Home Photoelektronen-Spektren und Moleküleigenschaften, 110 [1,2] Tricyanmethan-Derivate X—C(CN)3 / Photoelectron Spectra and Molecular Properties, 110 [1, 2] Tricyanomethane Derivatives X-C(CN)3
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Photoelektronen-Spektren und Moleküleigenschaften, 110 [1,2] Tricyanmethan-Derivate X—C(CN)3 / Photoelectron Spectra and Molecular Properties, 110 [1, 2] Tricyanomethane Derivatives X-C(CN)3

  • Hans Bock and Ralph Dammel
Published/Copyright: June 2, 2014
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Zeitschrift für Naturforschung B
From the journal Zeitschrift für Naturforschung B Volume 42 Issue 3

Received: 1986-9-12
Published Online: 2014-6-2
Published in Print: 1987-3-1

© 1946 – 2014: Verlag der Zeitschrift für Naturforschung

Articles in the same Issue

  1. Nitrido-Azido-Komplexe des Molybdän(VI): Synthese und Kristallstruktur von MoN(N3)2[HB(3,5-Me2pyz)3] und MoN(N3)Cl[HB(3,5-Me2pyz)3] / Nitrido Azido Complexes of Molybdenum(VI): Synthesis and Crystal Structure of MoN(N3)2[HB(3,5-Me2pyz)3] and MoN(N3)Cl[HB(3,5-Me2pyz)3]
  2. Ein weiteres P-Fluor-Ylid: [N(CH3)2]2PF=CH-CH(n-C4H9)-P[N(CH3)2]2 (4) Darstellung und NMR-Daten / A Further P-Fluoro-Ylide: [N(CH3)2]2 PF=CH-CH(n-C4H9)-P[N(CH3)2] 2 (4) Preparation and NMR Data
  3. Darstellung und Kristallstruktur des Bis(2-amino-1-ammonioethan)hexasulfids [H3N-(CH2)2-NH2]2S6 /Synthesis and Crystal Structure of Bis(2-amino-1-ammonioethan)hexasulfide, [H3N—(CH2)2-NH2]2S6
  4. Darstellung und Kristallstrukturen von [K(crypt-2.2.2)]2 S7 · (H2N-(CH2)2-NH2) und [K(crypt-2.2.2)]2S6 / Synthesis and Crystal Structures of [K(crypt-2.2.2)]2S7 · (H2N-(CH2)2-NH2) and [K(crypt-2.2.2)]2S6
  5. Säure-Base-Eigenschaften des zyklischen Triamins N,N′,N″-Trimethyl-1,4,7-triazacyclononan: Die Kristallstruktur seiner monoprotonierten Form [C9H22N3]ClO4) / Acid-Base Properties of the Cyclic Triamine N,N′,N″-Trimethyl-1,4,7-triazacyclononane and Crystal Structure of its Monoprotonated Form [C9H22N3](ClO4)
  6. closo-Halogenohydrohexaborate, I Darstellung der reinen closo-Halogenohydrohexaborate XnB6H6-n2-, n = 1— 6, X = Cl, Br, I, einschlieftlich der Stereoisomeren / closo-Halogenohydrohexaborate, I Preparation of the Pure closo-Halogenohydrohexaborates XnB6H6-n2-, n = 1— 6. X = Cl, Br, I, Including the Stereoisomers
  7. closo-Halogenohydrohexaborate, II 11B-NMR-Spektren der closo-Halogenohydrohexaborate XnB6H6-n2-, n = 0-6; X = Cl, Br, I / closo-Halogenohydrohexaborate, II 11B NMR Spectra of the closo-Halogenohydrohexaborates XnB6H6-n2-, n = 0-6; X = Cl, Br, I
  8. closo-Halogenohydrohexaborate, III Schwingungsspektren der closo-Halogenohydrohexaborate XnB6H6-n2-, n = 1-5; X = Cl, Br, I / closo-Halogenohydrohexaborate, III Vibrational Spectra of the closo-Halogenohydrohexaborates XnB6H6-n2-, n = 1-5; X = Cl, Br, I
