Synthesis and Characterization of Europium‐exchanged Titanate Nanoporous Phosphors

Eu_x(NH₄)_2‐2xTi₃O₇ nanoporous phosphor was prepared by ion exchange method. (NH₄)₂Ti₃O₇ nanotubes were employed as the host structure by treating H₂Ti₃O₇ with NH₄OH solution and the activator, Eu²⁺, was introduced into the host via ion exchange. This is an easy and feasible way to prepare a phosphor. The synthesized samples were characterized using TEM, XRD, N₂ adsorption‐desorption isotherm, TPR, and fluorescence spectrophotometer. Experimental results showed that a portion of Eu²⁺ ions was oxidized into Eu³⁺ ions during ion exchange, resulting in the present phosphor with blue‐emitting and red‐emitting. Moreover, the tubular structure of Eu_x(NH₄)_2‐2xTi₃O₇ was distorted as Eu²⁺ was placed into the host structure. This distortion is attributed to the electrostatic interaction between Eu²⁺ and the electric field of the host structure.     

Synthesis and crystal structure of 2‐amino‐3‐hydroxypyridinium dioxido(pyridine‐2,6‐dicarboxylato‐κ3O2,N,O6)vanadate(V) and its conversion to nanostructured V2O5

2‐Amino‐3‐hydroxypyridinium dioxido(pyridine‐2,6‐dicarboxylato‐κ³O²,N,O⁶)vanadate(V), (C₅H₇N₂O)[V(C₇H₃NO₄)O₂] or [H(amino‐3‐OH‐py)][VO₂(dipic)], (I), was prepared by the reaction of VCl₃ with dipicolinic acid (dipicH₂) and 2‐amino‐3‐hydroxypyridine (amino‐3‐OH‐py) in water. The compound was characterized by elemental analysis, IR spectroscopy and X‐ray structure analysis, and consists of an anionic [VO₂(dipic)]⁻ complex and an H(amino‐3‐OH‐py)⁺ counter‐cation. The V^V ion is five‐coordinated by one O,N,O′‐tridentate dipic dianionic ligand and by two oxide ligands. Thermal decomposition of (I) in the presence of polyethylene glycol led to the formation of nanoparticles of V₂O₅. Powder X‐ray diffraction (PXRD) and scanning electron microscopy (SEM) were used to characterize the structure and morphology of the synthesized powder.     

Regioselective synthesis and characterization of monovanadium‐substituted β‐octamolybdate [VMo7O26]5−

The monovanadium‐substituted polyoxometalate anion [VMo₇O₂₆]^5?, exhibiting a β‐octamolybdate archetype structure, was selectively prepared as pentapotassium [hexaikosaoxido(heptamolybdenumvanadium)]ate hexahydrate, K₅[VMo₇O₂₆]·6H₂O ( VMo₇ ), by oxidation of a reduced vanadomolybdate solution with hydrogen peroxide in a fast one‐pot approach. X‐ray structure analysis revealed that the V atom occupies a single position in the cluster that differs from the other positions by the presence of one doubly‐bonded O atom instead of two terminal oxide ligands in all other positions. The composition and structure of VMo₇ was also confirmed by elemental analyses and IR spectroscopy. The selectivity of the synthesis was inspected by a ⁵¹V NMR investigation which showed that this species bound about 95% of V^V in the crystallization solution. Upon dissolution of VMo₇ in aqueous solution, the [VMo₇O₂₆]^5? anion is substantially decomposed, mostly into [VMo₅O₁₉]^3?, α‐[VMo₇O₂₆]^4? and [V₂Mo₄O₁₉]^4?, depending on the pH.     

Chains of (4,4′‐bipyridyl)copper(I) bridged by dimolybdate units

The crystal structure of the title compound, poly­[bis‐[copper(I)‐μ‐(4,4′‐bipyridyl)‐N:N′]‐μ‐dimolybdato‐O:O′],[Cu₂(C₁₀H₈N₂)₂{Mo₂O₇}]_n, consists of {Mo₂O₇}^2? units (with the central O atom lying on twofold symmetry axes) and [Cu(4,4′‐bipy)]_nⁿ⁺ chains (bipy = bipyridyl); the chains are generated by a c‐glide‐plane operation. The {Mo₂O₇}^2? units are covalently bridged to two [Cu(4,4′‐bipy)]_nⁿ⁺ chains, forming a complex with a bridged double‐chain structure. The Cu—O and Cu—N distances are 2.191 (3) and 1.933 (3) Å, respectively.     

