Статті в журналах з теми "Heteroacenes"
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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 джерелаGong, Peng, Kaiqi Ye, Jingbo Sun, Peng Chen, Pengchong Xue, Hao Yang, and Ran Lu. "Electroluminescence and fluorescence response towards acid vapors depending on the structures of indole-fused phospholes." RSC Advances 5, no. 115 (2015): 94990–96. http://dx.doi.org/10.1039/c5ra19867d.
Повний текст джерелаMatsuda, Takanori, and Hirotaka Ito. "Synthesis of indole-fused heteroacenes by cascade cyclisation involving rhodium(ii)-catalysed intramolecular C–H amination." Organic & Biomolecular Chemistry 16, no. 36 (2018): 6703–7. http://dx.doi.org/10.1039/c8ob01837e.
Повний текст джерелаWu, Di, Jueting Zheng, Chenyong Xu, Dawei Kang, Wenjing Hong, Zheng Duan, and François Mathey. "Phosphindole fused pyrrolo[3,2-b]pyrroles: a new single-molecule junction for charge transport." Dalton Transactions 48, no. 19 (2019): 6347–52. http://dx.doi.org/10.1039/c9dt01299k.
Повний текст джерелаCheng, Na, Feng Chen, Colm Durkan, Nan Wang, Yuanyuan He, and Jianwei Zhao. "Electron transport behavior of quinoidal heteroacene-based junctions: effective electron-transport pathways and quantum interference." Physical Chemistry Chemical Physics 20, no. 45 (2018): 28860–70. http://dx.doi.org/10.1039/c8cp05901b.
Повний текст джерелаQu, Hemi, and Chunyan Chi. "Synthetic Chemistry of Acenes and Heteroacenes." Current Organic Chemistry 14, no. 18 (November 1, 2010): 2070–108. http://dx.doi.org/10.2174/138527210793351580.
Повний текст джерелаHu, Ben-Lin, Cunbin An, Manfred Wagner, Georgia Ivanova, Anela Ivanova, and Martin Baumgarten. "Three-Dimensional Pyrene-Fused N-Heteroacenes." Journal of the American Chemical Society 141, no. 13 (March 12, 2019): 5130–34. http://dx.doi.org/10.1021/jacs.9b01082.
Повний текст джерелаMüllen, K., P. Gao, D. Beckmann, H. Tsao, X. Feng, V. Enkelmann, M. Baumgarten, and W. Pisula. "Heteroacenes for Organic Field-Effect Transistors." Synfacts 2009, no. 03 (February 19, 2009): 0265. http://dx.doi.org/10.1055/s-0028-1087765.
Повний текст джерелаLaughlin, Feng Li, Nihal Deligonul, Arnold L. Rheingold, James A. Golen, Brynna J. Laughlin, Rhett C. Smith, and John D. Protasiewicz. "Fluorescent Heteroacenes with Multiply-Bonded Phosphorus." Organometallics 32, no. 23 (November 15, 2013): 7116–21. http://dx.doi.org/10.1021/om400838g.
Повний текст джерелаLepeltier, Marc, Olena Lukoyanova, Alex Jacobson, Shehzad Jeeva, and Dmitrii F. Perepichka. "ChemInform Abstract: New Azaborine-Thiophene Heteroacenes." ChemInform 42, no. 4 (December 30, 2010): no. http://dx.doi.org/10.1002/chin.201104188.
Повний текст джерелаBunz, Uwe H. F. "ChemInform Abstract: The Larger N-Heteroacenes." ChemInform 41, no. 39 (September 2, 2010): no. http://dx.doi.org/10.1002/chin.201039245.
Повний текст джерелаBunz, Uwe H. F., and Jens U. Engelhart. "The Palladium Way to N-Heteroacenes." Chemistry - A European Journal 22, no. 14 (February 17, 2016): 4680–89. http://dx.doi.org/10.1002/chem.201505018.
Повний текст джерелаYamaguchi, Shigehiro, Caihong Xu та Toshihiro Okamoto. "Ladder π-conjugated materials with main group elements". Pure and Applied Chemistry 78, № 4 (1 січня 2006): 721–30. http://dx.doi.org/10.1351/pac200678040721.
Повний текст джерелаShan, Xiang-Huan, Bo Yang, Jian-Ping Qu, and Yan-Biao Kang. "CuSO4-Catalyzed dual annulation to synthesize O, S or N-containing tetracyclic heteroacenes." Chemical Communications 56, no. 29 (2020): 4063–66. http://dx.doi.org/10.1039/d0cc01172j.
Повний текст джерелаWu, Yimin, Wei Li, Linfeng Jiang, Luoqiang Zhang, Jingbo Lan, and Jingsong You. "Rhodium-catalyzed ortho-heteroarylation of phenols: directing group-enabled switching of the electronic bias for heteroaromatic coupling partner." Chemical Science 9, no. 33 (2018): 6878–82. http://dx.doi.org/10.1039/c8sc02529k.
