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1996[X]
21Author    Herrn Prof, K. DrRequires cookie*
 Title    Reaktion  
 Abstract    von Ph3P=C=PPh3 mit Fe(CO)5; Molekülstrukturen von (CO)4Fe=C=C=PPh3 und Fe3(CO)9(/X3-r72-C=C-PPh3) Reaction o f Ph3P= C =P Ph3 w ith Fe(C O)5; M olecular Structures of (CO)4F e= C =C = P P h3 and Fe3(C O)9(/i3-/72-C = C -P P h 3). W olfgang P e tz * a, Frank W eller5 aGmelin- The ylide Ph3P=C=PPh3 reacts with Fe(CO)5 in toluene to give the metallacumulene (CO)4Fe=C=C=PPh3 (1) and 0=PPh3. A mixture of the ylide with its hydrolysis product Ph2P(0)-CH=PPh3 produces the trinuclear cluster Fe3(CO)9(^ 3-?/2-C=CPPh3) (2) in low yields which can also be obtained from 1 and Fe2(CO)9. Both compounds contain the same ligand bonded in a terminal (1) and in a bridging (2) manner. 1 and 2 crystallize in the monoclinic space groups P2(l)/n and P2(l)/c, respectively, with the unit cell parameters a = 1008.35(10), b= 1167.89(10), c = 1875.10(10) pm, ß = 99.824(10)° for 1 and a = 853.6(2), b = 1966.6(4), c = 1770.2(4) pm; ß = 99.05(3)° for 2. The compounds are further characterized by IR and NMR (l3C , 31P) spectroscopy and elemental analyses. 
  Reference    Z. Naturforsch. 51b, 1598—1604 (1996); eingegangen am 7. Juni 1996 
  Published    1996 
  Keywords    Crystal Structure, Hexaphenylcarbodiphosphorane, Iron Acetylide Complex, Metallacumulene 
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 Identifier    ZNB-1996-51b-1598 
 Volume    51 
22Author    Z. NaturforschRequires cookie*
 Title    On the Structure o f f-B utylam inotriphenylphosphonium Iodine D ichloride  
 Abstract    A del A m e ra, A n d rea M ayerb, D ouglas H o c, H ans Z im m erb * The structures of f-butylaminotriphenylphos-phonium iodine dibromide and iodine dichloride were determ ined by Raman spectroscopy and X-ray crystallographic structure analysis. The iodine dibromide [IBr2]~ species was assigned a centro­ symmetric nature, whereas the iodine dichloride [IC12]" possesses a non-centrosymmetric structure. 
  Reference    Z. Naturforsch. 51b, 1663—1665 (1996); received August 30 1995 
  Published    1996 
  Keywords    /-Butylaminotriphenylphosphonium Iodine D i­ chloride, Raman Spectra, Crystal Structure 
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 Identifier    ZNB-1996-51b-1663_n 
 Volume    51 
23Author    P. Eter, G. JonesRequires cookie*
 Title     
 Abstract    o ly su lfo n y la m in e, L X X V III [1] l-M e sy l-4 -d im e th y la m in o p y r id in iu m -d im esylam id : D a r ste llu n g und F estkörperstru ktur Polysulfonylam ines, L X X V III [1] l-M esyl-4-dim ethylam inopyridinium D im esylam ide: Synthesis and Solid State Structure A n d reas W irth, A rm an d B laschette Treating (MeSC^X^N with 4-dimethylaminopy-ridine in MeCN afforded the ionic title compound (monoclinic, space group P2j/c). The bond lengths of the 4-dimethylaminopyridinium moiety suggest a semiquinoid resonance form with a dou­ ble bond to the exocyclic nitrogen and two local­ ized carbon-carbon double bonds in the ring. The ring and the exocyclic N and S atoms of the cation are essentially coplanar. The S -N bond distances in the cation (173.4 pm) and the anion (159.1 and 159.6 pm) correlate with Pauling bond orders of 1.0 and 1.7, respectively. The anion displays a staggered conformation with approximate C2 symmetry (S -N -S 120.4°). 
