RICERCA ITALIANA     

Programmi di ricerca simili:

• 1 - Fattori stereodinamici che regolano la formazione e le proprietà dei microaggregati
• 2 - Complessi porfirinici autoorganizzati su scala nanoscopica: proprietà e applicazioni tecnologiche
• 3 - Proprietà reattive e spettroscopiche di aggregati molecolari in fasci supersonici e sviluppo di una modellistica unificante.
• 4 - CARATTERIZZAZIONE MICROSCOPICA DELLA DINAMICA DI PROCESSI CHIMICI
• 5 - ASPETTI MICROSCOPICI DELLA REATTIVITA' CHIMICA
• 6 - DNA a Quadrupla Elica: Studi Strutturali e Biologici Finalizzati alla Progettazione di Nuovi Farmaci ad Attività Antitumorale o Antivirale
• 7 - TRASFERIMENTI DI ENERGIA E DI CARICA A LIVELLO MOLECOLARE
• 8 - NANOSISTEMI AUTOASSOCIATIVI CON RICONOSCIMENTO TRA BASI COMPLEMENTARI DI DNA/RNA
• 9 - Processi molecolari in sistemi di non-equilibrio per applicazioni nel campo energetico e ambientale e per la sintesi di nuovi materiali.
• 10 - UN APPROCCIO INTEGRATO ALLA SINTESI, CARATTERIZZAZIONE E FUNZIONE DI BIOPOLIMERI EUMELANICI DERIVANTI DA 5,6-DIIDROSSIINDOLI E LORO MISCELAZIONE CON POLIMERI CONVENZIONALI E COMPOSITI

Classificazione scientifico-disciplinare

• Area scientifico disciplinare: Scienze chimiche
  • CHIMICA FISICA
  • CHIMICA GENERALE E INORGANICA
  • CHIMICA ORGANICA
  • FONDAMENTI CHIMICI DELLE TECNOLOGIE
• Area scientifico disciplinare: Scienze fisiche
  • FISICA APPLICATA (A BENI CULTURALI, AMBIENTALI, BIOLOGIA E MEDICINA)

Classificazione brevettuale

• CHEMISTRY; METALLURGY
  • COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL (by metallising textiles D06M11/83; decorating textiles by locally metallising D06Q1/04); CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL (for specific applications, see the relevant places, e.g. for manufacturing resistors H01C17/06); INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL (treating metal surfaces or coating of metals by electrolysis or electrophoresis C25D, C25F)
    • COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL (applying liquids or other fluent materials to surfaces in general B05; making metal-coated products by extrusion B21C23/22; covering with metal by connecting pre-existing layers to articles, see the relevant places, e.g. B21D39/00, B23K; working of metal by the action of a high concentration of electric current on a workpiece using an electrode B23H; metallising of glass C03C; metallising mortars, concrete, artificial stone, ceramics or natural stone C04B41/00; paints varnishes, laquers C09D; enamelling of, or applying a vitreous layer to, metals C23D; inhibiting corrosion of metallic material or incrustation in general C23F; single-crystal film growth C30B; manufacture of semiconductor devices H01L; manufacture of printed circuits H05K)
  • 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)

