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Facet section ZfN Section B:Volume 042 [X]
Facet Publication Year 1987 [X]

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1

1	Author	Michel Mégnamisi-Bélombé, Helmut Endres	Requires cookie*
	Title	Two Modifications of Tetraethylammonium tranis-Diiodobis(ethanedialdioximato)cobaltate(III) with and without Intermolecular 1--I Interactions
	Abstract	The structures of two modifications of [C 8 H 2 nN][C4H 6 Col2N 4 04], M r -617.11, have been deter-mined by X-rav investigations. Form 1 is orthorhombic, Pben, a = 8.417(2), b — 12.923(3), c = 18.444(3) A, V = 2006 Ä 3 , Z = 4, d c = 2.04 gem" 3 , final R w = 0.037 for 1989 reflections and 124 parameters. There are no unusual intermolecular interactions in this modification. From 2 is tetragonal, \A x md, a = 8.886(3), c = 25.841(6) Ä, V = 2040 Ä 3 , Z = 4, d c = 2.01 gem" 3 , final R w = 0.027 for 1629 reflections and 80 parameters. In this modification the metal complexes form strictly linear chains via short intermolecular I -I contacts, 3.722(1) Ä.
	Reference	(Z. Naturforsch. 42b, 1—4 [1987]; received August 21 1986)
	Published	1987
	Keywords	Structure, Dioxime Complex, Iodine Interactions, Linear Chain Compounds
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	TEI-XML for	default:Reihe_B/42/ZNB-1987-42b-0001.pdf
	Identifier	ZNB-1987-42b-0001
	Volume	42

2	Author	Helmut Endres	Requires cookie*
	Title	Two Modifications of Di[tetra(methylthio)tetrathiafulvalenium] Hexachlorodicuprate(II), [(TTM-TTF) + ] 2 [CU 2 C1 6 ] 2 "
	Reference	(Z. Naturforsch. 42b, 5—11 [1987]; received September 8 1986)
	Published	1987
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	TEI-XML for	default:Reihe_B/42/ZNB-1987-42b-0005.pdf
	Identifier	ZNB-1987-42b-0005
	Volume	42

3	Author	Manfred Lissel	Requires cookie*
	Title	Reaktionen mit Kaliumsuperoxid 3 [1] Über den Mechanismus der Ketonspaltung durch K0 2 Reactions with Potassium Superoxide 3 [1] On the Mechanism of the Cleavage of Ketones by K0 2
	Abstract	Some experiments on the mechanism of the oxidative cleavage of ketones are presented. The results show that the general mechanism of base catalysed autoxidation is operating.
	Reference	(Z. Naturforsch. 42b, 12—14 [1987]; eingegangen am 4. August/24. September 1986)
	Published	1987
	Keywords	Superoxide, Potassium Superoxide, Ketones
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	TEI-XML for	default:Reihe_B/42/ZNB-1987-42b-0012.pdf
	Identifier	ZNB-1987-42b-0012
	Volume	42

4	Author	Vicente Fernández, Moisés Morán, JuanCarlos Doadrio, Elke Conradi, Wolfgang Willing, Ulrich Müller	Requires cookie*
	Title	EPR-Spektren von Tetrachlorocupraten verschiedener Aminothiazoliumderivate. Die Kristallstrukturen von 2-Amino-2-thiazolinium-und 2-Amino-4-methylthiazoliumtetrachlorocuprat(II) EPR Spectra of Tetrachlorocuprates of Several Aminothiazolium Derivatives. The Crystal Structures of 2-Amino-2-thiazolinium and 2-Amino-4-methylthiazolium Tetrachlorocuprate(II)
	Abstract	The tetrachlorocuprates. of the 2-aminothiazolium ion and of four of its substitution products, of 2-aminothiazolinium, and of 2-amino-4-carboxyl-thiazolidinium ions were prepared from the cor-responding heterocyclic bases, hydrochloric acid and copper(II) chloride in ethanol. The thermo-chromic compounds were characterized by their IR and electronic spectra. The EPR spectra of solutions, frozen solutions, and of the solids show the CUC14 2 ~ ion to have the structure of a flattened tetrahedron; in the case of some of the solids, distortions from D 2 d symmetry are observed. This was confirmed by two X-ray crystal structure determinations. Crystal data: 2-amino-2-thiazolinium tetrachlorocuprate, monoclinic, space group C2/c, a = 2772.8, b = 780.0, c = 1560.0 pm, ß = 112.04°, Z = 8 (R = 0.047 for 2527 observed, independent reflexions); 2-amino-4-methylthiazolium tetrachlorocuprate, triclinic. PI, a = 780.4, b = 853.4, c — 1381.4 pm, a = 103.50, ß = 99.39, y = 104.17°, Z = 2 (R = 0.041 for 3319 reflexions). In both compounds the flattened CuCl 4 2 " tetrahedron is distorted and has two bond angles in the range between 130 and 141°. The heterocyclic cations are protonated at their ring N atoms; the corresponding H atoms and the H atoms of the amino groups are involved in N — H--C1 hydrogen bonding.
	Reference	(Z. Naturforsch. 42b, 15—22 [1987]; eingegangen am 31. Juli 1986)
	Published	1987
	Keywords	Aminothiazolium Derivates, Tetrachloro Cuprates, EPR Spectra, Crystal Structure
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	TEI-XML for	default:Reihe_B/42/ZNB-1987-42b-0015.pdf
	Identifier	ZNB-1987-42b-0015
	Volume	42

