Zobrazeno 1 - 10
of 123
pro vyhledávání: '"Marinella Catellani"'
Autor:
Marinella Catellani, Giovanni Marletta, Giovanni Li-Destri, Roberta Ruffino, Grazia M. L. Messina, Erika Kozma, Nunzio Tuccitto
Publikováno v:
The Journal of Physical Chemistry C. 123:8967-8974
The crystallization of a model semicrystalline polymer, namely, poly-3-hexylthiophene (P3HT), was studied as a function of the curvature at the nanometric scale and substrate surface free energy (SFE). Nanostructured substrates with a controlled loca
Autor:
Umberto Giovanella, Erika Kozma, Marco Paolino, Miriam Colombo, Marinella Catellani, Chiara Botta, Andrea Cappelli, Veronica Collico, Francesca Villafiorita-Monteleone
Publikováno v:
Dyes and pigments 149 (2018): 331–335. doi:10.1016/j.dyepig.2017.10.010
info:cnr-pdr/source/autori:Villafiorita-Monteleone F.; Kozma E.; Giovanella U.; Catellani M.; Paolino M.; Collico V.; Colombo M.; Cappelli A.; Botta C./titolo:Red and deep-red emissive polymeric nanoparticles based on polybenzofulvene and perylenediimide derivatives/doi:10.1016%2Fj.dyepig.2017.10.010/rivista:Dyes and pigments/anno:2018/pagina_da:331/pagina_a:335/intervallo_pagine:331–335/volume:149
info:cnr-pdr/source/autori:Villafiorita-Monteleone F.; Kozma E.; Giovanella U.; Catellani M.; Paolino M.; Collico V.; Colombo M.; Cappelli A.; Botta C./titolo:Red and deep-red emissive polymeric nanoparticles based on polybenzofulvene and perylenediimide derivatives/doi:10.1016%2Fj.dyepig.2017.10.010/rivista:Dyes and pigments/anno:2018/pagina_da:331/pagina_a:335/intervallo_pagine:331–335/volume:149
Polymeric nanoparticles obtained by co-aggregation of a polybenzofulvene derivative with bulky substituted perylene diimide dyes in tetrahydrofuran/water mixtures display emission color tunable from blue to red, or deep-red, thanks to energy transfer
Autor:
A. Andicsová Eckstein, Francesco Galeotti, Martin Danko, Erika Kozma, Alena Opálková Šišková, Vladimír Lukeš, Marinella Catellani, Wojciech Mróz
Publikováno v:
New journal of chemistry (1987) 42 (2018): 1061–1066. doi:10.1039/c7nj03860g
info:cnr-pdr/source/autori:Kozma, E.; Mroz, W.; Eckstein, A. Andicsova; Lukes, V.; Galeotti, F.; Siskova, A.; Danko, M.; Catellani, M./titolo:A joint experimental and theoretical study on the electro-optical properties of 1,6-and 1,7-fluorenyl disubstituted perylene diimide isomers/doi:10.1039%2Fc7nj03860g/rivista:New journal of chemistry (1987)/anno:2018/pagina_da:1061/pagina_a:1066/intervallo_pagine:1061–1066/volume:42
info:cnr-pdr/source/autori:Kozma, E.; Mroz, W.; Eckstein, A. Andicsova; Lukes, V.; Galeotti, F.; Siskova, A.; Danko, M.; Catellani, M./titolo:A joint experimental and theoretical study on the electro-optical properties of 1,6-and 1,7-fluorenyl disubstituted perylene diimide isomers/doi:10.1039%2Fc7nj03860g/rivista:New journal of chemistry (1987)/anno:2018/pagina_da:1061/pagina_a:1066/intervallo_pagine:1061–1066/volume:42
Core substituted perylene diimides (PDIs), obtained by introducing various functional groups into the perylenic bay positions, are well known as versatile materials for optoelectronic applications. The substitution of the perylene core affords mono-,
Autor:
Desta Antenehe Gedefaw, Marinella Catellani, Marco Cavazzini, Margherita Bolognesi, Erika Kozma, Mirko Seri, Mats Andersson, Michele Muccini
Publikováno v:
New Journal of Chemistry. 42:18633-18640
N-Substitution in perylene diimide (PDI) n-type semiconductors is critical for their performance in organic bulk heterojunction solar cells. In this work we synthesized and compared three perylene diimide-spirobifluorene derivatives, N-substituted wi
Publikováno v:
ChemistrySelect (2016): 3033–3037. doi:10.1002/slct.201600614
