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81	Author	OctahedraC. Wadewitz, Hk Müller-Buschbaum	Requires cookie*
	Title	Ba
	Abstract	(V0)4(As0 4)2(As20 7): Ein neues Divanadyl(IV)-Arsenat mit flächenverknüpften V20 8+1-Oktaederdoppeln Ba(V0)4(As0 4)2(As20 7): A New Divanadyl(IV)-Arsenate Containing Face Shared V20 8+, Double A new alkaline earth vanadyl arsenate Ba(V0)4(As0 4)2(As2 0 7) has been synthesized by solid state reactions in closed quartz tubes. X-ray investigations led to orthorhombic symmetry, space group D2£-Pnma, a = 17.540(2), b = 7.6223(8), c = 11.0633(12) A, Z = 4. The crystal structure is characterized by A s 0 4 single and As20 7 double tetrahedra and face shared asymmetric stretched V20 8+, double octahedra, forming a network of polyhedra. The incorporated Ba2+ ions show 12-fold coordination by oxygen. Ba(V 0)4(A s0 4)2(As20 7) is the first vanadyl compound containing V20 8 divanadyl groups originating from face sharing stretched V 0 5+l octahedra.
	Reference	(Z. Naturforsch. 52b, 83—87 [1997]; eingegangen am 21. August 1996)
	Published	1997
	Keywords	Barium, Vanadyl Arsenate, Crystal Structure
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	Identifier	ZNB-1997-52b-0083
	Volume	52

82	Author	Z. Naturforsch	Requires cookie*
	Title
	Abstract	The crystal structures of PbMe3I and BiPh2Cl have been determined by X-ray methods. Both compounds form polymeric chains via bent [i2-ha-logeno bridges and almost linear X-M-X units (X = I, Cl).
	Reference	Z. Naturforsch. 52b, 149—152 (1997); eingegangen am 20. September 1996
	Published	1997
	Keywords	Lead, Bismuth Compounds, Crystal Structure
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	Identifier	ZNB-1997-52b-0149_n
	Volume	52

83	Author	Amo Pfitzner, Eva Freudenthaler	Requires cookie*
	Title	(CuI)2Pi4* ein neues Phosphorpolymer in einer Kupferhalogenid-Matrix (CuI)2P 14: a Novel Phosphorus Polymer in a Copper Halide Matrix
	Abstract	(CuI)2Pi4 is a new adduct of copper iodide to a neutral phosphorus polymer. It is obtained by reaction of Cul and Pred at 400 °C. The compound crystallizes monoclinically, space group P2,/c (No. 14), a = 9.919(2), b = 9.718(2), c = 16.478(3) Ä, ß = 105.71(1)°, V = 1529.0(7) A3, with Z = 4. The crystal structure was refined to R\ = 0.029 for 2680 reflections and 173 parameters. It contains a new polymeric phosphorus allotrope with the translational unit P^° consisting of experimentally unknown [PI2] groups which are linked by [P2] fragments. The phosphorus rods consist of five-and six-membered rings, and are coordinated only by copper atoms.
	Reference	Z. Naturforsch. 52b, 199—202 (1997); eingegangen am 11. September 1996
	Published	1997
	Keywords	Phosphorus, Copper Compounds, Crystal Structure
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	Identifier	ZNB-1997-52b-0199
	Volume	52

84	Author	Olaf Reckeweg, H.-Jürgen Meyer	Requires cookie*
	Title	Unsymmetrische BN23'-Ionen in den Strukturen von Ca2ClBN2 und Sr2ClBN2. Unsymmetric BN23~-Ions in the Structures of Ca2ClBN2 and Sr2ClBN2
	Abstract	The new compounds Ca2ClBN2 (1) and Sr2ClBN2 (2) were prepared from the respective metal, its dihalide and h-BN in sealed tantalum ampoules at 1200 °C. The crystals obtained were transparent yellow (1) and blue (2), respectively. The crystal structures were determined from single crystal X-ray data. Ca2ClBN2 and Sr2ClBN2 are isotypic and crystallize in the orthorhombic space group Pnma (No. 62), Z = 4 (Ca2ClBN 2: a = 1166.7(2), b = 390.26(4), c = 899.8(1) pm, R 1 = 0.043, wR2 = 0.115 for 554 independent reflections; Sr-,C1BNT: a = 1242.8(1), b = 416.75(4), c = 920.8(1) pm, R\ = 0.031, wR2 = 0.054 for 6 6 2 'independent reflections). The structures contain two different layers of M 2+, C P and BN23~ alternating along the [010] direction. The bond angles N-B-N are 177.2(4)° for (1) and 176,6(5)° for (2), the bond distances of the BN23_ ions are dB_ N] = 134.6(5) pm for (1), 136,3(7) pm for (2) and dg_N2 = 132.4(5) pm for (1) and 131,3(7) pm for (2). The unsymmetric structure of the BN23~ ion, as is manifested particularly in the Sr compound (2), is caused by the coordination of N 1 to four cations while N2 is coordinated only to three.
	Reference	Z. Naturforsch. 52b, 340—344 (1997); eingegangen am 12. November 1996
	Published	1997
	Keywords	Boronitrides, Synthesis, Crystal Structure
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	Identifier	ZNB-1997-52b-0340
	Volume	52