5	Author	Ernst Egert, Ursula Kliebisch, Uwe Klingebiel, Dieter Schmidt	Requires cookie*
	Title	Cyclodi-und -trisilazane — Synthese, Reaktionen und Ringkopplungen Cyclodi-and -trisilazanes — Synthesis, Reactions and Ring Coupling
	Abstract	Contrary to our expectations, a cyclotrisilazane is obtained instead of a cyclodisilazane by the reaction of the lithiated di-rerf-butyldiamino-silane with Hal 2 SiMe 2 . Mono-and disubstitution takes place in reactions of lithiated tetra-isopropyl cyclodisilazane with halogeno-silanes and -boranes. A disubstituted ring reacts with LiOC 4 H 9 -formed from LiC 4 H y and THF — to give an unsymmetrically substituted four-membered ring as proved by a crystal structure determination. Coupling of four-and six-membered rings occurs in the reaction of SiF-substituted and lithiated rings.
	Reference	(Z. Naturforsch. 42b, 23—30 [1987]; eingegangen am 1. September 1986)
	Published	1987
	Keywords	Cyclosilazanes, Substitution, Ring Coupling, Crystal Structure
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	TEI-XML for	default:Reihe_B/42/ZNB-1987-42b-0023.pdf
	Identifier	ZNB-1987-42b-0023
	Volume	42

6	Author	ErhardT K Haupt, Heindirk Tom Dieck, PanayotR. Bontchev	Requires cookie*
	Title	Solution Structures of Pyrophthalones, I Structure and Conformation of l,3-Indandionato-2(2-pyridinium)-betai'n — a 1 H/ 13 C NMR Approach
	Abstract	receivedJune30/September8,1986 'H/ 13 C NMR, Pyrophthalones, Solvent Dependent Structure The complete analysis of the 'H/ 13 C NMR spectra of a-Pyrophthalone and related compounds demonstrates that the earlier static planar description of the molecules is invalid for polar sol-vents, and here the stability of any intramolecular hydrogen bond is small.
	Reference	(Z. Naturforsch. 42b, 31—36 [1987])
	Published	1987
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	Identifier	ZNB-1987-42b-0031
	Volume	42

