Macrocyclic, Molecular, and Supramolecular TTF Systems

作者: Jan Becher , Kent Nielsen , Jan O. Jeppesen

DOI: 10.1007/978-94-007-1027-6_1

关键词: Supramolecular chemistryCatenaneMoietyMolecular switchNanotechnologyDendrimerMolecular machineMaterials scienceTetrathiafulvaleneSolid-state chemistry

摘要: The sulfur-containing heterocycle, tetrathiafulvalene (TTF) and its derivatives have been intensively studied during the past two decades on account of their unique π electron donor properties. They were originally prepared for development electrically conducting materials have, as such, synonymous with molecular organic metals. However, few years, utility TTF building blocks in macrocyclic supramolecular chemistry has revealed that moiety is useful beyond field chemistry. Progress synthetic enabled preparation elaborate architectures consequently incorporated into a number systems, such cyclophanes, catenanes, rotaxanes, dendrimers, polymers. Molercular devices based host-guest interactions may act example sensors or switches. Among these systems mechanically-interlocked catenanes rotaxanes are now prime candidates construction artificial machines fabrication electronic devices.

参考文章(61)
Mogens Brøndsted Nielsen, Zhan-Ting Li, Jan Becher, Tetrathiafulvalenophanes and theircatenanes Journal of Materials Chemistry. ,vol. 7, pp. 1175- 1187 ,(1997) , 10.1039/A700129K
Jean-Paul Collin, Christiane Dietrich-Buchecker, Pablo Gaviña, Maria Consuelo Jimenez-Molero, Jean-Pierre Sauvage, Shuttles and Muscles: Linear Molecular Machines Based on Transition Metals† Accounts of Chemical Research. ,vol. 34, pp. 477- 487 ,(2001) , 10.1021/AR0001766
M. Asakawa, M. Higuchi, G. Mattersteig, T. Nakamura, A. R. Pease, F. M. Raymo, T. Shimizu, J. F. Stoddart, Current/Voltage Characteristics of Monolayers of Redox‐Switchable [2]Catenanes on Gold Advanced Materials. ,vol. 12, pp. 1099- 1102 ,(2000) , 10.1002/1521-4095(200008)12:15<1099::AID-ADMA1099>3.0.CO;2-2
Pierre Frère, Nuria Gallego-Planas, Philippe Blanchard, Gilles Mabon, David Rondeau, Access to 3,4-furan dithiolate: towards 3,4-dialkylsulfanylfurans and their Diels–Alder adducts with acrylonitrile Tetrahedron Letters. ,vol. 43, pp. 1825- 1828 ,(2002) , 10.1016/S0040-4039(02)00126-0
Pavel Anzenbacher,, Andrew C. Try, Hidekazu Miyaji, Karolina Jursíková, Vincent M. Lynch, Manuel Marquez, Jonathan L. Sessler, Fluorinated Calix[4]pyrrole and Dipyrrolylquinoxaline: Neutral Anion Receptors with Augmented Affinities and Enhanced Selectivities Journal of the American Chemical Society. ,vol. 122, pp. 10268- 10272 ,(2000) , 10.1021/JA002112W
Adolf Baeyer, Ueber ein Condensationsproduct von Pyrrol mit Aceton Berichte der deutschen chemischen Gesellschaft. ,vol. 19, pp. 2184- 2185 ,(1886) , 10.1002/CBER.188601902121
Eric W Wong, Charles P Collier, Martin Běhloradský, Françisco M Raymo, J Fraser Stoddart, James R Heath, None, Fabrication and Transport Properties of Single-Molecule-Thick Electrochemical Junctions Journal of the American Chemical Society. ,vol. 122, pp. 5831- 5840 ,(2000) , 10.1021/JA993890V
Philippe Blanchard, Bruno Jousselme, Pierre Frère, Jean Roncali, 3- and 3,4-Bis(2-cyanoethylsulfanyl)thiophenes as Building Blocks for Functionalized Thiophene-Based π-Conjugated Systems Journal of Organic Chemistry. ,vol. 67, pp. 3961- 3964 ,(2002) , 10.1021/JO025627+
Martin Adam, Volker Enkelmann, Hans-Joachim Räder, Jörg Röhrich, Klaus Müllen, A Donor Cage with Two Tetrathiafulvene Units Angewandte Chemie. ,vol. 31, pp. 309- 310 ,(1992) , 10.1002/ANIE.199203091
Kent Nielsen, Jan O. Jeppesen, Niels Thorup, Jan Becher, A pyrrolo-tetrathiafulvalene belt and its TCNQ complex: syntheses and X-ray crystal structures. Organic Letters. ,vol. 4, pp. 1327- 1330 ,(2002) , 10.1021/OL025622Z