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
Langmuir and Langmuir-Blodgett films of amphiphilic bistable rotaxanes.
Isaac C.Y. Lee,Curtis W. Frank,Tohru Yamamoto,Hsian-Rong Tseng,Amar H. Flood,J. Fraser Stoddart,Jan O. Jeppesen +6 more
TL;DR: Film balance and surface rheology experiments showed that the addition of the tetracationic cyclophane component and hydroxyl end groups markedly increased the stabilities and viscoelasticity of the films.
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Donor–Acceptor Oligorotaxanes Made to Order
Subhadeep Basu,Ali Coskun,Douglas C. Friedman,Mark A. Olson,Diego Benitez,Ekaterina Tkatchouk,Gokhan Barin,Jeffrey Yang,Albert C. Fahrenbach,William A. Goddard,J. Fraser Stoddart +10 more
TL;DR: Five donor-acceptor oligorotaxanes made up of dumbbells composed of tetraethylene glycol chains, interspersed with three and five 1,5-dioxynaphthalene units, and terminated by 2,6-diisopropylphenoxy stoppers, have been prepared by the threading of discrete numbers of cyclobis(paraquat-p-phenylene) rings, followed by a kinetically controlled stoppering protocol that relies
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A reverse donor-acceptor bistable [2]catenane.
TL;DR: A [2]catenane, composed of a bis-1,5-dioxynaphthalene[38]crown10 (BDNP38C10) ring, mechanically interlocked with a large macrocycle containing two disubstituted tetraarylmethane "speed bumps" and two different pi-electron-deficient units, undergoes equilibration to give approximately equal amounts of the other co-conformer.
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Mechanostereochemistry and the mechanical bond
TL;DR: This review highlights the range of template-directed synthetic methods being used currently in the preparation of MIMs; the syntheses of topologically complex knots and links in the form of stable molecular compounds; and the incorporation of bistable M IMs into many different device settings associated with surfaces, nanoparticles and solid-state materials in response to the needs of particular applications that are perceived to be fair game for mechanostereochemistry.
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High yielding template-directed syntheses of [2]rotaxanes
TL;DR: In this article, three dumbbell-shaped compounds incorporating terminal triisopropylsilyl stoppers, connected to a central 1,5-dioxynaphthalene recognition site by [−CH2CH2O]-n spacers (n = 1-3), have been synthesized.