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Showing 1 to 8 of 8 (0.019 seconds)Spelling suggestions: "subject:"paddlewheel"" "subject:"paddlewheels""
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Untersuchung von Dirhodium-Koordinationspolymeren mittels RasterkraftmikroskopieSteinbach, Daniel 24 August 2022 (has links)
Ein zentraler Nachteil der meisten Koordinationspolymere ist, dass sie elektrische Isolatoren sind. In dieser Arbeit wurden konjugierte Koordinationspolymere auf ihre Leitfähigkeit untersucht, die eine Rhodium-Paddle-Wheel-Struktur besitzen. Die Beschichtung auf einer funktionalisierten Oberfläche im Vorfeld der C-AFM-Messung wurde mittels eines selbstgebauten Dip-Coaters realisiert. Koordinationspolymere, die das [Rh2(ac)4]-Paddle-Wheel enthalten, sind unabhängig von den untersuchten Linkern Isolatoren. Werden die Acetatliganden mit drei oder vier Acetamidatliganden ausgetauscht, so ist das entstandene Koordinationspolymer leitfähig. Temperaturabhängige C-AFM-Messungen ergeben eine für hohe Feldstärken konstante Aktivierungsenergie, die je nach Koordinationspolymer zwischen 0,3 eV und 0,7 eV beträgt. Anhand der Ergebnisse wurde gezeigt, dass der Ladungstransport durch einen Hopping Mechanismus dominiert wird. C-AFM ist eine aussagekräftige Methode zur Charakterisierung leitfähiger Koordinationspolymere auf der Oberfläche.
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The Impact of Raceway Mixing and Light Penetration on Algal GrowthThanapisudwong, Thatchai January 2016 (has links)
No description available.
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Topological control of 3,4-connected frameworks based on the Cu2-paddle-wheel node: tbo or pto, and why?Müller, Philipp, Grünker, Ronny, Bon, Volodymyr, Pfeffermann, Martin, Senkovska, Irena, Weiss, Manfred S., Feng, Xinliang, Kaskel, Stefan 06 April 2017 (has links) (PDF)
Two trigonal tritopic ligands with different conformational degree of freedom: conformationally labile H3tcbpa (tris((4-carboxyl)phenylduryl)amine) and conformationally obstructed H3hmbqa (4,4′,4′′-(4,4,8,8,12,12-hexamethyl-8,12-dihydro-4H-benzo[9,1]quino-lizino[3,4,5,6,7-defg]acridine-2,6,10-triyl)tribenzoic acid) are assembled with square-planar paddle-wheel nodes with the aim of selective engineering of the frameworks with tbo and pto underlying net topologies. In the case of H3tcbpa, both topological types were obtained forming non-interpenetrated MOFs namely DUT-63 (tbo) and DUT-64 (pto). Whereas synthesis of DUT-63 proceeds under typical conditions, formation of DUT-64 requires an additional topology directing reagent (topological modifier). Solvothermal treatment of the conformationally hindered H3hmbqa ligand with the Cu-salt results exclusively in DUT-77 material, based on the single pto net. The possibility to insert the salen based metallated pillar ligand into networks with pto topology post-synthetically results in DUT-78 and DUT-79 materials (both ith-d) and opens new horizons for post-synthetic insertion of catalytically active metals within the above-mentioned topological type of frameworks.
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Měření průtoku kapalin / Liquid flow measurementHradil, Jiří January 2011 (has links)
In my master’s thesis, I consider with flow measurement. In shortness is described principle of flow sensors functionality, its advantages and disadvantages. I designed and made device for practice measurement of flow. On this device are installed three flowmeters The characteristic of this flowmeters were measured and evaluated. I made program in LabVIEW to collect and analyze information from instaled flowmeters.