7	Author	Bernward Engelen, Willi Buchmeier, HeinzDieter Lutz	Requires cookie*
	Title	Zur Polymorphie des Cadmiumsulfits, Kristallstrukturen von CdS0 3 -I, CdS0 3 -II und CdS0 3 -III Polymorphic Cadmium Sulfites, Crystal Structures of CdS0 3 -I, CdS0 3 -II, and CdSO r III
	Abstract	The crystal structures of the anhydrous cadmium sulfites CdS0 3 -I (¥2 x /c, Z=4), CdS0 3 -II (P2/C, Z=8), and CdS0 3 -III (R3, Z=18 for the hexagonal cell) have been determined by means of single crystal X-ray diffraction data. The final R for the 1475, 2349, and 2138 observed reflections are 0.040, 0.034, and 0.073. Coordination of Cd is trigonal-prismatic, a hitherto unknown coordination of Cd in salts of oxoacids, in CdS0 3 -I and CdS0 3 -II, and octahedral in CdS0 3 -III. The Cd0 6 -polyhedra are arranged in two-dimensional (CdS0 3 -I) and three-dimensional (CdS0 3 -II and CdS0 3 -III) networks. S0 3 2-groups act as monodentate and in CdS0 3 -I and CdS0 3 -II also as bidentate ligands. Cd—O distances range from 224.5(3) to 244.6(3) pm, with an average of 231.5 pm for the trigonal-prismatic and of 231.0 pm for the octahedral coordination. S—O dis-tances range from 152.3(3) to 155.3(3) pm with an average of 153.7 pm, the O —S—O angles from 99.2(2) to 106.7(3)° with an average of 103.2°.
	Reference	(Z. Naturforsch. 42b, 37—41 [1987]; eingegangen am 2. Juli/16. September 1986)
	Published	1987
	Keywords	Cadmium Sulfites, Crystal Structure, Sulfites
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	TEI-XML for	default:Reihe_B/42/ZNB-1987-42b-0037.pdf
	Identifier	ZNB-1987-42b-0037
	Volume	42

8	Author	FranzL. Dickert, MichaelW. Vonend	Requires cookie*
	Title	Konkurrierende Koordination von Kronenethern, Perchloratanionen und Lösungsmittelmolekülen am Co(II)-Ion — Eine Leitfähigkeits-und NMR-Studie in Nitromethan Anions and Solvent Molecules at Co(II)-Ions — A Conductivity and NMR Study on Nitromethane
	Abstract	The 1:1 complexes between Co(II) and the crown ethers dibenzo[24]crown-8, dibenzo[18]-crown-6 and [18]crown-6 show a molar conductivity in nitromethane which indicates coordination of even Perchlorate anions. The substitution of this anion by solvent molecules can be monitored by conductometric titrations. This procedure reveals that dibenzo[24]crown-8 and [18]crown-6 is a potent five dentate ligand whereas dibenzo[18]crown-6 strongly coordinates only via three donor atoms. The mixed complexes with crown ether and methanol show strong outer-sphere associa-tion with the Perchlorate anions, which can be confirmed by investigations with [15]crown-5 complexes.
	Reference	(Z. Naturforsch. 42b, 42—46 [1987]; eingegangen am 15. August/17. Oktober 1986)
	Published	1987
	Keywords	Crown Ether, Complex Formation Ionic Conductivity, NMR Spectra
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	TEI-XML for	default:Reihe_B/42/ZNB-1987-42b-0042.pdf
	Identifier	ZNB-1987-42b-0042
	Volume	42

9	Author	Roger Blachnik, Willi Buchmeier, Claudia Schneider, Ulrike Wickel	Requires cookie*
	Title
	Abstract	Phosphorus Selena Iodide, 5-Iodo-2,3,6,7-tetraselena-l,4,5-triphosphabicyclo[221]heptan. Reaction of Phosphorus Selenide with Iodine, Structure of P 3 Se 4 I, 31 P NMR Spectra P 3 Se 4 I is formed by the reaction of molten P 4 Se 3 and I 2 . P 3 Se 4 I is monoclinic, space group P2,/c with the lattice parameters of a = 1130.3(3) pm, b = 654.5(2) pm, c -1420.5(4) pm, ß — 117.64(2)°. d = 3.87 gem" 3 and d v = 3.82 gem" 3 for Z = 4. The structure of the molecule is derived from the structure of a-or /?-P 4 Se 3 I 2 by the substitution of a P—I group by a Se-atom. The P—I, P —P and Se — Se bond lengths are 249.9, 219.2 and 236.9 pm. resp. The mean P—Se bond length is 225.0 pm. The molecule is stabilized by two weak intramolecular P—Se and P—I bonds, comparable to the bonding situation in a-P 4 Se 3 I 2 . The 31 P NMR spectra reveal a coalescence effect, due to equilibrium between two isomeric forms of the molecules.
	Reference	(Z. Naturforsch. 42b, 47—51 [1987]; eingegangen am 16. Juni/21. Juli 1986)
	Published	1987
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	TEI-XML for	default:Reihe_B/42/ZNB-1987-42b-0047.pdf
	Identifier	ZNB-1987-42b-0047
	Volume	42

