π-electron-rich crown ethers incorporating either a binaphthol or two D-mannitol units have been synthesized and their abilities to bind bipyridinium guests demonstrated as discussed by the authors.
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Electron-catalysed molecular recognition
Yang Jiao,Yunyan Qiu,Long Zhang,Wei-Guan Liu,Haochuan Mao,Hongliang Chen,Yuanning Feng,Kang Cai,Dengke Shen,Bo Song,Xiao-Yang Chen,Xuesong Li,Xin‐Li Zhao,Ryan M. Young,Charlotte L. Stern,Michael R. Wasielewski,R. Dean Astumian,William A. Goddard,J. Fraser Stoddart +18 more
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Densely Charged Dodecacationic [3]- and Tetracosacationic Radial [5]Catenanes
Minh T. Nguyen,Daniel P. Ferris,Cristian Pezzato,Yuping Wang,J. Fraser Stoddart,J. Fraser Stoddart,J. Fraser Stoddart +6 more
TL;DR: In this article, a template-directed strategy for constructing mechanically interlocked molecules, consisting of multiply charged rings, represents a departure in chemistry and is capable of producing a blueprint for exploring a novel class of organic molecules that boast large numbers and high densities of like charges.
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A self-organised layered superstructure of arrayed [2]pseudorotaxanes
TL;DR: In this paper, a pseudorotaxane is built up from a macrocyclic cyclophane containing two atomatic π-acceptors and an acyclic molecular containing three aromatic πdonors, which has the ability to undergo self-organisation on crystallisation to form a layered superstructure of arrayed pseudo-drugs.