Ruthenium(V) Oxides from Low‐Temperature Hydrothermal Synthesis

Low‐temperature (200 °C) hydrothermal synthesis of the ruthenium oxides Ca_1.5Ru₂O₇, SrRu₂O₆, and Ba₂Ru₃O₉(OH) is reported. Ca_1.5Ru₂O₇ is a defective pyrochlore containing Ru^V/VI; SrRu₂O₆ is a layered Ru^V oxide with a PbSb₂O₆ structure, whilst Ba₂Ru₃O₉(OH) has a previously unreported structure type with orthorhombic symmetry solved from synchrotron X‐ray and neutron powder diffraction. SrRu₂O₆ exhibits unusually high‐temperature magnetic order, with antiferromagnetism persisting to at least 500 K, and refinement using room temperature neutron powder diffraction data provides the magnetic structure. All three ruthenates are metastable and readily collapse to mixtures of other oxides upon heating in air at temperatures around 300–500 °C, suggesting they would be difficult, if not impossible, to isolate under conventional high‐temperature solid‐state synthesis conditions.     

Two coordination polymers constructed by 5‐[(4‐carboxyphenoxy)methyl]benzene‐1,3‐dicarboxylic acid and 2,2′‐bipyridine: syntheses,structures and luminescence properties

Coordination polymers (CPs) have attracted increasing interest in recent years. In this work, two new CPs, namely poly[[aquabis(2,2′‐bipyridine‐κ²N,N′){μ₃‐5‐[(4‐carboxylatophenoxy)methyl]benzene‐1,3‐dicarboxylato‐κ⁴O¹,O^1′:O³:O⁵}(μ‐formato‐κ³O:O,O′)dicadmium(II)] monohydrate], {[Cd₂(C₁₆H₉O₇)(HCO₂)(C₁₀H₈N₂)₂(H₂O)]·H₂O}_n ( 1 ), and poly[[(2,2′‐bipyridine‐κ²N,N′){μ₃‐5‐[(4‐carboxylphenoxy)methyl]benzene‐1,3‐dicarboxylato‐κ⁴O¹,O^1′:O³:O⁵}manganese(II)] sesquihydrate], {[Mn(C₁₆H₁₀O₇)(C₁₀H₈N₂)]·1.5H₂O}_n ( 2 ), have been prepared using the tricarboxylic acid 5‐[(4‐carboxyphenoxy)methyl]benzene‐1,3‐dicarboxylic acid and 2,2′‐bipyridine under hydrothermal conditions. CP 1 displays a two‐dimensional layer structure which is further extended into a three‐dimensional (3D) supramolecular structure via intermolecular π–π interactions, while CP 2 shows a different 3D supramolecular structure extended from one‐dimensional ladder chains by intermolecular π–π interactions. In addition, the solid‐state luminescence spectra of 1 and 2 were studied at room temperature.     

Chemischer Transport fester Lösungen. 11 [1] Mischphasen und Chemischer Transport in den Systemen CrIII/InIII/GeIV/O,GaIII/InIII/GeIV/O,MnIII/InIII/GeIV/O und FeIII/InIII/GeIV/O

Chemical Vapor Transport of Solid Solutions. 11 Mixed Phases and Chemical Vapor Transport in the Systems Cr^III/In^III/Ge^IV/O, Ga^III/In^III/Ge^IV/O, Mn^III/In^III/Ge^IV/O und Fe^III/In^III/Ge^IV/O By means of chemical vapor transport methods the following mixed phases have been prepared: Cr_{0, 18}In_{1, 82}Ge₂O₇ (Cl₂, 950 → 850 °C), (Ga_{0, 6}In_{1, 4})₂Ge₂O₇ (Thortveitit‐type, Cl₂, 1050 → 950 °C), (Ga_{1, 9}In_{0, 1})₂Ge₂O₇ (Ga₂Ge₂O₇‐type, 1050 → 950 °C), (In_{1, 9}Mn_{0, 1})₂Ge₂O₇ (Thortveiti‐type, Cl₂, 1000 → 800 °C), mixed phase crystallizing in the Mn₂Ge₂O₇‐structure showing a composition near MnInGe₂O₇ (Cl₂, 1000 → 800 °C), Mn_{6, 5}In_{0, 5}GeO₁₂ (Braunit‐type, Cl₂, 1000 → 800 °C), (Fe_xIn_1‐x)Ge₂O₇ (Thortveitit‐type with x = 0…0, 94; Cl₂, 840 → 780 °C). Changing the compositions of the starting materials showed no effect on the composition of the deposit except for the system Fe₂O₃‐In₂O₃‐GeO₂.     

