Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Vito Maltese"'
Autor:
Giuseppina Anna Corrente, Francesco Parisi, Vito Maltese, Sante Cospito, Daniela Imbardelli, Massimo La Deda, Amerigo Beneduci
Publikováno v:
Molecules, Vol 26, Iss 22, p 6818 (2021)
Electrofluorochromic devices (EFCDs) that allow the modulation of the light emitted by electroactive fluorophores are very attractive in the research field of optoelectronics. Here, the electrofluorochromic behaviour of a series of squaraine dyes was
Externí odkaz:
https://doaj.org/article/169827409a174343a21c30ecb7738086
Autor:
Sante Cospito, Francesco Parisi, D. Imbardelli, Massimo La Deda, Giuseppina Anna Corrente, Vito Maltese, Amerigo Beneduci
Publikováno v:
Molecules, Vol 26, Iss 6818, p 6818 (2021)
Molecules
Molecules
Electrofluorochromic devices (EFCDs) that allow the modulation of the light emitted by electroactive fluorophores are very attractive in the research field of optoelectronics. Here, the electrofluorochromic behaviour of a series of squaraine dyes was
Autor:
Giuseppe Pandolfi, Sante Cospito, Giuseppe Chidichimo, Vito Maltese, Amerigo Beneduci, Antonio Tursi, Paolo Tassini
Publikováno v:
Liquid Crystals. 45:2132-2138
In this paper, we present a new type of parallax barrier, for switchable 2D/3D display vision, obtained by using a Reverse Mode Polymer Dispersed Liquid Crystal display (RV-PDLC). The parallax barr...
Autor:
Giuseppe Gigli, Sante Cospito, Giuseppe Ciccarella, Giuseppina Anna Corrente, Giuseppe Chidichimo, Agostina Lina Capodilupo, Vito Maltese, Amerigo Beneduci, Eduardo Fabiano
Publikováno v:
Chemical Communications. 53:8960-8963
Herein we present organic mixed-valence compounds with an innovative H-shape design, where four redox centres are bridged "vertically" via a dibenzofulvene backbone and "horizontally" via a bis-(dibenzofulvene)-thiophene bridge. These compounds are e
Autor:
Vito Maltese, Amerigo Beneduci, René A. J. Janssen, Nino Russo, Sante Cospito, Bruna Clara De Simone, Giuseppe Chidichimo
Publikováno v:
Chemistry : A European Journal, 22(29), 10179-10186. Wiley-VCH Verlag
Thienosquaraines are an interesting class of electroactive dyes that are useful for applications in organic electronics. Herein, the redox chemistry and electrochromic response of a few newly synthesized thienosquaraines are presented. These properti
Autor:
Bartolo Gabriele, Giuseppe Chidichimo, Chiara Santillo, Massimo La Deda, Finizia Auriemma, Claudio De Rosa, Lucia Veltri, Vito Maltese, Amerigo Beneduci, Sante Cospito
π-Conjugated ionic liquid crystals are a very interesting class of salts where the coupling of ionic and electronic functions with the anisotropy typical of liquid crystals may give rise to materials with advanced bulk properties. Defect-free active
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63283777907daf809cfcb13fc83f771e
http://hdl.handle.net/11588/670486
http://hdl.handle.net/11588/670486
Publikováno v:
The Journal of Organic Chemistry. 77:8657-8668
A variety of 3-yne-1,2-diol derivatives 1, bearing a primary or secondary alcoholic group at C-1, have been efficiently converted into high value added furan-3-carboxylic esters 2 in one step by PdI(2)/KI-catalyzed direct oxidative carbonylation, car
Autor:
Raffaella Mancuso, Bartolo Gabriele, Lucia Veltri, Mabel V. Vetere, Vito Maltese, Pierluigi Plastina
Publikováno v:
ChemInform. 44
CuCl2-catalyzed heterocyclodehydration of readily available 3-yne-1,2-diols and 1-amino-3-yn-2-ol derivatives afforded substituted furans and pyrroles, respectively, in good to high yields (53-99%) under mild conditions (MeOH as the solvent, 80-100
Autor:
Mabel V. Vetere, Raffaella Mancuso, Bartolo Gabriele, Pierluigi Plastina, Vito Maltese, Lucia Veltri
Publikováno v:
The Journal of organic chemistry. 78(10)
CuCl2-catalyzed heterocyclodehydration of readily available 3-yne-1,2-diols and 1-amino-3-yn-2-ol derivatives afforded substituted furans and pyrroles, respectively, in good to high yields (53-99%) under mild conditions (MeOH as the solvent, 80-100
Publikováno v:
ChemInform. 44
The reaction provides a convenient, mild, and widely applicable method to prepare substituted thiophenes under either conditions A) or B).