Статті в журналах з теми "Electron donating and electron accepting groups"
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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 джерелаSutradhar, Tanushree, and Anirban Misra. "Theoretical Study on the Nonlinear Optical Property of Boron Nitride Nanoclusters Functionalized by Electron Donating and Electron Accepting Groups." Journal of Physical Chemistry A 125, no. 12 (March 22, 2021): 2436–45. http://dx.doi.org/10.1021/acs.jpca.0c11101.
Повний текст джерелаJabłoński, Mirosław. "The Ultrashort Spike–Ring Interaction in Substituted Iron Maiden Molecules." Molecules 28, no. 5 (February 28, 2023): 2244. http://dx.doi.org/10.3390/molecules28052244.
Повний текст джерелаSchmitt, Volker, Stefan Glang, and Heiner Detert. "Synthesis, Optical and Electrical Properties of Oligo(phenylenevinylene)s Substituted with Electron-Accepting Sulfonyl Groups." Advances in Science and Technology 75 (October 2010): 103–7. http://dx.doi.org/10.4028/www.scientific.net/ast.75.103.
Повний текст джерелаKosaka, Yozo, and Toshiyuki Uryu. "Synthesis and Liquid Crystallinity of Polymethacrylate Systems Containing both Electron-Donating (Quinolinylmethylene)aniline and Electron-Accepting (4'-Nitrobenzylidene)aniline Groups." Macromolecules 28, no. 24 (November 1995): 8295–301. http://dx.doi.org/10.1021/ma00128a045.
Повний текст джерелаGreulich, Tobias W., Naoya Suzuki, Constantin G. Daniliuc, Aiko Fukazawa, Eriko Yamaguchi, Armido Studer, and Shigehiro Yamaguchi. "A biphenyl containing two electron-donating and two electron-accepting moieties: a rigid and small donor–acceptor–donor ladder system." Chemical Communications 52, no. 11 (2016): 2374–77. http://dx.doi.org/10.1039/c5cc03063c.
Повний текст джерелаMaleckaitė, Karolina, Domantas Narkevičius, Rugilė Žilėnaitė, Jelena Dodonova-Vaitkūnienė, Stepas Toliautas, Sigitas Tumkevičius, and Aurimas Vyšniauskas. "Give or Take: Effects of Electron-Accepting/-Withdrawing Groups in Red-Fluorescent BODIPY Molecular Rotors." Molecules 27, no. 1 (December 21, 2021): 23. http://dx.doi.org/10.3390/molecules27010023.
Повний текст джерелаZgierski, Marek Z., and Edward C. Lim. "On the mechanism of intramolecular charge transfer in para-disubstituted diphenylacetylenes containing electron-donating and electron-accepting groups: role of state in electron-transfer dynamics." Chemical Physics Letters 393, no. 1-3 (July 2004): 143–49. http://dx.doi.org/10.1016/j.cplett.2004.05.098.
Повний текст джерелаLabidi, N. S. "Nonlinear Optical Properties of Novel Mono-O-Hydroxy Bidentate Schiff Base: Quantum Chemical Calculations." International Journal of Metals 2013 (December 17, 2013): 1–5. http://dx.doi.org/10.1155/2013/964328.
Повний текст джерелаWieczorkiewicz, Paweł A., Halina Szatylowicz, and Tadeusz M. Krygowski. "Energetic and Geometric Characteristics of Substituents, Part 3: The Case of NO2 and NH2 Groups in Their Mono-Substituted Derivatives of Six-Membered Heterocycles." Symmetry 14, no. 1 (January 12, 2022): 145. http://dx.doi.org/10.3390/sym14010145.
Повний текст джерелаHou, Jiapeng, Deepak H. Veeregowda, Joop de Vries, Henny C. Van der Mei, and Henk J. Busscher. "Structured free-water clusters near lubricating surfaces are essential in water-based lubrication." Journal of The Royal Society Interface 13, no. 123 (October 2016): 20160554. http://dx.doi.org/10.1098/rsif.2016.0554.
