Статті в журналах з теми "Excited State Proton Transfer (ESPT)"
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Wu, Chia-Hua, Lucas José Karas, Henrik Ottosson, and Judy I.-Chia Wu. "Excited-state proton transfer relieves antiaromaticity in molecules." Proceedings of the National Academy of Sciences 116, no. 41 (September 25, 2019): 20303–8. http://dx.doi.org/10.1073/pnas.1908516116.
Повний текст джерелаJouvet, Christophe, Mitsuhiko Miyazaki, and Masaaki Fujii. "Revealing the role of excited state proton transfer (ESPT) in excited state hydrogen transfer (ESHT): systematic study in phenol–(NH3)n clusters." Chemical Science 12, no. 11 (2021): 3836–56. http://dx.doi.org/10.1039/d0sc06877b.
Повний текст джерелаWei, Qiang, Jiyu Wang, Meiyu Zhao, Meixia Zhang, Yuzhi Song, and Peng Song. "A theoretical investigation on excited-state single or double proton transfer process for aloesaponarin I." Canadian Journal of Chemistry 96, no. 1 (January 2018): 83–88. http://dx.doi.org/10.1139/cjc-2017-0533.
Повний текст джерелаPina, João, Mohamed Alnady, Anika Eckert, Ullrich Scherf, and J. Sérgio Seixas de Melo. "Alternating donor–acceptor indigo-cyclopentadithiophene copolymers: competition between excited state conformational relaxation, energy transfer and excited state proton transfer." Materials Chemistry Frontiers 2, no. 2 (2018): 281–90. http://dx.doi.org/10.1039/c7qm00439g.
Повний текст джерелаNovitasari, Dian, Hironari Kamikubo, Yoichi Yamazaki, Mariko Yamaguchi, and Mikio Kataoka. "Excited-State Proton Transfer in Fluorescent Photoactive Yellow Protein Containing 7-Hydroxycoumarin." Advanced Materials Research 896 (February 2014): 85–88. http://dx.doi.org/10.4028/www.scientific.net/amr.896.85.
Повний текст джерелаBasarić, Nikola, Nikola Cindro, Yunyan Hou, Ivana Žabčić, Kata Mlinarić-Majerski, and Peter Wan. "Competing photodehydration and excited-state intramolecular proton transfer (ESIPT) in adamantyl derivatives of 2-phenylphenols." Canadian Journal of Chemistry 89, no. 2 (February 2011): 221–34. http://dx.doi.org/10.1139/v10-102.
Повний текст джерелаYang, Dapeng, Jinfeng Zhao, Guang Yang, Nahong Song, Rui Zheng, and Yusheng Wang. "Elaborating the excited-state proton transfer behaviors for novel 3H-MC and P2H-CH." Organic Chemistry Frontiers 4, no. 10 (2017): 1935–42. http://dx.doi.org/10.1039/c7qo00398f.
Повний текст джерелаYang, Dapeng, and Ruiquan Qi. "Effects of intermolecular hydrogen bonding on the excited-state proton transfer properties of the cinnamonitrile–methanol complex." Canadian Journal of Chemistry 91, no. 3 (March 2013): 229–34. http://dx.doi.org/10.1139/cjc-2012-0368.
Повний текст джерелаJoshi, Hem C., and Liudmil Antonov. "Excited-State Intramolecular Proton Transfer: A Short Introductory Review." Molecules 26, no. 5 (March 9, 2021): 1475. http://dx.doi.org/10.3390/molecules26051475.
Повний текст джерелаZhao, Jinfeng, and Peng Li. "The investigation of ESPT for 2,8-diphenyl-3,7-dihydroxy-4H,6H-pyrano[3,2-g]-chromene-4,6-dione: single or double?" RSC Advances 5, no. 90 (2015): 73619–25. http://dx.doi.org/10.1039/c5ra14601a.
Повний текст джерелаGuo, Yang Xue, Xiang Hong Kong, Wei Yang, and Jia Jin Zheng. "Study on All Optical Switching Effect of Excited State Proton Transfer Organic Molecule 3-Hydroxyflavone." Advanced Materials Research 482-484 (February 2012): 830–34. http://dx.doi.org/10.4028/www.scientific.net/amr.482-484.830.
Повний текст джерелаAdamoczky, Anita, Tibor Nagy, Péter Pál Fehér, Veronika Pardi-Tóth, Ákos Kuki, Lajos Nagy, Miklos Zsuga, and Sándor Kéki. "Isocyanonaphthol Derivatives: Excited-State Proton Transfer and Solvatochromic Properties." International Journal of Molecular Sciences 23, no. 13 (June 29, 2022): 7250. http://dx.doi.org/10.3390/ijms23137250.
Повний текст джерелаYang, Dapeng, Min Jia, Xiaoyan Song та Qiaoli Zhang. "Elaborating a new excited state intramolecular proton transfer (ESPT) mechanism for a new π-conjugated dye 2, 2′-((5-(2-(4-methoxyphenyl)ethenyl)-benzene-1,1-diyl)-bis-(nitrilomethylylidene)-diphenol)". Canadian Journal of Chemistry 96, № 3 (березень 2018): 351–57. http://dx.doi.org/10.1139/cjc-2017-0628.
