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  • 1
    ISSN: 0044-2313
    Keywords: Tetrapnictidotitanate(IV) ; centered heterocubanes ; hierarchical derivative of Cr3Si and KGe ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Tetrapnictidotitanates(IV) M4TiX4 (M = Sr, Ba; X = P, As), hierarchical Derivatives of the KGe Structure K4□Ge4The four new tetrapnictidotitanates(IV) Sr4TiP4, Sr4TiAs4, Ba4TiP4 and Ba4TiAs4 are synthesized from the binary pnictides MX (M = Sr, Ba and X = P, As) and elementary titanium in tantalum ampoules. The compounds are isotypic and isoelectronic with Ba4SiAs4 (space group P43n (no. 218); cP72; Z = 8; Sr4TiP4: a = 1259.0(1) pm; Sr4TiAs4: a = 1288.3(4) pm; Ba4TiP4: a = 1316.6(2) pm; Ba4TiAs4: a = 1346.9(2) pm). The transition metal compounds form cubic, metallic reflecting crystals (Sr4TiP4 (green); Sr4TiAs4 (silver coloured); Ba4TiP4 (silver coloured); Ba4TiAs4 (violet). They are semiconducting and very sensitive against air and moisture. The structure is a hierarchical derivative of Cr3Si (A15) and KGe type: Cr6Si2 ≙ (□Ge4K4)6(□Ge4K4)2 ≙ (TiX4M4)6(TiX4M4)2, where Ti occupies the positions of the Cr3Si structure, and the alkaline-earth metal and pnicogen atoms occupy the positions of the KGe structure. Therefore, Ti is surrounded by four X and four more distant M atoms forming a heterocubane. The mean bond lengths are: d(Ti—P) = 238.0(5) pm; 307 ≤ d(Sr—P) ≤ 333 pm; d(Ti—As) = 245.9(4); 313 ≤ d(Sr—As) ≤ 341 pm; d(Ti—P) = 240.5(5); 324 ≤ d(Ba—P) ≤ 348 pm; d(Ti—As) = 248.3(3) pm; 331 ≤ d(Ba—As) ≤ 355 pm.
    Notes: Die vier neuen Tetrapnictidotitanate(IV) Sr4TiP4, Sr4TiAs4, Ba4TiP4 und Ba4TiAs4 wurden aus den binären Komponenten MX (M = Sr, Ba und X = P, As) und elementarem Titan in Tantalampullen dargestellt. Alle Verbindungen sind isotyp und isoelektronisch zu Ba4SiAs4 (Raumgruppe P43n (Nr. 218), cP72, Z = 8; Sr4TiP4: a = 1259.0(1) pm; Sr4TiAs4: a = 1288.3(4) pm; Ba4TiP4: a = 1316.6(2) pm; Ba4TiAs4: a = 1346.9(2) pm). Die Übergangsmetallverbindungen bilden würfelförmige, metallisch reflektierende Kristalle (Sr4TiP4 (grün), Sr4TiAs4 (silberfarben) Ba4TiP4 (silberfarben), Ba4TiAs4 (violett). Sie sind halbleitend und sehr empfindlich gegenüber Luft und Feuchtigkeit. Die Struktur ist eine hierarchische Variante vom Cr3Si- (A15) und KGe-Typ: Cr6Si2 ≙ (□Ge4K4)6(□Ge4K4)2 ≙ (TiX4M4)6(TiX4M4)2, in der die Ti-Atome die Positionen der Cr3Si-Struktur, die Erdalkalimetall- und Pnicogenatome die Positionen der KGe-Struktur besetzen. Ti ist deshalb von vier X-Atomen und von vier weiter entfernten M-Atomen in Form eines Heterokubans umgeben. Die mittleren Bindungslängen sind: d(Ti—P) = 238.0(5) pm, 307 ≤ d(Sr—P) ≤ 333 pm; d(T—As) = 245.9(4), 313 ≤ d(Sr—As) ≤ 341 pm; d(Ti—P) = 240.5(5), 324 ≤ d(Ba—P) ≤ 348 pm; d(Ti—As) = 248.3(3) pm, 331 ≤ d(Ba—As) ≤ 355 pm.
    Additional Material: 3 Ill.
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  • 2
    ISSN: 0044-2313
    Keywords: Tetrabariumtriphosphide, Ba4P3 ; preparation ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Chemistry and Structural Chemistry of Phosphides and Polyphosphides. 58. Tetrabariumtriphosphide, Ba4P3: Preparation and Crystal StructureBa4P3 is obtained from the elements in the molar ratio 4:3 or by reaction of Ba3P2 and Ba5P4 in the molar ratio 1:1 (steel ampoules with inner corundum crucibles; 1 490 K). The greyish black, easily hydrolysing compound crystallizes in a new structure type oP56. The structure shows two crystallographically independent dumbbells P24- (d(P—P) = 225 and 232 pm) and isolated ions P3- corresponding to (Ba2+)8(P24-)4(P3-)4. The partial structure of the Ba atoms forms a complex network of trigonal prisms with tetrahedral and square pyramidal holes, as well as polyhedra with 14 faces (CN 10) which are icosahedron derivatives. The P3- anions center trigonal prisms and the 14 face polyhedron. The P-atoms of the P24- dumbbells center neighboring trigonal prisms with common square faces. (Pbam (no. 55); a = 1 325.4(2) pm, b = 1 256.2(2) pm, c = 1 127.3 pm; Z = 8).
    Notes: Ba4P3 erhält man aus den Elementen im Molverhältnis 4:3 oder durch Umsetzung von Ba3P2 und Ba5P4 im Molverhältnis 1:1 (Korundinnentiegel; Stahlampullen; 1 490 K). Die grauschwarze, hydrolyseempfindliche Verbindung kristallisiert in einem neuen Strukturtyp oP56 mit zwei kristallographisch unabhängigen P24--Hanteln (d(P—P) = 225 und 232 pm und isolierten P3--Anionen entsprechend (Ba2+)8(P24-)(P3-)4. Die Partialstruktur der Ba-Atome bildet ein komplexes Netz trigonaler Prismen mit tetraedrischen und quadratisch-pyramidalen Lücken, sowie einem 14-Flächner (CN 10), der sich vom Ikosaeder ableitet. Die P3--Anionen zentrieren trigonale Prismen und den 14-Flächner, die Atome der P24--Hanteln jeweils benachbarte trigonale Prismen mit gemeinsamer Vierecksfläche. (Pbam (Nr. 55); a = 1 325,4(2) pm, b = 1 256,2(2) pm, c = 1 127,3(2) pm; Z = 8).
    Additional Material: 5 Ill.
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