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2000[X]
1Author    Bettina Eichhorn, Heinrich NöthRequires cookie*
 Title    New Diazasilaphosphetidines and their Precursors  
 Abstract    A series of aminosilanes (R 'H N bSiR : have been prepared. In case of bulky substituents R' the aminolysis of Ph^SiCb stops at the (R'HN)ClSiPh2 stage. Replacement of the Cl atom is achieved with LiNHR' which allows the synthesis o f mixed bisaminosilanes (R'HN)(R"HN)SiPh2. The X-ray structures of three of these compounds have been determined. There are no intermolecular N-H -N hydrogen bonds in these compounds in the solid state. Several 1,3,2,4-diazaphosphetidines have been synthesized using bis(N-lithioamino)silanes and bis(N-lithioamino)phosphanes . Amongst these the heterocycle 18 possesses an almost planar four membered N iSiP ring system. 
  Reference    Z. Naturforsch. 55b, 352—360 (2000); received January 18 2000 
  Published    2000 
  Keywords    Bis(monoorganylamino)diorganylsilanes, 1, 3, 2, 4-Diazasilaphosphetinides 
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 TEI-XML for    default:Reihe_B/55/ZNB-2000-55b-0352.pdf 
 Identifier    ZNB-2000-55b-0352 
 Volume    55 
2Author    ProfG. Dr, MlostonRequires cookie*
 Title    Metallkomplexe  
 Abstract    mit funktionalisierten Schwefelliganden, XV [1]. Reaktionen von Platin(0)-Komplexen mit 1,2,4-Trithiolanen, 1,2,4,5-Tetrathianen, 1,2,3,5,6-Pentathiepanen sowie Thioketonen. Kristallstrukturanalyse von (Ph3P)2Pt(772-Ph2C=S) M etal Com plexes o f Functionalized Sulfur C ontaining Ligands, XV [1]. Reactions of Platinum(O) Com plexes w ith 1,2,4-Trithiolanes, 1,2,4,5-Tetrathianes, 1,2,3,5,6-Penta-thiepanes as well as Thioketones. X -R ay Structure A nalysis o f (Ph3P)2Pt(/72-Ph2C=S) W olfgang W eigand2, R alf W ünsch3, C hristian R obl3, Grzegorz M lostonb, Heinrich N öthc und M anfred Schm idt0 3,3,5,5-Tetraphenyl-1,2,4-trithiolane (1) reacts with twofold excess of (Ph3P)2Pt(?/2-C2H4) (4) to give a 1:1 mixture of the complexes (Ph3P)2Pt (SCPh2S) (6a) and (Ph3P)2Pt(?/2-Ph2C=S) (7a). Treatment of 3,3,6,6-tetraphenyl-l,2,4,5-tetrathiane (2) with a fourfold excess of 4 yields [Pt2(PPh3)4(/j-S)2] (8) and the platinum(O) compound 7a. The reaction of the 1,2,3,5,6-pentathiepane 3 with a fourfold excess of 4 affords a 1:1:1 mixture of 8, the platinum(O) complex 7b and the bis-thiolato platinum(II) complex 6b. The thioketone complexes 7a-c were formed in smooth reactions of 4 with the thioketones 5a-c. The molecular structure of (Ph3P)2Pt(?/2-Ph2C=S) (7a) has been established by single-crystal X-ray analysis. 
  Reference    Z. Naturforsch. 55b, 453—458 (2000); eingegangen am 28. Februar 2000 
  Published    2000 
  Keywords    1, 2, 4-Trithiolanes, Thioketones, Platinum Complexes 
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 TEI-XML for    default:Reihe_B/55/ZNB-2000-55b-0453.pdf 
 Identifier    ZNB-2000-55b-0453 
 Volume    55 
3Author    Florian Breitsameter, Peter Mayer, Alfred SchmidpeterRequires cookie*
 Title    Die Kondensation von Ylidylchlorphosphanen mit Phosphanen und Bis(diphenylphosphanyl)methan und -amin The Condensation o f Ylidyl Chlorophosphines with Phosphines and Bis(diphenylphosphino)methane and -amine  
 Abstract    Ylidyl chlorophosphanes 1 and dichlorophosphanes 2 react with trimethylsilyl phosphanes to yield the ylidyl diphosphanes 3, 4,5, 7 and the 2-ylidyl triphosphanes 8. From the reaction of compounds 1 with lithium diphosphanyl amide and diphosphanyl methanide result the ylidyl diphosphonium ylides 11 and ylidyl diphosphinimines 13. The former rearrange to give the ylidyl triphosphanyl methanes 12. The chloromethyl diphosphinimine 13c enters a cyclization to give the 1,2,3,5-azatriphosphole derivative 14, the structure of which has been solved by X-ray analysis. From the reaction of ylidyl bis(chlorophosphanes) 17 and 20 with the same reagents the 1,2,4,5-tetraphosphinine derivative 18 and the 1,2,3,5,6-azatetraphosphinine derivatives 19 and 21 are obtained. 
