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7 results on '"Dimitri Matioszek"'

1. Chalcogeno[bis(phosphaalkenyl)] Germanium and Tin Compounds

Author

Jean Escudié, Dimitri Matioszek, Ionel Haiduc, Tibor-Gabor Kocsor, Annie Castel, Nathalie Saffon, Petronela M. Petrar, and Gabriela Nemes

Subjects
Stereochemistry, chemistry.chemical_element, Germanium, Ring (chemistry), Sulfur, Inorganic Chemistry, chemistry.chemical_compound, Crystallography, Monomer, chemistry, Physical and Theoretical Chemistry, Tin, Carbene, Single crystal, Derivative (chemistry)
Abstract

The first diphosphaalkenylstannylene stabilized through complexation with a carbene NHC-Sn[C(Cl)═PMes*](2)1 (Mes* = 2,4,6-tri-tert-butylphenyl; NHC = :C{N(iPr)C(Me)}(2)) was isolated and fully characterized including single crystal X-ray diffraction analysis. Its reaction with elemental sulfur rapidly gives the cyclic Sn(2)S(2) (dithiadistannetanne) derivative 3, presumably formed by dimerization of a stannathione intermediate. By contrast, its germanium analogue NHC-Ge[C(Cl)═PMes*](2)7 leads to the corresponding monomeric germathione 4 and germaselenone 5. The germaselenone was more stable than the germathione and could be structurally characterized. An unusual thermal cyclization reaction of the last one occurs with an excess of selenium to give the Ge(2)Se(3) (triselenadigermolane) ring derivative 6.

Published
2012
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3. Halogermanium(II) Complexes Having Phenylamidinate As Supporting Ligands: Syntheses, Characterizations, and Reactivities

Author

Nadia Katir, Dimitri Matioszek, Annie Castel, and Nathalie Saffon

Subjects
Denticity, Chemistry, Ligand, Organic Chemistry, Inorganic chemistry, chemistry.chemical_element, Germanium, Carbon-13 NMR, Cycloaddition, Inorganic Chemistry, Crystallography, Octahedral molecular geometry, Salt metathesis reaction, Chelation, Physical and Theoretical Chemistry
Abstract

Novel germylenes [{Me3SiNC(Ph)NSiMe3}GeX] (X = Cl, Br, I) and [{Me3SiNC(Ph)NSiMe3}2Ge] with the bidentate phenylamidinato ligand have been synthesized in high yields by a salt metathesis reaction between Cl2Ge·dioxane or I2Ge and the lithium salt of the ligand. They were characterized by 1H and 13C NMR and mass spectrometry and single-crystal X-ray structure analyses, which confirmed N-chelation and a three-coordinate germanium center. The cycloaddition reactions with o-quinone led to cycloadducts, whose structures were determined by X-ray analyses. The chelation of the ligand to the metal center was conserved, affording penta- and hexacoordinated germanium(IV) atoms. Complexation reactions with [codW(CO)4] and [nbdMo(CO)4] resulted in trinuclear bis(germanium(II)) transition-metal complexes in “trans” octahedral geometry.

Published
2010
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4. From rational design of organometallic precursors to optimized synthesis of core/shell Ge/GeO2 nanoparticles

Author

Heinz Gornitzka, A. Cornejo, Dimitri Matioszek, Hervé Martinez, M. Le Troedec, Wilfried-Solo Ojo, M. El Ezzi, Céline Nayral, Annie Castel, N. Katir, Fabien Delpech, Laboratoire Hétérochimie Fondamentale et Appliquée (LHFA), Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Institut de Chimie de Toulouse (ICT-FR 2599), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Institut de Recherche pour le Développement (IRD)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées, Laboratoire de physique et chimie des nano-objets (LPCNO), Institut de Recherche sur les Systèmes Atomiques et Moléculaires Complexes (IRSAMC), Institut National des Sciences Appliquées - Toulouse (INSA Toulouse), Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Centre National de la Recherche Scientifique (CNRS)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National des Sciences Appliquées - Toulouse (INSA Toulouse), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie de Toulouse (ICT-FR 2599), Université Fédérale Toulouse Midi-Pyrénées-Institut de Recherche pour le Développement (IRD)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Institut des sciences analytiques et de physico-chimie pour l'environnement et les materiaux (IPREM), Université de Pau et des Pays de l'Adour (UPPA)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de chimie de coordination (LCC), Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie de Toulouse (ICT-FR 2599), Université Fédérale Toulouse Midi-Pyrénées-Institut de Recherche pour le Développement (IRD)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS), POCTEFA Interreg project (MET-NANO EFA17/08), ANR-08-BLAN-0105,DeSiGeTin,Design de précurseurs organométalliques pour la synthèse contrôlée de nano-objets d'éléments du groupe 14(2008), Institut de Chimie de Toulouse (ICT), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS), Institut National des Sciences Appliquées (INSA)-Université de Toulouse (UT)-Institut National des Sciences Appliquées (INSA)-Université de Toulouse (UT)-Institut de Chimie de Toulouse (ICT), Université de Toulouse (UT)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Institut de Recherche sur les Systèmes Atomiques et Moléculaires Complexes (IRSAMC), and Université de Toulouse (UT)-Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)

Subjects
Trimethylsilyl, Thermal decomposition, chemistry.chemical_element, Nanoparticle, Germanium, [CHIM.MATE]Chemical Sciences/Material chemistry, Ring strain, Inorganic Chemistry, chemistry.chemical_compound, chemistry, Reagent, Organic chemistry, Physical chemistry, [CHIM]Chemical Sciences, Reactivity (chemistry), Single crystal
Abstract

