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1Author    M. A. Nabar, A. P. DalviRequires cookie*
 Title    Thermal Analysis of the Cadmium and Manganese Hydrogen Orthoarsenate Monohydrates (M HAs04 * H20, where M = Cd, Mn)  
 Abstract    The dehydration decomposition of cadmium and manganese hydrogen orthoarsenate monohydrates was studied by static isothermal and differential thermoanalytical methods. It was found that the dehydration decomposition takes place in a single stage forming the respective diarsenate, the peak minimum temperature being 458 K for the cadmium and 466 K for the manganese salt. 
  Reference    Z. Naturforsch. 33b, 1106—1 (1978); received April 17 1978 
  Published    1978 
  Keywords    Thermal Analysis, Cadmium, Manganese 
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 TEI-XML for    default:Reihe_B/33/ZNB-1978-33b-1106.pdf 
 Identifier    ZNB-1978-33b-1106 
 Volume    33 
2Author    S. P. Perlepes, ThF. Zafiropoulos, J. K. Kouinis, A. G. GalinosRequires cookie*
 Title    of the Group II B Metals, Part H [1] Etherate and Aniline Compounds of Cd(H)  
 Abstract    The preparation of new etherate and aniline compounds of the mixed complex halo-acids HCdCl2l and H2CdI2Cl2 is reported. Analytical, conductometric, spectral (UV and IR) and data from X-ray powder spectra were used for the characterization of the complexes. The structure of the aniline com-plexes, in the solid state, cannot be deduced with certainty. 
  Reference    Z. Naturforsch. 35b, 1241—1243 (1980); received April 24 1980 
  Published    1980 
  Keywords    Ether, Aniline, Cadmium, Mixed Haloacids 
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 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-1241.pdf 
 Identifier    ZNB-1980-35b-1241 
 Volume    35 
3Author    Thom As Fickenscher, G. Unter Kotzyba, Rolf-D Ieter, H. Offm, Ann, R. Ainer Pöttgen, H. P. FritzRequires cookie*
 Title    Synthesis, Structure, and Magnetic Properties of EuAgCd and YbAgCd  
 Abstract    New intermetallic compounds EuAgCd and YbAgCd were synthesized in quantitative yield by reaction of the elements in sealed tantalum tubes in a high-frequency furnace. Both com­ pounds were investigated by X-ray diffraction on powders and single crystals: KHg2 type, Imma, a = 490.41(8), b = 771.0(1), c = 834.4(2) pm, wR2 = 0.0624, 255 F values, 12 variables for EuAgCd, and MgZn2 type, Pb^/mmc, a = 584.66(5), c = 946.83(9) pm, wR2 = 0.0502, 187 F 2 values, 11 variables for YbAgCd. Owing to the very small difference in scattering power, no long range ordering of the silver and cadmium atoms is evident from the X-ray data, although Ag-Cd ordering is expected. The silver and cadmium atoms randomly occupy the mercury and zinc positions of the KHg2 and MgZn2 type structures, respectively. In EuAgCd the [AgCd] substructure consists of strongly puckered, orthorhombically distorted Ag3 Cd3 hexagons, while a three-dimensional network of face-and comer-sharing tetrahedra is observed in YbAgCd. The rare earth atoms fill the space between the Ag3 Cd3 hexagons (EuAgCd) or within the three-dimensional tetrahedral network (YbAgCd). Magnetic susceptibility measurements in­ dicate Pauli paramagnetism for YbAgCd and Curie-Weiss behavior above 60 K for EuAgCd with an experimental magnetic moment of 7.82(3) /j b/Eu indicating divalent ytterbium and europium. Ferromagnetic ordering at Tc = 28.0(5) K is observed for EuAgCd. At 2 K and 5 T the saturation magnetization is 5.85(5) /iß/Eu. 
