Добірка наукової літератури з теми "Electron donating and electron accepting groups"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся зі списками актуальних статей, книг, дисертацій, тез та інших наукових джерел на тему "Electron donating and electron accepting groups".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Статті в журналах з теми "Electron donating and electron accepting groups"
Cao, Wei, Kang Wang, Isabelle Ledoux-Rak, and Jianzhuang Jiang. "ABAB-type phthalocyanines simultaneously bearing electron donating and electron accepting groups. Synthesis, spectroscopy, and structure." Inorganic Chemistry Frontiers 3, no. 9 (2016): 1146–51. http://dx.doi.org/10.1039/c6qi00147e.
Повний текст джерелаGudimetla, Vittal B., Liqing Ma, Marlena P. Washington, John L. Payton, M. Cather Simpson, and John D. Protasiewicz. "meta-Terphenyl Phosphaalkenes Bearing Electron-Donating and -Accepting Groups." European Journal of Inorganic Chemistry 2010, no. 6 (February 2010): 854–65. http://dx.doi.org/10.1002/ejic.200900870.
Повний текст джерелаSugihara, Yoshiaki, Naoto Inai, Masayasu Taki, Thomas Baumgartner, Ryosuke Kawakami, Takashi Saitou, Takeshi Imamura, Takeshi Yanai, and Shigehiro Yamaguchi. "Donor–acceptor–acceptor-type near-infrared fluorophores that contain dithienophosphole oxide and boryl groups: effect of the boryl group on the nonradiative decay." Chemical Science 12, no. 18 (2021): 6333–41. http://dx.doi.org/10.1039/d1sc00827g.
Повний текст джерелаWierzbicka, Małgorzata, Irena Bylińska, Artur Sikorski, Cezary Czaplewski, and Wiesław Wiczk. "Experimental and theoretical studies of spectroscopic properties of simple symmetrically substituted diphenylbuta-1,3-diyne derivatives." Photochemical & Photobiological Sciences 14, no. 12 (2015): 2251–60. http://dx.doi.org/10.1039/c5pp00150a.
Повний текст джерелаZhang, Luqiong, Li Tian, Ming Li, Rongxing He, and Wei Shen. "A theoretical study on tuning the electronic structures and photophysical properties of newly designed platinum(ii) complexes by adding substituents on functionalized ligands as highly efficient OLED emitters." Dalton Trans. 43, no. 17 (2014): 6500–6512. http://dx.doi.org/10.1039/c3dt53209g.
Повний текст джерелаSetsoafia, Daniel Dodzi Yao, Kiran Sreedhar Ram, Hooman Mehdizadeh-Rad, David Ompong, and Jai Singh. "Density Functional Theory Simulation of Optical and Photovoltaic Properties of DRTB-T Donor-Based Organic Solar Cells." International Journal of Energy Research 2023 (October 19, 2023): 1–12. http://dx.doi.org/10.1155/2023/6696446.
Повний текст джерелаYang, Fang-Ling, Ka Lu, Xing Yang, Chao-Xian Yan, Rui Wang, Weichun Ye, Pan-Pan Zhou, and Zhaoyong Yang. "Computational investigations of intermolecular interactions between electron-accepting bromo- and iodo-pentafluorobenzene and electron-donating furan and thiophene." New Journal of Chemistry 42, no. 24 (2018): 20101–12. http://dx.doi.org/10.1039/c8nj04611e.
Повний текст джерелаYUASA, MAKOTO, BEAT STEIGER, and FRED C. ANSON. "Hydroxy-substituted Cobalt Tetraphenylporphyrins as Electrocatalysts for the Reduction of O2." Journal of Porphyrins and Phthalocyanines 01, no. 02 (April 1997): 181–88. http://dx.doi.org/10.1002/(sici)1099-1409(199704)1:2<181::aid-jpp22>3.0.co;2-r.
Повний текст джерелаJuma, Juma Mzume, and Said AH Vuai. "Computational studies of the thermodynamic properties, and global and reactivity descriptors of fluorescein dye derivatives in acetonitrile using density functional theory." Journal of Chemical Research 45, no. 7-8 (February 19, 2021): 800–805. http://dx.doi.org/10.1177/1747519821994518.
Повний текст джерелаYamaguchi, Isao, та Ryosuke Yamaji. "Synthesis of hydroxyoligophenylenes containing electron-donating, electron-accepting groups, or π-deficient aromatic ring and their solvatochromic behavior". Journal of Physical Organic Chemistry 30, № 10 (25 листопада 2016): e3671. http://dx.doi.org/10.1002/poc.3671.
Повний текст джерелаДисертації з теми "Electron donating and electron accepting groups"
Sutradhar, Tanushree. "Theoretical investigation on optoelectronic properties of nanoclusters and conjugates." Thesis, University of North Bengal, 2021. http://ir.nbu.ac.in/handle/123456789/4750.
Повний текст джерелаCheng, Hong-Yi, and 陳鴻儀. "The synthesis of porphyrins with electron-withdrawing and -donating groups." Thesis, 2008. http://ndltd.ncl.edu.tw/handle/64541561928294591379.
