ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    ISSN: 1520-6041
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the Chemistry of Asymmetrically Substituted Alkyne Complexes of Tungsten. Crystal Structure of [Na-15-Crown-5][WF5(Ph—C≡C—C≡C—SiMe3)] · CH3CN[WCl4(Ph—C≡C—C≡C—SiMe3)]2, which was described earlier, reacts with bromine at the free alkyne function under addition and formation of [WCl4(Ph—C≡C—C(Br)=C(Br)—SiMe3)]2. With sodium fluoride in acetonitrile in the presence of 15-crown-5, both alkyne complexes can be transformed into the fluoroderivatives [Na-15-crown-5][WF5(Ph—C≡C—C≡C—SiMe3)], and Na-15-crown-5[WF5(Ph—C≡C—C≡C—C(Br)=C(Br)—SiMe3)], respectively. They form orange-yellow, moisture sensitive diamagnetic crystal powders, which were characterized by their IR- and 13C-nmr spectra. [Na-15-crown-5][WF5(Ph—C≡C—C≡C—SiMe3)] crystallizes under inclusion of acetonitrile, which is easily given off in vacuo. Its crystal structure was determined by X-ray methods. Space group Pi, Z = 4, 8809 independent observed reflexions, R = 0.027. Lattice dimensions at -70°C: a = 1336.8(7), b = 1352.9(7), c = 1910.5(10) pm, α = 92.08(3)°, β = 106.83(3)°, γ = 105.71(3)°. The unit cell contains two symmetry-independent ion pairs, in which, besides the co-ordination by the five 0-atoms of the crown ether, the sodium ion is co-ordinated by two F-atoms of the [WF5(ph—C≡C—C≡C—SiMe3)]- ions with an average Na-F-distance of 230 pm. In the anion the tungsten atom is sevenfold surrounded by five F-atoms and by the two C-atoms of the side-on coordinate dialkyne ligand, which are adjoining the phenylring, with an average W—C-bond length of 202 pm.
    Notes: Das früher beschriebene [WCl4(Ph—C≡C—C≡C—SiMe3)]2 reagiert mit Brom an der freien Alkinfunktion unter Addition und Bildung von [WCl4(Ph—C≡C—C(Br)=C(Br)—SiMe3)]2. Beide Alkinkomplexe lassen sich mit Natriumfluorid in Acetonitril bei Anwesenheit von 15-Krone-5 in die Fluoroderivate [Na-15-Krone-5][WF5(Ph—C≡C—C≡C—SiMe3)] bzw. [Na-15-Krone-5][WF5(Ph—C≡C—C(Br)≡C(Br)—SiMe3)] überführen. Sie bilden orangegelbe, feuchtigkeitsempfindliche, diamagnetische Kristallpulver, die IR-spektroskopisch und durch ihre 13C-Kernresonanzspektren charakterisiert werden.[Na-15-Krone-5][WF5(Ph—C≡C—C≡C—SiMe3)] kristallisiert unter Einschluß von Acetonitril, das im Vakuum leicht abgegeben wird. Seine Kristallstrukturanalyse wurde mittels Röntgenmethoden gelöst. Raumgruppe P1, Z = 4, 8809 unabhängige beobachtete Reflexe, R = 2,7%. Die Gitterabmessungen betragen bei -70°C: a = 1326,8(7); b = 1352,9(7); c = 1910,5(10) pm; α = 92,08(3)°; β = 106,83(3)°; γ = 105,71(3)°. Die Elementarzelle enthält zwei symmetrieunabhängige Ionenpaare, in denen das Natriumion neben der Koordination durch die fünf O-Atome des Kronenethers noch durch zwei F-Atome des [WF5(Ph—C≡C—C≡C—SiMe3)]--Ions mit Na—F-Abständen von im Mittel 230 pm koordiniert ist. In dem Anion ist das Wolframatom siebenfach durch fünf F-Atome und durch die beiden dem Phenylring benachbarten C-Atome des seitlich koordinierten Dialkinliganden mit W—C-Abständen von im Mittel 202 pm umgeben.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    ISSN: 0044-2313
    Keywords: Molybdenum ; Tungsten ; Halogenonitrosyl Complexes ; Syntheses ; IR Spectra ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Halogeno-Nitrosyl Complexes of Molybdenum and Tungsten. Crystal Structures of [Na2(15-Crown-5)2(CH3CN)][MoCl4(NO)2] and [Na(15-Crown-5)]2[MoF4Cl(NO)]MoCl2(NO)2 and WCl2(NO)2, respectively, react with excess sodium fluoride in acetonitrile at room temperature and in the presence of 15-crown-5 to give crystalline mixtures, which consist of the title compounds, respectively of [Na(15-crown-5)]2[WCl4(NO)2] and [Na(15-crown-5)]2[WF4Cl(NO)], and which can be separated by selection. The complexes are characterized by their i.r. spectra, the molybdenum compounds additionally by crystal structure determinations.