Lorenzo Zani

ORCID: 0000-0003-0621-2648
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • TiO2 Photocatalysis and Solar Cells
  • Advanced Photocatalysis Techniques
  • Asymmetric Synthesis and Catalysis
  • Asymmetric Hydrogenation and Catalysis
  • Photochemistry and Electron Transfer Studies
  • Organic Light-Emitting Diodes Research
  • Conducting polymers and applications
  • Catalytic C–H Functionalization Methods
  • Chemical Synthesis and Analysis
  • Synthesis and Catalytic Reactions
  • Synthetic Organic Chemistry Methods
  • Catalytic Cross-Coupling Reactions
  • Polyoxometalates: Synthesis and Applications
  • Catalytic Alkyne Reactions
  • Photochromic and Fluorescence Chemistry
  • Pigment Synthesis and Properties
  • Advanced Nanomaterials in Catalysis
  • Organic Electronics and Photovoltaics
  • Orthopaedic implants and arthroplasty
  • Luminescence and Fluorescent Materials
  • Perovskite Materials and Applications
  • Quantum Dots Synthesis And Properties
  • Chemical Synthesis and Reactions
  • Analytical Chemistry and Sensors
  • Advanced Chemical Sensor Technologies

Institute for the Chemistry of OrganoMetallic Compounds
2016-2025

National Academies of Sciences, Engineering, and Medicine
2024

National Research Council
2020-2024

Loughborough University
2017-2023

Politecnico di Milano
1991-2017

Institute of Cancer Research
2014-2016

Cancer Research UK
2016

Institute of Cancer Research
2016

Nello Carrara Institute of Applied Physics
2015

Institute of Organic Synthesis and Photoreactivity
2012-2014

Acid treatment: Exposure of catalytically inactive (neutral) molecules to strong Brønsted acids generates cationic species (e.g. 1 and 2) that catalyze a wide range synthetically powerful transformations. These reactions give products with excellent ee values. TfO−=trifluoromethanesulfonate; TFA=trifluoroacetic acid.

10.1002/anie.200500154 article EN Angewandte Chemie International Edition 2005-03-08

Machining of micro SiCp/AA2124 composites remains a challenge with conventional machining yielding poor surface quality high tool wear. In this paper, we study two distinct and unique hybrid processes the aim improving outcome three types micro-SiC/AA2124 different particulate volume fractions sizes. The class studied is available commercially being used in industrial applications, thus assessing outcomes becomes even more pertinent. Vibratory where made to vibrate at ultrasonic frequencies,...

10.1016/j.jmapro.2022.12.045 article EN cc-by Journal of Manufacturing Processes 2023-01-01

The ability of Time-Dependent Density Functional Theory (TD-DFT) to provide excited state geometries and reproduce emission energies organic D-π-A dyes designed for DSSC applications is evaluated. performance six functionals (CAM-B3LYP, MPW1K, ωB97X-D, LC-BLYP, LC-ωPBE, M06-HF) in combination with three basis sets (cc-pVDZ, 6-31+G(d,p), 6-311+G(2d,p)) has been analyzed. Solvent effects have taken into account by means a Polarizable Continuum Model both LR SS formalisms. Our LR-PCM/TD-DFT...

10.1021/ct500328t article EN Journal of Chemical Theory and Computation 2014-07-23

Semitransparent dye-sensitized solar cells (DSSCs) for greenhouse integration were manufactured by using especially designed organic dyes featuring different heterocyclic moieties integrated into a thiazolo[5,4-<italic>d</italic>]thiazole-molecular scaffold.

10.1039/d0se00124d article EN cc-by Sustainable Energy & Fuels 2020-01-01

Visible light-driven production of fuels and value-added chemicals is currently one the most intensely investigated research topics across various scientific disciplines, due to its potential ease World s dependence on fossil fuels. In this perspective, we recapitulate some main features dye-sensitized photocatalytic systems aimed at solar H$_2$ production, focusing in particular TiO$_2$-based three-component assemblies with organic sensitizers. Relevant aspects include structural electronic...

10.1088/2515-7655/abe04b article EN cc-by Journal of Physics Energy 2021-01-27

Luminescent solar concentrators (LSCs) are a class of optical devices able to harvest, downshift, and concentrate sunlight, thanks the presence emitting materials embedded in polymer matrix. Use LSCs combination with silicon-based photovoltaic (PV) has been proposed as viable strategy enhance their ability harvest diffuse light facilitate integration built environment. LSC performances can be improved by employing organic fluorophores strong absorption center spectrum intense, red-shifted...

10.1021/acsaem.3c00362 article EN cc-by ACS Applied Energy Materials 2023-04-20

A one-pot, enantioselective synthesis of N-aryl propargylic amines, using alkynylation reagents obtained from dimethylzinc and terminal acetylenes in combination with various aldehydes o-methoxyaniline as starting materials, has been developed. Enantiopure beta-amino alcohols derived norephedrine were used non-covalent chiral auxiliaries, both stoichiometric or substoichiometric amount. After optimization, amines good to high yields (up 93%) moderate enantiomeric excesses 97% ee). The...

10.1002/chem.200601347 article EN Chemistry - A European Journal 2006-12-22

Three new thiazolo[5,4-d]thiazole-based organic dyes have been designed and synthesized for employment as DSSC sensitizers. Alternation of the electron poor thiazolothiazole unit with two propylenedioxythiophene (ProDOT) groups ensured very intense light absorption in visible region (ε up to 9.41 × 104 M−1 cm−1 THF solution). The were particularly suitable application transparent opaque thin-layer DSSCs (TiO2 thickness: 5.5–6.5 μm, efficiencies 7.71%), thus being good candidates production...

