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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 107 (1974), S. 3266-3274 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Structure of the Pyridine-N-oxide Complexes ZnI2L2, CdI2L and HgCl2L (L = C5H5NO)ZnI2L2 (L = pyridine-N-oxide, C5H5NO) crystallizes in the monoclinic space group P21/c with a = 14.319 Å, b = 13.362 Å, c = 8.192 Å, β = 102.68° and four formula units. The structure consists of discrete monomeric complexes with zinc atoms tetrahedrally bonded to two iodine atoms (ZN—I = 2.56 and 2.58 Å) and two oxygen atoms (Zn—O = 1.98 and 1.99 Å). CdI2L crystallizes in the monoclinic space groupe P21/a with a = 13.337 Å, b = 7.002 Å, c = 11.153 Å, β = 107.87° and four formula units. The structure is composed of infinite chains with units of [CdI] alternately bridged through two iodine atoms and two oxygen atoms. The environment of the penta coordinated Cd-atom corresponds largely to a trigonal bipyramid (Cd—I = 2.724, 2.834, 2.963 2.936 Å; Cd—O = 2.275, 2.383 Å). HgCl2L crystallizes in the triclinic space group P1¯ with a = 7.060 Å, b = 10.132 Å, c = 6.890 Å, α = 105.28°, β = 117.04°, γ = 75.35° and two formula units. The main feature of the structure are bent molecules HgCl2 (Hg—Cl = 2.316, 2.339 Å, β = 163°) held together in a two-dimensional network by markedly weaker mutual interactions and by C5H5NO-molecules (Hg—Cl° = 3.185, 3.318 Å, Hg—O = 2.59, 2.60 Å). Generally there is a layer structure with the atoms Hg, Cl and O in the inner region of the layers which is envelloped by pyridinrings.
    Notes: ZnJ2L2 (L = Pyridin-N-oxid, C5H5NO) kristallisiert monoklin in der Raumgruppe P21/c mit a = 14.319 Å, b = 13.362 Å, c = 8.192 Å, β = 102.68° und Z = 4 Formeleinheiten. Die Struktur wird aus isolierten Komplexen aufgebaut, in denen Zink tetraedrisch an je zwei Jod-bzw. Sauerstoffatome gebunden ist(Zn—J = 2.56 und 2.58 Å; Zn—O = 1.98 und 1.99 Å), CdJ2L kristallisiert monoklin in der Raumgruppe P21/a mit a = 13.337 Å,b = 7.002 Å. c = 11.153 Å, β = 107.87° und Z = 4 Formeleinheiten. Die Struktur enthält eindimensional unendliche Ketten, in denen [CdJ]-Einheiten abwechselnd über je zwei Jod-bzw. Sauerstoffatome verknüpft sind. Jedes Cd-Atom ist fünffach koordiniert, wobei das Koordinations-polyeder weitgehend einer trigonalen Bipyramide entspricht (Cd—J = 2.724, 2.834, 2.963 Å; Cd—O = 2.275, 2.383 Å). HgCl2L Kristallisiert triklin in der Raumgruppe P1¯ mit a = 7.060 Å, b = 10.132 Å, c = 6.890 Å, α = 105.28°, β = 117.04°, γ = 75.35° und Z = 2 Formeleinheiten. Hauptmerkmal der Struktur sind gewinkelte Moleküle HgCl2 (Hg—Cl′ = 2.316 bzw. 2.339 Å, β = 163°), die durch merklich schwächere Wechselwirkungen untereinander und über C5H5NO-Moleküle vernetzt sind (Hg—Cl′ = 3.185 bzw. 3.318 Å; Hg—O = 2.59 bzw. 2.60 Å). Insgesamt liegt ein Schichtengitter vor, wobei die Atome Hg, Cl und O einen inneren Bereich bilden, der durch die Pyridinringe eingehüllt wird.
    Additional Material: 4 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978), S. 3705-3710 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the Structure of the Octahedral Cations cis-[SiX2(bipy)2]2 +; the Crystal Structure of [Si(OH)2(bipy)2]I2 · 2H2OBy partial hydrolysis of SiI4(bipy)2 the dihydrate of [Si(OH)2(bipy)2]I2 is formed as a yellow crystalline compound which decomposes at 120°C. The compound crystallizes in the monoclinic space group I 2/c with 4 formula units per unit cell. The cis-octahedral cation [Si(OH)2(bipy)2]2 + has C2 symmetry. The bond distances Si — O = 164.3 pm are exceptionally short for an octahedral complex. The bond lengths Si — N in trans-position to the OH ligands are longer than the other ones (200.5 and 195.3 pm, respectively). The six-membered rings of the bipy ligands are bent against each other. Each H2O molecule hydrates exclusively one of the two OH ligands by hydrogen bonds. The entire structure can be compared with the CdI2 type.