[Na2(15-crown-5)2(CH3CN)][MoCl4(NO)2]: Space group P21, Z = 2, 5415 independent unique reflexions, R = 0.039. Lattice dimensions at -10°C: a = 984.3, b = 1231.1, c = 1483.0 pm, β = 105.67°. The compound consists of cations [Ne(l5-crown-5)(CH3CN)]+, in which the sodium ion is surrounded by the five O-atoms of the crown ether and by the N-atom of the acetonitrile molecule, as well as of anions, which form an ion pair {Na(15-crown-5)[MoCl4(NO)2]}-. In the in pairs the sodium ion is coordinated by the five oxygen atoms of the crown ether and by two chlorine atoms of the [MoCI4(NO)2]2- unit. The nitrosyl ligands take the cis-position a t the molybdenum atom which is in a distorted octahedrally fashion.[Na(15-crown-5)]2[MoF4Cl(NO)]. Space group C2/c, Z = 4, 1933 independent unique reflexions, R = 0.078. Lattice dimensions at -7O°C: D : 1.585.8, b = 1171.5, c = 1771.5 pm, β = 114.91°. The compound forms an ion triple, in which the sodium ions are linked to five oxygen atoms each of the crown ether molecules, and to two F-atoms of the [MoF4Cl(NO)]2- unit. The F-atom which is arranged in trans-position to the nitrosyl ligand coordinates with both sodium ions; thus an unusual T-shaped arrangement results for this F-atom. The sole terminal F-Atom and the Cl-atom are disordered in two positions.
    Notes: MoCl2(NO)2 bzw. WCl2(NO)2 reagieren mit überschüssigem Natriumfluorid in Acetonitril bei R.T. und Anwesenheit von 15-Krone-5 zu Kristallgemischen, die aus den Titelverbindungen bzw. aus [Na(15-Krone-5)]2[WCl4(NO)2] und [Na(15-Krone-5)]2[WF4Cl(NO)] bestehen, und die sich durch Auslesen trennen lassen. Die Komplexe werden durch ihre IR-Spektren, die Molybdänverbindungen zusätzlich durch Kristallstrukturanalysen charakterisiert.[Na2(15-Krone-5)2(CH3CN)][MoCl4(NO)2]: Raumgruppe P21, Z = 2, 5415 unabhängige beobachtete Reflexe, R = 3,9%. Gitterabmessungen bei -10°C: a = 984,3; b = 1 251,1; c = 1 483,0 pm, β = 105,67°. Die Verbindung besteht aus Kationen [Na(15-Krone-5)(CH3CN)]+, in denen das Natriumion von den fünf O-Atomen des Kronenethers und von dem N-Atom des Acetonitrilmoleküls umgeben ist, sowie aus Anionen, die ein Ionenpaar {Na(15-Krone-5)[MoCl4(NO)2]}- bilden. In ihnen ist das Natriumion durch die fünf O-Atome des Kronenethers und durch zwei Chloratome der [MoCl4(NO)2]2--Einheit koordiniert. Die Nitrosylliganden nehmen die cis-Positionen am verzerrt oktaedrisch koordinierten Molybdänatom ein.[Na(15-Krone-5)]2[MoF4Cl(NO)]: Raumgruppe C2/c, Z = 4, 1933 unabhängige beobachtete Reflexe, R = 7,8%. Gitterabmessungen bei -70°C: a = 1 585,8; b = 1 171,2; c = 1 771,5 pm; β = 114,91°. Die Verbindung bildet ein Ionentripel, in dem die Natriumionen mit je fünf O-Atomen der Kronenethermoleküle und mit zwei F-Atomen der [MoF4Cl(NO)]2--Einheit verbunden sind. Das in trans-Position zum Nitrosylliganden angeordnete F-Atom koordiniert mit beiden Natriumionen, so daß für dieses F-Atom eine ungewöhnliche T-förmige Anordnung resultiert. Das einzige terminal gebundene F-Atom und das Cl-Atom sind in zwei Positionen fehlgeordnet.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 596 (1991), S. 47-53 
    ISSN: 0044-2313
    Keywords: Mercury-N,N′-bis(trimethylsilyl)benzamidinate ; synthesis ; i.r. 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 Mercury(II)-N,N′-bis(trimethylsilyl)benzamidinate, Hg[Ph—C(NSiMe3)2]2The title compound has been synthesized by the reaction of N,N,N′-tris(trimethylsilyl)benzamidine with mercury(I)-acetate in boiling acetonitrile because of redox disproportionation, forming white crystal needles, which were characterized by IR spectroscopy as well as by an X-ray structure determination. Space group P1; Z = 2; 6846 observed unique reflections; R = 0.048. Lattice dimensions at -90 ° C: a = 1091.9, b = 1212.8, c = 1433.5 pm; α = 106.89°, β = 109.25°, γ = 90.62°. The compound forms a nearly centro-symmetric molecule structure with sp-hybridized Hg atom (r Hg—N = 207 pm).