85	Author	Uwe Klingebiel, Mathias Noltemeyer, Hans-Jörg Rakebrandt	Requires cookie*
	Title	Difluorphosphorylcyclosilazane -Synthese und Kristallstruktur Difluorophosphorylcyclosilazanes -Syntheses and Crystal Structure
	Abstract	The reaction of lithiated l,3-bis(fluorodimethyl)cyclotrisilazane with PF3 leads to the formation of a PF2-substituted six-membered Si-N ring (1). 1,5-Bis(difluorophosphanyl)-2,2,4,4,6,6,8,8-octamethyl-cyclotetrasilazane (2) is obtained in the reaction of the dilithium derivative of the cyclic tetrasilazane with trifluorophosphane in a molar ratio 1:2. The crystal structure of (F2P-N-SiMe2-NH-SiMe2)2 (2) has been determined.
	Reference	Z. Naturforsch. 52b, 775—777 (1997); eingegangen am 14. April 1997
	Published	1997
	Keywords	Fluorophosphorylcyclosilazanes, Silicon, Crystal Structure
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	Identifier	ZNB-1997-52b-0775
	Volume	52

86	Author	Pb2ln2si209, J.-P Werner, Hk Müller-Buschbaum	Requires cookie*
	Title	Zur Kenntnis eines synthetischen Kentrolits/Melanotekits des Indiums: On an Synthetic Kentrolite/Melanotekite of Indium: Pb2In2Si20 9
	Abstract	Single crystals of Pb2In2Si20 9 have been prepared by crystallisation from melts of Pb(N 03)2, ln20 3 and S i0 2. The compound crystallizes with orthorhombic symmetry, space group C2v-Pna2\| with the lattice constants a = 10.529(1),/?= 11.372(1) and c = 7.019(3) A, Z = 4. Despite the fact that the Kentrolite/Melanotekite structure is characterized by dissimilar occupied split positions of lead, Pb2In2Si20 9 shows completely filled and ordered point positions. The location of a dot like lone pair of Pb~+ is estimated by Coulomb term calculations of lattice energy. The results are discussed with respect to published Pb-lone pair distances using the electronic polarizability coefficient of the lone pair cation or simple geometrical considerations.
	Reference	Z. Naturforsch. 52b, 1213—1218 (1997); eingegangen am 8. Juli 1997
	Published	1997
	Keywords	Lead, Indium, Silicate, Crystal Structure
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	Identifier	ZNB-1997-52b-1213
	Volume	52

87	Author	Stefan Dick	Requires cookie*
	Title	Die Struktur von GaAs0 4 *2 H20 : Ein neues Mitglied der Variscit-Familie The Structure of GaAsC>4-2 H20 : A New M ember of the Variscite Family
	Abstract	GaAs0 4 -2 FF0 was synthesized hydrothermally from Ga2Ü3 and a K+-AsC>4~ solution at pH=2. A single crystal structure determination showed that GaAs0 4 -2H20 is isotypic with variscite and therefore the first gallium arsenate with octahedrally coordinated Ga(III). Crys tal data: space group Pbca, a = 1016,0(1), b = 886,2(1), c = 994. 1(1) pm, R g = 0,0266. GaAs0 4 -2 H2 0 dehydrates at 439 K with formation of an amorphous material and poor cry stalline GaAsC>4. The crystal data of all known compounds with variscite structure have been compiled.
	Reference	Z. Naturforsch. 52b, 1337—1340 (1997); eingegangen am 27. Juni 1997
	Published	1997
	Keywords	Gallium Arsenate, Crystal Structure, Variscite
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	Identifier	ZNB-1997-52b-1337
	Volume	52

