Zobrazeno 1 - 10 of 112 pro vyhledávání: '"Clara Baldoli"'
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Akademický článek
(Dimesityl)boron Benzodithiophenes: Synthesis, Electrochemical, Photophysical and Theoretical Characterization
Autor: Luigi Menduti, Dr. Clara Baldoli, Dr. Serena Arnaboldi, Prof. Dr. Andreas Dreuw, Duygu Tahaoglu, Dr. Alberto Bossi, Prof. Dr. Emanuela Licandro
Publikováno v: ChemistryOpen, Vol 11, Iss 1, Pp n/a-n/a (2022)
Abstract Triarylboranes containing linear or angular benzodithiophene moieties and bearing one or two dimesitylboron units were synthesized. The electrochemical and optical features of these compounds were investigated by cyclic voltammetry, UV/Vis a
Externí odkaz: https://doaj.org/article/7eaa6def03224415a9565aa084b69079
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(BO)2-Doped Tetrathia[7]helicene: A Configurationally Stable Blue Emitter
Autor: Luigi Menduti, Clara Baldoli, Simone Manetto, Michael Bolte, Hans‐Wolfram Lerner, Giovanna Longhi, Claudio Villani, Emanuela Licandro, Matthias Wagner
Publikováno v: Angewandte Chemie (International ed. in English).
Helicenes combine two central themes in chemistry: extended π-conjugation and chirality. Heteroatom doping preserves both characteristics and allows to modulate the electronic structure of a helicene. Herein, we report the (BO)2-doped tetrathia[7]he
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fb57473800ac4e4e10b5a67783a007b
https://pubmed.ncbi.nlm.nih.gov/36409523
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3
Diversified Syntheses of Tetrathia[7]helicenes by Metal‐Catalyzed Cross‐Coupling Reactions
Autor: D. Dova, Valentina Pelliccioli, Emanuela Licandro, Silvia Cauteruccio, Clara Baldoli, Claudia Graiff
Publikováno v: European journal of organic chemistry
3 (2021): 383–395. doi:10.1002/ejoc.202001382
info:cnr-pdr/source/autori:Pelliccioli V.; Dova D.; Baldoli C.; Graiff C.; Licandro E.; Cauteruccio S./titolo:Diversified Syntheses of Tetrathia[7]helicenes by Metal-Catalyzed Cross-Coupling Reactions/doi:10.1002%2Fejoc.202001382/rivista:European journal of organic chemistry (Print)/anno:2021/pagina_da:383/pagina_a:395/intervallo_pagine:383–395/volume:3
Efficient and versatile synthetic routes to functionalized tetrathia[7]helicenes (7-THs) are described. The key intermediates of these methodologies are 2-bromo-3,3?-bibenzo[1,2-b:4,3-b?]dithiophenes (1), synthesized through a palladium-catalyzed hom
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07ad5cbbeb5571dbb8ca0449d7bfa0af
https://doi.org/10.1002/ejoc.202001382
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6
Unusual Through‐Space Interactions between Oxygen Atoms that Mediate Inverse Morphochromism of an AIE Luminogen
Autor: Ben Zhong Tang, Lluís Blancafort, Alexander A. Voityuk, Jacky Wing Yip Lam, Yujie Tu, Nelson L. C. Leung, Herman H. Y. Sung, Ian D. Williams, Emanuela Licandro, Clara Baldoli, Ryan T. K. Kwok, Lucia Viglianti, Ni Xie
Publikováno v: Angewandte Chemie (Int. ed., Print) 59 (2020): 8552–8559. doi:10.1002/anie.201908573
info:cnr-pdr/source/autori:Viglianti L.; Xie N.; Sung H.H.Y.; Voityuk A.A.; Leung N.L.C.; Tu Y.; Baldoli C.; Williams I.D.; Kwok R.T.K.; Lam J.W.Y.; Licandro E.; Blancafort L.; Tang B.Z./titolo:Unusual Through-Space Interactions between Oxygen Atoms that Mediate Inverse Morphochromism of an AIE Luminogen/doi:10.1002%2Fanie.201908573/rivista:Angewandte Chemie (Int. ed., Print)/anno:2020/pagina_da:8552/pagina_a:8559/intervallo_pagine:8552–8559/volume:59
We have studied the photophysics of tetrafurylethene, an aggregation-induced emission luminogen with exceptionally short intramolecular O-O distances of 2.80 Å and a significant red-shifted morphochromism (27 nm) when going from the aggregate to the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f418bcdd97a32d61df406f5130b47cf5
