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1Author    Annette Jung, Gotthelf WolmershäuserRequires cookie*
 Title    Bromierung von "Poly(l,4-diselenobenzol)"  
 Abstract    Poly(l,4-diselenobenzene)", obtained by reaction of 1,4-dibromobenzene with disodiumdi-selenide is shown to contain many different polymer sequences. Bromination of the polymer yields a variety of low molecular weight species thus confirming the non-uniformity of the polymer and giving some hints about its composition. The aryl-selenium-bromine compounds 1,4-benzene-diselenenyldibromide, 4,4'-di(bromoselenenyl)-diphenylseleniumdibromide, and bromo-bis(4-bromophenyl)selenonium hexachloroantimonate were fully characterised inclu­ ding X-ray structure determinations. 
  Reference    Z. Naturforsch. 52b, 345—350 (1997); eingegangen am 11. November 1996 
  Published    1997 
  Keywords    Selenium Compounds, Polymers, Crystal Structure " 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-0345.pdf 
 Identifier    ZNB-1997-52b-0345 
 Volume    52 
2Author    H. Jacobs, E.Von OstenRequires cookie*
 Title    The Crystal Structure of a New Modification of Potassium Amide, KNH2  
 Abstract    In the temperature range from 54 to 75 °C a new modification of KNH2 was found, which crystallizes tetragonally a — 4.282 ±0.003 A, c = 6.182 ±0.003 A, and c/o= 1.444 (60 °C), in P 4/nmm -No. 129-, Z = 2, 2 K in 2c 0 1/2 z, z = 0.202(5), 2 N in 2c 0 1/2 z, z = 0.737(15). Its structure is of a deformed sodium chloride type. 
  Reference    (Z. Naturforsch. 31b, 385—386 [1976]; eingegangen am 24. November 1975) 
  Published    1976 
  Keywords    Potassium-Compound, Crystal Structures, Amides 
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 TEI-XML for    default:Reihe_B/31/ZNB-1976-31b-0385_n.pdf 
 Identifier    ZNB-1976-31b-0385_n 
 Volume    31 
3Author    Klaus Deller, Brigitte EisenmannRequires cookie*
 Title    The Crystal Structure of SrAs3  
 Abstract    The new intermetallic compound S1A.S3 crystallizes monoclinic, space group C2/m [a = 9.61(1) A, b = 7.63(1) A, c = 5.88(1) A, ß — 112.9(1)°). The anionic part of the struc-ture contains puckered layers of two-and threebonded As-atoms. 
  Reference    (Z. Naturforsch. 31b, 1550—1551 [1976]; eingegangen am 6. September 1976) 
  Published    1976 
  Keywords    Intermetallic Compounds, Arsenide, Crystal Structure 
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 TEI-XML for    default:Reihe_B/31/ZNB-1976-31b-1550_n.pdf 
 Identifier    ZNB-1976-31b-1550_n 
 Volume    31 
4Author    K. B. Plötz, Hk Müller-BuschbaumRequires cookie*
 Title    Oxoplumbate(II), IV Einbau von Sr 2+ in Pb9Al8021 Solid State Chemistry of Oxoplumbates(II), IV Incorporation of Sr 2+ in Pb9Al802i  
  Reference    (Z. Naturforsch. 37b, 108—109 [1982]; eingegangen am 29. September 1981) 
  Published    1982 
  Keywords    Crystal Structure, Lead, Aluminium, Strontium 
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 TEI-XML for    default:Reihe_B/37/ZNB-1982-37b-0108_n.pdf 
 Identifier    ZNB-1982-37b-0108_n 
 Volume    37 
5Author    Karl-Friedrich Tebbe, Roland FröhlichRequires cookie*
 Title    Beiträge zur Strukturchemie phosphorhaltiger Ketten und Ringe, V [1]  
 Abstract    Die Molekül-und Kristallstruktur des 1.2.3.4-Tetra-ferf-butyl-1.4-bis(trimethylsilyl)tetraphosphans, Me3Si-(«-BuP)4-SiMe3 Structural Chemistry of Phosphorus-Containing Chains and Rings, V [1] Molecular and Crystal Structure of 1,2,3,4-Tetra-ferf-butyl-1,4-bis(trimethylsilyl)tetraphosphane, (H3C)3Si-(f-BuP)4-Si(CH3)3 The compound l,2,3,4-tetra-£er£-butyl-l,4-bis(trimethylsilyl)tetraphosphane, Me3Si-(£-BuP)4-SiMe3, C22H54P4Si2, crystallizes monoclinically in the space group P2i/n (No. 14) with a = 889.9 pm, b = 2292.8 pm, c = 1568.0 pm, ß = 94.14° and Z = 4 formula units. The molecule forms a twisted Si-P4-Si-chain with two kinds of P-P-bonds. The atoms neighbouring the silicium atoms take part in bonds of length d(P-P) = 218.8 pm, whereas the central bond d(P-P) = 221.4 pm is much longer. A special feature of the structure is a short contact d(P-P) = 345.6 pm. Therefore, the inner region of the molecule has the shape of a nearly planar trapezium of the four phosphorus atoms. The periphery of the molecule is as expected. The average bond lengths are d(P-Si) = 228.5 pm, H(P-C) — 190.2 pm, d(Si-C) = 186.6 pm, d(C-C) = 151.8 pm and d(C-H) = 94 pm. 