10.1039/c4cc06160h article EN Chemical Communications 2014-09-11

Abstract Thiazolo[5,4‐ d ]thiazoles (TzTzs) are fused bicyclic heteroaromatic compounds characterized by a rigid planar backbone and an extended π‐conjugated electronic structure. Although they have been known for many decades, interest in their properties applications has begun to increase only recently, after incorporation into series of active materials used the field organic electronics. Recently, thiazolo[5,4‐ ]thiazole scaffold inserted new photoactive (both small‐molecule polymers)...

10.1002/ejoc.201501237 article EN European Journal of Organic Chemistry 2015-12-23

Conversion of sunlight into chemical energy has been the subject intense research efforts in recent years, due to possibility store enormous amount continuously provided by Sun form useful “solar fuels”. To allow such process, suitable photocatalysts are required, which usually obtained combination different inorganic materials or self‐assembly molecular components on semiconductor surfaces: accordingly, they capable carry out several processes as light harvesting, substrate binding,...

10.1002/ejic.201901174 article EN European Journal of Inorganic Chemistry 2019-11-29

In this paper, we present the design and synthesis of three organic dyes specially developed for fabrication dye-sensitized solar cells with potential application in greenhouses cladding.

10.1039/d0se01610a article EN cc-by Sustainable Energy & Fuels 2021-01-01

A hybrid-hybrid (ultrasonic-assisted + laser-assisted) turning study of silicon carbide reinforced aluminium metal matrix composite is presented. The results show a significant reduction average cutting force with an improved surface finish machined components compared to conventional machining, implying that this new and novel paradigm viable machining process.

10.1016/j.mfglet.2022.04.002 article EN cc-by Manufacturing Letters 2022-04-01

We report an efficient procedure to carry out palladium-catalyzed Miyaura borylation reactions of (hetero)aromatic halides and triflates in choline chloride (ChCl)-based deep eutectic solvents (DESs). The employs bis(pinacolato)diboron as a boron source catalyst prepared situ from readily available Pd2(dba)3 the phosphine ligand XPhos. Reactions proceed well different ChCl-based DESs, among which best results were provided by environmentally friendly biodegradable mixtures with glycerol...

10.1021/acs.joc.4c00357 article EN The Journal of Organic Chemistry 2024-05-08

A preparatively easy and efficient protocol for the resolution of racemic 2-aminocyclohexanol derivatives is described, delivering both enantiomers with >99% enantiomeric excess (ee) by sequential use (R)- (S)-mandelic acid. simple aqueous workup procedure permits isolation amino alcohols in analytically pure form almost quantitative recovery mandelic Debenzylation enantiopure trans-2-(N-benzyl)amino-1-cyclohexanol hydrogenation subsequent derivatization give access to a broad variety...

10.1021/jo052433w article EN The Journal of Organic Chemistry 2006-02-10

The treatment of various aromatic and aliphatic aldimines with a mixture terminal alkyne commercially available dimethylzinc solution in toluene yields the corresponding protected propargylic amines moderate to excellent yields. reaction proceeds absence any activator. These observations led development three-component synthesis which product was obtained upon mixing an aldehyde ortho-methoxyaniline phenylacetylene presence dimethylzinc, through situ formation imine.

10.1021/jo052273o article EN The Journal of Organic Chemistry 2006-01-20

Abstract Aryl alkyl‐, heteroaryl alkyl‐ and dialkyl ketones were readily reduced to their corresponding secondary alcohols in high yields, using the commercially available inexpensive polymeric silane polymethylhydrosiloxane (PMHS), as reducing agent. The reaction is catalyzed by an situ ‐generated iron complex, conveniently generated from iron(II) acetate N ‐heterocyclic carbene (NHC) precursor IPr·HCl. Copyright © 2011 John Wiley &amp; Sons, Ltd.

10.1002/aoc.1832 article EN Applied Organometallic Chemistry 2011-09-07

Abstract Four new D‐π‐A organic dyes incorporating either a thiazolo[5,4‐ d ]thiazole bicyclic system ( TTZ1 – 2 ) or benzo[1,2‐ :4,5‐ d′ ]bisthiazole tricyclic unit BBZ1 have been synthesized and fully characterized. The key steps of the synthesis include an efficient MW‐assisted preparation core selective functionalization two different dihalothienyl derivatives through Suzuki coupling. All compounds showed photo‐ electrochemical properties compatible with their employment in...

10.1002/ejoc.201201629 article EN European Journal of Organic Chemistry 2013-02-18

Five thiazolothiazole-based dyes, bearing electronrich ProDOT groups, were used as sensitizers in thin-layer DSSCs (active area: 0.25–3.6 cm<sup>2</sup>; TiO<sub>2</sub> thickness: 3.0–6.5 μm), giving efficiencies up to 7.71% coupled with excellent stability over 1000 h.

10.1039/c5ra03530a article EN RSC Advances 2015-01-01

Photostable donor–acceptor–donor fluorophores, which have a central quinoxaline acceptor nucleus, been used in LSCs, obtaining outstanding results for modern building-integrated photovoltaics (BIPV).

10.1039/d1tc02923a article EN cc-by-nc Journal of Materials Chemistry C 2021-01-01
Coming Soon ...