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41Author    H. Eribert, W. Adle, Kurt Dehnicke, D. Ieter FenskeRequires cookie*
 Title    (AsPh4)4[CrCl4(/J-N2S2)]4 * 8 CH2C12; Synthese, IR-Spektrum und Kristallstruktur (A sPh4)4[CrCl4(w-N2S2)]4 -8 CH 2C12; Synthesis, IR Spectrum and Crystal Structure  
 Abstract    Trithiazylchloride, (NSC1)3, reacts with metallic chrom ium, with chromium hexacarbonyl, with CrCl3-3 thf, as well as with chrom ium (VI) oxide to form mixtures, in which S4N 3®[CrCl4(N 2S2) ] 0 can be identified as the major product. This com pound reacts with tetraphenylarsonium chloride in dichlorom ethane to form the title com pound, which we have characterized by IR spectroscopy and an X-ray crystal structural analysis. (A sP h4)4[CrCl4(N 2S2)]4 -8 C H 2C12 crystallizes m onoclini-cally in the space group C 2 /c with four formula units per unit cell and with the follow ing lattice constants at —100 °C: a = 2146, b = 2033, c = 3137 pm; ß = 96.0° (9918 independent observed reflexions, R = 0.064). The com pound consists o f A sPh4® ions, tetrameric anions [CrCl4(N 2S2)]44e and included C H 2C12 m olecules. The chromium atom s of the anions occupy the corners o f a nearly ideal square; they are connected via the N -atom s o f planar N 2S2-rings, which are oriented perpendicularly to the Cr4-plane. The chromium atom s com plete their distorted octahedral coordination with four terminal chlorine atom s, the axial ones o f which form short Cl---S-contacts o f average 310 pm to the S-atom s o f the N 2S2-rings. 
  Reference    Z. Naturforsch. 40b, 1314—1319 (1985); eingegangen am 2. Mai 1985 
  Published    1985 
  Keywords    Trithiazylchloride, IR Spectra, Crystal Structure 
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 Identifier    ZNB-1985-40b-1314 
 Volume    40 
42Author    Siegfried Pohl, Wolfgang Saak, Detlev HaaseRequires cookie*
 Title    Darstellung und Kristallstrukturen von (Ph4P)4Sb8I28 und (Ph4P)Sb3l 10 (Ph = C6H5) Synthesis and Crystal Structures of (Ph4P)4Sb8I28 and (Ph4P)Sb3 l 1 0 (Ph = C6H 5)  
 Abstract    The compounds (Ph4P)4Sb8l 28 (1) and (Ph4P)Sb,Iio (2) were prepared by the reaction of Sbl3 and Ph4PI in acetonitrile (molar ratios 2:1 and 3:1 respectively). The structures of 1 and 2 were determined from single crystal X-ray diffraction data. 1 crystallizes in the triclinic space group P I with a = 1321.7(5), b = 1346.7(5), c = 2201.8(8) pm, a = 104.18(2), ß = 99.92(2), y = 100.33(2)°; 2: monoclinic, C2/c, a = 2371.1(2), b = 745.0(1), c = 2495.1(2) pm, ß = 100.75(1)°. Whereas 1 exhibits isolated SbsI284' ions, the anions of 2 are built up of polymeric chains [Sb3I 10_]x. In both compounds the distorted Sbl6 octahedra are linked by common edges. The Sb—I distances are in the range between 277.4 and 354.8 pm (1) and between 277.4 and 342.4 pm (2). The observed structures do not only depend on stoichiometry. the nature of the counter cations, and the possibility of oligomerisation but also on the wide variety of the Sb—I bond strengths and the different bridges formed by iodine. The lone pair of Sb(III) seems to be predominantly 5s: . 
