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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 621 (1995), S. 1466-1470 
    ISSN: 0044-2313
    Keywords: Synthesis ; Crystal structure ; Halides ; Clusters ; Lanthanides ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The First Bromide with Trigonal-Bipyramidal [M5(C2)] Clusters: [Pr5(C2)]Br9The bromide [Pr5(C2)]Br9 is obtained via metallothermic reduction of PrBr3 with rubidium in the presence of praseodymium and carbon in a sealed niobium container at 730°C as dark red single crystals. [Pr5(C2)]Br9 crystallizes in the monoclinic crystal system [P21/n; Z = 4; a = 1 006.9(1); b = 1 886.1(1); c = 1 045.9(1) pm; β = 108.130(1)°; Rint = 0.059; R1 = 0.038; wR2 = 0.077]. One edge in the base of the trigonal bipyramid in [Pr5(C2)]Br9 is usually long (440 pm). It is not brigded by a Bri ligand. In addition to the eight Bri, the cluster is coordinated by 12 terminal ligands (Bra). Except for the known Bra-a-a and Bri-a connections, Bri-a-a brigdes are observed for the first time for trigonal-bipyramidal clusters.
    Notes: Das Bromid [Pr5(C2)]Br9 erhält man durch metallothermische Reduktion von PrBr3 mit Rubidium in Gegenwart von Praseodym und Kohlenstoff in einer verschweißten Niobampulle bei 730°C in Form dunkelroter Kristalle. [Pr5(C2)]Br9 kristallisiert im monoklinen Kristallsystem [P21/n; Z = 4; a = 1 006,9(1); b = 1 886,1(1); c = 1 045,9(1) pm; β = 108,130(1)°; Rint = 0,059; R1 = 0,038; wR2 = 0,077]. Eine Kante in der Basis der trigonalen Bipyramide in [Pr5(C2)]Br9 ist mit 440 pm ungewöhnlich lang und wird nicht von einem Bri-Liganden überbrückt. Zusätzlich zu den acht Bri werden die Cluster von 12 terminalen Liganden koordiniert (Bra). Neben den bekannten Bra-a-a- und Bri-a-Brücken treten hier erstmals bei trigonal-bipyramidalen Clustern Bri-a-a-Brücken auf.
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  • 2
    ISSN: 0044-2313
    Keywords: Rare Earths ; Bromides ; Copper ; Synthesis ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Crystal Structure of (NH4)3Cu4Ho2Br13. Further Bromides of the (NH4)3Cu4M2Br13 Type (M = Dy—Lu, Y) and on Rb3Cu4Ho2Br13Single crystals of (NH4)3Cu4Ho2Br13 were obtained for the first time from the reaction of CuBr with HoBr3 which was contaminated with NH4Br: cubic, space group Pn3, Z = 2, a = 1101.71(5) pm. The crystal structure may be considered as a variant of the fluorite type according to [(HoBr6)4][(NH4)6(Cu4Br)2] ≡ Ca4F8. Pure products can be prepared from the binary halides in glass ampoules at 350°C. The bromides (NH4)3Cu4M2Br13 (M = Dy—Lu, Y) and Rb3Cu4Ho2Br13 are isotypic with (NH4)3Cu4Ho2Br13.
    Notes: Einkristalle von (NH4)3Cu4Ho2Br13 wurden erstmals bei der Reaktion von CuBr mit HoBr3, das mit NH4Br „verunreinigt“ war, erhalten: kubisch, Raumgruppe Pn3, Z = 2, a = 1101,71(5) pm. Die Kristallstruktur ist gemäß [(HoBr6)4][(NH4)6(Cu4Br)2] ≡ Ca4F8 als eine Variante des Flußspat-Typs aufzufassen. Reine Produkte können aus den binären Halogeniden bei 350°C in Glasampullen dargestellt werden. Die Bromide (NH4)3Cu4M2Br13 (M = Dy—Lu, Y) und Rb3Cu4Ho2Br13 sind mit (NH4)3Cu4Ho2Br13 isotyp.
    Additional Material: 2 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 593 (1991), S. 185-192 
    ISSN: 0044-2313
    Keywords: Calciumcarbide Chloride ; Synthesis ; Crystal Structure ; Allylenide Ion ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Crystal Structure of a Calciumcarbide Chloride Containing a C34- Unit, Ca3Cl2C3Ca3Cl2C3 was prepared from calcium, CaCl2 and graphite in sealed tantalum capsules. Red, transparent crystals were obtained from heating the mixture to 900°C (for one day) and annealing afterwards at 780°C for three days. The compound forms a layered structure (Cmcm, Z = 4, a = 384.24(9) pm, b = 1340.7(3) pm, c = 1152.6(3) pm, R = RW = 0.036 for 481 independent intensities) with alternating stacks of double layers of Ca2+ and monolayers of Cl-. The double layers of calcium contain allylenide ions, C34-. The latter exhibit C2v symmetry, a bond angle (C—C—C) of 169.0(6)° and a C—C separation of 134.6(4) pm.
