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'13C NMR Spectra' in keywords
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1Author    Bernd Wrackmeyer, Udo Dörfler, Wolfgang Milius, Max HerberholdRequires cookie*
 Title    Triferrocenylborane -Molecular Structure in Solution and in the Solid State  
 Abstract    According to a single crystal X-ray structure determination all three ferrocenyl substituents of triferrocenylborane (1) adopt the same orientation with respect to the BC3-plane [P 2 Jc\ monoclinic; Z = 4; a = 1353.5(3), b = 1695.6(3), c = 1056.4(2) pm, ß = 109.27(3)°]. The simu­ lated X-ray powder pattern of the single crystal is identical with the powder diagram o f a macroscopic sample, indicating the presence of a single diastereomer (l a) in the solid state. How ever, at low temperature (< -9 5 °C) in solution, the 13C NM R spectra suggest the pres­ ence of the second diastereomer (lb) in which one ferrocenyl group is oriented opposite to the other two with respect to the central BC3-plane. 
  Reference    Z. Naturforsch. 50b, 201—2 (1995); received July 25 1994 
  Published    1995 
  Keywords    Triferrocenylborane, 13C NMR Spectra, Dynamic Processes, X-Ray 
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 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-0201.pdf 
 Identifier    ZNB-1995-50b-0201 
 Volume    50 
2Author    W. Lübbe, W. PreetzRequires cookie*
 Title    undm-[(w-C4H9)4N][B6H5(CH2)2C6H4]  
 Abstract    Preparation, n B, 13C, 'H NM R Spectra and Vibrational Spectra o f 1,2-Xylylene-pentahydro-c/oso-hexaborate, cw-[B6H5(CH2)2C6H4]_ , and the Crystal Structures o f c/s-[P(C6H5)4][B 6H5(CIL,)2C6H4] and c/s-[(n-C4H9)4N ][B 6H5(CH2)2C6H4] 1,2-Xylylene-pentahydro-c/oso-hexaborat(1 -), ' By reaction of [B6H6]2-with u>,u/-dibromo-o-xylene in acetonitrile the 1,2-xylylene-pentahydro-c/oso-hexaborat, ds-[B 6H5(CH2)2C6H4]_ , is formed. The new ansa compound has been separated from excess [B6H6]2-and other reaction products by ion exchange chromatogra­ phy on diethylaminoethyl cellulose. The crystal structures of c/s-[P(C6H5)4][B6H5(CH2)2C6H4] (I) and as-[(n-C4H9)4N][B6H5(CH2)2C6H4] (II) have been determined by single crystal X-ray diffraction analysis: I is monoclinic, space group P 2 \/n with a = 13.715(5), b = 11.118(1) and c = 19.702(2) A, ß = 103.47(2)°; II is orthorhombic with a = 10.204(7), b = 13.352(4) and c = 20.824(8) A. The "B NMR spectrum confirms the structure with a hetero disubstituted octahedral B6 cage with local C2v symmetry. The l3C and 'H NMR spectra have been assigned in term of such a configuration. The IR and Raman spectra exhibit characteristic CH, BH, BC, B6 and arene vibrations. 
  Reference    Z. Naturforsch. 51b, 691—697 (1996); eingegangen am 25. August 1995 
  Published    1996 
  Keywords    H NMR Spectra, Vibrational Spectra, 13C NMR Spectra, 11B NMR Spectra 
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 TEI-XML for    default:Reihe_B/51/ZNB-1996-51b-0691.pdf 
 Identifier    ZNB-1996-51b-0691 
 Volume    51 
3Author    Susanna Kerschl, Bernd WrackmeyerRequires cookie*
 Title    Organoborierung von Alkinylstannanen, XIV [1]  
 Abstract    Organoborierung von Bis(alkinyl)stannanen: Mechanismus und Anwendung der 119Sn—NMR-Spektroskopie O rganoboration of Alkynylstannanes, XIV [1] O rganoboration of Bis(alkynyl)stannanes: M echanism and Application of 119Sn NM R Spectroscopy Dimethylbis(phenylethynyl)stannane (1) reacts with trialkylboranes, BR3 (2), to give bis(al-kenyl stannanes (5) (R = C2H5), l-bora-4-stanna-2,5-cyclohexadienes (6) (R = C2H5, C3H7'), 1-stanna-2,4-cyclopentadienes (7) (R = C2H5) and l-stanna-3-cyclopentenes (8) (R = CH3, C2H5). I3C and uySn NMR data prove the structure of the reaction products (5 to 8). 119Sn NMR is useful (i) for following the course of the reaction (mechanism!) and (ii) for quantitative analysis of the product distribution. Deorganoboration reactions play an important role in the formation of the various heterocyclic systems. 
