ZfN: Search Results

Browse byFacets

Bookbag ( 0 )

Facet Publication Year 1981 [X]
Facet section ZfN Section B [X]

Results 332 Items

1

1	Author	Joseph Grobe, BerndHeinz Schneider	Requires cookie*
	Title	Elektrochemische Synthesen, IV [1] Metallcarbonylverbindungen der Eisengruppe
	Abstract	The electrochemical synthesis of iron, cobalt, and nickel carbonyl compounds from metal acetylacetonates of oxidation state + II or + III and from metal anodes is de-scribed, solvent effects and the problem of cluster formation are discussed.
	Reference	(Z. Naturforsch. 36b, 1—7 [1981]; eingegangen am 15. Oktober 1980)
	Published	1981
	Keywords	Electrochemical Synthesis, Iron Carbonyl Compounds, Nickel Carbonyl Compounds, Cobalt Carbonyl Compounds
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0001.pdf
	Identifier	ZNB-1981-36b-0001
	Volume	36

2	Author	Joseph Grobe, BerndHeinz Schneider	Requires cookie*
	Title	Elektrochemische Synthesen, V [1] Phosphansubstituierte Metallcarbonyle der Eisengruppe
	Abstract	The electrochemical synthesis of iron, cobalt, and nickel carbonyl derivatives with phosphane ligands from metal anodes is described.
	Reference	(Z. Naturforsch. 36b, 8—13 [1981]; eingegangen am 15. Oktober 1980)
	Published	1981
	Keywords	Electrochemical Synthesis, Metal Carbonyls, Phosphane Ligands
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0008.pdf
	Identifier	ZNB-1981-36b-0008
	Volume	36

3	Author	F. Hulliger, T. Siegrist	Requires cookie*
	Title	The Crystal Structures of BaSe2 and BaSe3
	Abstract	Crystal Structure, Polyselenides BaSe2 crystallizes with a monoclinic cell, a = 9.820(5), 6 = 4.929(3), c = 9.335(5) A, ß = 118.48(5)°; Z = 4, space group C 2/c. BaSe3 is tetragonal, a = 7.2802(5), c = 4.2495(4) A; Z — 2, space group P42im. Both polyselenides are isotypic with the corresponding poly sulfides.
	Reference	(Z. Naturforsch. 36b, 14—15 [1981]; received September 9 1980)
	Published	1981
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0014.pdf
	Identifier	ZNB-1981-36b-0014
	Volume	36

4	Author	Gerd Becker, Gudrun Gresser, Werner Uhl	Requires cookie*
	Title	Acyl-und Alkylidenphosphane, XV [1] 2.2-Dimethylpropylidinphosphan, eine stabile Verbindung mit einem Phosphoratom der Koordinationszahl
	Abstract	In the presence of small amounts of solid sodium hydroxide, [2,2-dimethyl-l-(trimethyl-siloxy)propylidene]-trimethylsilylphosphine reacts at -f 20 °C to give hexamethyldisil-oxane and 2,2-dimethylpropylidynephosphine (2). In contrast to similar alkylidyne-phosphines this compound is stable at room temperature. The IR and mass spectrum are discussed, and iH, 13 C and 31 P NMR spectral data are given.
	Reference	(Z. Naturforsch. 36b, 16—19 [1981]; eingegangen am 3. Oktober 1980)
	Published	1981
	Keywords	Alkylidynephosphines, 2, 2-Dimethylpropylidynephosphine, P-C Triple Bond
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0016.pdf
	Identifier	ZNB-1981-36b-0016
	Volume	36

