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expandZfN Section B (126)
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1Author    Ulrich Wannagat, Merten Schlingmann, Horst AutzenRequires cookie*
 Title    Anorganische Fünfringsysteme auf der Basis Silicium/ Stickstoff/Heteroelement * Inorganic Fivemembered Ring Systems Basing upon Silicon, Nitrogen and "Hetero Elements"  
  Reference    (Z. Naturforsch. 31b, 621—640 [1976]; eingegangen am 2. Oktober 1975) 
  Published    1976 
  Keywords    Survey, Preparation, Properties, Structure, Spiranes 
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 TEI-XML for    default:Reihe_B/31/ZNB-1976-31b-0621.pdf 
 Identifier    ZNB-1976-31b-0621 
 Volume    31 
2Author    Fritz Seel, Fritz SchinnerlingRequires cookie*
 Title    Darstellung und thermische Zersetzung von Erdalkalimetall-Carbamoylphospliaten Preparation and Thermal Decomposition of Carbamoylphosphates of Alkaline-earth Metals  
 Abstract    After the formation of carbamoylphosphate through the reaction of KH2PO4 with KNCO in aqueous solution, unreacted phosphate and carbamoylphosphate can be separated by fractional precipitation with barium (first step) and calcium or strontium or barium salt solutions (second step) at low temperatures. The carbamoylphosphates of the alkaline earth metals are decomposed above 100 °C to yield predominantly diphosphates and urea. In aqueous suspensions the decomposition proceeds even at room temperature. -The chemical shifts of the phosphorus atom of the carbamoylphosphate ion between pH 6.5 and 8.2 are given. 
  Reference    Z. Naturforsch. 33b, 374—381 (1978); eingegangen am 31. Januar 1978 
  Published    1978 
  Keywords    Carbamoylphosphates, Preparation, Decomposition, NMR 
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 TEI-XML for    default:Reihe_B/33/ZNB-1978-33b-0374.pdf 
 Identifier    ZNB-1978-33b-0374 
 Volume    33 
3Author    Ulrich Wannagat, Gerd EiseleRequires cookie*
 Title    Neue Silaza-und Silaoxaza-spiro[4.4]nonane und [4.5]decane* Novel Silaza-and Silaoxaza-spiro[4,4]nonanes and [4,5]decanes  
 Abstract    The formerly unknown spiro systems C-F (Scheme I) with silicon in the spiral center and C, Si, N and O in the framework were synthesized via reactions 2-6 and confirmed in their structure by elemental analysis and spectroscopic data (Table I). 
  Reference    Z. Naturforsch. 33b, 471—474 (1978); eingegangen am 28. Februar 1978 
  Published    1978 
  Keywords    Preparation, Properties, Spiranes, Structure 
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 TEI-XML for    default:Reihe_B/33/ZNB-1978-33b-0471.pdf 
 Identifier    ZNB-1978-33b-0471 
 Volume    33 
4Author    A. P. Jekel, J. C. Van De GrampelRequires cookie*
 Title    Derivatives of eis-NPC12(NS0C1)2 and (NPC12)2NS0C1, Part XII [1] Triphenylphosphazenyl Derivatives of NPC12(NS0X)2 and (NPC12)2NS0X with X = F, Cl or Ph  
 Abstract    Reaction of the ring systems NPC12(NS0X)2 and (NPC12)2NS0X (X = F, Cl, Ph) with HNPPI13 in molar ratio 1:2 gives their mono(tripbenylphosphazenyl) derivatives. The compound NPCl(NPPh3)(NSOPh)2 forms a stable 1:1 adduct with acetonitrile. All compounds are characterized by NMR (31 P, 19 F), IR and mass spectra. 
