Giovanni Sotgiu

ORCID: 0000-0003-2841-9316
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Research Areas
  • Physics of Superconductivity and Magnetism
  • Silicon Nanostructures and Photoluminescence
  • Carbon dioxide utilization in catalysis
  • Chemical Synthesis and Reactions
  • CO2 Reduction Techniques and Catalysts
  • Asymmetric Hydrogenation and Catalysis
  • N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
  • Synthesis and Catalytic Reactions
  • Catalytic Cross-Coupling Reactions
  • ZnO doping and properties
  • Nanowire Synthesis and Applications
  • Oxidative Organic Chemistry Reactions
  • Semiconductor materials and devices
  • Ionic liquids properties and applications
  • Electrochemical Analysis and Applications
  • Asymmetric Synthesis and Catalysis
  • Electrocatalysts for Energy Conversion
  • Advanced Condensed Matter Physics
  • Cyclopropane Reaction Mechanisms
  • Thin-Film Transistor Technologies
  • Spectroscopy Techniques in Biomedical and Chemical Research
  • Radical Photochemical Reactions
  • Chemical Synthesis and Analysis
  • Advanced battery technologies research
  • Iron-based superconductors research

Roma Tre University
2016-2025

Engineering (Italy)
2022

Sapienza University of Rome
2000-2015

Bridge University
2009-2010

University of L'Aquila
2005

University of Basilicata
1989-1992

University of Bologna
1960

Medica (Italy)
1960

[reaction: see text] An efficient electrochemical synthesis of 5-methylene-1,3-oxazolidin-2-ones (2a-h) from acetylenic amines (1a-h) and carbon dioxide has been achieved by direct electrolysis solution MeCN Et4NPF6 containing the amine, with subsequent CO2 bubbling heating. The yields vary good to excellent, conditions are mild, use toxic harmful chemicals catalysts is avoided.

10.1021/jo0511804 article EN The Journal of Organic Chemistry 2005-08-12

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 200 leading journals. To access Abstract, please click on HTML or PDF.

10.1002/chin.200719058 article EN ChemInform 2007-04-18

Abstract The intrinsic chemistry of imidazolium‐based room‐temperature ionic liquids, related to the acidity C‐2 imidazolium cation, can be modified via cathodic cleavage C‐2/hydrogen bond. N‐Heterocyclic carbenes, electrogenerated by electrolysis are stable bases that strong enough deprotonate bromoamides 1a–k yielding azetidin‐2‐one ring C‐3/C4 bond formation. electrosynthesis β‐lactams 2a–k has been achieved under mild conditions, elevated yields and avoiding use toxic, volatile,...

10.1002/adsc.200800049 article EN Advanced Synthesis & Catalysis 2008-05-16

Despite the well-known favorable chemical and mechanical properties of titanium-based materials for orthopedic dental applications, poor osseointegration implants, bacteria adhesion, excessive inflammatory response from host remain major problems to be solved. Here, antioxidant anti-inflammatory enzyme-like abilities ceria (CeOx) were coupled advantageous features titanium nanotubes (TiNTs). Cost-effective fast methods, such as electrochemical anodization drop casting, used build active...

10.3390/nano11020445 article EN cc-by Nanomaterials 2021-02-10

Biopolymers have gained importance in various sectors such as biomedical, automotive and agriculture, well single‐use food packaging. However, to make them competitive with traditional plastics, biopolymers require certain modifications, including the addition of plasticizers and/or blending other macromolecules. This study aims develop biodegradable films using starch blended chitosan, plasticized by choline chloride [Ch][Cl], acetate [Ch][OAc], an ionic liquid derived from choline. The...

10.1002/cplu.202500072 article EN ChemPlusChem 2025-04-29

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTRegioselective opening of epoxy alcohols: mild chemo- and stereoselective preparation iodohydrins 1,2-diolsCarlo Bonini, Giuliana Righi, Giovanni SotgiuCite this: J. Org. Chem. 1991, 56, 21, 6206–6209Publication Date (Print):October 1, 1991Publication History Published online1 May 2002Published inissue 1 October 1991https://pubs.acs.org/doi/10.1021/jo00021a045https://doi.org/10.1021/jo00021a045research-articleACS PublicationsRequest reuse...

10.1021/jo00021a045 article EN The Journal of Organic Chemistry 1991-10-01

Abstract N ‐Heterocyclic carbenes (NHCs), generated by electrochemical reduction under galvanostatic control of 1,3‐dialkylimidazolium‐based ionic liquids, were employed as catalysts in transesterification reactions the parent, room temperature liquids (RTILs) solvents, without utilisation any volatile organic solvent or base. The reaction between isopropenyl ethyl acetate and an alcohol (not efficient absence catalyst) was induced presence electrogenerated NHC, which seems to assist proton...

10.1002/ejoc.201201023 article EN European Journal of Organic Chemistry 2012-11-12

Time of flight secondary ion mass spectrometry (ToF‐SIMS) has become a fundamental analytical technique in cultural heritage studies to obtain the identification and distribution organic components present artworks. A sample taken from soldier's golden shield decoration fresco Vela della Castità (San Francesco Lower Basilica, Assisi) was studied. The metal leaves for gilding on wall paintings are usually applied using an oil‐resin mordant as adhesive. In this work, inorganic compounds used...

10.1002/sia.5956 article EN Surface and Interface Analysis 2016-02-11

Despite the significant contribution of titanium and its alloys for hard tissue regenerative medicine, some major issues remain to be solved. Implants' long-term stability is threatened by poor osseointegration. Moreover, bacterial adhesion excessive inflammatory response are also considered in design a device intended integrated into human body. Here, cerium mixed oxide (CeOx) coating was realized on pristine nanotubular-structured Ti Ti6Al4V surfaces using simple layer-by-layer...

10.1021/acsbiomaterials.2c01461 article EN ACS Biomaterials Science & Engineering 2023-05-08

ADVERTISEMENT RETURN TO ISSUEPREVNoteNEXTThe Reaction of 1,2-Amino Alcohols with Carbon Dioxide in the Presence 2-Pyrrolidone Electrogenerated Base. New Synthesis Chiral Oxazolidin-2-onesM. Antonietta Casadei, Marta Feroci, Achille Inesi, Leucio Rossi, and Giovanni SotgiuView Author Information Dip. ICMMPM, Università "La Sapienza", via Castro Laurenziano, 7, I-00161 Roma, Italy, CICM, degli Studi, I-67040, Monteluco di Roio, L'Aquila, SCTSBA, P.le A. Moro, 5, I-00185 Ingegneria Elettronica,...

10.1021/jo0002386 article EN The Journal of Organic Chemistry 2000-07-01

Chiral 2-phenyl succinic ester derivatives have been obtained under mild conditions, in short times and with satisfactory yields by electrochemical reduction of chiral cinnamic acid a CO2 atmosphere. When 4R-(diphenylmethyl)-oxazolidin-2-one was used as auxiliary the two diastereoisomers could be easily separated flash chromatography R-isomer major product.

10.1039/b500570a article EN Organic & Biomolecular Chemistry 2005-01-01
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