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41	Author	Rolf Minkwitz, Thomas Hertel, Uwe Zachwieja	Requires cookie*
	Title	Reaktion von Cacodylsäure (CF^^AsOOH im System HF / MF5 (M = As, Sb) und Kristallstruktur von Difluordimethylarsonium- hexafluoroantimonat (CH3)2AsF2SbF6 Reaction of Cacodylic Acid (CH3)2AsOOH in the System HF / MF5 (M = As, Sb), and Crystal Structure of Difluorodimethylarsonium Hexafluoroantimonate
	Abstract	In the reaction of cacodylic acid (CH3)2AsOOH in the superacid system HF / MF5 (M = As, Sb) the difluorodimethylarsonium hexafluorometallates [(CH3)2AsF2]MF6 are formed and have been characterized by i.r. and Raman spectroscopy. The crystal structure of the hexafluoroanti monate has been determined at -100°C (orthorhombic space group Ibca with Z = 4, a = 10.973, b = 11.164, c = 14.200 pm).
	Reference	Z. Naturforsch. 52b, 1185—1190 (1997); eingegangen am 1. Juli 1997
	Published	1997
	Keywords	Difluorodimethylarsonium Hexafluorometallates, Cacodylic Acid, Crystal Structure, Super Acid
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	Identifier	ZNB-1997-52b-1185
	Volume	52

42	Author	Rolf Minkwitz, Thomas Hertel	Requires cookie*
	Title	Kristallstruktur von Bromnitrat BrONC>2 Crystal Structure of Bromine Nitrate BrONO?
	Abstract	The crystal structure of bromine nitrate BrONO, has been determined on a single crystal with M oK q radiation at -83°C. The structure is orthorhombic, space group P2,2 , 2 ,, Z = 4, and the cell dimensions are a = 403.2(2), b = 684.9(4), c = 1201.4(5) pm. An intermolecular Br.....O contact leads to the formation of chains within the crystal. Attempts to synthesize a bromine(III)-nitrate by oxidizing CF3Br and CCl3Br with C10N 02 were not successful. E inleitung
	Reference	Z. Naturforsch. 52b, 1307—1310 (1997); eingegangen am 8. August 1997
	Published	1997
	Keywords	Crystal Structure, Bromine Nitrate, Chlorine Nitrate
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	TEI-XML for	default:Reihe_B/52/ZNB-1997-52b-1307.pdf
	Identifier	ZNB-1997-52b-1307
	Volume	52

43	Author	Hk Wulff, Müller-Buschbaum	Requires cookie*
	Title	Planare C u 0 4-Polygone und eine einseitig offene Te4+0 3-Koordination in SrCuTe20 6 Planar C u 0 4 Polygons and a One-Sided Open Te4+0 3 Coordination in SrCuTe-,06 L
	Abstract	The new compound SrCuTe20 6 has been prepared by quenching single crystals grown from a flux of SrC 03, T e02 and C uC 03 C u(0H)2. X-ray investigations show cubic symmetry, space group 0 7-P4\| 32, lattice constant a = 12.473(1), Z = 12. The crystal structure is characterized by square planar C u 0 4 polygons and a one-sided open triangular oxygen coordination of Te4+, both incorporated in a Sr/O network. The one sided oxygen coordination of tellurium is completed by the lone pair of Te4+. Calculations of the Coulomb parts of lattice energy led to the position of the lone pair centre.
	Reference	Z. Naturforsch. 52b, 1341—1344 (1997); eingegangen am 26. August 1997
	Published	1997
	Keywords	Strontium, Copper, Tellurium Oxide, Crystal Structure
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	TEI-XML for	default:Reihe_B/52/ZNB-1997-52b-1341.pdf
	Identifier	ZNB-1997-52b-1341
	Volume	52

