RICERCA ITALIANA     

Programmi di ricerca simili:

• 1 - Complessi porfirinici autoorganizzati su scala nanoscopica: proprietà e applicazioni tecnologiche
• 2 - NANOSISTEMI AUTOASSOCIATIVI CON RICONOSCIMENTO TRA BASI COMPLEMENTARI DI DNA/RNA
• 3 - Progettazione ed auto-organizzazione di architetture molecolari per nanomagneti e sistemi optoelettronici
• 4 - Self-assembly gerarchico di architetture supramolecolari multi-componente
• 5 - Sistemi molecolari, polimeri coniugati e nanoparticelle per lo sviluppo di nuovi sensori chimici a trasduzione ottica
• 6 - Nano-Analytical Systems for Chem & bio-sEnsing - NASCE
• 7 - Fattori stereodinamici che regolano la formazione e le proprietà dei microaggregati
• 8 - Cromofori in nanostrutture organiche e ibride: controllo supramolecolare delle proprietà fotoniche
• 9 - Nuovi ligandi e modulatori per la caratterizzazione dei neurorecettori e per il trattamento delle relative disfunzioni
• 10 - Sistemi supramolecolari per la conversione dell'energia luminosa

Classificazione scientifico-disciplinare

• Area scientifico disciplinare: Scienze chimiche
  • CHIMICA FISICA
  • CHIMICA GENERALE E INORGANICA
  • CHIMICA ORGANICA

Classificazione brevettuale

• CHEMISTRY; METALLURGY
  • ORGANIC CHEMISTRY (such compounds as the oxides, sulfides, or oxysulfides of carbon, cyanogen, phosgene, hydrocyanic acid or salts thereof C01; products obtained from layered base-exchange silicates by ion-exchange with organic compounds such as ammonium, phosphonium or sulfonium compounds or by intercalation of organic compounds C01B33/44; macromolecular compounds C08; dyes C09; fermentation products C12; fermentation or enzyme-using processes to synthesise a desired chemical compound or composition or to separate optical isomers from a racemic mixture C12P; production of organic compounds by electrolysis or electrophoresis C25B3/00, C25B7/00)
    • ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM (metal-containing porphyrins C07D487/22)
    • GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR (preparation of carboxylic acid esters by telomerisation C07C67/47; telomerisation C08F)
• PERFORMING OPERATIONS; TRANSPORTING
  • MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR (punching, perforating, making articles by processing sheet metal, tubes, or profiles B21D; wire-working B21F; making pins, needles, or nails B21G; making chains B21L; grinding B24)
    • DETAILS, COMPONENTS, OR ACCESSORIES FOR MACHINE TOOLS, e.g. ARRANGEMENTS FOR COPYING OR CONTROLLING (tools of the kind used in lathes or boring machines B23B27/00); MACHINE TOOLS IN GENERAL CHARACTERISED BY THE CONSTRUCTION OF PARTICULAR DETAILS OR COMPONENTS; COMBINATIONS OR ASSOCIATIONS OF METAL-WORKING MACHINES, NOT DIRECTED TO A PARTICULAR RESULT [C9609]