  Reference    Z. Naturforsch. 55b, 519—526 (2000); eingegangen am 21. Februar 2000 
  Published    2000 
  Keywords    Phosphonium Ylides, Diphosphanes, 1, 2, 3, 5-Azatriphospholes 
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 TEI-XML for    default:Reihe_B/55/ZNB-2000-55b-0519.pdf 
 Identifier    ZNB-2000-55b-0519 
 Volume    55 
4Author    M.S S A A Haw AliRequires cookie*
 Title     
 Abstract    The synthesis and antimicrobial activity of a series of the title thiones were examined. Reaction of such thiones with hydrazonoyl halides, resulted in ring transformation to give 5-acylhydrazono derivatives of 1,3,4-thiadiazoles. The mechanisms of the studied reactions are discussed. 
  Reference    Z. Naturforsch. 55b, 546—552 (2000); received February 4. 2000 
  Published    2000 
  Keywords    Ring-Chain Tautomerism Heterocyclic Ring Transformation, 1, 3, 4-Thiadiazoles 
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 TEI-XML for    default:Reihe_B/55/ZNB-2000-55b-0546.pdf 
 Identifier    ZNB-2000-55b-0546 
 Volume    55 
5Author    Max Herberhold3, Yan-Xiang Chenga, Guo-Xin Jinb, Wolfgang Milius3Requires cookie*
 Title     
 Abstract    ,r-Di(terf-butyl)metallocenium Cations. The X-Ray Crystal Structures of [M(C5H4'Bu)2]PF6 (M = Fe, Co) and [ C o ^ H / B u ^ C o C ^ The hexafluorophosphate salts [Fe(C5H4'Bu)2]PF6 (1) and [C o ^H /B u ^lP F ö (2) crystal­ lize in isotypic structures with centrosymmetric cations which have a staggered (transoid) conformation of the exactly parallel ring ligands (conformational angle r = 180°). The 
  Reference    Z. Naturforsch. 55b, 814—820 (2000); received May 26 2000 
  Published    2000 
  Keywords    1, 1 '-Disubstituted Ferrocenes, Ferrocenium Cations, Cobaltocenium Salts 
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 TEI-XML for    default:Reihe_B/55/ZNB-2000-55b-0814.pdf 
 Identifier    ZNB-2000-55b-0814 
 Volume    55 
6Author    Jörg Fleischhauer3, Sven Gabriel3, Dieter Enders3, Anja Nühring3, Axel WollmerbRequires cookie*
 Title    CD-Spectroscopic Investigations for the Determination of the Absolute Configuration of a-Alkylated 1,4-CycIohexanedione Derivatives  
 Abstract    The absolute configuration of the conformationally flexible six membered ring system 2-me-thyl-and 2,6-dimethyl-l,4-cyclohexanedione monoethylene acetal was determined by compar­ ison of measured and calculated CD spectra. The rotational strengths were calculated by means of the CNDO/S-method assuming R at the stereogenic center. The results were compared with the predictions made by the octant rule. The enantiomerically pure material was synthesized via the corresponding SAMP-and RAMP-hydrazones. 
  Reference    Z. Naturforsch. 55b, 1011—1014 (2000); received July 3 2000 
  Published    2000 
  Keywords    1, 4-Cyclohexanedione Derivatives, Absolute Configuration, CD Spectra 
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 TEI-XML for    default:Reihe_B/55/ZNB-2000-55b-1011.pdf 
 Identifier    ZNB-2000-55b-1011 
 Volume    55