Vogel's Textbook of Practical Organic Chemistry, 5th Edition by Arthur Israel Vogel

By Arthur Israel Vogel

Most general, tested and revered reference handbook for the natural chemistry laboratory. accommodates new reactions and strategies now on hand to the natural chemist.

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Podzorov, V. M. Pudalov, M. E. Gershenson, Appl. Phys. Lett. 2003, 82, 1739–1741. V. Y. Butko, X. Chi, D. V. Lang, A. P. Ramirez, Appl. Phys. Lett. 2003, 83, 4773–4775. R. W. I. de Boer, M. E. Gershenson, A. F. Morpurgo, V. Podzorov, Phys. Stat. Sol. (a) 2004, 201, 1302–1331. S. E. Fritz, S. M. Martin, C. D. Frisbie, M. D. Ward, M. F. Toney, J. Am. Chem. Soc. 2004, 126, 4084–4085. D. J. Gundlach, J. A. Nichols, L. Zhou, T. N. Jackson, Appl. Phys. Lett. 2002, 80, 2925–2927. A. Hepp, H. Heil, W. Weise, M.

E. Lilienfeld, US Patent 1,745,175, 15 A. R. Brown, C. P. Jarrett, D. M. de 1930. D. Kahng, M. M. Atalla, in IRE Solid-State Devices Research Conference, Pittsburgh, PA, 1960; D. Kahng, US Patent 3,102,230, 1963. P. K. Weimer, Proc. IRE 1962, 50, 1462–1469. W. E. Spear, P. G. Le Comber, J. NonCryst. Solids 1972, 8–10, 727–738. G. W. Neudeck, A. K. Malhotra, Solid-State Electron. 1976, 19, 721–729. M. Pope, C. E. Swenberg, Electronic Processes in Organic Crystals and Polymers, Oxford University Press, New York, 1999.

The dependence is accounted for by a semi-empirical law depicted by Eq. (13): m ¼ KðVG À VT Þ g ð13Þ where K and g are empirical parameters. e. resistance multiplied by channel width) extracted from this model for both top- 15 16 1 Organic Transistors Equivalent circuit of a TFT including contact resistance. The bottom circuit also comprises head-to-toe diodes to account for non-linearity in the contact resistance. Fig. 11. contact and bottom-contact architecture was of the order of 10 3 W cm. Data obtained for sexithiophene with TC structure [36] were approximately ten times larger.

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