  Reference    Z. Naturforsch. 51b, 1666—1668 (1996); eingegangen am 20. August 1996 
  Published    1996 
  Keywords    l-Mesyl-4-dimethylaminopyridinium Dimesylamide, Synthesis, Crystal Structure 
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 Identifier    ZNB-1996-51b-1666_n 
 Volume    51 
24Author    Klaus Kopka, RainerM. AttesRequires cookie*
 Title    Ein  
 Abstract    zweikerniger Vanadium(V)-Komplex mit (r/1)-und (/x-772:?72)-gebundenen Hydrazido(2-)-Liganden A D inuclear V anadium (V) C om plex w ith (r/1)-and (^ -//2://2)-Bonded H ydrazido(2-) L igands The title complex was obtained by reaction of guanidinium dioxodipicolinatovanadate(V) and N-methyl-N-phenylhydrazine. According to the single crystal structure analysis the dinuclear anion [(/i-PhN NH)(/t-O CH 3){(M ePhN N (dipic)V)}2]~ with sevenfold coordinated metal cen­ ters contains two types of hydrazido ligands. The ligand [MePhNN]: ~ is terminally bonded, and the VNN unit is linear with extensive electron delocalisation. The V-N and N-N bond lengths are 167.9(5) and 131.9(6) pm, respectively. The bonding of the bridging ligand is of the hitherto unknown fi-rf'.rf type, with V-N and N-N bond lengths of 202.5(5) and 136.5(5) pm, respectively. The V (N 2)V moiety is not planar. The compound was also characterized by H and 1V NMR spectroscopy. 
  Reference    Z. Naturforsch. 51b, 1675—1678 (1996); eingegangen am 30. Juli 1996 
  Published    1996 
  Keywords    Vanadium(V) Compounds, Hydrazido(2-) Complexes, Crystal Structure 
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 Identifier    ZNB-1996-51b-1675 
 Volume    51 
25Author    Joachim Pickardt, Britta KühnRequires cookie*
 Title     
 Abstract    etallkom plexe m it C yanoguanidin als L iganden: K ristallstru k tu ren von [Cd(cnge)2F2]*3H20 , C d(cnge)2B r2 und Hg(cnge)Cl2 (enge = C yanoguanidin) M etal C om plexes with C yanoguanidine as Ligand: Crystal Structures o f [Cd(cnge)2F2]-3H 20 , C d(cnge)2 Br^ and H g(cnge)C l2 (cnge = Cyanoguanidine) Crystals of [Cd(cnge)2F2]-3H20 (1), Cd(cnge): Br2 (2) and Hg(cnge)Cl2 (3) (cnge = cya­ noguanidine) were obtained by crystallisation from solutions of CdF2, CdBr2 or HgCl2 and cyanoguanidine in water/ethanol or methanol. 1 crystallizes monoclinically, space group C2, Z = 2,a = 1629.2(4), b = 1056.6(4), c -353.9(1) pm, 3 = 101.05(2)°; 2 is monoclinic, space group P2,/n, Z = 2 , a = 3 9 1.9(I), b = 850.7(2), c = 1722.1(4) pm, ß = 94.06(2)°, 3 is triclinic, space group P I, Z = 1, a = 686.7(1), b = 693.0(5), c = 387.2(4) pm, a = 94.45(5)°, ß = 95.05(4)°, 7 = 78.58(5)°. In 1 and 2 each Cd atom is bonded to four halogen atoms to form polymeric (CdF2)" and (CdBr2)" chains, resp., and to two cyanoguanidine molecules. In 3 each Hg atom is bonded to four chlorine atoms also forming (HgCl2)" chains, which are connected via cyanoguanidine molecules acting as a bidentate bridging ligands to form a network. 
  Reference    Z. Naturforsch. 51b, 1701—1706 (1996); eingegangen am 30. Juli 1996 
  Published    1996 
  Keywords    Cyanoguanidine, Cadmium Halide Complexes, Mercuric Chloride Complex, Crystal Structure 
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 Identifier    ZNB-1996-51b-1701 
 Volume    51 
26Author    Ute Berger, Wolfgang SchnickRequires cookie*
 Title    Ba2Na(CN2)(CN)3, ein neues Cyanamid-cyanid mit interpenetrierenden Teilstrukturen Ba2Na(CN2)(CN)3, a Novel Cyanamide Cyanide with Interpenetrating Substructures  
 Abstract    Ba2Na(CN2)(CN)3 was obtained by the reaction of Ba2N with melamine and NaCN at 700 °C. The compound was structurally characterized by single-crystal X-ray investigations (Fd3m, a = 1518.8(3) pm, Z = 16). In the crystal structure the Ba"+ ions form a cubic close packed arrangement, the Na+ and the CN2_ ions occupy the octahedral interstices. The CN-ions are located within the close packed Ba2+ layers. The unit cell of Ba2Na(CN2)(CN)3 contains two interpenetrating substructures of the zinc-blende structure type, building up a variant of NaTl. A reversible phase transition has been observed during cooling of the compound. Whereas the Ba2(CN2)(CN)3 sublattice remains nearly unaffected in this process, the Na+ ions of the low-temperature phase are statistically distributed on two crystallographic positions. 
