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  • Inorganic Chemistry  (19)
  • Wiley-Blackwell  (19)
  • American Association for the Advancement of Science
  • Annual Reviews
  • International Union of Crystallography (IUCr)
  • 1990-1994  (19)
  • 1955-1959
  • 1994  (19)
Collection
Publisher
  • Wiley-Blackwell  (19)
  • American Association for the Advancement of Science
  • Annual Reviews
  • International Union of Crystallography (IUCr)
Years
  • 1990-1994  (19)
  • 1955-1959
Year
  • 1
    ISSN: 0009-2940
    Keywords: Cyclophosphahydrazides ; Dinitrogen-bridged ; Conformation ; Chair and Boat forms ; Dinuclear Mo(0) complexes ; 1,2,4,5,3,6-Tetrazadiphosphorinanes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of methylhydrazine with RPC12 (R = Et, tBu, and Ph) produced the cyclic phosphorus (III) hydrazides (1,2,4,5,3,6-tetrazadiphosphorinanes) [RPN(Me)N(H)2 (R = Et, 1; (Ph, 2; tBu, 3) in good yields. The 1H-and 31P-NMR spectroscopic analysis indicated that 1 exists in chair and boat conformations. However, it crystallizes in the chair conformation exclusively. The X-ray crystallographic investigation of all the three cyclo-phosphorus hydrazides 1-3 confirms the existence of these compounds in the chair conformations in the solid state. The reaction of Mo(CO)4-(NHC5H10)2 with 1 and 2 gives the dinuclear Mo(0) complexes [{Mo(CO)4(NHC5H10)}2(μ-[RPN(Me)N(H)]2}] (R = Et, 5; Ph, 6). Based on 1H- and 31P-NMR spectroscopic data, a bridging dinuclear dimetallic formulation is proposed for 5 and 6. The IR spectra indicate that the carbonyls are disposed in cis-geometry around the Mo(0) center.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1355-1357 
    ISSN: 0009-2940
    Keywords: Diphosphanylhydrazides ; Diphosphanes, dinitrogen-bridged ; Cycloplatinaphosphahydrazides ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: While the transition metal complexes of bis(phosphanyl)amines (PII-N-PIII) have been known for over three decades, the ligating properties of the next homologue PIII-N-N-PIII have been unprecedented so far. The X-ray structures of cycloplatinaphosphanehydrazides, [(OR)2PN(Me)N(Me)P(OR)2-PtCl2], reveal short distances for the P-N [1.639(5) Å] bonds.
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  • 3
    ISSN: 0009-2940
    Keywords: Bis(iminophosphoranes) ; Guanidines, bicyclic ; Aza Wittig reaction ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A one-pot synthesis of [5 + 6]-, [6 + 6]-, and [6 + 7]-rigid bicyclic guanidines (6, 8, 19, 21, 23) based on a bis(iminophosphorane)-mediated annulation strategy is reported. The crystal and molecular structure of the parent [5 + 6]-bicyclic guanidine 8 has been established by X-ray diffraction. The crystallographically independent molecule forms dimers through a centre of symmetry by N-H-N hydrogen bonds. The molecule, and therefore the dimer, is statistically disordered in a 65/35 ratio. A statistical study of N-H-N hydrogen bonds of this kind of dimers has been carried out by using the Cambridge Structural Database.
