Výsledky vyhledávání - "Jérémie Grolleau"

Toward Sustainable Organic Semiconductors from a Broad Palette of Green Reactions

Autor: Jérémie Grolleau, Magali Allain, Alexandre Faurie, Stéphanie Legoupy, Pierre Frère, Frédéric Gohier

Publikováno v: European Journal of Organic Chemistry. 2017:2707-2714

New conjugated materials, based on TPA-thiophene moieties and integrating azomethine bonds with dibenzofuran unit or cyanovinyl bond with phenyl-thiophene and bithiophene units, have been synthesized by using a wide range of green reactions such as d

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::031a5b77f57fc0f572a66d2e96176742
https://doi.org/10.1002/ejoc.201700317

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Synthesis via direct (hetero)arylation polymerization, electrochemical and optical properties of poly (3,4-disubstituted)thiophenes

Autor: Jérémie Grolleau, Pierre Frère, Stéphanie Legoupy, Frédéric Gohier

Publikováno v: Polymer
Polymer, 2019, 182, pp.121811. ⟨10.1016/j.polymer.2019.121811⟩

International audience; Some poly (3,4-disubstituted)thiophenes bearing both cyano and alkoxy or thioalkoxy groups have been synthesizedby direct (hetero)arylation polymerization (DHAP) of 2-iodo-3,4-disubstituted thiophenes. The electrondonor and ac

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db3651920e0a0a604ee1319ca7fbd1de
https://hal.archives-ouvertes.fr/hal-02307410/document

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Clean and Efficient Iodination of Thiophene Derivatives

Autor: Jérémie Grolleau, Pierre Frère, Frédéric Gohier

Publikováno v: SYNTHESIS
SYNTHESIS, Georg Thieme Verlag, 2015, 24 (47), pp.3901-3906. ⟨10.1055/s-0035-1560480⟩

International audience; Iodination of thiophene derivatives is realized using a simple, fast, and efficient methodology. Iodination of thiophene and 2- or 3-substituted or 3,4-disubstituted thiophenes with N-iodosuccinimide (NIS) activated with 4-tol

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3eadf0ba72aec883a4301004c36fa02
https://doi.org/10.1055/s-0035-1560480

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Rapid and green synthesis of complementary D-A small molecules for organic photovoltaics

Autor: Pierre Frère, Frédéric Gohier, Magali Allain, Jérémie Grolleau, Stéphanie Legoupy, Clément Cabanetos

Publikováno v: Organic Electronics
Organic Electronics, Elsevier, 2017, 42, pp.322-328. ⟨10.1016/j.orgel.2016.12.046⟩

International audience; Two push-pull molecules with close molecular structures have been synthesized through two green steps, direct heteroarylation and Knoevenagel condensation. The electronic properties and the basic bilayer heterojunction solar c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6703f7265640cd0a0d6ef8934ce8edcb
https://hal.archives-ouvertes.fr/hal-01447583

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Small D-π-A Systems witho-Phenylene-Bridged Accepting Units as Active Materials for Organic Photovoltaics

Autor: Dora Demeter, Philippe Blanchard, Antoine Leliège, Jean Roncali, Theodulf Rousseau, Magali Allain, Jérémie Grolleau

Publikováno v: Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2013, 19 (30), pp.9948-9960. ⟨10.1002/chem.201301054⟩

International audience; Donor-acceptor (D--A) systems that combine triarylamine donor blocks and dicyanovinyl (DCV) acceptor groups have been synthesized. Starting from the triphenylamine (TPA)thiopheneDCV compound (1) as a reference system, various

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64d7fe184d3f9c97f25322582583c33b
https://doi.org/10.1002/chem.201301054

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ChemInform Abstract: Clean and Efficient Iodination of Thiophene Derivatives

Autor: Pierre Frère, Jérémie Grolleau, Frédéric Gohier

Publikováno v: ChemInform. 47

Iodination of thiophene derivatives is realized using a simple, fast, and efficient methodology. Iodination of thiophene and 2- or 3-substituted or 3,4-disubstituted thiophenes with N-iodosuccinimide (NIS) activated with 4-toluenesulfonic acid in eth

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::73b65a031e81e0eb1fa7c9eaa1de1d21
https://doi.org/10.1002/chin.201619095

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Unprecedented Demonstration of Regioselective SE Ar Reaction giving Unsymmetrical Regioregular Oligothiophenes

Autor: Gurunathan Savitha, Frédéric Gohier, Charlotte Mallet, Pierre Frère, Magali Allain, Jérémie Grolleau, Simon Olivier, Chady Moussallem

Publikováno v: Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2016, 22 (19), pp.6510-6514. ⟨10.1002/chem.201600159⟩

International audience; Aromatization of 4-cyano-3-oxotetrahydrothiophene by sulfuryl chloride gives the new building block 4-cyano-3-pyrrolidylthiophene, which forms unsymmetrical regioregular oligothiophenes with a strict alternation of the donor a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3da712fbc50b5473ece5c5e583f17d72
https://pubmed.ncbi.nlm.nih.gov/26946039

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Syntheses via a direct arylation method of push-pull molecules based on triphenylamine and 3-cyano-4-hexyloxythiophene moieties

Autor: Magali Allain, Jérémie Grolleau, Pierre Frère, Clément Cabanetos, Frédéric Gohier, Stéphanie Legoupy

Publikováno v: Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2016, 14 (44), pp.10516-10522. ⟨10.1039/C6OB02036D⟩

International audience; Synthetic access to new push–pull molecules based on 3-cyano-4-hexyloxythiophene and triphenylamine moieties is presented herein using a clean methodology. The key step involves a direct heteroarylation coupling reaction in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8318c5b7b0058e0d17bbb5e14b4fbc60
https://hal.archives-ouvertes.fr/hal-01447587

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