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Hf-sputtered indium oxide films doped with tin (1978)

Hoffmann, H. ; Pickl, J. ; Schmidt, M. ; [et al.]

Springer

Applied physics 16 (1978), S. 239-246

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ISSN: 1432-0630

Keywords: 72.40 ; 73

Source: Springer Online Journal Archives 1860-2000

Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics

Notes: Abstract Indium oxide films doped with tin (ITO-films) have been hf-sputtered from an 80 at-%In2O3/20 at-%SnO2 target onto glass substrates. The sputter atmosphere contained mainly argon (10−2Torr) with addition of oxygen (0≦p O 2≦2·10−2Torr). The sputtered films aren-conductors. The conductivity and density of charge carriers depend on the oxygen content of the sputter gas. They could be varied by two orders of magnitude. In air or in oxygen atmosphere the films oxidize at the surface and for a certain depth beneath the surface, thus decreasing the conductivity. The Hall mobility of the sputtered films is smaller (≈10 cm2V−1 s−1) than one observes at ITO films produced by CVD sparaying or other methods. The conductivity of as sputtered films approached maximum values of about 1000Ώ−1cm−1.

Type of Medium: Electronic Resource

URL: http://dx.doi.org/10.1007/BF00885119

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Acyl- und Alkylidenphosphane. XXXII [1, 2]. Di-cyclo-hexoyl- und Diadamant-1-oylphosphan - Keto-Enol-Tautomerie und Struktur (1992)

Becker, G. ; Schmidt, M. ; Schwarz, W. ; [et al.]

Weinheim : Wiley-Blackwell

Zeitschrift für anorganische Chemie 608 (1992), S. 33-42

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ISSN: 0044-2313

Keywords: Diacylphosphines ; Di-cyclohexoylposphine ; Diadamant-1-oylphosphine ; keto-enol tautomerism ; NMR-parameters, thermodynamic data ; X-ray structure determination ; very short O‥H‥O bridge ; Chemistry ; Inorganic Chemistry

Source: Wiley InterScience Backfile Collection 1832-2000

Topics: Chemistry and Pharmacology

Description / Table of Contents: Acyl- and Alkylidenephosphines. XXXII. Di-cyclohexoyl- and Diadamant-1-oylphosphine - Keto-Enol Tautomerism and StructureLithium dihydrogenphosphide · DME (1) [12] and cyclo-hexoyl or adamant-1-oyl chloride react in a molar ratio of 3:2 to give lithium di-cyclo-hexoylphosphide · DME and the corresponding diadamant-1-oylphosphide.2THF (1) resp. Treatment of these two compounds with 85% tetrafluoroboric acid. diethylether adduct yields di-cyclo-hexoyl- (1b) and diadamant-1-oylphosphine (1c). In nmr spectroscopic studies 1b over a range of 203 to 343 K, a strong temperature dependence of the keto-enol equilibrium is found; thermodynamic data characteristic for the formation of the enol tautomer (ΔH0 = -4.3 kJ. mol-1; ΔS0 = -9.2 J. mol-1. K (-1) are compared of 1,3-diketones.The enol tautomer of diadamant-1-oylphosphine (E-1c) as obtained from a benzene solution in thin colourless plates, crystallizes in the monoclinic space group P21/c {a = 722.2(2); b = 1085.5(4); c = 2434.8(5) pm; ß = 96.43(2)° at -100 ± 3°C; Z = 4}. An X- ray structure analysis (Rw = 0.033) shows bond lengths and angles to be almost identical within the enolic system (P—C 179/180; C—O 130/129; C—C(adamant-1-yl) 152/153 pm; C—P—C 99°; P—C—O 124°/124°; P—C—C 120°/120°; C—C—O 116°/116°. The geometry of the very strong, but probably asymmetric O‥H‥O bridge is discussed (O—H 120/130, O‥O 245 pm).

Notes: Aus Lithium-dihydrogenphosphid · DME (1) [12] und cyclo-Hexoyl- bzw. Adamant-1-oyl-chlorid im Molverhältnis 3:2 zugängliches Lithium-di-cyclo-hexoylphosphid · DME und -diadamant-1-oylphosphid · 2THF 1) reagieren mit 85proz. Tetrafluoroborsäure · Diethylether-Addukt zu Di-cyclo-hexoyl- 1b) und Diadamant-1-oylphosphan (1 c). Die Lage des Keto-Enol-Gleichgewichts zwischen 203 und 343 K sowie thermodynamische Daten zur Bildung des Enol-Isomers ΔH0= -4,3kJ.Mol-1; ΔS0;=-9,2 J · mol-1 · K-1 () wurden NMR-spektroskopisch an einer 2 M Lösung des bei +20°C flüssigen Di-cyclo-Hexoyl-Derivates 1b in d8-Toluol ermittelt und mit Werten von 1,3-Diketonen verglichen.Das farblose, sich aus Benzol in dünnen Plättchen abscheidende Enol-Tautomer des Diadamant-1-oylphosphans (E-1 c) kristallisiert monoklin in der Raumgruppe P21/c {a = 722,2(2) b = 1085,5(4); c = 2434,8(5) pm; ß = 96,43(2)° bei - 100 ± 3°C; Z = 4}. Nach den Ergebnissen der Röntgenstrukturanalyse (Rw=0,033) weist das Molekül in beiden des Hälften des Enolrings nahezu identische Bindungslängen und -winkel auf P—C 179/180; C—O 130/129; C—C(Adamant-1-yl) 152/153 pm; C—P—C 99°; P—C—O 124°/124°; P—C—C 120°/120°; C—C—O 116°/116°. Die Geometrie der sehr starken, aber vermutlich asymmetrischen O‥H‥O-Brücke wird diskutiert (O—H 120/130; O‥O 245 pm).

Additional Material: 4 Ill.