η⇌μ exchange bonding mode of bidentate tmeda ligand. Molecular structure of [Y(tmhd)3]2(μ-tmeda)
摘要:
The reaction between the yttrium beta-diketonate complexes Y(tmhd)(3)(H2O)(x) (x = 0 or 1) and 0.5 or 1 equivalent of N,N,N',N'-tetramethylethylenediamine (tmeda = Me2NCH2CH2NMe2) in hexane at room temperature afforded [Y(tmhd)(3)](2)(tmeda) (1) and Y(tmhd)(3)(tmeda) (2) derivatives, respectively. They have been characterized by FT-IR, H-1 NMR spectroscopy and by single crystal X-ray diffraction for 1. Variable temperature 1 H NMR experiments indicated an equilibrium between 1 and 2. Their thermal behaviors were characterized by TGA and sublimation experiments. 2 is converted into compound 1 by heating over 100 degreesC. These precursors were used for the growth Of Y2O3 and YBa2Cu3O7-x films by pulsed injection metal organic chemical vapor deposition (PI-MOCVD). (C) 2003 Elsevier Science B.V. All rights reserved.
η⇌μ exchange bonding mode of bidentate tmeda ligand. Molecular structure of [Y(tmhd)3]2(μ-tmeda)
摘要:
The reaction between the yttrium beta-diketonate complexes Y(tmhd)(3)(H2O)(x) (x = 0 or 1) and 0.5 or 1 equivalent of N,N,N',N'-tetramethylethylenediamine (tmeda = Me2NCH2CH2NMe2) in hexane at room temperature afforded [Y(tmhd)(3)](2)(tmeda) (1) and Y(tmhd)(3)(tmeda) (2) derivatives, respectively. They have been characterized by FT-IR, H-1 NMR spectroscopy and by single crystal X-ray diffraction for 1. Variable temperature 1 H NMR experiments indicated an equilibrium between 1 and 2. Their thermal behaviors were characterized by TGA and sublimation experiments. 2 is converted into compound 1 by heating over 100 degreesC. These precursors were used for the growth Of Y2O3 and YBa2Cu3O7-x films by pulsed injection metal organic chemical vapor deposition (PI-MOCVD). (C) 2003 Elsevier Science B.V. All rights reserved.