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  • Synthesis  (24)
  • synthesis  (7)
  • syntheses  (5)
  • Nitrido ligand  (2)
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  • 11
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 619 (1993), S. 1023-1026 
    ISSN: 0044-2313
    Keywords: Phosphorane Iminato Complex of Vanadium(IV) ; Synthesis ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: [VCl3(NPPh3)(OPPh3)], a Phosphorane Iminato Complex of Vanadium(IV)The title compound has been prepared from vanadium tetrachloride and Me3SiNPPh3 in the presence of OPPh3 in CCl4 solution, forming orange-red, moisture sensitive crystals, which were characterized by an X-ray structure determination. Space group Cc, Z = 4, 2 560 observed unique reflections, R = 0.049. Lattice dimensions at 0°C: a = 1 018(1), b = 1 826(2), c = 1 859(2) pm, β = 93.65(9)° [VCl3(NPPh3)(OPPh3)] forms monomeric molecules, in which the vanadium atom is coordinated in a distorted square pyramidal fashion with the (NPPh3)- ligand in apical position. The three chlorine atoms and the oxygen atom of the OPPh3 molecule occupy the basal positions. The phosphorane iminato group V=N=PPh3 is nearly linear (bond angle VNP 161.4°), the bond lengths VN (169 pm) and PN (162 pm) correspond with double bonds.
    Notes: Die Titelverbindung entsteht aus Vanadiumtetrachlorid und Me3SiNPPh3 in Gegenwart von Triphenylphosphanoxid in CCl4. Die orangeroten, feuchtigkeitsempfindlichen Kristalle wurden durch eine röntgenographische Strukturanalyse charakterisiert: Raumgruppe Cc, Z = 4, 2 560 beobachtete unabhängige Reflexe, R = 4,9%. Gitterabmessungen bei 0°C: a = 1 018(1), b = 1 826(2), c = 1 859(2) pm, β = 93,65(9)°. [VCl3(NPPh3)(OPPh3)] bildet monomere Moleküle, in denen das Vanadiumatom eine verzerrte tetragonale Pyramide bildet mit dem (NPPh3)--Liganden in der Apicalposition. Die drei Chloratome und das O-Atom des OPPh3-Moleküls sind äquatorial angeordnet. Die Phosphaniminatogruppe V=N=PPh3 ist mit 161,4° nahezu gestreckt, die Abstände VN und PN entsprechen mit 169 und 162 pm Doppelbindungen.
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  • 12
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 621 (1995), S. 1171-1174 
    ISSN: 0044-2313
    Keywords: Selenium ; Phosphorane Iminato Complex of Selenium ; Synthesis ; IR Spectrum ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Crystal Structure of the Selenyl-Phosphoraneiminato Complex SeO(NPPh3)2SeO(NPPh3)2 has been prepared from SeO2 and Me3SiNPPh3 in a SeO2 suspension in acetonitrile, forming colourless crystals. The compound is characterized by IR spectroscopy and by a crystal structure determination. Space group P1, Z = 2, structure solution with 5 344 observed unique reflections, R = 0.064. Lattice dimensions at -40°C: a = 931.6, b = 947.6, c = 1 762 pm, α = 77.50°, β = 81.78°, γ = 79.23°. The compound forms monomeric molecules in which the selenium atom is ϕ-tetrahedrally surrounded with bond lengths SeO = 161.7 pm and SeN = 179.9 and 181.6 pm.
    Notes: SeO(NPPh3)2 entsteht in Form farbloser Kristalle bei der Reaktion einer Suspension von SeO2 mit Me3SiNPPh3 in Acetonitril. Die Verbindung wird durch das IR-Spektrum und durch eine Kristallstrukturanalyse charakterisiert. Raumgruppe P1, Z = 2, Strukturlösung mit 5 344 beobachteten unabhängigen Reflexen, R = 0,064. Gitterkonstanten bei -40°C: a = 931,6; b = 947,6; c = 1 762 pm, α = 77,50°, β = 81,78°, γ = 79,23°. Die Verbindung bildet monomere Moleküle, in denen das Selenatom verzerrt ϕ-tetraedrisch umgeben ist mit Abständen SeO = 161,7 pm und SeN = 179,9 und 181,6 pm.