10	Author	Yuzo Nishida, Masataka Takeuchi	Requires cookie*
	Title	Unique Reactivity of Peroxide Ion Trapped by Binuclear Iron(III) Complex
	Abstract	Binuclear Iron(III) Complex, Peroxide Ion The (1:1) peroxide adduct of the binuclear iron(III) complex exhibited high reactivity towards 1,3-diphenylisobenzofuran, one of the efficient singlet oxygen (] zl g) quencher. The activation of the peroxide ion in this molecule was discussed in relation to the monooxygenase function of this compound.
	Reference	(Z. Naturforsch. 42b, 52—54 [1987]; received April 23 1986)
	Published	1987
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	TEI-XML for	default:Reihe_B/42/ZNB-1987-42b-0052.pdf
	Identifier	ZNB-1987-42b-0052
	Volume	42

11	Author	Josef Geisenberger, Jürgen Erbe, Jürgen Heidrich, Ulrich Nagel, Wolfgang Beck	Requires cookie*
	Title	Pseudohalogenometallverbindungen, LXV [1] Synthese von Tetrazolen und Triazolen über die 1,3-dipolare Cycloaddition an die Azid-Liganden von polymeren Cobalt(III)-und PalIadium(II)-Komplexen. Darstellung und Struktur von 5-TrichlormethyItetrazol Pseudohalogeno Metal Compounds, LXV [1] Synthesis of Tetrazoles and Triazoles via 1,3-Dipolar Cycloaddition to the Azido Ligands of Polymerie Cobalt(III) and Palladium(II) Complexes. Synthesis and Structure of 5-Trichloromethyltetrazole
	Abstract	The cycloaddition of nitriles and of dimethylacetylenedicarboxylate to the azide ligand of polymeric Schiff Base cobalt(III) and phosphine palladium(II) complexes gives the corresponding tetrazolate and triazolate complexes from which the heterocycles could be cleaved by hydrogen chloride. Usually the yields are low; if the heterocycle is soluble in ether or sublimable, yields up to 30% have been obtained. Using this method the hitherto unknown 5-trichlormethyltetrazole could be prepared which was characterized by an X-ray structural analysis. Similarly, the cyclo-addition of azido(tetraphenylporphinato)cobalt(III) with nitriles, cyclohexylisocyanide and Me0 2 CC=CC0 2 Me affords the corresponding complexes with heterocyclic ligands. The prepa-ration of tetraphenylporphyrinato(tricyanmethanido)cobalt(III), (TPP)CoN-CC(CN) 2 , is reported.
	Reference	(Z. Naturforsch. 42b, 55—64 [1987]; eingegangen am 24. Juli 1986)
	Published	1987
	Keywords	Tetrazoles, Triazoles, Polymerie Schiff Base Cobalt(III) Complexes, Phosphine Palladium Complexes with Azide, Tetrazolate and Triazolate Ligands
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	TEI-XML for	default:Reihe_B/42/ZNB-1987-42b-0055.pdf
	Identifier	ZNB-1987-42b-0055
	Volume	42

12	Author	Max Herberhold, Wolfgang Bühlmeyer, Alfred Gieren, Thomas Hübner, J. Wu	Requires cookie*
	Title
	Abstract	Fragmentation of bis(rm-butyl) sulfur diimide, S(NBu') 2 (la), in the presence of Ru 3 (CO)i 2 leads to a yellow tetrahedrane-type complex Ru 2 (CO) 6 (Bu r NS) (3a) containing rer/-butyl sulfur imide as a six-electron ligand. According to the X-ray structure determination the N —S bond (1.716 Ä) is arranged perpendicular to the Ru —Ru axis (2.661 Ä).
	Reference	(Z. Naturforsch. 42b, 65—70 [1987]; eingegangen am 3. September 1986)
	Published	1987
	Keywords	Di(rm-butyl) Sulfur Diimide, tert-Butyl Sulfur Imide, Ruthenium Complex, Tetrahedrane Structures
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	Identifier	ZNB-1987-42b-0065
	Volume	42