44	Author	Peter Höhn, Matthias Ludwig, Rüdiger Kniep	Requires cookie*
	Title	Die Kristallstrukturen der isotypen Erdalkalimetall-Nitridowolfra- mat(VI)-Nitrid-Oxide Ca51[WN4]12N803 und Sr51[WN4]12N803 The Crystal Structures of the Isotypic Alkaline Earth-Nitridotungstate(VI)- Nitride-Oxides Ca5, [W N 4] 12N 80 3 and Sr5! [W N 4] l2N 80 3
	Abstract	Yellow single crystals of the isotypic phases Ca51 [WN4] 12N80 3 and Sr5\|[WN4] i2N80 3 (tri clinic, P I (#2); a= 1056.4(3) / 1 1 13.1(5) pm, b = 1239.7(3) / 1304.4(5) pm, c= 1598.2(3) / 1679.4(9) pm, q = 102.78(1)/102.47(2)°, = 95.15(1)/95.43(3)°, 7 = 109.89(1)/109.77(2)°; Z = 1) were grown in a Tl-flux (Ca:Tl, molar ratio 5:1, W-crucible; Tmax = 1273K; reaction with Ni, 1 atm, 36 h) or from pellets (Sr2N + W, molar ratio 6:1; Tmax = 1023K; reaction with N2, 1 atm, 36 h). The crystal structures contain tetrahedral anions [WN4]6" in addition to isolated nitride and isolated oxide ions, which are octahedrally coordinated by Ca and Sr, respectively.
	Reference	Z. Naturforsch. 52b, 1349—1358 (1997); eingegangen am 9. Juli 1997
	Published	1997
	Keywords	Nitridotungstate(VI), Nitride-Oxide, Preparation, Crystal Structure
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	TEI-XML for	default:Reihe_B/52/ZNB-1997-52b-1349.pdf
	Identifier	ZNB-1997-52b-1349
	Volume	52

45	Author	R. Üdiger, K. Niep	Requires cookie*
	Title	R
	Abstract	b[B2P20 8(0 H)] und Cs[B2P 2 0 8(0H)J: D ie ersten Borophosphate mit dreidimensional vernetzter Anionenteilstruktur R b[B 2P2O s(O H)] and C s[B 2P20 8(0 H)]: The First B oro p h o sp h ates with a T hree-dim ensional A nionic T etrahedral S tructure C ornelia Häuf, The isotypic borophosphates Rb[B2P20 8(0 H)] and Cs[B2P20 8(0 H)] were grown under hy drothermal conditions. The crystal structures were solved by single crystal methods (R b[B 2P20 8(0 H)]/C s[B 2 P20 8(0 H)]: monoclinic,
	Reference	Z. Naturforsch. 52b, 1432—1435 (1997); eingegangen am 28. Juli 1997
	Published	1997
	Keywords	Boron, Crystal Structure, Framework, Channel, Phosphorus
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	Identifier	ZNB-1997-52b-1432_n
	Volume	52

46	Author	Prof, Dr, Dr	Requires cookie*
	Title	Aluminiumphosphate mit nichtzentrosymmetrischen Schicht-und Raumnetzstrukturen aus topologisch verwandten Motiven: 2. KA12(P 0 4 )2 (0 H )* 2 H 20
	Abstract	Alum inum Phosphates w ith N on-C entrosym m etric Layer-and Fram ew ork-Structures o f Topologically R elated M otifs: 2. K A l2(P0 4)2(0 H)-2 H 20 Stefan D icka, Gisbert G roßm annb, G isela O hm sb, M anfred M üller0 KAl2(P04)2(0 H)-2H20 was obtained by the reaction of gibbsite with a potassium-phosphate solution of pH = 5.5 at 373 K. A single crystal X-ray structure analysis showed that it is an ordered, F-free K-analog of the microporous compound AIPO4-CI2 . Crystal data: orthorhombic space group P 2 \2 \2 \, a = 920.5(1), b = 970.7(2), c = 982.8(2) pm, Z -4. The structure consists of dimeric units of AIOö octahedra and AIO5 trigonal bipyramids, bridged by an OH and two bidentate phosphate groups. The dimers are linked by phosphate to form corrugated layers which are topologically related to the layers in KAl2(P04)2(0 H)-4H20 and minyulite. The layers are connected by Al-O-P and hydrogen bonds to a three dimensional framework structure with K ions in channel-like cavities. A neutron powder scattering experiment with KAb(P04)2(0 D)-2D20 showed that the bridging OD group and only one D of each water molecule are involved in hydrogen bonding. 31P MAS NMR spectra show two isotropic lines at 6iso = —6.9 and -18,7 ppm of the intensity ratio 1:1 and confirm the presence of two crystallographically independent P atoms in the unit cell. In the 'H MAS NMR spectra the water molecules and the bridging OH group show signals at 5.9 and 1.1 ppm, respectively.
	Reference	Z. Naturforsch. 52b, 1447—1455 (1997); eingegangen am 9. September 1997
	Published	1997
	Keywords	Crystal Structure, Neutron Scattering, MAS NMR, Aluminium Phosphate
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	TEI-XML for	default:Reihe_B/52/ZNB-1997-52b-1447.pdf
	Identifier	ZNB-1997-52b-1447
	Volume	52