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  • 13
    ISSN: 0044-2313
    Keywords: Phosphorane Iminato-Phosphaneimine Complex of Titanium ; Synthesis ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Crystal Structures of [TiF3(NPPh3)(HNPPh3)]2 and of HNPPh3The phosphoraneiminato-phosphaneimine complex [TiF3(NPPh3)(HNPPh3)]2 was obtained by the reaction of TiF4 with Me3SiNPPh3 in boiling dichloromethane. It crystallizes from 1,2-dichloroethane as yellow crystals which include four molecules C2H4Cl2 per dimeric formula unit. Space group P21/n, Z = 2, structure solution with 7270 independent reflections, R = 0.060 for reflections with I 〉 2σ(I). Lattice dimensions at -50°C: a = 1417.5, b = 1896.9, c = 1586.6 pm, β = 101.22°. The compound forms centrosymmetric dimeric molecules via μ2-F bridges with TiF distances of 194.6 and 223.3 pm, the longer one being in trans-position to the N atom of the (NPPh3)- ligand. Its TiN bond length of 177.7 pm corresponds with a double bond. The TiN bond length of the HNPPh3 donor molecule of 213.4 pm is typical for a donor acceptor bond.According to the crystal structure determination the phosphaneimine HNPPh3 forms monomeric molecules without intermolecular hydrogen bridges with a PN bond length of 152.4 pm. Space group P21/c, Z = 4, structure solution with 3229 independent reflections, R = 0.062 for reflections with I 〉 2σ(I). Lattice dimensions at -70°C: a = 1460.4, b = 928.9, c = 1096.6 pm, β = 93.35°.
    Notes: Der Phosphaniminato-Phosphanimin-Komplex [TiF3(NPPh3)(HNPPh3)]2 wird aus TiF4 und Me3SiNPPh3 in siedendem Dichlormethan erhalten. Er kristallisiert aus 1,2-Dichlorethan als gelbe Kristalle unter Einschluß von vier Molekülen C2H4Cl2 pro dimere Formeleinheit. Raumgruppe P21/n, Z = 2, Strukturlösung mit 7270 unabhängigen Reflexen, R = 0,060 für Reflexe mit I 〉 2σ(I). Gitterkonstanten bei -50°C: a = 1417,5; b = 1896,9; c = 1586,6 pm; β = 101,22°. Die Verbindung bildet zentrosymmetrische Dimere, in denen die Titanatome über μ2-F-Brücken mit TiF-Abständen von 194,6 und 223,3 pm verknüpft sind. Die lange Ti—F-Bindung befindet sich in trans-Position zum N-Atom des (NPPh3)--Liganden, dessen TiN-Bindung mit 177,7 pm einer Doppelbindung entspricht. Der vom HNPPh3-Liganden ausgehende Ti—N-Abstand beträgt 213,4 pm.Das Phosphanimin HNPPh3 bildet nach der Kristallstrukturanalyse monomere Moleküle mit einer PN-Bindungslänge von 152,4 pm ohne intermolekulare Wasserstoffbrücken. Raumgruppe P21/c, Z = 4, Strukturlösung mit 3229 unabhängigen Reflexen, R = 0,062 für Reflexe mit I 〉 2σ(I). Gitterkonstanten bei -70°C: a = 1460,4; b = 928,9; c = 1096,6 pm; β = 93,35°.
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  • 14
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 20 (1981), S. 413-426 
    ISSN: 0570-0833
    Keywords: Multiple bonds ; Bond theory ; Nitrido ligand ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Numerous nitrido complexes of transition metals show very short metal-nitrogen bond lengths, suggesting M≡N-triple bonds. At present, compounds of this type are being intensively investigated. In particular the molybdenum complexes are considered as model substances for the study of at least an intermediate step of N2-assimilation. This article contains a review of the structure and bonding, as well as syntheses and reactions of these complexes.
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  • 15
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 616 (1992), S. 191-194 
    ISSN: 0044-2313
    Keywords: Chloro-Cycloselenazenium Tetrachlorogallate ; Synthesis ; X-ray structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Crystal Structure of [Se3N2Cl]+GaCl4-[Se3N2Cl]+GaCl4- has been prepared by the reduction of [Se2NCl2]+GaC14- with SbPh3 in CH2Cl2 solution, forming red crystals, which were characterized by an X-ray structure determination. Space group P21/n, Z = 4, 1640 observed unique reflections, R = 0.050. Lattice dimensions at - 80 °C: a = 929.4(1), b= 1078.8(1), c = 1135.7(1) pm, β = 92.026(9)°. The cations from nearly planar Se3N2 five membered rings with Se—N bond lengths from 170 to 176pm and a Se—Se bond of 242.2 pm. One of the selenium atoms is bonded to the chlorine atom.