M3+(H2AsO4)(H2As2O7) (M3+ = Al,Ga) and In2(H2AsO4)2(H2As2O7)2: a new layer structure type and a new framework structure type containing the rare H2As2O72− group

The crystal structures of hydrothermally synthesized aluminium dihydrogen arsenate(V) dihydrogen diarsenate(V), Al(H₂AsO₄)(H₂As₂O₇), gallium dihydrogen arsenate(V) dihydrogen diarsenate(V), Ga(H₂AsO₄)(H₂As₂O₇), and diindium bis[dihydrogen arsenate(V)] bis[dihydrogen diarsenate(V)], In₂(H₂AsO₄)₂(H₂As₂O₇)₂, were determined from single‐crystal X‐ray diffraction data collected at room temperature. The first two compounds are representatives of a novel sheet structure type, whereas the third compound crystallizes in a novel framework structure. In all three structures, the basic building units are M ³⁺O₆ octahedra (M = Al, Ga, In) that are connected via one H₂AsO₄⁻ and two H₂As₂O₇²⁻ groups into chains, and further via H₂As₂O₇²⁻ groups into layers. In Al/Ga(H₂AsO₄)(H₂As₂O₇), these layers are interconnected by weak‐to‐medium–strong hydrogen bonds. In In₂(H₂AsO₄)₂(H₂As₂O₇)₂, the H₂As₂O₇²⁻ groups link the chains in three dimensions, thus creating a framework topology, which is reinforced by weak‐to‐medium–strong hydrogen bonds. The three title arsenates represent the first compounds containing both H₂AsO₄⁻ and H₂As₂O₇²⁻ groups.     

An investigation of polyhedral deformation in two mixed‐metal diarsenates: SrZnAs2O7 and BaCuAs2O7

Two isostructural diarsenates, SrZnAs₂O₇ (strontium zinc diarsenate), (I), and BaCuAs₂O₇ [barium copper(II) diarsenate], (II), have been synthesized under hydrothermal conditions and characterized by single‐crystal X‐ray diffraction. The three‐dimensional open‐framework crystal structure consists of corner‐sharing M2O₅ (M2 = Zn or Cu) square pyramids and diarsenate (As₂O₇) groups. Each As₂O₇ group shares its five corners with five different M2O₅ square pyramids. The resulting framework delimits two types of tunnels aligned parallel to the [010] and [100] directions where the large divalent nine‐coordinated M1 (M1 = Sr or Ba) cations are located. The geometrical characteristics of the M1O₉, M2O₅ and As₂O₇ groups of known isostructural diarsenates, adopting the general formula M1^IIM2^IIAs₂O₇ (M1^II = Sr, Ba, Pb; M2^II = Mg, Co, Cu, Zn) and crystallizing in the space group P2₁/n, are presented and discussed.     

Hydrogen bonding in two ammonium salts of 5‐sulfosalicylic acid: ammonium 3‐carboxy‐4‐hydroxybenzenesulfonate monohydrate and triammonium 3‐carboxy‐4‐hydroxybenzenesulfonate 3‐carboxylato‐4‐hydroxybenzenesulfonate