    Notes: Die Titelverbindung entsteht bei der Reaktion von N,N,N′-tris(trimethylsilyl)-benzamidin mit Quecksilber(I)-acetat in siedendem Acetonitril durch Redox-Disproportionierung in Form weißer Kristallnadeln, die durch das IR-Spektrum und durch eine röntgenographische Kristallstrukturanalyse charakterisiert werden. Raumgruppe P1, Z = 2, 6 846 beobachtete unabhängige Reflexe; R = 4, 8%. Gitterabmessungen bei -90 °C: a = 1091,9; b = 1212,8; c = 1433,5 pm; α = 106,89α β = 109,25°; γ = 90,62°. Die Verbindung bildet eine nahezu zentrosymmetrische Molekülstruktur mit sp-hybridisiertem Hg-Atom (r Hg—N = 207 pm).
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 596 (1991), S. 133-138 
    ISSN: 0044-2313
    Keywords: Benzamidinium hexachlorostannate ; synthesis ; crystal structure ; i.r. spectrum ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Benzamidinium Hexachlorostannate: Synthesis and Crystal Structure[Ph—C(NH2)2SnCl6] has been prepared by the reaction of hydrogen chloride with the amidinato complex [Ph—C(NSiMe3)2SnCl3] in CH2Cl2 solution, forming colourless crystals. which were characterized by IR spectroscopy as well as by an X-ray structure determination. Space group P21/c, Z = 4, 3070 observed unique reflexions, R = 0.029. Lattice dimensions at -50°C: a = 892.5, b = 1076.7, c = 1175.6 pm, β = 109.3°. The compound consists of benzamidinium ions C6H5—C(NH2)2+ and anions SnCl62-, which are connected by a network of N—H…Cl hydrogen bridges.
    Notes: [Ph—C(NH2)2]2SnCl6 entsteht in Form farbloser Einkristalle durch Einwirkung von Chlorwasserstoff auf eine Lösung des Amidinatokomplexes [Ph—C(NSiMe3)2SnCl3] in Dichlormethan. Die Verbindung wird durch das IR-Spektrum und durch eine röntgenographische Strukturanalyse charakterisiert. Raumgruppe P21/c, Z = 4, 3070 beobachtete unabhängige Reflexe, R = 2,9%. Gitterabmessungen bei -50°C: a = 892,5; b = 1076,7; c = 1175,6 pm; β = 109,3°. Die Verbindung besteht aus Benzamidinium-Kationen C6H5—C(NH2)2+ und SnCl62--Ionen, in denen ein Netz von N—H…Cl-Wasserstoffbrücken besteht.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    ISSN: 0044-2313
    Keywords: Phosphorane Iminato Complexes of Antimony ; 121Sb Mössbauer 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 Antimony. The Crystal Structures of [Sb2Cl5(NPMe3)2][SbCl6] · CH3CN and [SbCl(NPPh3)]2[SbCl6]2 · 6 CH3CNThe title compounds are formed by reaction of antimony pentachloride in acetonitrile solution with the phosphorane iminato complexes SbCl2(NPMe3) and SbCl2(NPPh3), respectively, which themselves are synthesized by reaction of antimony trichloride with Me3SiNPR3 (R = Me, Ph). The complexionic compounds are characterized by 121Sb Mössbauer spectroscopy and by crystal structure determinations.[Sb2Cl5(NPMe3)2][SbCl6] · CH3CN: Space group P41, Z = 4, 3 698 observed unique reflections, R = 0.022. Lattice dimensions at -60°C: a = b = 1 056.0(1), c = 2 709.6(2) pm. The structure consists of SbCl6- ions and cations [Sb2Cl5(NPMe3)2(CH3CN)]+, in which one SbIII atom and one SbV atom are bridged by the N atoms of the phosphorane iminato ligands.[SbCl(NPPh3)]2[SbCl6]2 · 6 CH3CN: Space group P1, Z = 2, 5 958 observed unique reflections, R = 0.033. Lattice dimensions at -60°C: a = 989.4(11), b = 1 273(1), c = 1 396(1) pm, α = 78.33(7), β = 77.27(8)°, γ = 86.62(8)°. The structure consists of SbCl6- ions and centrosymmetric cations [SbCl(NPPh3)(CH3CN)2]22+, in which the antimony atoms are bridged by the N atoms of the phosphorane iminato ligands.
