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1.
Ming‐Xue Li Su‐Zhi Li 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(11):m525-m526
The title novel manganese(II) coordination polymer, {(C10H10N2)[MnCl4]}n, consists of a one‐dimensional infinite zigzag chain composed of polymeric [MnCl4]2− units in which each Mn2+ ion is located on a twofold rotation axis and is coordinated to two terminal Cl atoms and four bridging chloro ligands. Adjacent Mn2+ ions are linked by double Cl bridges arranged about a centre of inversion, thus forming anionic chains of distorted edge‐sharing octahedra. Rows of approximately parallel 4,4′‐bipyridinium cations run side‐by‐side with the MnCl4 chains. A two‐dimensional layer structure is constructed via hydrogen bonds and by additional π–π stacking interactions. 相似文献
2.
Zoya A. Solodovnikova Sergey F. Solodovnikov 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(7):i53-i56
The crystal structures of dirubidium heptaoxodimolybdate, Rb2Mo2O7, and dicaesium heptaoxodimolybdate, Cs2Mo2O7, in the space groups Ama2 and P21/c, respectively, have been determined for the first time by single‐crystal X‐ray diffraction. The structures represent two novel structure types of monovalent ion dimolybdates, A2Mo2O7 (A = alkaline elements, NH4, Ag or Tl). In the structure of Rb2Mo2O7, Mo atoms are on a twofold axis, on a mirror plane and in a general position. One of the Rb atoms lies on a twofold axis, while three others are on mirror planes. Two O atoms attached to the Mo atom on a mirror plane are located on the same plane. Rubidium dimolybdate contains a new kind of infinite Mo–O chain formed from linked MoO4 tetrahedra and MoO6 octahedra alternating along the a axis, with two terminal MoO4 tetrahedra sharing corners with each octahedron. The chains stack in the [001] direction to form channels of an approximately square section filled by ten‐coordinate Rb ions. Seven‐ and eight‐coordinate Rb atoms are located between chains connected by a c translation. In the structure of Cs2Mo2O7, all atoms are in general positions. The MoO6 octahedra share opposite corners to form separate infinite chains running along the c axis and strengthened by bridging MoO4 tetrahedra. The same Mo–O polyhedral chain occurs in the structure of Na2Mo2O7. Eight‐ to eleven‐coordinate Cs atoms fill the space between the chains. The atomic arrangement of caesium dimolybdate has an orthorhombic pseudosymmetry that suggests a possible phase transition P21/c→Pbca at elevated temperatures. 相似文献
3.
Martin U. Schmidt Edith Alig Lothar Fink Michael Bolte Robin Panisch Volodymyr Pashchenko Bernd Wolf Michael Lang 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(7):m361-m364
Double‐layer structures consisting of alternating polar and non‐polar layers have been prepared using Mn2+ ions and o‐hydroxynaphthoic acids. The polar layers contain the Mn2+ ions, carboxylate groups, hydroxy groups and water molecules. The non‐polar layers are built up from the naphthalene moieties. In catena‐poly[[diaquamanganese(II)]bis(μ‐3‐hydroxy‐2‐naphthoato‐κ2O:O′)] (also called manganese 3‐hydroxy‐2‐naphthoate dihydrate), [Mn(C11H7O3)2(H2O)2]n, (I), the Mn2+ ions are connected by carboxylate groups to form two‐dimensional networks. This compound shows distinct antiferromagnetic interactions and long‐range ordering at low temperature. In contrast, tetraaquabis(1‐hydroxy‐2‐naphthoato‐κO)manganese(II), [Mn(C11H7O3)2(H2O)4], (II), which lacks a close linkage between the Mn2+ ions, reveals purely paramagnetic behaviour. In (II), the Mn2+ ion lies on an inversion centre. 相似文献
4.
Pierre F. Poudeu Poudeu Michael Ruck 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(5):i41-i43
The silver bismuth tridecasulfide Ag3.5Bi7.5S13 crystallizes in the monoclinic space group C2/m. Its structure is built up of two alternating kinds of layered modules parallel to (001). In the module denoted A, octahedra around the metal positions (M = Ag/Bi, M2 and an S atom on 2/m, other atoms on m) alternate with paired monocapped trigonal prisms around Bi. The NaCl‐type module B is composed of parallel eight‐membered chains of edge‐sharing octahedra running diagonally across it. Ag3.5Bi7.5S13 is the member with N = 8 of the pavonite homologous series NP of ternary compounds with the general formula [Bi2S3]2·[AgBiS2](N−1)/2. 相似文献
5.