  Reference    Z. Naturforsch. 37b, 534—541 (1982); eingegangen am 23. Dezember 1981 
  Published    1982 
  Keywords    Tetraphosphane, Phosphorus Chain, Crystal Structure 
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 TEI-XML for    default:Reihe_B/37/ZNB-1982-37b-0534.pdf 
 Identifier    ZNB-1982-37b-0534 
 Volume    37 
6Author    M. Pušelj, Z. Ban, A. DrašnerRequires cookie*
 Title    On the Crystal Structure of HgZn3  
 Abstract    The crystal structure of the intermetallic phase HgZn3 was determined using X-ray single crystal and powder diffraction methods. The phase belongs to the orthorhombic system, most probable space group being Cmc2i, and appears to be isostructural with /S'-Cu3Ti. Under standard preparative conditions a statistical distribution of both atomic species was observed. 
  Reference    Z. Naturforsch. 37b, 557—559 (1982); received December 14 1981 
  Published    1982 
  Keywords    Crystal Structure, Zinc, Mercury, Amalgam 
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 TEI-XML for    default:Reihe_B/37/ZNB-1982-37b-0557.pdf 
 Identifier    ZNB-1982-37b-0557 
 Volume    37 
7Author    Annegret Lipka, Dietrich MootzRequires cookie*
 Title    von Antimontribromid mit Biphenyl, 2 SbBr3 * C12H10 The Crystal Structure of the 2 : 1 Adduct of Antimony Tribromide with Biphenyl, 2SbBr3-Ci2Hio  
 Abstract    The crystal structure of 2 SbBr3 • biphenyl consists of pyramidally shaped SbBr3 molecules and planar biphenyl molecules which form a centrosymmetric complex through bonding of the Sb atoms to the phenyl rings. The distance of the Sb atoms to the phenyl ring planes is 323 pm. Taking into account intramolecular bonds Sb-Br at an average of 250.9 pm, an intermolecular Sb---Br contact at 369.5 pm and the .-r-donor-acceptor inter-action the Sb coordination is distorted -octahedral. The structure is discussed with regard to related compounds. 
  Reference    Z. Naturforsch. 37b, 695—698 (1982) 
  Published    1982 
  Keywords    Crystal Structure, Antimony Trihalides, Biphenyl 
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 TEI-XML for    default:Reihe_B/37/ZNB-1982-37b-0695.pdf 
 Identifier    ZNB-1982-37b-0695 
 Volume    37 
8Author    Helmut Endres, Nasser Kadkhodai-ElyaderaniRequires cookie*
 Title    Malonenamidoxim, Nickelkomplexe und deren ßeaktionsprodukte mit Sauerstoff und Kohlendioxid: Vergleichende Strukturuntersuchungen Malonenamide Oxime, Nickel Complexes, and their Reaction Products with Oxygen and Carbon Dioxide: Comparative Structural Studies  
 Abstract    Malonenamide oxime [HONC(NH2)CH2C(NH2)NOH = C3H8N402] (1), its bis-chelate complex with Ni(II) [Ni(C3HyN402)2] (2) and an ethanol solvate of this complex [Ni(C3H7N402)2 • 0.6 C2H5OH] (3) are characterized by X-ray structure analysis, as well as a paramagnetic tris-complex [Ni(C3H7N402)2(C3HsN402)] (4), which forms a catena structure in the crystal. The molecular structures of two reaction products of 2 with air are described: [Ni(C3H5N403)2(H20)2] • 4 H20 (5) has formed by oxidation of the methylene groups and may be taken as a complex of mesoxalamide oxime; [NiCsHieNsOs] • 6 H20 (6) has a macrocyclic ligand which is a derivative of orthocarbonic acid, formed by addition of carbon dioxide to the oxime groups. 