  Reference    (Z. Naturforsch. 51b, 1—8 [1996]; eingegangen am 7. Juni 1995) 
  Published    1996 
  Keywords    Cyanamide Cyanides, Synthesis, Crystal Structure, Vibrational Spectra 
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 Identifier    ZNB-1996-51b-0001 
 Volume    51 
27Author    S. Trojanov, A. Stiewe, E. KemnitzRequires cookie*
 Title    Synthese und Struktur saurer Ubergangsmetallsulfate - Ti(H50 2)(S 0 4)2(H20 ) 2 und Zr(H30 ) 2(S 0 4)3 Synthesis and Structure of Acid Transition Metal Sulfates - Ti(H50 2)(S 0 4)2(H20 )2 and Zr(H30 ) 2(S 0 4)3  
 Abstract    From the ternary system Mn(S 0 4)n/2 / S 0 3 / H20 (Mn+ = Zr4+, Ti3+) two new acid metal sulfates, Ti(H50 2)(S 0 4)2(H20)2 and Zr(H30) 2(S 0 4)3, have been synthesized and structurally characterized. Ti(H50 2)(S 0 4)2(H->0)i crystallizes in the orthorhombic space group Pnma with cell parameters a = 9.858(5), b = 18.32(2), c = 5.437(7)Ä (Z = 4); Zr(H30) 2(S 0 4)3 crystallizes in the triclinic space group PI with cell parameters a = 5.092(2), b = 8.533(3), c = 12.388(6)A, a = 92.95(3)°, ß = 90.89(3)°, 7 = 94.35(3)° (Z= 2). In the titanium compound there are slightly distorted T i0 6 octahedra with T i-0 distances between 1.99 and 2.09 A which are sharing corners with S 0 4 tetrahedra. Through hydrogen bonds layers are formed perpendicular to the 6-axis. These layers are connected by H30 + ions only. The structure of Zr(H30) 2(S 0 4)3 consists of three different S 0 4 tetrahedra and distorted Zr07 polyhedra which are connected via common corners and edges to form columns parallel to the a-axis. The Z r-0 distances vary from 2.13o to 2.18A for equatorial positions, significantly longer than the axial Zr-O distances with 2.05A. 
  Reference    (Z. Naturforsch. 51b, 19—24 [1996]; eingegangen am 13. Juni 1995) 
  Published    1996 
  Keywords    Synthesis, Crystal Structure, Titanium, Zirconium, Hydrogen Sulfates 
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 Identifier    ZNB-1996-51b-0019 
 Volume    51 
28Author    D. Frerichs, Hk Müller-BuschbaumRequires cookie*
 Title    Vier verschiedene Koordinationspolyeder um Cu2+ im Oxid-Arsenat-Phosphat Cu0  
 Abstract    (Cu,M g)3(As1_xPJt:0 4)2 (x = 0,3) Four Different Coordination Polyhedra Around Copper in the Oxide-Arsenate-Phosphate C u0(C u,M g)3(A s,_xP,.04)2 (x = 0.3) Single crystals of CuO(Cu,Mg)3[(As0.7P0.3)O4]2 have been prepared by crystallization from melts. The compound crystallizes with triclinic symmetry, space group C '-P l, a = 6.372(4), b = 7.643(7), c = 8.175(5) A, a = 98.59(6), ß = 112.26(3), 7 = 99.03(3)°, Z = 2. CuO(Cu,Mg)3[(Aso)7Po 3)0 4]2 is isotypic to Cu4(P 0 4)20 . X-ray investigations show square planar C u 04 polygons, twisted tetragonal C u 0 5 pyramids, C u 05 bipyramids and elongated (Cu,M g)06 octahedra. 