Повний текст джерелаMüller, Matthias, Lukas Ahrens, Victor Brosius, Jan Freudenberg, and Uwe H. F. Bunz. "Unusual stabilization of larger acenes and heteroacenes." Journal of Materials Chemistry C 7, no. 45 (2019): 14011–34. http://dx.doi.org/10.1039/c9tc04843j.
Повний текст джерелаBrier, Eduard, Christoph Wetzel, Michael Bauer, Elena Mena-Osteritz, Markus Wunderlin, and Peter Bäuerle. "S,N-Heteroacenes Up to a Tridecamer." Chemistry of Materials 31, no. 17 (June 20, 2019): 7007–23. http://dx.doi.org/10.1021/acs.chemmater.9b01652.
Повний текст джерелаAnthony, John E. "Functionalized Acenes and Heteroacenes for Organic Electronics." Chemical Reviews 106, no. 12 (December 2006): 5028–48. http://dx.doi.org/10.1021/cr050966z.
Повний текст джерелаNagahora, Noriyoshi, Tomoko Kushida, Kosei Shioji, and Kentaro Okuma. "Dicationic Heteroacenes Containing Thio- or Selenopyrylium Moieties." Organometallics 38, no. 8 (April 11, 2019): 1800–1808. http://dx.doi.org/10.1021/acs.organomet.9b00100.
Повний текст джерелаBunz, Uwe H. F. "ChemInform Abstract: The Larger Linear N-Heteroacenes." ChemInform 46, no. 35 (August 13, 2015): no. http://dx.doi.org/10.1002/chin.201535264.
Повний текст джерелаMishra, Amaresh. "Material perceptions and advances in molecular heteroacenes for organic solar cells." Energy & Environmental Science 13, no. 12 (2020): 4738–93. http://dx.doi.org/10.1039/d0ee02461a.
Повний текст джерелаLi, Guijie, Shaolin Zhou, Guowei Su, Yuanhong Liu, and Peng George Wang. "Improved Synthesis of Aryl-Substituted Anthracenes and Heteroacenes." Journal of Organic Chemistry 72, no. 25 (December 2007): 9830–33. http://dx.doi.org/10.1021/jo7017334.
Повний текст джерелаWang, Xinyang, Fan Zhang, Jun Liu, Ruizhi Tang, Yubin Fu, Dongqing Wu, Qing Xu, Xiaodong Zhuang, Gufeng He, and Xinliang Feng. "Ladder-Type BN-Embedded Heteroacenes with Blue Emission." Organic Letters 15, no. 22 (October 24, 2013): 5714–17. http://dx.doi.org/10.1021/ol402745r.
Повний текст джерелаHupf, Emanuel, Yuki Tsuchiya, Wayne Moffat, Letian Xu, Masato Hirai, Yuqiao Zhou, Michael J. Ferguson та ін. "A Modular Approach to Phosphorescent π-Extended Heteroacenes". Inorganic Chemistry 58, № 19 (10 вересня 2019): 13323–36. http://dx.doi.org/10.1021/acs.inorgchem.9b02213.
Повний текст джерелаOkamoto, Toshihiro, Kenichi Kudoh, Atsushi Wakamiya, and Shigehiro Yamaguchi. "General Synthesis of Thiophene and Selenophene-Based Heteroacenes." Organic Letters 7, no. 23 (November 2005): 5301–4. http://dx.doi.org/10.1021/ol0523650.
Повний текст джерелаXu, Wan, Mengjie Wang, Zhiying Ma, Zhen Shan, Chunli Li, and Hua Wang. "Selenophene-Based Heteroacenes: Synthesis, Structures, and Physicochemical Behaviors." Journal of Organic Chemistry 83, no. 19 (September 2, 2018): 12154–63. http://dx.doi.org/10.1021/acs.joc.8b02107.
Повний текст джерелаHu, Ben-Lin, Ke Zhang, Cunbin An, Dieter Schollmeyer, Wojciech Pisula, and Martin Baumgarten. "Layered Thiadiazoloquinoxaline-Containing Long Pyrene-Fused N-Heteroacenes." Angewandte Chemie 130, no. 38 (August 27, 2018): 12555–59. http://dx.doi.org/10.1002/ange.201803230.
Повний текст джерелаQu, Hemi, and Chunyan Chi. "ChemInform Abstract: Synthetic Chemistry of Acenes and Heteroacenes." ChemInform 42, no. 14 (March 14, 2011): no. http://dx.doi.org/10.1002/chin.201114237.
Повний текст джерелаGu, Xiao, Bowen Shan, Zikai He, and Qian Miao. "N-Phenylated N-Heteroacenes: Synthesis, Structures, and Properties." ChemPlusChem 82, no. 7 (October 11, 2016): 1034–38. http://dx.doi.org/10.1002/cplu.201600465.