  Reference    Z. Naturforsch. 37b, 1255—1265 (1982); eingegangen am 25. Mai 1982 
  Published    1982 
  Keywords    a, y-Diondioxime Complexes, Crystal Structure 
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 TEI-XML for    default:Reihe_B/37/ZNB-1982-37b-1255.pdf 
 Identifier    ZNB-1982-37b-1255 
 Volume    37 
9Author    Peter Pullmann, Karl Hensen, JanW. BatsRequires cookie*
 Title    Röntgenstrukturbestimmung von A1C13-Pyridin-Addukten: Der strukturelle Aufbau im fra7is-Dichlorotetrakis(pyridin)aluminium(III)- Tetrachloroaluminat(III) und im Trichlorotris(pyridin)aluminium(III) X-ray Diffraction Study of AICI3-Pyridine Adducts: The Crystal Structure of 7ra/?s-Dichlorotetrakis(pyridine)aluminium(III)tetrachloroaluminat(III) and of Trichlorotris(pyridine)aluminium(III)  
 Abstract    Crystals of [A1(C5H5N)4C12][A1C14] are orthorhombic, Pna2lf Z = 4, a = 18.522(7), b = 15.141(5), c = 9.593(3) A, V = 2690(2) A 3 , Dc = 1.440 g/cm 3 . The structure has been solved from 5968 diffractometer measured intensities and refined by full-matrix least squares to RW(F) = 0.032. The crystal structure shows the complex to be £ra»s-dichloro-tetrakis(pyridine)aluminium(III) tetrachloroaluminat(III). The mean trans Al-Cl-and trans Al-N-distances in the octahedron are 2.279(3) and 2.070(4) A, respectively. Crystals of Al(C5H5N)3Cl3 are monoclinic, P2i/c, Z = 4, a = 7.261(2), b = 29.961(4), c = 8.624(1) A, ß = 98.12(2)°, V -1857(1) A 3 , D0 = 1.326 g/cm 3 . The structure has been solved from 4707 diffractometer measured intensities and refined to RW(F) = 0.028. The crystal structure shows octahedral complexes AICI3 • 3 (C5H5N) with trans geometry. The Al-N-distance trans to chlorine (2.096(2) A) is significantly longer than the two other Al-N-distances (mean 2.072(2) A). 
  Reference    Z. Naturforsch. 37b, 1312—1315 (1982); eingegangen am 5. Mai 1982 
  Published    1982 
  Keywords    Aluminium Chloride, Pyridine, Crystal Structure 
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 TEI-XML for    default:Reihe_B/37/ZNB-1982-37b-1312.pdf 
 Identifier    ZNB-1982-37b-1312 
 Volume    37 
10Author    Bernt Krebs, Andreas Schäffer, Marita HuckeRequires cookie*
 Title    Oxotrihalogenoselenate(IV)  
 Abstract    Darstellung, Struktur und Eigenschaften von P(C6H5)4SeOCl3, P(C6H5)4SeOBr3 und As(C6H5)4SeOBr3 Oxotrihalogenoselenates(IV): Preparation, Structure and Properties of P(C6H5)4SeOCl3, P(C6H5)4SeOBr3 and As(C6H5)4SeOBr3 The novel oxotribromosolenate(IV) SeOBr3~ anion was prepared from the reaction of stoichiometric quantities of SeOBi'2 and bromide in acetonitrile solution, and it was isolated as the tetraphenylphosphonium and -arsonium salts in crystalline form. For the synthesis of the analogous SeOCl3 _ as P(C'6H5)4SeOCl3, SeCl4 was reacted in the presence of a small quantity of H«() with P(CeH5)4Cl in acetonitrile. Complete N-ray structural analyses of P(C6H5)4SeOCi3 (space group P I, a = 10.981(3), b = 11.059(3), c = 10.358(3) A, a = 73.77(2)°, ß = 83.33(2)°, -/ = 80.51(2)°, V -1187.9(6) A 3) and of P(C6H5)4SeOBr3 (space group P 2i/c, a = 11.719(4), b = 16.088(4), c = 13.124(4) A, ß = 94.72(3)°, V = 2466(1) A 3) show dimeric centrosymmetric Se202Cl6 2-and Se202Br6 2 -anions being present in the solid. In the anions two square-pyramidal (y-octahedral) SeOHal4 groups are connected through a common Hal-Hal edge. The axial oxygen ligands (Se-O: 1.597(4) and 1.584(6) A) cause a pronounced stereochemical iraws-activation of the inert pairs at the Se atoms. As(C6H5)4So()Br3 is isotypic with P(C6H5)4SeOCl3. 