    Notes: Das Dihydrat von [Si(OH)2(bipy)2]I2 entsteht als gelbe, kristalline Substanz bei der partiellen Hydrolyse von SiI4(bipy)2. Die Verbindung zersetzt sich bei 120°C. Sie kristallisiert monoklin in der Raumgruppe I 2/c mit 4 Formeleinheiten pro Elementarzelle. Das cis-oktaedrische Kation [Si(OH)2(bipy)2]2 + besitzt C2-Symmetrie. Die Abstände Si — O = 164.3 pm sind für einen oktaedrischen Komplex sehr kurz. Von den Si — N-Bindungen sind die zu den OH-Liganden trans-ständigen länger als die anderen (200.5 bzw. 195.3 pm). Die Sechsringe der bipy-Liganden sind gegeneinander geknickt. Die H2O-Moleküle hydratisieren ausschließlich je einen der beiden OH-Liganden über H-Brückenbindungen. Die gesamte Struktur kann mit dem CdI2-Typ verglichen werden.
    Additional Material: 1 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 112 (1979), S. 3104-3109 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Structure of the Plane 4,4′″,6,6′″ -Tetraazahexa-m-phenylene4,4′″,6,6′″- Tetraazahexa-m-phenylene (1) crystallizes in the monoclinic space group p21/n (No.14) with Z = 2 molecules per unit cell. The molecule has nearly D2h symmetry. The deviations of the molecule-plane are not greater than 5 pm. Strong H-H interactions occur as a result of this structure. The mean value for the short proton contacts is 202 pm. In the 18-membered ring system the mean bond lengths are 138.8 and 148.7 pm. resp., for the endocyclic and exocyclic C - C bonds. The deformations of bond lengths and bond angles are discussed as a result of proton-proton contact weakening.
    Notes: 4,4′″,6,6′″ -Tetraazahexa-m-phenylen (1) kristallisiert monoklin in der Raumgruppe p21/n (Nr. 14) mit Z = 2 Molekülen pro Elementarzelle. Das Molekül ist praktisch eben (Auslenkungen nicht größer als 5 pm) und weicht von der Symmetrie D2h kaum ab. Starke H-H-Wechselwirkungen sind die Folge dieser Struktur. Die kurzen Protonen-Kontakte betragen im Mittel 202 pm. Im 18-gliedrigen Ringsystem sind die mittleren Bindungslängen für die endocyclischen bzw. exocyclischen C-C-Bindungen 138.8 bzw. 148.7 pm. Die Veränderungen von Bindungslängen und Bindungswinkeln werden als Folge von Deformationen zur Abschwächung störender Protonenkontakte diskutiert.
    Additional Material: 2 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 109 (1976), S. 3728-3734 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Crystal and Molecular Structure of 1,1,2,2-Tetrachloro-1,2-dimethyldisilane-2,2′-BipyridylThe title compound crystallizes in the monoclinic space group P21/a (Z = 4). The monomeric complex molecule contains one tetrahedrally and one octahedrally bonded Si-atom Cl2MeSi-SiCl2MeN2. The bond lenghts Si - Si = 2.367 Ä and Si-CH3 = 1.90 Å correspond to normal tetrahedral bond lenghts. On the other hand the distances Si - Cl in the octahedral group (2.274 and 2.392 Å) are clearly lengthened compared with the distances Si - Cl in the tetrahedral group (2.081 Å). The two rings of the bipyridyl ligand are slightly bent against each other while the angles and distances correspond to those of the free bipyridyl molecule despite the transition from trans to cis configuration. - Per two of the complex molecules maximally one molecule of the solvent acetonitrile is incorporated.
    Notes: Die Titelverbindung kristallisiert monoklin in der Raumgruppe P21/a (Z = 4). Das monomere Komplex-Molekül besitzt ein tetraedrisch und ein oktaedrisch gebundenes Siliciumatom Cl2MeSi-SiCl2MeN2. Die Bindungslängen. Dagegen sind die Si - Si = 2.367 Ä und CH3 = 1.90 Å entsprechen den normalen tetraedrischen Bindungslängen. Dagegen sind die Si - Cl-Abstände in der Oktaedergruppe (2.274 und 2.392Å) gegenüber den Si - Cl-Abständen in der Tetraedergruppe (2.081 Å) deutlich verlängert. Die beiden Ringe des Bipyridyl-Linganden sind leicht gegeneinander geknickt, dabei entsprechen Winkel und Abstände trotz des Übergangs von der trans-zur cis-Konfiguration denen im freien Bipyridyl-Molekül - Pro zwei der Komplex-Moleküle ist maximal ein Molekül Acetonitril (Lösungsmittel) eingelagert.