88	Author	Hk Wulff, Müller-Buschbaum	Requires cookie*
	Title	Synthese und Kristallstruktur des Lanthan-Titanat-Tellurats LaTi
	Abstract	(Ti0 2 5Te0j 5)O6 und seine Verwandtschaft mit PbSb20 6 und Sr(MnTe)06 Synthesis and Crystal Structure of the Lanthanum Titanate Tellurate LaTi(Ti0 25Te0 75) 0 6 and its Relationship to PbSb20 6 and Sr(M nTe)06 L. Single crystals of LaTi(Ti0 25T e o .75) 0 6 have been prepared by solid state reactions. X-ray investigations led to trigonal symmetry, space group C3-P3 , a = 5.141(10), c = 5.218(10) A, Z = 1. The compound is characterized by a predominantly ordered distribution of Ti4+ and Te6+. Typical features of the crystal structure are staggered layers containing edge connected T i0 6 and (Ti,Te)06 octahedra. The layers are connected by La3+ ions receiving an octahedral coordination by the surrounding oxygen ions. The relationships to the PbSb20 6 type and the recently described compound Sr(M nTe)06 are discussed.
	Reference	Z. Naturforsch. 53b, 149—152 (1998); eingegangen am 25. November 1997
	Published	1998
	Keywords	Lanthanum, Titanate, Tellurate, Crystal Structure
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	Identifier	ZNB-1998-53b-0149
	Volume	53

89	Author	G. Waidmann, M. Jansen	Requires cookie*
	Title	Synthese und Charakterisierung des Fulleren-Kokristallisats C60SiH(C6H5)3 Synthesis and Characterisation of the Fullerene Co-Crystal C60SiH(C6H5)3
	Abstract	A new fullerene co-crystal C60*SiH(C6H5)3 has been synthesized by crystallisation from a melt of SiH(C6H5)3 and C60 in sealed duran tubes at 80°C. X-ray investigations led to triclinic symmetry, space group P i, a = 10.086(1),/? = 14.431(2), c = 14.911(2) Ä, a = 79.13(1), ß = 74.943(9), 7 = 88.33(1)°, V = 2058.0(4) A 3, Z = 2. The crystal structure consists of isolated fullerene and silane molecules. At -80°C, C60 is still rotationally disordered. Temperature dependent Guinier powder diagrams do not show any phase transformation between 25 and -165°C. The compound is stable in air.
	Reference	Z. Naturforsch. 53b, 161—164 (1998); eingegangen am 14. November 1997
	Published	1998
	Keywords	Fullerene C60, Synthesis, Crystal Structure
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	Identifier	ZNB-1998-53b-0161
	Volume	53

90	Author	Hk Wulff, Müller-Buschbaum	Requires cookie*
	Title	Isolierte trigonale S r 0 6-Prismen verknüpfen Kagome-Netze im Strontium-Manganat(I V)-Tellurat( VI): SrMnTe06 Kagome Layers Connected by Isolated Trigonal Sr06 Prisms in the Strontium Manganate(IV) Tellurate(VI): SrMnTe06 L
	Abstract	Single crystals of the hitherto unknown compound SrM nT e06 have been prepared from Sr(0H)2-8H20 , M n C 0 3(aq) and T e 0 2 in air by crystallization below the melt range. X-ray in vestigations showed hexagonal symmetry, space group D3h-P62m, lattice constants a = 5.143(1), c = 5.384(2) A, Z = 1. SrM nTe06 is characterized by staggered [(Mn/Te)60 18] Kagome layers along [001]. These layers are connected by Sr2+ ions, resulting in S r0 6 prisms isolated from each other. The structure is discussed with respect to the connection of Kagome nets in the quaternary oxides of the Ba3Ln40 9 type.
	Reference	Z. Naturforsch. 53b, 283—286 (1998); eingegangen am 7. November 1997
	Published	1998
	Keywords	Strontium, Manganese, Tellurate, Crystal Structure
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	Identifier	ZNB-1998-53b-0283
	Volume	53

