http://www.cnr.it/ontology/cnr/individuo/prodotto/ID48525
Functionalization of Oxide Surfaces by Terpyridine Phosphonate Ligands: Surface Reactions and Anchoring Geometry (Articolo in rivista)
- Type
- Label
- Functionalization of Oxide Surfaces by Terpyridine Phosphonate Ligands: Surface Reactions and Anchoring Geometry (Articolo in rivista) (literal)
- Anno
- 2010-01-01T00:00:00+01:00 (literal)
- Alternative label
Spampinato, V.; Tuccitto, N.; Quici, S.; Calabrese, V.; Marletta, G.; Torrisi, A.; Licciardello, A. (2010)
Functionalization of Oxide Surfaces by Terpyridine Phosphonate Ligands: Surface Reactions and Anchoring Geometry
in Langmuir
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Spampinato, V.; Tuccitto, N.; Quici, S.; Calabrese, V.; Marletta, G.; Torrisi, A.; Licciardello, A. (literal)
- Pagina inizio
- Pagina fine
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- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#note
- DOI: 10.1021/la9048314 (literal)
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- [Valentina Spampinato, Nunzio Tuccitto, Giovanni Marletta, Antonino Licciardello] LAMSUN, Laboratorio di Superfici Molecolari e Nanotecnologie, Dipartimento di Scienze Chimiche Università degli Studi di Catania, viale A. Doria 6, 95125 Catania, Italy; [Silvio Quici, Valentina Calabrese] Istituto di Scienze e Tecnologie Molecolari del CNR (ISTM), via C. Golgi 19, 20133 Milano, Italy, and Polo Scientifico e Tecnologico (PTS), Consiglio Nazionale delle Ricerche (CNR), via Fantoli 16/15, 20138 Milano, Italy]; [Alberto Torrisi] Dipartimento di Scienze Chimiche Università degli Studi di Catania, viale A. Doria 6, 95125 Catania, Italy (literal)
- Titolo
- Functionalization of Oxide Surfaces by Terpyridine Phosphonate Ligands: Surface Reactions and Anchoring Geometry (literal)
- Abstract
- A strategy for creating a general-purposes surface functionalization
platform is reported, based on direct attachment of phosphate groups
onto hydroxylated surfaces and subsequent formation of a
terpyridine-based monolayer. Such a platform is suitable for the
construction, onto technologically relevant oxide surfaces, of single-
and multilayer structures of interest in technological applications. In
particular, the paper describes the successful attachment of
4-(2,2':6',2 ''-terpyridine-4-yl)benzenephosphonic acid (I, PPTP) onto
a SiO2 surface previously functionalized by means of Zr-phosphate
groups. Two alternative anchoring strategies of the PPTP were explored:
(i) a direct one-step way, implying no protection of terpyridinie
functionality, and (ii) a three-step way, implying protection and
successive deprotection of this group. It was found that, in the First
case, the PPTP ligand anchoring to the Zr-containing phosphate layer
takes place by means of terpyridinic group. At variance of this, in the
second case, due to the protection or the terpyridinic functionality,
the anchoring process takes place through the phosphonic group, making
the terpyridinic moiety available for further reactions. i.e.,
multilayer constructs. X-ray photoelectron spectroscopy (XPS) and
time-of-flight secondary ion mass spectrometry (ToF-SIMS) were used to
study the functionalized surfaces, providing information on coverage,
chemical structure, and stoichiometry of the various functionalized
layers and, among the others, clear evidence of the PPTP linkage and
orientation. (literal)
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- Autore CNR
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