TY - JOUR A1 - Tacke, Reinhold A1 - Bentlagem, A. A1 - Towart, R. A1 - Meyer, H. A1 - Bossert, F. A1 - Vater, W. A1 - Stoepe, K. T1 - Sila-Analoga von Nifedipin-ähnlichen 4-Aryl-2.6-dimethyl-1.4-dihydropyridin-3.5-dicarbonsäure-dialkylestern, I N2 - no abstract available KW - Chemie Y1 - 1980 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-82430 ER - TY - JOUR A1 - Finze, Maik A1 - Reiss, Guido J. A1 - Frohn, Hermann-Josef T1 - 2,3,5,6-Tetrafluoro-1,4-bis(trimethylsilyl)benzene N2 - no abstract available KW - Chemie KW - single-crystal X-ray study KW - T = 199 K KW - R factor = 0.027 KW - wR factor = 0.068 KW - data-to-parameter ratio = 14.0. Y1 - 2012 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-75401 ER - TY - JOUR A1 - Finze, Maik A1 - Reiss, Guido J. T1 - Trimethyl­sulfonium 1-amino-6-fluoro-2,3,4,5,7,8,9,10,11,12-decaiodo-1-carba-closo-dodeca­borate N2 - no abstract available KW - Chemie KW - single-crystal X-ray study KW - T = 100 K KW - wR factor = 0.052 KW - data-to-parameter ratio = 20.8 Y1 - 2012 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-75397 ER - TY - JOUR A1 - Braunschweig, Holger A1 - Arnold, Thomas A1 - Gruss, Katrin T1 - cyclo-Tri-mu-oxido-tris{[(eta 5,eta 5)-1,2-bis(cyclopentadienyl)-1,1,2,2-tetramethyldisilane]zirconium(IV)}: atrimeric disila-bridged oxidozirconocene N2 - no abstract available KW - Chemie KW - single-crystal X-ray study KW - T = 174 K KW - R factor = 0.027 KW - wR factor = 0.069 KW - data-to-parameter ratio = 23.6. Y1 - 2011 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-74737 ER - TY - JOUR A1 - Hoffmann, Gerhard Georg A1 - Burschka, Christian T1 - (I\(_2\)GaS-i-C\(_3\)H\(_7\))\(_2\), das erste butterfly-Molekül mit vierfach koordiniertem Gallium T1 - The first "butterfly" molecule with four-coordinate gallium. Synthesis and structure of (I\(_2\)GaS-i-C\(_3\)H\(_7\))\(_2\) N2 - No abstract available KW - Chemie KW - Gallium Y1 - 1985 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-31432 ER - TY - JOUR A1 - Burschka, Christian A1 - Stroppel, Klaus A1 - Jutzi, Peter T1 - Die Struktur von μ-Dibromgermandiyl-bis(pentacarbonylwolfram)(W-W) N2 - No abstract available KW - Chemie Y1 - 1981 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-31852 ER - TY - JOUR A1 - Wieber, M. A1 - Hoehl, H. A1 - Burschka, Christian T1 - Diphenylantimonalkoxide und -thiolate als Liganden in Metallcarbonylkomplexen des Chroms und Molybdäns; Kristallstruktur von Tris[diphenyl(phenylthiolato)stiban]molybdäntricarbonyl T1 - Diphenylantimony Alkoxides and Thiolates as Ligands in Carbonyl Complexes of Chromium and Molybdenum; Crystal Structure of Tris [diphenyl(phenylthiolato)stibane] Molybdenum Tricarbonyl N2 - Diorganoantimonverbindungen R\(_2\)SbX (R = C\(_6\)H\(_5\) X = S-Organyl, O-Organyl) reagieren mit Cycloheptatrienylmolybdäntricarbonyl zu Produkten des Typs [R\(_2\)SbX]\(_3\)Mo(CO)\(_3\). Die analogen Komplexe des Chroms können durch Reaktion von Tris(acetonitril) chromtricarbonyl mit den Antimon-Liganden dargestellt werden. (1,5-Cyclooctadien)molybdäntetracarbonyl reagiert unter Substitution mit Diorganoantimonderivaten R\(_2\)SbX (R = C\(_6\)R\(_5\), X = S-Organyl) zu den Verbindungen [R\(_2\)SbX]\(_2\)Mo(CO)\(_4\) Synthese und Eigenschaften der StibanKomplexe sowie die Kristallstruktur der Verbindung [(C\(_6\)H\(_5\))\(_2\)SbSC\(_6\)H\(_5\)]\(_3\)Mo(CO)\(_3\) werden beschrieben. N2 - Diorganoantimony compounds R\(_2\)SbX (R = C\(_6\)H\(_5\), X = S-organyl, O-organyl) react with cycloheptatrienemolybdenum tricarbonyl to yield products of the type [R\(_2\)SbX]\(_3\)Mo(CO)\(_3\). Analogous complexes of chromium are prepared by reaction oftris(acetonitrile)chromium tricarbonyl with the stibane Ugands. Tetracarbonyl-l,5-cyclooctadienemolybdenum undergoes substitution reaction with