  Reference    (Z. Naturforsch. 51b, 25—28 [1996]; eingegangen am 27. Juli 1995) 
  Published    1996 
  Keywords    Copper, Magnesium, Arsenate, Phosphate, Crystal Structure 
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 Identifier    ZNB-1996-51b-0025 
 Volume    51 
29Author    A. Gordon, FrancisJ. DisalvoRequires cookie*
 Title    R obert  
 Abstract    The ternary compound Ce8Pd24Sb is very close in composition to the intermediate valent binary CePd3. A single crystal study yielded a cubic cell with a = 8.461 (1)A, Pm3m symmetry with wR2 = 0.0412 based on 1453 reflections (222 unique) and 16 parameters. This new structure type is composed of distorted perovskite and Cu3Au subcells arranged with the perovskite-like units centred on the corners of the cube. Fitting the magnetic susceptibility data above 100K to a Curie-Weiss expression yielded a Weiss constant of -15(3)K (anti­ ferromagnetic) and an effective high temperature moment per cerium of 2.45(4)/<B indicating trivalent cerium. No ordering was observed above 3K. 
  Reference    (Z. Naturforsch. 51b, 52—5 [1996]; received May 17 1995) 
  Published    1996 
  Keywords    Cerium Intermetallic, Crystal Structure, Magnetic Susceptibility 
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 Identifier    ZNB-1996-51b-0052 
 Volume    51 
30Author    HkM. Üller-Buschbaum, B. M. ErtensRequires cookie*
 Title    Single Crystal X-Ray Analysis of Ba3Ce R  
 Abstract    Single crystals of (I) Ba3C eRu20 9, (II) Ba3SmRu20 9, (III) Ba3D yR u20 9, (IV) Ba3ErRu20 9 and (V) Ba3Ti24Ru0.6O 9 have been prepared by high temperature solid state reactions. The compounds were exam ined by X-ray techniques. They crystallize with hexagonal symmetry, 
  Reference    (Z. Naturforsch. 51b, 79 [1996]; eingegangen am 18. Mai 1995) 
  Published    1996 
  Keywords    Barium, Rare Earth, Ruthenium Oxide, Titanium, Crystal Structure 
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 Identifier    ZNB-1996-51b-0079 
 Volume    51 
31Author    St Gallinat, Hk Müller-BuschbaumRequires cookie*
 Title    Two Examples of Partial and Total Defects in the B a«Ln2Mo4O i6-Type: BaCu0 41 ■o,59Pr2Mo4 0 16 and BaBYb2Mo4Ojg  
 Abstract    Single crystals of (I) BaCu0.4iPr2M o4O 16 and (II) BaYb2M o40 16 have been prepared by flux technique. Both compounds crystallize with m onoclinic symmetry, space group C2h-C 2 /c with (I): a = 5.352(11), b = 12.888(2), c = 19.399(4) A; ß = 90.89(3)°; (II): a = 5.181(7), b = 12.467(3), c -19.350(3) Ä , ß -91.93(2)°, Z = 4. The crystal structure is characterized by i [ B a M 0 12]-chains along [010]. In the first case the M positions are occupied by copper by about 41%, in the second case these positions remain com pletely unoccupied. With respect to the crystal chemistry of the reference compound Ba(Cu0.22Mg() 78)Nd2Mo4O 16 all substan­ ces of the composition BaLn2M o40 16 should be written as Ba»Ln2Mo40 16 indicating the holes in th e^ B a M O i^ -c h a in s by ■. 