  9. Gasphasen-Reaktionen, 58 [1, 2] β-Chlorethylazid: HCl-Eliminierung und Pyrolyse / Gas Phase Reactions, 58 [1, 2] β-Chloroethyl Azide: HCl Elimination and Pyrolysis
  10. Gasphasen-Reaktionen, 59 [1, 2] Die Pyrolysen von Trifluormethylazid und Hexafluorazomethan / Gas Phase Reactions, 59 [1, 2] The Pyrolyses of Trifluoromethylazide and Hexafluoroazomethane
  11. Photoelektronen-Spektren und Moleküleigenschaften, 110 [1,2] Tricyanmethan-Derivate X—C(CN)3 / Photoelectron Spectra and Molecular Properties, 110 [1, 2] Tricyanomethane Derivatives X-C(CN)3
  12. Über Polygermane, XVIII [1] Drucksynthese der mehrfach funktionellen Digermane Ph6-nGe2Cln (n = 2, 3, 4) und von Ph2GeCl2 / On Polygermanes, XVIII [1] Synthesis of the Multifunctional Digermanes Ph6-nGe2Cln (n = 2, 3, 4) and of Ph2GeCl2 under Pressure
  13. Beiträge zur Chemie des Phosphors, 174 [1] 1,3-Diaminotriphosphan(5), H2N-PH-PH-PH-NH2, ein neues Produkt der Spaltung von weißem Phosphor mit Natrium in flüssigem Ammoniak / Contributions to the Chemistry of Phosphorus, 174 [1] 1,3-Diaminotriphosphane(5), H2N-PH-PH-PH-NH2, a Novel Product of the Cleavage of White Phosphorus with Sodium in Liquid Ammonia
  14. Beiträge zur Chemie des Phosphors, 175 [1] Dinatrium-hexadecaphosphid: Darstellung durch Spaltung von weißem Phosphor mit Natrium / Contributions to the Chemistry of Phosphorus, 175 [1] Disodium Hexadecaphosphide: Preparation via Cleavage of White Phosphorus with Sodium
  15. Synthese, IR-, EPR-und Elektronenspektren der Dischwefel-dinitrid-Komplexe [CuCl2(CH3CN)]2 · (μ-S2N2) und [CuCl2]2 · (μ-S2N2) / Synthesis, IR, EPR, and Electronic Spectra of the Disulfur Dinitride Complexes [CuCl2(CH3CN)]2 · (μ-S2N2) and [CuCl2]2 -(μ-S2N2)
  16. Übergangsmetall-Komplexe mit Schwefelliganden, XXVII Synthese und Reaktivität der Nitrosyl-und Nitrido-Ruthenium-Komplexe mit 1,2-Benzoldithiolat-Liganden [Ru(NO)(S2C6H4) 2]- bzw. [Ru(N)(S2C6H4)2]- / Transition Metal Complexes with Sulfur Ligands, XXVII Synthesis and Reactivity of the Nitrosyl- and Nitrido-Ruthenium Complexes with 1,2-Benzenedithiolate Ligands [Ru(NO)(S2C6H4)2]- and [Ru(N)(S2C6H4)2]-, Respectively
  17. Synthese und absolute Konfiguration kettenverzweigter, Cimetidin-analoger Thioether / Synthesis and Absolute Configuration of Chain Branched Cimetidine Analogous Thioethers
  18. The 2-Thioanalogues of tRNA Components Derived from 5-Hydroxyuridine
  19. Transformation of Some tRNA “Wobble Uridines” to their 2-Thioanalogues
  20. Comparison between the Molecular and Crystal Structures of a Benzylpenicillin Ester and its Corresponding Sulfoxide with Drastically Reduced Biological Activity
  21. EPR and ENDOR of Sodium Complexes of Spin Labeled Monoazacrown Ethers
https://doi.org/10.1515/znb-1987-0311
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Articles in the same Issue