    Notes: [Se3N2Cl]+GaCl4- entsteht in Form leuchtend roter Kristalle bei der Reduktion von [Se2NCl2]+ GaC14- mit Triphenylantimon in Dichlormethanlösung. Die Verbindung wurde durch eine röntgenographische Strukturanalyse charakterisiert. Raumgruppe P21/n, Z = 4, 1640 beobachtete unabhängige Reflexe, R = 0,050. Gitterabmessungen bei - 80 °C: a = 929,4(1), b=1078,8(1) c = 1135,7(1) pm β = 92,026(9)°. Die Kationen bilden einen nahezu ebenen Se3N2-Fünfring mit SeN-Abständen zwischen 170 und 176 pm und einer Se—Se-Bindung von 242,2 pm. Eines der Selenatome ist mit dem Chloratom verbunden.
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  • 16
    ISSN: 0044-2313
    Keywords: Crown ether complexes of Sb3+ and Bi3+ ; synthesis ; IR spectra ; 121Sb Mössbauer spectrum ; X-ray structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: [Sb(12-Crown-4)2(CH3CN)][SbCl6]3 and [Bi(12-Crown-4)2(CH3CN)][SbCl6]3, first Trications of Antimony(III) and Bismuth(III)The crown ether complexes [M(12-crown-4)2(CH3CN)][SbCl6]3 with M = Sb and Bi are formed by the reaction of antimony trichloride and bismuth trichloride, respectively, with antimony pentachloride in acetonitrile solution in the presence of 12-crown-4. They form colourless, moisture sensitive crystals, which were characterized by X-ray structure determinations and by IR spectroscopy. The complex with M = Sb was also characterized by 121Sb Mössbauer spectroscopy.Both complexes crystallize isotypically in the orthorhombic space group Pbcn with four formula units per unit cell.M = Sb: 3 483 observed unique reflections, R = 0.038. M = Bi: 2 958 observed unique reflections, R = 0.036. The compounds consist of SbCl6- ions and trications [M(12-crown-4)2(CH3CN)]3+, in which the M3+ ions are ninefold coordinated by the eight oxygen atoms of the crown ether molecules and by the nitrogen atom of the acetonitrile molecule. The lone pair of the M3+ ions has no steric effect.
    Notes: Die Kronenetherkomplexe [M(12-Krone-4)2(CH3CN)][SbCl6]3 mit M = Sb und Bi entstehen durch Reaktion von Antimontrichlorid bzw. Bismuttrichlorid mit Antimonpentachlorid in Acetonitrillösung in Gegenwart von 12-Krone-4. Sie bilden farblose, feuchtigkeitsempfindliche Kristalle, die wir durch kristallographische Strukturanalysen und durch die IR-Spektren charakterisiert haben. Von dem Komplex mit M = Sb wurde ein 121Sb-Mößbauer-Spektrum aufgenommen.Beide Komplexe kristallisieren isotyp in der orthorhombischen Raumgruppe Pbcn mit vier Formeleinheiten pro Elementarzelle. M = Sb: 3 483 beobachtete unabhängige Reflexe, R = 0,038. M = Bi: 2 958 beobachtete unabhängige Reflexe, R = 0,036. Die Verbindungen enthalten neben den SbCl6--Ionen Trikationen [M(12-Krone-4)2(CH3CN)]3+, in denen die M3+-Ionen durch die acht O-Atome der beiden Kronenethermoleküle und durch das N-Atom des Acetonitrilmoleküls neunfach koordiniert sind. Das freie Elektronenpaar an den M3+-Ionen bleibt ohne sterische Wirksamkeit.
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  • 17
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 618 (1992), S. 93-97 
    ISSN: 0044-2313
    Keywords: Crown ether complex of antimony ; synthesis ; 121Sb-Mössbauer spectrum ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis, Crystal Structure, and 12Sb-Mössbauer Spectrum of [SbCl2(18-Crown-6)]+SbCl6-The title compound, which has been prepared by the reaction of antimony trichloride and antimony pentachloride in the presence of 18-crown-6 in acetonitrile solution, is characterized by its 121Sb-Mössbauer spectrum and by an X-ray structure determination. Space group P21, Z = 2, 2439 observed unique reflections, R = 0.045, wR = 0.043. Lattice dimensions at -80°C: a = 780.6(7), b = 1297.5(9), c = 1 278.5(10) pm, β = 100.56(7)°. The structure of [SbCl2(18-crown-6)]+SbCl6- contains cations in which the antimony atom in the first coordination sphere is surrounded in a φ-trigonal-bipyramidal fashion by two oxygen atoms of the crown ether in axial position as well as in the equatorial position by the two chlorine atoms and the lone electron pair.