5	Author	Ahmet Keçeci, Dieter Rehder	Requires cookie*
	Title	IR, 31 P-, 55 Mn-und 185 187 Re-NMR spektroskopische Untersuchungen an einigen Carbonylmangan-und -rhenium-Komplexen
	Abstract	The IR and NMR spectra of the complexes [M(CO)e]Cl • HCl (M = Mn: 1, M = Re: 2), M(C0)5C02Et (M = Mn: 3, M = Re: 4), [Mn(CO)5PR3][PF6] (5; PR3 = PPh(OPh)2: a, P(n-Pr)3: b, PHPh2: c, PPh(NEt2)2: d, P(p-C6H4F)3: e), [Be(CO)5PHPh8][FF6] (6 c), Mn2(CO)s(PR3)2 (7) and Re2(CO)g(PHPh2)2 (8c) are discussed in the context of a-and ^-interactions in the metal-ligand system and compared with 51 V NMR data of the analogous isoelectronic and isostructural carbonylvanadates (—I). On the basis of these results, the phosphines are arranged in the order of decreasing integral ligand strength according to a>b>c>d. The 55 Mn shielding of 5 is greater than that of 1, which is explained by strong (x-interactions and correspondingly large e-ai* splitting dominating the paramagnetic deshielding term in the pseudooctahedral complexes of type 5. The only rhenium compound accessible to NMR is 2, for which the 185 Re and 187 Re resonances were obtained. 31 P coordination shifts are positive for all complexes. Spectroscopic data for 7c show that this complex presumably has the structure (CO)sMn-Mn(CO)3(PHPh2)2, contrasting 7 a, 7 b, 7d and 7e (local D4d symmetry).
	Reference	(Z. Naturforsch. 36b, 20—26 [1981]; eingegangen am 6. Oktober 1980)
	Published	1981
	Keywords	Carbonylphosphinemanganese, Car bony lphosphinerhenium, IR Spectra, Manganese NMR Spectra, Rhenium NMR Spectra
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0020.pdf
	Identifier	ZNB-1981-36b-0020
	Volume	36

6	Author	Erwin Brechtel, Gerhard Cordier, Herbert Schäfer	Requires cookie*
	Title	Über Oxidpnictide s Zur Kenntnis von B^Mn^bgO und Ba2Mn2Bi20
	Abstract	The new oxide pnictides Ba2Mn2Sb20 and Ba2Mri2Bi20 crystallize in the hexagonal system (space group P63/mmc) with the following constants:
	Reference	(Z. Naturforsch. 36b, 27—30 [1981]; eingegangen am 14. Oktober 1980)
	Published	1981
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0027.pdf
	Identifier	ZNB-1981-36b-0027
	Volume	36

7	Author	Heinrich Nöth, Robert Rurländer, Peter Wolfgardt	Requires cookie*
	Title	Solutions of Lithium Tetrahydrido Aluminates in Ethers: a 'Li and 27 AI NMR Study
	Abstract	Solutions of LiAlH4 in tetrahydrofuran (THF), glycoldimethylether (monoglyme), diglycoldimethylether (diglyme) and triglycoldimethylether (triglyme) as well as solutions of LiAlH4/THF in toluene have been investigated by 7 Li and 27 A1 NMR. It was found that <5 27 A1 is nearly independent of the solvent as is 1 J(A1H). However, the line width of the 27 A1 NMR signal shows strong solvent influences and, in addition, concentration and temperature dependence. Intermolecular hydride exchange becomes rapid in solutions of monoglyme and triglyme at room temperature. This can also be shown by the H/D exchange between LiAlH4 and L1AID4. <5 7 Li data indicate that Li is hexacoordinated in the series of glycoldimethylethers, and LiAlH4 in diglyme seems to be the system in which the AIH4 moiety is least affected by ion pair or triple ion formation.
	Reference	(Z. Naturforsch. 36b, 31—41 [1981]; received July 28 1980)
	Published	1981
	Keywords	Lithium Tetrahydroaluminates, Lithium Tetradeuterioaluminates, 7 Li NMR Spectra, 27 A1 NMR Spectra
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0031.pdf
	Identifier	ZNB-1981-36b-0031
	Volume	36

