| 81 | Author
| J. Gosseick, W. W. Lötz | Requires cookie* | | Title
| Bentonit — ein Schichtsilikat — als Katalysator bei der elektrophilen aromatischen Substitution Bentonite, a Layered Silicate in Electrophilic Aromatic Substitution  | | | Abstract
| Bentonite is used as an heterogenous catalyst in the liquid-phase alkylation of benzene and toluene. Der Einsatz von Montmorillonit, einem in Schich-tengittern vorliegenden Aluminiumsilikat mit aus-tauschbaren Kationen, als Hochtemperatur-Kataly-sator für Alkylierungsreaktionen in der Gasphase ist seit längerem bekannt [1]. Im Rahmen unserer Untersuchungen über orga-nisch-chemische Reaktionsabläufe innerhalb zwei-dimensionaler Strukturen setzten wir Calcium-Bentonit -ein zu 78% aus Montmorillonit bestehen-des Aluminiumsilikat -als festen Katalysator in der flüssigen Phase ein. Als sich zeigte, daß Benzol und Brom bei 80 °C glatt in hoher Ausbeute (79%) Brombenzol ergaben, verwandten wir auch Alkyl-halogenide als Reaktionspartner von Aromaten. Mit Benzol erhielten wir monoalkylierte bzw. 1.4-dialkylierte Benzolderivate als Reaktionsprodukte, während mit Toluol als Monosubstitutionsprodukte 1.4-dialkylierte, daneben aber auch 1.3.5-trialky-lierte Benzole entstanden. Dabei ergab die Reaktion von Benzol mit den verschiedenen Butylbromiden eine deutliche | | |
Reference
| Z. Naturforsch. 33b, 346 (1978); eingegangen am 14. Dezember 1977 | | |
Published
| 1978 | | |
Keywords
| Bentonite, Catalyst, Friedel-Crafts-Alkylation | | |
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| default:Reihe_B/33/ZNB-1978-33b-0346_n.pdf | | | Identifier
| ZNB-1978-33b-0346_n | | | Volume
| 33 | |
82 | Author
| ViqarUddin Ahmad, Anwer Basha, Wasimul Haque, H.E J | Requires cookie* | | Title
| New Alkaloids from Prosopis julißora DC  | | | Abstract
| Prosopis juliflora, Piperidine Alkaloids The isolation of three new alkaloids from Prosopis julifiora is reported. A structure for the minor alkaloid julifloridine is suggested. | | |
Reference
| Z. Naturforsch. 33b, 347—348 (1978); received October 21 1977 | | |
Published
| 1978 | | |
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| default:Reihe_B/33/ZNB-1978-33b-0347_n.pdf | | | Identifier
| ZNB-1978-33b-0347_n | | | Volume
| 33 | |
86 | Author
| Marianne Baudler, Anna Marx, Josef Hahn | Requires cookie* | | Title
| Beiträge zur Chemie des Phosphors, 80 [1] Über die Phosphor-Bor-Dreiringverbindung (f-BuP)2BN(i-Pr)2 Contributions to the Chemistry of Phosphorus, 80 [1] About the Phosphorus Boron Three-Membered Ring Compound (£-BuP)2BN(i-Pr)2  | | |
Reference
| Z. Naturforsch. 33b, 355—360 (1978); eingegangen am 18. Januar 1978 | | |
Published
| 1978 | | |
Keywords
| l, 2-Di-£e^butyl-3-di-iso-propylamino-l, 2, 3-diphosphaborirane, Heterocyclophosphanes, Three-membered Ring Compounds, Cyclo-3-bora-l, 2-diphosphanes, Diphosphaboracyclopropanes | | |
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| default:Reihe_B/33/ZNB-1978-33b-0355.pdf | | | Identifier
| ZNB-1978-33b-0355 | | | Volume
| 33 | |
87 | Author
| Margret Sommer, Klaus Weidenhammer, Henning Wienand, ManfredL. Ziegler | Requires cookie* | | Title
| und die Röntgenstrukturanalyse von »? 6 -CH3-C-CH(CH3)-C7H7Mo(CO)3 II 0 Synthesis and Characterisation of the Species R-C7H7Mo(CO)3 and the X-ray Structure Determination of ^ 6 -CH3-C-CH(CH3)-C7H7Mo(CO)3 II 0  | | | Abstract