    Notes: Ca3Cl2C3 entsteht aus Calcium, CaCl2 und Graphit in verschweißten Tantal-Kapseln in Form roter, transparenter Kristalle durch Erhitzen des Reaktionsgemenges auf 900°C (1 Tag) und anschließendes dreitägiges Tempern bei 780°C. Die Verbindung kristallisiert in einer Schichtstruktur (Cmcm, Z = 4, a = 384,24(9) pm, b = 1 340,7(3) pm, c = 1 152,6(3) pm, R = RW = 0,036 für 481 unabhängige Intensitäten) mit einer alternierenden Anordnung von Doppelschichten aus Ca2+ und Schichten aus Cl-. In den Calcium-Doppelschichten liegen die Allylenidionen, C34-. Sie zeigen C2v-Symmetrie mit einem Bindungswinkel (C—C—C) von 169,0(6)° und dem C—C-Bindungsabstand von 134,6(4) pm.
    Additional Material: 2 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 614 (1992), S. 12-16 
    ISSN: 0044-2313
    Keywords: Europium(II) acetate ; Synthesis ; Crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: KEu(CH3COO)3, the First Ternary Europium(II) AcetateOn of EuCl2 with a melt of dry potassium acetate yields pale greenish-yellow single crystals (300°C, sealed glass ampoule, EuCl2 and K(CH3COO) in a molar ratio of 1 : 3). The crystal structure determination (orthorhombic, P212121 (no. 19), Z = 8, a = 1166.3(1) pm, b = 1288.4(2) pm, c = 1493.9(2) pm, R = 0.043, Rw = 0.032) revealed the composition KEu(CH3COO)3. The structure consists of one-dimensional chains built up by bridging acetate groups in the [100] and [001] directions in which potassium and europium alternate as central atoms. Eu2+ is surrounded by nine and eight and K+ by seven and six oxygen atoms, respectively. These chains are linked in the [010] direction so that a three-dimensional network is formed. The high coordination numbers of the acetate oxygen atoms of up to four are remarkable. Therefore, the acetate groups have highly bridging functions in addition to their chelating coordination of the cations.
    Notes: Bei der Umsetzung von EuCl2 mit einer Schmelze von trockenem Kaliumacetat im ungefähren Molverhältnis von 1 : 3 entstehen bei 300°C in einer abgeschmolzenen Glasampulle neben KCl blaß grünlichgelbe Kristalle. Die Röntgenstrukturanalyse (orthorhombisch, P212121 (Nr. 19), Z = 8, a = 1166,3(1) pm, b = 1288,4(2)pm, c = 1493,9(2)pm, R = 0,043, Rw = 0,032) ergab die Zusammensetzung KEu(CH3COO)3. Die Kristallstruktur wird von acetatverbrückten unendlichen Strängen in Richtung [100] und [001] bestimmt, in denen abwechselnd Kalium und Europium als Zentralteilchen aufeinanderfolgen. Dabei wird Eu2+ von 9 bzw. 8 Sauerstoffliganden, K+ aber nur von 7 bzw. 6 Sauerstoffatomen koordiniert. Durch zusätzliche Verknüpfungen der Stränge in Richtung [010] entsteht daraus ein dreidimensionales Netzwerk. Auffällig sind die ungewöhnlich großen Koordinationszahlen der Acetatsauerstoffatome von bis zu vier, so daß bei den Acetatgruppen neben der chelatisierenden Koordination zu den Kationen ihre Funktion als Brückenliganden im Vordergrund steht.
    Additional Material: 2 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 616 (1992), S. 141-144 
    ISSN: 0044-2313
    Keywords: Crystal structure ; Synthesis ; Thermolysis, Lanthanides ; Ternary ammonium nitrates ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis, Structure, and Thermolysis of the (NH4)3[M2(NO3)9] (M = La—Gd)The ternary ammonium nitrates (NH4)3[M2(NO3)9] (M = La-Gd) are obtained as single crystals from a solution of the respective sesquioxides in a melt of NH4NO3 and sublimation of the excess NH4NO3. In the crystal structure of (NH4)3[Pr2(NO3)9] (cubic, P4332, Z = 4, a = 1 377.0(1) pm, R = 0.038, Rw = 0.023) Pr3+ is surrounded by six bidentate nitrate ligands of which three are bridging to neighbouring Pr3+ ions. This results in a branched folded chain, held together by the NH4+ ions which occupy cavities in the structure. (NH4)3[Pr2(NO3)9] is the first intermediate product of the thermal decomposition of (NH4)2[Pr(NO3)5(H2O)2] · 2H2O.
