| 141 | Author
| Jochen Eilermann, Horst Schössner, HelmutA. Lindner | Requires cookie* | | Title
| Chemie polyfunktioneller Liganden  | | | Abstract
| , XLIV [1] Darstellung und Eigenschaften von l.l.l-Tris(diiodarsinomethyl)ethan Chemistry of Polyfunctional Ligands, XLIV [1] Preparation and Characterization of l,l,l-Tris(diiodarsinomethyl)ethane | | |
Reference
| Z. Naturforsch. 33b, 603—605 (1978); eingegangen am 23. März 1978 | | |
Published
| 1978 | | |
Keywords
| l, l, l-Tris(diiodarsinomethyl)ethane, Raman, IR, FIR, *H NMR | | |
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| default:Reihe_B/33/ZNB-1978-33b-0603.pdf | | | Identifier
| ZNB-1978-33b-0603 | | | Volume
| 33 | |
142 | Author
| Albrecht Mewis | Requires cookie* | | Title
| AB2X2-Verbindungen im CaAl2Si2-Typ, V [1] Zur Struktur der Verbindungen CaMn2P2, CaM^As*, SrMn2P2 und SrMn2As2  | | | Abstract
| Four ternary compounds with the formulas CaMn2P2, CaMn2As2, SrMn2P2, and SrMn2As2 have been prepared and investigated by X-ray methods. They are isotypic and crystallize trigonally in a CaAl2Si2-type structure (space group P 3 m 1-D3d) with the lattice constants: | | |
Reference
| Z. Naturforsch. 33b, 606—609 (1978); eingegangen am 20. März 1978 | | |
Published
| 1978 | | |
Keywords
| Strontium Compounds, Calcium Compounds, Manganese, Phosphides, Arsenides | | |
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| default:Reihe_B/33/ZNB-1978-33b-0606.pdf | | | Identifier
| ZNB-1978-33b-0606 | | | Volume
| 33 | |
145 | Author
| V. Propach, D. Reinen, H. Drenkhahn, Hk Müller-Buschbaum | Requires cookie* | | Title
| Über die Farbe von "NiO"  | | | Abstract
| Ligand Field Spectra, Non-Stochiometry Depending on the method of preparation ,,NiO"-single crystals of different colours can be synthesized. It is shown by ligand field spectroscopy that the ligand field and inter-electronic repulsion parameters are the same for the green, yellow and brown crystals. There is definite spectroscopic evidence, that the colour of stochiometric NiO is green. | | |
Reference
| Z. Naturforsch. 33b, 619—621 (1978); eingegangen am 30. Januar/17. April 1978 | | |
Published
| 1978 | | |
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| default:Reihe_B/33/ZNB-1978-33b-0619.pdf | | | Identifier
| ZNB-1978-33b-0619 | | | Volume
| 33 | |
146 | Author
| Norio Miyoshi, Giiti Tomita | Requires cookie* | | Title
| Production and Reaction of Singlet Oxygen in Aqueous Micellar Solutions Using Pyrene as Photosensitizer  | | | Abstract
| The reaction of singlet oxygen with 1,3-diphenylisobenzofuran was investigated in aqueous micellar solutions of sodium dodecyl sulfate and dodecyl trimethylammonium chloride using pyrene as photosensitizer. Singlet oxygen, produced by the photosensitiza-tion of pyrene bound to micelles, oxidized efficiently 1,3-diphenylisobenzofuran bound to micelles. The quantum yield for singlet oxygen production and the rate constant for furan oxidation were determined by the kinetic analysis for the oxidation reaction of furan. Quenching of singlet oxygen by sodium azide competed with the furan oxidation, and its rate constant was also determined. Results obtained were compared with those in methanolic solutions. The quantum yield for singlet oxygen production and the rate constant for furan oxidation were much higher in micellar solutions than those in methanolic solutions. Empty micelles w x as found to act as a considerably strong scavenger for singlet oxygen. The penetration probability of singlet oxygen from aqueous phase into the interior of micelles which bound furan was also estimated. | | |
Reference
| Z. Naturforsch. 33b, 622—627 (1978); received February 24 1978 | | |
Published
| 1978 | | |
Keywords
| Singlet Oxygen, Pyrene, Diphenylisobenzofuran, Micelles | | |
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| default:Reihe_B/33/ZNB-1978-33b-0622.pdf | | | Identifier
| ZNB-1978-33b-0622 | | | Volume
| 33 | |
148 | Author
| Friedrich Bölsing, Assadollah Hakim | Requires cookie* | | Title
| Präparative organische Chemie unter Verwendung einfach herzustellender Katalysatoren A Simple Method for Preparation of Catalysts for Preparative Organic Chemistry  | | | Abstract
