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    Rinaldo Psaro

    ... The specific surface area (295 m 2 /g) was obtained using the Brunauer–Emmett–Teller (BET) equation [12]. The palladium contents were determined by inductively coupled plasma atomic emission spectroscopy (ICP-AES) with a Intrepid Iris... more
    ... The specific surface area (295 m 2 /g) was obtained using the Brunauer–Emmett–Teller (BET) equation [12]. The palladium contents were determined by inductively coupled plasma atomic emission spectroscopy (ICP-AES) with a Intrepid Iris instrument (Thermo Elemental). ...
    The main methods for the design and preparation of single-site heterogeneous catalysts on inorganic oxide supports are described and reviewed. Catalytically active metal sites can be either introduced into the framework of porous... more
    The main methods for the design and preparation of single-site heterogeneous catalysts on inorganic oxide supports are described and reviewed. Catalytically active metal sites can be either introduced into the framework of porous materials via direct synthesis or added to a pre-existing support by post-synthesis techniques. Particular attention is paid to selected examples where the geometry, the nature and the chemical surroundings of the active single site is a key factor to obtain catalytic systems with enhanced chemo-, regio-and stereoselectivity. The ever-increasing capabilities of 'nanoarchitecture' at molecular level enable chemists to build ideal catalysts for the sustainable transformation of bulky and high added-value molecules.
    The preparation of a new amorphous mesoporous silica-titania (MST) is here reported. Following a modification of the standard procedure employed in the preparation of TS-1, a material showing a narrow pore size distribution in the... more
    The preparation of a new amorphous mesoporous silica-titania (MST) is here reported. Following a modification of the standard procedure employed in the preparation of TS-1, a material showing a narrow pore size distribution in the mesopore region (ca. 3 nm mean pore diameter) is obtained. The catalytic features, tested in the epoxidation of a series of unsaturated terpenic alcohols, were compared with those of an ordered mesoporous material as Ti-containing MCM-41. MST displayed mainly a higher activity than [Ti]-MCM-41 and a progressive increase in epoxidation rate was observed passing from bishomoallylic to allylic alcohols. Under these conditions, a global improvement in alkene conversion was achieved using methylacetate as solvent, without a remarkable loss in epoxide selectivity. During repeated recycles no significant changes in both catalytic performances and active metal content were recorded.
    ABSTRACT The structural evolution of non-acidic chemical-vapour deposition (CVD)-based Pt/KL catalyst has been investigated by in-situ extended X-ray absorption fine structure (EXAFS) spectroscopy. After in-situ reduction (H2, 400 °C),... more
    ABSTRACT The structural evolution of non-acidic chemical-vapour deposition (CVD)-based Pt/KL catalyst has been investigated by in-situ extended X-ray absorption fine structure (EXAFS) spectroscopy. After in-situ reduction (H2, 400 °C), EXAFS results suggested the presence of small metal particles which may be localized inside the KL-zeolite channels. After the reforming of methylcyclopentane at 500 °C (and 1 atm), no coke deposition was evidenced by EXAFS, in agreement with the non-acidic character of this catalyst.
