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  • 1
    ISSN: 0044-2313
    Keywords: Phosphoraneiminato Complexes of Manganese and Nickel ; Syntheses ; Crystal Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Phosphoraneiminato Complexes of Manganese(II) and Nickel(II) with Heterocubane Structure. Crystal Structures of [MCl(NPEt3)]4 with M = Mn and NiThe phosphoraneiminato complexes [MCl(NPEt3)]4 with M = manganese and nickel as well as [MnBr(NPEt3)]4 are formed from the anhydrous halides MX2 and excess phosphoraneimine Me3SiNPEt3 by fusion reaction. They form paramagnetic, moisture-sensitive, orange (M = Mn) and turquoisegreen (M = Ni) crystals, respectively, which are characterized by i.r. spectroscopy and by crystal structure determinations.[MnCl(NPEt3)]4 (1): Space group C2/c, Z = 4, structure solution with 3 591 unique reflections, (2 811 〉 2σ(I)) R = 0.036. Lattice dimensions at -50°C: a = 2104.3, b = 1100.6, c = 1966.5 pm, β = 115.87°.[NiCl(NPEt3)]4 (2): Space group C2/c, Z = 4, structure solution with 2 711 unique reflections, (1611 〉 2σ(I)) R = 0.056. Lattice dimensions at -50°C: a = 2051.6, b = 1099.2, c = 1954.6 pm, β = 115.80°.1 and 2 are isostructural with one another. They form heterocubane structures in which the metal atoms are linked via μ3-N-bridges of the phosphoraneiminato groups with M4N4 bridge-type bond angles close to 90°.
    Notes: Die Phosphaniminato-Komplexe [MCl(NPEt3)]4 mit M = Mangan und Nickel sowie [MnBr(NPEt3)]4 entstehen durch Schmelzreaktion aus den wasserfreien Halogeniden MX2 und überschüssigem Phosphanimin Me3SiNPEt3. Sie bilden paramagnetische, feuchtigkeitsempfindliche, orange (M = Mn) bzw. türkisgrüne (M = Ni) Kristalle, die wir IR-spektroskopisch und durch Kristallstrukturanalysen charakterisiert haben. [MnCl(NPEt3)]4 (1): Raumgruppe C2/c, Z = 4, Strukturlösung mit 3 591 unabhängigen Reflexen, (2811 〉 2σ(I)) R = 0,036. Gitterkonstanten bei -50°C: a = 2104,3; b = 1100,6; c = 1966,5 pm, β = 115,87°.[NiCl(NPEt3)]4 (2): Raumgruppe C2/c, Z = 4, Strukturlösung mit 2 771 unabhängigen Reflexen, (1 611 〉 2σ(I)) R = 0,056. Gitterkonstanten bei -50°C: a = 2051,6; b = 1 099,2; c = 1954,6 pm, β = 115,80°.1 und 2 sind miteinander isotyp. Sie bilden Heterocuban-Strukturen, in denen die Metallatome über μ3-N-Brücken der Phosphaniminato-Gruppen verknüpft sind mit M4N4-Brückenbindungswinkeln nahe bei 90°.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 622 (1996), S. 1847-1853 
    ISSN: 0044-2313
    Keywords: Selenium Halides ; Crystal Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Crystal Structures of SeCl3+SbCl6-, SeBr3+GaBr4-, PCl4+SeCl5-, and (PPh4+)2SeCl42- · 2 CH3CNThe crystal structures of the title compounds were determined by X-ray diffraction.SeCl3+SbCl6-: Space group P21/m, Z = 4, structure determination with 1795 observed unique reflections, R = 0.022. Lattice dimensions at -80°C: a = 940.9, b = 1066.3, c = 1234.9 pm, β = 102.79°. The compound forms ion pairs with the structure of a double octahedron with linked surfaces. SeBr3+GaBr4-: Space group Pc, Z = 2, structure determination with 1461 observed unique reflections, R = 0.058. Lattice dimensions at -60°C: a = 660.1, b = 655.3, c = 1431.3 pm, β = 101.177°. The compound crystallizes in the SCl3[AlCl4] lattice type. Between the ions there are two relatively short Se … Br—Ga contacts.PCl4+SeCl5-: Space group Ima2, Z = 8, structure determination with 1757 observed unique reflections, R = 0.029. Lattice dimensions at -50°C: a = 1651.6, b = 1201.2, c = 1166.4 pm. The SeCl5- ions are associated to chains via interionic Se—Cl … Se contacts along the crystallographic c-axis.(PPh4+)2SeCl42- · 2CH3CN: Space group P21/n, Z = 2, structure determination with 2578 observed unique reflections, R = 0.050. Lattice dimensions at -80°C: a = 1288.5, b = 726.0, c = 2585.8 pm, β = 101.65°. The compound includes planar-tetragonal SeCl42- ions, which almost meet D4h symmetry.