  Reference    Z. Naturforsch. 34b, 569—572 (1979); received December 27 1978 
  Published    1979 
  Keywords    Triphenylphosphazenyl Derivatives, Preparation, Characterization 
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 TEI-XML for    default:Reihe_B/34/ZNB-1979-34b-0569.pdf 
 Identifier    ZNB-1979-34b-0569 
 Volume    34 
5Author    Alain Schiff-Frangois, Gerhard Savelsberg, Herbert SchäferRequires cookie*
 Title    Darstellung und Struktur von  
 Abstract    Three sulfurapatites have been prepared. They crystallize in the hexagonal system (P63/m) with the following lattice constants: BaS(As04)2S04: a= 1052.6(5) pm, c= 773.7(4) pm, c/a = 0,735; SrS(As04)2S04: a = 1016.1(8) pm, c= 741(1) pm, c/a = 0.729; SrS(P04)2S04: a = 980.3(8) pm, c= 727(1) pm, c/a = 0.742. 
  Reference    Z. Naturforsch. 34b, 764—765 (1979); eingegangen am 16. Februar 1979 
  Published    1979 
  Keywords    Sulfur Apatite, Preparation, Crystal Structure 
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 TEI-XML for    default:Reihe_B/34/ZNB-1979-34b-0764_n.pdf 
 Identifier    ZNB-1979-34b-0764_n 
 Volume    34 
6Author    HansG. Kraft, BerndM. RodeRequires cookie*
 Title    The Compounds Mg(Hacac)2(C104)2 and Ca(Hacac)2(C104)2  
  Reference    Z. Naturforsch. 34b, 886—887 (1979); eingegangen am 25. Januar/15. März 1979 
  Published    1979 
  Keywords    Preparation, Complex Formation, Acetylacetone 
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 TEI-XML for    default:Reihe_B/34/ZNB-1979-34b-0886_n.pdf 
 Identifier    ZNB-1979-34b-0886_n 
 Volume    34 
7Author    Paul Binger, MichaelJ. Doyle, Carl Krüger, Yi-Hung TsayRequires cookie*
 Title    Metallacycloalkane, III [1] Darstellung und Charakterisierung von a.a'-Dipyridyl-Nickelacyclopentan Preparation and Characterisation of a,a'-Bipyridyl-nickelacyclopentane  
 Abstract    The title compound was synthesised from bis-l,5-cyclooctadienenickel, a,a'-bipyridyl and 1,4-dibromobutane in 83% yield and its structure determined by X-ray diffraction (a = 16.600, b = 10.837, c = 14.815 Ä; ß = 153.05°; C2/c, Z = 4; symmetry: C2 with square planar coordinated nickel; Ni-C: 1.949 A). a,a'-Bipyridylnickelcyclopentane reacts with maleic anhydride or methylacrylate under reductive elimination to give cyclobutane in 75 and 57% yield; considerable amounts of butenes are formed, in addition to cyclobutane, upon reaction with borontrifluoride-dibutylether or on thermolysis. 
  Reference    Z. Naturforsch. 34b, 1289—1292 (1979); eingegangen am 16. Mai 1979 
  Published    1979 
  Keywords    Nickelacyclopentane, Preparation, Metallacycloalkane, X-ray 
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 TEI-XML for    default:Reihe_B/34/ZNB-1979-34b-1289.pdf 
 Identifier    ZNB-1979-34b-1289 
 Volume    34 
8Author    Martin JansenRequires cookie*
 Title    Further Compounds A3NO3: K3NO3 and Rb3N03  
 Abstract    K3N03 and RbsNOa were prepared by solid state reaction of equimolar mixtures of K2O/KNO2 and Rb20/RbN02, respectively. According to X-ray powder photographs their crystal structures are derived from the perovs-kite structure. K3N03 is isostructural with Na3N03 (a = 521.7 pm, Z = 1), Rb3N03 represents a tetragonally distorted variant with a = 770.5, c = 550.8 pm and Z = 2. 
