Luigi Vaccaro

Prof. Luigi Vaccaro

Università degli Studi di Perugia
orcid

Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
28 June 2019 in Energy & Environmental Science
Verified
Journal Article
Closed access
PDF file
FVFederica Valentini
Federica Valentini
VKVadym Kozell
Vadym Kozell
CPChiara Petrucci
Chiara Petrucci
Assunta MarrocchiAssunta Marrocchi
Assunta Marrocchi
YGYanlong Gu
Yanlong Gu
Luigi VaccaroLuigi Vaccaro
Luigi Vaccaro
Formic acid is a main product from biomass-derived carbohydrates and is attracting ever more attention as a sustainable hydrogen source, owing to its high volumetric hydrogen density of 53 g of H2 per liter. In this review, we give an overview of the formic acid mediated transformations of biomass-based feedstocks into added-value products, including biofuels; attention will be primarily focused on the transformation of biomass-derived platform chemicals, with an emphasis on levulinic acid. Formic-acid mediated lignin depolymerization and biomass-oil upgrading will be also discussed.

20 March 2004 in The Journal of Organic Chemistry
Verified
Journal Article
Closed access
DADavid Amantini
David Amantini
RBRomina Beleggia
Romina Beleggia
FFFrancesco Fringuelli
Francesco Fringuelli
FPFerdinando Pizzo
Ferdinando Pizzo
Luigi VaccaroLuigi Vaccaro
Luigi Vaccaro

24 April 2014 in Green Chemistry
Verified
Journal Article
Closed access
PDF file
Luigi VaccaroLuigi Vaccaro
Luigi Vaccaro
DLDaniela Lanari
Daniela Lanari
Assunta MarrocchiAssunta Marrocchi
Assunta Marrocchi
GSGiacomo Strappaveccia
Giacomo Strappaveccia
Green chemistry and flow chemistry are ideal partners for accessing novel chemical spaces and define highly efficient synthetic tools.

10 March 2016 in Green Chemistry
Verified
Journal Article
Open access
PDF file
SSStefano Santoro
Stefano Santoro
SKSergei I. Kozhushkov
Sergei I. Kozhushkov
LALutz Ackermann
Lutz Ackermann
Luigi VaccaroLuigi Vaccaro
Luigi Vaccaro
This review summarizes the development of user-friendly, recyclable and easily separable heterogeneous catalysts for C–H activation during the last decade until December 2015.

27 August 2020 in Green Chemistry
Verified
Journal Article
Closed access
PDF file
FGFeng Gao
Feng Gao
RBRongxian Bai
Rongxian Bai
FFFrancesco Ferlin
Francesco Ferlin
Luigi VaccaroLuigi Vaccaro
Luigi Vaccaro
Minghao LiMinghao Li
Minghao Li
YGYanlong Gu
Yanlong Gu
Dipolar aprotic solvents (DMSO, DMF, DMAc, NMP, etc.) have been widely used in organic synthesis and pharmaceutical research because of their remarkable polarities and solubilities, while most of them are not green because of their detrimental effects on human health and hazards to the natural environment caused by their inescapable toxicity as well as large wastewater streams and high-energy-input requirements. This dangerous situation is further complicated by the surging demand of dipolar aprotic solvents in the research and development in the pharmaceutical industry and other chemical processes. Therefore, minimizing and avoiding the use of such solvents has become one of the most important facets of green chemistry. So far, substantial efforts have been devoted in response to this problem that has entailed the development of green and novel reaction systems that fulfill numerous requirements, which are also met by traditional dipolar aprotic solvents. In this context, this review summarizes the methods and strategies for replacing non-green polar aprotic solvents, which mainly include direct replacement with new green alternatives and utilization of polarized catalysts in common green solvents for avoiding the use of conventional polar aprotic solvents. Besides, the strengths and weaknesses of these two strategies are analyzed. Compared with the direct replacement strategy, the rational design of polarized catalysts not only expands the choice of green solvents, but also provides new possibilities for the design and preparation of multifunctional catalysts, suggesting a promising prospect in substitution strategies for non-green polar aprotic solvents. Certainly, other methods are being explored to realize the green and sustainable replacement of conventional dipolar aprotic solvents in an economical and handy tactic.

16 July 2012 in Energy & Environmental Science
Verified
Journal Article
Closed access
PDF file
Assunta MarrocchiAssunta Marrocchi
Assunta Marrocchi
DLDaniela Lanari
Daniela Lanari
AFAntonio Facchetti
Antonio Facchetti
Luigi VaccaroLuigi Vaccaro
Luigi Vaccaro
Poly(3-hexylthiophene) (P3HT) remains of significant importance as a prototypical benchmark hole conductor material in Organic Photovoltaics (OPVs). In this review we discuss synthetic strategies to P3HT, particularly focusing on those leading to the regioregular form and discussing key physical and morphological properties. Finally, a survey and a brief discussion of P3HT performance in bulk-heterojunction (BHJ) OPVs are also provided.