8	Author	B. P. Baranwal, G. K. Parashar, R. C. Mehrotra	Requires cookie*
	Title	Penta-Coordinated Complexes of Bis(2,4-pentanedionato) Copper(II) with Some Oxygen Donor Organic Solvents
	Reference	(Z. Naturforsch. 36b, 42—44 [1981]; received June 30 1980)
	Published	1981
	Keywords	Bis(2, 4-pentanedionato) Copper(II) Complexes, ER Spectra, Magnetic Moments, IR Spectra
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0042.pdf
	Identifier	ZNB-1981-36b-0042
	Volume	36

9	Author	Herbert Binder, Jürgen Palmtag	Requires cookie*
	Title	Zur Reaktion zwischen Bortrifluorid und Natrium-diethylphosphit Darstellung und Reaktionen von Tris(diethylphosphitoboran) The Reaction between Borontrifluoride and Sodium Diethylphosphite Synthesis and Reactions of Tris(diethylphosphitoborane)
	Abstract	Tris(diethylphosphitoborane) (2) can be synthesized by the reaction of BF3-0(C2H5)2 with sodium diethylphosphite. The chemical behaviour of this new compound and its NMR data are reported.
	Reference	(Z. Naturforsch. 36b, 45—47 [1981]; eingegangen am 22. Juli/9. September 1980)
	Published	1981
	Keywords	Tris(diethylphosphitoborane), Reactions, Rearrangement
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0045.pdf
	Identifier	ZNB-1981-36b-0045
	Volume	36

10	Author	Peter Dehnert, Joseph Grobe, Due Le Van	Requires cookie*
	Title	Perfluormethyl-Element-Liganden, XXTV [I]* Organozinnverbindungen als Reagenzien, DI [2] Spaltungsreaktionen der Element-Element-Bindung in Verbindungen des Typs RnE-ERTO (R = CH3, CF3-E =P, AS, Se, Te * n,m = l, 2)
	Abstract	A systematic study of the cleavage of element-element bonds in compounds of the type R"E-ERm (R = CH3, CF3; E = P, As, S, Se, Te; n,m = 1, 2) by the group IV A element hydrides Me3M'H (M' = Si, Ge, Sn; Me — CH3) has been carried out. To evaluate the reaction pathway, for a number of compounds the attack of H2O, CH3OH, HBr and HI has been investigated. Possible reaction intermediates have been synthesized by in-dependent routes and tested under comparable conditions.
	Reference	(Z. Naturforsch. 36b, 48—54 [1981]; eingegangen am 14. August 1980)
	Published	1981
	Keywords	Organoelement-Element Compounds, Perfluoromethyl Derivatives, NMR Spectra
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0048.pdf
	Identifier	ZNB-1981-36b-0048
	Volume	36

11	Author	Gertrud Kiel	Requires cookie*
	Title	Preparation and Crystal Structure of SbCl3 * I2 * 1,4-Dithiane
	Abstract	The darkred compound SbCl3 • I2 • S2C4H8 has been prepared and its crystal structure determined. This new compound crystallizes in the monoclinic system, space group P2i, with a = 849.2 pm, b = 904.2 pm, c = 923.6 pm and ß = 106.1° at a temperature of 113 K, and with a = 858.8(2) pm, b = 914.7(3) pm, c = 934.0(4) pm and ß = 106.62(3)° at a tem-perature of 293 K, respectively. The structure is buüt up from chains (SC2H4S-I-I-ClSbCl2) oo with a y-trigonal bipyramid around Sb.
	Reference	(Z. Naturforsch. 36b, 55—58 [1981]; eingegangen am 19. August/22. Oktober 1980)
	Published	1981
	Keywords	Iodine Antimony Trichloride 1, 4-Dithiane, Crystal Structure
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0055.pdf
	Identifier	ZNB-1981-36b-0055
	Volume	36

