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21Author    Manfred Weidenbruch, Claude Pierrard, Helge PeselRequires cookie*
 Title    Neue Siloxanverbindungen einiger Übergangsmetalle Silicon Compounds with Strong Intramolecular Steric Interactions, VIII [1] New Siloxane Compounds of Some Transition Metals  
 Abstract    Tri-£er£-butylsiloxane compounds of transition metals are obtained by two different routes, one of these involves condensation of tri-Zer£-butylsilanol with the binary oxides V2O5, CrC>3, M0O3, and Re2Ü7, while the other proceeds via a similar reaction between the chlorides VOCl3, NbCls, TaCls, Cr02Cl2, and the silanol. The new compounds, having good thermal stability and remarkable resistence to hydrolysis, are characterized by IR, 1 H NMR, and mass spectra. 
  Reference    Z. Naturforsch. 33b, 1468—47 (1978); eingegangen am 20. September 1978 
  Published    1978 
  Keywords    Tri-ierf-butylsiloxanes, Transition Metals, Steric Hindrance, Mass Spectra 
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 TEI-XML for    default:Reihe_B/33/ZNB-1978-33b-1468.pdf 
 Identifier    ZNB-1978-33b-1468 
 Volume    33 
22Author    Günter Schmid, Eckhard WelzRequires cookie*
 Title    Synthese und Eigenschaften von /^-Silandiyl-Eisencarbonylen [1] Synthesis and Properties of //2-Silanediyl Iron Carbonyls [1]  
 Abstract    The synthesis of dinuclear complexes of the types [(CO)4FeSiR 1 R 2 ]2 and Fe2(CO)7(SiR 1 R 2)2 is described. IR, mass and Mössbauer spectroscopic data are discussed. 
  Reference    Z. Naturforsch. 34b, 929—933 (1979); eingegangen am 29. Januar/27. März 1979 
  Published    1979 
  Keywords    ^2-Silanediyl, Iron Carbonyls, IR, Mass Spectra, Mössbauer Spectra 
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 TEI-XML for    default:Reihe_B/34/ZNB-1979-34b-0929.pdf 
 Identifier    ZNB-1979-34b-0929 
 Volume    34 
23Author    Werner Zeiß, Alfred SchmidpeterRequires cookie*
 Title    .3.4.2-Thiadiazaphospholin-2-thione l,3,4,2-Thiadiazaphospholine-2-thiones  
 Abstract    Perthiophosphonic anhydrides (1) and phos-phorus^) sulfide react with benzo-phenylhydra-zonoyl chloride (2) eliminating HCl and yielding the title compounds 3 and 4, which formally are cycloadducts of the monomeric units RPS2 and P2S5, respectively, and diphenyl nitrilimine. The corresponding cycloreversion is observed in their mass spectra. 
  Reference    Z. Naturforsch. 34b, 1042—1043 (1979); eingegangen am 26. März 1979 
  Published    1979 
  Keywords    Perthiophosphonic Anhydrides, Phosphorus(V) Sulfide, Cyclocondensation Reaction, NMR, Mass Spectra 
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 TEI-XML for    default:Reihe_B/34/ZNB-1979-34b-1042_n.pdf 
 Identifier    ZNB-1979-34b-1042_n 
 Volume    34 
24Author    Ertugrul Arpac, Lutz DahlenburgRequires cookie*
 Title    Oligophosphin-Liganden, I  
 Abstract    Einfache Synthesen der trimethylenverknüpften Triphosphine RP[(CH2)3PPh2]2 und ihrer Vorstufen Ph2P(CH2)3P(H)R (R Ph, Me) Oligophosphine Ligands, I Convenient Syntheses of the Trimethylene-linked Triphosphines RP[(CH2)3PPh2]2 and their Precursors Ph2P(CH2)3P(H)R (R = Ph, Me) The secondary-tertiary diphosphines Ph2P(CH2)3P(H)Ph (2) and Ph2P(CH2)3P(H)Me (3) have been prepared from Ph2P(CH2)3Cl (1) and NaP(H)Ph or LiP(H)Me, respectively. Metallation of 2 and 3 with n-butyl lithium and further reaction of the lithio-derivatives with one equivalent of 1 yields PhP[(CH2)3PPh2]2 (4) and MeP[(CH2)3PPh2]2 (5). The tritertiary phosphines 4 and 5 have likewise been obtained from RPLi2 (R = Ph, Me) and two equivalents of 1. The synthesis of 4 from PhPCl2 and two equivalents of the Grignard reagent of 1 is also reported. Each of the phosphines 1-5 was characterized by NMR and mass spectroscopy. 