Classificazione geografica

• Regione: Abruzzo

Bibliografia

[1] E .R. Bernstein, in: E.R. Bernstein (Ed.), Atomic and Molecular Clusters, Elsevier, Amsterdam, 1990.
[2] V. Even, A. Amirav, S. Lewtwyler, N. Ondrechen, Z. Berkovitch-Yellin, J. Jortner, Farad. Chem. Soc. 73 (1993) 153. ]. [3] B. Brutschy, Chem. Rev. 92 (1992) 11567.].
[4]. R. Taylor Electrophilic Aromatic Substitution, Wiley, New York, 1990.
[5]. C. A. Reed, K.-C. Kim, E. S. Stoyanov, D. Stasko, F. S. Tham, L. J. Mueller, P. D. W. Boyd J. Am. Chem. Soc. 2003, 125, 1796.
[6]. W. Jones, P. Boissel, B. Chiavarino, M. E. Crestoni, S. Fornarini, J. Lemaire, P. Maitre Angew. Chem. Int. Ed. Engl. 2003, 42, 2057
[7]. F. Terrier Chem. Rev. 1982, 82, 78.
[8]. T. Giroldo, L. A. Xavier, J. M. Riveros Angew. Chem. Int. Ed. 2004, 43, 3588.
[9]. (a) A. G. Marshall Int. J. Mass Spectrom. 2000, 200, 331; (b) C. L. Hendrickson, M. R. Emmett Annu. Rev. Phys. Chem. 1999, 50, 517.
[10]. (a) J. B. Fenn, M. Mann, C. K. Meng, S. F. Wong, C. M. Whitehouse Science 1989, 246, 64; (b) P. Kebarle J. Mass Spectrom. 2000, 35, 804.
[11]. (a) N.A. Cherepkov J. Phys. B. 1983, 16, 1543; (b) N.A. Cherepkov Chem. Phys. Lett. 1982, 87, 344; (c) B. Ritchie Phys. Rev. A 1976, 13, 1411.
[12]. (a) T. Likesch, N. Böwering, B. Schmidtke, N. Müller, T. Khalil, U. Heinzmann Phys. Rev. A 2004, 70, 022507; (b) G. A. Garcia, L. Nahon, M. Lebech, J. C. Houver, D. Dowek, I. Powis J. Chem. Phys. 2003, 119, 8781; (c) H. Hergenhahn, E. E. Rennie, O. Kugeler, S. Marburger, T. Lischke, I. Powis, G. A. Garcia J. Chem. Phys. 2004, 120 4553.
[13]. S. Turchini, N. Zema, G. Contini, G. Alberti, M. Alagia, S. Stranges, G. Fronzoni, M. Stener, P. Decleva, T. Prosperi Phys. Rev. A 2004, 70, 14502.
[14]. A. Giardini, D. Catone, S. Stranges, M. Satta, M. Tacconi, S. Piccirillo, S. Turchini, N. Zema, G. Contini, T. Prosperi, P. Decleva, D. Ditommaso, G. Fronzoni, M. Stener. A. Filippi, M. Speranza Chem. Phys. Chem. 2005, 6, 1164.
[15] Georgiu, S and Hillenkamp, F. Guest Eds.Tematic issue on Laser ablation of molecular substrates Chem. Rev., 2003, Vol 103 No.2, pp. 317ff.]
[16] Pulsed laser deposition of thin films. D. B. Chrisey and G. K. Hubler eds. John Wiley & Sons Inc. 1994.
[17] Laser ablation and desorption. J.C. Miller and R.F. Haglund eds. Academic Press 1998.
[18] P.R. Willmott and J.R. Huber, Rev. Modern Phys. 72, 2000, 315.
[19] Angular distribution of ablated material. K.L. Saenger, in Pulsed Laser Deposition of Thin Films, ed. D.B. Chrisey and G.K. Hubler, John Wiley & Sons, New York, 1994, p. 199.
[20] A.A. Puretzky, H. Schittenhelm, X. Fan, M.J. Lance, L.F. Allard, Jr., and D.B. Geohegan, Phys. Rev. B 65, 2002, 245425.
[21] A.A. Puretzky, D.B. Geohegan, X. Fan, S.J. Pennycook, Appl. Phys. A 70, 2000, 153.
[22] Femtochemitry and Femtobiology: Ultrafast Dynamics in Molecular Science. A. Douhal and J. Santamaria eds. World Scientific, Singapore, 2002.
[23] C. Cohen-Tannoudji, Review of Modern Physics 70(3), 1998, 707.
[24] A. Giardini, A. Paladini, D. Catone, S. Piccirillo, F. Rondino, M. Satta, A. Filippi, M. Speranza, S. Turchini, N. Zema, Chirality in press.
[25] F. Biondini, B.G. Brunetti, P. Candori, F. De Angelis, S. Falcinelli, F. Tarantelli, F. Pirani, F. Vecchiocattivi, J. Chem. Phys. 122, 164307 (2005).
[26] F. Biondini, B.G. Brunetti, P. Candori, F. De Angelis, S. Falcinelli, F. Tarantelli, F. Pirani, F. Vecchiocattivi, J. Chem. Phys. 122, 164308 (2005).
[27] B. Brunetti, P. Candori, S. Falcinelli, B. Lescop, G. Liuti, F. Pirani, F. Vecchiocattivi, Eur. Phys. J. D 38, 21(2006).
[28] Raghavachari, K. ; Anderson, J. B. J. Phys. Chem. 1996, 100, 12960.
[29] "Quantum-Mechanical Prediction of Thermochemical Data" Jerzy Cioslowski, Ed.. Kluwer academic publishers, Dordrecht 2001.
