GHIDINELLI, SIMONE

GHIDINELLI, SIMONE  

Dipartimento di Medicina Molecolare e Traslazionale  

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Titolo Data di pubblicazione Autore(i) File
Bilirubin and its congeners: conformational analysis and chirality from metadynamics and related computational methods 1-gen-2019 Ghidinelli, Simone; Longhi, Giovanna; Abbate, Sergio; Boiadjiev, Stefan E.; Lightner, David A.
Biliverdin chiral derivatives as chiroptical switches for pH and metal cation sensing 1-gen-2021 Ghidinelli, Simone; Abbate, Sergio; Mazzeo, Giuseppe; Boiadjiev, Stefan E.; Lightner, David A.; Longhi, Giovanna
Characterization of "Free Base" and Metal Complex Thioalkyl Porphyrazines by Magnetic Circular Dichroism and TDDFT Calculations 1-gen-2020 Ghidinelli, Simone; Abbate, Sergio; Santoro, Ernesto; Belviso, Sandra; Longhi, Giovanna
Characterization of tetrakis(thiadiazole)porphyrazine metal complexes by magnetic circular dichroism and magnetic circularly polarized luminescence 1-gen-2020 Ghidinelli, S.; Abbate, S.; Mazzeo, G.; Paoloni, L.; Viola, E.; Ercolani, C.; Donzello, M. P.; Longhi, G.
Circularly Polarized Luminescence of Some [2]Paracyclo[2](5,8)quinoliphane Derivatives with Planar and Central Chirality 1-gen-2021 Mazzeo, G.; Ghidinelli, S.; Ruzziconi, R.; Grandi, M.; Abbate, S.; Longhi, G.
Experimental and theoretical aspects of magnetic circular dichroism and magnetic circularly polarized luminescence in the UV, visible and IR ranges: A review 1-gen-2024 Fusè, Marco; Mazzeo, Giuseppe; Ghidinelli, Simone; Evidente, Antonio; Abbate, Sergio; Longhi, Giovanna
Insights into the Structures of Bilirubin and Biliverdin from Vibrational and Electronic Circular Dichroism: History and Perspectives 1-gen-2023 Longhi, Giovanna; Ghidinelli, Simone; Abbate, Sergio; Mazzeo, Giuseppe; Fusè, Marco; Boiadjiev, Stefan E; Lightner, David A
L-Stercobilin-HCl and d-Urobilin-HCl. Analysis of Their Chiroptical and Conformational Properties by VCD, ECD, and CPL Experiments and MD and DFT Calculations 1-gen-2018 Ghidinelli, Simone; Abbate, Sergio; Boiadjiev, Stefan E.; Lightner, David A.; Longhi, Giovanna
Magnetic circular dichroism of naphthalene derivatives: A coupled cluster singles and approximate doubles and time-dependent density functional theory study 1-gen-2021 Ghidinelli, S.; Longhi, G.; Abbate, S.; Hattig, C.; Coriani, S.
Magnetic circular dichroism spectra from resonant and damped coupled cluster response theory 1-gen-2020 Faber, R.; Ghidinelli, S.; Hattig, C.; Coriani, S.
MCD and Induced CD of a Tetraphenoxyperylene-Based Dye in Chiral Solvents: An Experimental and Computational Study 1-gen-2022 Ghidinelli, S; Fuse, M; Mazzeo, G; Abbate, S; Longhi, G
MCD and MCPL Characterization of Luminescent Si(IV) and P(V) Tritolylcorroles: The Role of Coordination Number 1-gen-2021 Ghidinelli, Simone; Abbate, Sergio; Mazzeo, Giuseppe; Paolesse, Roberto; Pomarico, Giuseppe; Longhi, Giovanna
New naphthyl derivatives from Aspergillus californicus 1-gen-2020 Guo, Y.; Ghidinelli, S.; de la Cruz, M.; Mackenzie, T. A.; Ramos, M. C.; Sanchez, P.; Vicente, F.; Genilloud, O.; Larsen, T. O.
On the aggregation of bilirubinoids in solution as evidenced by VCD and ECD spectroscopy and DFT calculations 1-gen-2018 Ghidinelli, Simone; Longhi, Giovanna; Mazzeo, Giuseppe; Abbate, Sergio; Boiadjiev, Stefan E.; Lightner, David A.
Solvent Effects and Aggregation Phenomena Studied by Vibrational Optical Activity and Molecular Dynamics: The Case of Pantolactone 1-gen-2020 Ghidinelli, S.; Abbate, S.; Koshoubu, J.; Araki, Y.; Wada, T.; Longhi, G.
Taxonomy Driven Discovery of Polyketides fromAspergillus californicus 1-gen-2021 Guo, Y.; Ding, L.; Ghidinelli, S.; Gotfredsen, C. H.; de la Cruz, M.; Mackenzie, T. A.; Ramos, M. C.; Sanchez, P.; Vicente, F.; Genilloud, O.; Coriani, S.; Larsen, R. W.; Frisvad, J. C.; Larsen, T. O.
The Antitumor Didox Acts as an Iron Chelator in Hepatocellular Carcinoma Cells 1-gen-2019 Asperti, Michela; Cantamessa, Luca; Ghidinelli, Simone; Gryzik, Magdalena; Denardo, Andrea; Giacomini, Arianna; Longhi, Giovanna; Fanzani, Alessandro; Arosio, Paolo; Poli, Maura
The role of chirality in a set of key intermediates of pharmaceutical interest, 3-aryl-substituted-γ-butyrolactones, evidenced by chiral HPLC separation and by chiroptical spectroscopies 1-gen-2017 Rossi, Daniela; Nasti, Rita; Collina, Simona; Mazzeo, Giuseppe; Ghidinelli, Simone; Longhi, Giovanna; Memo, Maurizio; Abbate, Sergio