Uwe Kolitsch 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(5):i35-i37
Sodium indium(III) chromate(VI) dihydrate, NaIn(CrO4)2·2H2O, synthesized from an aqueous solution at room temperature, is the first indium(III) member of the large family of compounds with kröhnkite [Na2CuII(SVIO4)2·2H2O]‐type chains. The crystal structure is based on infinite octahedral–tetrahedral [In(CrO4)2(H2O)2]− chains along [010], linked via charge‐balancing Na+ cations. The slightly distorted InO4(H2O)2 octahedra are characterized by a mean In—O distance of 2.125 Å. The CrO4 tetrahedra are strongly distorted (mean Cr—O = 1.641 Å). The Na atom shows an octahedral coordination, unprecedented among compounds with kröhnkite‐type chains. The NaO6 octahedra share opposite edges with the InO4(H2O)2 octahedra to form infinite [001] chains. The hydrogen bonds are of medium strength. NaIn(CrO4)2·2H2O belongs to the structural type F2 in the classification of Fleck, Kolitsch & Hertweck [Z. Kristallogr. (2002), 217 , 435–443], and is isotypic with KAl(CrO4)2·2H2O and MFe(CrO4)2·2H2O (M = K, Tl or NH4). All atoms are in special positions except one O atom. 相似文献
6.
Alexander A. Tsirlin Evgeny V. Dikarev Evgeny V. Antipov Roman V. Shpanchenko 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(2):i13-i15
Single crystals of a new complex phosphate, calcium sodium vanadium phosphate, Ca8.42Na1.16V(PO4)7, have been grown from a melt under an inert atmosphere. The crystal structure has rhombohedral (R3c) symmetry and belongs to the whitlockite structure type. Vanadium(III) ions occupy nearly regular octahedral sites (M5 with 3 point symmetry), which share corners with six PO4 tetrahedra to form isolated units. The calcium ions occupy eight‐ and nine‐coordinated sites. The sodium ions partially occupy one octahedral position and share one nine‐coordinated position with a Ca atom. 相似文献
7.
Mats Johnsson Helmuth Berger Richard Becker 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(8):i67-i69
Single crystals of tricobalt(II) tellurium(VI) hexaoxide, Co3TeO6, were synthesized via transport reactions using HCl as transporting agent. The compound crystallizes in the monoclinic system (space group C2/c). The Te atoms are positioned in 4b () and 8f positions, while the Co atoms are in 4e (2) and 8f positions. The structure consists of (100) oxygen layers packed in a hhchhc sequence, with TeVI in octahedral coordination and CoII in both octahedral and tetrahedral coordination. The structure contains face‐sharing CoO6 octahedra, as well as edge‐sharing CoO4 tetrahedra. Co3TeO6 is the first oxide that is isostructural with the β‐Li3MF6 family of compounds (M = Al, Cr, Ga, Ti and V). 相似文献
8.
Stefan T. Norberg Stefan Hoffmann Masahiro Yoshimura Nobuo Ishizawa 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(3):i35-i38
The compound Al6Ti2O13 (hexaaluminium dititanium tridecaoxide) has been synthesized using an arc‐imaging furnace, which allows fast cooling of melted oxides. The structure consists of infinite double chains of polyhedra running along the c axis. These chains are built up by four kinds of strongly distorted oxygen octahedra randomly occupied by either Ti or Al (point symmetry m or m2m), and by trigonal bipyramids exclusively occupied by Al (point symmetry m2m). 相似文献
9.
Michel Fleck Ladislav Bohatý 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(9):m412-m416
In catena‐poly[[[diaquanickel(II)]‐di‐μ‐glycine] dibromide], {[Ni(C2H5NO2)2(H2O)2]Br2}n, (I), the Ni atom is located on an inversion centre. In catena‐poly[[[tetraaquamagnesium(II)]‐μ‐glycine] dichloride], {[Mg(C2H5NO2)(H2O)4]Cl2}n, (II), the Mg atom and the non‐H atoms of the glycine molecule are located on a mirror plane. All other atoms are located on general positions. The atomic arrangements of both compounds are characterized by [MO6] octahedra (M = Ni or Mg) connected by glycine molecules, with the halogenide ions in the interstices. In (I), four of the coordinating O atoms are from glycine and two are from water molecules, building layers of octahedra and organic molecules. In (II), two of the coordinating O atoms are from glycine and four are from water molecules. The octahedra and organic molecules form chains. 相似文献
10.