47	Author	Joachim Pickardt, B. Enedikt Staub, E. Inleitu	Requires cookie*
	Title	Kristallstrukturen M etall(II)-Diazin Komplexe
	Abstract	von Cd(pyrazin)Br2, Cd(pyrazin)I2, Cu(pyrazin)Cl2 und Cd(pyrimidin)(N0 3)2*2 H2 0 M etal(II) D iazine Com plexes: Crystal Structures o f C d(pyrazine)B r2, C d(pyrazine)I2, C u(pyrazine)C l2, and C d (p y rim id in e)(N 0 3)2-2H20 . Single crystals of the compounds Cd(pyrazine)Br2, Cd(pyrazine)I2, Cu(pyrazine)Cl2 and Cd(pyrimidine)(N03)2-2H20 were obtained by crystallisation from aqueous solutions of the metal salts and solutions of the respective diazine in an organic solvent. The structures of the pyrazine complexes consist of "supramolecular" networks of -M-pyrazine-M-and -M -(^2-Hal)2-M-chains. The pyrimidine complex shows a three dimensional network due to -M-pyrimidine-M-chains connected via hydrogen bonds between H (H ,0) and 0 (0 N 0 2).
	Reference	Z. Naturforsch. 52b, 1456—1460 (1997); eingegangen am 27. August 1997
	Published	1997
	Keywords	Metal Halide Pyrazine Adducts, Cadmium Pyrimidine Complex, Crystal Structure
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	TEI-XML for	default:Reihe_B/52/ZNB-1997-52b-1456.pdf
	Identifier	ZNB-1997-52b-1456
	Volume	52

48	Author	P. Etra, W. Ollesen, JoachimW. Kaiser, W. Olfgang, Jeitschko	Requires cookie*
	Title	Quaternary Equiatomic Compounds LnZnSbO (Ln = La -Nd, Sm) with ZrCuSiAs-Type Structure
	Abstract	The five compounds LnZnSbO (Ln = La -Nd, Sm) were prepared by annealing cold-pressed pellets of the lanthanoids, zinc oxide, and antimony, or by reacting these components in a NaCl/KCl flux. They crystallize with the tetragonal ZrCuSiAs type structure, which was refined from single-crystal X-ray data of CeZnSbO : P 4/nmm, a = 419.76(4), c = 947.4(1) pm, Z = 2, R = 0.022 for 165 structure factors and 12 variable parameters. Chemical bonding in this and the formally isotypic compound CeZni-* Sbi is briefly discussed.
	Reference	Z. Naturforsch. 52b, 1467—1470 (1997); received August 8 1997
	Published	1997
	Keywords	Rare Earth Metals, Quaternary Pnictide Oxides, Crystal Structure
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	TEI-XML for	default:Reihe_B/52/ZNB-1997-52b-1467.pdf
	Identifier	ZNB-1997-52b-1467
	Volume	52

