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  • 1
    ISSN: 0948-1907
    Keywords: Ga2Se3 ; MOVPE ; TEM ; Wide-gap semiconductor ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: We present results of a study using metal-organic vapor phase epitaxy (MOVPE) to synthesize thin films of cubic Ga2Se3 on both nearly lattice matched GaP and mismatched GaAs substrates. We find that trimethylgallium (TMGa) pre-reacts with the hydride H2Se in the gas phase to yield films which are only partially epitaxial and that the combination of TMGa with ditertiarybutylselenide produces films of the best crystal quality under steady state flow conditions. We also show that GaAs is an unsuitable substrate for MOVPE growth of gallium selenide due to exchange reactions at the interface leading to poorly bonded films.
    Additional Material: 8 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Advanced Materials for Optics and Electronics 5 (1995), S. iii 
    ISSN: 1057-9257
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Electrical Engineering, Measurement and Control Technology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 5 (1994), S. 541-544 
    ISSN: 1042-7147
    Keywords: Metal alkyls ; Purification ; Poly(4-vinyl pyridine) ; Adduct ; Lewis base ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Poly(4-vinyl pyridine) is used as a polymeric ligand to react with metal alkyls, MenM (n = 3, M = Al, Ga or In; n = 2, M = Cd or Zn) to form adducts. The adducts are characterized by solid state 13C NMR, infrared spectroscopy, microanalyses and differential scanning calorimetry (DSC). All the adducts are nonpyrophoric and thermally dissociable, so they may have potential both for use in adduct purification processes or for use as safer metal alkyl sources for Metal-Organic Chemical Vapor Deposition.
    Additional Material: 3 Tab.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Advanced Materials for Optics and Electronics 7 (1997), S. 23-28 
    ISSN: 1057-9257
    Keywords: dimethylzinc ; purification ; adduct ; non-chelating diamine ; X-ray structure ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Electrical Engineering, Measurement and Control Technology , Physics
    Notes: The structure of the dimethylzinc adduct with the bidentate amine 1,3-bis(4-pyridyl)propane, [Me2Zn(C5H4N)CH2CH2CH2(C5H4N)]n, 1, has been determined by X-ray diffraction analysis. Crystals of 1 are monoclinic, space group P21/m, with two molecules within a unit cell of dimensions a=5.364(3) Å, b=12.839(3) Å, c=10.618(3) Å and β=92.76(3)°. The structure is polymeric, being composed of [Me2Zn(C5H4N)CH2CH2CH2(C5H4N)] units with the nitrogens within a specific 1,3-bis(4-pyridyl)propane ligand bonding to adjacent zinc centres. The zinc atom is four-co-ordinate, bonding to two carbon and two nitrogen atoms, with the C - Zn - C angle of 145.5(2)° intermediate between that of a linear and tetrahedral bond arrangement. As far as we know, this is the first example of a polymeric alkyl zinc/cadmium amine adduct to have been structurally characterised. © 1997 John Wiley & Sons, Ltd.
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  • 5
    ISSN: 1057-9257
    Keywords: barium ; volatile ; β-diketone ; X-ray structure ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Electrical Engineering, Measurement and Control Technology , Physics
    Notes: At 150 K [Ba(TDFND)2, tetraglyme] crystallises in the P1/c space group with a = 17.15(2) Å b = 10.735(5) Å, c = 22.830(7) A, β = 97.56 (7)°, V = 4165 (5) Å3, Z=4. R1 = 0.0435, wR2 = 0.1079. The barium atom is nine-co-ordinate, with binding to all the O atoms. The two BaTDFND rings are planar but tilted by 26° from being co-planar. The five O atoms of the tetraglyme ligand are also essentially co-planar, but this plane subtends angles of 88.8(1)° and 67.4(1)° to the two BaTDFND planes. The Ba—O (TDFND) bond lengths are longer than for other related compounds, but the Ba—O (tetraglyme) bond lengths are similar to those in [Ba(HFA)2.tetraglyme] (HFA ≡ CF3C(O)CHC(O)CF3). The low melting point and the fact that [Ba(TDFND)2.tetraglyme], alone of barium complexes of this kind, can be evaporated without decomposition at 1 atm are attributed to lower intermolecular forces for this compound and to its greater thermal stability.
    Additional Material: 3 Ill.
