Auswahl der wissenschaftlichen Literatur zum Thema „Pernigraniline“
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Zeitschriftenartikel zum Thema "Pernigraniline":
Leng, J. M., J. M. Ginder, R. P. Mccall, H. J. Ye, A. J. Epstein, Y. Sun, S. K. Manohar und A. G. Macdiarmid. „Photoexcitation spectroscopy of pernigraniline“. Synthetic Metals 41, Nr. 3 (Mai 1991): 1311–14. http://dx.doi.org/10.1016/0379-6779(91)91613-f.
Cao, Y., und A. J. Heeger. „Charged solitons in pernigraniline“. Synthetic Metals 39, Nr. 2 (Dezember 1990): 205–14. http://dx.doi.org/10.1016/0379-6779(90)90185-n.
Ginder, J. M., und A. J. Epstein. „Ring-rotational dimerization in pernigraniline“. Physical Review Letters 64, Nr. 10 (05.03.1990): 1184. http://dx.doi.org/10.1103/physrevlett.64.1184.
Long, S. M., K. R. Cromack, A. J. Epstein, Y. Sun und A. G. MacDiarmid. „ESR of pernigraniline base solutions revisited“. Synthetic Metals 62, Nr. 3 (Februar 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 und A. G. Macdiarmid. „Photoexcitation spectroscopy: Solutions in pernigraniline base“. Synthetic Metals 55, Nr. 1 (März 1993): 7–14. http://dx.doi.org/10.1016/0379-6779(93)90902-9.
Amaya, Toru, Izumi Kurata, Yuhi Inada, Tomohiro Hatai und Toshikazu Hirao. „Synthesis of phosphonic acid ring-substituted polyanilines via direct phosphonation to polymer main chains“. RSC Advances 7, Nr. 62 (2017): 39306–13. http://dx.doi.org/10.1039/c7ra04678b.
Liu, J., und D. C. Wu. „Combined polarons in a pernigraniline-base polymer“. Physics Letters A 244, Nr. 4 (Juli 1998): 292–94. http://dx.doi.org/10.1016/s0375-9601(98)00315-6.
dos Santos, M. C., und J. L. Brédas. „Protonation process of pernigraniline: A theoretical investigation“. Physical Review B 40, Nr. 17 (15.12.1989): 11997–2000. http://dx.doi.org/10.1103/physrevb.40.11997.
Sun, Yan, Alan G. MacDiarmid und Arthur J. Epstein. „Polyaniline: synthesis and characterization of pernigraniline base“. Journal of the Chemical Society, Chemical Communications, Nr. 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 und 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, Nr. 1 (November 1994): 399–405. http://dx.doi.org/10.1080/10587259408039269.
Dissertationen zum Thema "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).
Buchteile zum Thema "Pernigraniline":
dos Santos, M. C., und 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.
Konferenzberichte zum Thema "Pernigraniline":
Kwangjoon Kim, J. W. Blatchford, Liang Bih Lin, T. L. Gustafson, A. J. Epstein und 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 und 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 und 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.