1,924 research outputs found

    Biphenyl-bridged 6-(1-aryliminoethyl)-2-iminopyridyl-cobalt complexes: synthesis, characterization and ethylene polymerization behavior

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    A series of biphenyl-bridged 6-(1-aryliminoethyl)-2-iminopyridine derivatives reacted with cobalt dichloride in dichloromethane/ethanol to afford the corresponding binuclear cobalt complexes. The cobalt complexes were characterized by FT-IR spectroscopy and elemental analysis, and the structure of a representative complex was confirmed by single-crystal X-ray diffraction. Upon activation with either MAO or MMAO, these cobalt complexes performed with high activities of up to 1.2 × 10⁷ g (mol of Co)⁻¹ h⁻¹ in ethylene polymerization, which represents one of the most active cobalt-based catalytic systems in ethylene reactivity. These biphenyl-bridged bis(imino)pyridylcobalt precatalysts exhibited higher activities than did their mononuclear bis(imino)pyridylcobalt precatalyst counterparts, and more importantly, the binuclear precatalysts revealed a better thermal stability and longer lifetimes. The polyethylenes obtained were characterized by GPC, DSC, and high-temperature NMR spectroscopy and mostly possessed unimodal and highly linear features

    1,3-Bis[(4-nitro­benzyl­idene)amino­oxy]propane

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    The complete molecule of title compound, C17H16N4O6, is generated by a crystallographic twofold axis. Within the mol­ecule, the two benzene units are approximately perpen­dicular, making a dihedral angle of 85.91 (4)°. In the crystal, mol­ecules are linked into a three-dimensional network by C—H⋯O hydrogen bonds and short O⋯O and N⋯O inter­actions, with distances of 2.998 (2) and 2.968 (3) Å, respectively

    A review of combined phacoemulsification and endoscopic cyclophotocoagulation: efficacy and safety

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    As cataract occurs frequently in patients with glaucoma, combining phacoemulsification and endoscopic cyclophotocoagulation has been gaining attention recently due to its minimally invasive nature. A variety of studies had evaluated the efficacy and safety of this procedure and had shown extremely promising results. This review article has shown here that combined phacoemulsification and endoscopic cyclophotocoagulation procedure could effectively reduce intraocular pressure in medically uncontrolled glaucoma patients while avoiding serious complications associated with traditional cyclophotocoagulation procedure and adverse effects related to filtering surgery such as trabeculectomy

    5,5′-Dimeth­oxy-2,2′-[(pentane-1,5-diyl­dioxy)bis­(nitrilo­methyl­idyne)]diphenol

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    The mol­ecule of the title compound, C21H26N2O6, which lies across a crystallographic inversion centre, crystallizes with two unique half-molecules in the symmetric unit and adopts a linear configuration and the imino group is coplanar with the aromatic ring, making a dihedral angle of 3.26 (3)°. Strong intra­molecular O—H⋯N and weak inter­molecular O—H⋯O and C—H⋯O hydrogen bonds and weak inter­molecular π–π stacking inter­actions [centroid–centroid distance = 4.419 (2) Å]establish an infinite three-dimensional supra­molecular structure

    Interference theory of metamaterial perfect absorbers

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    The impedance matching in metamaterial perfect absorbers has been believed to involve and rely on magnetic resonant response, with a direct evidence from the anti-parallel directions of surface currents in the metal structures. Here we present a different theoretical interpretation based on interferences, which shows that the two layers of metal structure in metamaterial absorbers are linked only by multiple reflections with negligible near-field interactions or magnetic resonances. This is further supported by the out-of-phase surface currents derived at the interfaces of resonator array and ground plane through multiple reflections and superpositions. The theory developed here explains all features observed in narrowband metamaterial absorbers and therefore provides a profound understanding of the underlying physics.Comment: 8 pages, 4 figures, submitted to Optics Expres

    2,2′-{1,1′-[Butane-1,4-diyl­bis(oxy­nitrilo)]di­ethylidyne}di-1-naphthol

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    The title compound, C28H28N2O4, was synthesized by the reaction of 2-acetyl-1-naphthol with 1,4-bis­(amino­oxy)butane in ethanol. The molecule, which lies about an inversion centre, adopts a linear structure, in which the oxime groups and naphthalene ring systems assume an anti conformation. The intra­molecular inter­planar distance between parallel naphthalene rings is 1.054 (3) Å. Intra­molecular O—H⋯N hydrogen bonds are formed between the oxime nitro­gen and hydr­oxy groups

    {2,2′-[1,1′-(Ethyl­enedioxy­dinitrilo)diethyl­idyne]di-1-naphtholato}copper(II)

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    The title complex, [Cu(C26H22N2O4)], is isostructural with its Ni analogue. All intramolecular distances and angles are very similar for the two structures, whereas the packing of the molecules, including C—H⋯O and C—H⋯π interactions, are slightly different
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