  Reference    Z. Naturforsch. 56b, 598—603 (2001); received April 12 2001 
  Published    2001 
  Keywords    Cadmium, Crystal Structure, Magnetic Properties 
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 TEI-XML for    default:Reihe_B/56/ZNB-2001-56b-0598.pdf 
 Identifier    ZNB-2001-56b-0598 
 Volume    56 
4Author    S. Münchau, Hk Müller-BuschbaumRequires cookie*
 Title    Cd0,73 Cu0,27V2 O 6: A Com pound with Brannerite Structure  
 Abstract    Single crystals of Cd() 73Cu<,.27V 20 6 were prepared by solid state reactions. X-ray investiga­ tions lead to monoclinic symmetry, space group C \h-C2lm , a = 9.339, b = 3.5604, c = 6.893 A , ß = 111.85°, Z = 2. It belongs to the Brannerite structure, showing a statistical distribution of Cd2+ and Cu2+ on one point position. The crystal structure of Brannerites is discussed with respect to the distorted O 2-octahedra around V 5+ and the influence of the Jahn-Teller active Cu-+ ion to the shortened M2+Oa octahedra. 
  Reference    Z. Naturforsch. 49b, 927 (1994); eingegangen am 4. März 1994 
  Published    1994 
  Keywords    Cadmium, Copper, Vanadium, Oxide, Brannerite Type 
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 TEI-XML for    default:Reihe_B/49/ZNB-1994-49b-0927.pdf 
 Identifier    ZNB-1994-49b-0927 
 Volume    49 
5Author    S. Münchau, Hk Müller-BuschbaumRequires cookie*
 Title    Zur Kristallchemie eines Silber-Cadmium-Oxovanadats: AgCdV04 On the Crystal Chemistry of a Silver Cadmium Oxovanadate: A gC dV 04  
 Abstract    Single crystals of A gC dV 04 have been prepared in closed silver tubes using V20 5 as a flux. The light-orange crystals sho\v orthorhom bic symmetry, space group D2h-Pnm a, a = 9.786(2), b = 6.994(1), c = 5.439(1) A, Z = 4. The hitherto unknown A gC dV 04 is related to the Olivine structure but isotypic to Ag2C r 0 4 and NaCd4(V 0 4)3 respectively. The differences in crystal chemistry between the Olivine type, NaCd4(V 0 4)3 and A gC dV 04 are discussed. 
  Reference    Z. Naturforsch. 50b, 703—706 (1995); eingegangen am 10. O ktober 1994 
  Published    1995 
  Keywords    Silver, Cadmium, Vanadium, Oxide, Crystal Structure 
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 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-0703.pdf 
 Identifier    ZNB-1995-50b-0703 
 Volume    50 
6Author    Sabine Münchau, Karsten BluhmRequires cookie*
 Title    Zur Synthese und Kristallstruktur von Kupfercadmiumpyroboratoxid: Cu2Cd(B20 5) 0 Synthesis and Crystal Structure of Copper Cadmium Pyroborate Oxide: Cu2Cd(B20 5) 0  
 Abstract    Single crystals of the new compound Cu2C d(B20 5) 0 have been prepared by B 20 3/V 20 5 flux technique in a closed silver tube. Their structure is isotypic with Cu2C o(B 20 5) 0 but its preparation is quite different. X-ray investigations on single crystals led to the space group C |h-P 2 !/c (Nr. 14), a = 339.9(2); b = 1509.8(2); c -927,0(1) pm; ß = 93.19(1)°; Z -4. The structure contains isolated B 2O s groups and oxygen that is not coordinated to boron. Cad­ mium is octahedrally coordinated by oxygen, while copper exhibits a nearly square planar or a fivefold pyramidal coordination. 
  Reference    Z. Naturforsch. 50b, 1151 (1995); eingegangen am 19. Januar 1995 
  Published    1995 
  Keywords    Copper, Cadmium, Pyroborate, Oxide, Crystal Structure 
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 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-1151.pdf 
 Identifier    ZNB-1995-50b-1151 
 Volume    50 
7Author    VerbindungC., S. Münchau, Hk Müller-BuschbaumRequires cookie*
 Title    Synthese und Kristallstruktur einer mit dem Johillerit verwandten  
 Abstract    Single crystals of C dC u^M gx.5Pbo.5V30 12 have been prepared in closed steel tubes using V 20 5 as a flux. The orange crystals show monoclinic symmetry, space group C2h-C 2 /c , a = 12.417(5), b = 12.983(6), c = 6.911(3) Ä , ß = 113.02(1)°, Z = 4. CdCu1.5Mg1.5PbojV30 12 reveals a relationship to the Johillerite type, but it is characterized by an additional point position for cadmium, situated betw een the square planar C u 0 4 polygons of the Johillerite structure. 