    Notes: Die ternären Ammoniumnitrate (NH4)3[M2(NO3)9] (M = La—Gd) erhält man in Form von Einkristallen durch Auflösen der entsprechenden Sesquioxide in einer Schmelze von NH4NO3 und Entfernen des Überschusses durch Sublimation. Die Strukturanalyse am Beispiel von (NH4)3[Pr2(NO3)9] (kubisch, P4332, Z = 4; a = 1377,0(1) pm; R = 0,038; Rw = 0,023) zeigt, daß Pr3+ von sechs zweizähnigen Nitratliganden umgeben ist, von denen drei jeweils zu einem weiteren Pr3+-Ion verbrücken. Dadurch entsteht eine verzweigte, gefaltete Kette. Sie wird durch NH4+-Ionen zusammengehalten, die sich in Hohlräumen befinden. (NH4)3[Pr2(NO3)9] stellt die erste Stufe beim thermischen Abbau von (NH4)2[Pr(NO3)9(H2O)2] · 2H2O dar.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 618 (1992), S. 13-17 
    ISSN: 0044-2313
    Keywords: Ternary Lanthanide Chlorides ; Synthesis ; Crystal Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Ternary Halides of the A3MX6 Type I. A3YCI6 (A = K, NH4, Rb, Cs): Synthesis, Structures, Thermal Behaviour. Some Analogous Chlorides of the LanthanidesReaction of the trichlorides MCl3 (M = Y, Tb—Lu) with alkali chlorides AC1 (A = K, Rb, Cs) in evacuated silica ampoules at 850-900°C yields A3MCl6-type chlorides. (NH4)3YCl6 is obtained via the ammonium-chloride route. The crystal structure of Rb3YCl6 (monoclinic, C2/c (no. 15), Z = 8, a = 2583(1)pm, b = 788.9(4)pm, c = 1283.9(7)pm, p = 99.63(4)°, R = 0.062, Rw = 0.050) is that of Cs3BiCl6. The Rb3YCl6/Cs3BiCl6 structure and the closely related structures of K3MoCl6 and In2CI3 are derived from the elpasolite-type of structure (K2NaAlF6) making use of the model of closest-packed layer structures. Cell parameters for the chlorides Rb3MCl6 (M = Y, Tb—Lu) and Cs3YCl6 and Cs3ErCl6 as well, which are all isostructural with Rb3YCl6, are given. The “system” (K, NH4, Rb, Cs)YCl6 has been investigated by DTA and high-temperature X-ray powder diffractometry.
    Notes: Chloride vom Typ A3MCl6 (A = K, Rb, Cs; M = Y, Tb—Lu) werden durch Umsetzung der Trichloride MCl3 mit Alkalichloriden ACl in evakuierten Quarzglas-Ampullen bei 850-900°C dargestellt, (NH4)3YCl6 nach der “Ammoniumchlorid-Methode”. Die Röntgenstrukturanalyse an einem Einkristall von Rb3YCl6 (monoklin, C2/c (Nr. 15), Z = 8, a = 2583(1) pm, b = 788,9(4) pm, c = 1283,9(7) pm, β = 99,63(4)°, R = 0,062, Rw = 0,050) ergab Isotypie zu Cs3BiCl6. Ausgehend vom Elpasolith-Typ (K2NaAlF6) werden Cs3BiCl6 und nahe verwandte Strukturen (K3MoCl6, In2Cl3) mit dem Modell dichtest gepackter Schichten beschrieben. Für die zu Rb3YCl6 isotypen Chloride Rb3MCl6 (M = Y, Tb—Lu), sowie Cs3YCl6 und Cs3ErCl6 werden Gitterkonstanten angegeben. Das “System” (K, NH4, Rb, Cs)YCl6 wurde mittels DTA und Heiz-Guinier-Aufnahmen untersucht.