    Notes: Die Titelverbindungen entstehen durch Reaktion von Antimonpentachlorid in Acetonitrillösungen mit den Phosphaniminatokomplexen SbCl2(NPMe3) bzw. SbCl2(NPPh3), die ihrerseits aus Antimontrichlorid und Me3SiNPR3 (R = Me, Ph) hergestellt werden. Die ionisch aufgebauten Komplexe werden durch ihre 121Sb-Mößbauer-Spektren und durch Kristallstrukturanalysen charakterisiert.[Sb2Cl5(NPMe3)2][SbCl6] · CH3CN: Raumgruppe P41, Z = 4, 3 698 beobachtete unabhängige Reflexe, R = 0,022. Gitterabmessungen bei -60°C: a = b = 1 056,0(1); c = 2 709,6(2) pm. Die Struktur wird aus SbCl6--Ionen und Kationen [Sb2Cl5(NPMe3)2(CH3CN)]+ gebildet, in denen ein SbIII- und ein SbV-Atom über die N-Atome der Phosphaniminatoliganden verknüpft sind.[SbCl(NPPh3)]2[SbCl6]2 · 6 CH3CN: Raumgruppe P1, Z = 2, 5 958 beobachtete unabhängige Reflexe, R = 0,033. Gitterkonstanten bei -60°C: a = 989,4(11); b = 1 273(1); c = 1 396(1) pm; α = 78,33(7)°; β = 77,27(8)°; γ = 86,62(8)°. Die Verbindung besteht aus SbCl6--Ionen und zentrosymmetrischen Kationen [SbCl(NPPh3)(CH3CN)2]22+, in denen die beiden Antimonatome über die N-Atome der Phosphaniminatoliganden verknüpft sind.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    ISSN: 0009-2940
    Keywords: Co-operative effect ; Dinuclear alkyne complexes ; Alkyne oligomerisation ; Vinylallene complex ; Fluxional behavior ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Co-operative Effect in π-Ligand-Bridged Dinuclear Complexes, IX. - Influence of Cp′ - X - Cp′-Bridged Dinuclear CpM(CO)3 Complexes (M = Mo. W) on Reactions with AlkynesThe Cp′ — X — Cp′-bridged dinuclear complexes Me2Si[Cp′M(CO)3)2 (4, Cp′ = C5H4, M = Mo, W) react thermally as well as photochemically with alkynes RCCR′ to form the monoalkyne compounds {Me2Si(Cp′M(CO)2]2-μ-(η2:2-RCCR′)} (6, 7, 9) which possess M2C2 dimetallatetrahedrane units (X-ray structure analysis of 7a). A molecular fluxionality is shown for R = R′ (7) by NMR spectroscopy. The activation barrier for this process depends on the steric bulkiness of the alkyne substituents R. For this kind of dynamic behaviour a new mechanism is proposed. In the reaction of 4 (M = Mo) with the electron-rich alkyne bis(diethylamino)ethyne (R = R′ = NEt2) a novel bis(carbene) complex 8 is formed, which contains a 1,2-dimetallacyclobutadiene core in the central M2C2 unit. In some cases products are isolated and characterized, in which three (R = Ph, 10) and two (R = nPr, 11) alkyne units are co-ordinated under C - C linkage. Based on spectroscopic results a structural proposal is made for 10. By X-ray structure analysis of 11 it is shown that besides a dimerisation of the two alkynes an isomerisation occurs with formation of a complexed vinylallene.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    ISSN: 0044-2313
    Keywords: Reaction of dimeric di(tert-butyl)aluminium halides with tetramethylethylendiamine ; symmetrical and unsymmetrical cleavage ; aluminium cations ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: (N,N,N′,N′ -tetramethylethylendiamine) di(tert-butyl)aluminium Cations  -  Molecular Structure of [(Me3C)2Al(TMEDA)]⊕[(Me3C)2AlBr2]⊖Dimeric di(tert-butyl)aluminium halides (Me3C)2AlX (X = Cl, Br) react with N,N,N′,N′ -tetramethylethylendiamine (TMEDA) to give three compounds: the salt-like [(Me3C)2Al(TMEDA)]⊕[(Me3C)2AlX2]⊖ 1, characterized by crystal structure determination, and [(Me3C)2Al(TMEDA)]⊕X⊖ 3 both with chelating amine, and the more covalent, pentane soluble (Me3C)2AlX(TMEDA) 2 with TMEDA bound by only one nitrogen atom. The reaction resembles the symmetrical and unsymmetrical cleavage of diborane(6). 3 (X = Cl) is also formed by treatment of 1 with boiling n-hexane in the presence of TMEDA over a period of 24 hours, while for X = Br the more covalent 2 is the main product under similar conditions. In solution 2 decomposes slowly yielding different products in dependency of the solvent: in benzene 3 and in n-pentane 1 are formed.