12	Author	A. N. Garg, P. N. Shukla	Requires cookie*
	Title	Mössbauer Spectroscopic Studies of Monosubstituted Pentacyano Ferrate(II) Complexes, Na3 [Fe(CN)5RNH2] * nH20
	Abstract	A series of compounds Na3[Fe(CN)5RNH2] * nH20 where R = -H, -CH3, -C2H5, n-C3H7, n-C4H9 and -CH2C6H5 and RNH2 = C5H5N have been studied by Mössbauer spectroscopy. Quadrupole splitting (A EQ) values vary in a limited range (0.68-0.80 mm/sec) indicating only small distortions in the octahedral geometry of the compounds with the substitution of various amino groups. Isomer shift (6) values remain almost constant suggesting that s-electron density is not affected by substitution.
	Reference	(Z. Naturforsch. 36b, 59—61 [1981]; received September 19 1980)
	Published	1981
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0059.pdf
	Identifier	ZNB-1981-36b-0059
	Volume	36

13	Author	W. Preetz, H. Schulz	Requires cookie*
	Title	Darstellung und spektroskopische Charakterisierung von Tetrakis (chlor o -iodo ) oxalato -osmaten (IV )
	Abstract	On treatment of [OsLjox] 2-with Cl~ the mixed complexes [OsClnI4_nox] 2 -, n = 1, 2, 3, are formed. The isolation and complete separation of the differently coloured geometric isomers is achieved by ion exchange chromatography on diethylaminoethyl cellulose. The IR and Ra spectra are assigned according to point groups Czv, Cs, Ci. The mutual influence of ligands, especially by the high trans effect of I, is indicated by shifts of the distinct vibrational and electronic bands. The observed splittings of I -> Os transitions are attributed to the different groupings I-Os-I, I-Os-Cl, and I-Os-O, important for the distinction of stereoisomers. The CT-bands as well as the d-d-transitions show batho-chromic shifts with increasing number of I-ligands. Up to five spin-orbit components in the NIR region are well resolved. The assignment is improved by the electronic Ra spectra. The fine structure of some d-d-bands originates from coupling with symmetric vibrational modes.
	Reference	(Z. Naturforsch. 36b, 62—69 [1981]; eingegangen am 10. Oktober 1980)
	Published	1981
	Keywords	Tetrakis(chloro-iodo)oxalato-osmates(IV), UV-VIS-NIR Spectra, IR Spectra, Raman Spectra
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0062.pdf
	Identifier	ZNB-1981-36b-0062
	Volume	36

14	Author	Udo Praeckel, Friedo Huber	Requires cookie*
	Title	Darstellung und Charakterisierung von Monoorganobismut(III)-und Bismut(III)-Derivaten von Mercaptocarbonsäuren Preparation and Characterization of Monoorganobismuth(III) and Bismuth (III) Derivatives of Mercaptocarbonic Acids
	Abstract	Acidolysis, Triorganobismuthan, Bismuth(III) -mercaptocarboxylates, Monoorganobismuth(III)-mercaptocarboxylates. Cleavage of Bi-C-bonds in PhßBi (Ph = CßHs) by mercaptocarboxylic acids (H2Mc) depends on solvents and concentration. PhaBi in CHCI3 and H2MC (= mercaptoacetic, 3-and 2-mercaptopropionic, 2-mercaptobenzoic acid) reacted to give Bi(Mc)(HMc); in acetone at lower concentrations PhBi(Mc) (H2Mc — 2-mercaptopropionic, 2-mercapto-benzoic acid) was obtained. MesBi (Me = CH3) and H2Mc gave MeBi(Mc) at all concentra-tions used. Polymeric structures with bridging Mc-groups and four-coordinated Bi are proposed.
	Reference	(Z. Naturforsch. 36b, 70—73 [1981]; eingegangen am 20. Oktober 1980)
	Published	1981
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0070.pdf
	Identifier	ZNB-1981-36b-0070
	Volume	36

