Indane, 1-butyl 1-phenyl

Indan-[Pg.930]

Borsenberger et al. (1995a) measured electron mobilities of PS doped with a series of acceptor molecules 2-r-butyl-9,10-N,N -dicyanoanthraquinone-diimine (DCAQ), 2-methy 1-2-pentyl-1,3-bis(dicyanomethylene)indane (DCMI), 3,5-dimethyl-3, 5 -diisopropyl-4,4,-diphenoquinone (DPQ-A), N,N -bis(l, 2-di-methylpropyl)-l,4,5,8-naphthalenetetracarboxylic diimide (NTDI), and 1,1-dioxo-2-(4-methylphenyl)-6-phenyl-4-(dicyanomethylidene)thiopyran (PTS). The reduction potentials are -0.22, -0.34, -0.45, -0.56, and -0.15 V, respectively. The dipole moments are between 0.30 and 4.0 Debye. In all materials, the field and temperature dependencies were described as logu oc pE1/2 and -(T0/rP)2. Figure 33 shows the results for 40% NTDI doped PS. The results... 

Alcohol 3 (solid) (1 mmol) and 5% of iodine (0.05 mmol, 12.7 mg) were triturated in a glass mortar for 1 min, transferred to a 15-mL flask and heated at 70 °C for 3 h. an aqueous solution of Na2S203-5H20 (10%, 20 mL) was then poured into the cooled mixture and the crude product was extracted with tert-butyl methyl ether (35 mL) and washed with water. Pure l,l,3-trimethyl-3-phenyl-indane (5, colorless oil) was obtained by column chromatography (Si02, hexane-CH2C12 4 1) in 91% yield. 

Ethanol, 2-[(1,7,7-trimethylbicyclo [2.2.1] hept-2-yl) oxy], exo-. See (exo)-2-Camphanyl-P-hydroxyethyl ether Ethanol, undenatured. See Alcohol Ethanone, 1-(2,3-dihydro-1,1,2,3,3,6-hexamethyl-1H-inden-5-yl)-. See Acetyl hexamethyl indan Ethanone, 2,2-dimethoxy-1,2-diphenyl-. See 2,2-Dimethoxy-2-phenylacetophenone Ethanone, 1-(4-(1,1-dimethylethyl)-2,6-dimethyl-3,5-dinitrophenyl)-. See Musk ketone Ethanone, 1-[4-(1,1-dimethylethyl) phenyl]-. See p-t-Butyl acetophenone Ethanone, 1-(4-ethylphenyl)-. See4-Ethylacetophenone... 

Another view of the channel is shown in Figure 13, which shows that the walls of the channel consist of the ends of the indane moieties, the faces of the unsubstituted phenyl groups, and the butyl groups. The r-butyl group takes up two orientations in the crystal in approximately equal occupancies. 

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