Classificazione geografica

• Regione: Emilia Romagna

Bibliografia

1. R. F. Service, Science, 2001, 293, 785.
2. a) R. P. Feynman, Eng. Sci., 1960, 23, 22. b) Saturday Rev., 1960, 43, 45. Vedere anche: http://www.its.caltech.edu/~feynman.
3. V. Balzani: Small, 2005, 1, 278.
4. S-W. Hla, G. Meyer, K-H. Rieder, ChemPhysChem, 2001, 2, 361.
5. V. Johánek, M. Laurin, A. W. Grant, B. Kasemo, C. R. Henry, J. Libuda, Science, 2004, 304, 1639.
6. a) Nanotechnology. Innovation for tomorrow’s world European Commission, EUR 21 151, p. 1-56, 2004. www.cordis.lu/nanotechnology. b) S. J. Ainsworth, Chem. Eng. News, 2004, April 12, 17. c) S. R. Morrissey, Chem. Eng. News, 2004, April 19, 30.
7. J.-M. Lehn, Supramolecular Chemistry: Concepts and Perspectives, VCH, Weinheim, 1995.
8. V. Balzani, L. Moggi, F. Scandola in Supramolecular Photochemistry (Ed.: V. Balzani), Reidel, Dordrecth, 1987, p. 1.
9. V. Balzani, A. Credi, M. Venturi, Molecular Devices and Machines. A Journey into the Nanoworld, VCH-Wiley, Weinheim, 2003.
10. N. Koumura, R. W. Zijlstra, R. A. van Delden, N. Harada, B. L. Feringa, Nature, 1999, 401,152.
11. M. C. Jiménez, C. O. Dietrich-Buchecker, J.-P. Sauvage, Angew. Chem. Int. Ed., 2000, 39, 3248.
12. a) A. M. Brouwer, C. Frochot, F. G. Gatti, D. A. Leigh, L. Mottier, F. Paolucci, S. Roffia, G. W. H. Wurpel, Science, 2001, 291, 2124. b) P. R. Ashton, R. Ballardini, V. Balzani, A. Credi, R. Dress, E. Ishow, C. J. Kleverlann, O. Kocian, J. A. Preece, N. Spencer, J. F. Stoddart, M. Venturi, S. Wenger, Chem. Eur. J., 2000, 6, 3558.
13. J. D. Badjic, V. Balzani, A. Credi, S. Silvi, J. F. Stoddart, Science, 2004, 303, 1845.
14. a) G. Steinberg-Yfrach, J.-L. Rigaud, E. N. Durantini, A. L. Moore, D. Gust, T. A. Moore, Nature, 1998, 392, 479. b) I. M. Bennet, H. M. Vanegas Farfano, F. Bogani, A. Primak, P. A. Liddell, L. Otero, L. Sereno, J. J. Silber, A. L. Moore, T. A. Moore, D. Gust, Nature, 2002, 420, 398.
15. W. B. Sherman, N. C. Seeman, Nano Letters, 2004, 4, 1203.
16. H. Hess, G. D. Bachand, V. Vogel, Chem. Eur. J., 2004, 10, 2110.
17. D. S. Goodsell, Bionanotechnology, Wiley, New York, 2004.
18. Molecular Motors (Ed.: M. Schliwa) Wiley-VCH, Weinheim, 2003.
19. (a) V. Balzani, A. Credi, M. Venturi: “Molecular Devices and Machines”, Physics World, 2004, no. 11, 39. (b) K. Kinbara, T. Aida, Chem. Rev., 2005, 105, 1377. (c) Top. Curr. Chem., 2005, 262 (Special volume on Molecular Motors; ed. T.R Kelly). (d) H. Tian, Q.-C. Wang, Chem. Soc. Rev., 2006, 35, 361.
20. S. J. Rowan, S. J. Cantrill, G. R. L. Cousins, J. K. M. Sanders, J. F. Stoddart, Angew. Chem. Int. Ed., 2002, 41, 898.
21. J.-M. Lehn, Angew. Chem. Int. Ed. Engl., 1988, 27, 89.
22. a) A. Aviram, M. A. Ratner, Chem. Phys. Lett., 1974, 29, 277. b) Molecular Electronic Devices (Eds.: F. L. Carter, R. E. Siatkowski, H. Wohltjen), Elsevier, Amsterdam, 1988.
23. C. Joachim, J. P. Launay, Nouv. J. Chem., 1984, 8, 723.
24. a) V. Balzani, F. Scandola, Supramolecular Photochemistry, Horwood, Chichester, 1991. b) F. Vögtle, Supramolecular Chemistry. An Introduction, Wiley, Chichester, 1991. c) G. M. Whitesides, J. P. Mathias, C. T. Seto, Science, 1991, 254, 1312. d) D. B. Amabilino, J. F. Stoddart, Chem. Rev., 1995, 95, 2725.
25. R. Hoffmann, www.foresight.org/Updates/Update20/Update20.1.html#anchor176004
26. a) V. Balzani, M. Clemente-León, A. Credi, B. Ferrer, M. Venturi, A. H. Flood, J. F. Stoddart, “Autonomous artificial nanomotor powered by sunlight”, Proc. Natl. Acad. Sci., 2006, 103, 1178. b) V. Balzani, M.Clemente-Leon, A. Credi, M. Semeraro, M. Venturi, H-R. Tseng, S. Wegner, S. Saha, J.F. Stoddart, “A comparison of shuttling mechanisms in two sunlight powered nanomotors” Aust. J. Chem., 2006, 59, 193. c) G. Bergamini, P. Ceroni, V. Balzani, L. Cornelissen, J. van Heyst, S-K Lee, F. Vögtle, “Dendrimers based on a bis-Cyclam Core as Fluorescence Sensors for Metal Ions”, J. Mat. Chem., 2005, 15, 2959. d) V. Balzani, P. Ceroni, C. Giansante, V. Vicinelli, F.-G. Klärner, C. Verhaelen, F. Vögtle, U. Hahn, “Tweezering the Core of a Dendrimer: A Photophysical and Electrochemical Study”, Angew. Chem. Int. Ed., 2005, 44, 4574. e) J.D. Badji, V. Balzani, A. Credi, S. Silvi, J. F. Stoddart: “A Molecular Elevator”, Science, 2004, 303, 1845.