Günther J. Redhammer Georg Roth Georg Amthauer 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(4):i21-i24
The structure of copper(I,II) pentachromium(III) germanate, Cu(Cu0.44Cr4.56)Ge2O12, contains one Cu position (m2m), one Ge position (m) and three Cr positions (2/m, m and 2). The close‐packed structure is described in terms of slabs of edge‐sharing Cr3+O6 octahedra and isolated CuO4 and GeO4 tetrahedra. These slabs are aligned parallel to the bc plane and are separated from each other by GeO4 tetrahedra along a. The tetrahedral coordination observed for the Cu+/Cu2+ ions represents an unusual feature of the structure. The Cr—O and Cu—O bond lengths are compared with literature data. 相似文献
11.
Xin‐Qiang Wang Wen‐Tao Yu Dong Xu Guang‐Hui Zhang Yan‐Ling Geng 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(6):m278-m280
The title complex, [MnHg(NCS)4(C2H5NO)2]n, consists of slightly distorted MnN4O2 octahedra and HgS4 tetrahedra. Each MnII cation is bound to four N atoms of the NCS groups and two O atoms of the N‐methylformamide (NMF) ligands in a cis configuration. Each HgII cation is coordinated to four S atoms of NCS groups. Each pair of MnII and HgII cations is connected by an –NCS– bridge, forming an infinite three‐dimensional –Mn—NCS—Hg– network. 相似文献
12.
Michel Fleck Karolina Schwendtner Ana Hensler 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(4):m122-m125
In bis(glycine) lithium chromate monohydrate {systematic name: poly[aquadi‐μ‐glycinato‐μ‐tetraoxochromato(VI)‐dilithium(I)]}, [CrLi2(C2H5NO2)2O4(H2O)]n, (I) (space group P212121), and bis(glycine) lithium molybdate {systematic name: poly[di‐μ‐glycinato‐μ‐tetraoxomolybdato(VI)‐dilithium(I)]}, [Li2Mo(C2H5NO2)2O4]n, (II) (space group P21), all atoms are located on general positions. The crystal structure of (I) is characterized by infinite chains of corner‐sharing [LiO4] tetrahedra, which are connected by glycine molecules to form layers. [CrO4] tetrahedra are attached to the [LiO4] tetrahedra. Compound (II) contains dimers of [LiO4] tetrahedra which are connected by [MoO4] tetrahedra to form chains, which are in turn connected by glycine molecules to form double layers. 相似文献
13.
Abderrahmen Guesmi Ahmed Driss 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(1):i16-i17
The structure of the hydrothermally synthesized compound AgCo3PO4(HPO4)2, silver tricobalt phosphate bis(hydrogen phosphate), consists of edge‐sharing CoO6 chains linked together by the phosphate groups and hydrogen bonds. The three‐dimensional framework delimits two types of tunnels which accommodate Ag+ cations and OH groups. The title compound is isostructural with the compounds AM3H2(XO4)3 (A = Na or Ag, M = Co or Mn, and X = P or As) of the alluaudite structure type. 相似文献
14.
Xiao‐Hong Wen R.‐K. Li C.‐T. Chen 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(3):i21-i23
Single crystals of a new rubdidium beryllium borate, RbBe4(BO3)3, have been obtained by spontaneous nucleation from a high‐temperature melt. This new orthorhombic (Pnma) structure type contains [Be2BO4]− rings, made of two BeO4 tetrahedra and one BO3 triangle, which constitute the basic structural units. The m plane runs through the B and one of the O atoms and intersects the ring. These rings form chains in the a direction, which are connected in the b and c directions to form zeolite‐type cages in which the Rb+ cations are located, at sites of m symmetry. 相似文献
15.
Zoya A. Solodovnikova Evgeniya S. Zolotova Sergey F. Solodovnikov 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(1):i6-i8
Two new isotypic triple molybdates, namely tricesium lithium dicobalt tetrakis(tetraoxomolybdate), Cs3LiCo2(MoO4)4, and trirubidium lithium dizinc tetrakis(tetraoxomolybdate), Rb3LiZn2(MoO4)4, crystallize in the non‐centrosymmetric cubic space group I3d and adopt the Cs6Zn5(MoO4)8 structure type. In the parent structure, the Zn positions have 5/6 occupancy, while they are fully occupied by statistically distributed M2+ and Li+ cations in the title compounds. In both structures, all corners of the (M2/3Li1/3)O4 tetrahedra (M = Co and Zn), having point symmetry , are shared with the MoO4 tetrahedra, which lie on threefold axes and share corners with three (M,Li)O4 tetrahedra to form open mixed frameworks. Large alkaline cations occupy distorted cuboctahedral cavities with symmetry. The mixed tetrahedral frameworks in the structures are close to those of mayenite (12CaO·7Al2O3) and the related compounds 11CaO·7Al2O3·CaF2, wadalite (Ca6Al5Si2O16Cl3) and Na6Zn3(AsO4)4·3H2O, but the terminal vertices of the MoO4 tetrahedra are directed in opposite directions along the threefold axes compared with the configurations of Al(Si)O4 or AsO4 tetrahedra. The cation arrangements in Cs3LiCo2(MoO4)4, Rb3LiZn2(MoO4)4 and Cs6Zn5(MoO4)8 repeat the structure of Y3Au3Sb4, being stuffed derivatives of the Th3P4 type. 相似文献
16.