[30] Chaasinski, G.; Szczesniak, M. M. Chem. Rev. 2000, 100, 4227-4252; Rappé, A. K.; Bernstein, E. R.
J. Phys. Chem. 2000, 104, 6117-6128, and references therein.
[31] Mok, D. K. W.; Handy, N. C.; Amos, R. D. Mol. Phys. 1997, 92, 667.
[32] Schutz, M.; Rauhut, G.; Werner, H.-J. J. Phys. Chem. A 1998,102, 5997.
[33] Zhao, Y.; Truhlar, D. G. J. Chem. Theory Comput. 2005, 1, 415-432.
[34] Hobza, P.; Selzle, H. L.; Schlag, E. W. Chem. Rev. 1994, 94, 1767-1785.
[35] Gonzales, C.; Lim, E. C. J. Phys. Chem. A 2003, 107, 10105-10110.
[36] Kim, K. S.; Tarakeshwar, P.; Lee, J. Y. Chem. Rev. 2000, 100, 4145.
[37] J. C. Ma, D. A. Doughterty (1997) Chem Rev., 97, 1303.
[38] Zacharias, N.; Dougherty, D. A. Trends Pharmacol. Sci. 2002, 23, 281.
[39] Solari E.; Hesschenbrouck J.; Scopelliti R.; Floriani C.; Re N. Angew. Chem. Int. Ed. Engl. 2001, 40, 932.
[40] Marrone A.; Coletti C.; Re N. Organometallics 2004, 23, 4952-4963.
[41] Nunzi F.; Sgamellotti A.; Re N. Organometallics 2002, 21, 2219.
[42] Nunzi F.; Sgamellotti A.; Re N. J. Phys. Chem. B 2002 106, 10622-10633.
[43] Coletti, C.; Re, N. J Phys. Chem. A 2006, In press
[44] Hebbesen, T. W.; Hiura, H Adv. Mater. 1995, 7, 582]
[45] H. Vogelsang, O. Husberg, W. Von der Osten (2000) J. Luminescence, 86, 87.
[46] P Calandra, A. Longo, V. Marcianò, V. Turco Liveri (2003) J. Phys. Chem. B, 107, 6724.
[47] A. Ruggirello, V. Turco Liveri (2003) J. Coll. Int. Sci., 258, 123.
[48] D. Buongiorno, L Ceraulo, M Ferruggia, F Filizzola, A Longo, A Mele, A Ruggirello, V Turco Liveri, Internatinal Journal of Pharmaceutics, 312, 96-104, 2006
[49] D Buongiorno, L Ceraulo, M Ferrugia, F Filizzola, A Ruggirello, V Turco Liveri, ,Journal Pineal Research 38, 292-298, 2005
[50] K. Binnemans, C. Gorller-Walrand (2002) Chem. Rev., 102, 2303.
[51] T. Caronna, M. Catellani, S. Luzzati, L. Malpezzi, SV. Meille, A. Mele, C. Richter, R. Sinisi (2001) Chem. Mater., 13, 3906.
[52] C. Nuckolls, T. J. Katz, G. Katz, P. J. Collings, L. J. Castellanos (1999) J. Am. Chem. Soc., 121, 79.
[53] C. Nuckolls, T. J. Katz, (1998) J. Am. Chem. Soc., 120, 9541.
[54] K. E. S. Phillips, T. J. Katz, S. Jockusch, A. J. Lovinger, N. J. Turro (2001) J. Am. Chem. Soc., 123, 11899 ; C. Nuckolls, R.Shao, W.-G. Jang, N. A. Clark, D. M. Walba, J. Thomas, T. J. Katz, (2002) Chem. Mater., 14, 773; Fasel, R.; Parshau, M.; Ernst, K.-H. (2006)Nature, 439, 449-452.
[55] E.L. Eliel, S.H. Wilen (1994) Stereochemistry of Organic Compounds, J.Wiley & Sons, Inc., New York.
[56] D.A. Lightner, J.E. Gurst (2000) Organic Conformational Analysis and Stereochemistry from Circular Dichroism Spectroscopy,Wiley-VCH, New York, Chapter 13.
[57] F. Lebon, G. Longhi, F. Gangemi, S. Abbate, J. Priess, M. Juza, C. Bazzini, T. Caronna, A. Mele, "Chiroptical Properties of some mono-aza-penta-helicenes", J. Phys. Chem. A 108(2004)11752-11761
[58] F. Lebon, G. Longhi, F. Gangemi, S. Abbate, C. Bazzini, T. Caronna, M. Juza, "Experimental and Calculated CD spectra of a Series of monoaza[5]helicenes", Note 19, 10th International Conference on Circular Dichroism, August 2005, Destin, Florida, USA
[59] S. Abbate, C. Bazzini, T. Caronna, F. Fontana, C. Gambarotti, F. Gangemi, G. Longhi, I. natali Sora, A. Mele, W. Panzeri, Tetrahedron, 62 (2006)139-148
[60] E. Marcantoni, G. Roselli, L. Lucarelli, G. Renzi, A. Filippi, C. Trionfetti, M. Speranza, J. Org. Chem. 2005, 70, 4133; A. Filippi, C. Fraschetti, G. Renzi, G. Roselli, M. Speranza, Chem. Eur. J. 2006, in the press; P. Crotti, G. Renzi, G. Roselli, V. Di Bussolo, L. Lucarelli, M.R. Romano, Tetrahedron, 2005, 61, 7814.
[61] E. Marcantoni, A. Giuliani, M. Massaccesi, S. Lanari, G. Bartoli, L. Sambri, Adv. Synth. Catal. 2005, 347, 1673.

Parole Chiave

FASCI MOLECOLARI, COMPLESSI, SPETTROMETRIA DI MASSA, CALCOLI AB-INITIO, CHIRALITA', ELICENI, DICROISMO CIRCOLARE, NANOAGGREGATI, ABLAZIONE LASER