Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Tanguy Jousselin-Oba"'
Autor:
Tanguy Jousselin-Oba, Masashi Mamada, Karen Wright, Jérôme Marrot, Chihaya Adachi, Abderrahim Yassar, Michel Frigoli
Publikováno v:
Journal of Materials Chemistry C. 10:7717-7723
Bond lengths analysis highlights their closed-shell structures and gives insight on the bond lengths of diindenoacene diradicaloids. They are low band gap molecules with high electron affinity and exhibit ambipolar behavior in OFETs.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d8cf18f6570841e1936e637c90ef39b
https://doi.org/10.1039/d2tc01324j
https://doi.org/10.1039/d2tc01324j
Autor:
Tanguy Jousselin‐Oba, Masashi Mamada, Karen Wright, Jérome Marrot, Chihaya Adachi, Abderrahim Yassar, Michel Frigoli
Publikováno v:
Angewandte Chemie. 134
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8c573ccd5b9fab7eb8b02b5a3f2b437
https://doi.org/10.1002/ange.202112794
https://doi.org/10.1002/ange.202112794
Autor:
Jérôme Marrot, Tanguy Jousselin-Oba, Michael M. Haley, Lev N. Zakharov, Joshua E. Barker, Conerd K. Frederickson, Michel Frigoli, Takuya Kodama, Min K. Song, Richard P. Johnson
Publikováno v:
ChemPlusChem
ChemPlusChem, Wiley, 2019, Novel Aromatics, 84 (6), pp.665-672. ⟨10.1002/cplu.201800605⟩
ChemPlusChem, Wiley, 2019, Novel Aromatics, 84 (6), pp.665-672. ⟨10.1002/cplu.201800605⟩
International audience; The serendipitous isolation of very small amounts of two naphthocyclobutadiene (NCB) derivatives has led to the computational re-examination of the electrocyclization of Z,Z-3,5-octadiene-1,7-diyne as well as the experimental
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e51a2362008a536dacc60a42ebc3384c
https://doi.org/10.1002/cplu.201800605
https://doi.org/10.1002/cplu.201800605
Autor:
Masashi Mamada, Tanguy Jousselin-Oba, Karen Wright, Jérome Marrot, Chihaya Adachi, Abderrahim Yassar, Michel Frigoli
Publikováno v:
ECS Meeting Abstracts. :898-898
Recently, there has been increasing interest in a class of polycyclic aromatic hydrocarbons (PAHs) with peri-extension of acenes. These peri-fused systems, referred to as peri-acenes and acenoacenes, are considered to be nanographenes.[1–3] Thus, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c7b520964af28de736a3358a476befa
https://doi.org/10.1149/ma2022-0113898mtgabs
https://doi.org/10.1149/ma2022-0113898mtgabs
Autor:
Chihaya Adachi, Abderrahim Yassar, Karen Wright, Masashi Mamada, Michel Frigoli, Jérôme Marrot, Tanguy Jousselin-Oba
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, In press, ⟨10.1002/anie.202112794⟩
Angewandte Chemie International Edition, Wiley-VCH Verlag, In press, ⟨10.1002/anie.202112794⟩
International audience; We report the synthesis and optoelectronic properties of TIPS-peri-pentacenopentacene (TIPS-PPP), a vertical extension of TIPS-pentacene (TIPS-PEN) and a low-band-gap material with remarkable stability. We found the synthetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::872a4a2410a87212615b1f00dd4b296a
https://hal.archives-ouvertes.fr/hal-03442478
https://hal.archives-ouvertes.fr/hal-03442478
Autor:
Agnese Zangarelli, Masashi Mamada, Michel Frigoli, Fausto Ortica, Jérôme Marrot, Danilo Pannacci, Tanguy Jousselin-Oba, Chihaya Adachi
Publikováno v:
Photochemical & Photobiological Sciences
Photochemical & Photobiological Sciences, Royal Society of Chemistry, 2020, 19 (10), pp.1344-1355. ⟨10.1039/D0PP00202J⟩
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2020, 19 (10), pp.1344-1355. ⟨10.1039/d0pp00202j⟩
Photochemical & Photobiological Sciences, Royal Society of Chemistry, 2020, 19 (10), pp.1344-1355. ⟨10.1039/D0PP00202J⟩