The structures of two ammonium salts of 3‐carboxy‐4‐hydroxybenzenesulfonic acid (5‐sulfosalicylic acid, 5‐SSA) have been determined at 200 K. In the 1:1 hydrated salt, ammonium 3‐carboxy‐4‐hydroxybenzenesulfonate monohydrate, NH₄⁺·C₇H₅O₆S⁻·H₂O, (I), the 5‐SSA⁻ monoanions give two types of head‐to‐tail laterally linked cyclic hydrogen‐bonding associations, both with graph‐set R₄⁴(20). The first involves both carboxylic acid O—H...O_water and water O—H...O_sulfonate hydrogen bonds at one end, and ammonium N—H...O_sulfonate and N—H...O_carboxy hydrogen bonds at the other. The second association is centrosymmetric, with end linkages through water O—H...O_sulfonate hydrogen bonds. These conjoined units form stacks down c and are extended into a three‐dimensional framework structure through N—H...O and water O—H...O hydrogen bonds to sulfonate O‐atom acceptors. Anhydrous triammonium 3‐carboxy‐4‐hydroxybenzenesulfonate 3‐carboxylato‐4‐hydroxybenzenesulfonate, 3NH₄⁺·C₇H₄O₆S²⁻·C₇H₅O₆S⁻, (II), is unusual, having both dianionic 5‐SSA²⁻ and monoanionic 5‐SSA⁻ species. These are linked by a carboxylic acid O—H...O hydrogen bond and, together with the three ammonium cations (two on general sites and the third comprising two independent half‐cations lying on crystallographic twofold rotation axes), give a pseudo‐centrosymmetric asymmetric unit. Cation–anion hydrogen bonding within this layered unit involves a cyclic R₃³(8) association which, together with extensive peripheral N—H...O hydrogen bonding involving both sulfonate and carboxy/carboxylate acceptors, gives a three‐dimensional framework structure. This work further demonstrates the utility of the 5‐SSA⁻ monoanion for the generation of stable hydrogen‐bonded crystalline materials, and provides the structure of a dianionic 5‐SSA²⁻ species of which there are only a few examples in the crystallographic literature.     

One‐ and two‐dimensional CdII coordination polymers incorporating organophosphinate ligands

Reaction of cadmium nitrate with diphenylphosphinic acid in dimethylformamide solvent yielded the one‐dimensional coordination polymer catena‐poly[[bis(dimethylformamide‐κO)cadmium(II)]‐bis(μ‐diphenylphosphinato‐κ²O:O′)], [Cd(C₁₂H₁₀O₂P)₂(C₃H₇NO)₂]_n, (I). Addition of 4,4′‐bipyridine to the synthesis afforded a two‐dimensional extended structure, poly[[(μ‐4,4′‐bipyridine‐κ²N:N′)bis(μ‐diphenylphosphinato‐κ²O:O′)cadmium(II)] dimethylformamide monosolvate], {[Cd(C₁₂H₁₀O₂P)₂(C₁₀H₈N₂)]·C₃H₇NO}_n, (II). In (II), the 4,4′‐bipyridine molecules link the Cd^II centers in the crystallographic a direction, while the phosphinate ligands link the Cd^II centers in the crystallographic b direction to complete a two‐dimensional sheet structure. Consideration of additional π–π interactions of the phenyl rings in (II) produces a three‐dimensional structure with channels that encapsulate dimethylformamide molecules as solvent of crystallization. Both compounds were characterized by single‐crystal X‐ray diffraction and FT–IR analysis.     

SrB5O7F3 Functionalized with [B5O9F3]6− Chromophores: Accelerating the Rational Design of Deep‐Ultraviolet Nonlinear Optical Materials

Fluorooxoborates, benefiting from the large optical band gap, high anisotropy, and ever‐greater possibility to form non‐centrosymmetric structures activated by the large polarization of [BO_xF_4?x]^(x+1)? building blocks, have been considered as the new fertile fields for searching the ultraviolet (UV) and deep‐UV nonlinear optical (NLO) materials. Herein, we report the first asymmetric alkaline‐earth metal fluorooxoborate SrB₅O₇F₃, which is rationally designed by taking the classic Sr₂Be₂B₂O₇ (SBBO) as a maternal structure. Its [B₅O₉F₃]^6? fundamental building block with near‐planar configuration composed by two edge‐sharing [B₃O₆F₂]^5? rings in SrB₅O₇F₃ has not been reported in any other borates. Solid state ¹⁹F and ¹¹B magic‐angle spinning NMR spectroscopy verifies the presence of covalent B?F bonds in SrB₅O₇F₃. Property characterizations reveal that SrB₅O₇F₃ possesses the optical properties required for deep‐UV NLO applications, which make SrB₅O₇F₃ a promising crystal that could produce deep‐UV coherent light by the direct SHG process.     

