Zobrazeno 1 - 10
of 295
pro vyhledávání: '"Laure Vendier"'
Autor:
Livia Getzner, Damian Paliwoda, Laure Vendier, Latévi Max Lawson-Daku, Aurelian Rotaru, Gábor Molnár, Saioa Cobo, Azzedine Bousseksou
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-13 (2024)
Abstract Hofmann coordination polymers (CPs) that couple the well-studied spin transition of the FeII central ion with electron-responsive ligands provide an innovative strategy toward multifunctional metal-organic frameworks (MOFs). Here, we develop
Externí odkaz:
https://doaj.org/article/8cb2d2ada8e1443ba51051807dcd8f82
Autor:
Martin Jakoobi, Guillaume Carnide, Laure Vendier, Christian Bijani, Anne-Françoise Mingotaud, Richard Clergereaux, Myrtil L. Kahn
Publikováno v:
Proceedings, Vol 92, Iss 1, p 47 (2023)
In the early 1990s, the seminal work by B [...]
Externí odkaz:
https://doaj.org/article/b0b69eb7740c4248bfe010d984cf9dfe
Autor:
Anna Kapusterynska, Christian Bijani, Damian Paliwoda, Laure Vendier, Valérie Bourdon, Nicolas Imbert, Sandrine Cojean, Philippe Marie Loiseau, Deborah Recchia, Viola Camilla Scoffone, Giulia Degiacomi, Abdul Akhir, Deepanshi Saxena, Sidharth Chopra, Vira Lubenets, Michel Baltas
Publikováno v:
Molecules, Vol 28, Iss 13, p 5284 (2023)
Hydrazone compounds represent an important area of research that includes, among others, synthetic approaches and biological studies. A series of 17 hydrazones have been synthesized by mechanochemical means. The fragments chosen were phenolic and fur
Externí odkaz:
https://doaj.org/article/61eb728675e84df1b9da1c24b589c6b4
Autor:
Mirko Ruamps, Stéphanie Bastin, Lionel Rechignat, Alix Sournia-Saquet, Laure Vendier, Noël Lugan, Jean-Marie Mouesca, Dmitry A. Valyaev, Vincent Maurel, Vincent César
Publikováno v:
Molecules, Vol 27, Iss 12, p 3776 (2022)
The coordination chemistry of the N-heterocyclic carbene ligand IMes(NMe2)2, derived from the well-known IMes ligand by substitution of the carbenic heterocycle with two dimethylamino groups, was investigated with d6 [Mn(I), Fe(II)], d8 [Rh(I)], and
Externí odkaz:
https://doaj.org/article/b35208583e9f401ca5b85d36aab9219f
Publikováno v:
Acta Crystallographica Section E, Vol 69, Iss 12, Pp m659-m660 (2013)
In the title compound, [RuCl(C18H15P)(C26H31N2OP)](CF3O3S)·2C3H6O, the RuII ion is coordinated in a three-legged piano stool, half-sandwich-type geometry by a chlorido ligand, a triphenylphosphine and a tethered η6-(phenyl-p-O-methoxy) κ1-P N-diph
Externí odkaz:
https://doaj.org/article/b83e8b04527440c198920b3cf0cd1fb5
Publikováno v:
Acta Crystallographica Section E, Vol 69, Iss 12, Pp m640-m641 (2013)
In the cation of the title complex, [Ru(C31H32N3P2)(C10H8N2)2](PF6)(Br)2·2CH2Cl2·H2O, the ruthenium ion is coordinated in a distorted octahedral geometry by two 2,2′-bipyridine (bpy) ligands and a chelating cationic N-diphenylphosphino-1,3,4,6,7,
Externí odkaz:
https://doaj.org/article/687c7ee541b64f388e33f26c2a46f7e3
Publikováno v:
Acta Crystallographica Section E, Vol 65, Iss 9, Pp o2196-o2196 (2009)
The ten-membered fused ring of the title compound, C12H10N2O, is essentially planar in the two independent molecules of the asymmetric unit (r.m.s. deviations = 0.012 and 0.015 Å).
Externí odkaz:
https://doaj.org/article/321fb6de5aaa47fb8ba9f87790a50294
Publikováno v:
Acta Crystallographica Section E, Vol 64, Iss 11, Pp o2234-o2234 (2008)
The asymmetric unit of the title compound, C11H12N2O, contains two independent molecules. In the crystal structure, intermolecular C—H...O hydrogen bonds link the molecules. There are π–π contacts between the quinoxaline rings [centroid–centr
Externí odkaz:
https://doaj.org/article/241c06aa14b445f18b4a0079f2585e4a
Autor:
Ramaraj Ayyappan, Koushik Saha, Urminder Kaur, Sourav Gayen, Laure Vendier, Sylviane Sabo-Etienne, Sundargopal Ghosh, Sébastien Bontemps
Publikováno v:
Organometallics. 42:752-756
Autor:
Christina L. Koumpoura, Michel Nguyen, Christian Bijani, Laure Vendier, Elena G. Salina, Silvia Buroni, Giulia Degiacomi, Sandrine Cojean, Philippe M. Loiseau, Françoise Benoit-Vical, Alfonso T. García-Sosa, null Anne Robert, Michel Baltas
Publikováno v:
ACS Omega
ACS Omega, 2022, 7 (40), pp.35635-35655. ⟨10.1021/acsomega.2c03421⟩
ACS Omega, 2022, 7 (40), pp.35635-35655. ⟨10.1021/acsomega.2c03421⟩
International audience; The first effective synthetic approach to naphthofuroquinones via a reaction involving lawsone, various aldehydes, and three isocyanides under microwave irradiation afforded derivatives in moderate to good yields. In addition,