  Reference    Z. Naturforsch. 35b, 146—152 (1980); eingegangen am 26. Oktober 1979 
  Published    1980 
  Keywords    Secondary-tertiary Diphosphines, Tritertiary Phosphines, Preparation, NMR Spectra, Mass Spectra 
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 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0146.pdf 
 Identifier    ZNB-1980-35b-0146 
 Volume    35 
25Author    Ekkehard FluckRequires cookie*
 Title    Rüdiger Thamm  
 Abstract    Primary phosphanes, RPH2, react with carbonic ester chlorides, C1COOR', in the presence of K 2 C0 3 to yield the title compounds RPHCOOR' and RP(COOR') 2 . The NMR data of the novel compounds are presented and discussed. Other physical and some chemical properties are described. 
  Reference    Z. Naturforsch. 36b, 910—916 (1981); eingegangen am 11. Mai 1981 
  Published    1981 
  Keywords    Carbonic Ester Phosphides, Mass Spectra, IR Spectra, NMR Spectra 
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 TEI-XML for    default:Reihe_B/36/ZNB-1981-36b-0910.pdf 
 Identifier    ZNB-1981-36b-0910 
 Volume    36 
26Author    Alfred Schmidpeter, Konstantin KaraghiosoffRequires cookie*
 Title    4.5 -Dicyano-1.3.2A 3 -diazaphospholat - ein anionisches, als Monomer stabiles 1.3.2-Diazaphosphol [1] 4,5-Dicyano-1,3,2 A 3 -diazaphospholate -an Anionic 1,3,2-Diazaphosphole, Stable as a Monomer [1]  
 Abstract    Diamino-maleodinitrile and P(NMe2)3 condense at room temperature to the dimethyl -ammonium salt of the dicyano-1,3,2-diazaphosphole. Other products may result under different conditions. Mel methylates the ambivalent diazaphosphole anion at nitrogen. 
  Reference    Z. Naturforsch. 36b, 1273—1276 (1981); eingegangen am 17. Juli 1981 
  Published    1981 
  Keywords    Dicoordinate Phosphorus, Azaphospholes, Ambivalent System, 13 C NMR Spectra, Mass Spectra 
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 TEI-XML for    default:Reihe_B/36/ZNB-1981-36b-1273.pdf 
 Identifier    ZNB-1981-36b-1273 
 Volume    36 
27Author    Ekkehard Lindner, Claus-Peter Krieg, Sigurd Hoehne, Axel RauRequires cookie*
 Title    Darstellung und Eigenschaften von und Reaktionen mit metallhaltigen Heterocyclen, XXTTT [1] Untersuchungen zur P=S-heteroanalogen Cyclocotrimerisierung von Alkinen mit Nitrilen bzw. Isocyaniden Preparation and Properties of, and Reactions with, Metal-Containing Heterocycles, XXIII [1] Investigations on P=S-Heteroanalogous Cyclocotrimerization of Alkynes with Nitriles and Isocyanides, Respectively  
 Abstract    Structure of [(OC)4MnSP(CH 3)2]2, The dimanganadiphosphadithiacyclohexadiene [(OC)4MnSP(CH 3)2]2 (1) crystallizes in the H,C CH, \ / 3 / P =\ (OC).Mn Mn(CO), * \ / S=P /\ HjC CHj 1 /-PC CH * (OC)tMn I CH, * L Y\ CH, (OCULMn | CHj . CO \ ^ C" \R' L \ t-Bu C6H" C6H5 R'NC a b c PR'3 d R = C02CHJ 3a-d orthorhombic space group Pbca with Z = 4. Attempts to cyclotrimerize the intermediate 
  Reference    Z. Naturforsch. 36b, 1487—1492 (1981); eingegangen am 28. Juli 1981 
  Published    1981 
  Keywords    Isocyanide Complexes of Heteromanganacyclopentadienes, Mass Spectra, IR Spectra, NMR Spectra 
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 TEI-XML for    default:Reihe_B/36/ZNB-1981-36b-1487.pdf 
 Identifier    ZNB-1981-36b-1487 
 Volume    36 