    Notes: Die Kristallstrukturen der Titelverbindungen wurden röntgenographisch ermittelt.SeCl3+SbCl6-: Raumgruppe P21/m, Z = 4, Strukturlösung mit 1795 beobachteten unabhängigen Reflexen, R = 0,022. Gitterkonstanten bei -80°C: a = 940,9; b = 1066,3; c = 1234,9 pm; β = 102,79°. Die Verbindung bildet Ionenpaare mit der Struktur eines flächenverknüpften Doppeloktaeders.SeBr3+GaBr4-: Raumgruppe Pc, Z = 2, Strukturlösung mit 1461 beobachteten unabhängigen Reflexen, R = 0,058, Gitterkonstanten bei -60°C: a = 660,1; b = 655,3; c = 1431,3 pm; α = 101,17°. Die Verbindung kristallisiert im SCl3[AlCl4]-Strukturtyp. Zwischen den Ionen bestehen zwei relativ kurze Se … Br—Ga-Kontakte.PCl4+SeCl5-: Raumgruppe Ima2, Z = 8, Strukturlösung mit 1757 beobachteten unabhängigen Reflexen, R = 0,029. Gitterkonstanten bei -50°C; a = 1651,6; b = 1201,2; c = 1166,4 pm. Die SeCl5- -Ionen sind über interionische Se—Cl … Se-Kontakte entlang der kristallographischen c-Achse zu Ketten assoziiert.(PPh4+)2SeCl42- · 2CH3CN: Raumgruppe P21/n, Z = 2, Strukturlösung mit 2578 beobachteten unabhängigen Reflexen, R = 0,050. Gitterkonstanten bei -80°C: a = 1288,5; b = 726,0; c = 2585,8 pm; β = 101,65°. Die Verbindung enthält planar-quadratische SeCl42--Ionen, die nahezu D4h-Symmetrie erfüllen.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 622 (1996), S. 867-872 
    ISSN: 0044-2313
    Keywords: Phosphoraneiminato Complexes ; Cobalt ; Zinc ; Crystal Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Phosphoraneiminato Complexes of Cobalt and Zinc with Heterocubane Structure. Crystal Structures of [CoI(NPMe3)]4 and [ZnI(NPMe3)]4The title compounds have been prepared from CoI2 and ZnI2, respectively, and Me3SiNPMe3 by fusion reactions at 180°C in the presence of sodium fluoride. They crystallize from dichloromethane as dark green (Co) or colourless (Zn) single crystals including three molecules CH2Cl2 per formula unit, which were characterized by crystal structure determinations. [CoI(NPMe3)]4 · 3 CH2Cl2: Space group P3m1, Z = 2, structure solution with 2376 independent reflections, R = 0.033. Lattice dimensions at -50°C: a = b = 1455.8, c = 1270.5 pm.[ZnI(NPMe3)]4 · 3 CH2Cl2: Space group P3m1, Z = 2, structure solution with 2197 independent reflections, R = 0.043. Lattice dimensions at -60°C: a = b = 1454.9, c = 1270.5 pm. Both complexes are isostructural with one another. They form heterocubane structures in which the metal atoms are linked via μ3-N-bridges of the phosphoraneiminato groups with M4N4 bridge-type bond angles close to 90°.
    Notes: Die Titelverbindungen werden durch Reaktionen von CoI2 bzw. ZnI2 mit dem silylierten Phosphanimin Me3SiNPMe3 durch Schmelzreaktion bei 180°C in Gegenwart von Natriumfluorid synthetisiert. Sie kristallisieren aus Dichlormethan als dunkelgrüne (Co) bzw. farblose (Zn) Einkristalle mit drei Molekülen Dichlormethan pro Formeleinheit, die wir durch Kristallstrukturanalysen charakterisiert haben. [CoI(NPMe3)]4 · 3 CH2Cl2: Raumgruppe P3m1, Z = 2, Strukturlösung mit 2376 unabhängigen Reflexen, R = 0,033. Gitterkonstanten bei -50°C: a = b = 1455,8; c = 1270,5 pm.[ZnI(NPMe3)]4 · 3 CH2Cl2: Raumgruppe P3m1, Z = 2, Strukturlösung mit 2197 unabhängigen Reflexen, R = 0,043. Gitterkonstanten bei -60°C: a = b = 1454,9; c = 1270,5 pm. Die beiden miteinander isotypen Verbindungen bilden Heterocuban-Strukturen, in denen die Metallatome über μ3-N-Brücken der Phosphaniminato-Gruppen verknüpft sind mit M4N4-Brückenbindungswinkeln nahe bei 90°.
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  • 4
    ISSN: 0044-2313
    Keywords: Rare-Earth Complexes ; Syntheses ; Crystal Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Syntheses and Crystal Structures of the Rare-Earth Complexes [LaI2(THF)5]+I3-, [SmCl3(THF)4], [ErCl2(THF)5]+ [ErCl4(THF)2]-, [ErCl3(DME)2], and [Na(18-Crown-6)(THF)2]+[YbBr4(THF)2]-[LaI2(THF)5]+I3- (1) is obtained as red crystals from lanthanum powder and 1,2-diiodoethane in THF on exposure to light. Space group Pbcn, Z = 4, lattice dimensions at -83°C: a = 1264.9, b = 2218.9, c = 1199.1 pm, R = 0.031. The lanthanum atom of the cation of 1 is coordinated with iodine atoms in the axial positions in a pentagonal-bipyramidal way.[SmCl3(THF)4] (2) originates as colourless crystals on heating SmCl3 with excess THF in the presence of Me3SiNPEt3. Space group P21/c, Z = 8, lattice dimensions at -50°C: a = 3092.7, b = 826.2, c = 1758.3 pm, β = 93.85°, R = 0.054. Just like the known sample that crystallizes within the space group F2dd, 2 forms monomeric molecules in which the samarium atom is coordinated with two chlorine atoms in the axial positions in a distorted pentagonal-bipyramidal way.[ErCl2(THF)5]+[ErCl4(THF)2]- (3). Pale pink single crystals of 3 were prepared according to the described method by reaction of erbium powder with trimethylchlorosilane and methanol in THF. Space group C2/c, Z = 4, lattice dimensions at -50°C: a = 1246.3, b = 1145.7, c = 2726.0 pm, β = 91.293°, R = 0.036. The erbium atom of the cation of 3 has a pentagonal-bipyramidal coordination with the chlorine atoms in the axial positions. Within the anion the THF molecules are in trans-arrangement of the octahedrally coordinated erbium atom.[ErC13(DME)2] (4) originates as pink single crystals from 3 with excess boiling 1,2-dimethoxyethane. Space group P21/c, Z = 4, lattice dimensions at -50°C: a = 1137.2, b = 886.5, c = 1561.1 pm, β = 104.746°, R = 0.032. 4 forms monomeric molecules in which the erbium atom has a pentagonal-bipyramidal surrounding with two chlorine atoms in the axial positions.[Na(18-Krone-6)(THF)2]+ [YbBr4(THF)2]- (5) is formed as by-product by the reaction of YbBr3 with NaN(SiMe3)2 in THF in the presence-of 18-crown-6 forming colourless crystals. Space group P1, Z = 1, lattice dimensions at -70°C: a = 934.6, b = 988.9, c = 1208.0 pm, α = 73.82°, β = 72.98°, γ = 76.89°, R = 0.029. 5 contains isolated [YbBr4(THF)2]-ions, in which the THF molecules are arranged in trans-position.