    Notes: Die Titelverbindung entsteht aus Antimontrichlorid und Antimonpentachlorid in Gegenwart von 18-Krone-6 in Acetonitrillösung. Sie wird durch ihr 121Sb-Mößbauer-Spektrum und durch eine röntgenographische Strukturanalyse charakterisiert. Raumgruppe P21, Z = 2, 2439 beobachtete unabhängige Reflexe, R = 4,50%, wR = 4,25%. Die Gitterkonstanten betragen bei -80°C: a = 780,6(7); b = 1 297,5(9); c = 1 278,5(10) pm, β = 100,56(7)°. [SbCl2(18-Krone-6)]+SbCl6- enthält Kationen, in denen das Antimonatom in erster Koordinationssphäre φ-trigonal-bipyramidal von zwei O-Atomen des Kronenethers in Axialposition und von den beiden Cl-Atomen sowie dem freien Elektronenpaar äquatorial umgeben ist.
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  • 18
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 329-333 
    ISSN: 0044-2313
    Keywords: Phosphoraneiminato Complexes of Iodine ; Synthesis ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Phosphoraneiminato Complexes of Iodine. Syntheses and Crystal Structures of Ph3PNIO2 and Ph3PNSiMe3 · I2Ph3PNIO2 has been prepared as yellow crystals by the reaction of Ph3PNSiMe3 with I2O5 in boiling acetonitrile, whereas the molecular complex Ph3PNSiMe3 · I2 is formed as brown crystals by the reaction of Ph3PNSiMe3 with iodine in acetonitrile solution. Both complexes were characterized by crystal structure determinations.Ph3PNIO2: Space group P21/n, Z = 4, 2 858 observed unique reflections, R = 0.039. Lattice dimensions at 19°C: a = 972.8(2), b = 1 743.4(3), c = 1 073.7(2) pm, β = 115.46(3)°. The compound forms monomeric molecules with pyramidal geometry at the iodine atom. The bond angle PNI (126.9°) is unusually small; the PN bond length of 159.2 pm corresponds with a double bond.Ph3PNSiMe3 · I2: Space group P1, Z = 2, 3 560 observed unique reflections, R = 0.033. Lattice dimensions at 19°C: a = 941.2(2), b = 1 041.7(2), c = 1 287.4(3) pm, α = 78.34(1)°, β = 72.00(2)°, γ = 86.08(2)°. The compound forms monomeric molecules, in which the I2 molecule and the nitrogen atom of the phosphoraneimine molecule realize a linear N—I—I axis with a bond length N—I of 243.2 pm.
    Notes: Ph3PNIO2 entsteht als gelbe Kristalle durch Reaktion von Ph3PNSiMe3 und I2O5 in siedendem Acetonitril, während der Molekülkomplex Ph3PNSiMe3 · I2 aus Ph3PNSiMe3 und Iod bei Raumtemperatur in Acetonitril in Form brauner Kristallnadeln gebildet wird. Beide Komplexe haben wir durch röntgenographische Strukturanalysen charakterisiert.Ph3PNIO2: Raumgruppe P21/n, Z = 4, 2858 beobachtete unabhängige Reflexe, R = 0,039. Gitterabmessungen bei 19°C: a = 972,8(2); b = 1 743,4(3); c = 1 073,7(2) pm, β = 115,46(3)°. Die Verbindung bildet monomere Moleküle mit pyramidaler Geometrie am Iodatom. Der Bindungswinkel PNI ist mit 126,9° ungewöhnlich klein; der Abstand PN entspricht mit 159,2 pm einer Doppelbindung.Ph3PNSiMe3 · I2: Raumgruppe P1, Z = 2, 3 560 beobachtete unabhängige Reflexe, R = 0,033. Gitterabmessungen bei 19°C: a = 941,2(2); b = 1 041,7(2); c = 1 287,4(3) pm; α = 78,34(1)°; β = 72,00(2)°; γ = 86,08(2)°. Die Verbindung bildet monomere Moleküle, in denen das I2-Molekül mit dem N-Atom des Phosphanimins eine lineare N—I—I-Achse mit einem N—I-Abstand von 243,2 pm realisiert.