15	Author	Jörn Müller, Frerk Lüdemann	Requires cookie*
	Title	Stoßaktivierungs-Massenspektren von C6H6M + -und C7H7M + - Fragment-Ionen aus Übergangsmetall-^-Komplexen Collisional Activation Mass Spectra of C6H6M+ and C7H7M+ Fragment Ions from Transition Metal ^-Complexes
	Abstract	Comparative structure investigations of simple gaseous ions formed by electron impact of organometallic -complexes have been carried out by use of the collisional activation (CA) technique. The CA mass spectra of C6H6M+ ions (M — V, Cr, Fe) arising either from benzene or from methylcyclopentadienyl metal compounds show significant differences indicating different structures of these fragments. Similar observations were made with C7H7M+ ions produced from benzyl or cycloheptatrienyl chromium tricarbonyl derivatives, although the metal-free ligand ions exhibit identical CA mass spectra. The CeHßV 1 -ion arising from C5HsVC7H7 by a rearrangement fragmentation was shown to have the ^-benzene vanadium structure.
	Reference	(Z. Naturforsch. 36b, 74—77 [1981]; eingegangen am 21. Oktober 1980)
	Published	1981
	Keywords	Collisional Activation, Gas Phase Ion Structure Analysis, ^-Complexes
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0074.pdf
	Identifier	ZNB-1981-36b-0074
	Volume	36

16	Author	Reinhard Hemmer, HansAlbert Brune, Ulf Thewalt	Requires cookie*
	Title	Kristall-und Molekülstruktur des (Tetramethylcyclobutadien)cis-1.2-dicyano-ethen-1.2-dithiolato-nickel(II) Crystal and Molecular Structure of (Tetramethylcyclobutadiene)ciS-l,2-dicyano-ethene-l,2-dithiolato-nickel(II)
	Abstract	Nickel(II) Complex, (Tetramethylcyclobutadiene)cw-l,2-dicyano-ethene-l,2-dithiolato-nickel(II), Molecular Structure Single crystals of the title compound, A, have been prepared and studied structurally by X-ray analysis. A crvstallizes in the space group P 2i/n with Z = 4 and lattice parameters a = 11.174(3), b= 15.627(5), c= 8.148(3) A and ß = 92.82(3)°. Within the limits of error the -bonded cyclobutadiene ring is a square with an average C-C-bond distance of 1.465 A; the methyl groups are displaced away from the nickel atom, the average distance between the ring plane and the methyl C-atoms being 0.15 A. The sulfur containing five membered ring has a cyclic delocalized electron distribution.
	Reference	(Z. Naturforsch. 36b, 78—82 [1981]; eingegangen am 17. September 1980)
	Published	1981
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0078.pdf
	Identifier	ZNB-1981-36b-0078
	Volume	36

17	Author	D. Layek, G. C. Papavassiliou	Requires cookie*
	Title	Some New 1-D Compounds with Metal-Halide Chain
	Abstract	Some new mixed valence compounds of the type [M(L-L)2M(L-L)2X2]Y4 (where M = Pt or Pd, L-L = 2NH3 or ethylenediamine, X = Cl, Br or I and Y = HS04, 1/2 S04, C104 or 1/2 PtCU) have been synthesized. The polarized Raman spectra of single crystals show the anisotropic character and the presence of ---M(H)---X-M(IV)-X chains. The method of preparation and the chemical behaviour correspond to the mechanism of the formation of Magnus green salt oxidized product.
	Reference	(Z. Naturforsch. 36b, 83—86 [1981]; received July 28 1980)
	Published	1981
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0083.pdf
	Identifier	ZNB-1981-36b-0083
	Volume	36