    Notes: [LaI2(THF)5]+I3- (1) wird aus Lanthanpulver und 1,2-Diiodethan in THF unter Lichteinwirkung als rote Kristalle erhalten. Raumgruppe Pbcn, Z = 4, Gitterkonstanten bei -83°C: a = 1264,9; b = 2218,9; c = 1199,1 pm; R = 0,031. Das Lanthanatom des Kations von 1 ist pentagonal-bipyramidal koordiniert mit den Iodatomen in den Axialpositionen.[SmCl3(THF)4] (2) entsteht beim Erhitzen von SmCl3 mit überschüssigem THF in Gegenwart von Me3SiNPEt3 als farblose Einkristalle. Raumgruppe P21/c, Z = 8, Gitterkonstanten bei -50°C: a = 3092,7; b = 826,2; c = 1758,3 pm; β = 93,85°; R = 0,054. 2 bildet wie das bereits bekannte, in der Raumgruppe F2dd kristallisierende Präparat, monomere Moleküle, in denen das Samariumatom verzerrt pentagonal-bipyramidal koordiniert ist mit zwei Chloratomen in den Axialpositionen.[ErCl2(THF)5]+ [ErCl4(THF)2]- (3). Blaßrosa Einkristalle von 3 erhielten wir nach der literaturbekannten Methode durch Reaktion von Erbiumpulver mit Trimethylchlorsilan und Methanol in THF. Raumgruppe C2/c, Z = 4, Gitterkonstanten bei -50°C: a = 1246,3; b = 1145,7; c = 2726,0 pm; β = 91,293°; R = 0,036. Das Erbiumatom des Kations von 3 hat pentagonal-bipyramidale Koordination mit den Chloratomen in den Axialpositionen, im Anion befinden sich die THF-Moleküle in der trans-Anordnung des oktaedrisch koordinierten Erbiumatoms.[ErCl3(DME)2] (4) entsteht als rosa Einkristalle aus 3 mit überschüssigem, siedendem 1,2-Dimethoxyethan. Raumgruppe P21/c, Z = 4, Gitterkonstanten bei -50°C: a = 1137,2; b = 886,5; c = 1561,1 pm; β = 104,746°; R = 0,032. 4 bildet monomere Moleküle, in denen das Erbiumatom verzerrt pentagonal-bipyramidale Umgebung hat mit zwei Chloratomen in den Axialpositionen.[Na(18-Krone-6)(THF)2]+ [YbBr4(THF)2]- (5) entsteht als Begleitprodukt bei der Umsetzung von YbBr3 mit NaN(SiMe3)2 in THF in Gegenwart von 18-Krone-6 als farblose Kristalle. Raumgruppe P1, Z = 1, Gitterkonstanten bei -70°C: a = 934,6; b = 988,9; c = 1208,0 pm; α = 73,82°; β = 72,98°; γ = 76,89°; R = 0,029. 5 enthält isolierte [YbBr4(THF)2]--Ionen, in denen die THF-Moleküle in trans-Stellung angeordnet sind.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 623 (1997), S. 962-966 
    ISSN: 0044-2313
    Keywords: Phosphorane Iminato Complexes ; Sulfur Compounds ; Crystal Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Phosphorane Iminato Complexes of Sulfur. Crystal Structures of [S(NPEt3)3]Cl, [S(NPEt3)2]CI2 and [Me3SiOSO2NPPh3]The ionic phosphorane iminato complexes [S(NPEt3)3]Cl and [S(NPEt3)2]Cl2 are obtained as colourless, moisture sensitive crystals after reaction of Me3SiNPEt3 with disulfur dichloride from acetonitrile solutions. Both complexes, as well as the molecular complex [Me3SiOSO2NPPh3]. which is known from literature data, were characterized by crystal structure determinations.
    Notes: Die ionisch aufgebauten Phosphaniminato-Komplexe [S(NPEt3)3]Cl und [S(NPEt3)2]Cl2 entstehen als farblose, feuchtigkeitsempfindliche Kristalle nach Reaktion von Me3SiNPEt3 mit Dischwefeldichlorid in Acetonitrillösung. Beide Komplexe werden ebenso wie die literaturbekannte Molekülverbindung [Me3SiOSO2NPPh3] durch Kristallstrukturanalysen charakterisiert.