  Reference    (Z. Naturforsch. 51b, 85—8 [1996]; eingegangen am 7. Juni 1995) 
  Published    1996 
  Keywords    Barium, Copper, Rare Earth, Molybdenum Oxide, Crystal Structure 
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 Identifier    ZNB-1996-51b-0085 
 Volume    51 
32Author    O. Sedello, Hk Müller-BuschbaumRequires cookie*
 Title    Ein Oxometallat mit eindimensional flächenverknüpften Oktaederketten Synthesis and Crystal Structure of (C u,Fe)363M o3O i2. An Oxom etallate Showing One-Dimensional Chains of Face Sharing Octahedra  
 Abstract    Single crystals of (C u ,F e)3-63M o30 12 have been prepared by crystallisation from melts. X-ray investigations lead to orthorhombic symmetry, space group D : 2-P 2 12121, a = 5.0952(8), b = 10.637(2), c = 17.881(3) A , Z = 4. (C u ,F e)363M o3O i2 is isotypic to Cu385M o30 12 or (C u,Z n)3 75M o30 12. M olybdenum shows tetrahedral coordination by oxygen. Cu+ and Fe2+ are probably distributed statistically over four different point positions. Interesting features of the crystal structure are one-dim ensional chains of face shared (C u ,F e)0 6 octahedra. S y n t h e s e u n d K r i s t a l l s t r u k t u r v o n (C u , F e) 3 ,63 M o 3 0 12. 
  Reference    (Z. Naturforsch. 51b, 90—9 [1996]; eingegangen am 20. Juni 1995) 
  Published    1996 
  Keywords    Copper, Iron, M olybdenum, Oxide, Crystal Structure 
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 Identifier    ZNB-1996-51b-0090 
 Volume    51 
33Author    Stefan Horstmann, Wolfgang SchnickRequires cookie*
 Title    Synthese, Kristallstruktur und Eigenschaften von Tetraaminophosphoniumchlorid [P(NH2)4]C1 Synthesis, Crystal Structure, and Properties of Tetraaminophosphonium Chloride [P(NH2)4]C1  
 Abstract    [P(NH2)4]C1 has been prepared by ammonolysis of phosphorus pentachloride in liquid ammonia. The product was purified by reacting the byproduct, ammonium chloride, with diethylamine and removing the diethylamine hydrochloride. Suitable single crystals were obtained from an acetonitrile solution in a temperature gradient between 60 °C and room temperature. The crystal structure of [P(NH2)4]C1 has been determined by single crystal X-ray methods (Pbcn, a = 470.8(2), b = 1622.3(3), c = 756.3(2) pm, Z = 4). In the solid, [PfNH2)4]+ and Cl~ ions are found, resembling a Til-analogous structure. The N -H -C l distances indicate N -H — Cl hydrogen bonding interactions. The distortion of the P-N sceleton of the cation and the very short P -N H 2 distances (mean value: 161.2 pm) have been confirmed by ab initio calculations, which show a generalized anomeric effect of the electron pairs at nitrogen and pjrdjr bonding. 
  Reference    (Z. Naturforsch. 51b, 127—132 [1996]; eingegangen am 18. Mai 1995) 
  Published    1996 
  Keywords    Tetraaminophosphonium Salt, Synthesis, Crystal Structure, Vibrational Spectroscopic Data 
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 Identifier    ZNB-1996-51b-0127 
 Volume    51 
34Author    Ch Rabbow, O. Sfreddo, Hk Müller-BuschbaumRequires cookie*
 Title    Uber ein Barium-Lanthanoid-Oxozinkat-Platinat(IV): Ba17Ybi6Zn8Pt40 57 On a Barium Rare Earth Oxozincate-Platinate(IV): B a j 7 Yb 16Z n8Pt40 57  
 Abstract    Reactions of B a C 0 3, ZnO and Yb20 3 mixtures at temperatures up to 1300 °C using plati­ num crucibles led to yellow needles of B a17Y b 16Zn8Pt40 57. The compound crystallizes with a hitherto unknown tetragonal crystal structure, space group C-4h-I4/m, a = 22.731(1), c = 5.682(1) A , Z = 2. The crystal structure is characterized by P t 0 6 octahedra and tetragonal Z n 0 5 pyramids. Yb3+ shows a mono-capped trigonal prismatic coordination and Ba2+ several different coordination environments (C .N = 9 to 10, by O2"). The relationship to the Ba5Ln8M40 2i type is discussed. 