91	Author	B. Wedel, L. Wulff, Hk Müller-Buschbaum	Requires cookie*
	Title	Isolierte ^[TeOs]-Oktaederketten im Bleitellurat Pb2T e05 Isolated ^ [Te05] Chains of Octahedra in the Lead Tellurate Pb2T e05
	Abstract	Single crystals of Pb2T e0 5 have been prepared by flux techniques. X-ray investigations showed a new crystal structure with monoclinic symmetry, space group Cj-Cc, a = 13.099(3), b = 5.714(1), c = 7.520(2) Ä, ß = 123,80(3)°, Z = 4. Pb2T e 0 5 is characterized by o[o[Te05] chains of octahedra isolated from each other and incorporated into an edge, corner and face connected frame of P b 0 7 polyhedra. Possible positions o f the lone pair o f electrons of Pb2+ are estimated by calculations of Coulomb terms of lattice energy.
	Reference	Z. Naturforsch. 53b, 287—290 (1998); eingegangen am 17. November 1997
	Published	1998
	Keywords	Lead, Tellurate, Crystal Structure
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	Identifier	ZNB-1998-53b-0287
	Volume	53

92	Author	Thorsten Grob, FrankW. Eller, K. Urt, D. Ehnicke	Requires cookie*
	Title	Die Kristallstruktur von [Me3PN(H)PMe3]4l 28? einem Polyiodid mit I3~-, lg2--und I144"-Ionen Crystal Structure o f [M e3P N (H )P M e3]4I28, a Polyiodide w ith I3~, I82 -, and I 144~ Ions
	Abstract	Black-red single crystals of [Me3PN(H)PMe3]4I28 have been prepared by the reaction of [Me3PNPMe3]I with iodine in dichloromethane solution in the presence of Me3SiI and traces of water. The polyiodide crystallizes triclinically in the space group Pi with two formula units per unit cell with the lattice dimensions a = 831.2(1), b = 1661.2(3), c = 1739.0(3) pm, q = 87.26(1)°, ß = 79.48(1)°, 7 = 78.17(1)°. The structure consists of [Me3PN(H)PMe3]2+ ions, linear I3~ ions, z-shaped I8: ~ ions, and zig-zag chains of I I44-ions, the terminal iodine atoms of which form I-H -N hydrogen bridges to the cations.
	Reference	Z. Naturforsch. 53b, 552—556 (1998); eingegangen am 23. Februar 1998
	Published	1998
	Keywords	Polyiodide, Synthesis, Crystal Structure
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	Identifier	ZNB-1998-53b-0552
	Volume	53

93	Author	Andreas Mommertz, Gertraud Geiseier, Klaus Harms, Kurt Dehnicke	Requires cookie*
	Title	Kristallstrukturen von Me2Si[N(SiMe3)2]2 und [Me2Si(NPh)(NHPh)LiOEt2]2 Crystal Structures of Me2Si[N(SiM e3)2]2 and [Me2Si(NPh)(NHPh)Li-OEt2]2
	Abstract	The crystal structures of the title compounds are reported. Me2Si[N(SiMe3)2]2 : Space group Pbcn, Z = 4, lattice dimensions at 213 K: a = 1487.8(1), b = 1299.4(1), c = 1259.7(1) pm. The compound forms monomeric molecules with crystallographic C2 symmetry and Si-N bond lengths of 177.9(3), 171.6(3) and 175,2(3) pm. [Me2 Si(NPh)(NHPh)Li OEt2]2: Space group P2]/n, Z = 2, lattice dimensions at 190 K: a = 1082.7(3), b = 1038.8(2), c = 1641.3(4) pm, ß = 91.350(3)°. The compound forms centrosymmetric dimeric molecules in which the lithium atoms are members of a Li2N2 ring with Li-N bond lengths of 206.6(2) and 213.5(2) pm. The hydrogen atom at the nitrogen atom of the HNPh~ group is not involved in hydrogen bridging bonds.
	Reference	Z. Naturforsch. 53b, 977—980 (1998); eingegangen am 29. Mai 1998
	Published	1998
	Keywords	Silylamine, Lithium Amide, Crystal Structure
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	Identifier	ZNB-1998-53b-0977
	Volume	53