Повний текст джерелаLin, Haitao, Liyun Ding, Bingyu Zhang, and Jun Huang. "Detection of nitrite based on fluorescent carbon dots by the hydrothermal method with folic acid." Royal Society Open Science 5, no. 5 (May 2018): 172149. http://dx.doi.org/10.1098/rsos.172149.
Повний текст джерелаHamada, Tatsuo, Atsushi Nishida, and Osamu Yonemitsu. "Selective removal of electron-accepting p-toluene- and naphthalenesulfonyl protecting groups for amino function via photoinduced donor acceptor ion pairs with electron-donating aromatics." Journal of the American Chemical Society 108, no. 1 (January 1986): 140–45. http://dx.doi.org/10.1021/ja00261a023.
Повний текст джерелаFiodorova, Irina, Tomas Serevičius, Rokas Skaisgiris, Saulius Juršėnas, and Sigitas Tumkevicius. "Substituent effect on TADF properties of 2-modified 4,6-bis(3,6-di-tert-butyl-9-carbazolyl)-5-methylpyrimidines." Beilstein Journal of Organic Chemistry 18 (May 5, 2022): 497–507. http://dx.doi.org/10.3762/bjoc.18.52.
Повний текст джерелаXu, Zhiyuan, Zhen Yang, Hongping Wang, and Jie Jiang. "Assessing Redox Properties of Natural Organic Matters with regard to Electron Exchange Capacity and Redox-Active Functional Groups." Journal of Chemistry 2020 (April 14, 2020): 1–8. http://dx.doi.org/10.1155/2020/2698213.
Повний текст джерелаAbdullah, Kiran, Yanli Chen, and Jianzhuang Jiang. "Synthesis, fabrication of self-assembled film and ambipolar chemical sensing properties of triple-decker (phthalocyaninato) (porphyrinato) europium complex." Journal of Porphyrins and Phthalocyanines 21, no. 12 (December 2017): 893–99. http://dx.doi.org/10.1142/s1088424617500985.
Повний текст джерелаWei, Jinguang, Yang Xu, Minzhen Bao, Yanglun Yu, and Wenji Yu. "Effect of Resin Content on the Surface Wettability of Engineering Bamboo Scrimbers." Coatings 13, no. 1 (January 16, 2023): 203. http://dx.doi.org/10.3390/coatings13010203.
Повний текст джерелаKarabıyık, Hasan, Cumhur Kırılmış, and Hande Karabıyık. "Geometry dependence of electron donating or accepting abilities of amine groups in 4,4′-disulfanediylbis(methylene)dithiazol-2-amine: Pyramidal versus planar." Journal of Molecular Structure 1141 (August 2017): 650–59. http://dx.doi.org/10.1016/j.molstruc.2017.04.022.
Повний текст джерелаHan, Deming, Xiaoqiang Ji, Lihui Zhao, and Chunying Pang. "Theoretical insight on electronic structure and photophysical properties of a series of cyclometalated iridium(III) complexes bearing the substituted phenylpyrazole with different electron-donating or electron-accepting groups." Photochemical & Photobiological Sciences 20, no. 11 (October 28, 2021): 1487–95. http://dx.doi.org/10.1007/s43630-021-00125-8.
Повний текст джерелаMorales-Verdejo, Cesar, Ivonne Chávez, Rodrigo Faúndez, Francisco Castillo, Marcelo Preite, Eduardo Schott, Ximena Zarate, Juan Manriquez, and Elies Molins. "Novel and Convenient Synthesis of 2,7-Dialkyl-1,8-dihydro-as-indacenes." Synthesis 51, no. 02 (September 11, 2018): 441–49. http://dx.doi.org/10.1055/s-0037-1610631.
Повний текст джерелаHu, Zheyao, and Jordi Marti. "In Silico Drug Design of Benzothiadiazine Derivatives Interacting with Phospholipid Cell Membranes." Membranes 12, no. 3 (March 17, 2022): 331. http://dx.doi.org/10.3390/membranes12030331.