  Reference    Z. Naturforsch. 51b, 220 (1996); eingegangen am 10. Juli 1995 
  Published    1996 
  Keywords    Barium, Rare Earth, Zinc, Platinum, Crystal Structure 
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 Identifier    ZNB-1996-51b-0220 
 Volume    51 
35Author    S. Frenzen, Hk Müller-BuschbaumRequires cookie*
 Title    Uber ein neues Oxoiridat(V) vom Sr4P t0 6-Typ: NaSr3Ir06 On a New O xoiridate(V) of the Sr4P t 0 6 Type: NaSr3I r 0 6  
 Abstract    Single crystals of NaSr3I r 0 6 have been prepared by heating mixtures of Na20 2, SrO and iridium in closed silver tubes and were investigated by X-ray techniques^ NaSr3I r 0 6 crystal­ lizes with trigonal (rhombohedral) symmetry in the space group D 3d-R 3 c , a = 9.636(2), c = 11.556(3) A , Z = 6, and is isotypic to compounds of the Sr4P t 0 6 type. The substitution of Sr2+ by N a+ in NaSr3I r 0 6 led to an ordered metal distribution and an increase of the oxida­ tion state from IrIV to Irv. 
  Reference    Z. Naturforsch. 51b, 225 (1996); eingegangen am 2. Juni 1995 
  Published    1996 
  Keywords    Sodium, Strontium, Iridium Oxide, Crystal Structure 
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 Identifier    ZNB-1996-51b-0225 
 Volume    51 
36Author    Hk Müller-Buschbaum, St GallinatRequires cookie*
 Title    Zur Kristallchemie von CuDyMo20 8 und CuYbMo20 8 On the Crystal Chemistry o f C uD yM o20 8 and CuYbM o2O g  
 Abstract    Single crystals o f (I) C uD yM o20 8 and (II) CuYbM o20 8 have been prepared by crystalli­ sation from melts. Both com pounds crystallize with orthorhombic symmetry, space group D 2 5h~Pbca with (I): a = 10.195(1), b = 9.721(2), c = 14.563(3); (II): a = 10.094(6), b = 9.628(9), c = 14.467(8) A , Z = 8. The crystal structure is characterized by a triangular C u 0 3-polygon, a square antiprismatic coordination around the Rare Earth ions and the typical M o 0 4 tetra­ hedra. 
  Reference    Z. Naturforsch. 51b, 240 (1996); eingegangen am 18. Mai 1995 
  Published    1996 
  Keywords    Copper, Rare Earth M olybdenum Oxide, Crystal Structure 
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 Identifier    ZNB-1996-51b-0240 
 Volume    51 
37Author    A. Nne, M. Witte, Wolfgang JeitschkoRequires cookie*
 Title    Preparation and Crystal Structure of the Isotypic Carbides Ln3.67TC6 (Ln = rare earth elements; T = Mn, Fe, Ru) and Eu3 ,i6NiC6  
 Abstract    The 14 carbides Ln367MnC6 (Ln = La-Nd) and Ln367TC6 (Ln = La-Nd, Sm; T = Fe, Ru) were prepared from the elem ental components by arc-melting and subsequent annealing. Eu3 16N iC 6 was obtained from a lithium flux. The crystal structures of these nearly isotypic, hexagonal compounds (P63/m, Z = 2) were determined from single-crystal X-ray data; La3 67. FeC6: a = 878.7(2), c = 535.1(1) pm, R = 0.052 for 548 structure factors and 25 variable parameters; Eu316NiC6: a -860.0(1), c = 548.2(2) pm, R = 0.015 for 606 structure factors and 25 variables. The structures differ from the previously reported Gd3Mn2C6 structure by the occupancy of one manganese position by rare earth atoms. Since the lanthanum atoms are larger than the manganese atoms, only two thirds o f these manganese positions can be occupied by the lanthanum atoms in La3 67FeC6. Eu316NiC6 has similar atomic positions. The C-C bond distances in the C2 pairs are 130(2) and 126.5(5) pm in the La and Eu compounds, respectively. Magnetic susceptibility measurements with a SQ U ID m agnetom eter indicate La3 67FeC6 to be Pauli paramagnetic. A test for superconductivity was negative down to 3 K. 