| There are numerous simple chemical reactions in which reaction products arise, which compared with the materials at the outset, possess a considerably greater surface area. A significant example is the reaction of aluminium alcoholates with water. Reactions of this kind can, to a certain extent, be used as auxiliary reactions, in order to distribute other materials homogenously. In the chosen example, a material dissolved beforehand in the alcoholate, e.g. a solution of a metal salt, would be transferred in the course of the distributing reaction into the newly-developing structure of the reaction product. In this publication the application of some catalysts thus prepared to some classical organic chemical reactions is described by way of example. | | |
Reference
| Z. Naturforsch. 33b, 632—635 (1978); eingegangen am 9. Februar 1978 | | |
Published
| 1978 | | |
Keywords
| Catalysts, Hydrogenation, Dehydrogenation, Dehydration | | |
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| default:Reihe_B/33/ZNB-1978-33b-0632.pdf | | | Identifier
| ZNB-1978-33b-0632 | | | Volume
| 33 | |
149 | Author
| Horst Böhme, KurtHenning Ahrens, Hans-Joachim Drechsler, Georg Rumbaur | Requires cookie* | | Title
| Zur Synthese von N-(Chlormethyl)carbimidoylchloriden Synthesis of N-(Chloromethyl)carboximidoyl Chlorides  | | | Abstract
| N-(Chloromethyl)carboximidoyl Chlorides, N-(Chloromethyl)carboximidic Acid Chloromethylester, Tris(chloromethyl)amine, l,3-Bis(chloromethyl)-2,2,2,4,4,4-hexachloro-2,2,4,4-tetrahydro-l,3,2,4-diaz£kdiphosphetidine, N-Bis(chloromethyl)phosphoramidic Dichloride | | |
Reference
| Z. Naturforsch. 33b, 636—639 (1978); eingegangen am 22. Februar 1978 | | |
Published
| 1978 | | |
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| default:Reihe_B/33/ZNB-1978-33b-0636.pdf | | | Identifier
| ZNB-1978-33b-0636 | | | Volume
| 33 | |
152 | Author
| OttoJ. Scherer, Ngoc-Tram Külbach, Walter Glässel | Requires cookie* | | Title
| Elementorganische Amin/Imin-Verbindungen, XVIII [1] Amino-Imino-Thiophosphorane: er 3 , A 5 -Phosphazene Elementorganic Amino/Imino Compounds, XVIII [1] Aminoiminothiophosphoranes: o 3 , / 5 -Phosphazenes  | | | Abstract
| The reaction of the aminoiminothiophosphoranes (1) with methanol yields the bisamino-thiophosphoric acid derivatives (3). la and IV b ->VTb element halides form the new P-N element four membered rings 4->-7, which partially exist as a mixture of eis and trans isomers. Different ylide group transfer is observed on the reaction of la with trimethyl -phosphine or trimethyl phosphite. With trimethylphosphine (CH3)3P(S) and a phos-pha(III)azene are formed, with trimethyl phosphite (CH30)3P = NC(CH3)3 and the [2 + 2] cycloaddition product of la and (R3C)(R3Si)N-P = S (R = CH3) can be isolated. | | |
Reference
| Z. Naturforsch. 33b, 652—656 (1978); eingegangen am 16. Februar/13. März 1978 | | |
Published
| 1978 | | |
Keywords
| Ring Closure Reactions, Ylide Group Transfer, NMR | | |
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| default:Reihe_B/33/ZNB-1978-33b-0652.pdf | | | Identifier
| ZNB-1978-33b-0652 | | | Volume
| 33 | |
153 | Author
| M. P. Singh, A. K. Singh, Mandhir Kumar | Requires cookie* | | Title
| Mechanism of Hg(II) Oxidation of D-Galactose in Alkaline Medium  | | | Abstract
| D-Galactose, Nessler's Reagent The present paper deals with the kinetics of oxidation of D-galactose by Nessler's reagent in alkaline medium. The reaction is zero order with respect to Hg(II) and first order with respect to reducing sugar. The direct proportionality of the reaction rate at low hydroxide ion concentrations shows retarding trend at higher concentrations. The reaction rate is inversely proportional to iodide ion concentration. A mechanism has been proposed taking Hgl3~ as the reacting species. | | |
Reference
| Z. Naturforsch. 33b, 657—659 (1978); received February 27 1978 | | |
Published
| 1978 | | |
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| default:Reihe_B/33/ZNB-1978-33b-0657.pdf | | | Identifier
| ZNB-1978-33b-0657 | | | Volume
| 33 | |
154 | Author
| FathyA. Amer, AbdelHamid Harhash, MaryL. Awad | Requires cookie* | | Title
| Synthesis of 2-Methyl-l-phenylthiocarbamoylglyoxal Arylhydrazones and Diethyl(arylazo)(phenylthiocarbamoyl)malonate and their Reactions with Hydrazines  | | | Abstract