49	Author	Thomas Miekisch, Klaus Harms, Sigrid Wocadlo, Werner Massa, Bernhard Neumüller, Christoph Frommen, Kurt Dehnicke, Herrn Prof, J. Dr, Lorberth	Requires cookie*
	Title	[TiJv Cl8(NPMe3)3]Cl und [Vnw vCl4(NPPh3)3] Crystal Structures of the Phosphoraneiminato Complexes [Ti3v Cl8(NPMe3)3]Cl and [vl"/IVCl4(NPPh3)3]
	Abstract	[Ti3Cl8(NPMe3)3]Cl has been prepared by the reaction of TiCl3(THF)3 with Me3SiNPMe3 in dichloromethane forming green moisture sensitive crystals. According to the crystal structure determination the titanium atoms of the cation [Ti3Cl8(NPMe3)3]+ are linked by two /x3-N atoms of two NPMe3~ groups forming a distorted trigonal-bipyramidal arrangement. The third NPMe3_ group and two of the chlorine atoms have /i2-bridging functions. The mixed-valence complex [V2Cl4(NPPh3)3] is formed as dark green moisture sensitive crystals by the reaction of vanadium trichloride with Me3SiNPPh3 in boiling toluene. According to the crystal structure determination the vanadium atoms are linked by two /z2-N atoms of two NPPh3_ groups forming a nonplanar V2N2 four-membered ring with a V-V distance of 266.8(1) pm which corresponds to a (a, 1/27r) bond type. This is confirmed by the measurement of the magnetic susceptibility which leads to a magnetic moment of 1.45(5) B. M., corresponding to the remaining d 1 -electron.
	Reference	Z. Naturforsch. 52b, 1484—1490 (1997); eingegangen am 8. September 1997
	Published	1997
	Keywords	Phosphoraneiminato Complexes, Titanium, Vanadium, Crystal Structure
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	TEI-XML for	default:Reihe_B/52/ZNB-1997-52b-1484.pdf
	Identifier	ZNB-1997-52b-1484
	Volume	52

50	Author	LiAnsgar Bach, Michael Hoyer, Hans Hartl	Requires cookie*
	Title	Darstellung und Kristallstruktur der oligomeren Iodo-d10-metallate(II) [M(I)(CH3CN)4]4[Cd6I16] * 1,5 CH3CN mit M(I) = Cu, Li Synthesis and Crystal Structure of the Oligomeric Iodo-d10-Metalates(II) [M(I)(CH3CN)4]4[Cd6I16] * 1.5 CH3CN with M(I) = Cu
	Abstract	The reaction of Cul or Lil with Cdl2 in the polar solvent acetonitrile results in the formation of the iodocadmates [Cu(CH3CN)4]4[Cd6I16] • 1.5CH3CN (1) and [Li(CH3CN)4]4[Cd6I 16] • 1.5CH3CN (2) with the oligomeric anion [Cd6I16]4~. This new type of halometallate anion, which is found in both isotypic structures, is built up by six alternating corner and edge sharing Cdl4 tetrahedra. 1: Space group PI (No 2), a = 838.5(4), b = 1465.9(9), c = 1929.8(6) pm, q = 93.01(3), ß = 99.13(3), 7 = 105.11(3)°; 1: Space group P i (No 2), a = 841.7(8), b = 1470(9), c = 1945.5(9) pm, a = 93.27(5), ß = 99.13(5), 7 = 104.83(5)°.
	Reference	Z. Naturforsch. 52b, 1497—1500 (1997); eingegangen am 15. September 1997
	Published	1997
	Keywords	Iodocadmates, Lithium Iodocadmate, Copper Iodocadmate, Crystal Structure
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	Identifier	ZNB-1997-52b-1497
	Volume	52

