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Статті в журналах з теми "Heteroacenes"
Bunz, Uwe H. F. "N-Heteroacenes." Chemistry - A European Journal 15, no. 28 (July 13, 2009): 6780–89. http://dx.doi.org/10.1002/chem.200900990.
Повний текст джерелаBunz, Uwe H. F. "The larger N-heteroacenes." Pure and Applied Chemistry 82, no. 4 (March 20, 2010): 953–68. http://dx.doi.org/10.1351/pac-con-09-09-17.
Повний текст джерелаLepeltier, Marc, Olena Lukoyanova, Alex Jacobson, Shehzad Jeeva, and Dmitrii F. Perepichka. "New azaborine-thiophene heteroacenes." Chemical Communications 46, no. 37 (2010): 7007. http://dx.doi.org/10.1039/c0cc01963a.
Повний текст джерелаDing, Fangwei, Debin Xia, Congwu Ge, Zhenchao Kang, Yulin Yang, Ruiqing Fan, Kaifeng Lin, and Xike Gao. "Indenone-fused N-heteroacenes." Journal of Materials Chemistry C 7, no. 45 (2019): 14314–19. http://dx.doi.org/10.1039/c9tc04962b.
Повний текст джерелаFeofanov, Mikhail, Vladimir Akhmetov, Ryo Takayama, and Konstantin Amsharov. "Transition-metal free synthesis of N-aryl carbazoles and their extended analogs." Organic & Biomolecular Chemistry 19, no. 33 (2021): 7172–75. http://dx.doi.org/10.1039/d1ob00940k.
Повний текст джерелаZhang, Yubao, Jiulin Shi, Xingdao He, and Guoli Tu. "All-thiophene-substituted N-heteroacene electron-donor materials for efficient organic solar cells." Journal of Materials Chemistry A 4, no. 35 (2016): 13519–24. http://dx.doi.org/10.1039/c6ta03784d.
Повний текст джерелаZhang, Wanzheng, Yubin Fu, Peirong Qiang, Jens Hunger, Shuai Bi, Wenbei Zhang, and Fan Zhang. "syn-BN-heteroacene cored conjugated oligomers with finely tuned blue-violet luminescent properties." Organic & Biomolecular Chemistry 15, no. 34 (2017): 7106–11. http://dx.doi.org/10.1039/c7ob01679d.
Повний текст джерелаBulumulla, Chandima, Ruwan Gunawardhana, Sang Ha Yoo, Cody R. Mills, Ruvanthi N. Kularatne, Thomas N. Jackson, Michael C. Biewer, Enrique D. Gomez, and Mihaela C. Stefan. "The effect of single atom replacement on organic thin film transistors: case of thieno[3,2-b]pyrrole vs. furo[3,2-b]pyrrole." Journal of Materials Chemistry C 6, no. 37 (2018): 10050–58. http://dx.doi.org/10.1039/c8tc02887g.
Повний текст джерелаBunz, Uwe H. F. "The Larger Linear N-Heteroacenes." Accounts of Chemical Research 48, no. 6 (May 13, 2015): 1676–86. http://dx.doi.org/10.1021/acs.accounts.5b00118.
Повний текст джерелаDing, Fangwei, Debin Xia, Weipeng Sun, Wei Chen, Yulin Yang, Kaifeng Lin, Feibao Zhang, and Xugang Guo. "Sulfur‐Containing Bent N‐Heteroacenes." Chemistry – A European Journal 25, no. 66 (October 31, 2019): 15106–11. http://dx.doi.org/10.1002/chem.201902984.
Повний текст джерелаДисертації з теми "Heteroacenes"
Kulisic, Niksa. "Heteroacenes as potential materials for molecular electronics." Doctoral thesis, Università degli studi di Trieste, 2010. http://hdl.handle.net/10077/3609.
Повний текст джерелаIn this thesis, different strategies for obtaining azaacenes suitable for solution-based processing techniques have been investigated and developed. The first synthetic approach involved the condensation of commercially available compounds which include the diamines 2,3-diaminobenzene, 2,3-diaminonaphtalene and 2,3-diaminophenazine and the bromoanilic acid and embelin. This synthetic route yielded a series of dihydroazaacenes with 5 and 7 fused aromatic rings. The low overall solubility of this azaacenes did not permit an extensive characterization of the compounds. A second synthetic approach was developed to investigate both C-N exchange and lateral expansion of the π-conjugation. Through this approach a tetraazaoctacene derivative was obtained and characterized. However it lacked of solubility necessary for being compatible with solution-processing techniques. A third strategy was based on the introduction of solubilizing groups on such extended tetraazaoctacene core. While the di-substitution did not render the azaoctacene soluble in neutral media, tetra-substitution yielded a derivative with enhanced solubility in neutral solvent.
