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  • Inorganic Chemistry  (17)
  • 1,2-Dihydro-1,3,2λ5,4λ5-diazadiphosphete  (1)
  • Alkylation  (1)
  • 11
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 239-242 
    ISSN: 0009-2940
    Keywords: 1-Naphthalenecarbonitrile, photochemistry of ; Cyclobutanes ; Captodative substitution ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photoexcited 1-naphthalenecarbonitrile (1) adds 2-morpholinoacrylonitrile (2) in the [2 + 2] mode both at the C(1) - C(2) and C(7) - C(8) bond unidirectionally and with the formation of only one (3 and 4, respectively) of the two a priori possible stereoisomers in each case. The structure of 3 has been unambiguously confirmed by an X-ray structural analysis.
    Additional Material: 1 Ill.
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  • 12
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2041-2045 
    ISSN: 0009-2940
    Keywords: Imidazol-2-ylidene - Borane adducts ; Calculations, ab initio ; Borane - Imidazol-2-ylidene adducts ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Imidazole Derivatives, VI[1].  -  Stable Carbene BoranesStable imidazol-2-ylidene - borane adducts 8 and 9 are obtained from 1,3,4,5-tetraalkylimidazol-2-ylidenes 7 and Me2S BH3 or Et2O BF3. An X-ray structure analysis of 8b has been performed. An ab initio calculation [MP2(fu)/6-31G**] reveals a low energy difference between two rotamers. The bond orders of the cyclic bonds imply only a minor interaction between the N - C - N and the C - C fragment.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 13
    ISSN: 0009-2940
    Keywords: 1,2-Dihydro-1,3,2λ5,4λ5-diazadiphosphete ; Isomerization ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,2-Dihydro-1,3,2λ5,4λ5-diazadiphosphete - Synthesis, Structure and Isomerization to the „Inner Salt“ of 1,3,2,4λ5-Diazadiphosphetan-2-ium HydroxideThe photochemical reaction of the azidophosphane (iPr2N)2PN3 (1) with the tetraazaphospholene (3) and the bis(imino)phosphorane (Me3Si)2NP(=NSiMe3)2 (6) proceeds by elimination of N2 to yield (5) and by 1,3-silyl group shift to furnish (8) the structures of which were determined by means of NMR data and, in the case of 5, additionally by X-ray structure analysis.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 14
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Salts of S4N4O2 - Examples for the Dependence of the Structure of Cyclic Sulfur-Nitrogen Compounds on the Electron DensityThe reaction of S4N4O2 with nucleophiles (alcoholates, alcohols, azides, and isocyanates) in alcoholic solution leads to the salts 1a-h. The Structure of 1h was determined by means of an X-ray analysis. 1h crystallizes in the space group P21/n and contains a transannular S—S-bond with 248.2 (2) pm. The structure of 1h is considered in connection with the increase of electron density and compared with the results of the X-ray analysis of CH3Si(NSN)3SiCH3 (2). 2 is cubic (space group P4132). The bicyclic molecule (S—N 150.4(2), Si—N 173.7 (2) pm) has approximate D3h symmetry and shows no S—S bonds across the rings.
    Notes: Die Umsetzung von S4N4O2 mit Nucleophilen (Alkoholate, Alkohole, Azide und Isocyanate) in alkoholischem Medium führt zu den Salzen 1a-h. Für 1h wurde eine Röntgenstrukturanalyse durchgeführt. 1h kristallisiert in der Raumgruppe P21/n und enthält eine transannulare S—S Bindung mit 248.2 (2) pm. Die Struktur von 1h wird im Zusammenhang mit der Zunahme der Elektronendichte betrachtet und mit den Ergebnissen der Röntgenstrukturanalyse von CH3Si(NSN)3SiCH3 (2) verglichen. 2 kristallisiert kubisch (Raumgruppe P4132). Das bicyclische Molekül (S—N 150.4 (2), Si—N 173.7 (2)pm) hat praktisch D3h Symmetrie und zeigt keine S—S-Bindungen im Ring.
    Additional Material: 2 Ill.