  Reference    Z. Naturforsch. 42b, 1493—1499 (1987); eingegangen am 30. Juni 1987 
  Published    1987 
  Keywords    Iodoantimonates, Synthesis, Crystal Structure 
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 Identifier    ZNB-1987-42b-1493 
 Volume    42 
43Author    H.-Jürgen Meyer, Joachim PickardtRequires cookie*
 Title    Die Kristallstruktur von Calciumhexacyanoferrat(II)- Hexamethylentetramin-Wasser(l/l/6) Ca 2 [Fe(CN) 6 ] * C 6 H 12 N 4 * 6 H 2 0 The Crystal Structure of Calciumhexacyanoferrate(II)- Hexamethylenetetramine-Water(l/l/6) Ca 2 [Fe(CN) 6 ] * C 6 H 12 N 4 * 6 H : 0  
 Abstract    Ca 2 [Fe(CN) 6 ] • C t ,H 1 2N 4 -6H 2 0 crystallizes in the monoclinic space group B2lb with a = 1130,2(4), b = 1373,5(4), c = 1353,0(4) pm and y = 97,17°. The X-ray single crystal structure determination converged at R -0.055 (2057 reflections). Each of the four Fe(CN) 6 octahedra (Z = 4) in the unit cell is coordinated by six Ca atoms with mean N CY AN — Ca distances of 253.5(3) pm. The Ca atoms are bridged by hexamethylenetetramine and water molecules. 
  Reference    Z. Naturforsch. 43b, 135—137 (1988); eingegangen am 31. Juli 1987 
  Published    1988 
  Keywords    Crystal Structure, Hexacyanoferrate, Hexamethylenetetramine 
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 Identifier    ZNB-1988-43b-0135 
 Volume    43 
44Author    Walter Abriel, Hartmut EhrhardtRequires cookie*
 Title    Über hexakoordinierte gemischte Halogeno-Anionen des Te(IV): Kristallographische und Raman-spektroskopische Untersuchungen an Rb 2 TeBr 3 , 5 Cl 2 , 5 On Hexacoordinated Mixed Halogeno Anions of Te(IV): Crystallographic and Raman Spectroscopic Investigation of Rb 2 TeBr 3 5 C1 2 5  
 Abstract    The title compound contains the anions [TeBr 3 Cl 3 ] 2_ and [TeBr 4 Cl 2 ] 2_ in a 1:1 ratio. The corresponding point symmetries, detected by Raman spectroscopic methods, are 3 m and 4/mmm, respectively. The crystal structure analysis exhibits a random distribution of these anions: K 2 PtCl 6 -type, space group Fm3m with a = 10.4602(5) Ä and Z = 4, final R = 0.036 from 178 F n (MoKa). Einführung 
  Reference    Z. Naturforsch. 43b, 557—560 (1988); eingegangen am 7. Januar 1988 
  Published    1988 
  Keywords    Tellurates, Crystal Structure, Raman Spectra 
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 Identifier    ZNB-1988-43b-0557 
 Volume    43 
45Author    Gabi Reber, Jürgen Riede, Gerhard MüllerRequires cookie*
 Title    Molecular Structure of (o-Trimethylsilyl- benzyl)diphenylphosphine  
 Abstract    (o-Trimethylsilylbenzyl)diphenylphosphine (1) crystallizes in the monoclinic space group P2 Jn with a = 14.088(2), b = 8.712(1), c = 16.481(2)Ä, ß = 101.63(1)°, V -1981.3Ä\ Z = 4. There is no P-Si interaction in the solid state which is also found for the solution (31 P NMR, l3 C NMR). 
  Reference    Z. Naturforsch. 43b, 915—917 (1988); eingegangen am 18. März 1988 
  Published    1988 
  Keywords    Benzyl-phosphines, Conformation, Crystal Structure 
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 Identifier    ZNB-1988-43b-0915_n 
 Volume    43 
46Author    HerbertW. Roesky, Michael Zimmer, Regine Herbst, GeorgeM. Sheldrick, Prof Heinz, G. WagnerRequires cookie*
 Title    N,N'-Bis(diphenyIphosphino)-S,S-dimethylsulfodiimin — ein Ligand für cyclische Übergangsmetallkomplexe N,N'-Bis(diphenylphosphino)-S,S-dimethylsulfodiimine — a Ligand for Cyclic Transition Metal Complexes  
 Abstract    Me 2 SN 2 P 2 Ph 4 M(CO) 4 complexes (1) (M: la Cr, lb Mo, lc W) have been synthesized from Me 2 S(NPPh 2) 2 and C 7 H s M(CO) 4 . la—lc are stable at room temperature, lb crystallizes in the space group P2,2,2 with cell constants a = 2486.3(2); b = 1488.8(1); c = 882.0(1) pm. 
