Zobrazeno 1 - 10
of 101
pro vyhledávání: '"Mauro Bassetti"'
Autor:
Marco Valerio Fornaiolo, Piergiorgio Flamini, Paolo Mencarelli, Sara Mazzetti, Riccardo Salvio, Achille Antenucci, Sergio Di Silvio, Mauro Bassetti
Publikováno v:
Advanced synthesis & catalysis
361 (2019): 4517–4526. doi:10.1002/adsc.201900633
info:cnr-pdr/source/autori:Antenucci, Achille; Flamini, Piergiorgio; Fornaiolo, Marco Valerio; Di Silvio, Sergio; Mazzetti, Sara; Mencarelli, Paolo; Salvio, Riccardo; Bassetti, Mauro/titolo:Iron(III)-Catalyzed Hydration of Unactivated Internal Alkynes in Weak Acidic Medium, under Lewis Acid-Assisted Bronsted Acid Catalysis/doi:10.1002%2Fadsc.201900633/rivista:Advanced synthesis & catalysis (Print)/anno:2019/pagina_da:4517/pagina_a:4526/intervallo_pagine:4517–4526/volume:361
361 (2019): 4517–4526. doi:10.1002/adsc.201900633
info:cnr-pdr/source/autori:Antenucci, Achille; Flamini, Piergiorgio; Fornaiolo, Marco Valerio; Di Silvio, Sergio; Mazzetti, Sara; Mencarelli, Paolo; Salvio, Riccardo; Bassetti, Mauro/titolo:Iron(III)-Catalyzed Hydration of Unactivated Internal Alkynes in Weak Acidic Medium, under Lewis Acid-Assisted Bronsted Acid Catalysis/doi:10.1002%2Fadsc.201900633/rivista:Advanced synthesis & catalysis (Print)/anno:2019/pagina_da:4517/pagina_a:4526/intervallo_pagine:4517–4526/volume:361
Alkylarylalkynes are converted with full regioselectivity into the corresponding arylketones by formal hydration of the triple bond under weak acidic conditions, at times and temperatures (
Autor:
Riccardo Salvio, Mauro Bassetti
The review describes the state of the art in hydration reactions of alkynes by direct or indirect catalysis of first row transition metal complexes, covering mostly the literature of the last decade in which many examples based on these metal ions ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d704cd20bee992a3c22c4843dbc6395
http://hdl.handle.net/2108/274492
http://hdl.handle.net/2108/274492
Autor:
Roberto Iona, Mauro Bassetti
Publikováno v:
ChemistrySelect 5 (2020): 6666–6669. doi:10.1002/slct.202001372
info:cnr-pdr/source/autori:Iona Roberto; Bassetti Mauro/titolo:Dimerization of Aromatic Terminal Alkynes Featuring Hydrophilic Functional Groups under Ruthenium and Acid Promoted Catalysis. Competitive Alkyne Hydration upon Substituent Effect/doi:10.1002%2Fslct.202001372/rivista:ChemistrySelect/anno:2020/pagina_da:6666/pagina_a:6669/intervallo_pagine:6666–6669/volume:5
info:cnr-pdr/source/autori:Iona Roberto; Bassetti Mauro/titolo:Dimerization of Aromatic Terminal Alkynes Featuring Hydrophilic Functional Groups under Ruthenium and Acid Promoted Catalysis. Competitive Alkyne Hydration upon Substituent Effect/doi:10.1002%2Fslct.202001372/rivista:ChemistrySelect/anno:2020/pagina_da:6666/pagina_a:6669/intervallo_pagine:6666–6669/volume:5
The self-coupling (hydroalkynylation) process of aromatic terminal alkynes RC6H4CCH to give dimeric 1,4-diaryl-1-en-3- yne products (trans-RC6H4CCCH=CHC6H4R) is catalyzed by the complex [{RuCl(?-Cl)(?6-p-cymene)}2] with sodium acetate cocatalyst diss
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82526f241d0e0249d96510b07ae8779a
http://www.cnr.it/prodotto/i/428452
http://www.cnr.it/prodotto/i/428452
Autor:
Mauro Bassetti, Corrado Rizzoli, Elisa Viola, Maria Pia Donzello, Noemi Bellucci, Edoardo Raciti, Claudio Ercolani, Ida Pettiti
Publikováno v:
Inorganic chemistry (Online) 59 (2020): 8893–8905. doi:10.1021/acs.inorgchem.0c00699