  Reference    Z. Naturforsch. 35b, 237—238 (1980); eingegangen am 22. Oktober 1979 
  Published    1980 
  Keywords    Alkalioxidnitrites, Preparation, Crystal Data 
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 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0237_n.pdf 
 Identifier    ZNB-1980-35b-0237_n 
 Volume    35 
9Author    Peter Matje, Günter SchönRequires cookie*
 Title    Ag8SnTe6, ein neuer Vertreter der Argyrodite Ag8SnTe6 -a New Argyrodite  
 Abstract    AggSnTeö has been synthesized by different methods. The Dielectric Absorption Spectra point to a silver ion conductivity. Bei Arbeiten zur dielektrischen Untersuchung des quaternären Ag-Cu-Sn-Te-Systems konnte die Ver-bindung AgsSnTeö erstmals synthetisiert werden. Diese Verbindung ist nach den bisher vorliegenden Daten isotyp zu den schon bekannten argyrodit-analogen Telluriden mit Si und Ge. Nach Arbeiten von Gorochov [1] und anderen Autoren [2, 3] ist im System Ag2Te-SnTe-Te die Verbindung AggSnTee unter deren Bedingungen nicht existent. Es sollte ein Zerfall in mehrere Kom-ponenten wie AgSnTe2, AgzSni-xTe (x < 0,36), Ag5-zTe3 und Ag2Te stattfinden. Das von uns eindeutig als AggSnTee charakteri-sierte Produkt wurde wie folgt dargestellt: Ein stöchiometrisches Gemenge der Elemente (Ag: 99,999%, Sn: 99,999%, Te: 99,99%) wurde in saubersten, getrockneten und vorher evakuierten Quarzampullen eingeschmolzen, danach innerhalb von 24 h auf eine Temperatur von 800 °C geheizt und bei dieser anschließend einen Tag lang gehalten. Nach dem langsamen Abkühlen auf Raumtempera-tur wurde wieder auf diese Temperatur erhitzt, diese einen Tag lang beibehalten und dann innerhalb von zwei Tagen langsam abgekühlt. Das silbriggraue Produkt war gut kristallisiert. Die teilweise stark verwachsenen Kristalle hatten einen oktaedrischen Habitus. Die nach diesem Verfahren synthetisierte Sub-stanz konnte auch mit Spuren Iod als Transport-mittel kristallin erhalten werden (Temperaturen: 820-550 °C substanzseitig). Darüber hinaus gelang es, das nach den oben be-schriebenen Verfahren hergestellte AggSnTee in einer umgebenden B203-Schmelze in offenen Korund-oder Porzellantiegeln an Luft aufzuschmelzen. Zu diesem Zweck wurde innerhalb eines halben Tages auf eine Temperatur von 800 °C aufgeheizt, diese 
  Reference    Z. Naturforsch. 35b, 247 (1980); eingegangen am 31. Oktober 1979 
  Published    1980 
  Keywords    Ternary Chalcogenides, Preparation, Dielectric Spectroscopy 
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 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0247_n.pdf 
 Identifier    ZNB-1980-35b-0247_n 
 Volume    35 
10Author    R. Battaglia, H. Kisch, C. Krüger, L.-K LmRequires cookie*
 Title    Übergangsmetallkomplexe von Diazenen, XV [1] Darstellung und Eigenschaften von Heterodimetallkomplexen des Typs LMM-(C£S-RN=NR)-M'LOT Transition Metal Complexes of Diazenes, XV [1] Synthesis and Properties of Heterodimetal Complexes LnM-(ci<s-RN=NR)-M'Lm  
 Abstract    of type LnM(^ 2 -pentamethylenediazirine)M'L»», LnM/M'Lwj = (CO)5Cr/Mo(CO)5, (CO)5Cr/Fe(CO)4, (CO)5W/Fe(CO)4 and (CO)5Cr/Mn(CO)2 5 J?(-MeC5H4) were prepared from [M'Lm(THF)] or Fe2(CO)9 and (j? 1 -pentamethylenediazirine)MLn. The structure of the Cr/Mo complex was determined by X-ray analysis. The IR and UV-VIS data resemble those of the corresponding homodi-metal complexes. 
