Zobrazeno 1 - 10
of 74
pro vyhledávání: '"Patrizia Gentili"'
Autor:
David Rodríguez-Escribano, Rocío Pliego-Magán, Felipe de Salas, Pablo Aza, Patrizia Gentili, Petri Ihalainen, Thomas Levée, Valérie Meyer, Michel Petit-Conil, Sandra Tapin-Lingua, Michael Lecourt, Susana Camarero
Publikováno v:
Biotechnology for Biofuels and Bioproducts, Vol 15, Iss 1, Pp 1-19 (2022)
Abstract Background During the kraft process to obtain cellulosic pulp from wood, most of the lignin is removed by high-temperature alkaline cooking, released in the black liquors and usually incinerated for energy. However, kraft lignins are a valua
Externí odkaz:
https://doaj.org/article/3f6fbd1d7fe04c4a84040e8e47faeaad
Autor:
Irene, Antignano, Francesca, D'Acunzo, Davide, Arena, Stefano, Casciardi, Alessandra, Del Giudice, Francesca, Gentile, Maria, Pelosi, Giancarlo, Masci, Patrizia, Gentili
Publikováno v:
Langmuir : the ACS journal of surfaces and colloids. 38(46)
In this work, we compare nanoaggregation driven by pH-induced micellization (PIM) and by the standard solvent displacement (SD) method on a series of pH-, light-, and thermosensitive amphiphilic block copolymers. Specifically, we investigate poly(HIA
Autor:
Antonio Di Sabato, Francesca D’Acunzo, Dario Filippini, Fabrizio Vetica, Antonio Brasiello, Davide Corinti, Enrico Bodo, Cinzia Michenzi, Edoardo Panzetta, Patrizia Gentili
Photocyclization of carbonyl compounds (known as the Norrish-Yang reaction) to yield cyclobutanols is, in general, accompanied by fragmentation reactions. The latter are predominant in the case of aldehydes so that secondary cyclobutanols are not con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ee6b0894e8f6c32cf1f50248516cd7b
https://hdl.handle.net/11573/1656147
https://hdl.handle.net/11573/1656147
Autor:
Francesca D'Acunzo, L. Mancini, Antonella Dalla Cort, Linda Carbonaro, Patrizia Gentili, Francesca Leonelli, Antonio Di Sabato, Dario Filippini
Publikováno v:
European journal of organic chemistry (Online) 2021 (2021): 289–294. doi:10.1002/ejoc.202001303
info:cnr-pdr/source/autori:D'Acunzo F.; Carbonaro L.; Cort A.D.; Di Sabato A.; Filippini D.; Leonelli F.; Mancini L.; Gentili P./titolo:Click-Connected 2-(Hydroxyimino)aldehydes for the Design of UV-Responsive Functional Molecules/doi:10.1002%2Fejoc.202001303/rivista:European journal of organic chemistry (Online)/anno:2021/pagina_da:289/pagina_a:294/intervallo_pagine:289–294/volume:2021
info:cnr-pdr/source/autori:D'Acunzo F.; Carbonaro L.; Cort A.D.; Di Sabato A.; Filippini D.; Leonelli F.; Mancini L.; Gentili P./titolo:Click-Connected 2-(Hydroxyimino)aldehydes for the Design of UV-Responsive Functional Molecules/doi:10.1002%2Fejoc.202001303/rivista:European journal of organic chemistry (Online)/anno:2021/pagina_da:289/pagina_a:294/intervallo_pagine:289–294/volume:2021
Click chemistry is used to functionalize simple lipophilic and water-soluble molecules, a complex PEGylated phospholipid (DSPE-PEG2000), and two benzylic substrates with the 2-(hydroxyimino)aldehyde (HIA) group. To this end, two terminal alkynes bear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4f54f9ded43fa41abb5bea0f03ee1e3
https://publications.cnr.it/doc/443302
https://publications.cnr.it/doc/443302