    Additional Material: 2 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1981 (1981), S. 1826-1837 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and X-Ray Structure Determination of Bicyclo[4.2.1]non-3-ene-2-one DerivativesMethyl 4-chloro- and methyl 4-bromo-5-oxobicyclo[4.2.1]non-3-ene-1-carboxylate (2) and (3), respectively, 3-bromo-4-chlorobicyclo[4.2.1]non-3-ene-2-one (4), and methyl 5-oxobicyclo[4.2.1]-non-3-ene-1-carboxylate (5) have been prepared from the corresponding bicyclo[3.2.1]oct-2-ene derivatives via the dihalocarbene adducts, and X-ray structure analysis was carried out. In all cases a half-chair conformation was found for the five-membered rings whereas the seven-membered rings possess a twist-chair conformation. The enone system is almost planar in 3 and 5 but somewhat distorted in 2 and 4.
    Notes: 4-Chlor- und 4-Brom-5-oxobicyclo[4.2.1]non-3-en-1-carbonsäure-methylester (2) bzw. (3), 3-Brom-4-chlorbicyclo[4.2.1]non-3-en-2-on (4) und 5-Oxobicyclo[4.2.1]non-3-en-1-carbonsäure-methylester (5) wurden aus den entsprechenden Bicyclo[3.2.1]oct-2-en-Derivaten über die Dihalogencarbenaddukte dargestellt und einer Röntgenstrukturanalyse unterworfen. In allen Fällen liegt der Fünfring in einer Halbsesselkonformation vor, der Siebenring nimmt eine Twist-Sesselkonformation ein. In 3 und 5 ist das Enon-System annähernd planar, in 2 und 4 etwas verdrillt.
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 425 (1976), S. 1-9 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Formation of Organosilicon Compounds. LXVI. Crystal and Molecular Structure of Hexamethyl-heptasilahexacyclo-heptadecane Si7C16H361,3,7,9,11,13-Hexamethyl-1,3,5,7,9,11,13-heptasilahexacyclo-heptadecane Si7C16H36 crystallizes in the triclinic space group P1 with a = 11.393 Å, b = 11.819 Å, c = 10.583 Å, α = 83.73°, β = 67.42°, γ = 62.19° and Z = 2 formula units. The average bond lengths are CH—Si= 1.886, CH2—Si = 1.870 and CH3—Si = 1.883 Å. The steric interactions of CH2-groups and CH3-groups in the range of the eight-membered ring (1,14,13,12,11,10,9,15) lead to an increase of the bond angles Si—CH—Si within this ring (117.4°) and to a small but significant lowering of the symmetry from C2v to C2.
    Notes: 1,3,7,9,11,13-Hexamethyl-1,3,5,7,9,11,13-heptasilahexacyclo-heptadecan Si7C16H36 kristallisiert triklin in der Raumgruppe P1 mit a = 11,393 Å, b = 11,819 Å, c = 10,583 Å, α = 83,73°, β = 67,42°, γ = 62,19° und Z = 2 Formeleinheiten. Die mittleren Bindungslängen sind CH—Si = 1,886, CH2—Si = 1,870 und CH3—Si = 1,883 Å. Die sterischen Wechselwirkungen der CH3- und CH2-Gruppen im Bereich des Achtrings (1,14,13,12,11,10,9,15) führen dort zu einer Aufweitung der Bindungswinkel Si—CH—Si auf 117,4° und zu einer geringen, aber signifikanten Symmetrieerniedrigung von C2v auf C2.
    Additional Material: 2 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 399 (1973), S. 257-262 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Formation of Organosilicon Compounds. XXXXIX. Crystal and Molecular Structure of Octachlorohexasila-asteran Si6C6H8Cl8Octachlorohexasila-asteran Si6C6H8Cl8 crystallizes in the triclinic space group P1 with a = 8.588 Å, b = 8.612 Å, c = 8.053 Å, α = 67.8°, β = 66.7°, γ = 66.3° and 1 molecule in the unit cell. In this hexacyclic molecule the Si-atoms has significantly different mean bond length, i. e. Si—C = 1.815 ± 0.015 Å and Si—Cl = 2.056 ± 0.016 Å at the 〉 SiCl2 groups but Si—C = 1.890 ± 0.022 Å and Si—Cl = 2.025 ± 0.003 Å at the SiCl groups. Remarkable are the bond angles in the four membered rings because those at the Si-atoms (93°) are larger than those at the C-atoms (87°).
    Notes: Octachlorohexasila-asteran Si6C6H8Cl8 kristallisiert triklin in der Raumgruppe P1 mit a = 8,588 Å, b = 8,612 Å, α = 67,8°, β = 66,7° und γ = 66,3° (Z = 1). In dieser hexacyclischen Molekel treten signifikant verschiedene mittlere Bindungslängen an den Si-Atomen auf, nämlich Si—C = 1,815 ° 0,015 Å und Si—Cl = 2,056 ± 0,016 Å bei den 〉SiCl2-Gruppen bzw. Si—C = 1,890 ± 0,022 Å und Si—Cl = 2,025 ± 0,003 Å bei den SiCl-Gruppen. Beachtenswert sind die Bindungs-winkel in den 4-Ringen, die an den Si-Atomen (93°) größer sind als an den C-Atomen (87°).
    Additional Material: 2 Ill.
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  • 8
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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