Повний текст джерелаHu, Ben-Lin, Ke Zhang, Cunbin An, Dieter Schollmeyer, Wojciech Pisula, and Martin Baumgarten. "Layered Thiadiazoloquinoxaline-Containing Long Pyrene-Fused N-Heteroacenes." Angewandte Chemie International Edition 57, no. 38 (August 27, 2018): 12375–79. http://dx.doi.org/10.1002/anie.201803230.
Повний текст джерелаCampbell, Josh, and Graeme Day. "Structure prediction of N-heteroacenes as potential organic semiconductors." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C1621. http://dx.doi.org/10.1107/s2053273314083788.
Повний текст джерелаSanthini, P. V., Akhil Krishnan R, Sheba Ann Babu, Betna Shamlin Simethy, Gourab Das, Vakayil K. Praveen, Sunil Varughese, and Jubi John. "One-Pot MCR-Oxidation Approach toward Indole-Fused Heteroacenes." Journal of Organic Chemistry 82, no. 19 (September 25, 2017): 10537–48. http://dx.doi.org/10.1021/acs.joc.7b02039.
Повний текст джерелаBunz, Uwe H. F., and Jan Freudenberg. "N-Heteroacenes and N-Heteroarenes as N-Nanocarbon Segments." Accounts of Chemical Research 52, no. 6 (June 6, 2019): 1575–87. http://dx.doi.org/10.1021/acs.accounts.9b00160.
Повний текст джерелаBunz, Uwe H. F., Jens U. Engelhart, Benjamin D. Lindner, and Manuel Schaffroth. "Large N-Heteroacenes: New Tricks for Very Old Dogs?" Angewandte Chemie International Edition 52, no. 14 (February 18, 2013): 3810–21. http://dx.doi.org/10.1002/anie.201209479.
Повний текст джерелаYang, Shuaijun, Bowen Shan, Xiaomin Xu, and Qian Miao. "Extension of N-Heteroacenes through a Four-Membered Ring." Chemistry - A European Journal 22, no. 19 (March 30, 2016): 6637–42. http://dx.doi.org/10.1002/chem.201600918.
Повний текст джерелаBalaji, Ganapathy, Andrea M. Della Pelle, Bhooshan C. Popere, A. Chandrasekaran, and S. Thayumanavan. "Synthesis and properties of thienopyrrole based heteroacenes – indolodibenzothienopyrrole and dicarbazolodithienopyrrole." Organic & Biomolecular Chemistry 10, no. 17 (2012): 3455. http://dx.doi.org/10.1039/c2ob25087j.
Повний текст джерелаVerbitskiy, Egor V., Ekaterina M. Cheprakova, Nadezhda I. Makarova, Igor V. Dorogan, Anatoly V. Metelitsa, Vladimir I. Minkin, Pavel A. Slepukhin, et al. "Heteroacenes Bearing the Pyrimidine Scaffold: Synthesis, Photophysical and Electrochemical Properties." European Journal of Organic Chemistry 2016, no. 7 (February 8, 2016): 1420–28. http://dx.doi.org/10.1002/ejoc.201501450.
Повний текст джерелаHE, Yuan-Hang, Ren-Jie HUI, Yuan-Ping YI, and Zhi-Gang SHUAI. "Theoretically Rational Designs of Transport Organic Semiconductors Based on Heteroacenes." Chinese Journal of Chemistry 26, no. 6 (June 2008): 1005–10. http://dx.doi.org/10.1002/cjoc.200890179.
Повний текст джерелаMeng, Linghao, Debin Xia, Shihui Liu, Xiaoqing Yi, Fangwei Ding, Ruiqing Fan, and Yulin Yang. "Dimesitylboron Endcapped S,N-Heteroacenes: Syntheses, Photophysical and Fluoride-binding Properties." Chemistry Letters 49, no. 8 (August 5, 2020): 947–51. http://dx.doi.org/10.1246/cl.200290.
Повний текст джерелаWetzel, Christoph, Amaresh Mishra, Elena Mena-Osteritz, Andreas Liess, Matthias Stolte, Frank Würthner, and Peter Bäuerle. "Synthesis and Structural Analysis of Thiophene-Pyrrole-Based S,N-Heteroacenes." Organic Letters 16, no. 2 (December 20, 2013): 362–65. http://dx.doi.org/10.1021/ol403153z.
Повний текст джерелаZhang, You-Dan, Yishi Wu, Yanqing Xu, Qiang Wang, Ke Liu, Jian-Wei Chen, Jing-Jing Cao, Chunfeng Zhang, Hongbing Fu, and Hao-Li Zhang. "Excessive Exoergicity Reduces Singlet Exciton Fission Efficiency of Heteroacenes in Solutions." Journal of the American Chemical Society 138, no. 21 (May 19, 2016): 6739–45. http://dx.doi.org/10.1021/jacs.6b03829.
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