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 525-531 
    ISSN: 0009-2940
    Keywords: Alkynes ; Alkenes ; Nucleophilicity ; Carbenium ions ; Vinyl cations ; Kinetics ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Relative reactivities of alkenes and alkynes toward diarylmethyl cations have been determined by direct rate measurements and by competition experiments in dichloromethane. At -70°C alkynes are found to be one to two orders of magnitude less reactive than analogously substituted alkenes (e.g. phenylacetylene/styrene), but the reactivity difference reduces strongly as the temperature is raised. The stereochemistry of the vinyl chlorides produced by addition of benzhydryl chlorides to alkynes is characterized.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1851-1856 
    ISSN: 0009-2940
    Keywords: Grignard reagents, 1,3-di- ; Titanocene ; Zirconocene ; Platinum, complexes of ; Rhodium, complexes of ; Iridium, complexes of ; Metallacycles ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Five 1,8-naphthalenediyl transition metal compounds 2 were prepared by treating either 1,8-naphthalenediylmagnesium (1) or 1,8-dilithionaphthalene with the appropriate transition metal dichloride LnMCl2: LnM = Cp2Ti (2a), (PEt3)2Pt (2b), Cp* PPh3Rh (2c), Cp* PPh3Ir (2d), or Cp*2Zr (2e). The resulting metallacycles were characterized by NMR and mass spectrometry. X-ray crystal structure analyses were performed for (1,8-naphthalenediyl)titanocene (2a) and (1,8-naphthalenediyl)bis(triethylphosphane)platinum (2b). Despite the strain induced by the four-membered metal-containing rings, the naphthalene units show remarkably small distortions.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 1476-1478 
    ISSN: 0044-2313
    Keywords: Vanadiumpentoxide ; homogeneity range ; e.m.f. measurements ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: About the Homogeneity Range of V2O5 in the Temperature Range of 450°C to 620°CThe influence of the deposition temperature T1 on the homogeneity range of V2O5-crystalls was investigated by using a solid electrolyte cell. The deviation x in V2O5-x from the stoichiometric composition was obtained with: x = 0.0066 at T1 = 450°C up to x = 0.0326 at T1 = 620°C.
    Notes: Der Einfluß der Abscheidungstemperatur T1 auf die Phasenbreite chemisch transportierter V2O5-Kristalle wurde mit einer Festelektrolytzelle coulometrisch untersucht. Es ergab sich eine Phasenbreite x in V2O5-x von: x = 0,0066 bei T1 = 450°C bis zu x = 0,0326 bei T1 = 620°C.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 309-312 
    ISSN: 0044-2313
    Keywords: Barium vanadium oxide fluoride ; synthesis ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Kristallstruktur eines neuen azentrischen Oxidfluorids des VIV: BaVOF4Die Struktur von BaVOF4, erhalten durch hydrothermale Synthese, wurde röntgendiffraktometrisch aus Einkristalldaten bestimmt: Raumgruppe Fdd2 (azentrisch), Z = 16, a = 7,920(1), b = 27,608(2), c = 7,375(1) Å mit R = 0,0262, Rw = 0,0273 für 1 508 unabhängige Reflexe und 64 Parameter. Das Gitter wird von cis-verknüpften VOF5-Oktaedern aus gewinkelten unendlichen Ketten entlang [101] und [101] gebildet, die über Barium-Kationen verbunden sind. Die Lage der O2- und F- wird mittels Valenzband-Rechnungen diskutiert. Wie für BaTiOF4 und einige Verbindungen aus der Reihe AIIMIIIF5 (A = Ba, Sr und M = Ga, Al, Mn) kann die Struktur durch quasi-hexagonal dichteste Ebenen aus Stapeln von Ba2+, O2-- und F--Ionen beschrieben werden.
    Notes: The structure of BaVOF4 has been determined by X-ray diffraction data from a single crystal obtained by hydrothermal synthesis: S.G. Fdd2 (acentric), Z = 16, a = 7.920(1), b = 27.608(2) and c = 7.375(1) Å with R = 0.0262 and Rw = 0.0273 for 1 508 independent reflections and 64 parameters. The network is built up from cis-linked VOF5 octahedra forming infinite kinked chains running along the [101] and [101] directions, connected by barium cations. The location of O2- and F- ions is discussed using bond valence calculations. As for BaTiOF4 and some compounds in the series AIIMIIIF5 (A = Ba, Sr and M = Ga, Al, Mn), the structure can be described in terms of a quasi hexagonal compact planes stacking of Ba2+, O2- and F- ions.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 326-328 
    ISSN: 0044-2313
    Keywords: Lanthanum calcium copper gallate ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zur Kristallstruktur von LaCaCuGaO5Die Kristallstruktur von LaCaCuGaO5 wurde röntgenographisch an Einkristallen untersucht. Es kristallisiert orthorhombisch in der Raumgruppe C2v22-Ima2 mit a = 15,8467, b = 5,5077, c = 5,3188 Å, Z = 4. LaCaCuGaO5 gehört zum Brownmillerit-Typ und zeigt somit Schichten von eckenverknüpften CuO6-Oktaedern, die über GaO4-Tetraeder vernetzt sind. Die La3+- bzw. Ca2+-Ionen besetzen eine Punktlage statistisch.
