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Now showing 1 - 8 of 8
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    Nickel-Catalyzed Carbonylative Synthesis of Functionalized Alkyl Iodides
    (Amsterdam : Elsevier B.V., 2018) Peng, J.-B.; Wu, F.-P.; Xu, C.; Qi, X.; Ying, J.; Wu, X.-F.
    Chemistry; Catalysis; Organic Synthesis © 2018 The Author(s)Functionalized alkyl iodides are important compounds in organic chemistry and biology. In this communication, we developed an interesting nickel-catalyzed carbonylative synthesis of functionalized alkyl iodides from aryl iodides and ethers. With Mo(CO)6 as the solid CO source, both cyclic and acyclic ethers were activated, which is also a challenging topic in organic synthesis. Functionalized alkyl iodides were prepared in moderate to excellent yields with outstanding functional group tolerance. Besides the high value of the obtained products, all the atoms from the starting materials were incorporated in the final products and the reaction had high atom efficiency as well.
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    1-Di­phenyl­phosphanyl-2-(di­phenyl­phosphor­yl)hydrazine
    (Chester : IUCr, 2018) Höhne, Martha; Aluri, Bhaskar; Spannenberg, Anke; Müller, Bernd H.; Peulecke, Normen; Rosenthal, Uwe
    The title compound, C24H22N2OP2, is an asymmetrically substituted hydrazine derivative bearing a phosphoryl and a phosphanyl substituent. The PNNP backbone has a torsion angle of −131.01 (8)°. In the crystal, mol­ecules form centrosymmetric dimers by inter­molecular N—H...O hydrogen bonds, which are further linked into a three-dimensional network by weak C—H...O and C—H...π inter­actions.
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    Tetra­carbon­yl[N-(di­phenyl­phosphanyl-κP)-N,N′-diisoprop­yl-P-phenyl­phospho­rus di­amide-κP]molybdenum(0) with an unknown solvent
    (Chester : IUCr, 2018) Höhne, Martha; Gongoll, Marc; Spannenberg, Anke; Müller, Bernd H.; Peulecke, Normen; Rosenthal, Uwe
    The title complex, [Mo(C24H30N2P2)(CO)4], contains a molybdenum centre bearing a P,P′-cis-chelating Ph2PN(iPr)P(Ph)NH(iPr) and four carbonyl ligands in a distorted octa­hedral coordination geometry. This results in a nearly planar four-membered metallacycle. In the crystal, mol­ecules are linked by N—H...O and C—H...O hydrogen bonds to form layers parallel to the ac plane. For the final refinement, the contributions of disordered solvent mol­ecules were removed from the diffraction data with SQUEEZE in PLATON [Spek (2015). Acta Cryst. C71, 9–18]. The given chemical formula and other crystal data do not take into account the unknown solvent mol­ecule(s).
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    3,3′-Dimethyl-1,1′-methyl­enediimidazolium tetra­bromido­cobaltate(II)
    (Chester : IUCr, 2018) Peppel, Tim; Spannenberg, Anke
    The title compound, (C9H14N4)[CoBr4], was obtained as single crystals directly in very low yield as a side product in the reaction of 1,1′-bis­(1-methyl­imidazolium)acetate bromide and CoBr2. The title compound consists of an imidazolium-based dication and a tetra­bromido­cobaltate(II) complex anion, which are connected via C—H...Br inter­actions in the crystal. The dihedral angle between the imidazolium rings in the cation is 72.89 (16)°. The CoII ion in the anion is coordinated tetra­hedrally by four bromide ligands [Co—Br = 2.4025 (5)–2.4091 (5) Å and Br—Co—Br = 106.224 (17)–113.893 (17)°]. The compound exhibits a high melting point (>300°C) and is a light-blue solid under ambient conditions.
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    Tetra­carbonyl-2κ4C-[μ-5-methyl-1,1,3-triphenyl-2-(propan-2-yl)-2,4-di­aza-1,3-diphosphahexan-4-ido-1κN4:2κP1,P3](N,N,N′,N′-tetra­methyl­ethane-1,2-di­amine-1κ2N,N′)lithiummolybdenum
    (Chester : IUCr, 2018) Höhne, Martha; Spannenberg, Anke; Müller, Bernd H.; Peulecke, Normen; Rosenthal, Uwe
    The title complex, [LiMo(C6H16N2)(C24H29N2P2)(CO)4], contains a distorted octa­hedrally coordinated molybdenum centre bearing a li­thia­ted P,P′-cis-chelating PNPN ligand, which results in a nearly planar four-membered metallacycle. The Li atom is coordinated by one equivalent tetra­methyl­ethylenedi­amine. In the crystal, mol­ecules are linked via weak C—H...O inter­actions, forming a chain along the b-axis direction.
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    1,1-Bis(di­phenyl­phosphor­yl)hydrazine
    (Chester : International Union of Crystallography, 2018) Höhne, Martha; Aluri, Bhaskar R.; Spannenberg, Anke; Müller, Bernd H.; Peulecke, Normen; Rosenthal, Uwe
    The title compound, C24H22N2O2P2, contains a diphosphazane backbone, as well as a hydrazine entity. The P—N—P diphosphazane unit and the N-amine N atom are almost coplanar, and the O atoms of the Ph2P(O) units are oriented trans to each other with respect to the P...P axis. In the crystal, centrosymmetrically related mol­ecules are linked into dimers by pairs of N—H...O hydrogen bonds, forming rings of graph-set motif R22(10).
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    Palladium-catalyzed synthesis of aldehydes from aryl iodides and formic acid with propylphosphonic anhydride as the activator
    (London : Nature Publishing Group, 2018) Wu, Xiao-Feng
    An interesting palladium-catalyzed carbonylative procedure for the synthesis of aromatic aldehydes from aryl iodides has been developed. By using propylphosphonic anhydride as the activator for formic acid, moderate to good yields of the corresponding aldehydes were produced with formic acid as the carbonyl and hydrogen donors. Interestingly, neither additional phosphine ligand nor inert gas protection is needed here.
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    Tetra­carbon­yl[4,4-dimethyl-2-(pyridin-2-yl)-2-oxazoline-κ2N,N′]molybdenum(0)
    (Chester : IUCr, 2019) Steinlechner, Christoph; Spannenberg, Anke; Junge, Henrik; Beller, Matthias
    In the title compound, [Mo(C10H12N2O)(CO)4], the molybdenum(0) center is surrounded by a bidentate di­imine [4,4-dimethyl-2-(pyridin-2-yl)-2-oxazoline] and four carbonyl ligands in a distorted octa­hedral coordination geometry. The di­imine ligand coordinates via the two nitro­gen atoms.