13	Author	Heindirk Tom Dieck, Ingo Kleinwächter	Requires cookie*
	Title	Rutheniumkomplexe mit Diazadienen, VI [1] f/ 6 -Cycloheptatrien-und ?7 4 -Norbornadien-diazadien-ruthenium(0)-Komplexe Ruthenium Complexes with Diazadienes, VI [1] ^ 6 -Cycloheptatriene-and >; 4 -Norbornadiene-diazadiene-ruthenium(0) Complexes
	Abstract	Reduction of [(cyclo-C 7 H 8)RuCl 2 ]2 in the presence of a diazadiene RN-CH—CH=NR (DAD; R = 2-C3H7) gives red, airsensitive, sublimable ()/ 6 -C 7 H 8)Ru(DAD) (5). A rigid structure on the basis of the 'H NMR spectrum is excluded. On the other hand pentacoordinate complexes [(j/ 4 -ttor-C 7 H 8)Ru(DAD)P(C 6 H 5) 3 ] (8) or [(^ 4 -«or-C 7 H 8)Ru(DAD)CO] (9) have rigid, C s -sym-metric, square-pyramidal structures. They are obtained by chemical or irreversible electro-chemical reduction of [(>7 4 -rcor-C 7 H 8)Ru(DAD)Cl 2 ] to [(^ 4 -nor-C 7 H 8)Ru(DAD)(solv)] (7) (solv = tetrahydrofuran or acetonitrile) and addition of phosphine or carbon monoxide. 7, in non-coor-dinating solvents, is a stereospecific catalyst for the 1-alkene —trans-2,.. ,-alkene isomerization.
	Reference	(Z. Naturforsch. 42b, 71—76 [1987]; eingegangen am 1. September 1986)
	Published	1987
	Keywords	Ruthenium(O) Complexes, Diazadienes, Cycloheptatriene, Norbornadiene
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	TEI-XML for	default:Reihe_B/42/ZNB-1987-42b-0071.pdf
	Identifier	ZNB-1987-42b-0071
	Volume	42

14	Author	Udo Kunze, Rolf Tittmann	Requires cookie*
	Title	Phosphinsubstituierte Chelatliganden, XXIII [1] Darstellung und NMR-Spektren von Alkyl-arylphosphinothioformamiden, R(Ph)PC(S)NHMe Phosphine-Substituted Chelate Ligands, XXIII [1] Synthesis and NMR Spectra of Alkyl-arylphosphinothioformamides, R(Ph)PC(S)NHMe
	Abstract	A series of alkyl-arylsubstituted N-methyl phosphinothioformamides, R(Ph)PC(S)NHMe (2 a—g), with varying bulkiness of the alkyl rest was synthesized from the racemic secondary phosphines la—g and methyl isothiocyanate. 'H and 13 C NMR spectra of 2a—g reveal signal sets of diastereotopic nuclei due to the asymmetry of the molecule. The chemical shift and coupling constants were confirmed by simulation in case of 2b, c. The vicinal 31 P— 13 C cou-plings of the menthyl and neomenthyl compounds 2f, g show an "anti-Karplus" behaviour CJ(gauche) > ? J(trans)) and allow the conformational assignment of the alicyclic group. The 31 P chemical shifts of 2a—d give a linear correlation with the cone angle of the alkyl substituents quoted from literature.
	Reference	(Z. Naturforsch. 42b, 77—83 [1987]; eingegangen am 8. August 1986)
	Published	1987
	Keywords	Alkyl-arylphosphinothioformamides, Menthyl and Neomenthyl Derivatives, NMR Spectra, Conformational Analysis, Substituent Influence
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	Identifier	ZNB-1987-42b-0077
	Volume	42

15	Author	Richard Neidlein, Dagmar Knecht, Alfred Gieren, Catalina Ruiz-Pérez	Requires cookie*
	Title
	Abstract	The synthesis of 1 by reaction of phenanthro[9,10-c]-l,2,5-selenadiazole with ethylmagnesium-bromide and TeCI 4 is described; the X-ray structure analysis is reported.
	Reference	(Z. Naturforsch. 42b, 84—90 [1987]; eingegangen am 9. August 1986)
	Published	1987
	Keywords	Chalkogen-Diimides, 1, 2, 5-Telluradiazole, X-Ray
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	Identifier	ZNB-1987-42b-0084
	Volume	42