Polymorphism and photoluminescence properties of K3ErSi2O7

Two polymorphs of tripotassium erbium disilicate, K₃ErSi₂O₇, were synthesized by high‐temperature flux crystal growth during the exploration of the flux technique for growing new alkali rare‐earth elements (REE) containing silicates. Their crystal structures were determined by single‐crystal X‐ray diffraction analysis. One of them (denoted 1 ) crystallizes in the space group P6₃/mmc and is isostructural with disilicates K₃LuSi₂O₇, K₃ScSi₂O₇ and K₃YSi₂O₇, while the other (denoted 2 ) crystallizes in the space group P6₃/mcm and is isostructural with disilicates K₃NdSi₂O₇, K₃REESi₂O₇ (REE = Gd–Yb), K₃YSi₂O₇, K₃(Y_0.9Dy_0.1)Si₂O₇ and K₃SmSi₂O₇. In the crystal structure of polymorph 1 , the Er cations are in an almost perfect octahedral coordination, while in the crystal structure of polymorph 2 , part of the Er cations are in a slightly distorted octahedral coordination and the other part are in an ideal trigonal prismatic coordination environment. Sharing six corners, disilicate Si₂O₇ groups in the crystal structure of polymorph 1 link six ErO₆ octahedra, forming a three‐dimensional network and nine‐coordinated potassium cations are located in its holes. In the crystal structure of polymorph 2 , the disilicate Si₂O₇ groups connect four ErO₆ octahedra, as well as one ErO₆ trigonal prism. Three differently coordinated potassium cations are situated between them. Different site symmetries of the erbium cations in the crystal structures of polymorphs 1 and 2 affect their photoluminescence properties. Only polymorph 2 exhibits luminescence. Intense narrow lines in the emission spectrum are a result of the 4f–4f transition. The green emission line at 560 nm is the result of the Er³⁺ transition ⁴S_3/2→⁴I_15/2, and the luminescence line at 690 nm is the result of a ⁴F_9/2→⁴I_15/2 transition. The crystal morphologies of the two polymorphs are similar. Crystals of polymorph 1 are in the form of a hexagonal prism in combination with a hexagonal base, while crystals of polymorph 2 contain a dihexagonal prism in combination with a hexagonal base, although poorly developed faces of the dihexagonal pyramid can also be noticed.     

The first coordination polymer of lanthanum(III) with a naphthalene‐1,4,5,8‐tetracarboxylic 1,8‐anhydride derivative

The title compound, catena‐poly[[[heptaaqualanthanum(III)]‐μ‐1,3‐dioxo‐2‐oxa‐1H,3H‐phenalene‐6,7‐dicarboxylato‐κ²O⁶:O⁷] hemi(4,8‐dicarboxynaphthalene‐1,5‐dicarboxylate) dihydrate], {[La(C₁₄H₄O₇)(H₂O)₇](C₁₄H₆O₈)_0.5·2H₂O}_n, is a dihydrate of a coordination polymer between the dianion of naphthalene‐1,4,5,8‐tetracarboxylic 1,8‐anhydride and the heptahydrated lanthanum(III) ion, charge balanced by an additional 4,8‐dicarboxynaphthalene‐1,5‐dicarboxylate dianion that is located on an inversion centre and is not coordinated to the metal ion. The linear polymeric arrays adopt a comb‐like structure, and these pack in pairs with one chain interpenetrating another, like two parts of a zip, to optimize stacking interactions between their ligand fragments. All the components of this compound are further interlinked by an extensive pattern of O—H...O hydrogen bonds throughout the crystal structure. The main scientific significance of the results reported here is that they demonstrate for the first time the feasibility of coordination polymerization of the above organic ligand with lanthanide ions. The resulting polymer has a unique architecture. Finally, the reported structure is a rare example where the tetraacid and the diacid anhydride ligand species co‐exist in the same crystal.     

Sm2As4O9: Ein ungewöhnliches Samarium(III)‐Oxoarsenat(III) gemäß Sm4[As2O5]2[As4O8]