28Author    Jochen Eilermann, Martin LietzRequires cookie*
 Title    Chemie polyfunktioneller Liganden, 67 [1]  
 Abstract    Die Darstellung von l.l.l-Tris(dichlorarsinomethyl)ethan, Ethan-l.l.l-tris(methylarsonsäure), 1.1.1-Tris (arsinomethyl)ethan und einem neuen Organocyclotriarsan Chemistry of Polyfunctional Ligands, 67 [1] The Preparation of l.l.l-Tris(dichloroarsinomethyl)ethane, Ethane-l.l.l-tris(methylarsonic acid), l.l.l-Tris(arsinomethyl)ethane and of a New Organocyclotriarsane l,l,l-Tris(dichlorarsinomethyl)ethane, CH3C(CH2AsCl2)3 (5) can be obtained in the reaction of CH3C(CH2AsNC6H4CH3)3 (4) with gaseous HCl. The heteroadamantane CH3C(CH2AsO)3 (6) reacts with AsCl3 or PC13 yielding also 5. CH3C(CH2AsO)3, CH3C(CH2AsS)3 and CH3C(CH2AsI 2)3 are oxidized with H202 to give CH3C[CH2As(0)(0H)2]3 (7) and CH3C[CH2As(0)(0H)2]3 • H20 (7 a). CH3C(CH2AsI2)3 and C(CH2AsI2)4 can be reduced with LiAlH4 to give CH3C(CH2AsH2)3 (9) and C(CH2AsH2)4 (12). Oxidation of 9 and 12 leads to the cyclotriarsane compounds CH3C(CH2As)3 (10) and H2AsCH2C(CH2As)3 (13). 
  Reference    (Z. Naturforsch. 37b, 73—80 [1982]; eingegangen am 29. Juni/21. September 1981) 
  Published    1982 
  Keywords    Arsenic Compounds, Organocyclotriarsane, Vibrational Spectra, *H NMR Spectra, Mass Spectra 
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 TEI-XML for    default:Reihe_B/37/ZNB-1982-37b-0073.pdf 
 Identifier    ZNB-1982-37b-0073 
 Volume    37 
29Author    Rüdiger Thamm, Ekkehard FluckRequires cookie*
 Title    Kohlensäureesterphosphide -Synthese und Cyclisierungsreaktionen Carbonic Ester Phosphides -Synthesis and Cyclization Reactions  
 Abstract    Carbonic ester phosphides, RPHCOOR' and RP(COOR')2, have been prepared by the reaction of C1COOR' with primary phosphines RPH2 in the presence of K2CO3. Some compounds of RPHCOOR' series are transformed into P-heterocycles through addition of the P-H group to the C = C doubleboncl systems. The 31 P NMR data, IR and mass spectra of the novel compounds are presented and discussed. 
  Reference    Z. Naturforsch. 37b, 965—974 (1982); eingegangen am 8. März 1982 
  Published    1982 
  Keywords    Carbonic Ester Phosphides, Mass Spectra, IR Spectra, NMR Spectra 
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 TEI-XML for    default:Reihe_B/37/ZNB-1982-37b-0965.pdf 
 Identifier    ZNB-1982-37b-0965 
 Volume    37 
30Author    Umlagerung Synthese, Eigenschaften Diphenylphosphinosubstituierter Uracile, Jochen Ellermann, AlfonsA M DemuthRequires cookie*
 Title    Chemie polyfunktioneller Moleküle, 74 [1] [1] Synthesis, Rearrangement and Properties of Diphenylphosphino Substituted Uracils  
 Abstract    5-Bromo-uracil (2) with chloro-diphenylphosphine and triethylamine gives 5-bromo-N(1),N(3)-bis(diphenylphosphino)-uracil (3). In moist acetone, 3 is hydrolyzed to 5-bromo-N(l)-diphenylphosphino-uracil (4). 3 reacts with n-butyllithium under rearrangement and, with HCl, under elimination of a PPh2-group, forms C(5)-diphenylphosphino-uracil (7 a). Recrystallization of 7 a from ethanol yields the ethanol-1:1-adduct 7 b. Heating of 7 a in dimethylsulfoxide with D20 yields the N(l),N(3)-dideutero-C(5)-diphenylphosphino-uracil (7 c). All compounds were characterized by infrared, Raman, iH, 31 P NMR and mass spectra. 7 a shows a very small antitumor activity. 