27. a) V. Amendola, M. Boiocchi, L. Fabbrizzi, A. Palchetti, “Anion Receptors Containing -NH Binding Sites: Hydrogen-bonding Formation or Neat Proton Transfer?”, Chem. Eur. J., 2005, 11, 120. b) M. Boiocchi, L. Del Boca, D. Esteban-Gómez, L. Fabbrizzi, M. Licchelli, E. Monzani, “Anion-Induced Urea Deprotonation”, Chem. Eur. J., 2005, 11, 3097. c) D. Esteban Gómez, L. Fabbrizzi, M. Licchelli, “Why, on Interaction of Urea Based Receptors with Fluoride, Beautiful Colors Develop”, J. Org. Chem., 2005, 70, 5717. d) V. Amendola, M. Boiocchi, L. Fabbrizzi, A. Palchetti; “What Anions Do Inside a Receptor’s Cavity: A Trifurcate Anion Receptor Providing Both Electrostatic and Hydrogen-Bonding Interactions”; Chem. Eur. J., 2005, 11, 5648. e) V. Amendola, D. Esteban-Gómez, L. Fabbrizzi, M. Licchelli, E. Monzani, F. Sancenón, “Metal Enhanced H-bond Donor Tendencies of Urea and Thiourea Toward Anions. Ditopic Receptors for Silver (I) Salts”, Inorg. Chem., 2005, 44, 8690.
28. a) R. Cacciapaglia, S. Di Stefano, L. Mandolini, “Effective Molarities in Supramolecular Cataysis of Two-Substrate Reactions”, Acc. Chem. Res., 2004, 37, 113. b) R. Cacciapaglia, A. Casnati, L. Mandolini, D. N. Reinhoudt, R. Salvio, A. Sartori, R. Ungano, “Di- and Trinuclear Zn2+ Complexes of Calix[4]arene Based Ligands as Catalysts of Acyl and Phosphoryl Transfer Reactions”, J. Org. Chem., 2005, 70, 624. c) R. Cacciapaglia, A. Casnati, L. Mandolini, D. N. Reinhoudt, R. Salvio, A. Sartori, R. Ungano, “Calix[4]arene-Based Zn2+ Complexes as Shape- and Size-Selective Catalysts of Ester Cleavage”, J. Org. Chem., 2005, 70, 5398. d) A. Dalla Cort, L. Mandolini, L. Schiaffino, “Exclusive Transition State Stabilization in the Supramolecular Catalysis of Diels-Alder Reaction by a Uranyl Salophen Complex”, Chem. Commun., 2005, 3867. e) R. Cacciapaglia, S. Di Stefano, L. Mandolini, “Metathesis Reaction of Formaldehyde Acetals: An Easy Entry into the Dynamic Covalent Chemistry of Cyclophane Formation”, J. Am. Chem. Soc., 2005, 127, 13666.
29. a) E. Boseggia, M. Gatos, L. Lucatello, F. Mancin, S. Moro, M. Palumbo, C. Sissi, P. Tecilla, U. Tonellato, G. Fagotto, “Towards Efficient Zn(II)-based Artificial Nucleases”, J. Amer. Chem. Soc., 2004, 126, 4543. b) E. Brasola, F. Mancin, E. Rampazzo, P. Tecilla, U. Tonellato, “A fluorescence nanosensor for Cu2+ on silica particles”, Chem. Comm., 2003, 3028. c) F. Mancin; P. Scrimin; P. Tecilla, P. Tonellato, “Artificial Nucleases”, Chem. Comm, 2005, 2540. d) F. Mancin, E. Rampazzo, P. Tecilla, U. Tonellato, “Self-Assembled Fluorescent Chemosensors” Chem. Eur. J. 2006, 12, 1844. e ) T. Carofiglio, C. Fregonese, G.J. Mohr, F. Rastrelli, U. Tonellato, “Optical Sensor Arrays: One-pot, Multiparallel Synthesis and Cellulose Immobilization of pH and Metal Ion Sensitive Azo-dyes”, Tetrahedron, 2006, 62, 1502.
30. a) R. Ungaro, A. Casnati, F. Sansone, “Biomimetic Macrocyclic Receptors for Carboxylate Anion Recognition” in “Encyclopedia of Nanoscience and Nanotechnology, J. A. Schwarz, C. I. Contescu, K. Putyera Eds.; 2004, Marcel Dekker, New York, p. 295 – 309. b) F. Sansone, L. Baldini, A. Casnati, E. Chierici, G. Faimani, F. Ugozzoli, R. Ungano, “Chiral dimeric capsules from N,C-linked peptidocalix[4]arenes self-assembled through an antiparallel beta-sheetlike motif” J. Am. Chem. Soc. 2004, 126, 6204. c) A. Arduini; F. Ciesa, M. Frangassi, A. Pochini, A. Secchi, “Selective synthesis of two constitutionally isomeric oriented calix[6]arene-based rotaxanes”, Angew. Chem. Int. Ed., 2005, 43, 278. d) A. Arduini, A.; Demuru, D.; Pochini, A.; Secchi, A. “Recognition of quaternary ammonium cations by calix[4]arene derivatives supported on gold nanoparticles”, Chem.Commun.,2005, 645-647.

Parole Chiave

CHIMICA SUPRAMOLECOLARE, CONGEGNI MOLECOLARI, MACCHINE MOLECOLARI, SENSORI SUPRAMOLECOLARI, CATALISI SUPRAMOLECOLARE, NANOPARTICLELLE, DENDRIMERI, CALIXARENI, RICONOSCIMENTO MOLECOLARE