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1
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0348027681
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PABT: poly(4,4′-dialkyl-2,2′-bithiazol-5,5′-diyl)
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PABT: poly(4,4′-dialkyl-2,2′-bithiazol-5,5′-diyl).
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2
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19944383211
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Nanos, J. I.; Kampf, J. W.; Curtis, M. D.; Gonzalez, L.; Martin, D. C. Chem. Mater. 1995, 7, 2232.
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(1995)
Chem. Mater.
, vol.7
, pp. 2232
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Nanos, J.I.1
Kampf, J.W.2
Curtis, M.D.3
Gonzalez, L.4
Martin, D.C.5
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3
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35748980822
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(a) Yamamoto, T.; Suganuma, H.; Maruyama, T.; Kubota, K. J. Chem. Soc., Chem Commun. 1995, 1613.
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(1995)
J. Chem. Soc., Chem Commun.
, pp. 1613
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Yamamoto, T.1
Suganuma, H.2
Maruyama, T.3
Kubota, K.4
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4
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0001419575
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(b) Yamamoto, T.; Suganuma, H.; Maruyama, T.; Inoue, T.; Muramatsu, Y.; Arai, M.; Komarudin, D.; Ooba, N.; Tomaru, S.; Sasaki, S.; Kubota, K. Chem. Mater. 1997, 9, 1217.
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(1997)
Chem. Mater.
, vol.9
, pp. 1217
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Yamamoto, T.1
Suganuma, H.2
Maruyama, T.3
Inoue, T.4
Muramatsu, Y.5
Arai, M.6
Komarudin, D.7
Ooba, N.8
Tomaru, S.9
Sasaki, S.10
Kubota, K.11
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7
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0348027679
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note
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3 (MeOTf) at room temperature. The light yellow solution becomes orange and the greenish-yellow fluorescence of PNBT is replaced by an orange-reddish color under long-wavelength UV light. Further aliquots of MeOTf were added in 10 h intervals until 25 equiv of MeOTf was added. After 60 h, solvent and excess MeOTf were removed under vacuum. The product was analyzed for F (10.5%), corresponding to 55% methylation. With 4 equiv of MeOTf and a 10 h reaction time, the F analysis was 1.50%, corresponding to 6% methylation, whereas heating the PNBT solution with a large excess of MeOTf for 3 days gave 100% methylation (16% F).
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8
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0001164620
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Zhang, N. W.; Li, Q.; Pakbaz, K.; Yoon, C. O.; Wudl, F. Chem. Mater. 1993, 5, 1598.
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(1993)
Chem. Mater.
, vol.5
, pp. 1598
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Zhang, N.W.1
Li, Q.2
Pakbaz, K.3
Yoon, C.O.4
Wudl, F.5
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11
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0000436754
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(c) McCullough, R. D.; Tristram-Nagle, S.; Williams, S. P.; Lowe, R. D.; Jayaraman, M. J. Am. Chem. Soc. 1993, 115, 4910.
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(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 4910
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McCullough, R.D.1
Tristram-Nagle, S.2
Williams, S.P.3
Lowe, R.D.4
Jayaraman, M.5
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13
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0001714999
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(e) Chen, T.; Wu, X.; Rieke, R. D. J. Am. Chem. Soc. 1995, 117, 233-244.
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(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 233-244
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Chen, T.1
Wu, X.2
Rieke, R.D.3
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15
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0347396862
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note
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Thermal analyses were performed on a Perkin-Elmer Series 7 Thermal Analysis System. The TGA runs were under nitrogen with a heating rate of 40 °C/min, and the DSC results were obtained on samples in a crimped aluminum boat under nitrogen at 20 °C/min.
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18
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0348027676
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(c) Dalton, E. F.; Surridge, N. A.; Jernigan, J. C.; Wilbourn, K. O.; Facci, J. S.; Murray, R. W. Chem. Phys. 1990, 141, 1413.
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(1990)
Chem. Phys.
, vol.141
, pp. 1413
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Dalton, E.F.1
Surridge, N.A.2
Jernigan, J.C.3
Wilbourn, K.O.4
Facci, J.S.5
Murray, R.W.6
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19
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0006277627
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and references therein
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(d) Savéant, J.-M. J. Phys. Chem. 1988, 92, 4526, and references therein.
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(1988)
J. Phys. Chem.
, vol.92
, pp. 4526
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Savéant, J.-M.1
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20
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0040206106
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Yamamoto, T.; Zhou, Z.; Kanbara, T.; Shimura, M.; Kizu, K.; Maruyama, T.; Nakamura, Y.; Fukuda, T.; Lee, B.; Ooba, N.; Tomaru, S.; Kurihara, T.; Kaino, T.; Kubota, K.; Sasaki, S. J. Am. Chem. Soc. 1996, 118, 10389.
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(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 10389
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Yamamoto, T.1
Zhou, Z.2
Kanbara, T.3
Shimura, M.4
Kizu, K.5
Maruyama, T.6
Nakamura, Y.7
Fukuda, T.8
Lee, B.9
Ooba, N.10
Tomaru, S.11
Kurihara, T.12
Kaino, T.13
Kubota, K.14
Sasaki, S.15
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21
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0348027677
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note
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6 acetonitrile solution.
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23
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0346135859
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note
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2. I-V characteristics were measured with a Kiethley 236 Electrometer. EL spectra were recorded on a Tracer-Northern 1710A diode array spectrometer.
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24
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0347396863
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Brédas, J.-L., Chance, R. R., Eds.; Kluwer Academic Publishers: The Netherlands
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Eckhardt, H.; Jen, K. Y.; Shacklette, L. W.; Lefrant, S. In Conjugated Polymeric Materials: Opportunities in Electronics, Optoelectronics, and Molecular Electronics; Brédas, J.-L., Chance, R. R., Eds.; Kluwer Academic Publishers: The Netherlands, 1990; pp 305-320.
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(1990)
Conjugated Polymeric Materials: Opportunities in Electronics, Optoelectronics, and Molecular Electronics
, pp. 305-320
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Eckhardt, H.1
Jen, K.Y.2
Shacklette, L.W.3
Lefrant, S.4
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26
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0031208396
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He, Y.; Politis, J. K.; Cheng, H.; Curtis, M. D.; Kanicki, J. IEEE Trans. Electron. Dev. 1997, 44, 1282.
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(1997)
IEEE Trans. Electron. Dev.
, vol.44
, pp. 1282
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He, Y.1
Politis, J.K.2
Cheng, H.3
Curtis, M.D.4
Kanicki, J.5
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