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  • 7
    ISSN: 0044-2313
    Keywords: Rare-Earth Iodides ; Synthesis ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: [M9C4O]I8 (M = Y, Ho, Er, Lu), Reduced Rare-Earth Iodides with Waved Metal Double Layers and Two Different Interstitial Atoms[M9C4O]I8 (M = Y, Ho, Er, Lu) are examples of reduced rare-earth iodides with two different interstitial atoms. The compounds were synthesized from appropriate mixtures of MI3, M, C and M2O3 at 1 050°C in arc-welded tantalum containers. The X-ray structure analysis of a single crystal of [Y9C4O]I8 (orthorhombic, Pmmn (Nr. 59), Z = 2, a = 2 912.7(6) pm, b = 384.17(4) pm, c = 1 080.29(9) pm, R = 0.084, Rw = 0.053) exhibits octahedrally coordinated carbon in “plane” sections besides tetrahedrally coordinated oxygen in the “bend” of waved metal double layers. These double layers are stacked alternately with waved iodine double layers along [001].
    Notes: Mit [M9C4O]I8 (M = Y, Ho, Er, Lu) wurden reduzierte Selten-Erd-Iodide erhalten, die zwei verschiedene interstitielle Atomsorten enthalten. Die Synthese erfolgt aus geeigneten Gemengen von MI3, M, C und M2O3 bei 1 050°C in verschweißten Tantalampullen. Die Röntgenstrukturanalyse an einem Einkristall von [Y9C4O]I8 (orthorhombisch, Pmmn (Nr. 59), Z = 2, a = 2 912,7(6) pm, b = 384,17(4) pm, c = 1 080,29(9) pm, R = 0,084, Rw = 0,053) zeigt, daß neben oktaedrisch umgebenen Kohlenstoffatomen in “planaren” Abschnitten, tetraedrisch koordinierte Sauerstoffatome in “Knickstellen” gewellter Metall-Doppelschichten vorliegen. Diese Doppelschichten sind alternierend mit gewellten Iod-Doppelschichten längs [001] gestapelt.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 619 (1993), S. 1462-1464 
    ISSN: 0044-2313
    Keywords: Cesium Acetate ; Synthesis ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Crystal Structure of Cesium Acetate, Cs(CH3COO).The crystal structure of cesium acetate, Cs(CH3COO), was determined from single crystal fourcirclediffractometer data: hexagonal crystal system, P6/m (No. 175), Z = 6, a = 1 488.0(2), c = 397.65(5) pm, Vm = 76.54(2) cm3/mol, R = 0.045, Rw = 0.030. The structure consists of flat layers of acetate anions parallel (001) that are separated by layers of cesium cations. There is a close relationship with the CaF2 type according to CsO2(CCH3): each cesium cation has eight oxygen atoms as nearest neighbours. They form a heavily distorted cube with trapezoidal basal faces. In contrast to CaF2, these polyhedra are linked via three faces and two edges to a three-dimensional network.
    Notes: Die Kristallstruktur von wasserfreiem Caesiumacetat, Cs(CH3COO), wurde anhand von Vierkreisdiffraktometerdaten bestimmt: hexagonales Kristallsystem, P6/m (Nr. 175), Z = 6, a = 1 488,0(2), c = 397,65(5) pm, Vm = 76,54(2) cm3/mol, R = 0,045, Rw = 0,030. Die Struktur besteht aus ebenen Schichten von Acetationen parallel (001), die durch Caesium-Schichten separiert sind. Es besteht eine enge Verwandtschaft zum CaF2-Typ gemäß CsO2(CCH3): die Cs+-Ionen sind von 8 Sauerstoffatomen in Form eines stark verzerrten Würfels mit trapezoiden Grundflächen umgeben. Im Unterschied zu CaF2 sind die Würfel jedoch nur über drei gemeinsame Flächen und zwei Kanten zu einem dreidimensionalen Netzwerk verknüpft.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 619 (1993), S. 1465-1473 
    ISSN: 0044-2313
    Keywords: Cesium Lutetium(III) Acetate ; Synthesis ; Crystal Structure ; Thermolysis ; Evolved Gas Aalysis (EGA) ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Ternary Acetates of the Lanthanides with Cesium: Dimers in CsLu(CH3COO)4 and Trimers in Cs2[Lu3(CH3COO)10(OH)(H2O)]. Synthesis, Crystal Structures, ThermolysisSingle crystals of CsLu(CH3COO)4 and Cs2[Lu3(CH3COO)10(OH)(H2O)] were obtained from an aqueous solution of lutetium and cesium acetate in a 1:1 molar ratio. The crystal structures (CsLu(CH3COO)4: monoclinic, P21/n (no. 14), Z = 8, a = 1 293.1(2), b = 1 323.8(2), c = 1 622.5(3) pm, β = 92.01(2)°, Vm = 208.97(6) cm3/mol, R = 0.056, Rw = 0.034; Cs2[Lu3(CH3COO)10(OH)(H2O)]: monoclinic, C2/c (no.15), Z = 4, a = 2 138.5(6), b = 1 378.0(3), C = 1 482.9(4) pm, β = 106.15(2)°, Vm = 632.0(3) cm3/mol, R = 0.049, Rw = 0.036) were determined from four-circle-diffractometer data. The structures consist of dimers and trimers, respectively, that are built by bridging acetate groups. These units are fragments of the infinite chains of the Ho(CH3COO)3 type of structure. The isotypic compounds CsM(CH3COO)4 with M=Eu—Lu were synthesized and characterized by the X-ray Guinier technique. The thermal decomposition of CsLu(CH3COO)4 was examined with thermoanalytical methods (TG/DSC with coupled gas analysis) and the Guinier-Simon technique: it decomposes at 260°C in an endothermic reaction to Lu2O3 and Cs2CO3.
