Zobrazeno 1 - 10
of 240
pro vyhledávání: '"J. F. Stoddart"'
Autor:
J. D. Badjic, C. M. Ronconi, A. H. Flood, J. F. Stoddart, BALZANI, VINCENZO, SILVI, SERENA, CREDI, ALBERTO
Publikováno v:
Journal of the American Chemical Society. 128:1489-1499
Inspired by the concept of multivalency in living systems, two mechanically interlocked molecules have been conceived that incorporate not once or twice but thrice the features of a pH-switchable [2]rotaxane with two orthogonal recognition sites for
Publikováno v:
Advanced Functional Materials. 17:685-693
Autor:
Joaquín Barberá, J. F. Stoddart, José Luis Serrano, A. C. Garcés, Narayanaswamy Jayaraman, Ana Omenat
Publikováno v:
Advanced Materials. 13:175-180
The constitutional marriage between a classical thermotropic discotic molecule and carbohydrate-based amphiphiles (e.g., see Figure) is shown to result in hybrid compounds, where, for example, a triphenylene unit serves as the central core from which
Autor:
T. Nakamura, Toshimi Shimizu, Masahiro Higuchi, Anthony R. Pease, Françisco M. Raymo, Gunter Mattersteig, Masumi Asakawa, J. F. Stoddart
Publikováno v:
Advanced Materials. 12:1099-1102
Autor:
Lluïsa Pérez-García, Alberto Credi, Roberto Ballardini, Vincenzo Balzani, J. F. Stoddart, D. Marquis, Maria Teresa Gandolfi
Publikováno v:
European Journal of Organic Chemistry. 1998:81-89
A modified bis-p-phenylene-34-crown-10 ring in which one of the 1,4-dioxybenzene units has been replaced by a 9,10-dioxyanthracene unit has been employed as a template for the formation of cyclobis(paraquat-p-phenylene). The [2]catenane which results
Autor:
T. IJIMA, S. A. VIGNON, H. R. TSENG, T. JARROSSON, J. K. SANDERS, E. APOSTOLI, J. F. STODDART, MARCHIONI, FILIPPO, VENTURI, MARGHERITA, BALZANI, VINCENZO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4094::7c911dfc5d29443a610a1b99ee4248ec
http://hdl.handle.net/11585/713
http://hdl.handle.net/11585/713
Autor:
Christian G. Claessens, Françisco M. Raymo, J. F. Stoddart, L. Kuipers, Richard E. Palmer, P. Laitenberger
Publikováno v:
Chemical Physics Letters. 279:209-214
Recent advances in supramolecular chemistry enable the construction of novel nanostructures in solution and the solid state. We present an investigation of the supramolecular organisation of a prototypical charged macrocycle — the self-complementar
Publikováno v:
Accounts of Chemical Research. 30:393-401
For many decades, the construction of organic compounds in the laboratory has relied on the remarkable abilities of the 20th century ‘alchemists’ — namely, synthetic organic chemists — to make and break covalent bonds. Careful selection of fu
Autor:
Françisco M. Raymo, J. F. Stoddart
Publikováno v:
Pure and Applied Chemistry. 69:1987-1998
Slippage is a relatively simple phenomenon that provides an efficient way to self-assemble (nlrotaxanes. The procedure is based on the size complementarity between the dumbbell-shaped and macrocyclic components of the rotaxane. The macrocycle has to
Autor:
Françisco M. Raymo, Vincenzo Balzani, Luca Prodi, Douglas Philp, Peter R. Ashton, M. Belohradsky, Margherita Venturi, Neil Spencer, Roberto Ballardini, J. F. Stoddart, David J. Williams, M. V. Reddington, Maria Teresa Gandolfi
Publikováno v:
Journal of the American Chemical Society. 118:4931-4951
Synthetic approaches to self-assembling [n]rotaxanes incorporating π-electron deficient bipyridinium-based dumbbell-shaped components and π-electron rich hydroquinone-based macrocycles have been developed. In particular, the so-called slippage meth