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  • 6
    ISSN: 0044-2313
    Keywords: Phosphoraneiminato ; Complexes of Titanium ; Synthesis ; IR Spectra ; Crystal Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Phosphoraneiminato Complexes of Titanium. Synthesis and Crystal Structures of CpTiCl2(NPMe3), [TiCl3(NPMe3)]2, [Ti2Cl5(NPMe2Ph)3], and [Ti3Cl6(NPMe3)5][BPh4]The title compounds are formed from Cp2TiCl2 and titanium tetrachloride, respectively, and the corresponding phosphane imino compounds Me3SiNPMe3 and Me3SiNPMe2Ph. The tetraphenyl borate salt yielded from the reaction of [Ti3Cl6(NPMe3)5]Cl with NaBPh4. All compounds form yellow crystals which are sensitive to moisture. They were characterized by IR-spectroscopy and crystal structure analyses.CpTiCl2(NPMe3) (1): Space group Pbca, Z = 8, solution of the structure with 1632 observed independent reflections, R = 0.037. Lattice dimensions at 19°C: a = 1202.6, b = 1224.2, c = 1766.7 pm. The molecules of the compound are monomeric with the (NPMe3)- ligand in almost linear array (bond angle Ti—N—P 170.7°).[TiCl3(NPMe3)]2 (2): Space group Pbca, Z = 8, structure solution with 698 observed independent reflections, R = 0.030. Lattice dimensions at -60°C: a = 1140.5, b = 1112.2, c = 1589.4 pm. In 2 the titanium atoms, which occur in trigonal bipyramidal coordination, are linked by the N atoms of the (NPMe3)- groups to form a centrosymmetric dimer with Ti—N bond lengths of 184.3 and 208.2 pm.[Ti2Cl5(NPMe2Ph)3] · CH2Cl2 (3): Space group Pca21, Z = 4, structure solution with 8477 observed independent reflections, R = 0.051. The lattice dimensions at 20°C are: a = 1221.0; b = 1407.5, c = 2139.3 pm. 3 can be understood as a reaction product of TiCl2(NPMe2Ph)2 and TiCl3(NPMe2Ph). In the resulting, heavily distorted Ti2N2-four-membered ring the Ti—N bond lenghts are 1804., 194.4, 199.2, and 234.6 pm. The longest Ti—N bond is in trans-position to the N atom of the terminal (NPMe2Ph)- ligand, in which the Ti—N distance is 175.6 pm. .[Ti3CL6(NPMe3)5][BPh4] (4): Space group P21/n, structure solution with 2846 observed independent reflections, R = 0.062. The lattice dimensions at 20°C are: a = 1495.2, b = 2335.4, c = 155,8 pm, β = 93.28°. In the cation of 4 the three titanium atoms along with three (NPMe3)- groups with μ2- N functions and two (NPMe3)- groups with μ3- N functions form a nation number 6 with two terminal chlorine atoms.
    Notes: Die Titelverbindungen entstehen aus Cp2TiCl2 bzw. Titantetrachlorid und den entsprechenden silylierten Phosphaniminen Me3SiNPMe3 bzw. Me3SiNPMe2Ph. Das Tetraphenyloborat-Derivat erhielten wir durch Umsetzung von [Ti3Cl6(NPMe3)5]Cl mit NaBPh4. Alle Verbindungen bilden gelbe, feuchtigkeitsempfindliche Kristalle, die durch IR-Spektroskopie und durch Kristallstrukturanalysen charakterisiert wurden.CpTiCl2(NPMe3) (1): Raumgruppe Pbca, Z = 8, Strukturlösung mit 1632 beobachteten unabhängigen Reflexen, R = 0,037. Gitterabmessungen bei 19°C: a = 1202,6; b = 1224,2; c = 1766,7 pm. Die Verbindung bildet monomere Moleküle mit dem (NPMe3)--Liganden in nahezu gestreckter Anordnung TiNP (Bindungswinkel 170,7°).[TiCl3(NPMe3)]2 (2): Raumgruppe Pbca, Z = 8, Strukturlösung mit 698 beobachteten unabhängigen Reflexen, R = 0,030. Gitterabmessungen bei -60°C: a = 1140,5; b = 1112,2; c = 1589,4 pm. In 2 sind die trigonal-bipyramidal koordinierten Titanatome über die N-Atome der (NPMe3)- - Gruppen zu einem zentrosymmetrischen Dimer mit TiN-Abständen von 184,3 und 208,2 pm verknüpft.[Ti2Cl5(NPMe2Ph)3] · CH2Cl2 (3): Raumgruppe Pca21, Z = 4, Strukturlösung mit 8477 beobachteten unabhängigen Reflexen, R = 0,051. Gitterabmessungen bei 20°C: a = 1221,0; b = 1407,5; c = 2139,3 pm. 3 läßt sich als Dimerisierungsprodukt aus TiCl2(NPMe2Ph)2 und TiCl3(NPMe2Ph) auffassen, wobei ein stark verzerrter ebener Ti2N2-Vierring mit TiN-Abständen von 180,4, 194,4, 199,2, und 234,6 pm entsteht. Die längste TiN-Bindung befindet sich in trans-Stellung zu dem N-Atom des terminal gebundenen (NPMe2Ph)--Liganden, der eine TiN-Bindungslänge von 175,6 pm aufweist.[Ti3Cl6(NPMe3)5][BPh4] (4): Raumgruppe P21/n, Z = 4, Strukturlösung mit 2846 beobachteten unabhängigen Reflexen, R = 0,062. Gitterabmessungen bei 20°C: a = 1495,2; b = 2335,4; c = 1555,8 pm, β = 93,28°. In dem Kation von 4 bilden die drei Titanatome zusammen mit drei (NPMe3)--Gruppen mit μ2-N-Funktion und zwei (NPMe3)--Gruppen mit μ3-N-Funktion eine trigonale Bipyramide. Zusammen mit den terminal gebundenen Chloratomen erreichen die Titanatome die Koordinationszahl sechs.