51	Author	W. Olfgang Schneider, A.Lexander Sladek, A.Ndreas Bauer, Klaus Angermaier, H. Ubert, Schm Idbaur	Requires cookie*
	Title	Structural Investigation of Bis(isonitrile)gold(I) Complexes
	Abstract	The reaction of (MeNC)-, (PhNC)-and (MesNC)AuCl in tetrahydrofuran with an equimolar amount of the corresponding isonitrile ligand and one equivalent of Ag+X~ (X -= BF^ or CF3S O J) leads to the formation of the bis(isonitrile)gold(I) complexes (MeNC)aAu+ CFiSO ^ (1), (PhNC)2Au+ BF^ (2) and (M esNC)2Au+ BF^ (3). The crystal structures of 1, 2 and 3 have been determined. In compound 1 there are rod-like cations with a parallel packing into meandering puckered layers, in which the gold atoms have alternating A u-A u contacts of 3.611 and 3.624 A. In complex 2 the cations form long double-paddles, with the two paddles at an angle of 11.5°. The individual cations are well separated and have no sub-van-der-Waals A u-A u contacts. The crystal structure of 3 is similar, but with a smaller dihedral angle between the planes of the two mesityl rings (56.0°).
	Reference	(Z. Naturforsch. 52b, 53—56 [1997]; received September 18 1996)
	Published	1997
	Keywords	Gold(I) Complexes, Isonitrile Complexes, Crystal Structure, Supramolecular Chemistry
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	Identifier	ZNB-1997-52b-0053
	Volume	52

52	Author	Stefan Sawusch, Uwe Schilde, Erhard Uhlemann	Requires cookie*
	Title	Ligandenaustauschreaktionen
	Abstract	von ReCl4(PPh3)2 mit Salicylaldehyd-2-hydroxy(mercapto)anil. Struktur von Bis[salicylaldehyd-2-hydroxyanilato(2-)]rhenium(IV) Ligand Exchange Reactions of ReCl4(PPh3)2 with Salicylaldehyde-2-hydroxy(mercapto)anil. Molecular Structure of Bis[salicylaldehyde-2-hydroxyanilato(2-)]rhenium(IV)-hydroxyanilato(2-)]rhenium(IV) Ligand exchange reactions of tetrachloro-bis(triphenylphosphane)rhenium(IV) with sali-cylaldehyde-2-hydroxy(mercapto)anil were studied. The reaction products were characterized by mass spectroscopy. The crystal structure was determined by X-ray analysis for bisfsali-cylaldehyd-2-hydroxyanilato(2-)]rhenium(IV). Crystal data: a = 1987.1(18); b = 829.0(6), c -1296.9(7) pm, ß = 100.02(7) ; space group C
	Reference	(Z. Naturforsch. 52b, 61—64 [1997]; eingegangen am 17. Juni 1996)
	Published	1997
	Keywords	Rhenium(IV) Chelates, Tridentate Diacidic Ligands, Crystal Structure, Bis[salicylaldehyde-2
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	Identifier	ZNB-1997-52b-0061
	Volume	52

53	Author	O. V. Quinzania, S. Tarullia, O. E. Pirob, E. J. Baranc, E. E. Castellano0	Requires cookie*
	Title	Crystal Structure, Vibrational Spectra and Thermal Analysis of Bis(saccharinato)bis(pyridine)zinc(II)
	Abstract	The crystal structure of [Zn(sac)2(py)2] has been de termined by single-crystal X-ray diffrac-tometry. It crystallizes in the monoclinic space group C2/c with Z = 4. We propose and discuss an assignment of its IR and Raman spectra, compatible with the structural characteristics. Its thermal behavior was investigated by means of TG and DTA methods. Some comparisons with related compounds are made.
	Reference	Z. Naturforsch. 52b, 183—187 (1997); received July 1 1996
	Published	1997
	Keywords	Zinc, Saccharin/Pyridine, Crystal Structure, IR Spectra, Raman Spectra
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	Identifier	ZNB-1997-52b-0183
	Volume	52