  Reference    Z. Naturforsch. 50b, 1158—1162 (1995); eingegangen am 22. D ezem ber 1994 
  Published    1995 
  Keywords    Cadmium, Copper, Magnesium, Lead, Vanadium, Oxide, Crystal Structure 
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 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-1158.pdf 
 Identifier    ZNB-1995-50b-1158 
 Volume    50 
8Author    E. Kemnitz3, C. Werner3, A. Stiewe3, H. Worzalab, S. Trojanov3Requires cookie*
 Title    Synthese und Struktur von Zn(HS0 4)2(H2S0 4)2 und Cd(H S04)2 Synthesis and Structure of Z n(H S04)2(H2S 0 4)2 and C d(H S 04)2  
 Abstract    From the binary systems M2S 0 4/H2S 0 4 (M = Zn, Cd), two new hydrogen sulfates, (Zn(HS0 4)2(H2S04)2 and Cd(HS04)2, have been synthesized and structurally characteri­ zed. Both compounds crystallize in the monoclinic space group P2,/c with cell parameters a = 5.047(2), b = 15.430(4), c = 7.958(3) A and ß = 104.16(4)° (Z= 2) for Zn(HS04)2(H2S 0 4)2 and a = 5.339(1), b = 13.351(3), c = 8.508(2) A and ß = 92.22(3)° (Z = 4) for Cd(H S04)2. In the zinc compound there are slightly distorted centrosymmetric Z n 06 octahedra with Z n -0 distances of 2.05 -2.13 A which are sharing corners with S 0 4 tetrahedra. H S 04 and H2S 0 4 tetrahedra are linked via hydrogen bonds to form layers perpendicular to the c-axis. In the crystal structure of C d(HS04)2there exist two crystallographically different H S 04 tetrahedra. The C d06 octahedra with C d -0 distances between 2.24 and 2.31 A are strongly angle-distorted. Besides hydrogen bonds of medium strength (d0...o = 2.66 A) there are also much more weaker ones (d0...0 = 3.04 A). Considering these latter ones zigzag chains in z-direction can be recognized. The relatively low stability of Cd(H S04)2 in comparison with other metal-II-hydrogen sulfates is discussed with respect to its structural pecularities. 
  Reference    (Z. Naturforsch. 51b, 14—18 [1996]; eingegangen am 13. Juni 1995) 
  Published    1996 
  Keywords    Synthesis, Crystal Structure Zinc, Cadmium, Hydrogen Sulfate 
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 TEI-XML for    default:Reihe_B/51/ZNB-1996-51b-0014.pdf 
 Identifier    ZNB-1996-51b-0014 
 Volume    51 
9Author    S. Frenzen, Hk Müller-BuschbaumRequires cookie*
 Title    Zur Kristallchemie eines Natrium-Cadmium-Oxoiridats: Na3Cd2lr06 On the Crystal Chemistry of a Sodium Cadmium Oxoiridate: Na3C d-Jr06  
 Abstract    Single crystals of Na3Cd2Ir0 6 have been prepared by crystallization from melts in closed silver tubes. The crystal structure was investigated by X-ray techniques. Na^Cd^IrOf, crystallizes with monoclinic symmetry, space group Cih-C2/m; a = 5.663(2), b = 9.783(3), c = 5.689(2) A, ß = 109.95(2)°, Z = 2. It is isotypic to M+5A7+0 6 (M = Li, Na; A = Re, Os) and shows relations to the sodium chloride structure in spite of an ordered distribution of Na+, Cd2+ and Ir5+. 