  Reference    Z. Naturforsch. 43b, 933—936 (1988); eingegangen am 26. Februar 1988 
  Published    1988 
  Keywords    Crystal Structure, Chromium, Molybdenum, Tungsten 
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 Identifier    ZNB-1988-43b-0933 
 Volume    43 
47Author    Siegfried Pohl, Rainer Lötz, Detlev Haase, Wolfgang SaakRequires cookie*
 Title    Iodoantimonate der Zusammensetzung A + Sb 2 I 7 : Diskrete Anionen in (Me 4 N) 4 Sb 8 I 2 8 und (Me 3 S) 4 Sb 8 I 28 , polymere Ketten in (Me 3 NCH 2 Ph)Sb 2 I 7 (Me = CH 3 , Ph = C 6 H 5 ) Iodoantimonates of Composition A~Sb 2 I 7 ~: Discrete Anions in (Me 4 N) 4 Sb 8 I 28 and (Me 3 S) 4 Sb s I 28 , Polymerie Chains in (Me 3 NCH 2 Ph)Sb 2 I 7 (Me = CH 3 , Ph -C 6 H 5 )  
 Abstract    The reaction of Sbl 3 with Me 4 NI, Me ? SI, and Me^NCH^Phl in acetonitrile (molar ratios 2:1) yields (Me 4 N) 4 Sb 8 I 28 (1). (Me,S) 4 Sb K I 28 (2). and (Me,NCH 2 Ph)Sb : I 7 (3), respectively. The struc-tures of 1—3 were determined from single crystal X-ray diffraction data. 1—3 crystallize in the monoclinic space group P2,/«. 2: a -1434.2(3). b -1484.1(4). c = 2102.6(4) pm. ß = 105.4(1)°, Z = 2. 1: a = 1441.7(1), b = 1545.1(1). c = 2117.3(1) pm. ß = 106.4(1)°, Z = 2. 3: a = 1004.4(1). b = 1378.8(1). c = 1899.3(2) pm. ß = 94.2(1)°. Z = 4. The structures of 1 and 2 are very similar and consist of isolated cations and anions. The Sb s I 28 
  Reference    Z. Naturforsch. 43b, 1144—1150 (1988); eingegangen am 24. Mai 1988 
  Published    1988 
  Keywords    Iodoantimonates, Synthesis, Crystal Structure 
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 Identifier    ZNB-1988-43b-1144 
 Volume    43 
48Author    CarlD. Habben, Mathias NoltemeyerRequires cookie*
 Title    Molekül-und Kristallstruktur  
 Abstract    des l,l-Diethyl-3,5-dimethyl-lA 6 ,4,2,6,3,5-dithiadiazadiborins Molecular and Crystal Structure of l,l-Diethyl-3,5-dimethyl-H 6 ,4,2,6,3,5-dithiadiazadiborine The title compound, isolated from the reaction of SS-diethyl-N,N'-bistrimethylsilylsulfodiimide and 3.5-dimethyl-l,2,4-trithiadiborolane, crystallizes in space group Pbca with cell constants a — 1218.7(6), b = 1295.8(6), c = 1455.7(9) pm, V = 2.2987 nm 3 , Z = 8, Q — 1.167 MgirT 3 . The X-ray structure was refined to R = 0.053. 
