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  • 1
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 18 (1979), S. 1189-1192 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Environmental science & technology 8 (1974), S. 673-674 
    ISSN: 1520-5851
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 63 (1959), S. 1335-1336 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 66 (1962), S. 1639-1645 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Transition metal chemistry 12 (1987), S. 41-42 
    ISSN: 1572-901X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Reaction of MoCl5 or WCl6 with 1-methyl-1-phenylhydrazine or 1, 1-diphenylhydrazine hydrochloride results in the formation of MVI species [MCl4(NNRR′)]. These react with tertiary phosphines PR3 to form MV species [MCl3(NNRR′)(PR3) n ] (n=1 or 2). [MoCl3(NNMePh)(PMe3)2] can be reduced in the presence of PMe3 to the MoIV speciescis-mer-[MoCl2(NNMePh)(PMe3)3].
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  • 7
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions of Coordinated Ligands, VIII. Synthesis, Reactivity, and Structure of Molybdenum- and Nickel Carbonyl Complexes of 1,3-Bis(phenylphosphino)propane1,3-Bis(phenylphosphino)propane reacts with Ni(CO)4, C7H8Mo(CO)4, and Mo(CO)6 to produce complexes of the type (CO)nM(PhPH—C3H6—PPhH) (n = 4, M=Mo; n = 2, M=Ni) and oligomers thereof. These compounds were also obtained by the reaction of phosphido complexes (CO)nM(PhPHM′)2 (n = 4, M=Mo, M′=Li; n = 2, M=Ni, M′=Li, Na) with 1,3-dibromopropane. The complexes (CO)nM(PhPH—C3H6—PPhH) may be deprotonated with methyllithium. The reactions of the phosphido complexes thus obtained are discussed. From the meso-form of (CO)2Ni(PhPH—C3H6—PPhH), which crystallizes in the space group Cmc21, an x-ray structure analysis has been performed.
    Notes: 1,3-Bis(phenylphosphino)propan reagiert mit Ni(CO)4, C7H8Mo(CO)4 und Mo(CO)6 unter Bildung von Komplexen des Typs (CO)nM(PhPH—C3H6—PPhH) (n = 4, M=Mo; n = 2, M = Ni) und deren Oligomeren. Diese Verbindungen werden auch bei Umsetzung von Phosphidokomplexen (CO)nM(PhPHM′)2 (n = 4, M=Mo, M′=Li; n = 2, M=Ni, M′=Li, Na) mit 1,3-Dibrompropan erhalten. Die Komplexe (CO)nM(PhPH—C3H6—PPhH) lassen sich mit Methyllithium deprotonieren. Über Reaktionen der dabei gebildeten Phosphidokomplexe wird berichtet.  -  Von der Mesoform von (CO)2Ni(PhPH—C3H6—PPhH) (1), das in der Raumgruppe Cmc21 kristallisiert, wurde eine Röntgenstrukturanalyse durchgeführt.
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  • 8
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Linear Oligophosphaalkanes, III: Syntheses and stereochemistry of Palladium (II) Complexes of chiral Tetraphosphaalkanes H2-nRnP—[CH2]3 — PR′ — [CH2]m — PR′ — [CH2]3 — PRnH2-n(R, R′, = Me, tBu; m = 2, 3; n = 1, 2)The reaction of the chiral tetradentate ligands L of the title with K2PdCl4 affords the complexes Pd(L)Cl2 (2a - e), which for n = 1 may exist as ten (square pyramidal) or six (square planar coordination geometry) isomers. By suitable choice of the substituents R and size of the chelate rings (m + 3) the number of isomers may be reduced to two or three. The detailed investigation of the complexes 2a - e by means of 31P{1H} NMR spectroscopy offers the possibility to identify their stereochemistry. - Monodeprotonation of 2a (R = Me; m = 3; n = 1) and 2d (R = Me; m = 2; n = 1) by KOH or the OH- Form of anion exchange resin yields the phosphido complexes 3a and d (not isolated). Both compounds are oxidized by air with formation of the phosphanoxidophosphane complexes 4a and d, which exist as two or three configurational isomers with units Pd—P(O)Me—.
    Notes: Die Umsetzung der im Titel genannten vierzähnigen Liganden L mit k2PdCl4 liefert die Komplexe Pd(L)Cl2(2a-e)w, die für n = 1 in Form von zehn (quadratisch pyramidale Ligandenanordnung) bzw. sechs (planare Koordinationsgeometrie) Konfigurationsisomeren vorliegen können. Durch geeignete Wahl der substituenten R und der Chelatringgröße (m + 3) läßt sich die Zahl der Isomeren auf zwei bzw. drei reduzieren. Die detaillierte 31P{1H}-NMR-spektroskopische Untersuchung der Komplexe 2a - e erlaubt die Identifizierung der Stereochemie der Isomeren. - Die durch Monodeprotonierung von 2a (R = Me; m = 3; n = 1) und 2d(R = Me; m = 2; n = 1) mit KOH oder der OH- -Form eines Anionentauschers gebildeten Phosphidokomplexe 3a and d werden durch Luftsauerstoff zu den phosphanoxidophosphan-komplexen 4a und d oxidiert, bei denen zwei bzw. drei Konfigurationsisomere mit P-gebundenen Phosphanoxido-Einheiten Pd—P(O)Me— vorliegen.
