Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Sonia Ladeira"'
Autor:
Didier Bourissou, Karinne Miqueu, E. Daiann Sosa Carrizo, Sonia Ladeira, Stéphane Massou, Maxime Boudjelel, Ghenwa Bouhadir
Publikováno v:
ACS Catalysis
ACS Catalysis, American Chemical Society, 2018, 8 (5), pp.4459-4464. ⟨10.1021/acscatal.8b00152⟩
ACS Catalysis, American Chemical Society, 2018, 8 (5), pp.4459-4464. ⟨10.1021/acscatal.8b00152⟩
International audience; The o-phenylene bridged phosphine-borane iPr2P(o-C6H4)B(Fxyl)2 2 was prepared. Despite ring strain, it adopts a closed form, as substantiated by NMR, XRD, and DFT analyses. However, the corresponding open form is only slightly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4c79a81fea224704fcdf11c66a6d48f
https://hal.archives-ouvertes.fr/hal-01834610
https://hal.archives-ouvertes.fr/hal-01834610
Autor:
Dimitri Matioszek, Karinne Miqueu, Nathalie Saffon-Merceron, Sonia Ladeira, Jean-Marc Sotiropoulos, Dumitru Ghereg, Jean Escudié
Publikováno v:
Organometallics
Organometallics, American Chemical Society, 2012, 31 (3), pp.930-940. ⟨10.1021/om200968x⟩
Organometallics, American Chemical Society, 2012, 31 (3), pp.930-940. ⟨10.1021/om200968x⟩
cited By 5; International audience; The 1-arsa-3-germaallene Tip(t-Bu)Ge=C=AsMes* (1; Tip = 2,4,6-triisopropylphenyl, Mes* = 2,4,6-tri-tert-butylphenyl) reacts with selenium, fluorenone, N-tert-butylphenylnitrone, and 9,10-phenanthrenequinone as a 1,
Autor:
Karinne Miqueu, Maxime Mercy, Marie Sircoglou, Didier Bourissou, Ghenwa Bouhadir, Sonia Ladeira, Laurent Maron, Eric J. Derrah
Publikováno v:
Organometallics
Organometallics, American Chemical Society, 2011, 30 (4), pp.657-660. ⟨10.1021/om1011769⟩
Organometallics, 2011, 30 (4), pp.657-660. ⟨10.1021/om1011769⟩
Organometallics, American Chemical Society, 2011, 30 (4), pp.657-660. ⟨10.1021/om1011769⟩
Organometallics, 2011, 30 (4), pp.657-660. ⟨10.1021/om1011769⟩
cited By 42; International audience; The triphosphine-indane TPI ([o-i-Pr2P(C6H 4)]3In) has been prepared and found to react with [Pd(P-t-Bu3)2] and [AuCl(SMe2)]. According to X-ray diffraction analyses and DFT calculations, the ensuing complexes bot
Autor:
Nathalie Saffon, M. Sircoglou, Didier Bourissou, Laurent Maron, Karinne Miqueu, Sébastien Bontemps, Maxime Mercy, Ghenwa Bouhadir, Sonia Ladeira
Publikováno v:
Inorganic Chemistry
Inorganic Chemistry, American Chemical Society, 2010, 49 (9), pp.3983-3990. ⟨10.1021/ic901896z⟩
Inorganic Chemistry, 2010, 49 (9), pp.3983-3990. ⟨10.1021/ic901896z⟩
Inorganic Chemistry, American Chemical Society, 2010, 49 (9), pp.3983-3990. ⟨10.1021/ic901896z⟩
Inorganic Chemistry, 2010, 49 (9), pp.3983-3990. ⟨10.1021/ic901896z⟩
cited By 66; International audience; The monophosphino-boranes o-iPr2P(C6H 4)BR2 (1: R = Ph and 3: R = Cy) and diphosphino-boranes [o-R2P(C6H4)]2BPh (5: R = Ph and 6: R = iPr) readily react with CuCl to afford the corresponding complexes [o-iPr2P(C6H
Publikováno v:
Journal of the American Chemical Society
Journal of the American Chemical Society, American Chemical Society, 2012, 134 (15), pp.6560-6563. ⟨10.1021/ja301929n⟩
Journal of the American Chemical Society, American Chemical Society, 2012, 134 (15), pp.6560-6563. ⟨10.1021/ja301929n⟩
cited By 21; International audience; The paucity of boron-containing heteroalkene complexes prompted us to explore the coordination of phosphinoboranes. The complexes [R 2PB(C 6F 5) 2]Pt(PPh 3) 2 (R = Cy, t-Bu) were obtained by ethylene displacement.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdd90dbe08f115f900799b899ad5bf57
https://hal.archives-ouvertes.fr/hal-01613229
https://hal.archives-ouvertes.fr/hal-01613229