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  • 7
    ISSN: 0044-2313
    Keywords: Phosphorane Iminato Complexes of Niobium and Tantalum ; Synthesis ; IR spectra ; Crystal Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Phosphorane Iminato Complexes of Niobium and Tantalum. Crystal Structures of [NbCl4(NPiPr3)(CH3CN)], [NbCl3(NPiPr3)2], [TaCl4(NPiPr3)]2, and [TaCl3(NPiPr3)2]The title compounds have been prepared from the pentachlorides of niobium and tantalum with the silylated phosphorane imine Me3SiNPiPr3. They are characterized by IR spectroscopy and crystal structure determinations.NbCl4(NPiPr3)(CH3CN)]. Space group Pna21, Z = 4, 2102 observed unique reflections, R = 0.022. Lattice dimensions at -50°C: a = 1627.2, b = 876.3, c = 1335.3 pm. The compound forms monomeric molecules with the acetonitrile molecule in trans position to the phosphorane iminato group. This group shows a short NbN distance of 178.2 pm with a NbNP bond angle of 165.2°.[NbCl3(NPiPr3)2]. Space group Cc, Z = 4, 2534 observed unique reflections, R = 0.046. Lattice dimensions at 20°C: a = 1302.65, b = 1321.69, c = 1672.04 pm, β = 111.713°. The compound forms monomeric molecules with a distorted bipyramidal surrounding of the niobium atom and equatorially arranged phosphorane iminato groups.[TaCl4(NPiPr3)]2. Space group Pbca, Z = 4, 1537 observed unique reflections, R = 0.037. Lattice dimensions at -40°C: a = 1420.6, b = 1483.9, c = 1622.0 pm. The compound forms centrosymmetric dimeric molecules with dissimilarly long Ta2Cl2 bridges and equatorially arranged phosphorane iminato groups.[TaCl3(NPiPr3)2]. Space group Cc, Z = 4, 5737 observed unique reflections, R = 0.039. Lattice dimensions at -50°C: a = 1303.9, b = 1327.2, c = 1682.1 pm, β = 111,92°. The compound is isotypical with the corresponding niobium compound.
    Notes: Die Titelverbindungen werden aus den Pentachloriden von Niob und Tantal mit dem silylierten Phosphanimin Me3SiNPiPr3 erhalten und durch ihre IR-Spektren und Kristallstrukturanalysen charakterisiert.[NbCl4(NPiPr3)(CH3CN)]. Raumgruppe Pna21, Z = 4, 2102 beobachtete unabhängige Reflexe, R = 0,022. Gitterkonstanten bei -50°C: a = 1627,2; b = 876,3; c = 1335,3 pm. Die Verbindung bildet monomere Moleküle mit dem Acetonitril-Molekül in trans-Stellung zur Phosphaniminato-Gruppe, die einen kurzen NbN-Abstand von 178,2 pm aufweist bei einem NbNP-Bindungswinkel von 165,2°.[NbCl3(NPiPr3)2]. Raumgruppe Cc, Z = 4, 2534 beobachtete unabhängige Reflexe, R = 0,046. Gitterkonstanten bei 20°C: a = 1302,65; b = 1321,69; c = 1672,04 pm; β = 111,713°. Die Verbindung bildet monomere Moleküle mit verzerrt bipyramidaler Umgebung des Niobatoms und äquatorial angeordneten Phosphaniminato-Gruppen.[TaCl4(NPiPr3)]2. Raumgruppe Pbca, Z = 4, 1537 beobachtete unabhängige Reflexe, R = 0,037. Gitterkonstanten bei -40°C: a = 1420,6; b = 1483,9; c = 1622,0 pm. Die Verbindung bildet zentrosymmetrische dimere Moleküle mit ungleich langen Ta2Cl2-Brücken und äquatorial angeordneten Phosphaniminato-Gruppen.[TaCl3(NPiPr3)2]. Raumgruppe Cc, Z = 4, 5737 beobachtete unabhängige Reflexe, R = 0,039. Gitterkonstanten bei -50°C: a = 1303,9; b = 1327,2; c = 1682,1 pm; β = 111,92°. Die Verbindung ist isotyp mit der entsprechenden Niobverbindung.