Wilhelm Klein Jan Curda Martin Jansen 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(6):i63-i64
Pb2(Hg3O4)(CrO4) consists of [CrO4]2− tetrahedra, linear O—Hg—O dumbbells and divalent Pb atoms in [3+5]‐coordination. The HgO2 dumbbells are condensed into [Hg3O4]2− units and can be regarded as a section of the HgO structure. The [Hg3O4]2− complex anions are connected by interstitial Pb2+ ions, while the [CrO4]2− tetrahedra are isolated. 相似文献
17.
Ju‐Ying Hou Qi‐Yu Yang Han‐Hui Zhang Yi‐Ping Chen Jian‐Fu Xu Chang‐Cang Huang 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(6):i59-i60
A new three‐dimensional bimetallic tellurite, BaV2TeO8, was synthesized by the hydrothermal reaction of Ba(OH)2, TeO2 and V2O5, and characterized by single‐crystal X‐ray diffraction. The three‐dimensional framework is built up from anionic [V2TeO8]n2n− layers parallel to (101) and connected via Ba—O bonds. The anionic layers are formed by three types of polyhedra, namely VO5 tetragonal pyramids, VO4 tetrahedra and TeO4+2 `folded square' polyhedra. 相似文献
18.
Günther J. Redhammer Georg Roth Dan Topa Georg Amthauer 《Acta Crystallographica. Section C, Structural Chemistry》2008,64(3):i21-i26
Disodium hexamanganese(II,III) germanate is the first aenigmatite‐type compound with significant amounts of manganese. Na2(Mn5.26Na0.74)Ge6O20 is triclinic and contains two different Na positions, six Ge positions and 20 O positions (all with site symmetry 1 on general position 2i of space group P). Five out of the seven M positions are also on general position 2i, while the remaining two have site symmetry (Wyckoff positions 1f and 1c). The structure can be described in terms of two different layers, A and B, stacked along the [011] direction. Layer A contains pyroxene‐like chains and isolated octahedra, while layer B is built up by slabs of edge‐sharing octahedra connected to one another by bands of Na polyhedra. The GeO4 tetrahedra show slight polyhedral distortion and are among the most regular found so far in germanate compounds. The M sites of layer A are occupied by highly charged (trivalent) cations, while in layer B a central pyroxene‐like zigzag chain can be identified, which contains divalent (or low‐charged) cations. This applies to the aenigmatite‐type compounds in general and to the title compound in particular. 相似文献
19.
Julien Lesage Anne Guesdon Bernard Raveau 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(5):i44-i46
Rubidium trigallium bis(triphosphate), RbGa3(P3O10)2 has been synthesized by solid‐state reaction and studied by single‐crystal X‐ray diffraction at room temperature. This compound is the first anhydrous gallium phosphate containing both GaO4 tetrahedra (Ga1) and GaO6 octahedra (Ga2 and Ga3). The three independent Ga atoms are located on sites with imposed symmetry 2 (Wickoff positions 4a for Ga1 and 4b for Ga2 and Ga3). The GaO4 and GaO6 polyhedra are connected through the apices to triphosphate groups and form a three‐dimensionnal host lattice. This framework presents intersecting tunnels running along the [001] and <110> directions, where the Rb2+ cations are located on sites with imposed symmetry 2 (Wickoff position 4a). The structure also exhibits remarkable features, such as infinite helical columns created by the junction of GaO4 and PO4 tetrahedra. 相似文献
20.
Hiroyuki Hosomi Shigeru Ohba Yoshikatsu Ito 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(6):e260-e261
In the title two adducts, C3H12N22+·2C9H6NO4?, (I), and C6H16N22+·2C9H6NO4?, (II), hydrogen bonds between the diammonium and carboxylate ions form a two‐dimensional network parallel to the ab plane in (I) and one‐dimensional chains along the c axis in (II). The cyclohexanediammonium ion in (II) has a crystallographic twofold axis. 相似文献