  Reference    Z. Naturforsch. 51b, 249 (1996); received June 12 1995 
  Published    1996 
  Keywords    Lithium Flux, Crystal Structure, Ternary Carbides with C2 Pairs 
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 Identifier    ZNB-1996-51b-0249 
 Volume    51 
38Author    AnneU. Tzolino, K. Arsten BluhmRequires cookie*
 Title    Synthese und röntgenographische Charakterisierung von zwei neuen Verbindungen des Ludwigit-Strukturtyps: Co5Sn(B0 3)2 0 4 und Co5Mn(B0 3 )20 4  
 Abstract    Synthesis and X -R ay C haracterization o f Two New Com pounds with Ludw igite-Structure: C o5S n (B 0 3)20 4 and C o5M n (B 0 3)20 4 The compounds Co5Sn(B 03)20 4 (I) and Co5M n(B03)20 4 (II) were prepared by using a B20 3 flux technique. Single crystals were investigated by X-ray diffraction and showed orthorhombic symmetry, space group D2h-Pbam (No. 55), I a = 944.4; b = 1233.8; c = 310.5 pm; Z = 2 and II a = 925.07; b = 1241.67; c = 305.24 pm; Z = 2. Both compounds are isotypic to the mineral Ludwigite. All metal point positions show an octahedral oxygen coordination. Co2+ and M4+ (M = Sn or Mn) occupy one point position statistically. Both structures contain isolated, trigonal planar B 0 3 units and oxygen atoms that are not coordinated to boron. 
  Reference    Z. Naturforsch. 51b, 305—308 (1996); eingegangen am 28. September 1995 
  Published    1996 
  Keywords    Cobalt, Tin, Manganese, Borate Oxide, Crystal Structure 
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 TEI-XML for    default:Reihe_B/51/ZNB-1996-51b-0305.pdf 
 Identifier    ZNB-1996-51b-0305 
 Volume    51 
39Author    Park, K. Arsten BluhmRequires cookie*
 Title    Pb6(A s0 4)  
 Abstract    [B (A s04)4] -ein neuartiger Kristallstrukturtyp im System Pb0 /B2 0 3 /As2 0 5 mit einem Beitrag über P b(B A s05) Pb6(A s 0 4)[B (A s 0 4)4] -a New Crystal Structure Type in the System P b 0 /B 20 3/A s20 3 w ith R em arks about P b (B A s0 5) C heong- Single crystals of Pb6(A s04)[B(As04)4] (I) and Pb(BAs05) (II) were obtained by melting B->03, As20 5 and PbO at 800 °C. X-ray investigation led to the space group (I): S4 -P4 (Nr. 81) with a = 715.4(1), c = 976.2(3) pm, Z = 1 and (II): C | -P3, (Nr. 144) with a = 712.2(1), c = 693.5(2) pm, Z = 3. While (II) is isotypic to the Stillwellite structure, Pb^(As04)[B(As04)4] represents a completely novel type of crystal structure. Boron and arsenic are tetrahedrally coordinated by oxygen. These polyhedra form two kinds of isolated anions: A s04'~ and B(A s04)49_. Lead is eightfold coordinated by oxygen. 
  Reference    Z. Naturforsch. 51b, 313—318 (1996); eingegangen am 16. Oktober 1995 
  Published    1996 
  Keywords    Lead, Arsenic, Borate, Synthesis, Crystal Structure 
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 TEI-XML for    default:Reihe_B/51/ZNB-1996-51b-0313.pdf 
 Identifier    ZNB-1996-51b-0313 
 Volume    51 
40Author    Silke Busche, K. Arsten BluhmRequires cookie*
 Title    Ba2KZn3(B306)(B60 13)  
 Abstract    Single crystals of the new compound Ba2KZn3(B30 6)(B60 | 3) were obtained by using a B20 3 flux technique; they crystallize in an as yet unknown structure type. X-ray investigations led to the space group C '-P l (Nr.2) with lattice parameters a = 705.2(2), b = 712.5(2), c = 1880.3(6), a = 93.43(3)°, ß = 90.72(2)°, 7 = 119.57(2)°, Z = 2. The structure contains (B30 6)3~-rings and a new discrete (B60 13)8~ anion, which is composed of two B 0 4 and two B20 5 units. Zn-+ is tetrahedrally coordinated by oxygen and two out of three tenfold coordinated Ba-sites are statistically occupied by Ba2+ and K+. 
  Reference    Z. Naturforsch. 51b, 319—324 (1996); eingegangen am 26. September 1995 
  Published    1996 
  Keywords    Barium, Potassium, Zinc, Borate, Crystal Structure 
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 TEI-XML for    default:Reihe_B/51/ZNB-1996-51b-0319.pdf 
 Identifier    ZNB-1996-51b-0319 
 Volume    51 
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