Sm₂As₄O₉: An Unusual Samarium(III) Oxoarsenate(III) According to Sm₄[As₂O₅]₂[As₄O₈] Pale yellow single crystals of the new samarium(III) oxoarsenate(III) with the composition Sm₄As₈O₁₈ were obtained by a typical solid‐state reaction between Sm₂O₃ and As₂O₃ using CsCl and SmCl₃ as fluxing agents. The compound crystallizes in the triclinic crystal system with the space group (No. 2, Z = 2; a = 681.12(5), b = 757.59(6), c = 953.97(8) pm, α = 96.623(7), β = 103.751(7), γ = 104.400(7)°). The crystal structure of samarium(III) oxoarsenate(III) with the formula type Sm₄[As₂O₅]₂[As₄O₈] (≡ 2 × Sm₂As₄O₉) contains two crystallographically different Sm³⁺ cations, where (Sm1)³⁺ is coordinated by eight, but (Sm2)³⁺ by nine oxygen atoms. Two different discrete oxoarsenate(III) anions are present in the crystal structure, namely [As₂O₅]^4? and [As₄O₈]^4?. The [As₂O₅]^4? anion is built up of two Ψ¹‐tetrahedra [AsO₃]^3? with a common corner, whereas the [As₄O₈]^4? anion consists of four Ψ¹‐tetrahedra with ring‐shaped vertex‐connected [AsO₃]^3? pyramids. Thus at all four crystallographically different As³⁺ cations stereochemically active non‐binding electron pairs (“lone pairs”) are observed. These “lone pairs” direct towards the center of empty channels running parallel to [010] in the overall structure, where these “empty channels” being formed by the linkage of layers with the ecliptically conformed [As₂O₅]^4? anions and the stair‐like shaped [As₄O₈]^4? rings via common oxygen atoms (O1 – O6, O8 and O9). The oxygen‐atom type O7, however, belongs only to the cyclo‐[As₄O₈]^4? unit as one of the two different corner‐sharing oxygen atoms.     

Cyclic heterotetrameric and low‐dimensional hydrogen‐bonded polymeric structures in the morpholinium salts of ring‐substituted benzoic acid analogues

The morpholinium (tetrahydro‐2H‐1,4‐oxazin‐4‐ium) cation has been used as a counter‐ion in both inorganic and organic salt formation and particularly in metal complex stabilization. To examine the influence of interactive substituent groups in the aromatic rings of benzoic acids upon secondary structure generation, the anhydrous salts of morpholine with salicylic acid, C₄H₁₀NO⁺·C₇H₅O₃⁻, (I), 3,5‐dinitrosalicylic acid, C₄H₁₀NO⁺·C₇H₃N₂O₇⁻, (II), 3,5‐dinitrobenzoic acid, C₄H₁₀NO⁺·C₇H₃N₂O₆⁻, (III), and 4‐nitroanthranilic acid, C₄H₁₀NO⁺·C₇H₅N₂O₄⁻, (IV), have been prepared and their hydrogen‐bonded crystal structures are described. In the crystal structures of (I), (III) and (IV), the cations and anions are linked by moderately strong N—H…O_carboxyl hydrogen bonds, but the secondary structure propagation differs among the three, viz. one‐dimensional chains extending along [010] in (I), a discrete cyclic heterotetramer in (III), and in (IV), a heterotetramer with amine N—H…O hydrogen‐bond extensions along b, giving a two‐layered ribbon structure. With the heterotetramers in both (III) and (IV), the ion pairs are linked though inversion‐related N—H…O_carboxylate hydrogen bonds, giving cyclic R₄⁴(12) motifs. With (II), in which the anion is a phenolate rather than a carboxylate, the stronger assocation is through a symmetric lateral three‐centre cyclic R₁²(6) N—H…(O,O′) hydrogen‐bonding linkage involving the phenolate and nitro O‐atom acceptors of the anion, with extension through a weaker O—H…O_carboxyl hydrogen bond. This results in a one‐dimensional chain structure extending along [100]. In the structures of two of the salts [i.e. (II) and (IV)], there are also π–π ring interactions, with ring‐centroid separations of 3.5516 (9) and 3.7700 (9) Å in (II), and 3.7340 (9) Å in (IV).     

A novel copper(II) complex with 1,10‐phenanthroline and ciprofloxacin

The X‐ray structure analysis of the title compound, chloro[1‐cyclopropyl‐6‐fluoro‐1,4‐dihydro‐4‐oxo‐7‐(piperazin‐4‐ium‐1‐yl)‐3‐quinolinecarboxylate‐κ²O³,O⁴](1,10‐phenanthroline‐κ²N,N′)copper chloride dihydrate, [CuCl(C₁₇H₁₈FN₃O₃)(C₁₂H₈N₂)]Cl·2H₂O or [CuCl(cfH)(phen)]Cl·2H₂O, where cfH is 1‐cyclopropyl‐6‐fluoro‐1,4‐dihydro‐4‐oxo‐7‐(piperazin‐4‐ium‐1‐yl)‐3‐quinolinecarboxylate and phen is 1,10‐phenanthroline, shows that the geometry around the Cu ion is a slightly distorted square pyramid. Two O atoms of the carbonyl and carboxyl groups of ciprofloxacin and two N atoms of 1,10‐phenanthroline are coordinated to the metal centre in the equatorial plane, and a Cl⁻ ion is coordinated at the apical position. Extensive intermolecular hydrogen bonding produces a supramolecular structure that consists of alternating six‐ and 12‐membered rings.     

