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Long-range movement of large mechanically interlocked DNA nanostructuresIsolation by crystallization of translational isomers of a bistable donor-acceptor [2]catenane.Generation of a dynamic system of three-dimensional tetrahedral polycatenanesMeasurement of the ground-state distributions in bistable mechanically interlocked molecules using slow scan rate cyclic voltammetryDynamic donor-acceptor [2]catenanes.Efficient production of [n]rotaxanes by using template-directed clipping reactions.Photo-driven molecular devices.Design and synthesis of porphyrin-containing catenanes and rotaxanes.Profile of Jean-Pierre Sauvage, Sir J. Fraser Stoddart, and Bernard L. Feringa, 2016 Nobel Laureates in Chemistry.The application of CuAAC 'click' chemistry to catenane and rotaxane synthesis.Strategies and tactics for the metal-directed synthesis of rotaxanes, knots, catenanes, and higher order links.125 years of chemistry in the mirror of "angewandte".Disulfide exchange: exposing supramolecular reactivity through dynamic covalent chemistry.Progress in the synthesis and exploitation of catenanes since the Millennium.Catenanes: fifty years of molecular links.Solid surface vs. liquid surface: nanoarchitectonics, molecular machines, and DNA origami.A multicomponent molecular approach to artificial photosynthesis - the role of fullerenes and endohedral metallofullerenes.Synthesis and Dynamics of Nanosized Phenylene-Ethynylene-Butadiynylene Rotaxanes and the Role of Shape Persistence.The atom, the molecule, and the covalent organic framework.Surveying macrocyclic chemistry: from flexible crown ethers to rigid cyclophanes.From Chemical Topology to Molecular Machines (Nobel Lecture).Multistep energy and electron transfer processes in novel rotaxane donor-acceptor hybrids generating microsecond-lived charge separated states.A shape-persistent quadruply interlocked giant cage catenane with two distinct pores in the solid state.Rise of the Molecular Machines.Induced-fit binding of pi-electron-donor substrates to macrocyclic aromatic ether imide sulfones: a versatile approach to molecular assembly.Use of cleavable coordinating rings as protective groups in the synthesis of a rotaxane with an axis that incorporates more chelating groups than threaded macrocycles.An infinite catenane self-assembled by π···π interactions.Quantum Mechanical and Experimental Validation that Cyclobis(paraquat-p-phenylene) Forms a 1:1 Inclusion Complex with Tetrathiafulvalene.Poly[n]catenanes: Synthesis of molecular interlocked chains.An artificial molecular pump.Formation of Self-Templated 2,6-Bis(1,2,3-triazol-4-yl)pyridine [2]Catenanes by Triazolyl Hydrogen Bonding: Selective Anion Hosts for Phosphate.Mechanically Interlocked Molecules (MIMs)-Molecular Shuttles, Switches, and Machines (Nobel Lecture).Genesis of the Nanomachines: The 2016 Nobel Prize in Chemistry.The relationship between the conformational degree of freedom of template-containing threads and slippage in the formation of [2]rotaxane building blocks.Energy transfer and concentration-dependent conformational modulation: a porphyrin-containing [3]rotaxane.Mechanostereochemistry and the mechanical bond.Two-stage directed self-assembly of a cyclic [3]catenane.Substituent Effects in Parallel-Displaced π-π Stacking Interactions: Distance Matters.Synthesis and photophysical properties of new catenated electron donor-acceptor materials with magnesium and free base porphyrins as donors and C60 as the acceptor.125 Jahre Chemie im Spiegel der “Angewandten”
P2860
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P2860
description
wetenschappelijk artikel
@nl
наукова стаття, опублікована в жовтні 1989
@uk
name
A [2] Catenane Made to Order
@en
A [2] Catenane Made to Order
@nl
type
label
A [2] Catenane Made to Order
@en
A [2] Catenane Made to Order
@nl
prefLabel
A [2] Catenane Made to Order
@en
A [2] Catenane Made to Order
@nl
P2093
P356
P1476
A [2] Catenane Made to Order
@en
P2093
Angel E. Kaifer
Cristina Vicent
David J. Williams
Mark V. Reddington
Neil Spencer
Peter R. Ashton
Timothy T. Goodnow
P304
P356
10.1002/ANIE.198913961
P407
P577
1989-10-01T00:00:00Z