Повний текст джерелаMolski, Marcin. "Density Functional Theory Studies on the Chemical Reactivity of Allyl Mercaptan and Its Derivatives." Molecules 29, no. 3 (January 31, 2024): 668. http://dx.doi.org/10.3390/molecules29030668.
Повний текст джерелаMashweu, Adelaide R., Varsha P. Chhiba-Govindjee, Moira L. Bode, and Dean Brady. "Substrate Profiling of the Cobalt Nitrile Hydratase from Rhodococcus rhodochrous ATCC BAA 870." Molecules 25, no. 1 (January 6, 2020): 238. http://dx.doi.org/10.3390/molecules25010238.
Повний текст джерелаDuan, Jingtao, Zhiyuan Xu, Zhen Yang, and Jie Jiang. "Insight to Microbial Fe(III) Reduction Mediated by Redox-Active Humic Acids with Varied Redox Potentials." International Journal of Environmental Research and Public Health 18, no. 13 (June 24, 2021): 6807. http://dx.doi.org/10.3390/ijerph18136807.
Повний текст джерелаGallis, David E., James A. Warshaw, Bruce J. Acken та DeLanson R. Crist. "Electronic Nature of α-Methoxy, Amino, Cyano, and Mercapto Nitrones". Collection of Czechoslovak Chemical Communications 58, № 1 (1993): 125–41. http://dx.doi.org/10.1135/cccc19930125.
Повний текст джерелаZawadzka, Magdalena, Paweł Nitschke, Marta Musioł, Mariola Siwy, Sandra Pluczyk-Małek, Damian Honisz, and Mieczysław Łapkowski. "Naphthalene Phthalimide Derivatives as Model Compounds for Electrochromic Materials." Molecules 28, no. 4 (February 11, 2023): 1740. http://dx.doi.org/10.3390/molecules28041740.
Повний текст джерелаKharchenko, Oksana, Vitalii Smokal, and Oleksii Kolendo. "SYNTHESIS AND PHOTOCHEMICAL PROPERTIES OF NEW STYRYLQUINOLINE-CONTAINING POLYMERS." Ukrainian Chemistry Journal 88, no. 5 (June 24, 2022): 15–24. http://dx.doi.org/10.33609/2708-129x.88.05.2022.15-24.
Повний текст джерелаGudeika, D., R. Lygaitis, V. Mimaitė, J. V. Grazulevicius, V. Jankauskas, M. Lapkowski, and P. Data. "Hydrazones containing electron-accepting and electron-donating moieties." Dyes and Pigments 91, no. 1 (October 2011): 13–19. http://dx.doi.org/10.1016/j.dyepig.2011.02.002.
Повний текст джерелаScharl, Tobias, Alejandro Cadranel, Philipp Haines, Volker Strauss, Sarah Bernhardt, Sonia Vela, Carmen Atienza, Franziska Gröhn, Nazario Martín, and Dirk M. Guldi. "Fine-tuning the assemblies of carbon nanodots and porphyrins." Chemical Communications 54, no. 82 (2018): 11642–44. http://dx.doi.org/10.1039/c8cc05069d.
Повний текст джерелаMoon, Yejin, Chulyeon Lee, Hwajeong Kim, Jisu Park, and Youngkyoo Kim. "Synthesis of indacenodithienothiophene-based conjugated polymers containing electron-donating/accepting comonomers and their phototransistor characteristics." Polymer Chemistry 10, no. 46 (2019): 6324–33. http://dx.doi.org/10.1039/c9py01411j.
Повний текст джерелаWierzbicka, Małgorzata, Irena Bylińska, Cezary Czaplewski, and Wiesław Wiczk. "Experimental and theoretical studies of the spectroscopic properties of simple symmetrically substituted diphenylacetylene derivatives." RSC Advances 5, no. 37 (2015): 29294–303. http://dx.doi.org/10.1039/c5ra01077b.
