dat@UBFCdat@UBFC search : contributor:"Jérôme Husson"dat@UBFC websitehttps://search-data.ubfc.fr/custom/logo/icon/100.pnghttps://search-data.ubfc.fr/custom/logo/full/105h.pnghttps://search-data.ubfc.fr/search.php?s=contributor%3A%22J%C3%A9r%C3%B4me+Husson%22&format=atom&lang=en2023-07-17T10:20:54Z4’-(N-(2-cyanoethyl)pyrrol-2-yl)-2,2’:6’,2’’-terpyridinehttps://search-data.ubfc.fr/FR-13002091000019-2023-07-17_4-N-2-cyanoethyl-pyrrol-2-yl-2-2-6-2-terpyridin.html#maj202307171220542023-07-17T10:20:54Z2023-07-17T10:20:54ZJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-Jerome
<p>Data for the synthesis and caracterization of 4’-(N-(2-cyanoethyl)pyrrol-2-yl)-2,2’:6’,2’’-terpyridine.</p>
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<strong>Disciplines :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=discipline%3A%22chemistry%2C+organic%22">chemistry, organic</a>
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<div><strong>Collected date :</strong> Jun 2022</div>
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<strong>Creators :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22J%C3%A9r%C3%B4me+Husson%22">Jérôme Husson</a>
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Attribution4′-(N-(Propargyl)pyrrol-2-yl)-2,2′:6′,2′′-terpyridinehttps://search-data.ubfc.fr/FR-13002091000019-2023-07-06_4-N-Propargyl-pyrrol-2-yl-2-2-6-2-terpyridin.html#maj202307061826122023-07-06T16:26:12Z2023-07-06T16:26:12ZJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-JeromeLaurent GuyardJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-JeromeLaurent Guyard
<p>A new terpyridine molecule, bearing a N-propargylated pyrrole, was prepared and characterized. Its synthesis was based on a Krohnke-type reaction between 2-acetylpyridine and N-propargylpyrrole-2-carboxaldehyde in a basic medium. An allene-containing terpyridine was also obtained as a by-product.</p>
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<strong>Disciplines :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=discipline%3A%22chemistry%2C+organic%22">chemistry, organic</a>
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<div><strong>Collected date :</strong> from 2018 to 2019</div>
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<strong>Creators :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22J%C3%A9r%C3%B4me+Husson%22">Jérôme Husson</a>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Laurent+Guyard%22">Laurent Guyard</a>
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Attribution1-{4-[(Hexyloxy)methyl]pyridin-2-yl}ethanonehttps://search-data.ubfc.fr/FR-18008901306731-2018-03-15_1-4-Hexyloxy-methyl-pyridin-2-yl-ethanone.html#maj202301061433172018-03-15T16:39:08Z2023-01-06T13:33:17ZFlorian CharrierLaurent GuyardFlorian CharrierJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-Jerome
<p> A new member of the 2-acetylpyridine family has been prepared and characterized by NMR and IR spectroscopies.</p>
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<strong>Disciplines :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=discipline%3A%22chemistry%2C+organic%22">chemistry, organic</a>
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<div><strong>Collected date :</strong> 2016</div>
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<strong>Creators :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Florian+Charrier%22">Florian Charrier</a>
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Attribution1-(4-Formyl-2,6-dimethoxyphenoxy)-4-chlorobut-2-ynehttps://search-data.ubfc.fr/FR-18008901306731-2021-10-01-02_1-4-Formyl-2-6-dimethoxyphenoxy-4-chlorobut-2-yn.html#maj202110010857152021-10-01T06:57:15Z2021-10-01T06:57:15ZJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-JeromeJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-Jerome
<p>A reaction of biomass-derived aldehyde synringaldehyde and half an equivalent of 1,4-dichlorobut-2-yne was attempted in order to obtain a bis-aldehyde with an alkyne spacer. The reaction was carried out in a basic media to effect bis O-alkylation, as described in literature for the preparation of ...</p>
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<strong>Disciplines :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=discipline%3A%22chemistry%2C+organic%22">chemistry, organic</a>
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<div><strong>Collected date :</strong> from 2020 to 2021</div>
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<strong>Creators :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22J%C3%A9r%C3%B4me+Husson%22">Jérôme Husson</a>
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Attribution4′-(5-Methylfuran-2-yl)-2,2′:6′,2″-terpyridine: A New Ligand Obtained from a Biomass-Derived Aldehyde with Potential Application in Metal-Catalyzed Reactionshttps://search-data.ubfc.fr/FR-18008901306731-2021-10-01_4-5-Methylfuran-2-yl-2-2-6-2-terpyridine-A.html#maj202110010856442021-10-01T06:56:44Z2021-10-01T06:56:44ZJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-JeromeLaurent GuyardJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-JeromeLaurent Guyard
<p>The new ligand 4′-(5-methylfuran-2-yl)-2,2′:6′,2″-terpyridine (1) was prepared in one step from 2-acetylpyridine and 5-methylfurfural. The latter is an aldehyde that can be readily obtained from biomass. The new terpyridine molecule was characterized by 1H and 13C-NMR spectroscopy as well as by ...</p>
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<strong>Disciplines :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=discipline%3A%22chemistry%2C+organic%22">chemistry, organic</a>