diorganoantimony compounds R\(_2\)SbX (R = C\(_6\)R\(_5\), X = S-organyl) to give [R\(_2\)SbX]\(_2\)Mo(CO)\(_4\) Synthesis and properties of the stibane complexes as weil as an X-ray determination of [(C\(_6\)H\(_5\))\(_2\)SbSC\(_6\)H\(_5\)]\(_3\)Mo(CO)\(_3\) are described. KW - Chemie Y1 - 1990 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-31919 ER - TY - JOUR A1 - Wieber, M. A1 - Walz, J. A1 - Burschka, Christian T1 - Organostibonsäureester. II [1]: Darstellung und Eigenschaften von Methanstibonsäureestern. Struktur von Di-μ-methoxy-bis[dibromo-methoxy-methyl-antimon(V)] N2 - Dimere alkoxyverbrückte Verbindungen des Typs [CH\(_3\)SbX\(_2\)(OR)(μ-OR)]\(_2\) (X = Cl, Br; R = CH\(_3\), C\(_2\)H\(_5\)) können durch Oxidation von CH\(_3\)Sb(OR)\(_2\) mit Br\(_2\) oder S0\(_2\)Cl\(_2\) in CH\(_2\)Cl\(_2\) unterhalb -60°C als lichtempfindliche kristalline Feststoffe erhalten werden. Die Struktur der Verbindung [CH\(_3\)SbBr\(_2\)(OCH\(_3\))(μ-OCH\(_3\))]\(_2\) konnte mittels Röntgenstrukturanalyse bestimmt werden. Umsetzungen mit Natriumalkoholaten in den entsprechenden Alkoholen bei 0°C führen zu dimeren Tetraalkoxymethylstiboranen. Austauschreaktionen von Tetramethoxymethylstiboran mit Ethanol ergeben das Ethoxyderivat und mit Diolen symmetrische spirocyclische Methanstibonsäureester. N2 - Dimeric alkoxy-bridged compounds of the type [CH\(_3\)SbX\(_2\)(OR)(μ-OR)]\(_2\) (X = Cl, Br; R = CH\(_3\), C\(_2\)H\(_5\)) are prepared by oxidation of CH\(_3\)Sb(OR)\(_2\) with Br\(_2\) or S0\(_2\)Cl\(_2\) in CH\(_2\)Cl\(_2\) below -60°C as light sensitive erystals. The structure of [CH\(_3\)SbBr\(_2\)(OCH\(_3\))(μ-OCH\(_3\))]\(_2\) was determined by X-Ray analysis. By reaction with sodium alkoxides in the corresponding alcohol at 0°C dimeric tetraalkoxymethylstiboranes are obtained. Exchange reactions of tetramethoxymethylstiborane with ethanol give the ethoxy derivative and with diols symmetrie spirocyclic esters of methanestibonic acid. KW - Chemie Y1 - 1990 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-31909 ER - TY - JOUR A1 - Kaupp, Martin A1 - Schleyer, P. v. R. A1 - Stoll, H. A1 - Preuss, H. T1 - Pseudopotential Approaches to Ca, Sr and Ba Hybrides. Why are some Alkaline Earth MX\(_2\) Compounds Bent? N2 - Quasirelativistic and nonrelativistic lo-valence-electronp seudopotentialsf or Ca, Sr, and Ba are presented. Results of calculations with 6s6p5d basis sets for MH, MH\(^+\) , and MH\(_2\), are compared with all-electron and 2-valence-electron pseudopotential calculations with and , without core-polarization potentials. The lo-valence-electron pseudopotential approach agrees well with all-electron calculations. It circumvents problems for the 2-valence-electron pseudopotentials arising from an incomplete separation of valence and subvalence shells in polar molecular systems due to strongly contracted occupied (n - 1 )-d orbitals. All higherlevel calculations show SrH\(_2\) and BaII\(_2\), to be bent with angles of - 140° and 120°, respectively, while CaH\(_2\) is linear with a flat potential-energy surface for the bending motion. The use of a core-polarization potential together with the 2-valence-electronp seudopotentiala pproach allows an investigation of the relative importance of core-polarization vs direct d-orbital bonding participation as reasons for the bent structures. The calculations strongly suggest that both contribute to the bending in SrH\(_2\) and BaII\(_2\). Even at the Hartree-Fock level of theory lovalence- electronp seudopotentialc alculations given reasonablea nglesw hen the potentialenergy surface is not exceedingly flat, and only moderately contracted basis sets including both compact d functions and diffuse p functions are used. The effect of core-valence correlation and the importance off functions also are