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  • 6
    ISSN: 1057-9257
    Keywords: High Tc superconductors ; Precursors ; Copper ; Calcium ; Barium ; Yttrium ; Strontium ; Fluorinated β-dikeonates ; Ethanol ; Tetradecafluorononanedione ; Decafluoroheptanedione ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Electrical Engineering, Measurement and Control Technology , Physics
    Notes: The new β-diketone 1,1,1,2,2,3,3,7,7,8,8,9,9,9-tetradecafluorononane-4,6-dione (HTDFND) has been prepared and employed in the formation of complexes of Cu, Ca, Sr, Ba and Y. Complexes of the same metals derived from the β-diketone 1,1,1,2,2,3,3,7,7,7-decafluoroheptane-2,4-dione (HDFHD) have also been prepared. In general the compounds have the formula [M(TDFND)2H2O] or [M(DHFD)2H2O], although the yttrium complexes are [Y(β-diket)3] · xH2O (β-diket ≡ TDFND (x = 3) or DFHD (x = 2)). The complexes have been characterised by analytical and spectroscopic means and by a crystal structure of [Cu(TDFND)2EtOH] obtained by recrystallisation of [Cu(TDFND)2H2O] from aqueous ethanol. Crystal data for [Cu(TDFND)2EtOH]: triclinic, P̄1, a = 11.249(4) Å, b = 12.331 (2) Å, c = 12.890(2) Å, α = 96.89(2)°, β = 108.93(3)°, γ = 109.63(3)°, V = 1541.54 Å3, Z = 2. The complex is square pyramidal with the four oxygen atoms of the β-diketonates occupying the basal sites and the oxygen atom of the co-ordinated ethanol molecule in the apical position. The C3F7 ligands take up an extended staggered configuration in order to minimise steric repulsions. The complex is monomeric with intermolecular distances all greater than 4 Å. Simultaneous thermal analysis at 1 atm reveals that all the compounds lose water but then sublime, usually completely without decomposition. [Ba(TDFND)2H2O] is the first barium complex for which this is the case and it can be dehydrated to give [Ba(TDFND)2], which is also volatile but becomes less volatile with time. [Ba(TDFND)2H2O], [Sr(TDFND)2H2O] and [Ca(DFHD)2H2O] are suitable precursors for the growth of MF2 on silicon substrates. Complete orientation in the (111) direction is observed. Changes in the film growth rate with time for all the precursors are attributed to sample decomposition ([M(DFHD)2H2O], M ≡ Ca or Sr) or to slow reorganisation of the crystal structure ([Ba(TDFND)2H2O]). Layers with Y:Ba:Cu ratios close to the required 1:2:3 have been grown using [Y(DPM)3], [Cu(DPM)2] and [Ba(DFHD)2H2O] (DPM ≡ 2,2,6,6-tetramethylheptane-3,5-dionato).
    Additional Material: 6 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Advanced Materials for Optics and Electronics 3 (1994), S. 163-169 
    ISSN: 1057-9257
    Keywords: Zinc sulphide ; Zinc selenide ; t-butanethiol ; Precursors ; Purification ; Multilayers ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Electrical Engineering, Measurement and Control Technology , Physics
    Notes: A variety of problems in the growth of wide band gap II/VI materials by MOVPE has been addressed by the use of alternative precursors. The quality of grown layers of ZnSe has been greatly improved by adduct purification of Me2Zn. Using 4,4′-bipyridyl, the recovery of Me2Zn is variable because of the insolubility of 4,4′-bipyridyl in diethylether. Higher yields can be obtained using the ether-soluble base 1,3-bis(4-pyridyl)propane.tBuSH has been introduced for the growth of ZnS. Being a liquid, this compound is easy to handle and it allows growth of high-quality ZnS at temperatures down to 325°C with very little gas phase pre-reaction with Me2Zn. Growth of ZnSxSe1 - x at atmospheric pressure using H2S and Et2Se as the group 16 precursors allows excellent stoichiometric control, since the ratio of S : Se in the grown solid is similar to that of H2S : Et2Se in the gas phase for all compositions. Finally, multilayer structures have been grown at low pressure with excellent interface abruptness and goodquality material. However, the ternary layers are all much higher in sulphur than expected from the gas phase composition and the composition of the ternary appears to be influenced by the nature of the surface on which it is growing.
    Additional Material: 4 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 28 (1990), S. 510-514 
    ISSN: 0749-1581
    Keywords: Trimethylphosphine-o-xylidene-ruthenium complex ; 1H, 13C, 31P NMR ; P-H correlation spectroscopy ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1H, 13C and 31P NMR spectra of [Ru(CH2C6H4CH2)(PMe3)3], which contains a coordinated o-xylidene moiety, have been analysed. Parameters such as the geminal coupling in the methylene groups, P,H couplings and the chemical shifts of the quaternary ring carbon atoms all point to a metal-o-xylidene binding that is intermediate between σ2,π and π2. Spectral assignment is assisted by P-H correlation spectroscopy using the COLOC sequence. The best parameter for identifying the bonding mode is the chemical shift for the quaternary aromatic carbon atoms.
    Additional Material: 2 Ill.
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