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  • 19
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 619 (1993), S. 1127-1131 
    ISSN: 0044-2313
    Keywords: Polytellurido Complex of Cadmium ; Synthesis ; X-ray Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Crystal Structure of [Na(15-Crown-5)]4[Cd4Te12] · 8 DMFThe title compound has been prepared by reaction of Na2Te3 with cadmium acetate in DMF solution in the presence of 15-crown-5, forming black crystal needles, which were characterized by an X-ray structure determination. Space group P21/n, Z = 2, 5 716 observed unique reflections, R = 0.038. Lattice dimensions at -50°C: a = 1 622.9, b = 2 038.2, c = 1 739.8 pm, β = 92.26°. The compound has an ionic structure. The cations [Na(15-crown-5)(DMF)]+ and [Na(15-crown-5) · (DMF)2]+ together with two further DMF molecules form tetrameric units. In the centrosymmetric anions [Cd4Te12]4- the cadmium atoms are linked by μ2-Te2--, μ4-Te22--, and μ2-Te32--units.
    Notes: Die Titelverbindung entsteht in Form schwarzer Kristallnadeln bei der Einwirkung von Na2Te3 auf Cadmiumacetat in Dimethylformamidlösung in Gegenwart von 15-Krone-5. Sie wurde durch eine röntgenographische Strukturanalyse charakterisiert. Raumgruppe P21/n, Z = 2, Strukturbestimmung mit 5 716 beobachteten unabhängigen Reflexen, R = 3,8%. Gitterabmessungen bei -50°C: a = 1 622,9; b = 2 038,2; c = 1 739,8 pm; β = 92,26°. Die Verbindung hat ionischen Aufbau. Es liegen Kationen [Na(15-Krone-5) · (DMF)]+ und [Na(15-Krone-5)(DMF)2]+ vor, die zusammen mit je einem weiteren DMF-Molekül zu tetrameren Einheiten gepackt sind. In den zentrosymmetrischen [Cd4Te12]4--Anionen werden die Cadmiumatome durch μ2-Te2--, μ4-Te22-- und μ2-Te32--Einheiten verknüpft.
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  • 20
    ISSN: 0044-2313
    Keywords: Organometallic Nitrido Phosphoraneiminato Complex of Rhenium(VI) ; Synthesis ; X-ray structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Crystal Structure of [ReNCl(NPPh2C6H4)]2 · [Ph3PNH2]Cl · CH3CN, a Rhenium Organic Nitrido Phosphoraneiminato ComplexThe title compound is synthesized by the reaction of ReNCl4 with Me3SiNPPh3 in boiling acetonitrile, forming colourless crystals, which are characterized by an X-ray structure determination. Space group P1, Z = 2, 4 037 observed unique reflections, R = 0.043. Lattice dimensions at 19°C: a = 1 005.5; b = 1 695.2; c = 1 744.7 pm, α = 105.86°; β = 101.49°; γ = 104.45°. The structure consists of dimeric molecules [ReNCl(NPPh2C6H4)]2, triphenylphosphorane ammoniumchloride and included acetonitrile molecules. In the nitrido phosphoraneiminato complex the rhenium atoms are μ2-bridged via the N-Atoms of the phosphoraneiminato ligands. Because of this bridging and a Re—Re bond, one terminal nitrido ligand, one terminal chloro ligand, and a Re—C bond of an -C-atom of one phenylene group of Re-atoms attain co-ordination number six.
    Notes: Die Titelverbindung entsteht bei der Reaktion von ReNCl4 mit Me3SiNPPh3 in siedendem Acetonitril in Form farbloser Kristalle, die durch eine röntgenographische Strukturanalyse charakterisiert wurden. Raumgruppe P1, Z = 2, 4 037 beobachtete unabhängige Reflexe, R = 0,043. Gitterabmessungen bei 19°C: a = 1 005,5; b = 1 695,2; c = 1 744,7 pm, α = 105,86°; β = 101,49°; γ = 104,45°. Die Struktur besteht aus dimeren Molekülen [ReNCl(NPPh2C6H4)]2, Triphenylphosphanammoniumchlorid und eingelagerten Acetonitrilmolekülen. In dem Nitrido-Phosphaniminatokomplex sind die Rheniumatome über die N-Atome der Phosphaniminatoliganden μ2-verbrückt. Die Re-Atome erreichen dadurch sowie durch eine Re—Re-Bindung, durch je einen terminalen Nitrido- und Chloroliganden und durch eine Re—C-Bindung eines -C-Atoms einer Phenylengruppe die Koordinationszahl sechs.
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