discussed. KW - Chemie Y1 - 1991 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-31646 ER - TY - JOUR A1 - Kuehn, A. A1 - Burschka, Christian A1 - Werner, H. T1 - Synthesis and molecular structure of C\(_5\)H\(_5\)(P-/-Pr\(_3\))Pd(η\(^1\), η\(^3\)-C\(_3\)H\(_4\))Pd(P-/-Pr\(_3\))Br: a compound formed through insertion of allene into a metal-metal bond\(^1\) N2 - No abstract available KW - Chemie Y1 - 1982 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-46592 ER - TY - JOUR A1 - Burschka, Christian T1 - Erfahrungen mit einem Modelling-Paket T1 - Experience with a program package for molecular modeling N2 - Als Newcomer im Kreise der Anwender IIOn Molecular Modelling Software sieht man sich mit einer verwirrenden und ständig wachsenden Vielfalt von einschlägigen Programmen konfrontiert. die alle viel versprechen. Oie meisten bieten Grafik 110m Feinsten und eine beeindruckende Benutzeroberfläche. Unterschiede gibt es in der Funlctionalität, der Fehlerhäufigkeit, beim Support und natürlich im Preis. Seit ca. einem Jahr haben wir MOLEK 9000 auf einer IRIS 40351G im Einsatz. Hier ein erster Erfahrungsbericht. KW - Chemie Y1 - 1993 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-47169 ER - TY - JOUR A1 - Wieber, Markus A1 - Lang, Stefan A1 - Rohse, Stefan A1 - Habersack, Ralph A1 - Burschka, Christian T1 - Synthese und Kristallstruktur von Triphenyltelluroniumsulfid T1 - Synthesis and Crystal Structure of Triphenyltelluroniumsulfide N2 - No abstract available KW - Chemie KW - Triphenyltelluroniumsulfide KW - Synthesis KW - NMR Data KW - Crystal Structure KW - Secondary Bonding Y1 - 1994 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-47151 ER - TY - JOUR A1 - Baumann, Franz Erich A1 - Burschka, Christian A1 - Schenk, Wolfdieter A. T1 - Ligandensubstitution an cis-Mo(CO)\(_2\)(PPh\(_3\)h(MeCN)(\(\eta^2\)-S0\(_2\)), Kristall- und Molekülstruktur von cis-Mo(CO)\(_2\)(PMe\(_3\))\(_3\)(\(\eta^2\)-S0\(_2\)) [1] T1 - Ligand Substitution at cis-Mo(CO)\(_2\)(PPh\(_3\)h(MeCN)(\(\eta^2\)-S0\(_2\)), crystal and molecular structure of cis-Mo(CO)\(_2\)(PMe\(_3\))\(_3\)(\(\eta^2\)-S0\(_2\)) [1] N2 - No abstract available KW - Chemie KW - Molybdenum-Sulfur Dioxide Complexes KW - Ligand Displacement KW - Structure KW - Stereochemistry . Linkage Isomerism Y1 - 1986 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-47143 ER - TY - JOUR A1 - Wieber, Markus A1 - Fetzer-Kremling, Isa A1 - Reith, Hildegard A1 - Burschka, Christian T1 - Synthese und Struktur von Phenyltetra(acetato)stiboran T1 - Synthesis and structure of Phenyltetra(acetato)stiborane N2 - No abstract available KW - Chemie KW - Phenyltetra(acetato)stiborane KW - Synthesis KW - X-Ray Crystal Structure Y1 - 1987 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-47137 ER - TY - JOUR A1 - Schenk, Wolfdieter A1 - Rueb, Doris A1 - Burschka, Christian T1 - Die Koordinationschemie C=S-funktioneller Verbindungen V: Dithioester als \(\eta^1-, \eta^2-\), und \(\eta^3\)-Liganden in Übergangsmetallkomplexen N2 - No abstract available KW - Chemie Y1 - 1987 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-46736 ER - TY - JOUR A1 - Wieber, Markus A1 - Wirth, Dieter A1 - Burschka, Christian T1 - Synthese und Struktur einiger Methyl(dicarboxilato)stibane T1 - Syntheses and structure of Some Methyl(dicarboxilato)stibanes N2 - No abstract available KW - Chemie KW - Methyldiethoxistibane KW - Methyl(maleato)stibane KW - Methyl(phthalato)stibane KW - X-Ray Y1 - 1984 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-46741 ER - TY - JOUR A1 - Burschka, Christian A1 - Wieber, Markus T1 - Eine pentagonal pyramidale Koordination des Bismuts. Kristallstruktur von Methylbismutbis(dietyldithiocarbonat) T1 - A pentagonal pyramidal coordination of Bismut. Crystal structure of Methylbismuthbis(diethyldithiocar