Zobrazeno 1 - 10
of 457
pro vyhledávání: '"Jean, Roncali"'
Autor:
Yue Jiang, Magali Allain, Denis Gindre, Sylvie Dabos-Seignon, Philippe Blanchard, Clément Cabanetos, Jean Roncali
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Abstract The synthesis of a molecule constituted of two diarylamine-based push-pull chromophores covalently linked via their nitrogen atom is described. Comparison of the electronic properties with the parent monomer shows that dimerization has negli
Externí odkaz:
https://doaj.org/article/ba783f81e24b4170b4c79fe7d116fa21
Autor:
Andreea Petronela Diac, Ana-Maria Ţepeş, Albert Soran, Ion Grosu, Anamaria Terec, Jean Roncali, Elena Bogdan
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 825-834 (2016)
New indeno[1,2-c]pyran-3-ones bearing different substituents at the pyran moiety were synthesized and their photophysical properties were investigated. In solution all compounds were found to be blue emitters and the trans isomers exhibited significa
Externí odkaz:
https://doaj.org/article/e4f3b684b1754da29a2ee657eb3067f7
Autor:
Soomcc, Cluj-Napoca, Arany Janos str., Cluj-Napoca, Romania\\', Lorant Andras Szolga, Gavril-Ionel Giurgi, Ion Grosu, Jean Roncali, Andreea Crișan
Publikováno v:
Studia Universitatis Babeș-Bolyai Chemia. 66:97-105
Autor:
Antoine Labrunie, Teddy Lebailly, Amir Hossein Habibi, Clément Dalinot, Yue Jiang, Sylvie Dabos-Seignon, Jean Roncali, Philippe Blanchard, Clément Cabanetos
Publikováno v:
Metals, Vol 9, Iss 6, p 618 (2019)
The synthesis and characterization of a new molecular dyad consisting of a benzodithiophene-based push-pull linked to a fullerene derivative through the use of the well-known Copper Azide-Alkyne Huisgen Cycloaddition (CuAAC) reaction is reported here
Externí odkaz:
https://doaj.org/article/18cbad4b555c497c960dacaa55b0abac
Autor:
Atilla Bende, Ion Grosu, Jean Roncali, Alexandra Pop, Ioan Stroia, Cătălin C. Anghel, Niculina D. Hădade
Publikováno v:
RSC Advances. 11:9894-9900
We report herein our attempt to synthesize an analog of indacenedithiophene (IDT) based on a tetraphenylhexyl substituted, covalently bridged syn-terthienyl unit. Instead of the expected compound the adopted synthetic route led to the formation of an
Autor:
Ivan Ramirez, Amir Hossein Habibi, José María Andrés Castán, Clément Cabanetos, Pablo Simón Marqués, Martin Blais, Karsten Walzer, Pierre Josse, Jean Roncali, Philippe Blanchard
Publikováno v:
New Journal of Chemistry
New Journal of Chemistry, Royal Society of Chemistry, 2020, 44 (27), pp.11441-11447. ⟨10.1039/d0nj02019b⟩
New Journal of Chemistry, Royal Society of Chemistry, 2020, 44 (27), pp.11441-11447. ⟨10.1039/d0nj02019b⟩
Two push–pull derivatives based on a N,N-bis(4-biphenylyl)aniline (BPA) donor block connected to a dicyanovinyl accepting moiety by thienyl and bithienyl π-conjugated spacers have been synthesized and characterized. All-small-molecule planar-heter
Autor:
Chenchen Yang, Harry A. Atwater, Marc A. Baldo, Derya Baran, Christopher J. Barile, Miles C. Barr, Matthew Bates, Moungi G. Bawendi, Matthew R. Bergren, Babak Borhan, Christoph J. Brabec, Sergio Brovelli, Vladimir Bulović, Paola Ceroni, Michael G. Debije, Jose-Maria Delgado-Sanchez, Wen-Ji Dong, Phillip M. Duxbury, Rachel C. Evans, Stephen R. Forrest, Daniel R. Gamelin, Noel C. Giebink, Xiao Gong, Gianmarco Griffini, Fei Guo, Christopher K. Herrera, Anita W.Y. Ho-Baillie, Russell J. Holmes, Sung-Kyu Hong, Thomas Kirchartz, Benjamin G. Levine, Hongbo Li, Yilin Li, Dianyi Liu, Maria A. Loi, Christine K. Luscombe, Nikolay S. Makarov, Fahad Mateen, Raffaello Mazzaro, Hunter McDaniel, Michael D. McGehee, Francesco Meinardi, Amador Menéndez-Velázquez, Jie Min, David B. Mitzi, Mehdi Moemeni, Jun Hyuk Moon, Andrew Nattestad, Mohammad K. Nazeeruddin, Ana F. Nogueira, Ulrich W. Paetzold, David L. Patrick, Andrea Pucci, Barry P. Rand, Elsa Reichmanis, Bryce S. Richards, Jean Roncali, Federico Rosei, Timothy W. Schmidt, Franky So, Chang-Ching Tu, Aria Vahdani, Wilfried G.J.H.M. van Sark, Rafael Verduzco, Alberto Vomiero, Wallace W.H. Wong, Kaifeng Wu, Hin-Lap Yip, Xiaowei Zhang, Haiguang Zhao, Richard R. Lunt
Publikováno v:
Joule, 6(1), 8-15. Elsevier
Joule 6(1), 8-15 (2022). doi:10.1016/j.joule.2021.12.004
Joule 6(1), 8-15 (2022). doi:10.1016/j.joule.2021.12.004
Fair and meaningful device per- formance comparison among luminescent solar concentrator- photovoltaic (LSC-PV) reports cannot be realized without a gen- eral consensus on reporting stan- dards in LSC-PV research. There- fore, it is imperative to ado
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6055d7a2b3729a11ecb60be6d7c085b2
https://www.repository.cam.ac.uk/handle/1810/345600
https://www.repository.cam.ac.uk/handle/1810/345600
Autor:
Huojun Peng, Yue Jiang, Qikun Rong, Jean Roncali, Runsheng Mai, Jinwei Gao, Yuying Meng, Li Nian, Jun-Ming Liu, Guofu Zhou, Clément Cabanetos
Publikováno v:
Organic Electronics
Organic Electronics, Elsevier, 2019, 68, pp.200-204. ⟨10.1016/j.orgel.2019.01.012⟩
Organic Electronics, Elsevier, 2019, 68, pp.200-204. ⟨10.1016/j.orgel.2019.01.012⟩
Organic solar cells (OSCs) have reached a milestone with 15.6% efficiency through the development of active and interfacial materials. However, anode modifiers in the inverted structure, especially the interface of organic active layer/inorganic MoO3
Autor:
Jinwei Gao, Clément Cabanetos, Jun-Ming Liu, Guofu Zhou, Jean Roncali, Yuying Meng, Zhike Xian, Yue Jiang
Publikováno v:
Dyes and Pigments
Dyes and Pigments, Elsevier, 2019, 162, pp.697-703. ⟨10.1016/j.dyepig.2018.10.078⟩
Dyes and Pigments, Elsevier, 2019, 162, pp.697-703. ⟨10.1016/j.dyepig.2018.10.078⟩
The potential of three arylamine based molecules for electrochromic applications is investigated herein. The latter, by-product of a Buchwald-Hartwig reaction were fully characterized, instead of being thrown away, due to their structural analogy wit
Autor:
Ion Grosu, Andreea Petronela Crisan, Siriporn Jungsuttiwong, Niculina D. Hădade, Natalia Terenti, Jean Roncali, Alexandra Pop
Publikováno v:
Dyes and Pigments
Dyes and Pigments, Elsevier, 2021, 187, pp.109116-. ⟨10.1016/j.dyepig.2020.109116⟩
Dyes and Pigments, Elsevier, 2021, 187, pp.109116-. ⟨10.1016/j.dyepig.2020.109116⟩
Indacenodithiophene (IDT) is a major building block for the design of advanced functional π-conjugated polymers and nonfullerene electron-acceptor materials for organic photovoltaics. Preliminary results of a synthetic approach aiming at the modulat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfab08a60261bbad48ad09013bd41aec
https://hal.archives-ouvertes.fr/hal-03493643
https://hal.archives-ouvertes.fr/hal-03493643