  Reference    Z. Naturforsch. 37b, 1410—1417 (1982); eingegangen am 13. Mai 1982 
  Published    1982 
  Keywords    Oxohalogenoselenate, Crystal Structure, Selenium 
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 TEI-XML for    default:Reihe_B/37/ZNB-1982-37b-1410.pdf 
 Identifier    ZNB-1982-37b-1410 
 Volume    37 
11Author    HeinzDieter Lutz, Willi Buchmeier, Bernward EngelenRequires cookie*
 Title    Crystal Structure of Lead Sulfite  
 Abstract    The crystal structure of orthorhombic PbSOß (Pnma, Z = 4, a = 790.3(1), b = 548.8(1), c = 680.2(1) pm) has been determined using single crystal X-ray diffraction data (final R for 663 reflections with I > 2<r(I) = 0.052). The para-meters of the atoms in the asymmetric unit are: Pb(4c) 0.. The sulfite ion has S-O distances of 149.4(7) and 153.7(5) (twice) pm. The Pb-0 distances of the edge-connected Pb-0 7 polyhedra (distorted mono-capped trigonal prism) range from 253.4(5) to 284.8(5) pm. The structure is closely related to that of PbS04. 
  Reference    Z. Naturforsch. 38b, 523—525 (1983); eingegangen am 16. Dezember 1982 
  Published    1983 
  Keywords    Lead Sulfite, Crystal Structure, Sulfite 
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 TEI-XML for    default:Reihe_B/38/ZNB-1983-38b-0523_n.pdf 
 Identifier    ZNB-1983-38b-0523_n 
 Volume    38 
12Author    Karl-Friedrich Tebbe, Roland FröhlichRequires cookie*
 Title    Untersuchungen an Polypseudohalogeniden, II [1] Darstellung und Kristallstruktur des Rubidiumdicyanotriiodids, Rb[I(ICN)2] Preparation and Crystal Structure of Rb[I(ICN)2]  
 Abstract    The new compound Rb[I(ICN)2] can be prepared in aqueous solution by simple addition of two mole equivalents of ICN to one formula unit Rbl. The solid is isotypic with CS[I(ICN)2] and crystallizes in the orthorhombic space group Pmmn with a = 16.246 A, b = 6.795 A, c = 4.397 A and Z = 2. The crystal structure has been solved from diffracto-meter data and refined to R = 0.035 for 313 observed reflections. The structure may be interpreted as a layer-like package of Rb+ cations and pentahalide-analogous anions [I(ICN2]~. The anionic groups are angular with symmetry mm 2 and y(I-I--I) = 128.69°, 0>(I--I-C) = 175.5°, <p(I-C-N) = 177°, d(I~-I) = 3.271 A, d(I-C) = 2.11 A, d(C-N) = 1.13 A. The cation is surrounded by a distorted cube of iodine atoms with a minimum distance d(Rb-I) = 3.775 Ä. Some additional results on the reactions of alkali halides and halogenocyans in different solvents are mentioned and compared with those described elsewhere. 
