Zobrazeno 1 - 10
of 125
pro vyhledávání: '"Mario Gleria"'
Publikováno v:
Surface and Interface Analysis. 41:27-33
This paper investigates by means of XPS analysis the surface functionalization of soda-lime and fused quartz glass substrates with hexachlorocyclophosphazene (HCCP), obtained by simple immersion in solutions of phosphazene in anhydrous solvents. Seve
Autor:
Roberto Milani, Léon Gengembre, Roberta Bertani, Ahmed Mazzah, charafeddine Jama, Martine Frere, Mario Gleria, Roger De Jaeger
Publikováno v:
Journal of Applied Polymer Science
Journal of Applied Polymer Science, 2008, 108 (5), pp.3191-3199
Journal of Applied Polymer Science, Wiley, 2008, 108 (5), pp.3191-3199
Journal of Applied Polymer Science, 2008, 108 (5), pp.3191-3199
Journal of Applied Polymer Science, Wiley, 2008, 108 (5), pp.3191-3199
In this article, we describe the synthesis and characterization of surface-modified polyamide-6, using polydichlorophosphazene and hexachlorocyclophosphazene as coupling agents. The solid surface of this polymer was modified first by the introduction
Autor:
Riccardo Po, Giorgio Giannotta, Giovanni Depaoli, Roberto Milani, Alfonso Venzo, Luisa Fiocca, Mario Gleria
Publikováno v:
Designed monomers and polymers
11 (2008): 243–260. doi:10.1163/156855508X316854
info:cnr-pdr/source/autori:1-Fiocca L.; 1-Po' R.; 1-Giannotta G.; 2-Gleria M.; 2-Venzo A.; 3-Milani R.; 3-De Paoli G./titolo:Oxazoline-containing phosphazene derivatives. Parte III. Synthesis and characterization of novel cyclophosphazenes functionalized with chiral 2-oxazoline groups./doi:10.1163%2F156855508X316854/rivista:Designed monomers and polymers (Print)/anno:2008/pagina_da:243/pagina_a:260/intervallo_pagine:243–260/volume:11
Fiocca, L, Pó, R, Giannotta, G, Gleria, M, Venzo, A, Milani, R & Depaoli, G 2008, ' Oxazoline-containing phosphazene derivatives, part III : Synthesis and characterization of novel cyclophosphazenes functionalized with chiral 2-oxazoline groups ', Designed Monomers and Polymers, vol. 11, no. 3, pp. 243-260 . https://doi.org/10.1163/156855508X316854
11 (2008): 243–260. doi:10.1163/156855508X316854
info:cnr-pdr/source/autori:1-Fiocca L.; 1-Po' R.; 1-Giannotta G.; 2-Gleria M.; 2-Venzo A.; 3-Milani R.; 3-De Paoli G./titolo:Oxazoline-containing phosphazene derivatives. Parte III. Synthesis and characterization of novel cyclophosphazenes functionalized with chiral 2-oxazoline groups./doi:10.1163%2F156855508X316854/rivista:Designed monomers and polymers (Print)/anno:2008/pagina_da:243/pagina_a:260/intervallo_pagine:243–260/volume:11
Fiocca, L, Pó, R, Giannotta, G, Gleria, M, Venzo, A, Milani, R & Depaoli, G 2008, ' Oxazoline-containing phosphazene derivatives, part III : Synthesis and characterization of novel cyclophosphazenes functionalized with chiral 2-oxazoline groups ', Designed Monomers and Polymers, vol. 11, no. 3, pp. 243-260 . https://doi.org/10.1163/156855508X316854
In this paper we describe the synthesis and the characterization of a series of cyclophosphazenes substituted with 2-oxazoline-containing moieties, with and without optical activity. These products could be obtained by reacting cyclophosphazenes cont
Autor:
Alessandro Sassi, Mario Gleria, S. Carturan, G. Della Mea, Roberto Milani, Gianluigi Maggioni
Publikováno v:
Surface and Coatings Technology. 201:5829-5835
In this work the surface of silicon substrates has been modified with organic ligands by exploiting chlorinated phosphazene as coupling agent. Hexachlorocyclophosphazene-derived thin films were deposited by Glow-Discharge-induced Sublimation (GDS) an
Publikováno v:
Designed monomers and polymers
info:cnr-pdr/source/autori:1-Milani R.; 2-Sassi A.; 2-Venzo A.; 3-Bertani R.; 4-Fambri L.; 2-Gleria, M./titolo:Surface Functionalization with Phosphazene Substrates. Part IV. Silica and Si(100) Surface Functionalization Using Cyclophosphazenes Partially Substituted with Trialkoxysilane Derivatives and PEG-750-Monomethylether, 2,2,3,3-Tetrafluoropropanol and 4-Hydroxyazobenes/doi:/rivista:Designed monomers and polymers (Print)/anno:2007/pagina_da:555/pagina_a:573/intervallo_pagine:555–573/volume:10
info:cnr-pdr/source/autori:1-Milani R.; 2-Sassi A.; 2-Venzo A.; 3-Bertani R.; 4-Fambri L.; 2-Gleria, M./titolo:Surface Functionalization with Phosphazene Substrates. Part IV. Silica and Si(100) Surface Functionalization Using Cyclophosphazenes Partially Substituted with Trialkoxysilane Derivatives and PEG-750-Monomethylether, 2,2,3,3-Tetrafluoropropanol and 4-Hydroxyazobenes/doi:/rivista:Designed monomers and polymers (Print)/anno:2007/pagina_da:555/pagina_a:573/intervallo_pagine:555–573/volume:10
This paper deals with the possibility of functionalizing the surface of silicon-based materials by exploiting cyclophosphazenes containing suitable substituent groups. Thus, phosp-hazene trimers were prepared, containing about 50% of the reactive sit
Publikováno v:
Journal of inorganic and organometallic polymers and materials
16 (2006): 327–341.
