Academic literature on the topic 'Charge-transfer-Komplex'

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Journal articles on the topic "Charge-transfer-Komplex"

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Steinfeld, Gunther, Vasile Lozan, Hans-Jörg Krüger, and Berthold Kersting. "Stabilisierung eines Thiolat→Dibrom-Charge-Transfer-Addukts durch einen makrocyclischen Dinickel-Komplex und dessen Überführung in einen Arensulfenylbromid-Komplex." Angewandte Chemie 121, no. 11 (2009): 1988–91. http://dx.doi.org/10.1002/ange.200805028.

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Kubiniok, Silvia, Wolf-Walther Du Mont, Siegfried Pohl, and Wolfgang Saak. "Das Reagens Diphenyldiselan/Iod: Kein „Phenylselenenyliodid”, sondern ein Charge-Transfer-Komplex mit cyclischen Einheiten." Angewandte Chemie 100, no. 3 (1988): 434–35. http://dx.doi.org/10.1002/ange.19881000332.

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Kuhn, Norbert, and Hans Schumann. "[(C5H5)4FeNi](BF4)2; ein charge-transfer-komplex aus elektronenreichen und elektronenarmen metallocen-fragmenten." Journal of Organometallic Chemistry 314, no. 1-2 (1986): C39—C42. http://dx.doi.org/10.1016/0022-328x(86)80378-3.

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Stein, D., H. Sitzmann, R. Boese, E. Dormann, and H. Winter. "Ein charge-transfer komplex von decaethylferrocen mit 2,3,5,6-tetrafluoro-7,7′,8,8′-tetracyano-p-chinodimethan." Journal of Organometallic Chemistry 412, no. 1-2 (1991): 143–55. http://dx.doi.org/10.1016/0022-328x(91)86050-z.

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Bartley, Stuart L., та Kim R. Dunbar. "[{Re2Cl4(dppm)2}2(μ-TCNQ)], ein neuartiger Charge-Transfer-Komplex mit einem Donor mit Metall-Metall-Mehrfachbindung". Angewandte Chemie 103, № 4 (1991): 447–50. http://dx.doi.org/10.1002/ange.19911030424.

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Sellmann, Dieter, Daniel Häußinger, Torsten Gottschalk-Gaudig, and Frank W. Heinemann. "Übergangsmetallkomplexe mit Schwefelliganden, 145 [1]. [Ru(NO)('pybuS4')]Br, ein Komplex mit [Ru(NO)(NS4)]-Gerüst, aktivierten CH2-Gruppen und interionischen Wechselwirkungen im Festkörper ['pybuS4'2- = 2,6-Bis(2-mercapto-3,5-di-terM>utylphenylthio) dimethylpyridin(2-)] / Transition Metal Complexes with Sulfur Ligands, 145 [1]. [Ru(NO)('pybuS4 ')]Br, a Complex with [Ru(NO)(NS4)] Core, Activated CH2 Groups, and Interionic Interactions in the Solid State ('pybuS4'2- = 2,6-Bis(2-mercapto-3,5-di-terf-butylphenylthio)dimethylpyridine(2-))." Zeitschrift für Naturforschung B 55, no. 8 (2000): 723–29. http://dx.doi.org/10.1515/znb-2000-0809.

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Abstract In the search for soluble and reactive ruthenium nitrosyl complexes, [Ru(NO)('pybuS4')]Br ([2]Br) was synthesized by template alkylation of NBu4[Ru(NO)('buS2')2] with py(CH2,Br)2 ['pybuS4'2-= 2,6-bis(2-mercapto-3,5-di-tert-butyl-phenylthio)dimethylpyridine(2-); 'buS2'2- = 2-mercapto-3,5-di-tert-butylphenylthiolate(2-); py(CH2Br)2 = 2,6-bis(bromomethyl)pyridine]. The solid state structure of 2 has been determined by X-ray diffraction, which reveals a head-to-head O-O interaction between the linear Ru-NO entities. The ligand CH2 protons of [2]+ are activated and exchange with D+ under a
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Dissertations / Theses on the topic "Charge-transfer-Komplex"

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Pochekailov, Sergii. "Elektrické, optické a senzorové vlastnosti organických polovodičů." Doctoral thesis, Vysoké učení technické v Brně. Fakulta chemická, 2009. http://www.nusl.cz/ntk/nusl-233292.

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There is big interest in cheap, sensitive and selective gas sensors. In this work, substituted soluble phthalocyanines are proposed as a sensing materials for several gases. Optical, electrical and gas sensing properties of several phthalocyanines were studied and the mechanisms of their interaction with several analyte gases are described. It was found, that sulfo-substituted Pcs has good sensitivity to humidity. Sulfonamide-substituted phthalocyanines are promising for nitrogen dioxide and volatile organic compounds detection. tert-Butyl-substituted phthalocyanines are sensitive to NO2 under
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Habániková, Shannelle Diana. "Využití kvantitativní elektronové paramagnetické rezonance (EPR) a komerčně dostupných EPR standardů při studiu elektrochemické oxidace substituovaných tetrathiafulvalenů." Master's thesis, 2019. http://www.nusl.cz/ntk/nusl-396694.

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Tetrathiafulvalene derivatives are remarkable molecules, with various application, reported relatively recently. The radical cation of these compounds has very inter- esting optical, electronic, electrocatalytic superconducting and magnetic properties that have been intensively studied recently. Quantitative in-situ EPR voltammetric spectroelectrochemistry studies of 2-(2-hydroxyethylsulfanyl)-3-(benzylsulfanyl)-6,7- bis(octadecylsulphanyl)tetrathiafulvalene (TTF-Der3) have been carried out with the aim to confirm the oxidation sites, follow-up reactions (after the first electron transfer), an
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Warzecha, Tomáš. "Syntéza pi-elektronových oligomerů a studium jejich vlastností." Master's thesis, 2012. http://www.nusl.cz/ntk/nusl-310422.

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The pi-electron oligomers: Their synthesis and properties This diploma thesis is focused on the synthesis of p-oligophenyleneethynylene rods (dimer and trimer) containing laterally attached naphtalenediimide units as electron acceptor groups. These functionalised short oligomers are intended to serve as model oligodentate acceptors in the study on multiple interactions with electron rich molecules. The oligomers were assembled from building blocks such as aryl iodides and aryl alkynes bearing a naphthalenediimide unit. The functionalised monomers were combined in a stepwise way by using Sonoga
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Wagener, Philipp. "Photodissoziation von Polyhalogenmethanen in Fluiden: Kurzzeitdynamik und Mechanismen." Doctoral thesis, 2008. http://hdl.handle.net/11858/00-1735-0000-0006-ACB1-4.

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Faukner, Tomáš. "Iontové polymery a polymerní sítě polyacetylenického typu připravené metodou kvaternizační polymerizace." Doctoral thesis, 2016. http://www.nusl.cz/ntk/nusl-353396.

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(Doctoral Thesis, 2016, Mgr. Tomáš Faukner, IONIC POLYACETYLENE TYPE POLYMERS AND POLYMER NETWORKS BY CATALYST FREE QUATERNIZATION POLYMERIZATION) The composition and structure of a series of ionic π-conjugated poly(monosubstituted acetylene)s prepared via catalyst-free quaternization polymerization (QP) of 2-ethynylpyridine (2EP) activated with equimolar amount of alkyl halide [RX = ethyl bromide, ethyl iodide, nonyl bromide and haxadecyl (cetyl) bromide] as a quaternizing agent (QA) have been studied in detail. The performed QPs gave ionic polymers well soluble in polar solvents, with approx
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