  Reference    Z. Naturforsch. 43b, 1683—1684 (1988); eingegangen am 11. August 1988 
  Published    1988 
  Keywords    Crystal Structure, Synthesis, Dithiadiazadiborines 
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 Identifier    ZNB-1988-43b-1683_n 
 Volume    43 
49Author    Petra Krieger-Beck, A. Ndreas Brodbeck, Joachim SträhleRequires cookie*
 Title    Synthesis and Structure of K2A u3, a New Phase in the System Potassium —Gold  
 Abstract    K2A u 3 is obtained from the elem ents in a sealed Ta am poule as air-sensitive needles with a golden lustre. It crystallizes in the orthorhom bic space 
  Reference    Z. Naturforsch. 44b, 237—239 (1989); eingegangen am 18. O ktober 1988 
  Published    1989 
  Keywords    Dipotassium Triauride, Synthesis, Crystal Structure 
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 Identifier    ZNB-1989-44b-0237_n 
 Volume    44 
50Author    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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 Identifier    ZNB-1989-44b-0249 
 Volume    44 
51Author    HansG. Eorg Stammler, Johannes WeissRequires cookie*
 Title    Synthese  
 Abstract    und Kristallstruktur von (S4N3)2Se2Cl10, (S4N3)2Se2CI6 und [(S4N3)SeCl5]n Synthesis and Crystal Structure of (S4N3)2Se2C l10, (S4N3)2Se2Cl6, and [(S4N 3)SeCl5]" (S4N 3)2S e2C l10, (S4N 3)2Se2Clft and [(S4N 3)SeC l5]" are formed by the reaction o f S4N 4, Se2Cl2, and SO C l2. The structures o f the three com pounds where determ ined by X-ray diffraction. The yellow crystals o f (S4N 3)2Se2C l10 are monoclinic, space group P 2,/a, a = 817.5(2) pm , b = 1790.4(5) pm, c = 843.1(6) pm, ß = 104.31(4)°, Z = 2. The Se2C l102~ anion consists o f 2 Cl-bridged distorted octahedra. (S4N 3)2Se2Cl6 forms red m onoclinic crystals, space group P2,/c, a = 1036.5(3) pm , b = 1376.5(5) pm , c = 1400.4(4) pm ,/3 = 100.65(2)°, Z = 4. In the Se2Cl62" anion the Se atoms have a square planar environm ent. The yellow crystals o f (S4N 3)SeC l5 are orthorhom bic, space group P 2 12 12 1, a = 734.2(3) pm , b — 989.4(4) pm , c = 1627.4(6) pm , Z = 4. In the SeC l5_ anion the Se atom has an octahedral environm ent o f chlorine atom s, thus forming a polym eric structure. 
  Reference    Z. Naturforsch. 44b, 1483 (1989); eingegangen am 5. Mai 1989 
  Published    1989 
  Keywords    Thiotrithiazyl-chloroselenates, Synthesis, Crystal Structure 
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 Identifier    ZNB-1989-44b-1483 
 Volume    44 
52Author    SylviaM. Agull, Bernhard Neumüller, K. Urt DehnickeRequires cookie*
 Title    Synthese und Kristallstrukturen der Polyselenido-Mercurate (PPh4)2|H g(Se4)2| und |Cs(18-Krone-6)|2|H g2(Se4)3l Syntheses and Crystal Structures of the Polyselenido M ercurates (PPh4)2[Hg(Se4)2] and [Cs(18-Crown-6)]2[Hg2(Se4)3]  
 Abstract    (PPh4)2[Hg(Se4)J has been prepared by the reaction o f (PPh4)2[Sn(Se4)3] with H g(C H 3COO)2 in dimethylformamide (D M F) solution. [Cs(18-crown-6)]2[Hg2(Se4)3] has been prepared by the reaction o f a lithium polyselenide solution in D M F with H g(C H 3COO)2 in the presence o f CsBr and 18-crown-6. Both com pounds are obtained as dark red crystals and characterized by X-ray structure determinations. (PPh4) 2[H g(Se4) 2]: Space group P 2,/c, Z = 4, 3021 observed unique reflexions, R = 0.082. Lattice dim ensions at 20 °C: a = 1046.0(3), b = 2129.4(2), c = 2213.1(3) pm,/? = 97.62(2)°. The com pound consists o f PPh4+ ions and anions [Hg(Se4)2]2", in which the mercury atom is a spi-rocenter o f puckered HgSe4 rings. [ Cs(18-crown-6) J2[H g2(Se4)3J: Space group la, Z = 4, 2859 observed unique reflexions, R = 0.074. Lattice dimensions at 20 °C: a = 2018(1), b = 1097.0(2), c = 2317.1(5) pm, ß = 99.40(3)°. The compound forms an ion triple which originates from Cs-Se contacts o f 382 to 390 pm with the [Hg2(Se4)3]2~ ion. The latter can be described as a [FlgtSe^JJ2-ion, which has contacts with a HgSe4 fragment. 