Autor:
Francesca Martini, Maria Assunta Navarra, Polyssena Renzi, Francesca Nardelli, Francesca D'Acunzo, Marco Geppi, Carmine Mancone, Lucia Mazzapioda, Patrizia Gentili
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c8c3ccef16a72513c0bcbc9ba16de09
http://hdl.handle.net/11568/1051991
http://hdl.handle.net/11568/1051991
Autor:
Francesca D'Acunzo, Martina Nardi, Paolo Cambise, Alessandro Pinna, Marco D'Abramo, Emanuele Ussia, Irene Antignano, Patrizia Gentili
Publikováno v:
Chemistry-A European Journal 24 (2018): 7683–7694. doi:10.1002/chem.201800059
info:cnr-pdr/source/autori:Gentili P. (a,b); Nardi M. (a,b); Antignano I. (a); Cambise P. (a); D'Abramo M. (a); D'Acunzo F. (b); Pinna A. (a); Ussia E. (a)/titolo:2-(Hydroxyimino)aldehydes: Photo-and Physicochemical Properties of a Versatile Functional Group for Monomer Design/doi:10.1002%2Fchem.201800059/rivista:Chemistry-A European Journal/anno:2018/pagina_da:7683/pagina_a:7694/intervallo_pagine:7683–7694/volume:24
info:cnr-pdr/source/autori:Gentili P. (a,b); Nardi M. (a,b); Antignano I. (a); Cambise P. (a); D'Abramo M. (a); D'Acunzo F. (b); Pinna A. (a); Ussia E. (a)/titolo:2-(Hydroxyimino)aldehydes: Photo-and Physicochemical Properties of a Versatile Functional Group for Monomer Design/doi:10.1002%2Fchem.201800059/rivista:Chemistry-A European Journal/anno:2018/pagina_da:7683/pagina_a:7694/intervallo_pagine:7683–7694/volume:24
In the context of our research on stimuli-responsive polymers bearing the 2-(hydroxyimino)aldehyde (HIA) group, we have explored the photochemical behavior and physicochemical properties of a number of HIAs. Interpretation of the experimental data is
Publikováno v:
Polymer chemistry
8 (2017): 4233–4245. doi:10.1039/c7py00975e
info:cnr-pdr/source/autori:Nardi M. (a,b); D'Acunzo F. (b); Clemente M. (a); Proietti G. (a); Gentili P. (a,b)/titolo:A first study on copolymers of a methacrylate containing the 2-(hydroxyimino) aldehyde group and OEGMA. RAFT polymerization and assessment of thermal and photoresponsive polymer behavior/doi:10.1039%2Fc7py00975e/rivista:Polymer chemistry (Print)/anno:2017/pagina_da:4233/pagina_a:4245/intervallo_pagine:4233–4245/volume:8
8 (2017): 4233–4245. doi:10.1039/c7py00975e
info:cnr-pdr/source/autori:Nardi M. (a,b); D'Acunzo F. (b); Clemente M. (a); Proietti G. (a); Gentili P. (a,b)/titolo:A first study on copolymers of a methacrylate containing the 2-(hydroxyimino) aldehyde group and OEGMA. RAFT polymerization and assessment of thermal and photoresponsive polymer behavior/doi:10.1039%2Fc7py00975e/rivista:Polymer chemistry (Print)/anno:2017/pagina_da:4233/pagina_a:4245/intervallo_pagine:4233–4245/volume:8
We report the first synthesis of 4-[(hydroxyimino) aldehyde] butyl methacrylate and its RAFT copolymerization with oligo(ethylene glycol) monomethylether methacrylate. For comparison, 6-(hydroxyimino) hexyl methacrylate, containing a free oxime group
Autor:
Alicia Virseda-Jerez, Ángel T. Martínez, Felipe de Salas, Gerard Santiago, Patrizia Gentili, Jesper Vind, Rubén Cañadas, Victor Guallar, Susana Camarero, Inés G. Muñoz
Publikováno v:
International Journal of Biological Macromolecules
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digital.CSIC. Repositorio Institucional del CSIC