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Purushothaman, Balaji. "PARTIALLY HALOGENATED ACENES AND HETEROACENES FOR ORGANIC ELECTRONICS." UKnowledge, 2011. http://uknowledge.uky.edu/gradschool_diss/124.
Повний текст джерелаGrimminger, Marsha Loth. "PERIODIC TRENDS IN STRUCTURE FUNCTION RELATIONSHIP OF ORGANIC HETEROACENES." UKnowledge, 2011. http://uknowledge.uky.edu/gradschool_diss/850.
Повний текст джерелаAppleton, Anthony Lucas. "Synthesis and characterization of large linear heteroacenes and their derivatives." Diss., Georgia Institute of Technology, 2010. http://hdl.handle.net/1853/37225.
Повний текст джерелаPaulus, Fabian [Verfasser], and Uwe H. F. [Akademischer Betreuer] Bunz. "N-Heteroacenes in Organic Field-Effect Transistors / Fabian Paulus ; Betreuer: Uwe Bunz." Heidelberg : Universitätsbibliothek Heidelberg, 2016. http://d-nb.info/1180615247/34.
Повний текст джерелаGranger, Devin B. "ACENES, HETEROACENES AND ANALOGOUS MOLECULES FOR ORGANIC PHOTOVOLTAIC AND FIELD EFFECT TRANSISTOR APPLICATIONS." UKnowledge, 2017. http://uknowledge.uky.edu/chemistry_etds/76.
Повний текст джерелаDoan, Thu Hong. "Synthesis, self-assembly and photophysical evaluation of fluorophores derived from acenes, heteroacenes and quinazolines." Thesis, Normandie, 2018. http://www.theses.fr/2018NORMC205.
Повний текст джерелаOrganic semiconductors (OSCs) are a highly attractive research field due to their potentials as active layers in optoelectronic devices such as organic field-effect transistors (OFETs), organic photovoltaic (OPVs) and organic light emitting diodes (OLEDs). Polycyclic aromatic compounds as well as heteroaromatics are considered as promising materials for OSCs due to their semi conductivity properties, optical properties and geometric structures. The mentioned systems and their photophysical properties were investigated in three chapters of my thesis. In the first chapter, a study on a set of linear, angular and condensed acenes consisting of heteroatom linkages with unique aggregations was described and analyzed. The angular and π-extended N-fused heteroacenes are the main class studied in the second chapter. Their synthesis is based on the Suzuki-Miyaura coupling and the Cadogan reactions. Besides acenes and N-fused heteroacenes, N-heteroaromatics have gained attention in material area. One of them is the quinazoline class that is known as an electron withdrawing unit in push-pull structures for intramolecular charge transfer (ICT). The investigation of the relationships between the electron donor-acceptor-donor (D-A-D) quinazoline-based structures and their photoluminescence properties is the main work mentioned in the third chapter
Wong, Hok-lai, and 黃學禮. "Design, synthesis, photochromic and photophysical studies of dithienylethene-containing heteroacenes, alkynyls, diimines and theirmetal complexes." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2011. http://hub.hku.hk/bib/B45874748.
Повний текст джерелаLevick, Matthew Thomas. "Connective-Pummerer cyclisations and SmI2-mediated cascade reactions for the synthesis of nitrogen-containing heteroacenes." Thesis, University of Manchester, 2013. https://www.research.manchester.ac.uk/portal/en/theses/connectivepummerer-cyclisations-and-smi2mediated-cascade-reactions-for-the-synthesis-of-nitrogencontaining-heteroacenes(762eea6e-0dc0-4397-8af0-07413517db63).html.
Повний текст джерелаKast, Hannelore [Verfasser]. "Fused S,N-heteroacenes and thiophene-substituted Ruthenium(II) complexes for organic solar cells / Hannelore Kast." Ulm : Universität Ulm, 2016. http://d-nb.info/1105590380/34.
Повний текст джерелаЧастини книг з теми "Heteroacenes"
Anthony, John E., and Adolphus G. Jones. "Silylethyne-Substituted Acenes and Heteroacenes." In Organic Electronics II, 105–36. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527640218.ch4.
Повний текст джерелаТези доповідей конференцій з теми "Heteroacenes"
Sakai, K., Y. Okada, S. Kitaoka, J. Tsurumi, Y. Ohishi, A. Fujiwara, H. Sato, et al. "Heteroacene-based organic single crystal transistors under high pressure." In 2013 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2013. http://dx.doi.org/10.7567/ssdm.2013.ps-10-9.
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