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1	Molecular polygons self-assembled from conjugated 1,1'-Ferrocenediyl Bridged Bis(pyridines), Bis(2,2'-bipyridines), and Bis(1,10-phenanthrolines) and transition metals as building blocks Zong, Ruifa. January 2002 (has links) Tübingen, Univ., Diss., 2002. Polygon. Ferrocen.
2	Macrocylic Di- and Tetranuclear Osmacycloferrocenophanes Ayasse, Christoph Stefan. January 2002 (has links) Tübingen, Univ., Diss., 2002.
3	Aminoferrocene als Steuerliganden in der Katalyse : Synthese, Eigenschaften und Anwendungen / Nikolaides, Katharina R. A. January 2009 (has links) Zugl.: München, Techn. Universiẗat, Diss., 2008. Ferrocen. Amine. Ligand. Katalyse.
4	Sandwich- und Halbsandwich-substituierte Diborene – Synthese, Eigenschaften und Reaktivität / Sandwich- and half sandwich-substituted diborenes – synthesis, properties and reactivity Schmidt, Uwe January 2022 (has links) (PDF) Innerhalb der vorliegenden Arbeit ist es gelungen, durch das Einführen von Cymantrenylresten neue Diborene darzustellen, welche Halbsandwich-Substituenten tragen und somit das Substitutionsmuster von basenstabilisierten Diborenen um eine weitere Verbindungsklasse zu erweitern. Neben Cymantrenylresten gelang es auch, Ferrocenylreste als weitere Substituenten in entsprechende Diborensysteme einzuführen. Über die Darstellung neuer Diborensysteme hinaus, waren Reaktivitätsstudien am Diboraferrocenophan 29 ebenso ein wesentlicher Bestandteil der vorliegenden Arbeit. Es konnte gezeigt werden, dass 29 mit kleinen Lewis-Basen, Element-Wasserstoff-Verbindungen und Hydrierungsreagenzien zur Reaktion gebracht werden kann. / The work in this project resulted in the synthesis of new diborenes with cymantrenyl substituents. With these half-sandwich substituents it was possible to expand the substitution pattern of base-stabilized diborenes by further examples. In addition to cymantrenyl substituents, ferrocenyl substituents were introduced into the corresponding diborene systems. In addition to the synthesis of new diborene systems, reactivity studies on the diboraferrocenophane 29 constituted another major component of the present work. It was shown that 29 reacts with small Lewis-bases, element-hydrogen compounds, and hydrogenation reagents. Diborene Mehrfachbindung Cymantren Ferrocen ddc:546
5	From early to late transition metal complexes syntheses, structures and electrochemical properties = Von frühen zu späten Übergansmetallverbindungen : Darstellung, Strukturen und elektrochemische Eigenschaften / Köcher, Stefan, January 2008 (has links) Chemnitz, Techn. Univ., Diss., 2008.
6	Synthese und Untersuchung konjugierter metallorganischer Hybridpolymere durch ADMET-Polymerisation Weychardt, Holger. Unknown Date (has links) (PDF) Darmstadt, Techn. Universiẗat, Diss., 2008.
7	Neue redoxfunktionalisierte Schwefel-Tripodliganden für selbstassemblierende monomolekulare Filme auf Goldoberflächen Hossbach, Jens Uwe Unknown Date (has links) (PDF) Kassel, Univ., Diss., 2008
8	Cellulosederivate mit lateralen Übergangsmetall-Chelatkomplexen Synthese und Eigenschaften in verdünnter Lösung / Laube, Bettina. January 2002 (has links) (PDF) Darmstadt, Techn. Univ., Diss., 2002.
9	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. Ferrocen Kristallographie Nitril Pyrrol Technische Universität Chemnitz Publikationsfonds Ferrocen Kristallographie Nitril Paddle-Wheel Pyrrol Negishi-Coupling Technische Universität Chemnitz Publication funds ddc:546 ddc:547 ddc:548 Ferrocen Kristallographie Pyrrol
10	Fabrication of a label-free electrochemical immunosensor using a redox active ferrocenyl dendrimer Chandra, Sudeshna, Gäbler, Christian, Schliebe, Christian, Lang, Heinrich, Bahadur, Dhirendra 06 March 2017 (has links) (PDF) We report an IgG (=immunoglobulin) electrochemical immunosensor using a newly synthesized redox-active ferrocenyl dendrimer of generation 2 (G2Fc) as a voltammetric transducer. The ferrocenyl dendrimer N(CH2CH2C(O)NHCH2CH2NHC(O)Fe(η5-C5H4)(η5-C5H5))(CH2CH2N(CH2CH2C(O)NHCH2CH2NHC(O)Fe(η5-C5H4)(η5-C5H5))2)2 (G2Fc) was used as a functional moiety to immobilize the antibody on the surface of the electrode. A sandwich immunosensor of the type IgG/Bovine serum albumin (BSA)/anti-IgG/G2Fc/glassy carbon electrode (GCE) was fabricated. The electrochemical properties of G2Fc were thoroughly studied in aqueous and non-aqueous electrolytes with varying scan rates. The incubation time was optimized for better analytical performance of the immunosensor. It is found that the developed amperometric immunosensor is sensitive to a concentration of IgG as low as 2 ng mL−1. / Dieser Beitrag ist aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich. immunoglobulin immune-sensor ferrocene polyamidoamine dendrimer spectroelectrochemistry cancer biomarkers electrochemical immuno-sensor ddc:540 Ferrocen Spektroelektrochemie

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