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2 results on '"Dolgushin, Fedor M."'

1. An Unusual Conversion of Paramagnetic [3-Cl-3,3,8-{Ph2P(CH2)nPPh-µ-(H8] (n = 3 and 4) to Form the First 18-Electron P-Phenylene ortho-Cycloboronated closo-Ruthenacarboranes with a Dioxygen Ligand

Author

Kostukovich, Alexander Y., D’yachihin, Dmitrii I., Dolgushin, Fedor M., Smol’yakov, Alexander F., Godovikov, Ivan A., and Chizhevsky, Igor T.

Subjects
NMR-spectra, Oxygen, oxygen-type ligands, Molecular Structure, X-Ray Diffraction, ruthenacarboranes, Ligands, Article
Abstract

Treatment of [3-Cl-3,3,8-[Ph2P(CH2)nPPh-µ-(C6H4-ortho)]-1,2-Me2-closo-3,1,2-RuIIIC2B9H8] (1, n=3; 2, n=4) with an excess of KOH in a 1:1 benzene/methanol mixture at room temperature in air affords new dioxygen closo-ruthenacarborane complexes [3-(η2-O2)-3,3,8-[Ph2P(CH2)nPPh-µ-(C6H4-ortho)]-1,2-Me2-closo-3,1,2-RuIIIC2B9H8] (3, n=3) and (4, n=4) in 42.5% and 45.8% yield respectively. The structures of dioxygen complexes 3 and 4 were established by single-crystal X-ray diffraction. The IR and multinuclear NMR data [1H, 13C{1H}, 31P{1H} and 11B{1H}] along with 2D HSQC correlation spectra for the new dioxygen closo-ruthenacarboranes are discussed.

Published
2014

2. Hydrido complexes of yttrium and lutetium supported by bulky guanidinato ligands [Ln(mu-H){(Me3Si)(2)NC(NCy)(2)}(2)](2) (Ln = Y, Lu): Synthesis, structure, and reactivity

Author

Lyubov, Dmitrii M., Bubnov, Alexey M., Fukin, Georgy K., Dolgushin, Fedor M., Antipin, Miklail Yu., Pelcé, Olivier, Schappacher, Michèle, Guillaume, Sophie M., Trifonov, Alexander A., Russian Acad Sci, GA Razunaev Inst Organomet Chem, Russian Academy of Sciences [Moscow] (RAS), A. N. Nesmeyanov Institute of Organoelement Compounds (INEOS), Laboratoire de Chimie des polymères organiques (LCPO), Centre National de la Recherche Scientifique (CNRS)-École Nationale Supérieure de Chimie et de Physique de Bordeaux (ENSCPB)-Université Sciences et Technologies - Bordeaux 1-Institut de Chimie du CNRS (INC), Institut des Sciences Chimiques de Rennes (ISCR), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Ecole Nationale Supérieure de Chimie de Rennes (ENSCR)-Institut National des Sciences Appliquées - Rennes (INSA Rennes), Institut National des Sciences Appliquées (INSA)-Université de Rennes (UNIV-RENNES)-Institut National des Sciences Appliquées (INSA), Team 1 LCPO : Polymerization Catalyses & Engineering, Laboratoire de Chimie des Polymères Organiques (LCPO), Centre National de la Recherche Scientifique (CNRS)-Institut Polytechnique de Bordeaux-Ecole Nationale Supérieure de Chimie, de Biologie et de Physique (ENSCBP)-Université de Bordeaux (UB)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut Polytechnique de Bordeaux-Ecole Nationale Supérieure de Chimie, de Biologie et de Physique (ENSCBP)-Université de Bordeaux (UB)-Institut de Chimie du CNRS (INC), Université Sciences et Technologies - Bordeaux 1 (UB)-École Nationale Supérieure de Chimie et de Physique de Bordeaux (ENSCPB)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Université de Rennes (UR)-Institut National des Sciences Appliquées - Rennes (INSA Rennes), Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Ecole Nationale Supérieure de Chimie de Rennes (ENSCR)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), and Université de Bordeaux (UB)-Ecole Nationale Supérieure de Chimie, de Biologie et de Physique (ENSCBP)-Institut Polytechnique de Bordeaux-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université de Bordeaux (UB)-Ecole Nationale Supérieure de Chimie, de Biologie et de Physique (ENSCBP)-Institut Polytechnique de Bordeaux-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)

Subjects
guanidinato ligands, rare earths, alkyl complexes, [CHIM.POLY]Chemical Sciences/Polymers, polymerization, hydrosilylation, hydrido complexes
Abstract

International audience; Lewis base free hydrido complexes of yttrium and lutetium supported by bulky cyclohexyl- substituted guanidinato ligands, [Ln(mu-H){(Me3Si)(2)NC(NCy)(2)}(2)](2) (Ln = Y, Lu), were synthesized and characterized. Single-crystal X-ray diffraction studies revealed dimeric structures. H-1 NMR spectroscopy shows that complex [Y(mu-H){(Me3Si)(2)NC(NCy)(2)}(2)](2) retains its dimeric structure in C6D6 solution. Scrambling of the hydrido complexes [Ln(mu-H){(Me3Si)(2)NC(NCy)(2)}(2)](2) (Ln = Y, Lu) in C6D6 resulted in an equilibrium mixture containing the heterodimetallic species [{(Me3Si)(2)NC(NCy)(2)}(2)Y(mu-H)(2)-Lu{(Me3Si)(2)NC(NCy)(2)}(2)], indicating the dissociation of dimers and the presence of monomeric species in solution. Both compounds initiate the polymerization of ethylene: the activity of the cyclohexyl- substituted yttrium complex, [Y(mu-H){(Me3Si)(2)NC(NCy)(2)}(2)](2), is much lower than that of the isopropyl-substituted analogue, [Y(mu-H){(Me3Si)(2)NC(NiPr)(2)}(2))(2), while in the case of lutetium the activities of [Ln(mu-H){(Me3Si)(2)NC(NR)(2)}(2)](2) (R = iPr, Cy) are similar. Complexes [Ln(mu-H){(Me3Si)(2)NC(NR)(2)}(2)](2) (Ln = Y, Lu; R = iPr, Cy) were shown to catalyze efficiently the hydrosilylation of 1-nonene with PhSiH3 (at a 1:1 substrates mol ratio) to give the terminal silane PhSiH2(n-C9H19) exclusively. If the hydrosilylation reaction is carried out in the presence of a twofold molar excess of 1-nonene, double addition takes place and leads to the formation of tertiary silane PhSiH(n-C9H19)2, which was obtained in 96% yield. The hydrido complexes [Ln(mu-H){(Me3Si)(2)NC(NiPr)(2)}(2)](2) (Ln = Y, Lu) efficiently initiate the ring-opening polymerization of epsilon-caprolactone to give polymers with molar mass up to 80000. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008).

Published
2008

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