| Synthesis of R-C7H7Mo(CO)3, X-ray The species R-C7H7Mo(CO)3 (R=-CH2COCH3,-CH(CH3)COCH3,-CH(CH)(CH3)2COCH3) have been synthesized by electrolysing [^ 7 -C7H7Mo(CO)3] + , 7? 7 -C7H7Mo(CO)2Br and the dimers [C7H7Mo(CO)3]2 and (C7H7)2Mo(CO)3, respectively, in suitable ketones and HBr. *H NMR spectra and the X-ray structure determination of (CH3-CO-CH(CH3)-C7H7)Mo(CO)3 revealed the CH3-CO-CH(CH3)-group being bonded to the cycloheptatriene ligand via the a-carbon atom of the ethyl group. | | |
Reference
| Z. Naturforsch. 33b, 361—365 (1978); eingegangen am 30. Dezember 1977 | | |
Published
| 1978 | | |
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| default:Reihe_B/33/ZNB-1978-33b-0361.pdf | | | Identifier
| ZNB-1978-33b-0361 | | | Volume
| 33 | |
88 | Author
| Dieter Messer | Requires cookie* | | Title
| Die Kristallstruktur yon RbGeCl3 The Crystal Structure of RbGeCl3  | | | Abstract
| Structure Determination, Trigonal Pyramidal Ions RbGeCb is prepared from RbCl and Ge(II) in 6 N HCl or by reaction of RbCl with HGeCl3. The compound crystallizes monoclinic, space group P2i/m, with a = 798.8, b = 694.1, c = 580.0 pm, ß = 106.34° and Z = 2. The crystal structure has been deter-mined by SHELX and refined till R = 0.067. RbGeCl3 is built up by Rb+ and pyramidal GeCl3~-units. The coordination of Ge and the anionic framework is discussed. | | |
Reference
| Z. Naturforsch. 33b, 366—369 (1978); eingegangen am 16. Januar 1978 | | |
Published
| 1978 | | |
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| default:Reihe_B/33/ZNB-1978-33b-0366.pdf | | | Identifier
| ZNB-1978-33b-0366 | | | Volume
| 33 | |
89 | Author
| Gerhard Savelsberg, Herbert Schäfer | Requires cookie* | | Title
| Ternäre Pnictide und Chalkogenide von Alkalimetallen und IB-bzw. IIB-Elementen On Ternary Pnictides and Chalkogenides of Alkaline Metals and IB-resp. II B-Elements  | | | Abstract
| The new compounds NaCuSe, NaCuTe, KCuSe, KCuTe and KZnP were prepared and their structures -together with those of KZnSb, NaCdSb and NaZnSb -determined. NaCuSe, NaCuTe and NaZnSb crystallize in a PbFCl type, while NaCdSb forms the awta'-PbCl2-structure. KCuSe, KCuTe, KZnP and KZnSb build up the Ni2ln-structure. | | |
Reference
| Z. Naturforsch. 33b, 370—373 (1978); eingegangen am 31. Januar 1978 | | |
Published
| 1978 | | |
Keywords
| Intermetallic Compounds, Crystal Structure, Ternary Pnictides, Ternary Chalkogenides | | |
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| default:Reihe_B/33/ZNB-1978-33b-0370.pdf | | | Identifier
| ZNB-1978-33b-0370 | | | Volume
| 33 | |
91 | Author
| Albrecht Mewis | Requires cookie* | | Title
| AB2X2 Compounds with the CaAl2Si2 Structure, IV [1]  | | | Abstract
| The four ternary compounds CaZn2Sb2, CaCd2Sb2, SrZn2Sb2, and SrCd2Sb2 have been prepared and investigated by X-ray methods. They are isotypic and crystallize trigönally in a CaAl2Si2-type structure (space group P3ml-D3d) with the following constants: CaZn2Sb2 a = 4.441 ± 0.001 A, c = 7.464 ± 0.002 A; CaCd2Sb2 a = 4.649 ± 0.001 A, c = 7.597 ± 0.002 A; SrZn2Sb2 a = 4.500 ± 0.001 A, c = 7,716 ± 0.002 A; SrCd2Sb2 a = 4.709 ± 0.001 A, c = 7.822 ± 0.003 A. | | |
Reference
| Z. Naturforsch. 33b, 382—384 (1978); eingegangen am 23. Januar 1978 | | |
Published
