Letteratura scientifica selezionata sul tema "Pernigraniline"
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Articoli di riviste sul tema "Pernigraniline":
Leng, J. M., J. M. Ginder, R. P. Mccall, H. J. Ye, A. J. Epstein, Y. Sun, S. K. Manohar e A. G. Macdiarmid. "Photoexcitation spectroscopy of pernigraniline". Synthetic Metals 41, n. 3 (maggio 1991): 1311–14. http://dx.doi.org/10.1016/0379-6779(91)91613-f.
Cao, Y., e A. J. Heeger. "Charged solitons in pernigraniline". Synthetic Metals 39, n. 2 (dicembre 1990): 205–14. http://dx.doi.org/10.1016/0379-6779(90)90185-n.
Ginder, J. M., e A. J. Epstein. "Ring-rotational dimerization in pernigraniline". Physical Review Letters 64, n. 10 (5 marzo 1990): 1184. http://dx.doi.org/10.1103/physrevlett.64.1184.
Long, S. M., K. R. Cromack, A. J. Epstein, Y. Sun e A. G. MacDiarmid. "ESR of pernigraniline base solutions revisited". Synthetic Metals 62, n. 3 (febbraio 1994): 287–89. http://dx.doi.org/10.1016/0379-6779(94)90219-4.
Coplin, K. A., J. M. Leng, R. P. Mccall, A. J. Epstein, S. K. Manohar, Y. Sun e A. G. Macdiarmid. "Photoexcitation spectroscopy: Solutions in pernigraniline base". Synthetic Metals 55, n. 1 (marzo 1993): 7–14. http://dx.doi.org/10.1016/0379-6779(93)90902-9.
Amaya, Toru, Izumi Kurata, Yuhi Inada, Tomohiro Hatai e Toshikazu Hirao. "Synthesis of phosphonic acid ring-substituted polyanilines via direct phosphonation to polymer main chains". RSC Advances 7, n. 62 (2017): 39306–13. http://dx.doi.org/10.1039/c7ra04678b.
Liu, J., e D. C. Wu. "Combined polarons in a pernigraniline-base polymer". Physics Letters A 244, n. 4 (luglio 1998): 292–94. http://dx.doi.org/10.1016/s0375-9601(98)00315-6.
dos Santos, M. C., e J. L. Brédas. "Protonation process of pernigraniline: A theoretical investigation". Physical Review B 40, n. 17 (15 dicembre 1989): 11997–2000. http://dx.doi.org/10.1103/physrevb.40.11997.
Sun, Yan, Alan G. MacDiarmid e Arthur J. Epstein. "Polyaniline: synthesis and characterization of pernigraniline base". Journal of the Chemical Society, Chemical Communications, n. 7 (1990): 529. http://dx.doi.org/10.1039/c39900000529.
Epstein, A. J., J. W. Blatchford, K. Kim, L.-B. Lin, T. L. Gustafson, K. A. Coplin e A. G. Macdiarmid. "Long Lived Neutral Solitons in Pernigraniline Base". Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 256, n. 1 (novembre 1994): 399–405. http://dx.doi.org/10.1080/10587259408039269.
Tesi sul tema "Pernigraniline":
Leng, Jingmin. "Photoexcited solitons and polarons of pernigraniline base". The Ohio State University, 1992. http://rave.ohiolink.edu/etdc/view?acc_num=osu1343061168.
Coplin, Kimberly A. "Photoexcitation of pernigraniline base : the role of neutral solitons /". The Ohio State University, 1993. http://rave.ohiolink.edu/etdc/view?acc_num=osu1343058811.
Molapo, Kerileng Mildred. "Electro chemiluminescence and organic electronics of derivatised poly(aniline sulphonic acid) light-emitting diodes". University of the Western Cape, 2011. http://hdl.handle.net/11394/8437.
Electrochemiluminescence (EeL) is applied for industrial applications that have considerable potential, such as clinical diagnostic, analytical chemistry, and light-emitting devices, due to selectivity, sensitivity for detection and quantification of molecules through generation of fluorescence light when electric current is applied on the materials. In EeL the electrochemical reaction allows for precise control over the time and position of the light emitting reaction. The control over time allows one to synchronise the luminescence and the biochemical reaction under study and control over position not only improves sensitivity of the instrument by increasing the signal to noise ratio, but also allows multiple analytical reactions in the same sample to be analyzed using an electrode array. The EeL generation fluorescent materials are based on inorganic semiconductor materials for light-emitting devices. Further progress in this EeL field mainly depends on discovery of new advanced materials, interfacial films and nanoparticle coatings, advances in microfluidics leading to total increase in EeL properties. There has been extensive use of polymers for enhancement of EeL properties. Electrochemiluminescent conjugated polymers constitute a new class of fluorescent polymers that emit light when excited by the flow of an electric current. These new generation fluorescent materials may now challenge the domination by inorganic semiconductor materials for the commercial market of light-emitting devices such as lightemitting diodes and polymer laser devices (PLDs).
Capitoli di libri sul tema "Pernigraniline":
dos Santos, M. C., e J. L. Brédas. "Oxidized Polyaniline: Effects of Protonation on the Electronic Structure of Pernigraniline". In Springer Series in Solid-State Sciences, 325–29. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-83833-0_61.
Atti di convegni sul tema "Pernigraniline":
Kwangjoon Kim, J. W. Blatchford, Liang Bih Lin, T. L. Gustafson, A. J. Epstein e A. G. MacDiarnid. "Dynamics of photoexcited states in pernigraniline base polymer". In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835649.
Libert, J., R. Lazzaroni e J. L. Bredas. "Theoretical investigation of neutral and charged defects in the pernigraniline base form of polyaniline". In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835219.
Quillard, S., K. Berrada, G. Louam e S. Lefrant. "Polyanilines and substituted polyanilines: a comparative study of the Raman spectra of leucoemeraldine, emeraldine and pernigraniline". In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835642.