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Crystal structure of 3-ferrocenyl-1-phenyl-1H-pyrrole, [Fe(η5-C5H4cC4H3NPh)(η5-C5H5)]Pfaff, Ulrike, Korb, Marcus, Lang, Heinrich 13 May 2016 (has links) (PDF)
The molecular structure of the title compound, [Fe(C 5 H 5 )(C 15 H 12 N)], consists of a ferrocene moiety with an N-phenylpyrrole heterocycle bound to one cyclopentadienyl ring. The 1,3-disubstitution of the pyrrole results in an L- shaped arrangement of the molecule with plane intersections of 2.78 (17)° between the pyrrole and the N-bonded phenyl ring and of 8.17 (18)° between the pyrrole and the cyclopentadienyl ring. In the crystal, no remarkable intermolecular interactions are observed.
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Topological control of 3,4-connected frameworks based on the Cu2-paddle-wheel node: tbo or pto, and why?Müller, Philipp, Grünker, Ronny, Bon, Volodymyr, Pfeffermann, Martin, Senkovska, Irena, Weiss, Manfred S., Feng, Xinliang, Kaskel, Stefan 06 April 2017 (has links)
Two trigonal tritopic ligands with different conformational degree of freedom: conformationally labile H3tcbpa (tris((4-carboxyl)phenylduryl)amine) and conformationally obstructed H3hmbqa (4,4′,4′′-(4,4,8,8,12,12-hexamethyl-8,12-dihydro-4H-benzo[9,1]quino-lizino[3,4,5,6,7-defg]acridine-2,6,10-triyl)tribenzoic acid) are assembled with square-planar paddle-wheel nodes with the aim of selective engineering of the frameworks with tbo and pto underlying net topologies. In the case of H3tcbpa, both topological types were obtained forming non-interpenetrated MOFs namely DUT-63 (tbo) and DUT-64 (pto). Whereas synthesis of DUT-63 proceeds under typical conditions, formation of DUT-64 requires an additional topology directing reagent (topological modifier). Solvothermal treatment of the conformationally hindered H3hmbqa ligand with the Cu-salt results exclusively in DUT-77 material, based on the single pto net. The possibility to insert the salen based metallated pillar ligand into networks with pto topology post-synthetically results in DUT-78 and DUT-79 materials (both ith-d) and opens new horizons for post-synthetic insertion of catalytically active metals within the above-mentioned topological type of frameworks.
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A catalytically active porous coordination polymer based on a dinuclear rhodium paddle-wheel unitNickerl, Georg, Stoeck, Ulrich, Burkhardt, Ulrich, Senkovska, Irena, Kaskel, Stefan 02 December 2019 (has links)
Two new coordination polymers, DUT-82 and DUT-83 (DUT – Dresden University of Technology), were synthesized by a solvothermal reaction in methanol of rhodium(II) acetate and the tricarboxylic acid H₃btc (btc – benzene-1,3,5-tricarboxylate) or H₃btb (btb – benzene-1,3,5-tribenzoate), respectively. After drying using supercritical carbon dioxide, aerogels with specific surface areas of up to 1150 m² gˉ¹ and pore volumes of up to 2.26 cm³ gˉ¹ were obtained. Although there is no long range order in the materials, the presence of rhodium paddle-wheel units and thus a local order was proven by X-ray absorption spectroscopy measurements. DUT-82 shows good performance in the adsorption of hydrogen and a high affinity for carbon monoxide, which is rarely observed for metal–organic frameworks. Catalytic investigations demonstrate the activity of DUT-82 in the heterogeneous hydrogenation of styrene as a model system. DUT-82 can be recycled for at least ten cycles underlining the stability during the course of reaction.
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Crystal structure of 3-ferrocenyl-1-phenyl-1H-pyrrole, [Fe(η5-C5H4cC4H3NPh)(η5-C5H5)]Pfaff, Ulrike, Korb, Marcus, Lang, Heinrich 13 May 2016 (has links)
The molecular structure of the title compound, [Fe(C 5 H 5 )(C 15 H 12 N)], consists of a ferrocene moiety with an N-phenylpyrrole heterocycle bound to one cyclopentadienyl ring. The 1,3-disubstitution of the pyrrole results in an L- shaped arrangement of the molecule with plane intersections of 2.78 (17)° between the pyrrole and the N-bonded phenyl ring and of 8.17 (18)° between the pyrrole and the cyclopentadienyl ring. In the crystal, no remarkable intermolecular interactions are observed.
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