18	Author	ThF. Zafiropoulos, S. P. Perlepes, P. V. Ioannou, J. M. Tsangaris, A. G. Galinos	Requires cookie*
	Title	Non Deprotonated Metal Complexes of the Bis-amide Tetradentate Ligand N,N' -(Dipicolyl) -1,8-naphthylenediamine
	Abstract	Complexes of the general formula M(LH2)Cl2 • 2 H2O, where LH2 = N,N'-(dipicolyl)-1,8-naphthylenediamine and M = Mn, Ni and Cu, have been prepared. None of the metal ions used promote amide deprotonation on coordination: LH2 acts as a tetradentate ligand. Distorted octahedral stereochemistries for the complexes in the solid state have been proposed utilising microanalyses, magnetic susceptibilities, molar conductance measure-ments and IR and visible spectral data. The Ni(II) complex exhibits evidence of a poly-meric structure.
	Reference	(Z. Naturforsch. 36b, 87 [1981]; received July 14 1980)
	Published	1981
	Keywords	N, N'-(Dipicolyl)-l, 8-naphthylenediamine, Bis-amide Tetradentate Ligand, Secondary Acid Amide Groups, Non-Deprotonated Complexes, IR Spectra
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0087.pdf
	Identifier	ZNB-1981-36b-0087
	Volume	36

19	Author	Helmut Burdorf, Christoph Eischenbroich	Requires cookie*
	Title	Metall-rr-Komplexe yon Benzolderivaten, XIII [1] Bis(methylthio-/-beiizol)chrom(0) Darstellung und Einsatz als zweizähniger Chelatligand
	Abstract	The thioanisole-7r-complexes (methylthio-^-benzene)-(^-benzene)-chromium (2) and bis(methylthio-r/-benzene)chromium (3) have been prepared via lithiation of bis(rj-benzene)-chromium and consecutive reaction with dimethyldisulfide. H NMR and 13 C NMR spectra of 2 and 3 as well as ESR-spectra of the corresponding radical cations 2t and 3t were recorded and analyzed. In contrast to C(»?.arene)-Si and C(r/-arene)-P bonds, C(1/.arene)-S bonds are stable to solvolysis. With (norbornadiene)tetracarbonylmolybdenum, 3 readily forms [bis(methylthio-?j-benzene)chromium]tetracarbonylmolybdenum (6) wherein 3 functions as a chelating ligand. H and 13 C NMR evidence suggests, that at room temperature 6 undergoes rapid conformational interconversions.
	Reference	(Z. Naturforsch. 36b, 94—101 [1981]; eingegangen am 9. September 1980)
	Published	1981
	Keywords	Thioanisole Sandwich Complexes, X H NMR Spectra, 13 C NMR Spectra, ESR Spectra, Coordination Chemistry
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0094.pdf
	Identifier	ZNB-1981-36b-0094
	Volume	36

20	Author	K. K. Chacko, W. Saenger	Requires cookie*
	Title	The Crystal and Molecular Structure of 2-{8-(2-Aminophenoxy)-3,6-dioxaoctyloxy}benzoic Acid * NaC104, a Linear Polyether with Terminal Amino and Carboxyl Functions' 4
	Abstract	Polyether, Zwitterion, X-ray, 2-{8-(2-Amino phenoxy)-3,6-dioxaoctyloxy}benzoic acid • NaC104 The title compound, C19H23NO6 • NaC104, crystallizes in the monoclinic space group P2i/c with cell dimensions a = 16.374(5), 6 = 9.856(4), c = 27.245(8) A, 0 = 91.88(5)° and Z = 8. The structure of this polyether complex was solved on the basis of 4501 diffracto-meter measured reflections and refined to an Rw of 0.091. There are two molecules per asymmetric unit which are related to each other by an approximate non-crystallographic centre of symmetry. Both complex molecules exist in the favourable zwitterion configura-tion with ion pair attraction between the amino (NH3+) and carboxyl(COO _) end groups of the polyether ligand. The Na+ion is circulary coordinated to all except the oxygen atoms of the aminophenoxy end group of the polyether ligand suggesting that this oxygen has reduced electronegativity. All C-C and C-0 bonds of the ligand exist in favourable gauche and trans conformations.
	Reference	(Z. Naturforsch. 36b, 102—107 [1981]; received October 20 1980)
	Published	1981
	Similar Items	Find
	DEBUG INFO
	TEI-XML for	default:Reihe_B/36/ZNB-1981-36b-0102.pdf
	Identifier	ZNB-1981-36b-0102
	Volume	36

1