info:cnr-pdr/source/autori:G. Grisci, W. Mròz, M. Catellani, E. Kozma, F. Galeotti/titolo:Off-On Fluorescence Response of a Cysteine-based Perylene Diimide for Mercury Detection in Water/doi:10.1002%2Fslct.201600614/rivista:ChemistrySelect/anno:2016/pagina_da:3033/pagina_a:3037/intervallo_pagine:3033–3037/volume
info:cnr-pdr/source/autori:G. Grisci, W. Mròz, M. Catellani, E. Kozma, F. Galeotti/titolo:Off-On Fluorescence Response of a Cysteine-based Perylene Diimide for Mercury Detection in Water/doi:10.1002%2Fslct.201600614/rivista:ChemistrySelect/anno:2016/pagina_da:3033/pagina_a:3037/intervallo_pagine:3033–3037/volume
The development of simple, low-cost and selective methods for quantitative detection of mercury ions in aqueous media is still a challenge. Herein, we employ a cysteine based perylene diimide (PDI-Cys) as sensing probe for Hg2+ ions in water. The pro
Autor:
Wojciech Mróz, Anita Eckstein-Andicsová, Katiuscia Pagano, Giorgio Grisci, Marinella Catellani, Erika Kozma, Francesco Galeotti
Publikováno v:
Dyes and pigments 125 (2016): 201–209. doi:10.1016/j.dyepig.2015.10.019
info:cnr-pdr/source/autori:Erika Kozma, Giorgio Grisci, Wojciech Mróz, Marinella Catellani, Anita Eckstein-Andicsovà, Katiuscia Pagano, Francesco Galeotti/titolo:Water-soluble aminoacid functionalized perylene diimides: the effect of aggregation on the optical properties in organic and aqueous media/doi:10.1016%2Fj.dyepig.2015.10.019/rivista:Dyes and pigments/anno:2016/pagina_da:201/pagina_a:209/intervallo_pagine:201–209/volume:125
info:cnr-pdr/source/autori:Erika Kozma, Giorgio Grisci, Wojciech Mróz, Marinella Catellani, Anita Eckstein-Andicsovà, Katiuscia Pagano, Francesco Galeotti/titolo:Water-soluble aminoacid functionalized perylene diimides: the effect of aggregation on the optical properties in organic and aqueous media/doi:10.1016%2Fj.dyepig.2015.10.019/rivista:Dyes and pigments/anno:2016/pagina_da:201/pagina_a:209/intervallo_pagine:201–209/volume:125
We report on the straightforward preparation and photophysical characterization of four symmetrically substituted water soluble perylene diimides, obtained by functionalizing the imide positions with l -threonine, l -aspartic acid, l -cysteine and l
Autor:
Margherita Bolognesi, a Desta Gedefaw, b, e Marco Cavazzini, c Marinella Catellani, d Mats R. Andersson, e Michele Muccini, a Erika Kozma*d, Mirko Seri*f
Publikováno v:
New journal of chemistry (Online) (2018).
info:cnr-pdr/source/autori:Margherita Bolognesi,a Desta Gedefaw,b,e Marco Cavazzini,c Marinella Catellani,d Mats R. Andersson,e Michele Muccini,a Erika Kozma*d and Mirko Seri*f/titolo:Side chain modification on PDI-spirobifluorene based molecular acceptors and its impact on organic solar cell performances/doi:/rivista:New journal of chemistry (Online)/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume
info:cnr-pdr/source/autori:Margherita Bolognesi,a Desta Gedefaw,b,e Marco Cavazzini,c Marinella Catellani,d Mats R. Andersson,e Michele Muccini,a Erika Kozma*d and Mirko Seri*f/titolo:Side chain modification on PDI-spirobifluorene based molecular acceptors and its impact on organic solar cell performances/doi:/rivista:New journal of chemistry (Online)/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume
N-substitution in perylene diimide (PDI) n-type semiconductors is critical for their performance in organic bulk heterojunction solar cells. In this work we synthesized and compared three perylene diimide-spirobifluorene derivatives, N-substituted wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::72b4008e9d571381d98f261a571e7b1d
http://www.cnr.it/prodotto/i/393223
http://www.cnr.it/prodotto/i/393223
Autor:
Marinella Catellani, Luisa Barba, William Porzio, Francesco Galeotti, Giorgio Grisci, Guido Scavia, Gianmichele Arrighetti, Erika Kozma
Publikováno v:
Surface science 675 (2018): 15–25. doi:10.1016/j.susc.2018.04.008
info:cnr-pdr/source/autori:E. Kozma, F. Galeotti, G. Grisci, L. Barba, G. Arrighetti, M. Catellani, G. Scavia, W. Porzio/titolo:Perylene diimide cysteine derivatives self-assembled onto (111) gold surface: Evidence of ordered aggregation/doi:10.1016%2Fj.susc.2018.04.008/rivista:Surface science/anno:2018/pagina_da:15/pagina_a:25/intervallo_pagine:15–25/volume:675
info:cnr-pdr/source/autori:E. Kozma, F. Galeotti, G. Grisci, L. Barba, G. Arrighetti, M. Catellani, G. Scavia, W. Porzio/titolo:Perylene diimide cysteine derivatives self-assembled onto (111) gold surface: Evidence of ordered aggregation/doi:10.1016%2Fj.susc.2018.04.008/rivista:Surface science/anno:2018/pagina_da:15/pagina_a:25/intervallo_pagine:15–25/volume:675
Perylene diimide derivatives containing pendant cysteine residues are subjected to a strong self-assembly onto [1 1 1] Au films due to the presence of thiol functionality. The preparation of two different Au surfaces easies the understanding of both
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcc9328a8266330619141bfe28c4dcef
https://publications.cnr.it/doc/386689
https://publications.cnr.it/doc/386689
Autor:
Marinella Catellani, Marco Cavazzini, Alberto Bossi, Erika Kozma, Silvia Luzzati, D. Kotowski, Guido Scavia
Publikováno v:
Dyes and pigments (2015). doi:10.1016/j.dyepig.2015.04.006
info:cnr-pdr/source/autori:Dariusz Kotowski, Silvia Luzzati, Guido Scavia, Marco Cavazzini, Alberto Bossi, Marinella Catellani, Erika Kozma/titolo:The effect of perylene diimides chemical structure on the photovoltaic performance of P3HT%2Fperylene diimides solar cells/doi:10.1016%2Fj.dyepig.2015.04.006/rivista:Dyes and pigments/anno:2015/pagina_da:/pagina_a:/intervallo_pagine:/volume
info:cnr-pdr/source/autori:Dariusz Kotowski, Silvia Luzzati, Guido Scavia, Marco Cavazzini, Alberto Bossi, Marinella Catellani, Erika Kozma/titolo:The effect of perylene diimides chemical structure on the photovoltaic performance of P3HT%2Fperylene diimides solar cells/doi:10.1016%2Fj.dyepig.2015.04.006/rivista:Dyes and pigments/anno:2015/pagina_da:/pagina_a:/intervallo_pagine:/volume
Core substituted perylene diimides are promising n-type semiconductor materials for organic photovoltaic applications. We have prepared three Donor-Acceptor-Donor perylene diimide molecules, substituted in bay positions with bithiophene, spirobifluor
Autor:
Alberto Bossi, Silvia Luzzati, D. Kotowski, Simonetta Orlandi, Erika Kozma, Fabio Bertini, Marinella Catellani, Marco Cavazzini
Publikováno v:
Materials chemistry and physics
163 (2015): 152–160. doi:10.1016/j.matchemphys.2015.07.025
info:cnr-pdr/source/autori:Kozma E.; Kotowski D.; Catellani M.; Luzzati S.; Cavazzini M.; Bossi A.; Orlandi S.; Bertini F./titolo:Design of perylene diimides for organic solar cell: Effect of molecular steric hindrance and extended conjugation/doi:10.1016%2Fj.matchemphys.2015.07.025/rivista:Materials chemistry and physics (Print)/anno:2015/pagina_da:152/pagina_a:160/intervallo_pagine:152–160/volume:163
163 (2015): 152–160. doi:10.1016/j.matchemphys.2015.07.025
info:cnr-pdr/source/autori:Kozma E.; Kotowski D.; Catellani M.; Luzzati S.; Cavazzini M.; Bossi A.; Orlandi S.; Bertini F./titolo:Design of perylene diimides for organic solar cell: Effect of molecular steric hindrance and extended conjugation/doi:10.1016%2Fj.matchemphys.2015.07.025/rivista:Materials chemistry and physics (Print)/anno:2015/pagina_da:152/pagina_a:160/intervallo_pagine:152–160/volume:163
Core-substituted perylene diimides (PDI) are promising candidates as n-type semiconductor materials for organic photovoltaics. The chemical functionalization of perylene diimides in the bay positions is a versatile tool to obtain a series of electron