| 1978 | | |
Keywords
| Calcium Compounds, Strontium Compounds, 2 B-Elements, Antimonides, Crystal Structure | | |
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| default:Reihe_B/33/ZNB-1978-33b-0382.pdf | | | Identifier
| ZNB-1978-33b-0382 | | | Volume
| 33 | |
93 | Author
| Cr Simionescu, S. Dumitriu, V. Bulacovschi, V. I. Popa, B. Simionescu | Requires cookie* | | Title
| Molekulare Reaktionen in kalten Methan-Wasser-Plasmen und die Wirkung von UV-Bestrahlung Molecular Reactions in Cold Methane-Water Plasma and the Effect of UV Irradiation  | | | Abstract
| After passage of methane-water mixtures through the state of a cold plasma, numerous products were identified, especially aldehydes, ketones, alcohols and acids. Their concen-tration was dependent on the methane/water ratio. Irradiation with UV light during or after the process gave transformations of the above compounds to more complex combi-nations. For the formation of ketones, aldehydes, alcohols and acids a detailed mechanism is proposed. | | |
Reference
| Z. Naturforsch. 33b, 390—395 (1978); eingegangen am 8. April 1976 | | |
Published
| 1978 | | |
Keywords
| Methane-Water Plasma, Aldehydes, Ketones, Alcohols, Acids | | |
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| default:Reihe_B/33/ZNB-1978-33b-0390.pdf | | | Identifier
| ZNB-1978-33b-0390 | | | Volume
| 33 | |
95 | Author
| N. Gottstein, H. J. Keller | Requires cookie* | | Title
| .3-Diondioxime und ihre Metall(II)-Komplexe mit den Ionen Nickel(II), Palladium(II) und Platin(II) 1,3-Dionedioximes and their Metal(II) Complexes with Ions Niekel(II), Palladium(II) and Platinum(II)  | | | Abstract
| Planar d 8 -Transition Metal Complexes Several alkyl and aryl substituted 1,3-dionedioximes, like acetylacetonedioxime, have been reacted with nickel(II), palladium(II) and platinum(II) in aqueous or alcoholic solution. Two kinds of complexes were obtained: (i) those with stoichiometry metal: ligand =1:1 and (ii) bis(l,3-dionedioximato)metal(II) complexes. None of the isolated solid compounds showed any sign of appreciable intermolecular metal metal interactions. An attempt to enhance intermolecular interaction by oxidizing the compounds with iodine lead to the destruction of all of the complexes. | | |
Reference
| Z. Naturforsch. 33b, 399—402 (1978); eingegangen am 13. Dezember 1977 | | |
Published
| 1978 | | |
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| default:Reihe_B/33/ZNB-1978-33b-0399.pdf | | | Identifier
| ZNB-1978-33b-0399 | | | Volume
| 33 | |
97 | Author
| Henri Brunner, Manfred Muschiol, Wilfried Nowak | Requires cookie* | | Title
| Optisch aktive Übergangsmetall-Komplexe, LVII [1]  | | | Abstract
| (+)-und (—)-C5H5M(CO)(P02R*)X mit M = Fe, "Fe und X = 1, COCH3, CH3 Optically Active Transition Metal Complexes, LVII [1] (+)-and (—)-C5H5M(CO)(P02R*)X with M = Fe, "Fe, and X = I, COCH3, CH3 In the reaction of C5H5Fe(CO)2l and CsHsFefCO^CHa, respectively, with S-(+)-(C6H5)2PN(CH3)CH(CH3)(C6H5) (abbreviated P02R*) the complexes C5H5Fe(CO)(P02R*)I(l),C5H5Fe(CO)(P02R*)COCH3(2),andC5H5Fe(CO)(P02R !,t)CH3(3) are formed as pairs of diastereoisomers the components of which differ only in the configu-ration at the iron atom. CsH5Fe(CO)(P02R*)CH3 (3) can be obtained in higher yield by photochemical decarbonylation of C5H5Fe(CO)(P02R*)COCH3 (2). The (+)s85-and (—)365-diastereoisomers of each pair exhibit different chemical shifts in the X H NMR spectra. Diastereoisomer separation can be achieved by fractional crystallization. Starting with 57 Fe metal (—)365-C5H5 57 Fe(CO)(P02R*)I was prepared via 57 FeI2, 57 Fe(CO)4l2, C5H5 57 Fe(CO)2l, and C5H5 57 Fe(CO)(P02R*)I in order to demonstrate optical activity of a 57 Fe compound in the y region by Mössbauer polarimetry in later experiments to be reported elsewhere. | | |