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  • 8
    ISSN: 0044-2313
    Keywords: Chromium ; Palladium ; Copper Phosphaneimine Complexes ; Syntheses ; IR Spectra ; Crystal Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Silylated Phosphaneimine Complexes of Chromium(II), Palladium(II), and Copper(II). The Crystal Structures of [CrCl2(Me3SiNPMe3)2], [PdCl2(Me3SiNPEt3)2], and [CuCl2(Me3SiNPMe3)]2The title compounds have been prepared by the reaction of the silylated phosphaneimines Me3SiNPR3 (R = CH3, C2H5) with CrCl2(THF)2, PdCl2 and CuCl2, respectively, in dichloromethane suspensions. All donor-acceptor complexes were characterized by IR spectroscopy and by crystal structure determinations.[CrCl2(Me3SiNPMe3)2]: Space group Pccn, Z = 4, structure determination with 2104 observed unique reflections, R = 0.045. Lattice dimensions at -70°C: a = 1326.3, b = 1562.5, c = 1171.5 pm. Within the monomeric molecular structure the chromium atom is planarly coordinated within the trans-configuration of the Cl atoms and the N atoms with distances of Cr—Cl = 235.94 pm and Cr—N = 211.7 pm.[PdCl2(Me3SiNPEt3)2]: Space group P21/n, Z = 2, structure determination with 2412 observed unique reflections, R = 0.031. Lattice dimensions at 20°C: a = 917.3, b = 1390.2, c = 1161.7 pm, β = 95.80°. Within the monomeric molecular structure the palladium atom is planarly coordinated within the trans-configuration of the Cl atoms and the N atoms with distances of Pd—Cl = 222.9 pm and Pd—N = 209.5 pm.[CuCl2(Me3SiNPMe3)2]: Space group Pbca, Z = 4, structure determination with 1861 observed unique reflections, R = 0.067. Lattice dimensions at -70°C: a = 1440.2, b = 1205.1, c = 1536.5 pm. The compound forms centrosymmetric dimeric molecules, in which the Cu atoms are linked via almost symmetrical chloro-bridges with Cu—Cl distances of 231.4 pm. The distance Cu—N is 196.7 pm.
    Notes: Die Titelverbindungen entstehen bei der Einwirkung der silylierten Phosphanimine Me3SiNPR3 (R = CH3, C2H5) auf CrCl2(THF)2, PdCl2 und CuCl2 in Dichlormethan-Suspension. Die drei Donor-Acceptor-Komplexe werden durch ihre IR-Spektren und durch Kristallstrukturanalysen charakterisiert.[CrCl2(Me3SiNPMe3)2]: Raumgruppe Pccn, Z = 4, Strukturlösung mit 2104 unabhängigen beobachteten Reflexen, R = 0,045. Gitterkonstanten bei -70°C: a = 1326,3; b = 1562,5; c = 1171,5 pm. In der monomeren Molekülstruktur ist das Chromatom planar in der trans-Konfiguration von den Cl-Atomen und den N-Atomen der Phosphanimin-Liganden koordiniert mit Abständen Cr—Cl = 235,94 pm und Cr—N = 211,7 pm.[PdCl2(Me3SiNPEt3)2]: Raumgruppe P21/n, Z = 2, Strukturlösung mit 2412 unabhängigen beobachteten Reflexen, R = 0,031. Gitterkonstanten bei 20°C: a = 917,3; b = 1390,2; c = 1161,7 pm, β = 95,80°. In der monomeren Molekülstruktur ist das Palladiumatom planar in der trans-Konfiguration von den Cl-Atomen und den N-Atomen der Phosphaniminliganden koordiniert mit Abständen Pd—Cl = 222,9 pm und Pd—N = 209,5 pm.[CuCl2(Me3SiNPMe3)]2: Raumgruppe Pbca, Z = 4, Strukturlösung mit 1861 unabhängigen beobachteten Reflexen, R = 0,067. Gitterkonstanten bei -70°C: a = 1440,2; b = 1205,1; c = 1536,5 pm. Die Verbindung bildet zentrosymmetrische dimere Moleküle, in denen die Cu-Atome über nahezu symmetrische Chlorobrücken mit Cu—Cl-Abständen von 231,4 pm verknüpft sind. Der Abstand Cu—N beträgt 196,7 pm.
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  • 9
    ISSN: 0044-2313
    Keywords: Phosphoraneiminato Complexes ; Boron Compounds ; Crystal Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Phosphaneimine and Phosphoraneiminato Complexes of Boron. Synthesis and Crystal Structures of [BF3(Me3SiNPEt3)], [BCl2(NPPh3)]2, [BCl2(NPEt3)]2, [B2Cl3(NPEt3)2]+BCl4-, and [B2Cl2(NPiPr3)3]+BCl4-The title compounds have been prepared from the corresponding silylated phosphaneimines and boron trifluoride etherate and boron trichloride, respectively. The compounds form white moisture sensitive crystals, which were characterized by 11B-nmr-spectroscopy, IR-spectroscopy and by crystal structure determinations.[BF3(Me3SiNPEt3)]: Space group P21/c, Z = 4, R = 0.032 for reflections with I 〉 2σ(I). Lattice dimensions at -70°C: a = 1361.0, b = 819.56, c = 1422.5 pm, β = 109.86°. The donor acceptor complex forms monomeric molecules with a B—N bond length of 157.8 pm.[BCl2(NPPh3)]2 · 2 CH2Cl2: Space group P21/c, Z = 2, R = 0.049 for reflections with I 〉 2σ(I). Lattice dimensions at -50°C: a = 1184.6, b = 2086.4, c = 843.0 pm, β = 96.86°. The compound forms centrosymmetric dimeric molecules in which the boron atoms are linked to B2N2 four-membered rings with B—N distances of 152.7 pm via μ2-N bridges of the NPPh3 groups.[BCl2(NPEt3)]2: Space group Pbca, Z = 4, R = 0.029 for reflections with I 〉 2σ(I). Lattice dimensions at -90°C: a = 1269.5, b = 1138.7, c = 1470.3 pm. The compound has a molecular structure corresponding to the phenyl compound with B—N ring distances of 151.0 pm.[B2Cl3(NPEt3)2]+BCl4-: Space group Pbca, Z = 8, R = 0.034 for reflections with I 〉 2σ(I). Lattice dimensions at -70°C: a = 1309.3, b = 1619.8, c = 2410.7 pm. Within the cations the boron atoms are linked to planar, asymmetrical B2N2 four-membered rings with B—N distances of 155.1 and 143.1 pm via the μ2-N atoms of the NPEt3 groups.[B2Cl2(NPiPr3)3]+BCl4- · CH2Cl2: Space group Pna2, Z = 4, R = 0.033 for reflections with I 〉 2σ(I). Lattice dimensions at -70°C: a = 1976.5, b = 860.2, c = 2612.7 pm. Within the cations the boron atoms are linked to planar, asymmetrical B2N2 four-membered rings with B—N distances of 153.7 and 150.5 pm via the μ2-N atoms of two of the NPiPr3 groups. The third NPiPr3 group is terminally connected to the sp2-hybridized boron atom with a B—N distance of 133.5 pm and with a B—N—P bond angle of 165.3°.