info:cnr-pdr/source/autori:Raciti E.; Donzello M.P.; Viola E.; Bassetti M.; Pettiti I.; Bellucci N.; Rizzoli C.; Ercolani C./titolo:Palladium(II) and Platinum(II) Mononuclear Complexes and Tendency to Undergo Dehydrogenation of the Multiple N-Donor Ligand Di-(2-pyridyl)dihydropyrazine/doi:10.1021%2Facs.inorgchem.0c00699/rivista:Inorganic chemistry (Online)/anno:2020/pagina_da:8893/pagina_a:8905/intervallo_pagine:8893–8905/volume:59
info:cnr-pdr/source/autori:Raciti E.; Donzello M.P.; Viola E.; Bassetti M.; Pettiti I.; Bellucci N.; Rizzoli C.; Ercolani C./titolo:Palladium(II) and Platinum(II) Mononuclear Complexes and Tendency to Undergo Dehydrogenation of the Multiple N-Donor Ligand Di-(2-pyridyl)dihydropyrazine/doi:10.1021%2Facs.inorgchem.0c00699/rivista:Inorganic chemistry (Online)/anno:2020/pagina_da:8893/pagina_a:8905/intervallo_pagine:8893–8905/volume:59
The already known di(2-pyridyl)dihydropyrazine (dhdpp) was prepared and isolated also in the form of a bis-hydrated species, i.e., dhdpp·2H2O. As established by X-ray work, a small amount of single crystals of di(2-pyridyl)-pyrazine (dpp) was also o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::041e49059ee893fa79637d31da054562
http://hdl.handle.net/11573/1461011
http://hdl.handle.net/11573/1461011
Autor:
Chiara Battocchio, Laura Fontana, Sara Cerra, Mauro Bassetti, Roberto Matassa, Ilaria Fratoddi, Giuseppe Familiari, Laura Carlini, Enrico Rossi, Iole Venditti
Publikováno v:
Inorganica Chimica Acta (Testo stamp.) 516 (2021). doi:10.1016/j.ica.2020.120170
info:cnr-pdr/source/autori:Cerra Sara; Fontana Laura; Rossi Enrico; Bassetti Mauro; Battocchio Chiara; Venditti Iole; Carlini Laura; Matassa Roberto; Familiari Giuseppe; Fratoddi Ilaria/titolo:Binuclear organometallic Pt(II) complexes as stabilizing ligands for gold and silver metal nanoparticles/doi:10.1016%2Fj.ica.2020.120170/rivista:Inorganica Chimica Acta (Testo stamp.)/anno:2021/pagina_da:/pagina_a:/intervallo_pagine:/volume:516
info:cnr-pdr/source/autori:Cerra Sara; Fontana Laura; Rossi Enrico; Bassetti Mauro; Battocchio Chiara; Venditti Iole; Carlini Laura; Matassa Roberto; Familiari Giuseppe; Fratoddi Ilaria/titolo:Binuclear organometallic Pt(II) complexes as stabilizing ligands for gold and silver metal nanoparticles/doi:10.1016%2Fj.ica.2020.120170/rivista:Inorganica Chimica Acta (Testo stamp.)/anno:2021/pagina_da:/pagina_a:/intervallo_pagine:/volume:516
The bifunctional hybrid thioester ligands containing square planar Pt(II) centers 2,7-bis[2-(trans-acetylthio-bis-(tributylphosphine)platinumII)ethynyl]-9,9-didodecyl-9H-fluorene (1) and trans-4,4′-bis[2-(trans-acetylthio-bis-(tributylphosphine)pla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ace14b3823ada149abf9919c1717994
https://hdl.handle.net/11590/375657
https://hdl.handle.net/11590/375657
Autor:
Denise Gradella Villalva, Giovanna Mancini, Maria Grazia Nemi, Donatella Capitani, Sara Battista, Anatoly P. Sobolev, Mauro Bassetti, Alessandro Mauceri, Luisa Giansanti, Luciano Galantini
Publikováno v:
Langmuir 36 (2020): 12168–12178. doi:10.1021/acs.langmuir.0c01735
info:cnr-pdr/source/autori:Mauceri, Alessandro; Giansanti, Luisa; Capitani, Donatella; Sobolev, Anatoly; Galantini, Luciano; Bassetti, Mauro; Nemi, Maria Grazia; Villalva, Denise Gradella; Battista, Sara; Mancini, Giovanna/titolo:Cationic Amphiphiles Bearing a Diacetylenic Function in the Headgroup: Aggregative Properties and Polymerization/doi:10.1021%2Facs.langmuir.0c01735/rivista:Langmuir/anno:2020/pagina_da:12168/pagina_a:12178/intervallo_pagine:12168–12178/volume:36
