Spettrometro NMR ad alto campo operante in soluzione alla frequenza di 400 MHz

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NMR Multinucleare AVANCE III HD 400MHz (Bruker) MR in grado di registrare spettri in soluzione a temperatura variabile e dotato di autocampionatore. Questa analisi rappresenta lo strumento principe per l'identificazione della struttura chimica di materiali organici, sia puri sia in miscela.

Edificio
U9; ; Laboratorio NMR
Responsabile scientifico
Immagine
Immagine Cover

Pubblicazioni

  • Macher, S; Sassi, M; Beverina, L; Posset, U; Schott, M; Giffin, G; Lobmann, P (2021) Electrochromic Polymer Ink Derived from a Sidechain-Modified EDOT for Electrochromic Devices with Colorless Bright State. Dettaglio
  • Bodlos, W; Mattiello, S; Perinot, A; Gigli, L; Demitri, N; Beverina, L; Caironi, M; Resel, R (2021) Cold Crystallization of the Organic n-Type Small Molecule Semiconductor 2-Decyl-7-phenyl-[1]benzothieno[3,2- b][1]benzothiophene S, S, S′, S′-Tetraoxide. Dettaglio
  • Bonizzoni, S; Stilli, P; Lohmann-Richters, F; Oldani, C; Ferrara, C; Papagni, A; Beverina, L; Mustarelli, P (2021) Facile Chemical Modification of Aquivion® Membranes for Anionic Fuel Cells. Dettaglio
  • Beverina, L (2021) Sustainable access to conjugated materials in interface rich and water based microheterogeneous environments. Dettaglio
  • Pallini, F; Sangalli, E; Sassi, M; Roth, P; Mattiello, S; Beverina, L (2021) Selective photoredox direct arylations of aryl bromides in water in a microfluidic reactor. Dettaglio
  • Fortunato, A; Sanzone, A; Mattiello, S; Beverina, L; Mba, M (2021) The pH- And salt-controlled self-assembly of [1]benzothieno[3,2-b][1]-benzothiophene-peptide conjugates in supramolecular hydrogels. Dettaglio
  • Hofer, S; Bodlos, W; Novak, J; Sanzone, A; Beverina, L; Resel, R (2021) Molecular packing analysis of the crystal smectic E phase of a benzothieno-benzothiophene derivative by a combined experimental / computational approach. Dettaglio
  • Hofer, S; Unterkofler, J; Kaltenegger, M; Schweicher, G; Ruzie, C; Tamayo, A; Salzillo, T; Mas-Torrent, M; Sanzone, A; Beverina, L; Geerts, Y; Resel, R (2021) Molecular Disorder in Crystalline Thin Films of an Asymmetric BTBT Derivative. Dettaglio
  • Bodlos, W; Mattiello, S; Perinot, A; Fischer, R; Beverina, L; Caironi, M; Resel, R (2021) Controlled recrystallization from the melt of the organic n-type small molecule semiconductor 2-decyl-7-phenyl-[1]benzothieno[3,2-b][1]benzothiophene S,S,S′,S′-tetraoxide. Dettaglio
  • Zablocki, J; Schulz, M; Schnakenburg, G; Beverina, L; Warzanowski, P; Revelli, A; Gruninger, M; Balzer, F; Meerholz, K; Lutzen, A; Schiek, M (2020) Structure and Dielectric Properties of Anisotropic n-Alkyl Anilino Squaraine Thin Films. Dettaglio
  • Sassi, M; Mattiello, S; Beverina, L (2020) Syntheses of Organic Semiconductors in Water. Recent Advancement in the Surfactants Enhanced Green Access to Polyconjugated Molecules. Dettaglio
  • Gandini, M; Villa, I; Beretta, M; Gotti, C; Imran, M; Carulli, F; Fantuzzi, E; Sassi, M; Zaffalon, M; Brofferio, C; Manna, L; Beverina, L; Vedda, A; Fasoli, M; Gironi, L; Brovelli, S (2020) Efficient, fast and reabsorption-free perovskite nanocrystal-based sensitized plastic scintillators. Dettaglio
  • Sanzone, A; Calascibetta, A; Monti, M; Mattiello, S; Sassi, M; Corsini, F; Griffini, G; Sommer, M; Beverina, L (2020) Synthesis of conjugated polymers by sustainable Suzuki polycondensation in water and under aerobic conditions. Dettaglio
