@article{RiesAlbrightSilvestreetal.1986, author = {Ries, Wolfgang and Albright, Thomas and Silvestre, Jerome and Bernal, Ivan and Malisch, Wolfgang and Burschka, Christian}, title = {Unusual structural features of a siloxane}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-31925}, year = {1986}, abstract = {Crystals of the R, S diastereoisomer of [Cp(CO)\(_2\)-FeSiCH\(_3\)F]\(_2\)O are monoclinic, space group ndc (No. 14), with a = 846.0(3) [836.4(1»), b = 768.0(3) [757.1(1»), c = 1548.5(4) [1522.3(2)] pm, {3 = 97.34(3t [97.47(3t] at 300 K [120 K] with Z = 2. Even at 120 K the Si-O-Si fragment is found to be strictly linear due to crystallographically imposed symmetry. To explain the unusual electron distribution derived from the X-ray data collected, several types of possible disorders are discussed, none of which leads to a satisfying explanation. Retaining the Ci symmetry (linear Si-O-Si fragment in the final model) the important bond lengths are Fe-Si 226.7(1) [226.5(1)] pm, Si-F 160.9(2) [161.8(2)] pm, Si-O 160.3(1) [161.1(1)] pm, Si-C 185.0(3) [185.6(3)] pm. The electronic features of this compound were probed via molecular orbital calculations of the extended Hiickel type. It was found that the lone pairs on the siloxane oxygen were tipped away from cylindrical symmetry. The tipping was directed toward the fluorine substituents on the silicon atoms and away from the CpFe(CO)\(_2\) units. A pertubational approach was utilized to rationalize this effect.}, subject = {Chemie}, language = {en} } @article{TackeLinkJoppienetal.1986, author = {Tacke, Reinhold and Link, Matthias and Joppien, Hartmut and Ernst, Ludger}, title = {Sila-Substitution des Akarizids Fenbutatinoxid und einiger seiner Derivate: Synthese und Eigenschaften von Hexakis[(dimethylphenylsilyl)methyl]distannoxan und Tris[(dimethylphenylsilyl)methyl](1,2,4-triazol-1-yl)stannan}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-86937}, year = {1986}, abstract = {No abstract available.}, subject = {Chemische Synthese}, language = {de} } @article{TackeBentlageFeltenLinohetal.1986, author = {Tacke, Reinhold and Bentlage-Felten, Anke and Linoh, Haryanto and Magda, Stephen}, title = {Sila-Analoga des Triparanols und Ethamoxytriphetols: Synthese sowie pharmakologische und toxikologische Eigenschaften}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-86940}, year = {1986}, abstract = {No abstract available.}, language = {de} } @article{BaumannBurschkaSchenk1986, author = {Baumann, Franz Erich and Burschka, Christian and Schenk, Wolfdieter A.}, title = {Ligandensubstitution an cis-Mo(CO)\(_2\)(PPh\(_3\)h(MeCN)(\(\eta^2\)-S0\(_2\)), Kristall- und Molek{\"u}lstruktur von cis-Mo(CO)\(_2\)(PMe\(_3\))\(_3\)(\(\eta^2\)-S0\(_2\)) [1]}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-47143}, year = {1986}, abstract = {No abstract available}, subject = {Chemie}, language = {de} } @article{GrossBurschkaMalisch1986, author = {Groß, Elisabeth and Burschka, Christian and Malisch, Wolfgang}, title = {Hauptgruppenelement-{\"U}bergangsmetall-Mehrfachbindungen, IV. Katalytische Assistenz von [Cp(C0)\(_3\)Mo]\(_2\) bei der Aggregation von Metallo-arsanen {\"u}ber Arsen-Metall-Doppelbindungskomplexe}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-31424}, year = {1986}, abstract = {The metallo-arsanes CP(CO)\(_3\)M - AsMc\(_2\) (1 a, b) (M = Mo, W) are convcrted to the double arsenido-bridged dinuclear complexes [(η-AsMe\(_2\))Mo(CO)\(_2\)Cp]\(_2\) (3a, b) in the presence of [CP(CO)\(_3\)Mo]\(_2\). Due to the unusual mild conditions of aggregation the intermediate formation of the double bonded species Cp(CO)\(_2\)M = AsMe\(_2\) (2a, b) is postulated. The crystal structure of 3a is reported, which shows mutual trans arrangement of the cyclopentadienyl and CO ligands.}, subject = {Chemie}, language = {de} } @article{ZilchTacke1986, author = {Zilch, H. and Tacke, Reinhold}, title = {Fluorid-induzierte Fragmentierung von Acetyldimethylphenylsilan}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-63802}, year = {1986}, abstract = {Acetyldimethylphenylsilane (2) reacts with TBAF · 3H\(_2\)O in THF and with KF in DMSO/H\(_2\)0, respectively, to give [(CH\(_3\) )\(_2\)SiO]\(_x\) and 1-Phenylethanol (3) which can be isolated with a nearly quantitative yield. The way 2 reacts with F\(^-\) contrasts with that of some aroyl- and heteroaroyltrimethylsilanes, described in the literature. A reaction mechanism is discussed which involves among others a 1 ,2-phenyl shift and a Brook rearrangement.}, subject = {Anorganische Chemie}, language = {de} }