  Reference    Z. Naturforsch. 38b, 1165—1172 (1983); eingegangen am 19. Mai 1983 
  Published    1983 
  Keywords    Diphenylphosphino Substituted Uracils, Rearrangement, NMR Spectra, Vibrational Spectra, Mass Spectra 
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 TEI-XML for    default:Reihe_B/38/ZNB-1983-38b-1165.pdf 
 Identifier    ZNB-1983-38b-1165 
 Volume    38 
31Author    Ekkehard Lindner, E. Rnst, Ulrich KüsterRequires cookie*
 Title    Preparation and Properties of, and Reactions with, M etal-Containing H eterocycles, XX X V I [1] Novel Phosphane Ligands Containing Asymmetric Phosphorus or Carbon Atoms  
 Abstract    The functionalized ligands (H3C)PhP—(CH2)"-C1 (1, 2) [n = 2 (1), 3 (2)] and 
  Reference    (Z. Naturforsch. 39b, 115—117 [1984]; eingegangen am 25. Juli 1983) 
  Published    1984 
  Keywords    o>-Chloroalkyl(methyl)phenylphosphanes, Menthoxymethyl(diphenylphosphane), Mass Spectra, NMR Spectra 
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 TEI-XML for    default:Reihe_B/39/ZNB-1984-39b-0115_n.pdf 
 Identifier    ZNB-1984-39b-0115_n 
 Volume    39 
32Author    H.E JRequires cookie*
 Title    A tta-ur-Rahm an*, M ehrun Nisa, and Talat Zamir  
 Abstract    A new alkaloid, "papilicine", has been isolated from the leaves of Buxus papilosa to which structure (1) has been assigned on the basis of spectroscopic studies. Buxus species have been used in the indigenous system of medicine as febrifuge, for relief of rheumatism and for the treatm ent of a num ber of other ailments. Buxus papilosa C. K. Schn., Linn. 
  Reference    (Z. Naturforsch. 39b, 127—128 [1984]; received March 23 1983) 
  Published    1984 
  Keywords    Buxus papilosa, Alkaloids, Structure Elucidation, NMR Spectra, Mass Spectra 
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 TEI-XML for    default:Reihe_B/39/ZNB-1984-39b-0127_n.pdf 
 Identifier    ZNB-1984-39b-0127_n 
 Volume    39 
33Author    Atta-Ur -Rahman, Mehrun Nisa, Talat Zamir, H.E J, Wolfgang VoelterRequires cookie*
 Title    The Isolation and Structure of "Papilinine" a New Alkaloid from Buxus papilosa  
 Abstract    A new alkaloid "Papilinine" has been isolated from the leaves of Buxus papilosa to which structure 1 has been assigned. 
  Reference    Z. Naturforsch. 40b, 565—566 (1985); received June 28 1984 
  Published    1985 
  Keywords    Buxus papilosa, Steroidal Alkaloids, Structure Elucidation, NMR Spectra, Mass Spectra 
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 TEI-XML for    default:Reihe_B/40/ZNB-1985-40b-0565_n.pdf 
 Identifier    ZNB-1985-40b-0565_n 
 Volume    40 
34Author    Edmund Maliński3, Jósef Kusmierz3, Janusz Szafranek3, Eligiusz Dubisb, Janusz Poplawskib, JerzyT W Ró Belb, W. Ilfried, A. KönigcRequires cookie*
 Title    Cuticular Hydrocarbons of the Colorado Beetle Leptinötarsa decemlineata say  
 Abstract    The cuticular hydrocarbons o f the C olorado beetle Leptinotarsa decemlineata say consist of 2-m ethylalkanes, internally branched m onom ethylalkanes, dim ethyl-, trimethyl-and tetramethyl-alkanes. The hydrocarbons differ from those o f m ost o f the other insects so far investigated. The major com ponents were found to be the dim ethyl branched alkanes, 2,6-and/or 7,22-dimethyl-octacosane and the tetram ethylalkane, 3,10,16,23-tetram ethyltritriacontane. The hydrocarbons identified are m embers o f hom ologous series which differ by two m ethylene groups. The identifi­ cation of hydrocarbons was achieved by mass spectrom etry and gas chromatographic determ ina­ tion o f Kovats retention indices on two high efficiency capillary colum ns coated with D exsil 300 and O V-1. 