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  • 9
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions of Coordinated Ligands, VII. Syntheses and Reactions of Transition Metal Carbonyl Complexes of PH-Functional Di-, Tri-, and TetraphosphanesThe synthesis of complexes of PH-functional diphosphanes (CO)mM(PhPH—PR2)n (M=Mo, m = 4, 5, n = 2, 1, R=Ph, tBu; M=Fe, m = 4, n = 1, R=Ph) (7 - 10) and of 1,2,3-triphenyltriphosphane (CO)mM—PPhH—PPh—PPhH—M(CO)m (M=Mo, Fe, m = 5, 4) (13, 14) is reported. The availability of PH-functional groups as well as uncoordinated P-atoms in these compounds permits the formation of new P—P-bonds and of heterometallic complexes such as (CO)5Mo(PhPH—PPh2)Ni(CO)3 (16) or (CO)5Mo—PPhH—PPh[Ni(CO)3]PPhH—Mo-(CO)5 (17). The 1H- and 31P NMR spectra of the complexes 4 - 10 and 13 - 20 are discussed. For complexes of 1,1,2,3,3-pentaphenyltriphosphane, (Ph2P)2PPh—M(CO)m (M=Mo, Fe, m = 5, 4) the migration of the (CO)mM group from the medial to the terminal position of the P3-skeleton could be observed by means of 31P{1H} NMR spectroscopy.
    Notes: Die Synthese von Komplexen PH-funktioneller Diphosphane (CO)mM(PhPH—PR2)n (M=Mo, m = 4, 5, n = 2, 1, R=Ph, tBu; M=Fe, m = 4, n = 1, R=Ph) (7 - 10) und des 1,2,3-Triphenyltriphosphans (CO)mM—PPhH—PPh—PPhH—M(CO)m (M=Mo, Fe, m = 5, 4) (13, 14) wird beschrieben. Die Verfügbarkeit von PH-Funktionen sowie von nicht-koordinativ gebundenen P-Atomen in diesen Verbindungen erlaubt die Knüpfung weiterer P—P-Bindungen und die Bildung heterometallischer Komplexe, z. B. (CO)5Mo(PhPH—PPh2)Ni(CO)3 (16) oder (CO)5Mo—PPhH—PPh[Ni(CO)3]PPhH—Mo(CO)5 (17). Die 1H- und 31P-NMR-Spektren der Komplexverbindungen 4 - 10 sowie 13 - 20 werden diskutiert. Für Komplexe des 1,1,2,3,3-Pentaphenyltriphosphans, (Ph2P)2PPh—M(CO)m (M=Mo, Fe, m = 5, 4) (18, 19) konnte 31P{1H}-NMR-spektroskopisch die Wanderung der (CO)mM-Fragmente von der medialen in die terminale Position des P3-Gerüstes nachgewiesen werden.
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  • 10
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Linear Oligophosphaalkanes, IV. Synthesis and Structure of Nickel(II) Complexes of Chiral Tetraphosphaalkanes RR′P—[CH2]3—PMe—[CH2]m—PMe—[CH2]3—PRR′ (R = Me; R′ = H, Me; m = 2, 3)Nickel(II) bromide and the tetraphosphaalkanes RR′P—[CH2]3—PMe—[CH2]m—PMe—[CH2]3—PRRL′ (R = Me; R′ = H, Me; m = 2, 3) (1a-d) form complexes of composition [NiBrL]Br (L = 1a-d). According to 31P{1H}-NMR investigations, these complexes exist as two, four or more configurational isomers. UV/VIS spectra indicate a square pyramidal coordination at the nickel atom. - The X-ray analysis of a configurational isomer of [Ni(1c)Br]Br reveals the ionic structure and shows a slightly distorted square pyramidal geometry at the nickel atom. The two chelate-six-rings exist in the chair form while the chelate-five-ring is twisted. In the cation [Ni(1c)Br]+ the distances Ni—P are 217.0, 216.7, 207.8, and 227.0 pm and Ni—Br 268.9 pm.
    Notes: Nickel(II)-bromid bildet mit den Tetraphosphaalkanen RR′P—[CH2]3 - PMe —[CH2]m — PMe — [CH2]3 — PRR′ (R = Me; R′ = H, Me; m = 2, 3) (1a-d) Komplexe der Zusammensetzung [NiBrL]Br (L = 1a-d), die nach den Ergebnissen der 31P{1H}-NMR-spektroskopischen Untersuchung in Form von zwei, vier oder mehr Konfigurationsisomeren vorliegen. Die UV/VIS-Spektren der Komplexverbindungen deuten auf eine quadratisch-pyramidale Koordination am Nickel hin. - Die Röntgenstrukturanalyse eines Konfigurationsisomeren von [Ni(1c)Br]Br bestätigt die ionische Struktur und zeigt eine leicht verzerrte quadratisch-pyramidale Ligandenanordnung am Nickelatom. Die beiden Chelat-Sechsringsysteme liegen in der Sesselform, der Chelatfünfring in der Twistform vor. Im Kation [Ni(1c)Br]+ betragen die Abstände Ni—P 217.0, 216.7, 207.8 und 227.0 pm, während für Ni—Br 268.9 pm gefunden werden.
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