    A comparative study of the hydrogenation of various heterocycles, model compounds in raw oil materials, by either Ru(II) complex immobilized on mesoporous silica or Ru(0) nanoparticles deposited on the same support has been performed. The... more
    A comparative study of the hydrogenation of various heterocycles, model compounds in raw oil materials, by either Ru(II) complex immobilized on mesoporous silica or Ru(0) nanoparticles deposited on the same support has been performed. The single-site catalyst contains the molecular precursor [Ru(NCMe)3(sulphos)](OSO2CF3) tethered to partially dehydroxylated high-surface-area silica through hydrogen bonds between silanol groups of the support and SO3− groups
    An operando study of CO oxidation by Ce0.5Zr0.5O2 catalysts under dynamic conditions was performed using a prototype gas flow DRIFTS reaction chamber coupled with a MS. Previous studies conducted under oscillating CO/O2 feedstream... more
    An operando study of CO oxidation by Ce0.5Zr0.5O2 catalysts under dynamic conditions was performed using a prototype gas flow DRIFTS reaction chamber coupled with a MS. Previous studies conducted under oscillating CO/O2 feedstream conditions, allowed the identification of carbonates as the C-containing storage species on the catalyst surface, with their decomposition being the origin of CO2 evolution dynamics during O2
    Cluster-derived FeIr/MgO catalysts prepared from [Et4N]2[Fe2Ir4(CO)16] and [Et4N]2[Fe2Ir2(CO)12] exhibit high activity in methanol synthesis from CO + H2. The catalyst performance improves significantly upon raising the Fe:Ir ratio in the... more
    Cluster-derived FeIr/MgO catalysts prepared from [Et4N]2[Fe2Ir4(CO)16] and [Et4N]2[Fe2Ir2(CO)12] exhibit high activity in methanol synthesis from CO + H2. The catalyst performance improves significantly upon raising the Fe:Ir ratio in the precursor from 2:4 to 2:2; with the latter sample, at 488–523 K and 6.1 MPa, methanol productivities up to 100 mol/molir h are obtained with selectivity around 90%. Preliminary extended
    ... 1 I , 80333 Miinchen, Germany Horacio Treviiio, 2. Conrad Zhangt and WMH Sachtler V. N. lpatieff Laboratory, Center for Catalysis and Surface Science, Departments ... t Present address : Catalytic System Division, Johnson Matthey, 456... more
    ... 1 I , 80333 Miinchen, Germany Horacio Treviiio, 2. Conrad Zhangt and WMH Sachtler V. N. lpatieff Laboratory, Center for Catalysis and Surface Science, Departments ... t Present address : Catalytic System Division, Johnson Matthey, 456 Devon Park Drive, Wayne, PA 19087, USA ...
    ABSTRACT ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select... more
    ABSTRACT ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
    The one-step transformation of (+)-citronellal into (-)-menthol has been realised with yield ∼90% and stereoselectivity up to 80% under mild conditions in the presence of Cu/SiO2 by exploiting the presence of acidic and hydrogenation... more
    The one-step transformation of (+)-citronellal into (-)-menthol has been realised with yield ∼90% and stereoselectivity up to 80% under mild conditions in the presence of Cu/SiO2 by exploiting the presence of acidic and hydrogenation sites on the catalyst surface, the unusual reducibility of an olefinic bond under these conditions and the chemoselectivity of the process.
    ... a Dipartimento di Chimica Inorganica, Metallorganica e Analitica, University of Milano Milan Italy. b CNR Center 'CSSCMTBSO' Via Venezian, 21 20133 Milan Italy. Received 2 September 1997; revised 5 May 1998; accepted 11 May... more
    ... a Dipartimento di Chimica Inorganica, Metallorganica e Analitica, University of Milano Milan Italy. b CNR Center 'CSSCMTBSO' Via Venezian, 21 20133 Milan Italy. Received 2 September 1997; revised 5 May 1998; accepted 11 May 1998. Available online 2 September 1998. ...
    ... Dipartimento di Scienze CC, FF, MM, Università degli Studi dell'Insubria, Via Valleggio 11, 22100 Como, Italy. Rinaldo Psaro, Achille Fusi, and Renato ... the active sites are probably formed by two copper centers with a favorable... more
    ... Dipartimento di Scienze CC, FF, MM, Università degli Studi dell'Insubria, Via Valleggio 11, 22100 Como, Italy. Rinaldo Psaro, Achille Fusi, and Renato ... the active sites are probably formed by two copper centers with a favorable geometric arrangement for the N−N bond formation ...
    ... Dominique Roberto,*9+ Elena Cariati,? Rinaldo Psaro,J: and Renato Ugot Dipartimento di Chimica Inorganica, Metallorganica e Analitica and Centro CNR, Universita di Milano, Via Venezian, 21, 20133 Milano, Italy ... 1993, 35, 261. (7)... more
    ... Dominique Roberto,*9+ Elena Cariati,? Rinaldo Psaro,J: and Renato Ugot Dipartimento di Chimica Inorganica, Metallorganica e Analitica and Centro CNR, Universita di Milano, Via Venezian, 21, 20133 Milano, Italy ... 1993, 35, 261. (7) Tanaka, K; Watters, K. L.; Howe, RFJ Cutal. ...
    The increasing need for new materials capable of solar fuel generation is central in the development of a green energy economy. In this contribution, we demonstrate that black TiO(2) nanoparticles obtained through a one-step... more
    The increasing need for new materials capable of solar fuel generation is central in the development of a green energy economy. In this contribution, we demonstrate that black TiO(2) nanoparticles obtained through a one-step reduction/crystallization process exhibit a bandgap of only 1.85 eV, which matches well with visible light absorption. The electronic structure of black TiO(2) nanoparticles is determined by the unique crystalline and defective core/disordered shell morphology. We introduce new insights that will be useful for the design of nanostructured photocatalysts for energy applications.