    Notes: Die Verbindungen CsLu(CH3COO)4 und Cs2[Lu3(CH3COO)10(OH)(H2O)] konnten aus wäßriger Lösung von Cs(CH3COO) und Lu(CH3COO)10 (OH)(H2O) dargestellt werden. Ihre Kristallstrukturen (CsLu(CH3COO)4: monoklin, P21/n (Nr. 14), Z = 8, a = 1293,1(2), b = 1323,8(2), c = 1 622,5(3) pm, β = 92,01(2)°, Vm = 208,97(6) cm3/mol, R = 0,056, Rw = 0,034; Cs2[Lu3(CH3COO)10(OH)(H2O)]: monoklin, C2/c (Nr. 15), Z = 4, a = 2138,5(6), b = 1378,0(3), C = 1 482,9(4) pm, β = 106,15(2)°, Vm = 632,0(3) cm3/mol, R = 0,049, Rw = 0,036) wurden anhand von Vierkreisdiffraktometerdaten bestimmt. In den Kristallstrukturen liegen zwei- bzw. dreikernige Baueinheiten vor, die durch verbrückende Acetatgruppen aufgebaut werden und Fragmente der unendlichen Ketten im Ho(CH3COO)3-Typ darstellen. Die isotypen Verbindungen CsM(CH3COO)4, M=Eu—Lu, wurden hergestellt und mittels Pulver-Röntgenmethoden charakterisiert. Das thermische Verhalten von CsLu(CH3COO)4 wurde mittels TG/DSC und simultaner Gasanalyse (EGA) einerseits und mit Hilfe der Guinier-Simon-Technik andererseits untersucht: Es zersetzt sich ab 260°C in Cs2CO3 und Lu2O3.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 438-443 
    ISSN: 0044-2313
    Keywords: Praseodymium(III) Acetate ; Synthesis ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Pr(CH3COO)3, an Anhydrous Rare-Earth Acetate with a Network StructurePr(CH3COO)3 may be prepared by dehydration of Pr(CH3COO)3 · 1,5 H2O at 180°C as an amorphous green powder. Single crystals were grown from the powder by addition of (NH4)CH3COO as „mineralisator“ at 180°C in a sealed glass ampoule. The crystal structure (tetragonal, P421c (no. 114), Z = 24, a = 2106.5(3), c = 1323.6(1) pm, Vm = 147.39(3) cm3/mol, R = 0.055, Rw = 0.029) was determined from four-circle-diffractometer data. The Pr3+ ions occupy three crystallographically independent positions and are surrounded by 9 and 10 oxygen atoms, respectively. Acetate ions connect the cations to a complicated three-dimensional network.
    Notes: Pr(CH3COO)3 entsteht beim Entwässern von Pr(CH3COO)3 · 1,5 H2O bei 180°C als amorphes Pulver. Einkristalle konnten daraus mit Hilfe von (NH4)CH3COO als „Mineralisator“ ebenfalls bei 180°C in einer geschlossenen Glasampulle gezüchtet werden. Die Kristallstruktur (tetragonal, P421c (Nr. 114), Z = 24, a = 2106,5(3), c = 1323,6(1) pm, Vm = 147,39(3) cm3/mol, R = 0,055, Rw = 0,029) wurde anhand von Vierkreis-Diffraktometerdaten bestimmt. Pr3+-Ionen besetzen drei unterschiedliche kristallographische Positionen und sind von 9 bzw. 10 Sauerstoffatomen umgeben. Acetationen verbinden die Kationen auf unterschiedliche Weise zu einem komplizierten dreidimensionalen Netzwerk.
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