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  • 15
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 112 (1979), S. 1751-1755 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Planar Threefold Coordination of Sulfur(VI): Crystal and Molecular Structures of (R3SiN)3S and (R3CN)3S (R=CH3) at -130°CThe crystal structures of the title compounds were determined from single crystal X-ray data (measured at -130°C) and refined to unweighted R-values of 0.034 for (R3SiN)3S (1) and 0.047 for (R3CN)3S(2). 2 crystallizes in the triclinic space group P1 and 1 in the hexagonal space group P63/m. Both structures exhibit a planar threefold nitrogen coordination of the sulfur but the large coefficients of the temperature factors perpendicular to the SN3 planes in 1 and 2 might indicate a disorder due to small deviations from planarity. The S—N bond lengths were found to be 150.4 (1) and 151.5 pm (2, mean).
    Notes: Die Strukturen der Titelverbindungen wurden aus Diffraktometer-Einkristalldaten (gemessen bei -130°C) bestimmt und zu ungewichteten R-Werten von 0.034 für (R3SiN)3S )(1) und 0.047 für (R3CN)3S (2)verfeinert. 2 kristallisiert triklin, P1. Und 1 hexagonal, P63/m. In beiden Strukturen wird eine trigonal planare Koordination des zentralen Schwefelatoms beobachtet, doch deuten die relativ großen Koeffizienten der anisotropen Temperaturfaktoren senkrecht zu den SN3-Ebenen in 1 und 2 auf eine Fehlordnung als Folge geringer Abweichungen von der Planarität in den einzelnen Molekülen hin. Die S—N-Abstände betragen 150.4 pm (1) und 151.5 pm (2, Mittelwert).
    Additional Material: 1 Ill.
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  • 16
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation of trans-[Mo6Cl8]Cl4Br22- Starting from Crystalline [Mo6Cl8]Cl4(H2O)2 and Crystal Structure of [(C6H5)4As]2[Mo6Cl8]Cl4Br2The synthesis of the title compound is successful if the crystallized [(Mo6Cl8)Cl4(H2O)2] containing the H2O molecules in trans-position reacts with HBr + [(C6H5)4As]Br in ethanol in a heterogeneous reaction. The X-ray structure investigation confirms the existence of discrete trans-Br-substituted cluster anions of composition [(Mo6Cl8)Cl4Br2]2- in the crystal. The reaction in homogeneous solutions proceeds to Br-enriched compounds. [(C6H5)4As]2[(Mo6Cl8)Cl4Br2] crystallizes in the triclinic space group P¯1 with a = 11.071(2), b = 11.418(2), c = 12.813(2) Å, α = 116.10(2), β = 95.27(2) and γ = 94.41(2)° (-133°C). The crystal structure at -133°C was determined from single crystal X-ray diffraction data (R1 = 0.026). The [(Mo6Cl8)Cl4Br2]2--anions are not completely ordered but distributed statistically among the three positions which are possible within the limits of the ordered [Mo6Cl8]-cores (ratio 11:5:4). The frameworks of the anions consist of Mo6 cluster units with (slightly distorted) octahedral arrangement of the metal atoms (d(Mo—Mo): 2.600(1) up to 2.614(1) Å), which are coordinated by the halogeno ligands in a square-pyramidal manner. The details of the structure will be discussed and compared with similar [(Mo6X8)Y4] cluster units (X, Y = Cl, Br).
