http://www.cnr.it/ontology/cnr/individuo/prodotto/ID48600
Synthesis and Catalytic Activity of Titanium Silsesquioxane Frameworks as Models of Titanium Active Surface Sites of Controlled Nuclearity (Articolo in rivista)
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- Synthesis and Catalytic Activity of Titanium Silsesquioxane Frameworks as Models of Titanium Active Surface Sites of Controlled Nuclearity (Articolo in rivista) (literal)
- Anno
- 2010-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/om100636h (literal)
- Alternative label
Giovenzana, T.; Guidotti, M.; Lucenti, E.; Orbelli Biroli, A.; Sordelli, L.; Sironi, A.; Ugo, R. (2010)
Synthesis and Catalytic Activity of Titanium Silsesquioxane Frameworks as Models of Titanium Active Surface Sites of Controlled Nuclearity
in Organometallics; ACS, American chemical society, Washington, DC (Stati Uniti d'America)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Giovenzana, T.; Guidotti, M.; Lucenti, E.; Orbelli Biroli, A.; Sordelli, L.; Sironi, A.; Ugo, R. (literal)
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- Department of Inorganic, Metallorganic and Analytical Chemistry 'Lamberto Malatesta', University of Milan, Via Venezian 21, 20133 Milan, Italy
Institute of Molecular Science and Technology of CNR, Via Golgi 19, 20133 Milan, Italy
Department of Structural Chemistry and Inorganic Stereochemistry, University of Milan, Via Venezian 21, 20133 Milan, Italy
Italian InteruniVersity Consortium on Materials Science and Technology (INSTM) - Research Unit of Milan, Via Giusti 9, 50121 Firenze, Italy (literal)
- Titolo
- Synthesis and Catalytic Activity of Titanium Silsesquioxane Frameworks as Models of Titanium Active Surface Sites of Controlled Nuclearity (literal)
- Abstract
- The synthesis and catalytic activity of some new titanium(IV) complexes with incompletely condensed Cy6Si6O7(OH)4 and endo-Cy8Si8O11(OH)2 (Cy = c-C6H11) silsesquioxane cages have been carried out with the aim of investigating new Ti silsesquioxane frameworks as molecular models of titanium active sites of catalysts prepared by grafting Ti(IV) precursors on the surface or in a matrix of mesoporous silica. The silsesquioxane Cy6Si6O7(OH)4, which bears four potentially reactive OH groups, when reacted with TiCpCl3 (Cp = ?5-C5H5) affords the new species [Cy6Si6O12Ti2(Cp)2], with two titanium atoms connected through one oxygen bridge, as confirmed by a XANES and EXAFS spectroscopic investigation. By reaction of endo-Cy8Si8O11(OH)2 with [Ti(o-C6H4O2)(OCH2CH3)2] the new complex [Cy8Si8O11O2]2Ti was obtained, which exhibits a tetrapodal coordination of Ti, as shown by a X-ray diffraction investigation. The catalytic
activity of these two new Ti silsesquioxane complexes was investigated for the catalytic epoxidation of cyclohexene with tert-butylhydroperoxide and compared with the catalytic activity of the known [Cy7Si7O12TiCp], widely used to model very active tripodal titanium single sites. It appears that a tripodal coordination of Ti sites facilitates the catalytic activity that is in contrast quite low for the two new complexes investigated in this work, probably due to the higher stability toward dissociation to generate a tripodal coordination of the Ti-O-Ti bond and to the steric hindrance of Ti tetrapodal coordination. (literal)
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