    Notes: Die Titelverbindungen werden aus den entsprechenden silylierten Phosphaniminen Me3SiNPR3 und Bortrifluorid-Etherat bzw. Bortrichlorid hergestellt. Die Verbindungen bilden weiße, feuchtigkeitsempfindliche Kristalle, die wir durch 11B-NMR- und IR-Spektren sowie durch Kristallstrukturanalysen charakterisiert haben.[BF3(Me3SiNPEt3)]: Raumgruppe P21/c, Z = 4, R = 0,032 für Reflexe mit I 〉 2σ(I). Gitterkonstanten bei -70°C: a = 1361,0; b = 819,56; c = 1422,5 pm, β = 109,86°. Der Donor-Akzeptor-Komplex bildet monomere Moleküle mit einer B—N-Bindungslänge von 157,8 pm.[BCl2(NPPh3)]2 · 2 CH2Cl2: Raumgruppe P21/c, Z = 2, R = 0,049 für Reflexe mit I 〉 2σ(I). Gitterkonstanten bei -50°C: a = 1184,6; b = 2086,4; c = 843,0 pm; β = 96,86°. Die Verbindung bildet zentrosymmetrische dimere Moleküle, in denen die Boratome über μ2-N-Brücken der NPPh3-Gruppen zu B2N2-Vierringen mit B—N-Abständen von 152,7 pm verknüpft sind.[BCl2(NPEt3)]2: Raumgruppe Pbca, Z = 4, R = 0,029 für Reflexe mit I 〉 2σ(I). Gitterkonstanten bei -90°C: a = 1269,5; b = 1138,7; c = 1470,3 pm. Die Verbindung hat einen zu der Phenylverbindung entsprechenden Aufbau mit B—N-Ringabständen von 151,0 pm.[B2Cl3(NPEt3)2]+BCl4-: Raumgruppe Pbca, Z = 8, R = 0,034 für Reflexe mit I 〉 2σ(I). Gitterkonstanten bei -70°C: a = 1309,3; b = 1619,8; c = 2410,7 pm. In den Kationen sind die Boratome über die μ2-N-Atome der NPEt3-Gruppen zu planaren, asymmetrischen B2N2-Vierringen mit B—N-Abständen von 155,1 und 143,1 pm verknüpft.[B2Cl2(NPiPr3)3]+BCl4- · CH2Cl2: Raumgruppe Pna21, Z = 4, R = 0,033 für Reflexe mit I 〉 2σ(I). Gitterkonstanten bei -70°C: a = 1976,5; b = 860,2; c = 2612,7 pm. In den Kationen sind die Boratome durch die μ2-N-Atome zweier NPiPr3-Gruppen zu planaren, asymmetrischen B2N2-Vierringen mit B—N-Abständen von 153,7 und 150,5 pm verknüpft. Die dritte NPiPr3-Gruppe ist mit dem sp2-hybridisierten Boratom terminal mit einem B—N-Abstand von 133,5 pm verbunden bei einem B—N—P-Bindungswinkel von 165,3°.