info:cnr-pdr/source/autori:Mauceri, Alessandro; Giansanti, Luisa; Capitani, Donatella; Sobolev, Anatoly; Galantini, Luciano; Bassetti, Mauro; Nemi, Maria Grazia; Villalva, Denise Gradella; Battista, Sara; Mancini, Giovanna/titolo:Cationic Amphiphiles Bearing a Diacetylenic Function in the Headgroup: Aggregative Properties and Polymerization/doi:10.1021%2Facs.langmuir.0c01735/rivista:Langmuir/anno:2020/pagina_da:12168/pagina_a:12178/intervallo_pagine:12168–12178/volume:36
In the wide panorama of diacetylenic lipids, the photoresponsive conjugated 1,3-diyne function is usually encased into the hydrocarbon chain of the amphiphile at a variable distance from the headgroup. Therefore, the polydiacetylene network obtained
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cde0a3edd3513f34fc413d18c4a46c8e
http://hdl.handle.net/11573/1521692
http://hdl.handle.net/11573/1521692
Publikováno v:
Colloids and surfaces. A, Physicochemical and engineering aspects
532 (2017): 282–289. doi:10.1016/j.colsurfa.2017.05.005
info:cnr-pdr/source/autori:Fontana L. (a); Bassetti M. (b); Battocchio C. (c); Venditti I. (a); Fratoddi I. (a)/titolo:Synthesis of gold and silver nanoparticles functionalized with organic dithiols/doi:10.1016%2Fj.colsurfa.2017.05.005/rivista:Colloids and surfaces. A, Physicochemical and engineering aspects (Print)/anno:2017/pagina_da:282/pagina_a:289/intervallo_pagine:282–289/volume:532
532 (2017): 282–289. doi:10.1016/j.colsurfa.2017.05.005
info:cnr-pdr/source/autori:Fontana L. (a); Bassetti M. (b); Battocchio C. (c); Venditti I. (a); Fratoddi I. (a)/titolo:Synthesis of gold and silver nanoparticles functionalized with organic dithiols/doi:10.1016%2Fj.colsurfa.2017.05.005/rivista:Colloids and surfaces. A, Physicochemical and engineering aspects (Print)/anno:2017/pagina_da:282/pagina_a:289/intervallo_pagine:282–289/volume:532
In this work commercially available bifunctional organic dithiols, 4,4′-dithiol-biphenyl (BI), 4,4′-dithiolterphenyl (TR) and the on purpose prepared precursor of 4,4′-dithiol- trans -stilbene (ST), have been used for the stabilization of gold
Autor:
Sara Cerra, Francesca D’Acunzo, Giovanni Pulci, Chiara Pasquini, Federico Cruciani, Ilaria Fratoddi, Andrea D'Annibale, Mauro Bassetti
Publikováno v:
Synthetic metals 269 (2020): 116538. doi:10.1016/j.synthmet.2020.116538
info:cnr-pdr/source/autori:Cruciani F.; Pasquini C.; D'Acunzo F.; D'Annibale A.; Fratoddi I.; Cerra S.; Pulci G.; Bassetti M./titolo:Synthesis and characterization of stereoregular conjugated polyarylenynes, (-Ar-(E)-CH=CHC-C-)n, decorated with branched bis-alkoxy side chains/doi:10.1016%2Fj.synthmet.2020.116538/rivista:Synthetic metals/anno:2020/pagina_da:116538/pagina_a:/intervallo_pagine:116538/volume:269
info:cnr-pdr/source/autori:Cruciani F.; Pasquini C.; D'Acunzo F.; D'Annibale A.; Fratoddi I.; Cerra S.; Pulci G.; Bassetti M./titolo:Synthesis and characterization of stereoregular conjugated polyarylenynes, (-Ar-(E)-CH=CHC-C-)n, decorated with branched bis-alkoxy side chains/doi:10.1016%2Fj.synthmet.2020.116538/rivista:Synthetic metals/anno:2020/pagina_da:116538/pagina_a:/intervallo_pagine:116538/volume:269
Novel poly(p-phenyleneethynylenevinylene)s (PPEV) have been synthesized by step-growth oligomerization of 2,5-diethynyl-1,4-dialkoxybenzene monomers promoted by the ruthenium pre-catalyst [{RuCl(μ-Cl)(η6-p-cymene)}2] in the solvent mixture AcOH/CH2