  Reference    Z. Naturforsch. 35b, 719—723 (1980); eingegangen am 7. Februar 1980 
  Published    1980 
  Keywords    Diazene Complexes, Preparation, Structure Complexes 
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 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0719.pdf 
 Identifier    ZNB-1980-35b-0719 
 Volume    35 
11Author    Hidenari Inoue, Ekkehard FluckRequires cookie*
 Title    Darstellung und Charakterisierung von Berlinerblau-Analoga des Typs Ti[MB(CN)6] Preparation and Characterization of Prussian Blue Analogs of the Type Ti[MB(CN)6]  
 Abstract    Three compounds of the type Ti[MB(CN)6] (MB = Co, Rh, and Ir) have been synthesized and characterized by means of their X-ray diffraction powder patterns, magnetic measurements, infrared, electronic, and X-ray photoelectron spectra. All compounds crystallize in the face-centered cubic system and form a three-dimensional framework of two octahedral coordination units MBC6 and TiN6. Upon the formation of Ti[MB(CN)6] from the corresponding potassium salt, the jz back-donation in the [MD(CN)6]3-moiety is enhanced by the bridge formation through the cyanide ligand. 
  Reference    Z. Naturforsch. 39b, 185 (1984); eingegangen am 12. Oktober 1983 
  Published    1984 
  Keywords    Preparation, Characterization, Prussian Blue Analogs 
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 TEI-XML for    default:Reihe_B/39/ZNB-1984-39b-0185.pdf 
 Identifier    ZNB-1984-39b-0185 
 Volume    39 
12Author    IhsanA M JasimRequires cookie*
 Title    Zur Reaktion von Hexamethyldistannoxan und Hexamethyldistannthian mit Phosphor-oxo-bzw. -thio-halogeniden. Schwingungsspektren von (Me2PS)20 und (Me2PS)2S A bdel-Fattah Shihada  
 Abstract    M e3S n 0 2PCl2 and (M e2PS)20 are prepared from the reactions o f (M e3Sn)20 with PO C l3 (1:1) and with M e2PSCl (1 :2), respectively. The reactions of (M e3Sn)2S with M e2PSCl and with PSBr3 lead to the formation o f (M e2PS)2S and P4S9, respectively. PO C l3 reacts with (M e3Sn)2S to give unidentified products as a result o f O/S exchange. The i.r. and Raman spectra o f the solids (M e2P S)20 and (M e2PS)2S and the Raman spectra of the m olten com pounds are reported and the frequencies assigned. 
  Reference    Z. Naturforsch. 39b, 783—787 (1984); eingegangen am 16. Januar 1984 
  Published    1984 
  Keywords    R eactions, Preparations, Vibrational Spectra 
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 TEI-XML for    default:Reihe_B/39/ZNB-1984-39b-0783.pdf 
 Identifier    ZNB-1984-39b-0783 
 Volume    39 
13Author    Gerhard Beber, Jürgen Hanich, Kurt DehnickeRequires cookie*
 Title    Reaktionen von Yanadiumtetrachlorid mit Trithiazylchlorid Reactions of Vanadium Tetrachloride with Trithiazylchloride Vanadiumtrichloride-Thiazylchoride Adduct, Tetrachlorovanadate(III)-S 2 N 2  
  Reference    (Z. Naturforsch. 40b, 9—12 [1985]; eingegangen am 24. September 1984) 
  Published    1985 
  Keywords    Adduct, Preparation, IR Spectra 
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 TEI-XML for    default:Reihe_B/40/ZNB-1985-40b-0009.pdf 
 Identifier    ZNB-1985-40b-0009 
 Volume    40 
14Author    KurtO. KleppRequires cookie*
 Title    Darstellung und Kristallstruktur von Tl 2 TiS 4 : Ein Perthiotitanat(IV) mit i-[TiS 4 2 "]-Ketten Preparation and Crystal Structure of Tl 2 TiS 4 : A Perthiotitanate(IV) with ^-[TiS 4 2 ~]-Chains  
 Abstract    Tl 2 TiS 4 is orthorhombic, space group Pbca, with a = 22.176(7), b = 9.484(4), c = 6.3977(9) A, Z = 8. The crystal structure was solved by direct methods and refined to a conventional R of0.058 for 704 reflections with I^3a(I). The crystal structure is characterized by infinite perthioanions, i-[TiS 4/2 (S 2) 2 -], which are separated by Tl + -cations. The anion chains are built up by distorted octahedra which share two skew edges to form infinite cis-chains running along [001], The two unshared S-atoms of each octahedron are connected via a S —S-single bond of 2.10 A length. The crystal structure is described as a mixed packing of TI-and S-atoms, composed of puckered T1S 2 -layers, in which the Ti-atoms occupy the octahedral interstices. The relationship of the ^-[XiS^ -]-chains to the anionic groups of Cs 2 TiS 3 is discussed. 