https://doi.org/10.1002/anie.201908573
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β-Diketonate ancillary ligands in heteroleptic iridium complexes: a balance between synthetic advantages and photophysical troubles
Autor: Alberto Bossi, Marta Penconi, Davide Ceresoli, Marco Cazzaniga, Clara Baldoli, Patrizia R. Mussini, Sagar Kesarkar
Publikováno v: Photochemical & photobiological sciences
17 (2018): 1169–1178. doi:10.1039/c8pp00052b
info:cnr-pdr/source/autori:Penconi, Marta; Cazzaniga, Marco; Kesarkar, Sagar; Baldoli, Clara; Mussini, Patrizia R.; Ceresoli, Davide; Bossi, Alberto/titolo:beta-Diketonate ancillary ligands in heteroleptic iridium complexes: a balance between synthetic advantages and photophysical troubles/doi:10.1039%2Fc8pp00052b/rivista:Photochemical & photobiological sciences (Print)/anno:2018/pagina_da:1169/pagina_a:1178/intervallo_pagine:1169–1178/volume:17
beta-Diketones are an important class of bidentate cyclometalating compounds, used in organometallic chemistry as ancillary ligands because of their wide commercial availability and easy synthesis. They are employed to finely tune the electronic, spe
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad36b603ed3d5b981278da51bf33aefa
https://doi.org/10.1039/c8pp00052b
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A Comparative Study of Electrochemical, Spectroscopic and Structural Properties of Phenyl, Thienyl and Furyl Substituted Ethylenes
Autor: Chiara Botta, Emanuela Licandro, Silvia Cauteruccio, Emanuele Ortoleva, Francesca Villafiorita-Monteleone, Lucia Viglianti, Patrizia R. Mussini, Clara Baldoli
Publikováno v: ChemistrySelect 2 (2017): 2763–2773. doi:10.1002/slct.201700109
info:cnr-pdr/source/autori:Viglianti, Lucia; Villafiorita-Monteleone, Francesca; Botta, Chiara; Mussini, Patrizia R.; Ortoleva, Emanuele; Cauteruccio, Silvia; Licandro, Emanuela; Baldoli, Clara/titolo:A Comparative Study of Electrochemical, Spectroscopic and Structural Properties of Phenyl, Thienyl and Furyl Substituted Ethylenes/doi:10.1002%2Fslct.201700109/rivista:ChemistrySelect/anno:2017/pagina_da:2763/pagina_a:2773/intervallo_pagine:2763–2773/volume:2
a detailed electrochemical and photophysical comparative study of three parallel series of phenyl, thienyl and furyl substituted ethylenes has been carried out, implemented by the computational calculation of selected terms. Relationships have been h
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad2f36f9f0fc99e21d94f84492dd1a5f
https://doi.org/10.1002/slct.201700109
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10
Synthesis of luminescent 2,3-diphenylmaleimide-labelled peptide nucleic acid oligomers
Autor: Prasanna Ramani, Silvia Cauteruccio, Emanuela Licandro, Clara Baldoli
Publikováno v: Tetrahedron letters 59 (2018): 2229–2231. doi:10.1016/j.tetlet.2018.03.060
info:cnr-pdr/source/autori:Ramani P.; Cauteruccio S.; Licandro E.; Baldoli C./titolo:Synthesis of luminescent 2,3-diphenylmaleimide-labelled peptide nucleic acid oligomers/doi:10.1016%2Fj.tetlet.2018.03.060/rivista:Tetrahedron letters/anno:2018/pagina_da:2229/pagina_a:2231/intervallo_pagine:2229–2231/volume:59
A lys-GTAGATCACT-lys peptide nucleic acid (PNA) decamer labelled with the luminescent 2,3-diphenyl maleimido (DPM) group on the e-position of the terminal lysine residue was prepared through an automated solid phase synthesis. Fluorescence emission o
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9ec19b0063eb65015bf6b28b5388150
http://www.cnr.it/prodotto/i/388690
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