Повний текст джерелаRajamalli, Pachaiyappan, Dongyang Chen, Wenbo Li, Ifor D. W. Samuel, David B. Cordes, Alexandra M. Z. Slawin, and Eli Zysman-Colman. "Enhanced thermally activated delayed fluorescence through bridge modification in sulfone-based emitters employed in deep blue organic light-emitting diodes." Journal of Materials Chemistry C 7, no. 22 (2019): 6664–71. http://dx.doi.org/10.1039/c9tc01498e.
Повний текст джерелаYue, Yuankai, Tod Grusenmeyer, Zheng Ma, Peng Zhang, Russell H. Schmehl, David N. Beratan, and Igor V. Rubtsov. "Electron transfer rate modulation in a compact Re(i) donor–acceptor complex." Dalton Transactions 44, no. 18 (2015): 8609–16. http://dx.doi.org/10.1039/c4dt02145b.
Повний текст джерелаSchmelzer, M., M. Burghard, S. Roth, and P. Báurle. "New LB Heterostructures Containing Electron Donating and Accepting Molecules." Molecular Crystals and Liquid Crystals 253, no. 1 (August 1, 1994): 173–81. http://dx.doi.org/10.1080/10587259408055256.
Повний текст джерелаKnysh, Iryna, Anna Kozakiewicz-Piekarz, Andrzej Wojtczak, Damian Plażuk, Glib Baryshnikov, Rashid Valiev, Rinat Nasibullin, et al. "Less is more: on the effect of benzannulation on the solid-state emission of difluoroborates." Journal of Materials Chemistry C 9, no. 44 (2021): 15820–30. http://dx.doi.org/10.1039/d1tc03316f.
Повний текст джерелаPang, Xuelei, Xudong Yu, Dongyan Xie, Yajuan Li, Lijun Geng, Jujie Ren, and Xiaoli Zhen. "Tunable multicolor emissions in a monocomponent gel system by varying the solvent, temperature and fluoride anion." Organic & Biomolecular Chemistry 14, no. 47 (2016): 11176–82. http://dx.doi.org/10.1039/c6ob02007k.
Повний текст джерелаJeon, Young Pyo, Kyu Sung Kim, Kyeong Kyun Lee, In Kyu Moon, Dong Chul Choo, Jun Yeob Lee, and Tae Whan Kim. "Blue phosphorescent organic light-emitting devices based on carbazole/thioxanthene-S,S-dioxide with a high glass transition temperature." Journal of Materials Chemistry C 3, no. 24 (2015): 6192–99. http://dx.doi.org/10.1039/c5tc00279f.
Повний текст джерелаÖztürk, Gülsiye, Hasan Karabıyık, Muhittin Aygün, Serap Alp, and Serdar Özçelik. "Tuning Photoinduced Intramolecular Electron Transfer by Electron Accepting and Donating Substituents in Oxazolones." Journal of Fluorescence 23, no. 4 (March 15, 2013): 733–44. http://dx.doi.org/10.1007/s10895-013-1198-6.
Повний текст джерелаHonório, K. M., and A. B. F. Da Silva. "An AM1 study on the electron-donating and electron-accepting character of biomolecules." International Journal of Quantum Chemistry 95, no. 2 (2003): 126–32. http://dx.doi.org/10.1002/qua.10661.
Повний текст джерелаGuzauskas, Matas, Dmytro Volyniuk, Ausra Tomkeviciene, Anna Pidluzhna, Algirdas Lazauskas, and Juozas Vidas Grazulevicius. "Dual nature of exciplexes: exciplex-forming properties of carbazole and fluorene hybrid trimers." Journal of Materials Chemistry C 7, no. 1 (2019): 25–32. http://dx.doi.org/10.1039/c8tc04708a.
Повний текст джерелаNakanotani, Hajime, Taro Furukawa, Kei Morimoto, and Chihaya Adachi. "Long-range coupling of electron-hole pairs in spatially separated organic donor-acceptor layers." Science Advances 2, no. 2 (February 2016): e1501470. http://dx.doi.org/10.1126/sciadv.1501470.
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