Повний текст джерела國立中興大學
化學系所
96
Abstract A series of zinc porphyrins with both electron donor and acceptor groups were synthesized for use as NLO chromophores in optoelectronic materials and devices.The porphyrin bridge connecting D and A groups should provide a pathway for strong electronic coupling between D and A. Organic molecules with strong electron donor and electron aceptor groups that are connected by a large conjugated π– electron system usually show high β values, so we utilized a ethynyl unit to extendπ– conjugation of the systems. The preparation of porphyrins with ethyne-linked functional groups can be achieved by the sonogashira cross-coupling method. Light - harvesting arrays that consist of porphyrin and perylene units were synthesized. These arrays show broad absorption in the visible region. The energy transfer between porphyrin and perylene pigments was investigated by fluorescence spectroscopy. We except that porphyrin – perylene systems have high energy conversion efficiency in solar cells.
Частини книг з теми "Electron donating and electron accepting groups"
Bachrach, Steven M. "More Hard Truths." In Thinking Like a Physical Organic Chemist, 130—C13F6. Oxford University Press, 2023. http://dx.doi.org/10.1093/oso/9780197640371.003.0013.
Повний текст джерелаVinduja, Puttanveedu, and Karuvanthodi Muraleedharan. "Theoretical Studies on Anti-Oxidant Activity of the Phytochemical, Coumestrol and Its Derivatives." In Functional Foods - Phytochemicals and Health Promoting Potential. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.96967.
Повний текст джерелаAgrawal, Pratibha S., M. K. N. Yenkie, M. G. Bhotmange, B. D. Deshpande, and S. J. Dhoble. "Degradation of Substituted Benzoic Acids Related to Structural Reactivity." In Water Pollution Sources and Purification: Challenges and Scope, 75–89. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/9789815050684122010006.
Повний текст джерелаHore, P. J. "Chemical shifts." In Nuclear Magnetic Resonance. Oxford University Press, 2015. http://dx.doi.org/10.1093/hesc/9780198703419.003.0002.
Повний текст джерелаKeeler, James, and Peter Wothers. "Transition metals." In Chemical Structure and Reactivity. Oxford University Press, 2013. http://dx.doi.org/10.1093/hesc/9780199604135.003.0019.
Повний текст джерелаMellor, Sarah L., and Donald A. Wellings. "Synthesis of modified peptides." In Fmoc Solid Phase Peptide Synthesis. Oxford University Press, 1999. http://dx.doi.org/10.1093/oso/9780199637256.003.0010.
Повний текст джерелаТези доповідей конференцій з теми "Electron donating and electron accepting groups"
Runser, Claude, Marguerite Barzoukas, Alain Fort, Mireille Blanchard-Desce, and Jean-Marie Lehn. "Push-pull polyenes with enhanced quadratic nonlinear susceptibilities." In The European Conference on Lasers and Electro-Optics. Washington, D.C.: Optica Publishing Group, 1994. http://dx.doi.org/10.1364/cleo_europe.1994.cwf42.
Повний текст джерелаChittibabu, K. G., L. Li, X. Wang, J. Kumar, and S. K. Tripathy. "Thiophene based Nonlinear Optical Chromophore functionalized Epoxy Polymers for Electro-Optic Applications." In Organic Thin Films for Photonic Applications. Washington, D.C.: Optica Publishing Group, 1997. http://dx.doi.org/10.1364/otfa.1997.thc.4.
Повний текст джерелаWong, Ken-Tsung. "Exciplex-forming Systems for High Efficiency OLEDs." In Solar Energy and Light-Emitting Devices. Washington, D.C.: Optica Publishing Group, 2023. http://dx.doi.org/10.1364/seled.2023.stu2d.2.
Повний текст джерелаSmith, David A. M., Scott Williams, P. Jenkner, Robert D. Miller, E. J. Ginsburg, and Robin M. Hochstrasser. "Localization of excitations in silicon chains by electron donating side groups." In Optics Quebec, edited by Roger A. Lessard. SPIE, 1994. http://dx.doi.org/10.1117/12.166345.
Повний текст джерелаLiu, Li, Jie-Ping Shi, Hong-Wen Hu, and Guo-Yuan Lu. "Photophysical properties of tribranched chromophores Based on 1,3,5-triazine core and 3,4-ethyllenedioxythiophene electron-donating end-groups." In 2011 IEEE 4th International Nanoelectronics Conference (INEC). IEEE, 2011. http://dx.doi.org/10.1109/inec.2011.5991650.
Повний текст джерелаMOTOYOSHIYA, J., T. TANAKA, M. KUROE, and Y. NISHII. "CHEMILUMINESCENCE OF 9-BENZYLIDENE-10-METHYLACRIDANS WITH ELECTRON-DONATING GROUPS BY CHEMICALLY GENERATED SINGLET OXYGEN – APPLICATION TO METAL ION SENSING USING AZACROWNED COMPOUND." In Proceedings of the 15th International Symposium. WORLD SCIENTIFIC, 2008. http://dx.doi.org/10.1142/9789812839589_0054.
Повний текст джерела