Michel Frigoli
Overview
Explore the profile of Michel Frigoli including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
35
Citations
116
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Pennachio M, Wei Z, Mamada M, Frigoli M, Petrukhina M
Chem Commun (Camb)
. 2024 Aug;
60(71):9526-9529.
PMID: 39139141
Chemical reduction of a vertically expanded pentacene, TIPS--pentacenopentacene (TIPS-PPP), with sodium metal in THF readily afforded a doubly-reduced product isolated as [{Na(THF)}(TIPS-PPP2-)]. Single-crystal X-ray diffraction revealed the formation of a...
2.
Jousselin-Oba T, Mamada M, Wright K, Marrot J, Adachi C, Yassar A, et al.
Angew Chem Int Ed Engl
. 2021 Nov;
61(1):e202112794.
PMID: 34727416
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 conditions to avoid...
3.
Jousselin-Oba T, Mamada M, Okazawa A, Marrot J, Ishida T, Adachi C, et al.
Chem Sci
. 2021 Jun;
11(44):12194-12205.
PMID: 34094431
Biradicaloid compounds with an open-shell ground state have been the subject of intense research in the past decade. Although diindenoacenes are one of the most developed families, only a few...
4.
Frigoli M, Jousselin-Oba T, Mamada M, Marrot J, Zangarelli A, Pannacci D, et al.
Photochem Photobiol Sci
. 2020 Aug;
19(10):1344-1355.
PMID: 32780060
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...
5.
Barker J, Kodama T, Song M, Frederickson C, Jousselin-Oba T, Zakharov L, et al.
Chempluschem
. 2020 Jan;
84(6):665-672.
PMID: 31944015
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 and computational...
6.
Richard M, Al-Ajaji A, Ren S, Foti A, Tran J, Frigoli M, et al.
Adv Colloid Interface Sci
. 2019 Dec;
275:102080.
PMID: 31809990
Printed organic electronics has attracted considerable interest in recent years as it enables the fabrication of large-scale, low-cost electronic devices, and thus offers significant possibilities in terms of developing new...
7.
Jousselin-Oba T, Mamada M, Marrot J, Maignan A, Adachi C, Yassar A, et al.
J Am Chem Soc
. 2019 May;
141(23):9373-9381.
PMID: 31117656
Designing stable open-shell organic materials through the modifications of the π-topology of molecular organic semiconductors has recently attracted considerable attention. However, their uses as an active layer in organic field-effect...
8.
Jousselin-Oba T, Deal P, Fix A, Frederickson C, Vonnegut C, Yassar A, et al.
Chem Asian J
. 2018 Dec;
14(10):1737-1744.
PMID: 30548168
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...
9.
Sbargoud K, Mamada M, Marrot J, Tokito S, Yassar A, Frigoli M
Chem Sci
. 2018 Mar;
6(6):3402-3409.
PMID: 29511505
Diindeno[1,2-:2',1'-]perylene, a new derivative of the indenoacene family was synthesized, and its electronic, electrochemical, and electrical properties were investigated. This material has a closed shell electronic configuration which corresponds to...
10.
Ianni F, Scorzoni S, Gentili P, Di Michele A, Frigoli M, Camaioni E, et al.
J Sep Sci
. 2017 Dec;
41(6):1266-1273.
PMID: 29232048
Two chloromethyl phenylcarbamate-based chiral stationary phases, one containing an amylose-type chiral selector (Lux Amylose 2, from Phenomenex) and the other a cellulose-type one (Lux Cellulose-4, from Phenomenex), were successfully used...