16	Author	Rahman, Sajida Khanum, Yasmin Badar, Kaneez Fatima, Yusuf Ahmad, H.E J	Requires 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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	Identifier	ZNB-1987-42b-0091
	Volume	42

17	Author	M. Hammouda, W. S. Hamama, E. M. Afsah	Requires cookie*
	Title	A Study on the Mannich Reaction with l-Phenylamino-3-indenone
	Abstract	Mannich Reaction. l-Phenylamino-3-indenone Mannich reaction of the title compound 1 with formaldehyde and morpholine, piperidine or piperazine afforded the Mannich bases 3—5 respectively, whereas the indeno[1.2-d]pyrimidines (6—7) were obtained where primary amines were used. Treatment of 2 with formaldehyde gave benz[b]indeno-diazepine (8). The reaction of formaldehyde with 1 was also investigated.
	Reference	(Z. Naturforsch. 42b, 94—96 [1987]; received May 9. 1986)
	Published	1987
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	Identifier	ZNB-1987-42b-0094
	Volume	42

18	Author	RolfW. Saalfrank, Franz Schütz, Hans-Ulrich Hummel	Requires cookie*
	Title	Vinylacetylene aus 1.3-Bis(dialkylamino) -1,3-diethoxyallenen und Alkylidenmalonylchloriden. Kristall-und Molekülstruktur von 3-(Diphenyl)methylen-6-diisopropylamino-5-diisopropyIaminocarbonyl- 2.4-dioxo-3,4-dihydro-2H-pyran [1] Vinylacetylenes from l,3-Bis(dialkylamino)-l,3-diethoxyallenes and Alkylidenemalonyl Chlorides. Crystal and Molecular Structure of 3-(Diphenyl)methylene-6-diisopropylamino-5-diisopropylaminocarbonyl- 2,4-dioxo-3,4-dihydro-2H-pyrane [1]
	Reference	(Z. Naturforsch. 42b, 97—100 [1987]; eingegangen am 14. Juli 1986)
	Published	1987
	Keywords	Tetra Donor Substituted Allenes, Vinylacetylenes, 3-Methylene-2, 4-dioxo-3, 4-dihydro-2H-pyranes, Crystal Structure
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	Identifier	ZNB-1987-42b-0097
	Volume	42

19	Author	Karl Folkers, Cyril Bowers, Xiao Shao-Bo, Pui-Fun, Louisa Tang, Minoru Kubota, Janusz Stepinski, Teresa Kubiak	Requires cookie*
	Title	Activities of Antagonists of the Luteinizing Hormone Releasing Hormone with Emphasis on Positions 1, 5 and 6 and on Positions 1, 2 and 3
	Abstract	Analogs of the luteinizing hormone releasing hormone (LHRH) which are antagonists for controlling ovulation require potency and negligible release of histamine as a side effect. Forty analogs were designed, synthesized and bioassayed in two groups with emphasis upon positions 1, 5 and 6 and upon positions 1, 2 and 3. N-Ac-D-2-Nal 1 , D-pClPhe 2 , D-3-Pal 3 , Ser 4 , Tyr 5 . D-Lys 6 ,
	Reference	(Z. Naturforsch. 42b, 101—106 [1987]; received July 18 1986)
	Published	1987
	Keywords	Luteinizing Hormone Releasing Hormone, a«f/-Ovulatory Activity, Peptide, Antagonist, Histamine Release
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	Identifier	ZNB-1987-42b-0101
	Volume	42

20	Author	Abdel Moneim El-Torgoman, Mohamed Salah, El-Kousy, Zaghloul El, -Shahat Kandeel	Requires cookie*
	Title	Nitriles in Heterocyclic Synthesis: The Reaction of 2-Thiocarbamoyl Cinnamonitriles with Active Methylene Reagents
	Abstract	Heterocyclic Synthesis, 2-Thiocarbamoyl Cinnamonitriles Substituted pyridin-2-thiones, 2-pyridones, thiopyrans and pyranoazoles could be synthesized via the reaction of 2-thiocarbamoyl cinnamonitriles with some active methylene reagents.
	Reference	(Z. Naturforsch. 42b, 107—111 [1987]; received March 25/July 31 1986)
	Published	1987
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	Identifier	ZNB-1987-42b-0107
	Volume	42

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