  Reference    Z. Naturforsch. 39b, 1037—1041 (1984); eingegangen am 24. Februar 1984 
  Published    1984 
  Keywords    et Alkynylstannanes, Organoboration, Mechanism, 1, ySn NMR Spectra, 13C NMR Spectra 
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 TEI-XML for    default:Reihe_B/39/ZNB-1984-39b-1037.pdf 
 Identifier    ZNB-1984-39b-1037 
 Volume    39 
4Author    Eberhard Bessler, BrowdoM. Arins Barbosa, Wolfgang Hiller, Johann WeidleinRequires cookie*
 Title    Synthese und Eigenschaften von Tetrakis(trimethylsilylisocyanid)nickel(0), N i(C = N -S iM e 3)4 Synthesis and Properties of Tetrakis(trimethylsilylisocyanide)nickel(0), N i(C = N -S iM e 3)4  
 Abstract    Ni(CNSiMe3)4 (Me = CH,), the first homoleptic isocyanosilane complex, has been prepared by reaction of bis(1,5-cyclooctadiene)nickel(0) with trimethylcyanosilane in ether and charac­ terized by its infrared, Raman spectra, ,3C NMR spectra. 
  Reference    Z. Naturforsch. 46b, 490—494 (1991); eingegangen am 8. November 1990 
  Published    1991 
  Keywords    Tetrakis(trimethylsilylisocyanide)nickcl(0), Synthesis, Vibrational Spectra, 13C NMR Spectra 
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 TEI-XML for    default:Reihe_B/46/ZNB-1991-46b-0490.pdf 
 Identifier    ZNB-1991-46b-0490 
 Volume    46 
5Author    W. Lübbe, W. PreetzRequires cookie*
 Title    Darstellung, n B-, 13C-, !H-NMR-und Schwingungsspektren von //-Methylen-bis  
 Abstract    hexahydro-c/öso-hexaborat, [B6H6(CH2)B6H6]2_, und Kristallstruktur von [As(C6H5)4]2[B6H6(CH2)B6H6]* V2(CH3)2CO Preparation, "B , 13C, NM R and Vibrational Spectra of //-M ethylene-bis-hexahydro-doso-hexaborate, [B6H 6(C H 2)B6H 6]2~, and Crystal Structure of [As(C6H 5)4]2[B6H 6(C H 2)B6H 6] • V2 (CH3)2CO ^-M ethylene-bis-hexahydro-c/oso-hexaborate(2-), ' 
  Reference    Z. Naturforsch. 51b, 545 (1996); eingegangen am 19. Septem ber 1995 
  Published    1996 
  Keywords    H NM R Spectra, Vibrational Spectra, 13C NMR Spectra, n B NMR Spectra 
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 TEI-XML for    default:Reihe_B/51/ZNB-1996-51b-0545.pdf 
 Identifier    ZNB-1996-51b-0545 
 Volume    51 
6Author    HildegardD. Inter, Rudolf Hänsel, Andrew PelterRequires cookie*
 Title    from Zingiber cassumunar (roxb.)  
  Reference    Z. Naturforsch. 35c, 156—158 (1980); received September 17 1979 
  Published    1980 
  Keywords    Zingiber cassumunar roxb, Alflabene and Cassumunene, 2-(3', 4'-dimethoxystyryl)-ethanol, Phenylbutene Derivatives, 13C NMR Spectra, Diels-Alder Reactions 
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 TEI-XML for    default:Reihe_C/35/ZNC-1980-35c-0156_n.pdf 
 Identifier    ZNC-1980-35c-0156_n 
 Volume    35 
7Author    T. Koch, W. PreetzRequires cookie*
 Title    Darstellung, n B-, 13C -,1 H-NMR-und Schwingungsspektren  
 Abstract    von 2,2' -Bipyridylundecahydro-c/oso-dodecaborat(1-) sowie Kristallstruktur von (Ph4As)[(2,2-C10H8N2)B12Hn ] CH3CN Synthesis, n B, 13C, 'H NMR and Vibrational Spectra of 2 ,2 '-Bipyridyl-undecahydro-c/o5o-dodecaborate(l-) and Crystal Structure of (Ph4As)[(2 ,2 '-C10H8N2)B 12H 1 1 ]-CH3CN 
  Reference    Z. Naturforsch. 52b, 1165—1168 (1997); eingegangen am 17. Juli 1997 
  Published    1997 
  Keywords    2, 2'-Bipyridyl-undecahydro-c/oso-dodecaborate(l-), Crystal Structure, n B NMR Spectra, 1H NMR Spectra, 13C NMR Spectra, Vibrational Spectra 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-1165.pdf 
 Identifier    ZNB-1997-52b-1165 
 Volume    52