  Reference    Z. Naturforsch. 51b, 822—825 (1996); eingegangen am 29. November 1995 
  Published    1996 
  Keywords    Sodium, Cadmium, Iridium Oxide, Crystal Structure 
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 TEI-XML for    default:Reihe_B/51/ZNB-1996-51b-0822.pdf 
 Identifier    ZNB-1996-51b-0822 
 Volume    51 
10Author    S. Meyer, B. Mertens, Hk Müller-BuschbaumRequires cookie*
 Title    SrZn  
 Abstract    (V0)(P04)2 und BaC d(V 0)(P04)2: Zum BaZn(V0)(P04)2-Typ verwandte, jedoch nicht isotype Vanadylphosphate SrZ n(V 0)(P 04)2 and B a C d (V 0)(P 04)2: Vanadylphosphates Related but not Isotypic to the B aZ n (V 0)(P 04)2 Type Single crystals of the compounds S rZ n (V 0)(P 0 4)2 (I) and B aC d(V 0)(P04)2 (II) ha­ ve been prepared by solid state reactions in evacuated quartz tubes. X-ray investigati­ ons confirmed orthorhombic symmetry, space group D ^-P bca, lattice constants a/b/c (I): 9.066(1)/9 .0 1 2 (l)/l7.513(1) A and (II); 8.838(4)/8.915(4)/19.374(9) Ä, Z = 8. Initially assu­ med isotypies of (I) and (II) to B aZ n(V 0)(P 04)2 proved to be erroneous considering significant details of the connectivity of the Z n 0 4 and P 0 4 tetrahedra (I) and the coordination sphere of cadmium (II), respectively. The similarities and differences of the crystal chemistry relation to (I) and (II) are discussed with respect to B a Z n(V 0)(P 04)2. The Coulomb terms of the lattice energies of vanadyl M2(V 0)(P 0 4)2 and divanadyl M (V 0)2(P 0 4)2 phosphates are shown. 
  Reference    Z. Naturforsch. 52b, 985—988 (1997); eingegangen am 20. Mai 1997 
  Published    1997 
  Keywords    Barium, Strontium, Cadmium, Zinc, Vanadium Phosphate 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-0985.pdf 
 Identifier    ZNB-1997-52b-0985 
 Volume    52 
11Author    B. Mertens, Hk Müller-BuschbaumRequires cookie*
 Title    Uber ein cadmiumreiches Orthovanadat Ba2,5Cd11(V 04)9 mit Cadmium in oktaedrischer und tetragonal pyramidaler Koordination On a Cadmium Rich Orthovanadate Ba-, 3Cd, |( V 0 4)9 Showing Cadmium in Octahedral and Square Pyramidal Coordination  
 Abstract    Single crystals of Ba2 ^C di^V O ^g have been prepared by solid state reactions. The new compound crystallizes with orthorhombic symmetry, space group D ^-Pbcn, a = 20.842(6), b = 13.471(3), c = 11.838(9) A, Z = 4. The crystal structure is characterized and dominated by C d 0 6 octahedra and unusual square pyramids of 0 2~ around Cd2+ forming a three-dimensional [C d ]|0 36] network. The interstices are occupied by V 5+ and Ba2+ ions. This results in V 0 4 tetrahedra and irregular BaO 10 polyhedra isolated from each other. Occupation of the barium positions is deficient in agreement with the valence state V5+ and calculations of the coulomb terms of lattice energy. 
  Reference    Z. Naturforsch. 52b, 989—993 (1997); eingegangen am 26. Mai 1997 
  Published    1997 
  Keywords    Barium, Cadmium, Vanadium Oxide, Crystal Structure 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-0989.pdf 
 Identifier    ZNB-1997-52b-0989 
 Volume    52 
12Author    Reint Eujen, Ralf HaigesRequires cookie*
 Title    Reaktionen des donorfreien (C F 3 )2Cd mit Phosphor(V)halogeniden: Difluorcarben-Einschiebungen und Direktsynthese von (C F 3)3PF2 Reactions of Donor-Free (CF3)2Cd with Phosphorus(V) Halides: Insertion of Difluorocarbene and Direct Synthesis of (CF3)3PF2  
 Abstract    Difluorocarbene which is quantitatively eliminated from donor-free bis(trifluoromethyl)-cadmium below 0 °C inserts smoothly into the P-F bonds o f PF5 to form (CF3)3PF2 in high yield. Due to the fast conversion of P-Cl bonds into P-F bonds by cadmium fluoride, PC15 forms (CF3)3PF2 as well, and a direct synthesis of (CF3)3PF2 with ca. 70 % yield starting from CdEt2, CF3I and PC15 is reported. Whereas no insertion o f CF2 into the axial bonds o f (CF3)3PF2 has been detected, reaction o f (CF3)2Cd with (CF3)3PC12 gives the new tetra-kis(haloalkyl)fluorophosphoranes (CF3)3(CF2C1)PF, (CF3)3(CFC12)PF, (CF3) 2 (CF2C1)2PF and (CF3)3(CC13)PF. The NMR spectra of these and related compounds and of their hydrolysis products (CF3)3(CF3_"Cln)PO are reported. The formation of the higher chlorinated phos­ phoranes is discussed in terms o f an isomerization mechanism presumably involving carbene elimination-reinsertion processes. 