  Reference    Z. Naturforsch. 38b, 549—553 (1983); eingegangen am 14. Februar 1983 
  Published    1983 
  Keywords    Rubidiumdicyanotriiodide, Polypseudohalide, Pseudopentahalide, Crystal Structure 
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 TEI-XML for    default:Reihe_B/38/ZNB-1983-38b-0549.pdf 
 Identifier    ZNB-1983-38b-0549 
 Volume    38 
13Author    Wilhelm Isenberg, NaylaK. Homsy, Jens Anhaus, HerbertW. Roesky, GeorgeM. SheldrickRequires cookie*
 Title    Synthese und Struktur von N2S3C1 + SbCI^ Synthesis and Structure of N2S3C1+ SbCl6~  
 Abstract    N2S3C1+ SbClö -was prepared by chlorination of N4S4 • SbCls with elemental chlorine. The crystals are monoclinic, P2i/c, with a = 1492.4(4), b = 1233.6(2), c = 1437.5(4) pm, ß = 91.40(2)°, and R = 0.059 for 3663 observed reflections. There are two independent cations and anions in the asymmetric symmetric unit. The appreciable interionic inter-action results in a high density of q = 2.642 g • cm -3 (calcd). In einer vorausgegangenen Arbeit berichteten wir u.a. über Reaktionen des Chlortrithiadiazylchlorids 1 mit Lewis-Säuren [1], Bei diesen Reaktionen wird im allgemeinen nur das ionogen gebundene Cl sub-stituiert, so daß sich Verbindungen der Formel N2S3C1+ MCI4-(M = AI, Fe) ergeben. Lediglich SbCls reagiert mit 1 unter Substitution beider Cl zu N2S3(SbCle)2. Die Bildung der monosubstituierten Verbindung N2S3C1+ SbCls -2 wurde nicht beob-achtet. Nun gelang uns die Darstellung von 2 durch Chlorierung des Addukts N4S4 • SbCls [2] mit ele-mentarem Chlor. Experimenteller Teil 
  Reference    Z. Naturforsch. 38b, 808—810 (1983); eingegangen am 25. März 1983 
  Published    1983 
  Keywords    Chlorotrithiadiazol, Hexachloroantimonate, Crystal Structure 
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 TEI-XML for    default:Reihe_B/38/ZNB-1983-38b-0808.pdf 
 Identifier    ZNB-1983-38b-0808 
 Volume    38 
14Author    Walter AbrielRequires cookie*
 Title    Die Kristallstruktur von [Na(H20)3]2TeBr6, ein Hydrat mit Ketten aus flächenkondensierten Na(H20)6-Oktaedern The Crystal Structure of [Na(H20)3]2TeBr6, a Hydrate with Chains of Face-Sharing Na(H20)6 Octahedra  
 Abstract    Using 293 K diffractometer intensity data the structure of [Na(H20)3]2TeBr6 has been determined by single crystal X-ray technique and refined to a final Rw of 0.048. The crystals are monoclinic (space group C2/m) with a — 13.039(4) A, b = 10.899(8) A, c = 6.838(3) A, ß = 115.89(2)° and Z = 2. The structure contains infinite chains parallel [001] built up by face-sharing Na(H20)6-octahedra. Isolated TeBrß 2-octahedra between these chains represent the anion part of the structure, which can be regarded as a packing of layers based on a 3 3 .4 2 .-net consisting of oxygen and bromine atoms. 
  Reference    Z. Naturforsch. 38b, 1543—1547 (1983); eingegangen am 20. Juli 1983 
  Published    1983 
  Keywords    Crystal Structure, Hydrates, Tellurates 
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 TEI-XML for    default:Reihe_B/38/ZNB-1983-38b-1543.pdf 
 Identifier    ZNB-1983-38b-1543 
 Volume    38 
15Author    Willi Buchm, Bernward Engelen, HeinzD. Ieter LutzRequires cookie*
 Title    Kristallstrukturen von NaM g20 H ( S 0 3)2 * H ,(), NaMn20 H ( S 0 3)2 * H20 , N aFe20 H ( S 0 3)2 * H20 , NaCo2O H (S 0 3)2 H 20 und NaZn20 H ( S 0 3)2 H 20 Crystal Structures of NaMg20 H ( S 0 3)2-H 20 , N aM n20 H ( S 0 3)2 * H 20 , N aFe20 H ( S 0 3)2 H 20 , NaCo2OH(SC>3)2 * H 20 , and N aZ n20 H ( S 0 3)2-H 20  
 Abstract    The crystal structures of the isotypic hydroxosulfitom etalates N aM 20 H (S 0 3)2-1 H 20 with M = 
  Reference    Z. Naturforsch. 41b, 852 (1986); eingegangen am 11. März 1986 
  Published    1986 
  Keywords    Sulfites, Crystal Structure, Hydroxosulfitom etalates 
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 TEI-XML for    default:Reihe_B/41/ZNB-1986-41b-0852.pdf 
 Identifier    ZNB-1986-41b-0852 
 Volume    41 