54	Author	X. =. Cl, I. V. Br, W. Lorenzen, Preetz	Requires cookie*
	Title	Kristallstrukturen von Oi-Bu4N)
	Abstract	[B6C16], (w-Bu4N)[B6Br6] und (Ph3P=N=PPh3)[B6I6] sowie Schwingungsspektren und Normal-koordinatenanalyse der Hexahalogeno-c/osö-Hexaboratradikal-anionen [B6X6]~, X = Cl, Br, I Crystal Structures of («-Bu4N)[B6C16], (rc-Bu4N)[B6Br6], and (Ph3P=N=PPh3)[B6I6], and Vibrational Spectra and Normal Coordinate Analysis of the Hexahalogeno-c/oso-hexaborate Radical Anions [B6X6]-, Oxidation of hexahalogeno-c/oso-hexaborates [B6X6]2_, X = Cl, Br, I, with (NH4)2[Ce(N03)6] in ethanol yields coloured radical ions [B6X6]~. X-ray structure determina tions have been performed on single crystals of («-Bu4N)[B6Cl6] (1) (monoclinic, space group P2,/c,a = 13.144(2),6 = 12.594(2),c = 17.688(5) A,ß = 107.29(2)°,Z=4),(«-B u4N)[B6Br6] (2) (monoclinic, space group P2,/c, a = 13.529(5), b = 13.096(5), c = 17.863(5) Ä, ß = 107.20(5)°, Z = 4) and (Ph3P=N=PPh3)[B6I6] (3) (triclinic, space group P I, a = 9.3137(8), b = 10.6988(10), c = 11.8760 A, a = 102.220(7), ß = 99.34J(8), 7 = 96.030(7)°, Z = 1). The average B-B distan ces are nearly equal (1.733 Ä (1), 1.728 A (2), 1.728 A (3)) while the B-X distances increase (1.762 A (1), 1.912 A (2), 2.120 A (3)). Using the molecular parameters, normal coordinate analyses have been performed and a good agreement of observed and calculated frequencies of 11B and 1 'B labelled derivatives has been achieved. The valence force constants fd(BB) and fd(BX) of [B6X6]" are 1.17 and 4.17 (X = Cl), 1.18 and 3.34 (Br) and 1.18 and 2.60 mdyn/A (I), respectively.
	Reference	Z. Naturforsch. 52b, 565—572 (1997); eingegangen am 19. Februar 1997
	Published	1997
	Keywords	Hexahalogenohexaborates( 1 -), Crystal Structure, Vibrational Spectra, Normal Coordinate Analysis
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	Identifier	ZNB-1997-52b-0565
	Volume	52

55	Author	Antje Albert, D. Ietrich, M. Ootz	Requires cookie*
	Title	Formation and Crystal Structures of the Hydrates of 18-Crown-6 [1]
	Abstract	The melting diagram of the system 18-crown-6/water has been set up and the existence of four binary hydrates confirmed. Crystal structures have been determined for three of these, in addition to that for the hexahydrate already published. The hydrates are monoclinic, a tetrahydrate (previously reported as a 4.5-hydrate) with space group P2\|/c and Z = 2 formula units per unit cell, an octahydrate with I2/a and Z = 4, and a dodecahydrate with P2i/n and Z= 2. In each structure the crown ether molecule has the (pseudo) D.^ conformation common for many of its complexes, and is immediately hydrogen-bonded by a group of four water molecules in a similar, characteristic pattern. In the tetrahydrate, with one of the waters disordered, the total connectivity is that of a 1D chain, while the overall structures of the octa-and dodecahydrate are 3D networks. Four of the six independent water molecules in the dodecahydrate are linked with each other into a rare 2D ice-like layer.
	Reference	Z. Naturforsch. 52b, 615—619 (1997); received January 15 1997
	Published	1997
	Keywords	Crown Ether, Crystal Structure, Hydrate, Hydrogen Bonding, Melting Diagram
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	Identifier	ZNB-1997-52b-0615
	Volume	52