| Treatment of a-phenylthiocarbamoyl acetyl acetone (1) with aromatic diazonium salts effects acetyl cleavage with the formation of 2-methyl-l-phenylthiocarbamoylglyoxal arylhydrazones (2a-c), which afford the anilinopyrazoles (5a-c) and the phenylimino-2-pyrazolines (6a-c) on treatment with hydrazine or phenyl hydrazine respectively. Treatment of diethyl a-phenylthiocarbamoyl malonate with aryl diazonium salts gave diethyl (arylazo)(phenylthiocarbamoyl) malonate which afford the 7-phenyl-5-(arylazo)-2,3,7-triazabicyclo[3,2,0]hept-l-ene-4,6-dione (9a, b) and its 3-phenyl derivatives (9c, d) with hydrazines and phenyl hydrazine respectively. | | |
Reference
| Z. Naturforsch. 33b, 660—662 (1978); received January 5 1978 | | |
Published
| 1978 | | |
Keywords
| Hydrazines, Pyrazoles, Arylhydrazones | | |
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| default:Reihe_B/33/ZNB-1978-33b-0660.pdf | | | Identifier
| ZNB-1978-33b-0660 | | | Volume
| 33 | |
156 | Author
| BarryJ. Parsons, Dietrich Schulte-Frohlinde, Clemens Von Sonntag | Requires cookie* | | Title
| Reaction of Br3' 2 -with 2-Deoxy-D-ribose. A Preferred Attack at C-l  | | | Abstract
| In the photolysis of 5-bromouracil containing DNA Br atoms are expected inter mediates. In order to evaluate the possible site of attack of the Br atom at the sugar moiety of DNA the reaction of 2-deoxy-D-ribose with the Br atom (complexed with two bromide ions) was investigated. Hydroxyl radicals generated by the radiolysis of N20 saturated aqueous solutions were converted into Br3 -2_ radicals by 1 M bromide ions. Br3-2-reacts with 2-deoxy-D-ribose (k = 3.7 • 10 4 M -1 s -1 , pulse radiolysis). The major product is 2-deoxy-D-erythro-pentonic acid (G = 2.4, y-radiolysis). It is formed by hydrogen abstraction from C-l and oxidation of this radical by other radicals. An alternative route via the radical at C-2 is neglible. It follows that Br3-2 ~ reacts preferentially at C-l of 2-deoxy-£>-ribose. | | |
Reference
| Z. Naturforsch. 33b, 666—668 (1978); received March 15 1978 | | |
Published
| 1978 | | |
Keywords
| Pulse Radiolysis, y-Radiolysis, 2-Deoxy-D-ribose, G-values, Radical Reactions | | |
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| default:Reihe_B/33/ZNB-1978-33b-0666.pdf | | | Identifier
| ZNB-1978-33b-0666 | | | Volume
| 33 | |
159 | Author
| W. Maringgele, A. Meiler, H. Nöth, R. Schroen | Requires cookie* | | Title
| Darstellung und Assoziation einiger Phosphiniminoborane Preparation and Association of Some Phosphiniminoboranes  | | | Abstract
| Triphenylphosphiniminodihalogenoboranes, Triphenylphosphindiorganylboranes, NMR N -Trimethylsily 1 -triphenylphosphinimine re -acts with halogenoboranes R2BX (R = organyl, F, Cl, Br; X = F, Cl, Br) to yield triphenylphos-phiniminodihalogenoboranes and triphenylphos-phiniminodiorganylboranes, respectively. In so-lution, the dihalogeno compounds are associated, probably dimeric, while the diorganyl derivatives are monomeric. Mass spectroscopic data of the compounds show them to be monomeric in the vapor phase. | | |
Reference
| Z. Naturforsch. 33b, 673—675 (1978); eingegangen am 14. März 1978 | | |
Published
| 1978 | | |
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| default:Reihe_B/33/ZNB-1978-33b-0673_n.pdf | | | Identifier
| ZNB-1978-33b-0673_n | | | Volume
| 33 | |
160 | Author
| Klaus Deller, Brigitte Eisenmann | Requires cookie* | | Title
| BaSb3, ein Antimonid mit einem zwei- dimensional unendlichen [Sb3 2 ] n-Poly anion BaSb3, an Antimonide with an Infinite Twodimensional [Sb3 2 ~]n -Anion  | | | Abstract
| The new compound BaSb3 has been prepared and its structure determined. It crystallizes monoclinic (C 2/m, a = 1080.7(5) pm, b = 851.9(5) pm, c = 647.1(5) pm, ß = 112.66(4)°). The Sb-atoms build up 14-rings of two-and threebonded Sb, which are connected to puckered nets. | | |
Reference
| Z. Naturforsch. 33b, 676—677 (1978); eingegangen am 17. März 1978 | | |
Published
| 1978 | | |
Keywords
| Barium Antimonide, Crystal Structure, Intermetallic Compound | | |
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| default:Reihe_B/33/ZNB-1978-33b-0676_n.pdf | | | Identifier
| ZNB-1978-33b-0676_n | | | Volume
| 33 | |
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