  Reference    Z. Naturforsch. 41b, 567 (1986); received D ecem ber 10 1985 
  Published    1986 
  Keywords    Insect Cuticular Hydrocarbons, Colorado B eetles, Mass Spectra, Gas Chromatography 
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 TEI-XML for    default:Reihe_B/41/ZNB-1986-41b-0567.pdf 
 Identifier    ZNB-1986-41b-0567 
 Volume    41 
35Author    Rahman, Sajida Khanum, Yasmin Badar, Kaneez Fatima, Yusuf Ahmad, H.E JRequires cookie*
 Title    Atta-ur  
 Abstract    Continuing studies on the leaves of Rhazya stricta have resulted in the isolation of a new Picralima alkaloid, N h -methyl strictamine 2. 
  Reference    (Z. Naturforsch. 42b, 91—93 [1987]; received June 10 1986) 
  Published    1987 
  Keywords    Rhazya stricta, Alkaloids, Indolenine, 13 C NMR Spectra, Mass Spectra 
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 TEI-XML for    default:Reihe_B/42/ZNB-1987-42b-0091.pdf 
 Identifier    ZNB-1987-42b-0091 
 Volume    42 
36Author    G. Hagenow3, H.-W Jochims3, J. Sawatzkib, R. Minkwitzb, H. Baumgärtel3Requires cookie*
 Title    Photoionisationsmassenspektren von MethyI(trifluormethyl)sulfan CH3SCF3 [1] Photoionization Mass Spectra of Methyl(trifluoromethyl)sulfan CH 3SCF3 [1]  
 Abstract    The ionization potential of C H 3SCF3 and the appearance potentials of fragm ent ions have been m easured in the photon energy range 9 —19 eV using synchrotron, radiation. From these results thermochem ical data of C H 3SCF3, C H 3SCF3+ and fragment ions have been evaluated. 
  Reference    (Z. Naturforsch. 44b, 17 [1989]; eingegangen am 29. A ugust 1988) 
  Published    1989 
  Keywords    Sulfane, H eat of Form ation, Photoionization, Bond Energy, Mass Spectra 
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 TEI-XML for    default:Reihe_B/44/ZNB-1989-44b-0017.pdf 
 Identifier    ZNB-1989-44b-0017 
 Volume    44 
37Author    JörnM. Üller, Corinna Hänsch, Joachim PickardtRequires cookie*
 Title    ;r-01efin-Iridium-Komplexe, XV [1] Kationische Bis(2.3-dimethylbutadien)iridium-L-Verbindungen mit verschiedenen Donorliganden L jr-Olefin Iridium Complexes, XV [1] Cationic Bis(2.3-dim ethylbutadiene)iridium-L Compounds with Various D onor Ligands L  
 Abstract    (dm b)2IrCH , (dm b = 2.3-dim ethylbuta-l,3-diene) reacts with Ph,CBF4 in C H 2C12 to form the 
  Reference    Z. Naturforsch. 44b, 278 (1989); eingegangen am 10. Oktober 1988 
  Published    1989 
  Keywords    Synthesis, IR Spectra, NM R Spectra, Mass Spectra, Crystal Structure 
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 TEI-XML for    default:Reihe_B/44/ZNB-1989-44b-0278.pdf 
 Identifier    ZNB-1989-44b-0278 
 Volume    44 
38Author    Winfried Plass3, M. Anfred Spahna, G. Ernot Heckmann3, Ekkehard FluckRequires cookie*
 Title    Neue Carbodiphosphorane. Notiz zur Reaktion zwischen Bis(dimethylamino)fluormethylidenphosphoran und /i-Butyllithium New C arbodiphosphoranes. N ote on the Reaction between Bis(dimethylamino)fluoromethylidene-phosphorane and «-Butyllithium  
 Abstract    The main product from the reaction between bis(dimethylamino)fluoromethylidene-phos-phorane (1) and «-butyllithium in the presence of tetramethylethylenediamine is /j-butyl-di-methylamino-methyl-{[tris(dimethylamino)phosphoranylidene]methylene}-phosphorane (7). As a by-product from the reaction between methyl-bis(dimethylamino)difluorophosphorane and rt-butyllithium bis(dimethylamino)-methyl-{[«-butyl-bis(dimethylamino)phosphor-anylidene]methylene}-phosphorane (9) was isolated in small yield. The new carbodiphosphor­ anes 7 and 9 are characterized by their 'H , 13C, and 31P N M R and mass spectra. 