  Reference    Z. Naturforsch. 40b, 229—234 (1985); eingegangen am 27. September 1984 
  Published    1985 
  Keywords    Thallium Perthiotitanate, Preparation, Crystal Structure 
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 TEI-XML for    default:Reihe_B/40/ZNB-1985-40b-0229.pdf 
 Identifier    ZNB-1985-40b-0229 
 Volume    40 
15Author    Rolf Minkwitz, Rüdiger NaßRequires cookie*
 Title    Darstellung und Eigenschaften von Monofluoramin, H 2 NF Preparation and Properties of Monofluoramine, H 2 NF  
 Abstract    Monofluoramine H ; NF is prepared by thermolysis of H 3 NF + HF 2 ~ -nHF and selective absorp-tion of HF on activated KF. In the solid state H 2 NF is stable below 170 K, and immediately decomposes in NH 4 HF 2 " and N 2 by melting. 
  Reference    Z. Naturforsch. 43b, 1478—1480 (1988); eingegangen am 29. April/22. Juni 1988 
  Published    1988 
  Keywords    Preparation, Spectra, Chemical Properties 
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 TEI-XML for    default:Reihe_B/43/ZNB-1988-43b-1478.pdf 
 Identifier    ZNB-1988-43b-1478 
 Volume    43 
16Author    Brigitte Eisenmann, Roland ZaglerRequires cookie*
 Title    Selenoantimonate  
 Abstract    (V): Darstellung und Struktur von Na3SbSe4, K3SbSe4 und [Ba(en)4]2[Ba(en)3](SbSe4)2 Selenoantim onates(V): Preparation and Crystal Structure of N a3SbSe4, K3SbSe4 and [Ba(en)4]2[Ba(en)3](SbSe4) 2 The crystal structures of N a 3SbSe4, K3SbSe4 and [B a(en)4]2[B a(en)3](SbSe4)2 contain isolated tetrahedral anions SbSe43 -, which are the first exam ples o f selenoantim onates(V). Na3SbSe4 
  Reference    Z. Naturforsch. 44b, 249 (1989); eingegangen am 24. Oktober 1988 
  Published    1989 
  Keywords    Selenoantim onates, Preparation, Crystal Structure 
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 TEI-XML for    default:Reihe_B/44/ZNB-1989-44b-0249.pdf 
 Identifier    ZNB-1989-44b-0249 
 Volume    44 
17Author    Rolf Minkwitz, G. Abriele NowickiRequires cookie*
 Title    Darstellung von SC12F+MF6 (M = A s, Sb) und zusammenfassende  
 Abstract    Betrachtung der Kationen SC1"F3_IJ+ (n = 0 —3) [1] Preparation of SC12F +MF6~ (M = As, Sb) and a Comprehensive Discussion of the Cations SC1"F3_"+ (n = 0 -3) [1] The preparations and characterizations of com pounds SC12F +M F6" (M = As, Sb) are reported. They are yellowish hydrolysable solids, with a strong tendency towards sym metrization in solu­ tion. The mass spectra data indicate the form ation of SC12F2 on thermolysis. The series of SCl"F3_n+-cations (n = 0 —3) is now com plete, and a comprehensive discussion of the spectro­ scopic data is given. 
