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Maurizio Ballico

Researcher at University of Udine

Publications -  23
Citations -  634

Maurizio Ballico is an academic researcher from University of Udine. The author has contributed to research in topics: Transfer hydrogenation & Ruthenium. The author has an hindex of 11, co-authored 21 publications receiving 539 citations.

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BMP tests of source selected OFMSW to evaluate anaerobic codigestion with sewage sludge

TL;DR: The best codigestion BMP test has highlighted an increase of 47% in methane production respect sewage sludge digestion, and the maximum methane yield was observed for restaurant and canteens organic wastes.
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New Benzo[h]quinoline‐Based Ligands and their Pincer Ru and Os Complexes for Efficient Catalytic Transfer Hydrogenation of Carbonyl Compounds

TL;DR: New benzo[h]quinoline ligands (HCN'N) containing a CHRNH2 function in the 2-position were prepared and used to prepare ruthenium and osmium complexes, which are excellent catalysts for the transfer hydrogenation (TH) of ketones.
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Osmium Pyme Complexes for Fast Hydrogenation and Asymmetric Transfer Hydrogenation of Ketones

TL;DR: Compounds 1, 2, 5 and the mixture of isomers 3/4 efficiently catalyze the transfer hydrogenation (TH) of different ketones in refluxing 2-propanol and in the presence of NaOiPr.
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Role of the NH2 functionality and solvent in terdentate CNN alkoxide ruthenium complexes for the fast transfer hydrogenation of ketones in 2-propanol.

TL;DR: The reaction of [RuCl(CNN)(dppb)] with NaOiPr in 2-propanol/C6D6 affords the alcohol adduct alkoxide, containing the Ru-NH2 linkage, which is very close to the enantiomeric excess of the alcohol (R)-CF3CH(OH)(4-C6H4F) formed in catalysis, thus suggesting that diastereoisomeric alkoxides with the Ru
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Pincer CNN Ruthenium(II) Complexes with Oxygen-Containing Ligands (O2CR, OAr, OR, OSiR3, O3SCF3): Synthesis, Structure, and Catalytic Activity in Fast Transfer Hydrogenation

TL;DR: The pincer complexes [RuX(CNN)(dppb)] and [RuCl(CNN) as discussed by the authors have been obtained in high yield by substitution of the chloride with sodium or thallium compounds or protonation of the alkoxide.