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Naphthalenetetracarboxylic Diimides

Murray et al. (1996) measured electron and hole mobilities of vapor-deposited N-(p-(di-p-tolylamino)phenyl)-N,-(l,2-dimelthylpiopyl)-l,4,5,8-naphthalenetet-racaiboxylic diimide (TAND). The TAND molecule contains a naphthalene [Pg.576]


N, N,-bis(l,2-dimethylpropyl)-l,4,5,8-naphthalenetetracarboxylic diimide (NTDI). NTDI is a weakly polar acceptor compound with a dipole moment of... [Pg.563]

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... [Pg.565]

Katz, H.E. et al., Naphthalenetetracarboxylic diimide-hased n-chaimel transistor semi-... [Pg.227]

Katz, H.E. et al., Naphthalenetetracarboxylic diimide-based -channel transistor semiconductors Structural variation and thiol-enhanced gold contacts, J. Am. Chem. Soc. 122, 7787-7792, 2000. [Pg.417]

Chen. G. Lean. J.T. Alcala. M. Mallouk, T.E. Modular synthesis of ir-acceptor cyclophanes derived from 1,4,5,8-naphthalenetetracarboxylic diimide and 1.5-dinitro-naphthalene. J. Org. Chem. 2001. 66. 3027-3034. [Pg.430]


See other pages where Naphthalenetetracarboxylic Diimides is mentioned: [Pg.418]    [Pg.265]    [Pg.315]    [Pg.715]    [Pg.576]    [Pg.585]    [Pg.586]    [Pg.586]    [Pg.633]    [Pg.723]    [Pg.724]    [Pg.775]    [Pg.3559]    [Pg.3625]    [Pg.339]    [Pg.384]    [Pg.228]    [Pg.104]    [Pg.408]   


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