bamate) N2 - The crystal structure of the title compound, recrystallized from ethanol, was solved by means of X-ray diffraction methods and could be refined to an R-value of 0.050 with 2126 reflections observed. In contrast to its behaviour in benzene solution, where the compound is monomerie, in the crystalline state dimerie units are formed by intermoleeular Bi-S-interactions. The bismuth atoms are coordinated in form of a slightly distorted pentagonal pyramid with the free electron pair presumably directed opposite the apical C-atom. KW - Chemie Y1 - 1979 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-46750 ER - TY - JOUR A1 - Jutzi, Peter A1 - Karl, Alfons A1 - Burschka, Christian T1 - Synthese, Reaktionen und Struktur von Tricarbonyl(1R,1R',2,3,4,5-Tetraphenyl-1-Germacyclopentadien) Eisen-Komplexen N2 - Die Tricarbonyl(germacy~lopentadien)eisen-Komplexe VI-X werden durch Umsetzung der Germacyclopentadiene I-V niit Fe(CO)\(_5\) dargestellt. In l,l-Dialkyl- und -Diaryl-l-gemiacyclopentadien-Komplexen kann die Ge-C( exo )-Bindung durch verschiedene Elementhaloge~de gespalten werden, wobei die I-Halogen-l-germacyclopentadien-Komplexe XII, XIII, XV-XVII gebildet werden. Eine Entkomplexierung des Komplexes XI tritt bei der Reaktion mit Me\(_3\)NO oder TiCl\(_4\) ein. Das Tricarbonyl(l-chlor-l-germacyclopentadien)eisen XII reagiert mit AgF, NaJ, NaOMe und LiAIH\(_4\) zu den Komplexen XIXXXII. Das German XXII kann mit CCl\(_4)\ in XII überführt werden. Die Tricarbonyleisen-Komplexe XI, XII, XVI, XVII und XIX reagieren photochemisch mit Trimethylphosphan zu den Dicarbonyl(trimethylphosphan)-Komplexen XXIII-XXVII. Die Kristallstruktur des Tricarbonyl(l-exo-fluor-1-endo-methyl-2,3,4,5-tetraphenyl-1-germacyclopentadien)eisen wird beschrieben. N2 - The tricarbonyl(germacyclopentadiene)iron complexes VI-X are synthesized by the reaction of the germacyclopentadienes I-V with Fe(CO)\(_5\). In l,l-dialkyl- and -diaryi-l-germacyclopentadiene complexes the Ge-C(exo) bond can be split by different element halides, whereby the I-halo-l-germacyclopentadiene complexes XII. XIII. XV-XVII are formed. Decomplexation takes place by the reaction of complex XI with Me\(_3\)NO or TiCl\(_4\). Tricarbonyl(l-chloro-1-germacyclopentadiene)iron (XII) reacts with AgF. NaI. NaOMe and LiAIH\(_4\) to the complexes XIX-XXII. The germane XXII can be transferred to XII with CCl\(_4)\. The tricarbonyliron complexes XI. XII. XVI. XVII and XIX react photochemicaIly with trimethylphosphane to the dicarbonyl(trimethylphosphane) complexes XXIII-XXVll. The crystal structure of tricarbonyl(1-exo-fluoro-l-endo-methyl-2,3,4,5-tetraphenyl-l-germacyclopentadiene) iron is described. KW - Chemie Y1 - 1981 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-46723 ER - TY - JOUR A1 - Burschka, Christian T1 - Kristallstruktur von NH\(_4\)CuS\(_4\) T1 - The crystal structure of NH\(_4\)CuS\(_4\) N2 - NH4CuS4 was prepared according to syntheses reported in the literature. Orthorhombic crystals could be grown (P21 21 21 , a = 5.249(1), b = 8.444(2), c = 12.782(2) A, Z = 4), the structure of which was solved from X-ray diffractometer data. (R = 0.031 for 767 obs. reflections). In the solid state (CuS4)- chelate rings are linked via additional Cu-S-bonds to form one-dimensional polymerie anions. KW - Chemie KW - Crystal Structure KW - Copper Polysulfides KW - Chain Polymers Y1 - 1980 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-46763 ER - TY - JOUR A1 - Wieber, Markus A1 - Burschka, Christian A1 - Baudis, Ulrich T1 - Darstellung und Molekülstruktur von 2-Methylthio-1,3,2-benzodithiastibol T1 - Preparation and X-ray structure of 2-Methylthio-l,3,2-benzodithiastibole N2 - No abstract available KW - Chemie Y1 - 1978 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-46772 ER -