instname
13 p.-7 fig.-2 tab
Fungal laccases have great potential as biocatalysts oxidizing a variety of aromatic compounds using oxygen as co-substrate. Here, the crystal structure of 7D5 laccase (PDB 6H5Y), developed in Saccharomyces cerevisiae and over
Fungal laccases have great potential as biocatalysts oxidizing a variety of aromatic compounds using oxygen as co-substrate. Here, the crystal structure of 7D5 laccase (PDB 6H5Y), developed in Saccharomyces cerevisiae and over
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62e40266ff9c108ec2a7f236d0166801
http://hdl.handle.net/10261/190477
http://hdl.handle.net/10261/190477
Autor:
Angela La Bella, Patrizia Gentili, Giovanna Mancini, Manuela Petaccia, Denise Gradella Villalva, Marco D'Abramo, Luisa Giansanti, Neva Bešker, Francesca Leonelli
Publikováno v:
Colloids and surfaces. B, Biointerfaces
140 (2016): 121–127. doi:10.1016/j.colsurfb.2015.12.020
info:cnr-pdr/source/autori:Petaccia M.; Gentili P.; Besker N.; D'Abramo M.; Giansanti L.; Leonelli F.; La Bella A.; Gradella Villalva D.; Mancini G./titolo:Kinetics and mechanistic study of competitive inhibition of thymidine phosphorylase by 5-fluoruracil derivatives/doi:10.1016%2Fj.colsurfb.2015.12.020/rivista:Colloids and surfaces. B, Biointerfaces (Print)/anno:2016/pagina_da:121/pagina_a:127/intervallo_pagine:121–127/volume:140
140 (2016): 121–127. doi:10.1016/j.colsurfb.2015.12.020
info:cnr-pdr/source/autori:Petaccia M.; Gentili P.; Besker N.; D'Abramo M.; Giansanti L.; Leonelli F.; La Bella A.; Gradella Villalva D.; Mancini G./titolo:Kinetics and mechanistic study of competitive inhibition of thymidine phosphorylase by 5-fluoruracil derivatives/doi:10.1016%2Fj.colsurfb.2015.12.020/rivista:Colloids and surfaces. B, Biointerfaces (Print)/anno:2016/pagina_da:121/pagina_a:127/intervallo_pagine:121–127/volume:140
In a previous investigation, cationic liposomes formulated with new 5-FU derivatives, differing for the length of the polyoxyethylenic spacer that links the N(3) position of 5-FU to an alkyl chain of 12 carbon atoms, showed a higher cytotoxicity comp
Publikováno v:
Polymer (Amsterdam. Online) 55 (2014): 5043–5049. doi:10.1016/j.polymer.2014.08.041
info:cnr-pdr/source/autori:F. D'Acunzo, P. Gentili, G. Masci, O. Ursini/titolo:Towards controlled cationic polymer growth from inorganic oxide defects: Directing the mechanism of polystyrene grafting from g-irradiated silica/doi:10.1016%2Fj.polymer.2014.08.041/rivista:Polymer (Amsterdam. Online)/anno:2014/pagina_da:5043/pagina_a:5049/intervallo_pagine:5043–5049/volume:55
info:cnr-pdr/source/autori:F. D'Acunzo, P. Gentili, G. Masci, O. Ursini/titolo:Towards controlled cationic polymer growth from inorganic oxide defects: Directing the mechanism of polystyrene grafting from g-irradiated silica/doi:10.1016%2Fj.polymer.2014.08.041/rivista:Polymer (Amsterdam. Online)/anno:2014/pagina_da:5043/pagina_a:5049/intervallo_pagine:5043–5049/volume:55
Most studies on surface-initiated controlled polymerizations for the synthesis of polymeric covalent organic-inorganic hybrid materials focus on chemical methods requiring specific modifications of the inorganic substrate. Few mechanistically-aware a