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  • 10
    ISSN: 0044-2313
    Keywords: Phosphoraneiminato Complexes ; Boron Compounds ; Crystal Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Phosphoraneiminato Complexes of Boron. Syntheses and Crystal Structures of [BBr2(NPMe3)]2, [B2Br3(NPiPr3)2]Br, [B2(NPEt3)4]Br2, [B2Br2(NPPh3)3]BBr4 and [{B2(NMe2)2}2(NPEt3)2]ClThe bromoderivatives of the title compounds are prepared from the corresponding silylated phosphoraneimines Me3SiNPR3 and boron tribromide. The boron subcompound [{B2(NMe2)2}2(NPEt3)2]Cl2 derives from Me3SiNPEt3 and B2Cl2(NMe2)2. All complexes are characterized by NMR and IR spectroscopy as well as by crystal structure determinations.[BBr2(NPMe3)]2 (1): Space group P21/n, Z = 2, R = 0.031. Lattice dimensions at -50°C: a = 723.8, b = 894.2, c = 1305.4 pm, β = 92.35°. 1 forms centrosymmetric molecules in which the boron atoms are linked via μ2-N bridges of the NPMe3- groups of from B2N2 four-membered rings with B—N distances of 149.9 and 150.9 pm.B2Br3(NPiPr3)2]Br (2): Space group P21, Z = 2, R = 0.059. Lattice dimensions at -80°C: a = 817.6, b = 2198.7, c = 851.5 pm, β = 115.09°. In the cations of 2 the boron atoms are lined via the μ2-N atoms of the NPiPr3- groups to form planar, asymmetric B2N2 four-membered rings with B—N distances of 143 and 156 pm.[B2(NPEt3)4[Br2·4CH2Cl2 (3): Space group C2/c, Z = 4, R = 0.042. Lattice dimensions at -50°C: a = 1946.1, b = 1180.3, c = 2311.3 pm, β = 101.02°. The structure contains centrosymmetric dications in which both the boron atoms are lined by the N atoms of two of the NPEt3- groups to form a B2N2 four-membered ring with B—N distances of 149.6 pm. The remaining two NPEt3- groups are terminally bonded with very short B—N distances of 133.5 pm.B2Br2(NPPh3)3]BBr4 (4): Space group P1, Z = 2, R = 0.065. Lattice dimension at -50°C: a = 1025.7, b = 1496.1, c = 1807.0 pm, α = 85.09°, β = 82.90°, γ = 82.72°. In the cation the boron atoms are lined via the μ2-N atoms of two of the NPPh3- groups to form a nearly planer B2N2 four-membered ring with B—N distances of 149.3-153.1 pm. The third NPPh33 group is terminally connected with teh sp2 hybridized boron atom and with a B—N distance of 134.1 pm along with an almost linear BNP bond angle of 173.6°.[{B2(NMe2)2}2(NPEt2)2]Cl2 · 3CH2Cl2 (5): Space group C2/c, Z = 4, R = 0.098. Lattice dimensions at -70°C: a = 1557.9, b = 1294.7, c = 2122.9 pm, β = 96.08°. The structure of 4 contains centrosymmetric dications in which two by two B-B dumb-bells are linked via the μ2-N atoms of the two NEPt3- groups to form B4N2 six-membered rings with B—N distances of 150 and 156 pm and B-B distances of 173 pm. The B—N distances of the terminally bonded NMe2- groups correspond to 138 pm double bonds.
    Notes: Die Bromoderivate der Titelverbindungen werden aus den entsprechenden silylierten Phosphaniminen Me3SiNPR3 und Bortribromid hergestellt. Die Borsubverbindung [{B2(NMe2)2}2(NPEt3)2]Cl2 entsteht aus Me3SiNPEt3 und B2Cl2(NMe2)2. Alle Komplexe werden durch NMR- und IR-Spektren sowie durch Kristallstrukturanalysen charakterisiert.[BBr2(NPMe3)]2 (1): Raumgruppe P21/n, Z = 2, R = 0,031. Gitterkonstanten bei -50°C: a = 723,8; b = 894,2; c = 1305,4 pm; β = 92,35°. 1 bildet zentrosymmetrische Moleküle, in denen die Boratome über μ2-N-Brücken der NPMe3--Gruppen zu B2N2-Vierringen mit B—N-Abständen von 149,9 und 150,9 pm verknüpft sind.[B2Br3(NPiPr3)2]Br (2): Raumgruppe P21, Z = 2, R = 0,059. Gitterkonstanten bei -80°C: a = 817,6; b = 2198,7; c = 851,5 pm; β = 115,09°. In den Kationen von 2 sind die Boratome über die μ2-N-Atome der NPiPr3--Gruppen zu planaren, asymmetrischen B2N2-Vierringen mit B—N-Abständen von 143 und 156 pm verknüpft.[B2(NPEt3)4]Br2 · 4 CH2Cl2 (3): Raumgruppe C2/c, Z = 4, R = 0,042. Gitterkonstanten bei -50°C: a = 1946,1; b = 1180,3; c = 2311,3 pm; β = 101,02°. Die Struktur enthält zentrosymmetrische Dikationen, in denen die N-Atome zweier NPEt3--Gruppen die beiden Boratome zu einem B2N2-Vierring mit B—N-Abständen von 149,6 pm verknüpfen. Die beiden übrigen NPEt3--Gruppen sind terminal gebunden mit sehr kurzen B—N-Abständen von 133,5 pm.[B2Br2(NPPh3)3]BBr4 (4): Raumgruppe P1, Z = 2, R = 0,065. Gitterkonstanten bei -50°C: a = 1025,7; b = 1496,1; c = 1807,0 pm; α = 85,09°; β = 82,90°; γ = 82,72°. In dem Kation sind die Boratome über die μ2-N-Atome zweier NPPh3--Gruppen zu einem nahezu planaren B2N2-Vierring mit B—N-Abständen von 149,3-153,1 pm verknüpft. Die dritte NPPh3--Gruppe ist mit dem sp2-hybridisierten Boratom terminal mit einem B—N-Abständ von 134,1 pm verbunden bei einem fast linearen BNP-Bindungswinkel von 173,6°.[{B2(NMe2)2}2(NPEt3)2]Cl2 · 3 CH2Cl2 (5): Raumgruppe C2/c, Z = 4, R = 0,098. Gitterkonstanten bei -70°C: a = 1557,9; b = 1294,7; c = 2122,9 pm; β = 96,08°. Die Struktur von 4 enthält zentrosymmetrische Dikationen, in denen je zwei B—B-Hanteln über die μ2-N-Atome der beiden NPEt3--Gruppen zu B4N2-Sechsringen mit B—N-Abständen von 150 und 156 pm sowie B—B-Abständen von 173 pm verknüpft sind. Die B—N-Abstände der terminal gebundenen NMe2--Gruppen entsprechen mit 138 pm Doppelbindungen.
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