94	Author	Z. Naturforsch	Requires cookie*
	Title	Pentacoordinated Nitrogen Atoms in the Structure of Hexalithium Bis[methylsilyl-tris(methylimide)] Hexakis(tetrahydrofuran)
	Abstract	Lithiation of tris(methylamino)wt'f/7v/silane using an excess of n -butyllithium affords the cor responding trifunctional lithium amide in high yield. The compound crystallizes from tetrahy-drofuran as a dimer with six donor molecules: {[M eSi(NM eLi)3]2(thf)6}. The cluster is a cage structure grouped around a crystallographic center of inversion. The silicon and lithium atoms are tetrahedrally tetracoordinated, but the nitrogen atoms are pentacoordinated and have a square pyramidal environment of one carbon, one silicon, and three lithium atoms. Parallels can be drawn to other species with polymetallated nitrogen functions. An analogous compound was prepared from tris(methylamino)vwv/silane.
	Reference	(Z. Naturforsch. 54b, 8—12 [1999]; received September 1 1998)
	Published	1999
	Keywords	Silylamines, Silylamides, Crystal Structure
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	Identifier	ZNB-1999-54b-0008
	Volume	54

95	Author	Joachim Pethe, Joachim Strähle	Requires cookie*
	Title	Synthese und Kristallstruktur von [Au(AuNCO)(AuPPh3)8]Cl Synthesis and Crystal Structure of [Au(AuNCO)(AuPPh3)8]Cl
	Abstract	The photolysis of Cr(CO)6 and Ph3PAuN3 (1:2) in thf yields the unstable cluster cation [(Ph3PAu)5Cr(CO)4]+ that slowly decomposes to form the new homometallic gold cluster [Au(AuNCO)(AuPPh3)8]Cl. The cluster compound crystallizes in form of red needles in the tetragonal space group 14 with a = 2214.1(3), c = 1408.9(2) pm, and Z = 2. The inner skeleton of the cluster with the symmetry C4 consists of a centered square antiprism of nine Au atoms with the square faces of the antiprism being bridged by the AuNCO group, and a C P anion, respectively. The shortest Au-Au distances exist between the central and the 8+1 peripheral Au atoms ranging between 263.5(1) and 270.6(3) pm, the four Au-Cl distances are 280(1) pm.
	Reference	Z. Naturforsch. 54b, 381—384 (1999); eingegangen am 3.Dezember 1998
	Published	1999
	Keywords	Gold Cluster, Synthesis, Crystal Structure
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	Identifier	ZNB-1999-54b-0381
	Volume	54

96	Author	M. Ludwig3, R. Niewab, R. Kniep	Requires cookie*
	Title	Dimers [A12N6]12-and Chains J j A lN ^ ] in the Crystal Structures of Ca6[Al2N6] and Ba3[Al2N4]
	Abstract	Pale yellow transparent single crystals of Ca6[Al2Nö] (P 2\/c, No. 14, a = 693.7(3), b = 614.9(3), c = 987.1(5) pm, ß = 94.01(5)°; Z = 4) and colourless transparent single crystals of Ba.^ALN*] (Pnna, No. 52, a = 617.9(2), b = 1005.2(4), c = 1023.0(4) pm; Z = 4) were obtained from reactions of mixtures of the representative metals with nitrogen at Tmax = 1000 °C. The crystal structure of CaöfALNft] contains isolated units [ALNftJ12-built of two edge-sharing tetrahedra. Ba3[ALN4] is an isotype of S r^A bN ^. The crystal structure contains infinite chains ^ [A1N^T2] of trans edge-sharing tetrahedra.
	Reference	Z. Naturforsch. 54b, 461—465 (1999); received December 18 1998
	Published	1999
	Keywords	Nitridoaluminates, Preparation, Crystal Structure
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	Identifier	ZNB-1999-54b-0461
	Volume	54