  Reference    Z. Naturforsch. 53b, 1455—1460 (1998); eingegangen am 3. Juli 1998 
  Published    1998 
  Keywords    Phosphoranes, Trifluoromethyl Compounds, Difluorocarbene, Cadmium, NM R Data 
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 TEI-XML for    default:Reihe_B/53/ZNB-1998-53b-1455.pdf 
 Identifier    ZNB-1998-53b-1455 
 Volume    53 
13Author    AnthonyJ. Arduengo, JensR. Iiia, Fredric Goerlicha, WilliamJ. Davidsonb, Marshall5Requires cookie*
 Title    Carbene Adducts of Dimethylcadmium  
 Abstract    The first examples of carbene-cadmium complexes are reported from the reactions of a variety of imidazol-2-ylidenes or imidazolin-2-ylidenes with dimethylcadmium. Four new carbene complexes are characterized by NMR spectroscopy ('H , i?C and 1 n Cd). The cadmium centers are strongly shifted downfield (100 -1 5 0 ppm) by interaction with the carbenes. X-ray structures are reported for three carbene-cadmium 1:1 adducts. The cadmium centers exhibit distorted trigonal-planar geometries in which the carbene ligands have an average 18.2 pm longer bond distance to cadmium compared to the methyl groups. The planes of cadmium coordination are twisted with respect to the plane of the imidazole ring. The more basic imidazolin-2-ylidene is shown to displace imidazol-2-ylidenes from the cadmium center. 
  Reference    Z. Naturforsch. 54b, 1350—1356 (1999); received June 16 1999 
  Published    1999 
  Keywords    Carbene, Cadmium, Ylide, Carbene Complex, Imidazol-2-ylidene 
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 TEI-XML for    default:Reihe_B/54/ZNB-1999-54b-1350.pdf 
 Identifier    ZNB-1999-54b-1350 
 Volume    54 
14Author    Florian Stadler, Thomas Fickenscher, Rainer PöttgenRequires cookie*
 Title    Synthesis and Structure of RE2Rh2Cd (RE = La, Ce, Pr, Nd, Sm)  
 Abstract    New intermetallic cadmium compounds /?£2Rh2Cd (r e = La, Ce, Pr, Nd, Sm) were syn­ thesized from the elements in sealed tantalum tubes in a high-frequency furnace. They were characterized through X-ray powder data: Mo2FeB2 type, space group P4/mbm, Z = 2. Single crystal data of the cerium compound (a = 762.8(1), c = 377.8(1) pm, wR2 = 0.0662, 199 F2 values, and 13 variable parameters) revealed small defects on the rhodium position leading to the composition Ce2R h186(3)Cd for the investi­ gated crystal. According to the course of the cell volumes Ce2Rh2Cd may be classified as a mixed-valent compound. The Ce2Rh2Cd structure is an intergrowth of slightly distorted A1B2 and CsCl related slabs of compositions CeRh2 and CeCd. Within the CeRh2 slab short Ce-Rh contacts (284-300 pm) are indicative of strong Ce-Rh bonding. The Rh-Rh distance within the A1B2 re­ lated slab is 289 pm. 
  Reference    Z. Naturforsch. 56b, 1241—1244 (2001); received September 10 2001 
  Published    2001 
  Keywords    Cadmium, Solid State Synthesis, Mixed Valence 
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 TEI-XML for    default:Reihe_B/56/ZNB-2001-56b-1241_n.pdf 
 Identifier    ZNB-2001-56b-1241_n 
 Volume    56 
15Author    Requires cookie*
 Abstract    AB2 X 2 Compounds with the CaAl2Si2 Structure, I I 1 (A = C a; B = Zn, Cd; X = P, As) P e t e r K l ü f e r s u n d A l b r e c h t M e w i s In stitu t Four new ternary calcium compounds of zinc (cadmium) with a 5 B-element have been prepared. Analytic, pycnometric and X-ray powder data are given. The compounds are supposed to crystallize trigonally in a CaAl2 Si2-type structure. 