International audience; The synthesis of germanium nanoparticles has been carried out, thanks to the design of novel aminoiminate germanium(II) precursors: (ATI)GeZ (with Z = OMe, NPh2, and ATI = N,N′-diisopropyl-aminotroponiminate) and (Am)2Ge (Am = N,N′-bis(trimethylsilyl)phenyl amidinate). These complexes were fully characterized by spectroscopic techniques as well as single crystal X-ray diffraction. The thermolysis of both complexes yielded NPs which display similar features that are a Ge/GeO2 core/shell structure with a mean diameter close to 5 nm with a narrow size distribution (300 °C) classically reported in the literature for the preparation of germanium-based NPs were necessary for thermolysis of the complexes (ATI)GeZ, the use of amidinate-based precursors allows the preparation at an unprecedented low temperature (160 °C) for the thermolytic route. As suggested by a mechanistic study, the lower reactivity of (ATI)GeZ (for which the concomitant use of high temperature and acidic reagent is required) was explained in terms of lower ring strain compared to the case of (Am)2Ge.

Published
2015
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5. Synthesis and structure of some heterobimetallic complexes having a polyalkyl-s-indacenyl spacer

Author

Ivonne Chávez, Juan M. Manriquez, Dimitri Matioszek, Annie Castel, Pierre Rivière, Iván Martínez, Desmond Mac-Leod Carey, Nathalie Saffon, Cesar Morales-Verdejo, and Elies Molins

Subjects
Inorganic Chemistry, Nickel, Crystallography, chemistry.chemical_compound, chemistry, Stereochemistry, Materials Chemistry, Moiety, chemistry.chemical_element, Lithium, Manganese, Physical and Theoretical Chemistry, Derivative (chemistry)
Abstract

Three heterobimetallic complexes LmM(s-Ic′)M′Ln (M = Fe,Ru or Mn; M′ = Ni) having the same Cp∗ nickel moiety and based on a polyalkyl-s-indacenyl spacer (s-Ic′ = 2,6-diethyl-4,8-dimethyl-s-indacenyl) were synthesized by reacting Cp∗Ni(acac) with the lithium derivative of the parent monometalated complex. All three compounds were fully characterized and shown to adopt a trans geometry by X-ray crystallography.

Published
2013

6. Bis(amidinato)germylenerhodium complexes: synthesis, structure, and density functional theory calculations

Author

Jean-Marc Sotiropoulos, Dimitri Matioszek, Annie Castel, Karinne Miqueu, Jean Escudié, Nathalie Saffon, Structure Fédérative Toulousaine en Chimie Moléculaire (SFTCM), Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS), Institut Pluridisciplinaire de Recherche sur l'Environnement et les Matériaux (IPREM), Université de Pau et des Pays de l'Adour (UPPA)-Centre National de la Recherche Scientifique (CNRS), Institut des sciences analytiques et de physico-chimie pour l'environnement et les materiaux (IPREM), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Pau et des Pays de l'Adour (UPPA), Laboratoire Hétérochimie Fondamentale et Appliquée (LHFA), Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Institut de Chimie de Toulouse (ICT-FR 2599), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie du CNRS (INC)-Institut National Polytechnique (Toulouse) (Toulouse INP), and Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)

Subjects
Steric effects, chemistry.chemical_classification, 010405 organic chemistry, Ligand, [CHIM.ORGA]Chemical Sciences/Organic chemistry, Oxide, chemistry.chemical_element, Germanium, Nuclear magnetic resonance spectroscopy, [CHIM.CATA]Chemical Sciences/Catalysis, 010402 general chemistry, Photochemistry, 01 natural sciences, 0104 chemical sciences, Divalent, Rhodium, Inorganic Chemistry, [CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry, chemistry.chemical_compound, Crystallography, [CHIM.POLY]Chemical Sciences/Polymers, chemistry, Density functional theory, [CHIM.COOR]Chemical Sciences/Coordination chemistry, Physical and Theoretical Chemistry
Abstract

cited By 23; International audience; The first monogermylenerhodium complexes stabilized by bulky amidinato ligands on the divalent germanium center have been synthesized and characterized by NMR spectroscopy and X-ray crystallography. Their stability strongly depends on the steric hindrance of the amidinato ligand. With trimethysilyl groups on the nitrogen atoms of the amidinato ligand, only the germylene oxide rhodium complex could be obtained; by contrast, with t-Bu groups, the germylenerhodium complex was isolated. In both cases, the formation of amidinatorhodium complexes was observed. The donating ability of the germylene ligand has been assessed from the CO stretching frequency of the corresponding dicarbonylrhodium complex and was confirmed by density functional theory calculations. © 2012 American Chemical Society.

Published
2012
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7. Phosphaalkenyl germylenes and their gold, tungsten and molybdenum complexes

Author

Dimitri Matioszek, Gabriela Nemes, Annie Castel, Nathalie Saffon, Tibor-Gabor Kocsor, and Jean Escudié

Subjects
Denticity, Chemistry, Inorganic chemistry, Metals and Alloys, chemistry.chemical_element, Germanium, General Chemistry, Tungsten, Catalysis, Surfaces, Coatings and Films, Electronic, Optical and Magnetic Materials, Crystallography, Molybdenum, Phosphorus atom, Atom, Materials Chemistry, Ceramics and Composites
Abstract

The new bis(phosphaalkenyl) germanium(II) compound (NHC)Ge(CCl=PMes*)(2) reacts with L(2)M(CO)(4) (M = Mo, W) to give bidentate complexes with an unexpected coordinating behaviour involving the Ge(II) centre and one phosphorus atom, and with AuI or Me(2)SAuCl to afford the monodentate complexes coordinated at the germanium(II) atom.

Published
2012

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