56	Author	Hans-Christian Böttcher, Kurt Merzweiler, Clemens Bruhn	Requires cookie*
	Title	Synthesis and X -R a y C rysta l Structure o f the Heterobim etallic Com plex [F eR h (/x-C O )(C O )3(/i-P B u '2)(M -Ph2PC H 2PPh2)]
	Abstract	The reaction of the phosphido-bridged metal carbonyl [FeRh(CO)ö(At-PBu2)] (1) with dppm [dppm = bis(diphenylphosphino)methane] leads to the heterobimetallic complex [FeRh(/z-CO)(CO)3()U-PBu2)(/i-dppm)] (2) in good yields. The molecular structure of 2 was determined at room temperature [triclinic, space group Pi, a = 9.509(6), b = 13.637(5), c = 14.926(8) A, q = 81.38(4), ß = 82.75(4), 7 = 71.25(4)°]. The compound acts as a homogeneous catalyst precursor in the hydroformylation reaction of ethylene, but it decomposes during this process.
	Reference	Z. Naturforsch. 52b, 810—814 (1997); received April 15 1997
	Published	1997
	Keywords	Dinuclear Iron Rhodium Complex, Phosphido-Bridged, Crystal Structure, Homogeneous Catalysis, Hydroformylation
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	Identifier	ZNB-1997-52b-0810
	Volume	52

57	Author	Z. Naturforsch	Requires cookie*
	Title	Mechanismus der Cyclotrimerisierung von Phenylvinylketonen und die Kristallstrukturen von 1-((1R,2S,3R,5S)-und 1-((1R,2S,3R,5R)- 3.5-Dibenzoyl-2-hydroxy-2-phenylcyclohexylmethyl)-pyrrolidin-2-on
	Abstract	T h e M e ch a n ism o f C y c lo trim e risa tio n o f P h e n y lv in y lk e to n e s a n d th e C ry sta l S tru c tu re s o f 1-((1R ,2S,3R ,5S)-an d 1 -((1 R * ,2 S * ,3 R * ,5 R )-3 .5 -D ib e n zo y l-2 -h y d ro x y -2 -p h e n y lcy c lo h e x y lm e th y l)-p y rro lid in -2 -o n H . M ö h rle 3 , R. W ille3, B. M id d e lh a u v e b, D. M o o tz b, H . W u n d e rlic h 1 5 H errn Prof. Dr. E. R eim ann zu m 60. G ebu rtstag g e w id m e t The cyclotrimerisation of l-phenyl-2-propyn-l-ol (1) with pyrrolidin-2-one (2) to the tri-benzoylcyclohexanes 4 and 5 produced -with modifications of the reaction conditions -the phenylvinylketone adducts 17 and 18 as intermediates and additionally the cyclohexylmethyl-pyrrolidin-2-ones 8 and 9. Obviously the mechanism consists of a primary attack of pyrroli-din-2-onat (2a) to a phenylketone (7) followed by a series of consecutive Michael reactions, which give rise to 4 and 5 as well as to 8 and 9. The latter two have been identified by X-ray crystal structure analyses. They crystallize in the monoclinic space group P2j/c, Z=4, with 8: a = 1786,8(6), b = 636.7(2), c = 2280.9(8) pm,y3 = 102.33(3)°; 9: a = 1119.9(7), b = 1165.1(3), c = 2198.6(5) pm, ß = 118.24(4)°.
	Reference	Z. Naturforsch. 52b, 859—872 (1997); eingegangen am 16. April 1997
	Published	1997
	Keywords	Michael Reaction, Polysubstituted Cyclohexanes, Diastereomeres, Consecutive Reactions, Crystal Structure
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	TEI-XML for	default:Reihe_B/52/ZNB-1997-52b-0859.pdf
	Identifier	ZNB-1997-52b-0859
	Volume	52