16Author    Bernward Engelen, Willi Buchmeier, HeinzDieter LutzRequires 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 
17Author    Roland Zagler, Brigitte Eisenmann, Herbert SchäferRequires cookie*
 Title    Tritelluride mit komplexierten Kationen: Darstellung und Kristallstruktur von [Ba(en) 3 ]Te 3 und [Ba(en) 4;5 ]Te 3 Tritellurides of Complex Cations: Synthesis and Crystal Structure of [Ba(en) 3 ]Te 3 and [Ba(en) 4 5 ]Te 3  
 Abstract    The two title compounds have been prepared by reaction of appropriate mixtures of the elements in ethylenediamine. The structures have been determined on the basis of single crystal data. [Ba(en) 3 ]Te 3 crystallizes in the monoclinic system, space group P2 (/c with a = 918.0(4), b — 1203.7(6), c = 1639.9(6) pm, ß = 93.4(1)°. In the structure there are bent tritelluride anions Te 3 2 ~ (bond lengths 273.9—278.5 pm, bond angle 105.7°). The Ba 2+ cations are six coordinate by the bidentate ligand ethylenediamine. [Ba(en) 4 5 ]Te 3 crystallizes in the monoclinic system, space group Cc with a = 1752.8(6), b = 938.9(4), c = 3041.7(8) pm, ß = 91.3(1)°. In this structure the bond lengths in the Te 3 2 ~ anions are shorter (272.1—273.1 pm, bond angles 110.9—112.2°). The cations are coordinated by four bidentate ligands, and are connected into pairs by a further ethylenediamine molecule. The resulting dinuclear [Ba(en) 4 ]en[Ba(en) 4 ] 4+ units have the Ba 2+ cations in CN 9. 
  Reference    Z. Naturforsch. 42b, 151—156 (1987); eingegangen am 7. 0ktober/20. November 1986 
  Published    1987 
  Keywords    Tellurides, Polyanions, Crystal Structure 
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 TEI-XML for    default:Reihe_B/42/ZNB-1987-42b-0151.pdf 
 Identifier    ZNB-1987-42b-0151 
 Volume    42 
18Author    H. Erbert, W. Roesky, Nasreddine Benm, Oham Ed, Klaus Keller, Nayla Keweloh, M. Athias, N. Oltem Eyer, GeorgeM. SheldrickRequires cookie*
 Title    Synthesis and Crystal Structure of Seven-M em bered Sulfur Nitrogen Rings Containing Carbon  
 Abstract    The reaction of C1SCF2CF2SC1 and (Me3SiN)2SR2 proceeds with formation of the seven-mem-bered ring compounds 4a, R = CH3, and 4b, R = C2H 5. 4a was shown by an X-ray structure determination to contain a non-planar ring system. 
  Reference    Z. Naturforsch. 42b, 1249—1252 (1987); eingegangen am 5. Mai 1987 
  Published    1987 
  Keywords    Crystal Structure, Sulfur, Nitrogen 
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 TEI-XML for    default:Reihe_B/42/ZNB-1987-42b-1249.pdf 
 Identifier    ZNB-1987-42b-1249 
 Volume    42 
19Author    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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 Identifier    ZNB-1996-51b-0599_n 
 Volume    51 
20Author    Joachim Pethe, Joachim SträhleRequires cookie*
 Title    Synthese und Kristallstruktur von [Au(AuNCO)(AuPPh3)8]Cl Synthesis and Crystal Structure of [Au(AuNCO)(AuPPh3)8]Cl  
 Abstract    The photolysis of Cr(CO)6 and Ph3PAuN3 (1:2) in thf yields the unstable cluster cation [(Ph3PAu)5Cr(CO)4]+ that slowly decomposes to form the new homometallic gold cluster [Au(AuNCO)(AuPPh3)8]Cl. The cluster compound crystallizes in form of red needles in the tetragonal space group 14 with a = 2214.1(3), c = 1408.9(2) pm, and Z = 2. The inner skeleton of the cluster with the symmetry C4 consists of a centered square antiprism of nine Au atoms with the square faces of the antiprism being bridged by the AuNCO group, and a C P anion, respectively. The shortest Au-Au distances exist between the central and the 8+1 peripheral Au atoms ranging between 263.5(1) and 270.6(3) pm, the four Au-Cl distances are 280(1) pm. 
  Reference    Z. Naturforsch. 54b, 381—384 (1999); eingegangen am 3.Dezember 1998 
  Published    1999 
  Keywords    Gold Cluster, Synthesis, Crystal Structure 
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 Identifier    ZNB-1999-54b-0381 
 Volume    54 
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