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2020, 19 (10), pp.1344-1355. ⟨10.1039/d0pp00202j⟩
International audience; Five new N-phenyl-carbazole benzopyrans bearing different substitutions on one of the phenyl rings at the sp3 carbon have been synthesized. Their molecular structures were investigated by X-ray and NMR analyses and through qua
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1668bb1fe963eedd5c2187477ac2c91
https://hal.archives-ouvertes.fr/hal-02989119/document
https://hal.archives-ouvertes.fr/hal-02989119/document
Autor:
Kamal Sbargoud, Michel Frigoli, Francesco Meinardi, Abderrahim Yassar, Tanguy Jousselin-Oba, G. Vaccaro
Publikováno v:
Chemistry – A European Journal. 23:16184-16188
The extension of the pyrene ring from dimethyl 2,2′-(pyrene-1,6-diyl)dibenzoate derivatives by an intramolecular Friedel–Crafts acylation can be realized in an efficient and regioselective manner using triflic acid as proton source. Naphtho-tetra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::851c2b65dca7f48b6068369644c22e62
https://doi.org/10.1002/chem.201704116
https://doi.org/10.1002/chem.201704116
Autor:
Abderrahim Yassar, Tanguy Jousselin-Oba, Michel Frigoli, Jérôme Marrot, Antoine Maignan, Chihaya Adachi, Masashi Mamada
Publikováno v:
Journal of the American Chemical Society
Journal of the American Chemical Society, American Chemical Society, 2019, 141 (23), pp.9373-9381. ⟨10.1021/jacs.9b03488⟩
Journal of the American Chemical Society, 2019, 141 (23), pp.9373-9381. ⟨10.1021/jacs.9b03488⟩
Journal of the American Chemical Society, American Chemical Society, 2019, 141 (23), pp.9373-9381. ⟨10.1021/jacs.9b03488⟩
Journal of the American Chemical Society, 2019, 141 (23), pp.9373-9381. ⟨10.1021/jacs.9b03488⟩
International audience; Designing stable open-shell organic materials through the modifications of the π-topology of molecular organic semiconductors have attracted recently considerable attention. However, their uses as an active layer in organic f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c98dbe5fb796a52ea8fa37cae02f951a
https://pubmed.ncbi.nlm.nih.gov/31117656
https://pubmed.ncbi.nlm.nih.gov/31117656
Autor:
Abderrahim Yassar, Parker E. Deal, Conerd K. Frederickson, Chris L. Vonnegut, Tanguy Jousselin-Oba, Michael M. Haley, Lev N. Zakharov, Michel Frigoli, Aaron G. Fix
Publikováno v:
Chemistry, an Asian journal. 14(10)
A set of fully-conjugated indenofluorenes has been synthesized and confirmed by solid-state structure analysis. The indeno[2,1-c]fluorenes and their benzo-fused analogues all contain the antiaromatic as-indacene core. The molecules possess high elect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b91982e502928b096ef6ca6253fcb271
https://pubmed.ncbi.nlm.nih.gov/30548168
https://pubmed.ncbi.nlm.nih.gov/30548168
Autor:
Cecilie Lindholm Andersen, Mads Mansø, Ole Hammerich, Mogens Nielsen, Michel Frigoli, Tanguy Jousselin-Oba, Søren Lindbæk Broman
Publikováno v:
Broman, S L, Andersen, C L, Jousselin-Oba, T, Mansø, M, Hammerich, O, Frigoli, M & Nielsen, M B 2017, ' Tetraceno[2,1,12,11-opqra ]tetracene-extended tetrathiafulvalene-redox-controlled generation of a large PAH core ', Organic & Biomolecular Chemistry, vol. 15, no. 4, pp. 807-811 . https://doi.org/10.1039/c6ob02666d
Two tetraceno[2,1,12,11-opqra]tetracene-extended tetrathia-fulvalenes were prepared and found to undergo reversible conversion into their planar polycyclic aromatic hydrocarbons (PAHs) upon electrochemical oxidation – at potentials probing the best
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::615d742989dd77405925cb42bea5ab22
https://pubmed.ncbi.nlm.nih.gov/28054066
https://pubmed.ncbi.nlm.nih.gov/28054066