58	Author	T. Koch, W. Preetz	Requires cookie*
	Title	Darstellung, n B
	Abstract	,13 C -,1 H-NMR-und Schwingungsspektren von Phenylundecahydro-c/oso-dodecaborat(2-) sowie Kristallstruktur von [As(C6H5)4]2[(C6H5)B12H n ] Preparation, n B, 13C, 'H NMR and Vibrational Spectra of Phenylundecahydro-c/oso-dodecaborate(2-) and Crystal Structure o f [As(C6H5)4]2[(C6H5)B 12H n ]
	Reference	Z. Naturforsch. 52b, 935—938 (1997); eingegangen am 2. Mai 1997
	Published	1997
	Keywords	Phenylundecahydro-c/oso-dodecaborate(2-), Crystal Structure, 'H NMR Spectra, Vibrational Spectra
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	TEI-XML for	default:Reihe_B/52/ZNB-1997-52b-0935.pdf
	Identifier	ZNB-1997-52b-0935
	Volume	52

59	Author	U. Steiner, W. Reichelt	Requires cookie*
	Title	Zum System Ca/Mo/O: Phasendiagramm, Synthese und Charakterisierung der ternären Verbindungen On the System Ca/Mo/O: Phase Diagram, Synthesis and Characterization of Ternary Compounds
	Abstract	The phase diagram of the ternary system Ca/Mo/O has been determined. Powder samples of the ternary compounds CaM o04, CaM o03, CaMo50 8, Ca16 5Mo,3 5O40 and Ca5 45Moi80 32 were prepared by solid state reactions. Rietveld analysis based on powder X-ray diffraction data shows that the compound CaMo50 8 has monoclinic structure (P2,/c) with a = 7.549, b = 9.064, c = 9.974 A, 3 = 110.04°. CaMo.O, Ca I. <Moit sOjo and Ca« 4sMoieO-i9 are semiconductors over the temperature range 75 to 300 K.
	Reference	Z. Naturforsch. 52b, 1169—1174 (1997); eingegangen am 14. August 1997
	Published	1997
	Keywords	Calcium Molybdate, Phase Diagram, Synthesis, Crystal Structure, Electric Properties
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	TEI-XML for	default:Reihe_B/52/ZNB-1997-52b-1169.pdf
	Identifier	ZNB-1997-52b-1169
	Volume	52

60	Author	Joachim Pickardt, Sven Wiese, Pirka Wischlinski	Requires cookie*
	Title	Reaktionen von Cadmium-und Quecksilber(II)halogeniden und -pseudohalogeniden mit Kronenethern: Kristallstrukturen der Komplexe von Benzo-18-krone-6 mit CdX2 und HgX2 (X = CI, Br) und von Dibenzo-18-krone-6 mit Hg(CN)2 Reactions of Cadmium and Mercury(II) Halides and Pseudohalides with Crown Ethers: Crystal Structures of the Complexes of Benzo-18-crown-6 with CdX2 and HgX2 (X = Cl, Br) and of Dibenzo-18-crown-6 with Hg(CN)2
	Abstract	The reactions of benzo-18-crown-6 with MeX2 (Me = Cd, Hg; X = Cl. Br), and of dibenzo-18-crown-6 with Hg(CN)2 afford the compounds [Me(benzo-18-crown-6)X2] (1-4) and [Hg(dibenzo-18-crown-6)(CN)2 (5), resp., the crystal structures of which were determined. They consist of isolated neutral molecules, the crystalline Cd complexes and 5 contain one molecule of water of crystallization per formula unit, which however is not coordinated to the metal atom. The metal atoms are coordinated by the six O atoms of the ligands and the two halide atoms, or the two CN groups for 5, resp., the coordination being more unsymmetrical for the benzo than for the dibenzo ligand.
	Reference	Z. Naturforsch. 52b, 1296—1300 (1997); eingegangen am 11. August 1997
	Published	1997
	Keywords	Crown Complexes, Cadmium Halides, Mercuric Halides, Mercuric Cyanide, Crystal Structure
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	TEI-XML for	default:Reihe_B/52/ZNB-1997-52b-1296.pdf
	Identifier	ZNB-1997-52b-1296
	Volume	52

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