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<div><strong>Collected date :</strong> from 2017 to 2018</div>
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<strong>Creators :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22J%C3%A9r%C3%B4me+Husson%22">Jérôme Husson</a>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Laurent+Guyard%22">Laurent Guyard</a>
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Attribution4,4″-Dichloro-4′-(2-thienyl)-2,2′:6′,2″-terpyridinehttps://search-data.ubfc.fr/FR-18008901306731-2021-09-24-02_4-4-Dichloro-4-2-thienyl-2-2-6-2-terpyridin.html#maj202109241053562021-09-24T08:53:56Z2021-09-24T08:53:56ZJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-JeromeLaurent GuyardJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-JeromeLaurent Guyard
<p>A new thiophene-substituted terpyridine derivative has been prepared and characterized. This ligand features a thiophene heterocycle (as an electrochemically polymerizable unit) as well as two chlorine atoms for further functionalization.</p>
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<strong>Disciplines :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=discipline%3A%22chemistry%2C+organic%22">chemistry, organic</a>
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<div><strong>Collected date :</strong> from 2017 to 2018</div>
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<strong>Creators :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22J%C3%A9r%C3%B4me+Husson%22">Jérôme Husson</a>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Laurent+Guyard%22">Laurent Guyard</a>
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Attribution4′-(N-(Propan-1,2-dienyl)pyrrol-2-yl)-2,2′:6′,2″-terpyridinehttps://search-data.ubfc.fr/FR-18008901306731-2021-09-24_4-N-Propan-1-2-dienyl-pyrrol-2-yl-2-2-6-2-terpyridin.html#maj202109241053362021-09-24T08:53:36Z2021-09-24T08:53:36ZLaurent GuyardJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-JeromeLaurent GuyardJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-Jerome
<p>A new pyrrole-substituted terpyridine derivative that possesses an allene moiety was obtained as an “unexpected” sole product during an attempt to alkylate the N-atom of pyrrole with propargyl bromide in order to obtain an alkyne-functionalized terpyridine. </p>
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<strong>Disciplines :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=discipline%3A%22chemistry%2C+organic%22">chemistry, organic</a>
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<div><strong>Collected date :</strong> from 2018 to 2019</div>
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<strong>Creators :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22J%C3%A9r%C3%B4me+Husson%22">Jérôme Husson</a>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Laurent+Guyard%22">Laurent Guyard</a>
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Attribution4′-(5-n-Propylthiophen-2-yl)-2,2′:6′,2″-terpyridine https://search-data.ubfc.fr/FR-18008901306731-2021-04-12-05_4-5-n-Propylthiophen-2-yl-2-2-6-2-terpyridine.html#maj202109101650172021-04-12T12:01:31Z2021-09-10T14:50:17ZJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-JeromeLaurent GuyardJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-JeromeLaurent Guyard
<p>A new thiophene-substituted terpyridine derivative has been prepared through the reaction between 5-n-propylthiophene-2-carboxaldehyde and 2-acetylpyridine. This terpyridine derivative bears an alkyl chain linked via a thiophene heterocycle. </p>
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<strong>Disciplines :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=discipline%3A%22chemistry%2C+organic%22">chemistry, organic</a>
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<div><strong>Collected date :</strong> 2020</div>
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<strong>Creators :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22J%C3%A9r%C3%B4me+Husson%22">Jérôme Husson</a>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Laurent+Guyard%22">Laurent Guyard</a>
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AttributionDiethyl 2,2'-(1,4-phenylenedioxy)diacetatehttps://search-data.ubfc.fr/FR-18008901306731-2016-07-19-04_Diethyl-2-2-1-4-phenyl-enedi-oxy-diacetate.html#maj201608231700052016-07-19T10:36:16Z2016-08-23T15:00:05ZYoann RousselinJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-JeromeMichael Knorrhttps://www.utinam.cnrs.fr/?Michael-KNORRMarek M. Kubicki
<p>In the title compound, C14H18O6, a crystallographic center at the centroid of the aromatic ring generates the complete mol­ecule which is planar within 0.085 (1) Å for the non-H atoms. In the crystal, weak C—H⋯O and C—H⋯π inter­actions link the molecules.</p>
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<strong>Disciplines :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=discipline%3A%22chemistry%2C+organic%22">chemistry, organic</a>
<a href="https://search-data.ubfc.fr/search.php?s=discipline%3Acrystallography">crystallography</a>
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<div><strong>Collected date :</strong> 2010</div>
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<strong>Creators :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22J%C3%A9r%C3%B4me+Husson%22">Jérôme Husson</a>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Michael+Knorr%22">Michael Knorr</a>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Marek+M.+Kubicki%22">Marek M. Kubicki</a>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Yoann+Rousselin%22">Yoann Rousselin</a>
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Attribution, Non Commercial, Share Alike