97	Author	MarkusF. Zumdick, Rainer Pöttgen	Requires cookie*
	Title	Condensed [Ru4Sn6] Units in the Stannides LnRu4Sn6 (Ln = La, Pr, Nd, Sm, Gd) -Synthesis, Structure, and Chemical Bonding
	Abstract	The stannides LnRu4Sn6 (Ln = La, Pr, Nd, Sm, Gd) were prepared by reaction of the elements in an arc-melting furnace and subsequent annealing at 1120 K. The praseodymium, the neodymium, and the samarium stannide were obtained for the first time. The LnRu4Sn6 stannides were investigated by X-ray diffraction both on powders and single crystals. They adopt the YRu4Sn6 type structure which was refined from single crystal X-ray data for the samarium and the gadolinium compound: /42m, a = 686.1 (1), c = 977.7(2) pm, wR2 = 0.0649, 483 F2 values for SmRu4Sn6, and a = 685.2(1), c = 977.6(3) pm, wR2 = 0.0629, 554 F2 values for GdRu4Sn6 with 19 variables for each refinement. The striking structural motif of these stannides are distorted RuSnö octahedra with Ru-Sn distances ranging from 257 to 278 pm. Four of such octahedra are condensed via common edges and faces forming [Ru4Snö] units which are packed in a tetragonal body-centered arrangement. The rare-earth atoms fill the voids between the [Ru4Sn6] units. Based on an extended Hückel calculation, strong bonding interactions were found for the Ru-Sn and the various Sn-Sn contacts.
	Reference	Z. Naturforsch. 54b, 863—869 (1999); received March 29 1999
	Published	1999
	Keywords	Stannides, Crystal Structure, Chemical Bonding
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	Identifier	ZNB-1999-54b-0863
	Volume	54

98	Author	Rolf Minkwitz, Michael Berkei, Sonderdruckanforderungen An, ProfR. Dr, Minkwitz	Requires cookie*
	Title	Neuuntersuchung der Kristallstruktur von a-ICl Novel Investigation on the Crystal Structure of a-ICl
	Abstract	The redetermination of the crystal structure of a-iodine monochloride, a-ICl, is described. It cry stallises monoclinically in the space group P2j/c with a = 1216.2(1), b = 428.6(1), c = 1188.9(1) pm, ß= 117.50(1)° and eight formula units per unit cell.
	Reference	Z. Naturforsch. 54b, 1615—1617 (1999); eingegangen am 10. September 1999
	Published	1999
	Keywords	Iodine Monochloride, Redetermination, Crystal Structure
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	Identifier	ZNB-1999-54b-1615_n
	Volume	54

99	Author	Ratikanta Mishra, Rolf-Dieter Hoffmann, Rainer Pöttgen	Requires cookie*
	Title	New Magnesium Compounds /fcE2Cu2Mg (RE = Y, La -Nd, Sm, Gd -Tm, Lu) with Mo2FeB2 Type Structure
	Abstract	The title compounds were synthesized by reaction of the elements in sealed tantalum tubes in a water-cooled sample chamber in a high-frequency furnace. These magnesium intermetallics crystallize with the tetragonal Mo2FeB2 type structure, space group PMmbm. The lattice pa rameters of all compounds were refined from X-ray powder data. Single crystal X-ray data yielded a = 792.09(6), c = 396.31(8) pm, wR2 = 0.0396, 315 F 2 values for La2Cu2Mg, a = 778.30(5), c = 384.04(5) pm, wR2 = 0.0954, 214 F 2 values for Nd2Cu2Mg, and a = 762.65(5), c = 374.09(3) pm, wR2 = 0.0566, 186 F 2 values for Y2Cu2Mg with 12 variable parameters for each refinement. The /?£, 2Cu2Mg structures can be described as an intergrowth of distorted A1B2 and CsCl related slabs of compositions RECui and REMg. Chemical bonding in La2Cu2Mg was investigated on the basis of extended Hückel calculations and compared to isotypic La2Cu2ln. This structure was also refined from single crystal X-ray data: PMmbm, a = 780.8(2), c = 400.1(2) pm, wR2 = 0.0351, 211 F 2 values and 12 variable parameters.
	Reference	Z. Naturforsch. 56b, 239—244 (2001); received January 25 2001
	Published	2001
	Keywords	Intermetallic Compounds, Magnesium, Crystal Structure
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	Identifier	ZNB-2001-56b-0239
	Volume	56

100	Author	N. O. Rb, E. Rt, W. M. Itzel, Christian Lustig	Requires cookie*
	Title	Crystal Structure of a Lithium Chloride Cubane Cluster Solvated by Diethyl Ether
	Reference	Z. Naturforsch. 56b, 443 (2001); received March 2 2001
	Published	2001
	Keywords	Lithium Chloride, Aggregation, Crystal Structure
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	Identifier	ZNB-2001-56b-0443_n
	Volume	56

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