info:cnr-pdr/source/autori:Silvestrelli, PL; Gleria, M; Milani, R; Boscoletto, AB/titolo:Surface functionalization with phosphazene substrates. Part II. Theoretical and experimental investigations of the interactions of hexachlorocyclophosphazene with hydroxylated silicon-based surfaces/doi:/rivista:Journal of inorganic and organometallic polymers and materials (Print)/anno:2006/pagina_da:327/pagina_a:341/intervallo_pagine:327–341/volume:16
16 (2006): 327–341.
info:cnr-pdr/source/autori:Silvestrelli, PL; Gleria, M; Milani, R; Boscoletto, AB/titolo:Surface functionalization with phosphazene substrates. Part II. Theoretical and experimental investigations of the interactions of hexachlorocyclophosphazene with hydroxylated silicon-based surfaces/doi:/rivista:Journal of inorganic and organometallic polymers and materials (Print)/anno:2006/pagina_da:327/pagina_a:341/intervallo_pagine:327–341/volume:16
The interaction of hexachlorocyclophosphazene (HCCP) with the hydroxylated silicon-based surfaces is studied by a combination of XPS experimental analysis and theoretical ab initio simulations, including the estimate of the energy barriers via CI-NEB
Autor:
Roberta Bertani, Giovanni Vitulli, Mario Gleria, Giacomo Facchin, Roberto Milani, Paolo Pertici
Publikováno v:
Macromolecular symposia 235 (2006): 98–114.
info:cnr-pdr/source/autori:Pertici P., Vitulli G., Gleria M., Facchin G., Milani R., Bertani R./titolo:Metal-containing poly(organophosphazenes)/doi:/rivista:Macromolecular symposia/anno:2006/pagina_da:98/pagina_a:114/intervallo_pagine:98–114/volume:235
info:cnr-pdr/source/autori:Pertici P., Vitulli G., Gleria M., Facchin G., Milani R., Bertani R./titolo:Metal-containing poly(organophosphazenes)/doi:/rivista:Macromolecular symposia/anno:2006/pagina_da:98/pagina_a:114/intervallo_pagine:98–114/volume:235
In this paper we highlighted the general situation of metal containing poly(organophosphazenes) and we presented the status of the art in this area in terms of interactions between phosphazene materials and different types of metals. Possible practic
Publikováno v:
Designed Monomers and Polymers. 9:627-647
In this paper we report the utilization of phosphazene substrates for the surface functionalization of silicon-based materials (e.g., silica gel beads and crystalline silicon(100) wafers) and for the preparation of monoliths by means of a sol-gel tec
Autor:
Luigi Botta, Roberto Scaffaro, Domenico Acierno, Roberta Bertani, Pierluigi Magagnini, Mario Gleria, F. P. La Mantia
Publikováno v:
Polymer Degradation and Stability. 90:234-243
Poly(butylene terephthalate) (PBT) and a sample of polyamide have been melt processed in the presence of two new phosphazene compounds, namely 2,2-dichloro-4,4,6,6-bis[spiro(2′,2″dioxy-1′,1″biphenyl)]cyclotriphosphazene (2Cl-CP) and 2,2-bis-(
Autor:
Nico Scalera, Andrea Spitaleri, Manh Hoang, Mario Gleria, Terence W. Turney, Giovanni Vitulli, Paolo Pertici
Publikováno v:
Inorganica Chimica Acta. 352:61-71
Supported Ru nanoparticles on a number of polyorganophosphazenes were prepared and tested for the hydrogenation of unsaturated compounds. The complex Ru(η6-cycloocta-1,3,5-triene)(η4-cycloocta-1,5-diene) was found to be a suitable precursor to depo