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1
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0003938641
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Marcel Dekker, New York
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P. M. Borsenberger, D. S. Weiss, Organic Photoreceptors for Xerography, Marcel Dekker, New York, 1998, pp. 234-242.
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Organic Photoreceptors for Xerography
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Borsenberger, P.M.1
Weiss, D.S.2
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5
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79956038122
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D. J. Gundlach, J. A. Nichols, L. Zhou, T. N. Jackson, Appl. Phys. Lett. 2002, 80, 2925-2927.
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Appl. Phys. Lett.
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Gundlach, D.J.1
Nichols, J.A.2
Zhou, L.3
Jackson, T.N.4
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6
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0031103927
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a) D. J. Gundlach, Y.-Y. Lin, T. N. Jackson, S. F. Nelson, D. G. Schlom, IEEE Electron Device Lett. 1997, 18, 87-89;
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IEEE Electron Device Lett.
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Gundlach, D.J.1
Lin, Y.-Y.2
Jackson, T.N.3
Nelson, S.F.4
Schlom, D.G.5
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7
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0031382876
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b) Y.-Y. Lin, D. J. Gundlach, S. F. Nelson, T. N. Jackson, IEEE Electron Device Lett. 1997, 18, 606-608.
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IEEE Electron Device Lett.
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Lin, Y.-Y.1
Gundlach, D.J.2
Nelson, S.F.3
Jackson, T.N.4
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8
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0034873221
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The oligomer approach for OFETs is the most successful in oligothiophene semiconductors, see a) H. E. Katz, Z. Bao, S. L. Gilat, Acc. Chem. Res. 2001, 34, 359-369;
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Acc. Chem. Res.
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Katz, H.E.1
Bao, Z.2
Gilat, S.L.3
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9
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0000816323
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b) F. Garnier, A. Yassar, R. Hajlaoui, G. Horowitz, E Deloffre, B. Servet, S. Ries, P. Alnot, J. Am. Chem. Soc. 1993, 115, 8716-8721.
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J. Am. Chem. Soc.
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Garnier, F.1
Yassar, A.2
Hajlaoui, R.3
Horowitz, G.4
Deloffre, E.5
Servet, B.6
Ries, S.7
Alnot, P.8
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10
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0000778553
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Oligo(p-phenylene)s for OFETs: D. J. Gundlach, Y.-Y. Lin, T. N. Jackson, D. G. Schlom, Appl. Phys. Lett. 1997, 71, 3853-3855.
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(1997)
Appl. Phys. Lett.
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Gundlach, D.J.1
Lin, Y.-Y.2
Jackson, T.N.3
Schlom, D.G.4
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12
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84989446720
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In crystalline oligo(9,10-anthrylene)s, the dihedral angles between anthracene moieties were more than 75° as a consequence of steric hindrance: a) U. Müller, M. Adam, K. Müllen, Chem. Ber. 1994, 127, 437-444;
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Chem. Ber.
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Müller, U.1
Adam, M.2
Müllen, K.3
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13
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33751391936
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b) H.-D. Becker, V. Langer, J. Sieler, H.-C. Becker, J. Org. Chem. 1992, 57, 1883-1887.
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J. Org. Chem.
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Becker, H.-D.1
Langer, V.2
Sieler, J.3
Becker, H.-C.4
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14
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0012588769
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See Supporting Information for the experimental details
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See Supporting Information for the experimental details.
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15
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0002812967
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Dehalogenation is a side reaction of the Suzuki coupling and responsible for the low yields of the anthracene oligomers: N. Miyaura, Top. Curr. Chem. 2002, 219, 11-59.
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Top. Curr. Chem.
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Miyaura, N.1
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16
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0012580640
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note
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This is in agreement with the result of PM3 calculations: The HOMO-LUMO energy gaps decrease in the order 2A (6.94 eV) > DH-2 A (6.91 eV) > 3A (6.86 eV) > DH-3 A (6.82 eV).
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17
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0030737247
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Interestingly, 2A is isoelectronic (14π x 2) with p-type OFET materials such as bis(benzodithiophene) and bis(dithienothiophene): a) J. G. Laquindanum, H. E. Katz, A. J. Lovinger, A. Dodabalapur, Adv. Mater. 1997, 9, 36-39;
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Adv. Mater.
, vol.9
, pp. 36-39
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Laquindanum, J.G.1
Katz, H.E.2
Lovinger, A.J.3
Dodabalapur, A.4
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18
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0032507252
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b) X.-C. Li, H. Sirringhaus, F. Garnier, A. B. Holmes, S. C. Moratti, N. Feeder, W. Clegg, S. J. Teat, R. H. Friend, J. Am. Chem. Soc. 1998, 120, 2206-2207.
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J. Am. Chem. Soc.
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Li, X.-C.1
Sirringhaus, H.2
Garnier, F.3
Holmes, A.B.4
Moratti, S.C.5
Feeder, N.6
Clegg, W.7
Teat, S.J.8
Friend, R.H.9
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19
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0035913765
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Also, see references [6a] and [6b]
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OFET materials with self-assembly properties by alkyl groups: H. Meng, Z. Bao, A. J. Lovinger, B.-C. Wang, A. M. Mujsce, J. Am. Chem. Soc. 2001, 123, 9214-9215. Also, see references [6a] and [6b].
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J. Am. Chem. Soc.
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, pp. 9214-9215
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Meng, H.1
Bao, Z.2
Lovinger, A.J.3
Wang, B.-C.4
Mujsce, A.M.5
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20
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0012580641
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note
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Atomic force microscopy (AFM) images of 2 A films prepared at 50-70°C showed a series of terraces with the step height of 2.0 nm. See Supporting Information.
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21
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0000815529
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-1, respectively): F. Garnier, R. Hajlaoui, A. E. Kassmi, G. Horowitz, L. Laigre, W. Porzio, M. Armanini, F. Provasoli, Chem. Mater. 1998, 10, 3334-3339.
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Chem. Mater.
, vol.10
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Garnier, F.1
Hajlaoui, R.2
Kassmi, A.E.3
Horowitz, G.4
Laigre, L.5
Porzio, W.6
Armanini, M.7
Provasoli, F.8
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