Reference
| Z. Naturforsch. 33b, 407—411 (1978); eingegangen am 24. Januar 1978 | | |
Published
| 1978 | | |
Keywords
| Diastereoisomer Separation, X H NMR, Optical Activity, Transition Metal Complexes | | |
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| default:Reihe_B/33/ZNB-1978-33b-0407.pdf | | | Identifier
| ZNB-1978-33b-0407 | | | Volume
| 33 | |
98 | Author
| Reinhold Tacke, Roland Niedner | Requires cookie* | | Title
| Sila-Pharmaka, 9. Mitt. [1] Darstellung und Eigenschaften potentiell curarewirksamer Silicium-Verbindungen, I Preparation and Properties of Silicon Compounds with Potential Curare-Like Activity, I  | | | Abstract
| Organosilicon compounds 8, 9 and 10 with potential curare-like action and their precursors 5, 6 and 7 were synthesized for the first time. 5-10 were characterized by their physical and chemical properties, and their structures were confirmed by analyses, 1 H NMR and mass spectroscopy (only for 5-7). The pharmacological and toxicological data of 8, 9 and 10 are reported. | | |
Reference
| Z. Naturforsch. 33b, 412—416 (1978); eingegangen am 3. Februar 1978 | | |
Published
| 1978 | | |
Keywords
| Silicon Compounds, Pharmacological Properties, Toxicological Properties, Curare-Like Activity | | |
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| default:Reihe_B/33/ZNB-1978-33b-0412.pdf | | | Identifier
| ZNB-1978-33b-0412 | | | Volume
| 33 | |
100 | Author
| Claudia Bäk, Klaus Praefcke | Requires cookie* | | Title
| Aromatische Photosubstitutionsreaktionen halogenierter Benzoesäurebenzylester [1] Aromatic Photosubstitution Reactions of Halogenated Benzoic Acid Benzylesters [lj  | | | Abstract
| Aromatic Photosubstitutions A photorearrangement of the benzylester of benzoic acid in ethanol as discribed under formation of 2-benzyl-resp. 4-benzylbenzoic acid does not occur. In dependence of irradiation time and used UV lamp the only definate product found is benzoic acid in different yields (5-21%). On irradiation through Pyrex or Solidex filter glass the benzyl -ester does not react. Benzylesters of 2-halogenated resp. 2,4-or 2,6-dichlorated benzoic acids undergo a photosubstitution of halogens in 2-position against hydrogen or phenyl from the solvent ethanol or benzene resp. A photochemical cleavage of the C-Cl-bond in 4-position as well eis a substitution of halogens against benzyl under formation of 2-benzyl-or 4-benzyl-benzoic acids are not observed. But in some cases benzoic acid or benzylhalides are isolated. | | |
Reference
| Z. Naturforsch. 33b, 420—424 (1978); eingegangen am 30. Dezember 1977 | | |
Published
| 1978 | | |
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| default:Reihe_B/33/ZNB-1978-33b-0420.pdf | | | Identifier
| ZNB-1978-33b-0420 | | | Volume
| 33 | |
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