  1. Nitrido-Azido-Komplexe des Molybdän(VI): Synthese und Kristallstruktur von MoN(N3)2[HB(3,5-Me2pyz)3] und MoN(N3)Cl[HB(3,5-Me2pyz)3] / Nitrido Azido Complexes of Molybdenum(VI): Synthesis and Crystal Structure of MoN(N3)2[HB(3,5-Me2pyz)3] and MoN(N3)Cl[HB(3,5-Me2pyz)3]
  2. Ein weiteres P-Fluor-Ylid: [N(CH3)2]2PF=CH-CH(n-C4H9)-P[N(CH3)2]2 (4) Darstellung und NMR-Daten / A Further P-Fluoro-Ylide: [N(CH3)2]2 PF=CH-CH(n-C4H9)-P[N(CH3)2] 2 (4) Preparation and NMR Data
  3. Darstellung und Kristallstruktur des Bis(2-amino-1-ammonioethan)hexasulfids [H3N-(CH2)2-NH2]2S6 /Synthesis and Crystal Structure of Bis(2-amino-1-ammonioethan)hexasulfide, [H3N—(CH2)2-NH2]2S6
  4. Darstellung und Kristallstrukturen von [K(crypt-2.2.2)]2 S7 · (H2N-(CH2)2-NH2) und [K(crypt-2.2.2)]2S6 / Synthesis and Crystal Structures of [K(crypt-2.2.2)]2S7 · (H2N-(CH2)2-NH2) and [K(crypt-2.2.2)]2S6
  5. Säure-Base-Eigenschaften des zyklischen Triamins N,N′,N″-Trimethyl-1,4,7-triazacyclononan: Die Kristallstruktur seiner monoprotonierten Form [C9H22N3]ClO4) / Acid-Base Properties of the Cyclic Triamine N,N′,N″-Trimethyl-1,4,7-triazacyclononane and Crystal Structure of its Monoprotonated Form [C9H22N3](ClO4)
  6. closo-Halogenohydrohexaborate, I Darstellung der reinen closo-Halogenohydrohexaborate XnB6H6-n2-, n = 1— 6, X = Cl, Br, I, einschlieftlich der Stereoisomeren / closo-Halogenohydrohexaborate, I Preparation of the Pure closo-Halogenohydrohexaborates XnB6H6-n2-, n = 1— 6. X = Cl, Br, I, Including the Stereoisomers
  7. closo-Halogenohydrohexaborate, II 11B-NMR-Spektren der closo-Halogenohydrohexaborate XnB6H6-n2-, n = 0-6; X = Cl, Br, I / closo-Halogenohydrohexaborate, II 11B NMR Spectra of the closo-Halogenohydrohexaborates XnB6H6-n2-, n = 0-6; X = Cl, Br, I
  8. closo-Halogenohydrohexaborate, III Schwingungsspektren der closo-Halogenohydrohexaborate XnB6H6-n2-, n = 1-5; X = Cl, Br, I / closo-Halogenohydrohexaborate, III Vibrational Spectra of the closo-Halogenohydrohexaborates XnB6H6-n2-, n = 1-5; X = Cl, Br, I
  9. Gasphasen-Reaktionen, 58 [1, 2] β-Chlorethylazid: HCl-Eliminierung und Pyrolyse / Gas Phase Reactions, 58 [1, 2] β-Chloroethyl Azide: HCl Elimination and Pyrolysis
  10. Gasphasen-Reaktionen, 59 [1, 2] Die Pyrolysen von Trifluormethylazid und Hexafluorazomethan / Gas Phase Reactions, 59 [1, 2] The Pyrolyses of Trifluoromethylazide and Hexafluoroazomethane
  11. Photoelektronen-Spektren und Moleküleigenschaften, 110 [1,2] Tricyanmethan-Derivate X—C(CN)3 / Photoelectron Spectra and Molecular Properties, 110 [1, 2] Tricyanomethane Derivatives X-C(CN)3
  12. Über Polygermane, XVIII [1] Drucksynthese der mehrfach funktionellen Digermane Ph6-nGe2Cln (n = 2, 3, 4) und von Ph2GeCl2 / On Polygermanes, XVIII [1] Synthesis of the Multifunctional Digermanes Ph6-nGe2Cln (n = 2, 3, 4) and of Ph2GeCl2 under Pressure
  13. Beiträge zur Chemie des Phosphors, 174 [1] 1,3-Diaminotriphosphan(5), H2N-PH-PH-PH-NH2, ein neues Produkt der Spaltung von weißem Phosphor mit Natrium in flüssigem Ammoniak / Contributions to the Chemistry of Phosphorus, 174 [1] 1,3-Diaminotriphosphane(5), H2N-PH-PH-PH-NH2, a Novel Product of the Cleavage of White Phosphorus with Sodium in Liquid Ammonia
  14. Beiträge zur Chemie des Phosphors, 175 [1] Dinatrium-hexadecaphosphid: Darstellung durch Spaltung von weißem Phosphor mit Natrium / Contributions to the Chemistry of Phosphorus, 175 [1] Disodium Hexadecaphosphide: Preparation via Cleavage of White Phosphorus with Sodium
  15. Synthese, IR-, EPR-und Elektronenspektren der Dischwefel-dinitrid-Komplexe [CuCl2(CH3CN)]2 · (μ-S2N2) und [CuCl2]2 · (μ-S2N2) / Synthesis, IR, EPR, and Electronic Spectra of the Disulfur Dinitride Complexes [CuCl2(CH3CN)]2 · (μ-S2N2) and [CuCl2]2 -(μ-S2N2)
  16. Übergangsmetall-Komplexe mit Schwefelliganden, XXVII Synthese und Reaktivität der Nitrosyl-und Nitrido-Ruthenium-Komplexe mit 1,2-Benzoldithiolat-Liganden [Ru(NO)(S2C6H4) 2]- bzw. [Ru(N)(S2C6H4)2]- / Transition Metal Complexes with Sulfur Ligands, XXVII Synthesis and Reactivity of the Nitrosyl- and Nitrido-Ruthenium Complexes with 1,2-Benzenedithiolate Ligands [Ru(NO)(S2C6H4)2]- and [Ru(N)(S2C6H4)2]-, Respectively
  17. Synthese und absolute Konfiguration kettenverzweigter, Cimetidin-analoger Thioether / Synthesis and Absolute Configuration of Chain Branched Cimetidine Analogous Thioethers
  18. The 2-Thioanalogues of tRNA Components Derived from 5-Hydroxyuridine
  19. Transformation of Some tRNA “Wobble Uridines” to their 2-Thioanalogues
  20. Comparison between the Molecular and Crystal Structures of a Benzylpenicillin Ester and its Corresponding Sulfoxide with Drastically Reduced Biological Activity
  21. EPR and ENDOR of Sodium Complexes of Spin Labeled Monoazacrown Ethers
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