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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 619 (1993), S. 608-612 
    ISSN: 0044-2313
    Keywords: Irondiiodide complexes ; irontriiodide complexes ; tetramethylurea ; synthesis ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Complexes of FeI2 and FeI3 with Tetramethylurea[FeI2(OC(NMe2)2)2] (1, [Fe2I4(OC(NMe2)2)2] (2), and [FeI3(OC(NMe2)2] (3) were prepared by the reaction of FeI2 and FeI2/iodine, respectively, with tetramethylurea.The structures of 1 and 3 were determined from single crystal X-ray diffraction data. 1 crystallizes in the triclinic space group P1, with a = 809.9(1), b = 923.2(1), c = 1 374.6(1) pm, α = 106.80(1), β = 90.47(1), γ = 101.55(1)°; Z = 2; R = 0.045., 3: monoclinic, P21/c, a = 1 311.4(1), b = 783.3(1), c = 1 409.1(1) pm, β = 97.36(1)°; Z = 4; R = 0.047.1 and 3 are isolated neutral complexes with distorted tetrahedral coordination of iron. 3 is the first FeI3-complex with an O-donor ligand.The IR-spectra exhibit strong shifts of n̈C = O and n̈asC - N of tetramethylurea especially on coordinating to FeI3.
    Notes: [FeI2(OC(NMe2)2)2] (1), [Fe2I4(OC(NMe2)2)2] (2) und [FeI3(OC(NMe2)2] (3) werden durch Reaktion von FeI2 bzw. FeI2 und Iod mit Tetramethylharnstoff dargestellt.Die Kristallstrukturen von 1 und 3 wurden durch Röntgenbeugung bestimmt. 1 kristallisiert triklin, P1, mit a = 809,9(1), b = 923,2(1), c = 1 374,6(1) pm, α = 106,80(1), β = 90,47(1), γ = 101,55(1)°; Z = 2; R = 0,045. 3: monoklin, P21/c, a = 1 311,4(1), b = 783,3(1), c = 1 409,1(1) pm, β = 97,36(1)°; Z = 4; R = 0,047.1 und 3 enthalten isolierte neutrale Komplexe mit verzerrt tetraedrischer Koordination von Eisen. 3 ist der erste FeI3-Komplex mit einem O-Donorliganden. Die Schwingungsspektren zeigen starke Verschiebungen von n̈C = O und n̈asC - N für Tetramethylharnstoff besonders bei der Koordination an FeI3.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 619 (1993), S. 727-730 
    ISSN: 0044-2313
    Keywords: Antimonytriiodide complex with trithiacyclononane ; synthesis ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Crystal and Molecular Structure of SbI3 · 9S3 (9S3 = 1.4.7-Trithiacyclononane).SbI3 forms a 1:1 adduct with 1.4.7-trithiacyclononane. The crystal structure exhibits discrete complexes with a distorted octahedral coordination of antimony(III). In comparison with molecular SbI3 the Sb—I distances are elongated from 271.9 to 290.4 pm (mean). The mean value of the Sb—S distances is 287.5 pm. The planes through iodine and sulfur atoms, respectively, are nearly coplanar. There is no significant stereochemical influence of the Sb(III) lone pair.
    Notes: SbI3 bildet ein 1:1-Addukt mit 1,4,7-Trithiacyclononan. Die Kristallstruktur enthält diskrete Komplexe mit verzerrt oktaedrischer Koordination von Antimon(III). Im Vergleich zum molekularen SbI3 ist der Sb—I-Abstand von 271,9 auf 290,4 pm aufgeweitet. Der mittlere Sb—S-Abstand beträgt 287,5 pm. Die Ebenen durch die drei Iod- und drei Schwefelatome sind nahezu koplanar. Ein signifikanter stereochemischer Einfluß des nichtbindenden Elektronenpaares von Sb(III) ist nicht zu erkennen.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0044-2313
    Keywords: Iron(II) phosphane complexes ; synthesis ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Iron(II) Phosphane Complexes. Synthesis and Crystal Structures of [Fe2I4(dppe)2], [Fe2(SR)4(dppe)2], [Fe(SR′)2(dppp)] and [Fe(SR)2(PMePh2)2] (dppe = Ph2P(CH2)2PPh2; dppp = Ph2P(CH2)3PPh2; R = 2,4,6-Me3C6H2; R′ = 2,4-tBuC6H3)The title compounds were isolated and their structures determined by crystallographic methods. [Fe2I4(dppe)2] (1) and [Fe2(SR)4(dppe)2] (2) form dimeric complexes with the bidentate phosphane binding to different iron atoms. The resulting ten-membered rings of both compounds exhibit a nearly identical conformation. The central FeS2P2 units of the mononuclear complexes [Fe(SR′)2(dppp)] (3) and [Fe(SR)2(PMePh2)2] (4) show like 2 large deviations from ideal C2v symmetry with bonding angles around the central iron atom ranging from 97.2, 92.5, and 96.5° (angle P—Fe—P in 2, 3, and 4, respectively) to 129.0, 129.9, and 133.6° (angle S—Fe—S in 2, 3, and 4, respectively).
    Notes: Die Titelverbindungen wurden dargestellt und ihre Strukturen mit kristallographischen Methoden bestimmt. [Fe2I4(dppe)2] (1) und [Fe(SR)4(dppe)2] (2) bilden zweikernige Komplexe, in denen die zweizähnigen Phosphinliganden jeweils an unterschiedliche Fe-Atome gebunden sind. Die daraus resultierenden zehngliedrigen Ringe sind für beide Verbindungen nahezu identisch. Die zentrale FeS2P2-Einheit der einkernigen Komplexe [Fe(SR′)2(dppp)] (3) und [Fe(SR)2(PMePh2)2] (4) zeigen, wie auch diese Gruppierung in 2, große Abweichungen von der idealen C2v-Symmetrie mit Bindungswinkeln um das zentrale Eisenatom zwischen 97,2, 92,5 und 96,5° (P—Fe—P-Winkel in 2, 3 bzw. 4) und 129,0, 129,9 und 133,6° (S—Fe—S-Winkel in 2, 3 bzw. 4).
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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