    Notes: Die Darstellung der in der Überschrift genannten Verbindung gelingt, wenn das kristallisierte [(Mo6Cl8)Cl4(H2O)2], das die H2O-Molekeln in trans-Stellung enthält, in Ethanol mit HBr + [(C6H5)4As]Br in heterogener Reaktion umgesetzt wird. Die röntgenographische Untersuchung bestätigt, daß im Kristall das isolierte trans-Br-substituierte Clusteranion [(Mo6Cl8)Cl4Br2]2- vorliegt. In homogener Lösung läft die Reaktion weiter zu Br-reicheren Produkten. [(C6H5)4As]2[(Mo6Cl8)Cl4Br2] kristallisiert in der triklinen Raumgruppe P¯1 mit a = 11,071(2), b = 11,418(2), c = 12,813(2) Å, α = 116,10(2), β = 95,27(2) und γ = 94,41(2)° (-133°C). Die Kristallstruktur bei -133°C wurde aus Einkristalldiffraktometerdaten bestimmt (R1 = 0,026). Die [(Mo6Cl8)Cl4Br2]2--Anionen sind im Kristall nicht vollständig geordnet, sondern verteilen sich statistisch im Verhältnis 11:5:4 auf die bei definiertem [Mo6Cl8]-Gerüst möglichen drei Positionen mit trans-ständiger Anordnung der Br-Liganden. Die Gerüste der Anionen bestehen aus Mo6-Clustern mit (leicht verzerrter) oktaedrischer Anordnung der Metallatome (d(Mo—Mo): 2,600(1) bis 2,614(1) Å), die quadratischpyramidal von Halogenatomen koordiniert sind. Die Einzelheiten der Struktur werden im Vergleich mit analog gebauten [(Mo6X8)Y6]-Clustern (X, Y = Cl, Br) diskutiert.
    Additional Material: 2 Ill.
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  • 17
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 524 (1985), S. 95-100 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 18C6 Crown Complex of Amidosulfuric AcidThe title compound (3) has been obtained from reaction of the crown ether 18C6 (1) with amidosulfuric acid (2) in water, methanol, and ethanol. The structure of the substance was elucidated with X-ray diffraction and IR data. The two constituents of 3 are connected through three oxygen-hydrogen bridges. 3 is ideally suited for the isolation and recovery of 1 from aqueous solutions.
    Notes: Durch Umsetzung des Kronenethers 18C6 (1) mit Amidoschwefelsäure (2) in Wasser, Methanol und Ethanol konnte die Titelverbindung (3) dargestellt werden. Die Struktur der Substanz wurde durch Röntgenstrukturanalyse und durch ihr IR-Spektrum aufgeklärt. Die beiden Komponenten von 3 sind durch drei Sauerstoff-Wasserstoff-Brücken miteinander verknüpft. 3 eignet sich hervorragend für die Isolierung und die Rückgewinnung von 1 aus wäßrigen Lösungen.
    Additional Material: 2 Ill.
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  • 18
    ISSN: 0044-2313
    Keywords: Potassium dithiocarbiminate ; dithiolates ; X-ray structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Structure of [ImNCS2K] (ImN = 1,3-Dimethylimidazoline-2-imino): a Novel Potassium DithiocarbiminateThe reaction of the 2-iminoimidazoline 4 with KMe gives the potassium imidate 7 from which the potassium 1,1-dithiolate 8 is obtained in almost quantitative yield. Crystals of C6H8N3S2K · 1/6 CH3CN (8 · 1/6 CH3CN) are triclinic, space group P1, Z = 6, a = 10.988(4), b = 13.597(8), c = 13.622(9) Å, α = 113.003, β = 105.53(3), γ = 105.62(3)°, V = 1636.90 Å3. The structure consists of a complicated 3-dimensional framework in which the K2 units bridged by the four sulfur atoms of two thiolate ligands are connected by nitrogen and sulfur bridges.
    Notes: Die Umsetzung des 2-Iminoimidazolins 4 mit KMe ergibt das Kaliumimidat 7, aus dem das Kalium-1,1-dithiolat 8 in fast quantitativer Ausbeute erhältlich ist. C6H8N3S2K · 1/6 CH3CN (8 · 1/6 CH3CN) kristallisiert triklin, Raumgruppe P1, Z = 6, a = 10.988(4), b = 13.597(8), c = 13.622(9) Å, α = 113.00(3), β = 105.53(3), γ = 105.62(3)°, V = 1636.90 Å3. Die komplexe Raumnetzstruktur besteht aus den durch die 4 Schwefelatome zweier Dithiolat-Liganden verbrückten K2-Einheiten, die ihrerseits über Stickstoff- und Schwefelatome verbunden sind.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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