  Reference    (Z. Naturforsch. 32b, 353—354 [1977]; eingegangen am 3. Dezember 1976) 
  Published    1977 
  Keywords    Calcium Compounds, Zinc, Cadmium, 5 B-elements, Crystal Data 
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 TEI-XML for    default:Reihe_B/32/ZNB-1977-32b-0353_n.pdf 
 Identifier    ZNB-1977-32b-0353_n 
 Volume    32 
16Author    Reinhard Matthes, Hans-Uwe SchusterRequires cookie*
 Title    Synthese und Struktur der Phasen K2CdSn und K2CdPb Synthesis and Structure of the Phase K2CdSn and K2CdPb  
 Abstract    orthorhombically, with space group Ama2 = Cmc2, a = 645.8 pm, b = 860.2 pm, c — 1095.5 pm. The structure is built of a potassium-3D-net forming eight-edged channels parallel to the a-axis; these channels are penetrated by infinite Cd-Pb-zigzag-chains. The powder-diagram shows the homologous phase K2CdSn (a = 643.2 pm, b = 854.3 pm, c = 1087.7 pm) to be isotypic to K2CdPb. 
  Reference    Z. Naturforsch. 34b, 541—543 (1979); eingegangen am 28. Dezember 1978 
  Published    1979 
  Keywords    Ternary Phases, Potassium, Cadmium, 4B-Element, Crystal Data K2CdPb crystallizes 
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 TEI-XML for    default:Reihe_B/34/ZNB-1979-34b-0541.pdf 
 Identifier    ZNB-1979-34b-0541 
 Volume    34 
17Author    Reinhard Matthes, Hans-Uwe SchusterRequires cookie*
 Title    Ternäre Natriumphasen mit Cadmium bzw. Quecksilber und Zinn bzw. Blei Ternary Sodium Phases with Cadmium or Mercury and Tin or Lead  
 Abstract    Four ternary sodium phases with the formula Na2BX (B = Cd, Hg; X = Sn, Pb) were prepared and structurally investigated. The structures of the cubic phases Na2HgSn, Na2CdPb and Na2HgPb (space group F43m) are closely related to LiaBi, that of Na2CdSn (space group P63mmc) to the hexagonal structure of NaßAs. 
  Reference    Z. Naturforsch. 35b, 778—780 (1980); eingegangen am 8. Februar 1980 
  Published    1980 
  Keywords    Ternary Intermetallic Phases, Sodium, Cadmium, Mercury, Tin, Lead, Crystal Structures 
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 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0778_n.pdf 
 Identifier    ZNB-1980-35b-0778_n 
 Volume    35 
18Author    Jörg Adel, Frank Weller, Kurt DehnickeRequires cookie*
 Title    Synthese und Kristallstrukturen der spirocyclischen Polyselenido-Komplexe [Na-15-Krone-5] 2 [M(Se 4 ) 2 ] mit M = Zink, Cadmium und Quecksilber Sythesis and Crystal Structures of the Spirocyclic Polyselenido Complexes [Na-15-Crown-5] 2 [M(Se 4 ) 2 ] with M = Zink, Cadmium, and Mercury  
 Abstract    The title compounds have been prepared by reactions of the metal acetates of zink, cadmium, and mercury with ethanolic solutions of sodium polyselenides in the presence of 15-crown-5. They form dark red crystals, which were characterized by their IR specta as well as by X-ray crystal structure determinations. All complexes [Na-15-crown-5] 2 [M(Se 4) 2 ] with M = Zn (1), Cd (2), Hg (3) crystallize isotypically in the space group C2/c with 4 formula units per unit cell. In the anions [M(Se 4) 2 ] 2 ^ the metal atoms are coordinated tetrahedrally by four selenium atoms of two Se 4 2 ~ units, thus forming a spiro-bicyclus. The complex cations [Na-15-crown-5] + have a Na---Se contact of approximately 299 pm with two selenium atoms of a MSe 4 group, allowing formulation of triple ion species. 
  Reference    Z. Naturforsch. 43b, 1094—1100 (1988); eingegangen am 4. Mai 1988 
  Published    1988 
  Keywords    Polyselenide Complexes of Zink, Cadmium, Mercury, Syntheses, Crystal Structure 
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 TEI-XML for    default:Reihe_B/43/ZNB-1988-43b-1094.pdf 
 Identifier    ZNB-1988-43b-1094 
 Volume    43