    Notes: Die dimeren Di(tert-butyl)halogenalane (Me3C)2AlX (X = Cl, Br) reagieren mit N,N,N′,N′-Tetramethylethylendiamin (TMEDA) in heißem Benzol zu insgesamt drei Verbindungen: den salzartigen Derivaten [(Me3C)2Al (TMEDA)]⊕[(Me3C)2AlX2]⊖ 1, die, wie die Kristallstrukturbestimmung am entsprechenden Bromderivat zeigt, im Festkörper isolierte Anionen und Kationen aufweisen, den ebenfalls salzartigen [(Me3C)2Al(TMEDA)]⊕X⊖ 3 und den eher kovalenten, in n-Pentan löslichen (Me3C)2AlX(TMEDA) 2, in denen das Amin nicht mehr chelatartig an das Aluminiumatom, sondern nur noch über ein Stickstoffatom gebunden ist. Die Reaktion gleicht damit der symmetrischen und unsymmetrischen Spaltung des Diborans(6). 2 ist in Lösung unbeständig und wandelt sich je nach Lösungsmittel zu unterschiedlichen Produkten um: in Benzol bildet sich 3, aus n-Pentan scheidet sich 1 ab. Mehrstündiges Behandeln von 1 mit siedendem n-Hexan in Gegenwart von wenig TMEDA ergibt für X = Cl das Monohalogenidderivat 3, für X = Br aber die kovalente Verbindung 2.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 615 (1992), S. 35-38 
    ISSN: 0044-2313
    Keywords: Zirconocene-phosphido complexes ; (tricyclohexyltriphosphane-1,3-diyl)zirconocene(IV) ; preparation ; 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 meso-(1,2,3-Tricyclohexyltriphosphane-1,3-diyl)zirconocene(IV), Cp2(Cp = η5-C5H5, Cy = C6H11)Cp2ZrCl2 reacts with Li(THF)2PHCy (Cy = C6H11) to yield the metallacyclic compound Cp2 1., The 31P{1H} NMR spectrum of 1, shows a coupling pattern for an A2X system, indicating the presence of only the meso-forms in solution, which are also present in the solid state. 1, crystallizes in the monoclinic space group P21/n (No. 14) with a = 12.984(8), b = 9.241(7), c = 23.05(1) Å, β = 93.48(4)°, V = 2760.1 Å3 and four formula units in the unit cell (2718 independent observed reflections, R = 7.3%). The central ZrP3 ring in 1, is almost planar. The Zr—P bond lengths of 2.618(4) and 2.628(4) Å are nearly identical.
    Notes: Cp2ZrCl2 setzt sich mit Li(THF)2PHCy (Cy = C6H11) zu der metallacyclischen Verbindung Cp2 1, um. Im 31P{1H}-NMR-Spektrum von 1, tritt das für ein A2X-System zu erwartende Aufspaltungsmuster auf, was auf das Vorliegen der meso-Formen in Lösung hinweist. Auch im Festkörper liegen nur die meso-Formen vor. 1, kristallisiert monoklin in der Raumgruppe P21/n (Nr. 14) mit a = 12,984(8), b = 9,241(7), c = 23,05(1) Å, β = 93,48(4)°, V = 2760,1 Å3 und vier Formeleinheiten pro Elementarzelle (2718 unabhängige beobachtete Reflexe, R = 7,3%). Der zentrale ZrP3-Ring in 1, ist angenähert planar. Die Zr—P-Bindungslängen sind mit 2,618(4) und 2,628(4) Å fast gleich.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...