  Reference    Z. Naturforsch. 46b, 985—9 (1991); eingegangen am 12. Dezember 1990 
  Published    1991 
  Keywords    Polyselenido Mercurates, Synthesis, Crystal Structure 
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 Identifier    ZNB-1991-46b-0985 
 Volume    46 
53Author    Bernhard NeumüllerRequires cookie*
 Title    Darstellung und Kristallstruktur von [(Me3Si)2CH(7-Pr)InCll2 Synthesis and Crystal Structure o f [(Me3Si)2CH(/-Pr)InCl]2  
 Abstract    The title com pound 1 has been prepared by the reaction o f z-PrlnCl, with LiC H (SiM e3)2 in diethylether at -3 0 °C. The colorless substance 1 was characterized by N M R , IR, and RE spectroscopy, as well as by mass spectrometry. 1 is dimer in solution and the solid state and crystallizes in the space group P 2 ,/c with the cell parameters a = 1206.4(3) pm, b = 905.7(2) pm, c = 1591.2(5) pm, and ß = 101.18(2)°. The unit cell contains two centrosymmetri-cal dimeric molecules. 
  Reference    Z. Naturforsch. 46b, 1539—1543 (1991); eingegangen am 12. April 1991 
  Published    1991 
  Keywords    Diorganoindiumchloride, Synthesis, Crystal Structure 
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 Identifier    ZNB-1991-46b-1539 
 Volume    46 
54Author    K. Arin Ruhlandt-Senge, AlfredDirk Bacher, G. Ertraude Koellner, Birgit Siewert, Ulrich MüllerRequires cookie*
 Title    Tetraphenylphosphonium-nonachlorodivanadat(III), (PPh4)3[V2Cl9l * 7 CH2C12 Tetraphenylphosphonium Nonachlorodivanadate(III), (PPh4)3[V2Cl9] * 7 C H 2C12  
  Reference    Z. Naturforsch. 47b, 814—818 (1992); eingegangen am 14. O ktober 1991 
  Published    1992 
  Keywords    N onachlorodivanadate, Synthesis, Crystal Structure 
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 Identifier    ZNB-1992-47b-0814 
 Volume    47 
55Author    G.Erhard Müller, Joachim Lachm, Jürgen RiedebRequires cookie*
 Title    Molekülstrukturen von (o-Brombenzyl)diphenylphosphan und l,3-Bis(diphenylphosphinomethyl)benzol M olecular Structures of (o-Bromobenzyl)diphenylphosphine and l,3-Bis(diphenylphosphinomethyl)benzene  
  Reference    Z. Naturforsch. 47b, 823—828 (1992); eingegangen am 3. Februar 1992 
  Published    1992 
  Keywords    Benzylphosphines, Conformation, Crystal Structure 
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 Identifier    ZNB-1992-47b-0823 
 Volume    47 
56Author    Z. NaturforschRequires cookie*
 Title    Über Sulfide und Oxidsulfide des Samariums  
 Abstract    Stoichiometric oxidation o f SmCl2 with sulfur in the presence o f NaCl (evacuated silica ves­ sel, 850 °C, 7 d) results in the formation o f A -S m -,S 3 (orthorhombic, Pnma (no. 62), a = 737.64(5), b = 397.44(3), c = 1536.26(9) pm, Z = 4, /?w = 0.017). In contrast, C ~ S m 2S3 (cubic, I4 3 d (no. 220), a = 844.71(3) pm, Z = 5.333, Rw = 0.017) is obtained upon reaction o f the 
  Reference    Z. Naturforsch. 47b, 1614 (1992); eingegangen am 1. Juli 1992 
  Published    1992 
  Keywords    Samarium, Sulfides, Oxysulfides, Crystal Structure 
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 Identifier    ZNB-1992-47b-1614 
 Volume    47 
57Author    Gudrun Stieglitz, Bernhard Neumüller, K. Urt DehnickeRequires cookie*
 Title    Synthesen und Kristallstrukturen der Lithiumphosphide { Li(DME)[P(f-Bu)2]} 2 und [Li(DM E)PPh2l00 Syntheses and Crystal Structures of the Lithium Phosphides {Li(DME)[P(/-Bu)2]}2 and [Li(DM E)PPh2]0 0  
 Abstract    The title com pounds have been prepared by the reaction o f rc-butyllithium with the corre­ sponding diorganophosphanes H PR 2 (R = r-Bu, Ph) in D M E solutions. Both compounds were characterized by crystal structure determinations. {Li(DM E)[P(f-Bu)2]}2: Space group P 1, Z = 1, 2027 observed unique reflections, R = 0.055. Lattice dimensions at —80 °C: a = 879.9(3), b = 986.3(1), c = 1064.0(2) pm, a = 70.69(1)°, ß = 70.63(2)°, y -69.89(2)°. The com pound forms centrosymmetric dimers o f symmetry Q with L i-P bond lengths o f 260.0 and 257.3 pm for the Li2P2 four-membered ring. [Li(DM E)PPh2]0C : Space group P 2 ,/«, Z = 4. 3437 observed unique reflections, R = 0.055. Lattice dimensions at -8 0 °C: a = 1034.8(2), b = 812.48(9), c = 1978.4(3) pm, ß = 103.30(2)°. The com pound forms polymeric chains via LiP bridges with L i-P bond lengths o f 256.3 and 254.1 pm. 