  Reference    Z. Naturforsch. 44b, 1343 (1989); eingegangen am 6. Juni 1989 
  Published    1989 
  Keywords    Chlorofluorosulfonium Salts, Preparation, Spectra 
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 TEI-XML for    default:Reihe_B/44/ZNB-1989-44b-1343.pdf 
 Identifier    ZNB-1989-44b-1343 
 Volume    44 
18Author    A. Bdel-Fattah, Shihada, HekmatR. YousifRequires cookie*
 Title    Preparation and Vibrational Spectra of M e2S n (0 2PM e2)2, Cl2S n (0 2PMe2)2 and A l( 0 2PM e2)3  
 Abstract    M e2S n (0 2PM e2)2 has been prepared from the reaction o f M e2P 0 2H and M e2SnS in benzene, and A l(0 2PM e2)3 and Cl2S n (0 2PM e2)2 have obtained from the reaction o f M e2P 0 2H with AlClj and SnCl4, respectively in C H 2C12. The vibrational spectra o f the com pounds were found to be consistent with polymeric structures with hexacoordinated metal atoms. 
  Reference    Z. Naturforsch. 46b, 1568—1570 (1991); eingegangen am 29. April 1991 
  Published    1991 
  Keywords    Reactions, Preparations, Vibrational Spectra 
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 TEI-XML for    default:Reihe_B/46/ZNB-1991-46b-1568.pdf 
 Identifier    ZNB-1991-46b-1568 
 Volume    46 
19Author    Peter Remmert, Edmund Fischer, Hans-Ulrich HummelRequires cookie*
 Title    Phasenuntersuchungen im System 2 H a -T a S 2-2 H c -M o S 2 Investigations on Phases in the System 2 H a -T a S 2-2 H c -M o S 2  
 Abstract    Ternary phases in the system TaS2-M o S 2 have been obtained by thermal reactions at 1050 °C of binary layered disulfides and N H 4C1 as promotor. Ternary phases Taj_*Mo*S2 exist in the range 0.5 < jc< 0.9. In the range of 0.25 < * < 0.55 the reactions are quantitative and the phase-compositions are determined by the amounts of the starting materials. For x < 0 .2 lT -T a S 2 and for jc> 0.60 2 H c -M o S 2 are contaminating the resulting ternary phases. Ternary phases have been characterized by X-ray powder diffraction and are indexed rhombohedrally on the basis o f a 3 R-structure with metals in trigonal-prismatic coordination. The phases Tal jcMo*S2 with 0.25 < * < 0.55 show a reversible transition of higher order asso­ ciated with a change in the electrical conductivity mechanism. B elow 420 K the phases show semiconductivity while above 460 K metallic conductivity is observed. 
  Reference    Z. Naturforsch. 49b, 1175—1178 (1994); eingegangen am 15. April 1994 
  Published    1994 
  Keywords    Ternary Phases, Preparation, Phase Transition 
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 TEI-XML for    default:Reihe_B/49/ZNB-1994-49b-1175.pdf 
 Identifier    ZNB-1994-49b-1175 
 Volume    49 
20Author    Rolf Minkwitz, RaimUnd Bröchler, Hans PreutRequires cookie*
 Title    Low-Temperature Crystal Structure of the Inclusion Compound {[N(CH3)4+C1]2] * CH 3CN * h 2o  
 Abstract    The crystal structure of {[N(CH3)4+C1]2}-CFI3C N H 20 is reported. Cry-stalls are orthorhombic, space group Pnma, with a = 1622.9(15), b = 671.3(6), c = 1511.2(11) pm, V = 1646(2) 106 pm3 and Z = 4. 
  Reference    Z. Naturforsch. 51b, 599—601 (1996); eingegangen am 3. August 1995 
  Published    1996 
  Keywords    Preparation, Crystal Structure, Inclusion Compound 
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 TEI-XML for    default:Reihe_B/51/ZNB-1996-51b-0599_n.pdf 
 Identifier    ZNB-1996-51b-0599_n 
 Volume    51 
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