  • Calascibetta, A; Mattiello, S; Sanzone, A; Facchinetti, I; Sassi, M; Beverina, L (2020) Sustainable Access to π-Conjugated Molecular Materials via Direct (Hetero)Arylation Reactions in Water and under Air. Dettaglio
  • Ceriani, C; Ghiglietti, E; Sassi, M; Mattiello, S; Beverina, L (2020) Taming troublesome suzuki-miyaura reactions in water solution of surfactants by the use of lecithin: A step beyond the micellar model. Dettaglio
  • Mattiello, S; Sanzone, A; Bruni, F; Gandini, M; Pinchetti, V; Monguzzi, A; Facchinetti, I; Ruffo, R; Meinardi, F; Mattioli, G; Sassi, M; Brovelli, S; Beverina, L (2020) Chemically Sustainable Large Stokes Shift Derivatives for High-Performance Large-Area Transparent Luminescent Solar Concentrators. Dettaglio
  • Macher, S; Schott, M; Sassi, M; Facchinetti, I; Ruffo, R; Patriarca, G; Beverina, L; Posset, U; Giffin, G; Loebmann, P (2020) New Roll-to-Roll Processable PEDOT-Based Polymer with Colorless Bleached State for Flexible Electrochromic Devices. Dettaglio
  • Mattioli, G; Mattiello, S; Sassi, M; Beverina, L (2020) Ab Initio Simulations of Interfaces between SAM-Modified Gold Electrodes and n-Type or p-Type Organic Semiconductors Based on the Benzothieno-Benzothiophene (BTBT) Architecture. Dettaglio
  • Zanotti, G; Angelini, N; Mattioli, G; Paoletti, A; Pennesi, G; Caschera, D; Sobolev, A; Beverina, L; Calascibetta, A; Sanzone, A; Di Carlo, A; Berionni Berna, B; Pescetelli, S; Agresti, A (2020) [1]Benzothieno[3,2-b][1]benzothiophene-Phthalocyanine Derivatives: A Subclass of Solution-Processable Electron-Rich Hole Transport Materials. Dettaglio
  • Sanzone, A; Mattiello, S; Maria Garavaglia, G; Calascibetta, A; Ceriani, C; Sassi, M; Beverina, L (2019) Efficient synthesis of organic semiconductors by Suzuki-Miyaura coupling in an aromatic micellar medium. Dettaglio
  • Sanzone, A; Cimò, S; Mattiello, S; Ruffo, R; Facchinetti, I; Bonacchini, G; Caironi, M; Sassi, M; Sommer, M; Beverina, L (2019) Front Cover: Preparation of Naphthalene Dianhydride Bithiophene Copolymers by Direct Arylation Polycondensation and the Latent Pigment Approach (ChemPlusChem 9/2019). Dettaglio
  • Beverina, L (2019) Green organic chemistry for advanced optoelectronic applications. Dettaglio
  • Della Sala, P; Buccheri, N; Sanzone, A; Sassi, M; Neri, P; Talotta, C; Rocco, A; Pinchetti, V; Beverina, L; Brovelli, S; Gaeta, C (2019) First demonstration of the use of very large Stokes shift cycloparaphenylenes as promising organic luminophores for transparent luminescent solar concentrators. Dettaglio
  • Beverina, L (2019) Bench-top, sustainable access to conjugated materials: how far you can go with tap water, a stirring plate, very little palladium and a little soap. Dettaglio
  • Vaghi, L; Coletta, M; Coghi, P; Andreosso, I; Beverina, L; Ruffo, R; Papagni, A (2019) Fluorine substituted non-symmetric phenazines: A new synthetic protocol from polyfluorinated azobenzenes. Dettaglio
  • Ronchi, A; Brazzo, P; Sassi, M; Beverina, L; Pedrini, J; Meinardi, F; Monguzzi, A (2019) Triplet-triplet annihilation based photon up-conversion in hybrid molecule-semiconductor nanocrystal systems. Dettaglio
  • Sanzone, A; Cimò, S; Mattiello, S; Ruffo, R; Facchinetti, I; Bonacchini, G; Caironi, M; Sassi, M; Sommer, M; Beverina, L (2019) Preparation of Naphthalene Dianhydride Bithiophene Copolymers by Direct Arylation Polycondensation and the Latent Pigment Approach. Dettaglio