Unexpected Luminescence Properties of Sr0.25Ba0.75Si2O2N2:Eu2+—A Narrow Blue Emitting Oxonitridosilicate with Cation Ordering

Owing to a parity allowed 4f⁶(⁷F)5d¹→4f⁷(⁸S_7/2) transition, powders of the nominal composition Sr_0.25Ba_0.75Si₂O₂N₂:Eu²⁺ (2 mol % Eu²⁺) show surprising intense blue emission (λ_em=472 nm) when excited by UV to blue radiation. Similarly to other phases in the system Sr_1?xBa_xSi₂O₂N₂:Eu²⁺, the described compound is a promising phosphor material for pc‐LED applications as well. The FWHM of the emission band is 37 nm, representing the smallest value found for blue emitting (oxo)nitridosilicates so far. A combination of electron and X‐ray diffraction methods was used to determine the crystal structure of Sr_0.25Ba_0.75Si₂O₂N₂:Eu²⁺. HRTEM images reveal the intergrowth of nanodomains with SrSi₂O₂N₂ and BaSi₂O₂N₂‐type structures, which leads to pronounced diffuse scattering. Taking into account the intergrowth, the structure of the BaSi₂O₂N₂‐type domains was refined on single‐crystal diffraction data. In contrast to coplanar metal atom layers which are located between layers of condensed SiON₃‐tetrahedra in pure BaSi₂O₂N₂, in Sr_0.25Ba_0.75Si₂O₂N₂:Eu²⁺ corrugated metal atom layers occur. HRTEM image simulations indicate cation ordering in the final structure model, which, in combination with the corrugated metal atom layers, explains the unexpected and excellent luminescence properties.     

A New Cu, Al Fluoride Disilicate CuAl2F2(Si2O7) and its Relations to Topaz

CuAl₂F₂(Si₂O₇) has been prepared by hydrothermal synthesis and its crystal structure was determined by single crystal X‐ray diffraction: space group Pnma, a = 8.8697(9), b = 14.084(2), c = 4.7553(5) Å, wR₂ = 0.056, R = 0.022. Cu²⁺ shows elongated square pyramidal coordination. Edge‐ and corner‐sharing [AlO₄F₂] octahedra with fluorine atoms in cis position form layers parallel to the ac plane. Along b these layers are linked by Si₂O₇ groups to form a three‐dimensional framework [Al₂F₂(Si₂O₇]^2–. In addition, the [CuO₅] pyramides connect two Al octahedra of neighbouring layers. The crystal structure is discussed as a derivative from topaz structure. The modular (or polysomatic) approach is used for this purpose, and for modelling hypothetical related compounds.     

2,3‐Dimethoxy‐10‐oxostrychnidinium 2‐(2,4,6‐trinitroanilino)benzoate monohydrate: a 1:1 proton‐transfer salt of brucine with o‐picraminobenzoic acid

In the structure of the title 1:1 proton‐transfer compound of brucine with 2‐(2,4,6‐trinitroanilino)benzoic acid, C₂₃H₂₇N₂O₄⁺·C₁₃H₇N₄O₈⁻·H₂O, the brucinium cations form classic undulating ribbon substructures through overlapping head‐to‐tail interactions, while the anions and the three related partial solvent water molecules (having occupancies of 0.73, 0.17 and 0.10) occupy the interstitial regions of the structure. The cations are linked to the anions directly through N—H...O_COO− hydrogen bonds and indirectly by the three water molecules, which form similar conjoint cyclic bridging units [graph set R²₄(8)] through O—H...O_C=O and O—H...O_COO− hydrogen bonds, giving a two‐dimensional layered structure. Within the anion, intramolecular N—H...O_COO− and N—H...O_nitro hydrogen bonds result in the benzoate and picrate rings being rotated slightly out of coplanarity [inter‐ring dihedral angle = 32.50 (14)°]. This work provides another example of the molecular selectivity of brucine in forming stable crystal structures, and also represents the first reported structure of any form of the guest compound 2‐(2,4,6‐trinitroanilino)benzoic acid.