  Reference    Z. Naturforsch. 47b, 947—951 (1992); eingegangen am 11. Dezember 1991 
  Published    1992 
  Keywords    Diam inofluorom ethylidenephosphorane, Carbodiphosphoranes, N M R Spectra, Mass Spectra 
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 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0947.pdf 
 Identifier    ZNB-1992-47b-0947 
 Volume    47 
39Author    Ion Neda, Michael Farkens, Axel Fischer, PeterG. Jones, R. Einhard SchmutzlerRequires cookie*
 Title    Zur Chemie der l,3,5-Triaza-2-phosphinan-4,6-dione, Teil V* Darstellung der Phosphoryl(III)(A4P)-und Thiophosphoryl(III)(A4P)-Derivate der l,3,5-Triaza-2-phosphinan-4,6-dione. Umsetzungen mit Ketonen  
 Abstract    Chemistry of the l,3,5-Triaza-2-phosphinane-4,6-diones, Part V Synthesis of Phosphoryl(III)(^4P) and Thiophosphoryl(III)(/!.4P) Derivatives of 1.3.5-Triaza-2-phosphinane-4,6-diones. Reactions with Ketones 18. M ärz 1993 1.3.5-Trimethyl-Substituted l,3,5-Triaza-2-oxo-and 1.3.5-Triaza-2-thio-2/.4-phosphinane-4, 
  Reference    Z. Naturforsch. 48b, 860—866 (1993); eingegangen am 
  Published    1993 
  Keywords    6-diones, N M R Spectra, Mass Spectra, X-Ray 
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 TEI-XML for    default:Reihe_B/48/ZNB-1993-48b-0860.pdf 
 Identifier    ZNB-1993-48b-0860 
 Volume    48 
40Author    Anne-Kathrin Duhme, Henry StrasdeitRequires cookie*
 Title    Ligandenmangelkomplexe des Cadmiums. Synthese und spektroskopische Charakterisierung molekularer (Pentafluorphenyl)cadmium-Thiolate und die Struktur des Cubankomplexes [{Cd(C6F5)(SBur)}4] Ligand-Deficient Complexes of Cadmium. Synthesis and Spectroscopic Characterization o f Molecular Pentafluorophenyl Cadmium Thiolates and the Structure o f the Cubane Complex [{Cd(C6F5)(SBuf)}4]  
 Abstract    In toluene, bis(pentafluorophenyl)cadmium(II) and thiols RSH (R = Bu', 2,4,6-Pr'3C6H2, 2,4,6-Bu'3C6H2) react to give soluble pentafluorophenyl cadmium thiolates [(Cd(C6F5)(SR)} J. The compounds [{Cd(C6F 5)(SBu')}4] (1)0 .5 C6H5CH3, [ {Cd(C6F5)(SC6H2Pr'3-2,4,6)} J (2)-ca. 0.25n C6H 5CH3, and [{Cd(C6F5)(SC6H2Bu'3-2,4,6)} J (3) ca. 0.25« C6H5CH3 have been prepared in 65, 59 and 78% yield, respectively. 1-0.5 C6H5CH3 crystallizes in the triclinic space group PI with a = 11,635(1)Ä, b = 11.583(1)Ä, c = 21.480(2)Ä, a = 82.12(1)°, ß = 76.26(1)°, y — 89.35(1)°, and Z = 2. 1 is a cubane-type complex with a {Cd4(/z3-SBur)4}4+ core. Each Cd atom is coordinated by three bridging thiolato ligands and one terminal C6F5 group (C d -S 2.62 A, C d -C 2.15Ä (mean values)). The central C atoms of the Bu'S" ligands of 1 show a remarkable low-field shift o f their 13C N M R resonance (12.3 ppm relative to the value of the free thiol). A characteristic spectral feature of (Cd(C6F5) } + complexes is the large value of the coupling constant 2/ (19F ,13C) o f the ipso-C atom (1, 2: 68 Hz; 3: 67 Hz). The complexes [Cd(C6F5)(SR) + H]+, [Cd(SR)2 + H]+, and [Cd2(SR)3]+ were identified in the Cl mass spectra (/50-butane) of 2 and 3. 
  Reference    (Z. Naturforsch. 49b, 119—127 [1994]; eingegangen am 17. August 1993) 
  Published    1994 
  Keywords    Cadmium Complexes, Thiolates, Crystal Structure, NMR Spectra, Mass Spectra 
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 TEI-XML for    default:Reihe_B/49/ZNB-1994-49b-0119.pdf 
 Identifier    ZNB-1994-49b-0119 
 Volume    49