    Notes: The crystal structure of LaCaCuGaO5 has been investigated by single crystal X-ray analysis. It crystallizes with orthorhombic symmetry, space group C2v22-Ima2, a = 15.8467, b = 5,5077, c = 5.3188 Å, Z = 4. LaCaCuGaO5 belongs to the mineral Brownmillerite showing layers of corner connected CuO6 octahedra linked by GaO4 tetrahedra. The La3+ and Ca2+ ions are distributed statistically over one crystallographic point position.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 977-980 
    ISSN: 0044-2313
    Keywords: Mercury(II) lead(II) oxide chloride ; synthesis ; crystal structure ; structural comparison ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: HgPb2O2Cl2, a “Perforated” Lead(II) OxideSingle crystals of HgPb2O2Cl2 were grown in a HgCl2 flux by reaction of PbO with HgCl2. Crystal structure analysis by single crystal X-ray methods were carried out. HgPb2O2Cl2 crystallizes monoclinic with a = 11.788(2) Å, b = 3.910(1) Å, c = 7.749(2) Å, β = 122.64(3)°, space group C2/m (No. 12) and Z = 2. HgPb2O2Cl2 is the first member of a new structure type, closely related to the structure of PbO.
    Notes: Einkristalle von HgPb2O2Cl2 wurden durch Umsetzung von PbO und HgCl2 in HgCl2-Schmelzen gezüchtet. An ihnen wurde der Aufbau mittels Einkristallröntgenstrukturanalyse bestimmt. HgPb2O2Cl2 kristallisiert monoklin mit a = 11,788(2) Å, b = 3,910(1) Å, c = 7,749(2) Å, β = 122,64(3)°, Raumgruppe C2/m (Nr. 12) und Z = 2. HgPb2O2Cl2 ist der erste Vertreter eines neuen Strukturtyps, der kristallchemisch von der Struktur von PbO ableitbar ist.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 1307-1311 
    ISSN: 0044-2313
    Keywords: Copper ; lead ; oxide ; preparation ; structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Structure of the First Ternary Lead(II) Copper(I) Oxide: PbCu2O2PbCu2O2 can be prepared by solid state reaction or by precipitation from a basic aqueous solution. Single crystals of the new compound were prepared by recrystallisation from a molten mixture (PbO—Cu2O) and investigated by X-ray diffractometer technique. PbCu2O2 crystallizes isotypically with the homologue silver compound PbAg2O2 (monoclinic with a = 8.223 Å, b = 8.289 Å, c = 6.015 Å, β = 132.62°, Z = 4, space group C2h6—C 1 2/c 1). The crystallographic data from the X-ray investigation are reported. The structure is built by endless ∞1[PbO4/4]- and ∞1[CuO2/4]-chains. Pb2+ has a one-sided asymmetric coordination with four next oxygen neighbours and Cu+ forms a stretched dumbbell with two oxygen atoms.
    Notes: PbCu2O2 kann durch Feststoffreaktion oder aus alkalischer, wässeriger Lösung erhalten werden. Einkristalle der neuen Verbindung wurden aus einer erstarrten Oxidschmelze (PbO—Cu2O) präpariert und mit Vierkreisdiffraktometertechnik röntgenographisch untersucht. PbCu2O2 ist isotyp mit der homologen Silberverbindung PbAg2O2 (monoklin mit a = 8,223 Å, b = 8,289 Å, c = 6,015 Å, β = 132,62°, Z = 4; Raumgruppe C2h6—C 1 2/c 1). Die kristallographischen Daten der Röntgenstrukturanalyse werden mitgeteilt. Die Kristallstruktur ist durch ∞1[PbO4/4]- und ∞1[CuO2/4]-Ketten charakterisiert. Pb2+ hat eine einseitige Koordination mit vier nächsten Sauerstoffnachbarn. Cu+ bildet mit zwei Sauerstoffatomen eine gestreckte Hantel.
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