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
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 1321-1325 
    ISSN: 0009-2940
    Keywords: Alkenes ; Nickel complexes ; Stannenes ; Metal-metal bonds ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: {Bis[bis(trimethylsilyl)methyl]stannio(II)}bis(η2-ethene)nickel(O) and Related Compounds, Part IThe reaction of Ni(C2H4)3 and bis{bis(trimethylsilyl)methyl}-stannene affords the crystalline, coordinatively unsaturated complex (C2H4)2Ni = Sn{CH(SiMe3)2}2 (1). The NMR spectra of 1 show for the tin moiety a temperature-dependent solvate complex formation (thf) and for the nickel moiety a hindered rotation of the ethene ligands at low temperature. X-ray structure analysis indicates Sn - Ni multiple-bond character. Upon addition of donor molecules to 1 the addition compounds (C2H4)2Ni - Sn{CH(SiMe3)2}2(donor) [donor = NH3: 2a; pyridine: 2b; (Me2N)3PO: 2c] are obtained. According to the low-temperature NMR spectra the complexes are asymmetric in their ground state. Similar to the formation of the adducts 2a - c, the title compound 1 reacts with LiHAliBu3 as a source of LiH in ether/tmeda to form the hydride adduct [Li(tmeda)2]+ [(C2H4)2Ni - Sn{CH(SiMe3)2}2}2(H)]ominus; (2d). Displacement of the ethene ligands in 1 by CO yields with conservation of the Ni - Sn bond the complex (CO)3Ni= Sn{CH(SiMe3)2}2 (3). From this complex the donor adducts (CO)3Ni - Sn{CH(SiMe3)2}2(donor) [donor = NH3: 4a; pyridine: 4b; (Me2N)3PO: 4c] are prepared. For the donor-ligand carbonyl complexes the ground state has been shown to be asymmetric by low-temperature NMR spectra.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 103-106 
    ISSN: 0009-2940
    Keywords: Alkynes ; Nickel complexes ; Stannenes ; Metallacycloalkenes ; Kinetic and thermodynamic reaction control ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis, Structure, and Reactivity of a Stanna(II)-nickela(III)-cyclobutene KomplexesThe (ethyne)nickel(0) complex (iPr2PC2H4PiPr2)Ni(C2H2) (1) reacts with the stannene Sn[CH(SiMe3)2]2 below -30°C to yield the stanna(II)-nickela(II)-cyclobutene complex (iPr2PC2H4PiPr2)YYNiCH=YYCHSn[CH(SiMe3)2]2 (2; 83%) as the kinetically controlled product; 2 has been characterized by IR and NMR spectroscopy and an X-ray crystal-structure determination. The latter shows the central four-membered ring to be planar with a long Ni - Sn bond [2.626(1) Å]. According to the temperature-dependent NMR spectra, 2 dissociates reversibly in solution to the starting components. The synthesis reaction thus represents an equilibrium as long as the temperature is below 20°C. These observations indicate that the structural lability of the stanna(II)-nickela(II)-cyclobutene moiety is associated with the weakness of the Ni - Sn bond. The bonding situation in 2 is best described as an “inner complex” in which a stannyl anion is coordinated to a nickel(II) cation. An ethereal solution of 2 undergoes an oxidative addition of one ethyne C - H bond to the stannene at 20°C to give the Ni(0)/Sn(IV) complex iPr2PC2H4PiPr2)Ni({η2-HC≡CSn(H)[CH(SiMe3)2]2} (3) as the thermodynamically controlled product. Reaction of 3 with CO liberates the new alkyne ligand.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 653-655 
    ISSN: 0009-2940
    Keywords: 1,6-Diynes ; Nickel complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis and Structure of (R3P)Ni(1,6-Heptadiin) ComplexesDisplacement of the alkene ligand in Ligand-Ni(0)(1,6-diene) complexes by 1,6-heptadiyne, the parent 1,6-diyne, affords the complexes (Me3P)Ni(η2,η2-C7H8) (1) and (Ph3P)Ni(η2,η2-C7H8) (2). According to an X-ray structure analysis of the PMe3 derivative 1 the nickel atom is ideally trigonal-planar coordinated by the phosphane and both C≡C bonds. The increased stability of the complexes as compared to Ligand-Ni(HC≡CH)2 complexes is referred to the strong chelating effect which is special to the 1,6-functionalization. The compounds can be considered to be model complexes for the key intermediates of numerous transition metal-mediated coupling reactions of (substituted and unsubstituted) 1,6-diynes.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    ISSN: 0009-2940
    Keywords: (η2-Alkene)(η5-cyclopentadienyl)organylnickel(II) complexes, stability and reactivity of ; Cyclopentadienyl ligands, substituted ; Chelating alkenylcyclopentadienyl ; Nickel complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Various Coordinations in (η2-Alkene)(η5-cyclopentadienyl)organylnickel(II) ComplexesA series of (η2-alkene)(η5-cyclopentadienyl)organylnickel(II) complexes with substituted cyclopentadienyl ligands is synthesized in order to compare the structures, the thermal stabilities, and chemical reactivities. In (allyl)(η5-Cp')Ni compounds the allyl moiety is η3-coordinated when Cp'=C5H5, C5Me5 (1), C5Ph5 (2), indenyl (3), [Hydridotri(pyrazolyl)borato] (4) (as an equivalent of the cyclopentadienyl ligand), and [C5H4((CH2)3CH=CH2)] (22). It is found that the [(η2-alkene)alkyl(η5-Cp')nickel] compounds [Cp'=C5Me5; alkene=C2H4, alkyl=Me (10), Et (9) or alkene=(1 - 2-η2)-1,3-butadiene, alkyl=Me (11); Cp'=C5Ph5; alkene=C2H4, alkyl=Me (12)] are thermally more stable and less reactive than their η5;- C5H5 analogues; the largest increase in thermal stability is observed when the η5-Cp' and the η2-alkene functions are connected by substitution of the cyclopentadienyl ligand with an alkenyl group of suitable chain length. In the case of compounds of the general type [(η5-C5R4((CH2)nCH=CH2))-(ligand)Ni(II)] with Ph3P as the ligand these complexes are cationic [R=H, n=3 (14+) or R=Me, n=2 (17+)]. On the other hand, the compounds with anionic ligands are neutral complexes (R=H, n=3, ligand=methyl (19), ethyl (20), isopropyl (21) or R=Me, n=3 and ligand=iodide (24), bromide (25), methyl (26), ethyl (27)]. In 14+, 17+, 19 - 21 and 24 - 27 the C=C bond of the alkenyl group is η2-coordinated to the nickel atom. X-ray structures have been determined for 4 and 25.
    Additional Material: 2 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...