Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Ilir Pecnikaj"'
Autor:
David Possetto, Ilir Pecnikaj, Gabriela Marzari, Simonetta Orlandi, Silvia Sereno, Marco Cavazzini, Gianluca Pozzi, Fernando Fungo
Publikováno v:
Chemphyschem : a European journal of chemical physics and physical chemistry.
A clear case of relationship between the monomer molecular structure and the capability of tuning the morphology of electrodeposited gas bubbles template polymer thin films is shown. To this end, a series of fluorene-bridged dicarbazole derivatives c
Autor:
Fiorella Meneghetti, Raffaella Bucci, Michele Penso, Carlo Castellano, Francesca Foschi, Ilir Pecnikaj, Maria Luisa Gelmi
Publikováno v:
European Journal of Organic Chemistry. 2019:6707-6713
Autor:
Simonetta Orlandi, Laura Hernandez, Maximiliano Andres Zensich, Fernando Fungo, Gianluca Pozzi, María Victoria Cappellari, Gabriela Lorena Marzari, Luciana Fernandez, Ilir Pecnikaj
Publikováno v:
Langmuir 35 (2019): 8732–8740. doi:10.1021/acs.langmuir.9b01141
info:cnr-pdr/source/autori:Pecnikaj, Ilir; Orlandi, Simonetta; Pozzi, Gianluca; Cappellari, María Victoria; Marzari, Gabriela; Fernández, Luciana; Zensich, Maximiliano Andrés; Hernandez, Laura; Fungo, Fernando/titolo:Improving the Electropolymerization Properties of Fluorene-Bridged Dicarbazole Monomers through Polyfluoroalkyl Side Chains/doi:10.1021%2Facs.langmuir.9b01141/rivista:Langmuir/anno:2019/pagina_da:8732/pagina_a:8740/intervallo_pagine:8732–8740/volume:35
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
info:cnr-pdr/source/autori:Pecnikaj, Ilir; Orlandi, Simonetta; Pozzi, Gianluca; Cappellari, María Victoria; Marzari, Gabriela; Fernández, Luciana; Zensich, Maximiliano Andrés; Hernandez, Laura; Fungo, Fernando/titolo:Improving the Electropolymerization Properties of Fluorene-Bridged Dicarbazole Monomers through Polyfluoroalkyl Side Chains/doi:10.1021%2Facs.langmuir.9b01141/rivista:Langmuir/anno:2019/pagina_da:8732/pagina_a:8740/intervallo_pagine:8732–8740/volume:35
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
The facile functionalization of the fluorene scaffold at the 2,7-positions was utilized to provide access to two soluble carbazole-π-carbazole derivatives CFC-H1 and CFC-F1 featuring fully hydrogenated and polyfluorinated alkyl chains at the 9-posit
Autor:
Ilir Pecnikaj, Gianluca Pozzi, Simonetta Orlandi, Luis Otero, Marco Cavazzini, Fernando Fungo, Daniela Minudri
Publikováno v:
New journal of chemistry (1987) 41 (2017): 7729–7738. doi:10.1039/c7nj01516j
info:cnr-pdr/source/autori:Pecnikaj I.; Minudri D.; Otero L.; Fungo F.; Cavazzini M.; Orlandi S.; Pozzi G./titolo:Fluorous molecules for dye-sensitized solar cells: Synthesis and properties of di-branched, di-anchoring organic sensitizers containing fluorene subunits/doi:10.1039%2Fc7nj01516j/rivista:New journal of chemistry (1987)/anno:2017/pagina_da:7729/pagina_a:7738/intervallo_pagine:7729–7738/volume:41
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
info:cnr-pdr/source/autori:Pecnikaj I.; Minudri D.; Otero L.; Fungo F.; Cavazzini M.; Orlandi S.; Pozzi G./titolo:Fluorous molecules for dye-sensitized solar cells: Synthesis and properties of di-branched, di-anchoring organic sensitizers containing fluorene subunits/doi:10.1039%2Fc7nj01516j/rivista:New journal of chemistry (1987)/anno:2017/pagina_da:7729/pagina_a:7738/intervallo_pagine:7729–7738/volume:41
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Four organic sensitizers having a di-branched molecular structure D-(π-A)2 (D = para-substituted arylamine, π = 9,9-dibutylfluorene, A = cyanoacrylic acid) were synthesized, characterized, and applied in the development of dye-sensitized solar cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3671236dbc46d20a03b16e01e31c2b6f
https://publications.cnr.it/doc/374834
https://publications.cnr.it/doc/374834
Publikováno v:
NATO Science for Peace and Security Series A: Chemistry and Biology ISBN: 9789402411126
Exposure of human populations to cadmium (Cd) and Lead (Pb) from food and products thereof may produce effects in organssuch as the kidneys, liver, lungs, cardiovascular, immune and reproductive systems. Since Cd and Pb have been identified as a huma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7b455f0f875f81446d610543d7f1a44
https://doi.org/10.1007/978-94-024-1113-3_19
https://doi.org/10.1007/978-94-024-1113-3_19
Publikováno v:
Organic letters. 19(1)
The synthesis of enantiopure 2,6-disubstituted morpholines was realized through sequential ring opening of two different optically pure oxiranes by a tosylamide, under solid–liquid phase-transfer catalysis (SL-PTC) conditions, mono-O-sulfonylation
Autor:
Stefano Caramori, Ilir Pecnikaj, Gianluca Pozzi, Stefano Tortelli, Rita Boaretto, Simonetta Orlandi, Marco Cavazzini
Publikováno v:
Journal of fluorine chemistry
188 (2016): 110–116. doi:10.1016/j.jfluchem.2016.06.012
info:cnr-pdr/source/autori:Stefano Tortelli, Marco Cavazzini, Simonetta Orlandi, Gianluca Pozzi, Ilir Pecnikaj, Stefano Caramori, Rita Boaretto/titolo:Property tuning in unsymmetrical alkoxy zinc phthalocyanines by introduction of perfluoro-tert-butoxy end groups/doi:10.1016%2Fj.jfluchem.2016.06.012/rivista:Journal of fluorine chemistry (Print)/anno:2016/pagina_da:110/pagina_a:116/intervallo_pagine:110–116/volume:188
188 (2016): 110–116. doi:10.1016/j.jfluchem.2016.06.012
info:cnr-pdr/source/autori:Stefano Tortelli, Marco Cavazzini, Simonetta Orlandi, Gianluca Pozzi, Ilir Pecnikaj, Stefano Caramori, Rita Boaretto/titolo:Property tuning in unsymmetrical alkoxy zinc phthalocyanines by introduction of perfluoro-tert-butoxy end groups/doi:10.1016%2Fj.jfluchem.2016.06.012/rivista:Journal of fluorine chemistry (Print)/anno:2016/pagina_da:110/pagina_a:116/intervallo_pagine:110–116/volume:188
Two peripherally octasubstituted zinc phthalocyanines (ZnPcs) bearing six alkoxy residues and two adjacent carboxylic acid anchoring groups were synthesized in order to assess the benefits deriving from the insertion of fluorocarbon domains at the pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7432cd4a33913e4ef1dcc27d70c28350
http://www.sciencedirect.com/science/article/pii/S0022113916301580
http://www.sciencedirect.com/science/article/pii/S0022113916301580
Autor:
Ilir Pecnikaj, Michele Penso, Voichita Mihali, Aaron Tagliabue, Tullio Pilati, Francesca Foschi
Publikováno v:
ChemInform. 44
An interesting protocol is described to convert single enantiomeric sulfonamides (I) in a stereodivergent fashion into sultams.
Autor:
Francesca Foschi, Michele Penso, Ilir Pecnikaj, Aaron Tagliabue, Tullio Pilati, Voichita Mihali
Publikováno v:
Organic letters (Online) 15 (2013): 3686–3689. doi:10.1021/ol401557v
info:cnr-pdr/source/autori:Foschi F.; Tagliabue A.; Mihali V.; Pilati T.; Pecnikaj I.; Penso M./titolo:Memory of chirality approach to the enantiodivergent synthesis of chiral benzo[ d ]sultams/doi:10.1021%2Fol401557v/rivista:Organic letters (Online)/anno:2013/pagina_da:3686/pagina_a:3689/intervallo_pagine:3686–3689/volume:15
info:cnr-pdr/source/autori:Foschi F.; Tagliabue A.; Mihali V.; Pilati T.; Pecnikaj I.; Penso M./titolo:Memory of chirality approach to the enantiodivergent synthesis of chiral benzo[ d ]sultams/doi:10.1021%2Fol401557v/rivista:Organic letters (Online)/anno:2013/pagina_da:3686/pagina_a:3689/intervallo_pagine:3686–3689/volume:15
The "memory of chirality" stereodivergent synthesis of polyfluorobenzo[d]sultams has been developed. The interest of this protocol resides in the possibility of using the chirality of a starting sulfonamide single enantiomer to synthesize the target
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c49df38ae4d258120b3b434729c5c705
http://hdl.handle.net/11383/2097247
http://hdl.handle.net/11383/2097247
Publikováno v:
ChemInform. 38