  • Beverina, L (2019) Sustainable approaches for the design and synthesis of organic dyes and pigments for printed electronics. Dettaglio
  • Beverina, L (2018) Efficient Suzuki-Miyaura micellar Cross-Coupling in water, at room temperature and under aerobic atmosphere. Organic materials go green. Dettaglio
  • Sanzone, A; Calascibetta, A; Ghiglietti, E; Ceriani, C; Mattioli, G; Mattiello, S; Sassi, M; Beverina, L (2018) Suzuki-Miyaura Micellar One-Pot Synthesis of Symmetrical and Unsymmetrical 4,7-Diaryl-5,6-difluoro-2,1,3-benzothiadiazole Luminescent Derivatives in Water and under Air. Dettaglio
  • Beverina, L; Rooney, M; Ruffo, R; Sassi, M; Carulli, F; Luzzati, S; Resel, R; Schrode, B (2018) Diketopyrrolopyrrole latent pigment-based bilayer solar cells. Dettaglio
  • Rooney, M; Mattiello, S; Stara, R; Sanzone, A; Brazzo, P; Sassi, M; Beverina, L (2018) Suzuki-Miyaura cross-coupling of latent pigments in water/toluene emulsion under aerobic atmosphere. Dettaglio
  • Facchinetti, I; Ruffo, R; Beverina, L; Sassi, M; Fontanesi, C; Vanossi, D (2018) The role of electrolyte ions on the electrochemical properties of thiophene based conducting polymers. Dettaglio
  • Vaghi, L; Sanzone, A; Sassi, M; Pagani, S; Papagni, A; Beverina, L (2018) Synthesis of Fluorinated Acridines via Sequential Micellar Buchwald-Hartwig Amination/Cyclization of Aryl Bromides. Dettaglio
  • Sassi, M; Salamone, M; Beverina, L; Longoni, G; Fontanesi, C; Vanossi, D; Cigarini, L; Ruffo, R (2017) An Integrated theoretical/experimental study of quinolinic-isoquinolinic derivatives acting as reversible electrochromes. Dettaglio
  • Beverina, L (2017) Sustainable approaches for the design and synthesis of organic semiconductors. Dettaglio
  • Caranzi, L; Pace, G; Sassi, M; Beverina, L; Caironi, M (2017) Transparent and Highly Responsive Phototransistors Based on a Solution-Processed, Nanometers-Thick Active Layer, Embedding a High-Mobility Electron-Transporting Polymer and a Hole-Trapping Molecule. Dettaglio
  • Beverina, L; Brazzo, P; Sassi, M; Mattiello, S; Rooney, M (2017) Latent pigments with extended conjugation. Resourceful materials for organic electronics.. Dettaglio
  • Beverina, L (2017) Organic based electrochromic materials: design, characterization and integration in flexible devices. Dettaglio
  • Mattiello, S; Rooney, M; Sanzone, A; Brazzo, P; Sassi, M; Beverina, L (2017) Suzuki-Miyaura Micellar Cross-Coupling in Water, at Room Temperature, and under Aerobic Atmosphere. Dettaglio
  • Bianchi, G; Po, R; Sassi, M; Beverina, L; Chiaberge, S; Spera, S; Cominetti, A (2017) Synthesis of Dithienocyclohexanones (DTCHs) as a Family of Building Blocks for π-Conjugated Compounds in Organic Electronics. Dettaglio
  • Maqueira-Albo, I; Ernesto Bonacchini, G; Dell'Erba, G; Pace, G; Sassi, M; Rooney, M; Resel, R; Beverina, L; Caironi, M (2017) A latent pigment strategy for robust active layers in solution-processed, complementary organic field-effect transistors. Dettaglio
  • Salamone, M; Ruffo, R; Mari, C; Beverina, L (2017) Redox Switchable Organic Conjugated Materials for Flexible Electrochromic Devices. Dettaglio
  • Wang, B; Di Carlo, G; Turrisi, R; Zeng, L; Stallings, K; Huang, W; Bedzyk, M; Beverina, L; Marks, T; Facchetti, A (2017) The Dipole Moment Inversion Effects in Self-Assembled Nanodielectrics for Organic Transistors. Dettaglio