Publikováno v:
Organometallics
Organometallics, American Chemical Society, 2012, 31 (17), pp.6001-6004. ⟨10.1021/om3006905⟩
Organometallics, American Chemical Society, 2012, 31 (17), pp.6001-6004. ⟨10.1021/om3006905⟩
cited By 18; International audience; The diphosphine-disilane iPr 2(o-C 6H 4)SiMe 2SiMe 2(o-C 6H 4)PiPr 2 reacts with AuCl(SMe 2) via coordination of the two phosphines and oxidative addition of the σ-Si-Si bond. The ensuing bis(silyl) gold(III) com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53f0be14b75b4b3d2fe27f909b16346f
https://hal.archives-ouvertes.fr/hal-01613237
https://hal.archives-ouvertes.fr/hal-01613237
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2011, 50 (36), pp.8320-8324. ⟨10.1002/anie.201103719⟩
Angewandte Chemie International Edition, 2011, 50 (36), pp.8320-8324. ⟨10.1002/anie.201103719⟩
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2011, 50 (36), pp.8320-8324. ⟨10.1002/anie.201103719⟩
Angewandte Chemie International Edition, 2011, 50 (36), pp.8320-8324. ⟨10.1002/anie.201103719⟩
cited By 38; International audience; Gold can do it! The activation of disilanes at gold was observed experimentally and analyzed theoretically. Upon chelation with two or even only one phosphine donor, the oxidative addition of σ-Si-Si bonds procee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::995f878d933fe017a1be9ac6ca29b623
https://hal.archives-ouvertes.fr/hal-01613246
https://hal.archives-ouvertes.fr/hal-01613246
Publikováno v:
Chemical Communications
Chemical Communications, Royal Society of Chemistry, 2011, 47 (30), pp.8611-8613. ⟨10.1039/c1cc12477c⟩
Chemical Communications, Royal Society of Chemistry, 2011, 47 (30), pp.8611-8613. ⟨10.1039/c1cc12477c⟩
cited By 26; International audience; The reaction of the diphosphine-phosphine oxide ligand [o-iPr 2P-(C6H4)]2P(O)Ph with Pd(PtBu 3)2 proceeds with cleavage of the Ph-P(O) bond to give an original κP,P(O),P-pincer complex. According to DFT calculati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee1b960dae61ac32b171f0b184053a45
https://hal.archives-ouvertes.fr/hal-01613243
https://hal.archives-ouvertes.fr/hal-01613243
Publikováno v:
Journal of the American Chemical Society
Journal of the American Chemical Society, 2011, 133 (12), pp.4257-4259. ⟨10.1021/ja200789z⟩
Journal of the American Chemical Society, American Chemical Society, 2011, 133 (12), pp.4257-4259. ⟨10.1021/ja200789z⟩
Journal of the American Chemical Society, 2011, 133 (12), pp.4257-4259. ⟨10.1021/ja200789z⟩
Journal of the American Chemical Society, American Chemical Society, 2011, 133 (12), pp.4257-4259. ⟨10.1021/ja200789z⟩
cited By 27; International audience; Over the last decades, our understanding of σ-bond activation at transition metals has progressed considerably from both fundamental and synthetic points of view thanks to the preparation and characterization of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e137516e0b080ef0d46dbaf7f457d6cb
https://hal.science/hal-01613241
https://hal.science/hal-01613241
Autor:
Ghenwa Bouhadir, Didier Bourissou, Sonia Ladeira, Karinne Miqueu, Eric J. Derrah, Carmen Martín
Publikováno v:
Dalton Transactions
Dalton Transactions, Royal Society of Chemistry, 2012, 41 (47), pp.14274-14280. ⟨10.1039/c2dt31848b⟩
Dalton Transactions, Royal Society of Chemistry, 2012, 41 (47), pp.14274-14280. ⟨10.1039/c2dt31848b⟩
cited By 6; International audience; Gold, silver and rhodium complexes of the diphosphine-phosphine oxide DPPO = [o-iPr2P-(C6H4)]2P(O)Ph have been prepared and characterized. Thanks to its polyfunctional character, DPPO features versatile coordinatio