  Reference    Z. Naturforsch. 48b, 156 (1993); eingegangen am 8. Oktober 1992 
  Published    1993 
  Keywords    Lithium Phosphides, Synthesis, Crystal Structure 
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 Identifier    ZNB-1993-48b-0156 
 Volume    48 
58Author    Jorge Blanco, Eduardo Gayoso, JoseManuel Vila, Miguel Gayoso, CäciliaM. Aichle, -. M. Össmer, Joachim SträhleRequires cookie*
 Title    Synthesis and Structure of Di-I/i-acetato(0,0')-ferrocenylmethyliden- 2,4,6-trimethylaniline(N,C)-palladium(II)l  
 Abstract    Di-[//-acetato(0,0')-ferrocenylmethylidene-2,4,6-trimethylaniline(N,C)-palladium(II)], 
  Reference    Z. Naturforsch. 48b, 906—910 (1993); received M arch 8 1993 
  Published    1993 
  Keywords    Cyclometallation, Synthesis, Crystal Structure 
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 Identifier    ZNB-1993-48b-0906 
 Volume    48 
59Author    Enno Lork, Ulrich Behrens, G. Ünter Steinke, Rüdiger MewsRequires cookie*
 Title    Die Kristallstruktur von trans-l,3?5-Trichloro-l,3>5-trioxo  
 Abstract    1 A6, 3 A6, 5 A6,2,4,6-trithiatriazin (/?-Sulfanurchlorid) The Crystal Structure o f /raws-1,3,5-Trichloro-1,3,5-trioxo-1 X6, 3/i6, 516, 2,4,6-trithiatriazine (/?-Sulfanuric Chloride) The crystal structure o f /?-(N S(0)C l)3 is reported. 
  Reference    Z. Naturforsch. 49b, 437 (1994); eingegangen am 22. November 1993 
  Published    1994 
  Keywords    Trichlorotrioxotrithiatriazines, Sulfanuric Chlorides, Crystal Structure 
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 Identifier    ZNB-1994-49b-0437 
 Volume    49 
60Author    Siegfried Pohl, Michael Peters, Detlev Haase, Wolfgang SaakRequires cookie*
 Title    Bildung von Iodoantimonaten und -bismutaten. Kristallstrukturen von (PhCH2NEt3)4 [Sb6l 2 2 L (PhCH2NEt3)4 [Bi6l 2 2 ] und (Ph4P)3[Bi5I18] Form ation of Iodoantim onates and Bismutates. Crystal Structures of (PhCH 2N E t3)4[Sb6I22], (PhC H 2N Et3)4[Bi6l22] and (Ph4P)3[Bi5I 18]  
 Abstract    The formation and the crystal structures of the title compounds are reported. (PhCH2N E t3)4[Sb6l 22] and (PhCH 2N E t3)4[Bi6l 22] are isotypic and contain a novel [E6I22]4~ anion (E = Sb, Bi). The anion of (Ph4P)3[Bi5I18] consists of a linear chain of five face-sharing [B il6] octahedra. 
  Reference    Z. Naturforsch. 49b, 741—7 (1994); eingegangen am 27. Januar 1994 
  Published    1994 
  Keywords    Iodoantimonates, Iodobismutates, Crystal Structure 
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 TEI-XML for    default:Reihe_B/49/ZNB-1994-49b-0741.pdf 
 Identifier    ZNB-1994-49b-0741 
 Volume    49 
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