    The complex Rh(cod)(sulfos) (Rh(I); sulfos = (-)O(3)S(C(6)H(4))CH(2)C(CH(2)PPh(2))(3); cod = cycloocta-1,5-diene), either free or supported on silica, does not catalyze the hydrogenation of benzene in either homogeneous or heterogeneous... more
    The complex Rh(cod)(sulfos) (Rh(I); sulfos = (-)O(3)S(C(6)H(4))CH(2)C(CH(2)PPh(2))(3); cod = cycloocta-1,5-diene), either free or supported on silica, does not catalyze the hydrogenation of benzene in either homogeneous or heterogeneous phase. However, when silica contains supported Pd metal nanoparticles (Pd(0)/SiO(2)), a hybrid catalyst (Rh(I)-Pd(0)/SiO(2)) is formed that hydrogenates benzene 4 times faster than does Pd(0)/SiO(2) alone. EXAFS and DRIFT measurements of in situ and ex situ prepared samples, batch catalytic reactions under different conditions, deuterium labeling experiments, and model organometallic studies, taken together, have shown that the rhodium single sites and the palladium nanoparticles cooperate with each other in promoting the hydrogenation of benzene through the formation of a unique entity throughout the catalytic cycle. Besides decreasing the extent of cyclohexa-1,3-diene disproportionation at palladium, the combined action of the two metals activates the arene so as to allow the rhodium sites to enter the catalytic cycle and speed up the overall hydrogenation process by rapidly reducing benzene to cyclohexa-1,3-diene.
    Specific studies carried in Milan laboratory in the application of metal carbonyl clusters to preparation of supported catalysts are reviewed. Examples are reported of catalysis by heterogeneous organometallic surface species, such as... more
    Specific studies carried in Milan laboratory in the application of metal carbonyl clusters to preparation of supported catalysts are reviewed. Examples are reported of catalysis by heterogeneous organometallic surface species, such as 1-butene isomerisation catalysed by silica-anchored osmium carbonyl species, or of catalysis by very small metal particles produced under catalytic conditions, such as ethylene hydroformylation using silica supported [Rh12(CO)30]2−
    Cyclooligosiloxanolate complexes of higher valent transition metals and lanthanides were synthesized and characterized by single-crystal X-ray diffraction experiments, spectra, cyclic voltammetry, conductivity and magnetic behaviour.... more
    Cyclooligosiloxanolate complexes of higher valent transition metals and lanthanides were synthesized and characterized by single-crystal X-ray diffraction experiments, spectra, cyclic voltammetry, conductivity and magnetic behaviour. These complexes are sandwich-type clusters containing assemblies of 4 to 8 metals between siloxanolate ligand ‘layers’. A high degree of electron delocalization in the metal containing fragment of these complexes is detected by electrochemical and
    ... Journal of Molecular Catalysis A: Chemical Volumes 204-205, 15 September 2003, Pages 465-472 In honour of Prof. R. Ugo on the occasion of his 65th. Birthday. ... Dedicated to Professor Renato Ugo on the occasion of his 65th birthday.... more
    ... Journal of Molecular Catalysis A: Chemical Volumes 204-205, 15 September 2003, Pages 465-472 In honour of Prof. R. Ugo on the occasion of his 65th. Birthday. ... Dedicated to Professor Renato Ugo on the occasion of his 65th birthday. ...
    ... Vladimiro Dal Santo*a, Alessandro Galloa, Marco M. Gatti†b, Valentina De Grandib, Rinaldo Psaroa, Laura Sordellia and Sandro Recchiac. a ISTM-CNR, Via C. Golgi, 19, 20133 Milan, Italy. ... 20, L. Basini, A. Guarinoni, Int. Pat. Appl.,... more
    ... Vladimiro Dal Santo*a, Alessandro Galloa, Marco M. Gatti†b, Valentina De Grandib, Rinaldo Psaroa, Laura Sordellia and Sandro Recchiac. a ISTM-CNR, Via C. Golgi, 19, 20133 Milan, Italy. ... 20, L. Basini, A. Guarinoni, Int. Pat. Appl., 2003, WO 2 003 099 712 . ...

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