Повний текст джерелаDonati, Greta, and Nadia Rega. "Direct or Indirect ESPT Mechanism in CFP psamFP488? A Theoretical-Computational Investigation." International Journal of Molecular Sciences 23, no. 24 (December 9, 2022): 15640. http://dx.doi.org/10.3390/ijms232415640.
Повний текст джерелаSahu, Saugata, Minati Das, Aditya Kumar Bharti, and G. Krishnamoorthy. "Proton transfer triggered proton transfer: a self-assisted twin excited state intramolecular proton transfer." Physical Chemistry Chemical Physics 20, no. 42 (2018): 27131–39. http://dx.doi.org/10.1039/c8cp03835j.
Повний текст джерелаKerdpol, Khanittha, Rathawat Daengngern, Chanchai Sattayanon, Supawadee Namuangruk, Thanyada Rungrotmongkol, Peter Wolschann, Nawee Kungwan та Supot Hannongbua. "Effect of Water Microsolvation on the Excited-State Proton Transfer of 3-Hydroxyflavone Enclosed in γ-Cyclodextrin". Molecules 26, № 4 (5 лютого 2021): 843. http://dx.doi.org/10.3390/molecules26040843.
Повний текст джерелаTang, Longteng, Liangdong Zhu, Miles Taylor, Yanli Wang, S. Remington, and Chong Fang. "Excited State Structural Evolution of a GFP Single-Site Mutant Tracked by Tunable Femtosecond-Stimulated Raman Spectroscopy." Molecules 23, no. 9 (September 1, 2018): 2226. http://dx.doi.org/10.3390/molecules23092226.
Повний текст джерелаHu, Shanshan, Kun Liu, Yuanzuo Li, Qianqian Ding, Wei Peng, and Maodu Chen. "Investigation of excited-state intramolecular proton transfer coupled charge transfer reaction of paeonol." Canadian Journal of Chemistry 92, no. 4 (April 2014): 274–78. http://dx.doi.org/10.1139/cjc-2013-0286.
Повний текст джерелаNelson, Kacie J., Paige J. Brown, Holly E. Rudel, and Kana Takematsu. "Divergent excited state proton transfer reactions of bifunctional photoacids 1-ammonium-2-naphthol and 3-ammonium-2-naphthol in water and methanol." Physical Chemistry Chemical Physics 21, no. 44 (2019): 24383–92. http://dx.doi.org/10.1039/c9cp05269k.
Повний текст джерелаLiu, Lei, and Bingqing Sun. "pH-related fluorescence quenching mechanism of pterin derivatives and the effects of 6-site substituents." Canadian Journal of Chemistry 96, no. 4 (April 2018): 404–10. http://dx.doi.org/10.1139/cjc-2017-0644.
Повний текст джерелаQuina, Frank H., Paulo F. Moreira, Carolina Vautier-Giongo, Daniel Rettori, Rita F. Rodrigues, Adilson A. Freitas, Palmira F. Silva, and António L. Maçanita. "Photochemistry of anthocyanins and their biological role in plant tissues." Pure and Applied Chemistry 81, no. 9 (August 19, 2009): 1687–94. http://dx.doi.org/10.1351/pac-con-08-09-28.
Повний текст джерелаBailey-Darland, Sullivan, Taylor D. Krueger, and Chong Fang. "Ultrafast Spectroscopies of Nitrophenols and Nitrophenolates in Solution: From Electronic Dynamics and Vibrational Structures to Photochemical and Environmental Implications." Molecules 28, no. 2 (January 6, 2023): 601. http://dx.doi.org/10.3390/molecules28020601.
Повний текст джерелаBasari?, Nikola, and Peter Wan. "Excited state proton transfer (ESPT) from phenol to nitrogen and carbon in (2-hydroxyphenyl)pyridines." Photochemical & Photobiological Sciences 5, no. 7 (2006): 656. http://dx.doi.org/10.1039/b600826g.
Повний текст джерелаTseng, Huan-Wei, Jiun-Yi Shen, Ting-Yi Kuo, Ting-Syun Tu, Yi-An Chen, Alexander P. Demchenko, and Pi-Tai Chou. "Excited-state intramolecular proton-transfer reaction demonstrating anti-Kasha behavior." Chemical Science 7, no. 1 (2016): 655–65. http://dx.doi.org/10.1039/c5sc01945a.
Повний текст джерелаLI, YUANZUO, SHASHA LIU, LILI ZHAO, MAODU CHEN, FENGCAI MA, and YONG DING. "EXCITED-STATE INTRAMOLECULAR ELECTRON TRANSFER COUPLED WITH EXCITED-STATE INTRAMOLECULAR PROTON TRANSFER IN PHOTOINDUCED ENOL TO KETO TAUTOMERIZATION." Journal of Theoretical and Computational Chemistry 08, supp01 (January 2009): 1073–86. http://dx.doi.org/10.1142/s0219633609005246.
Повний текст джерелаLiu, Xiumin, Heyao Yuan, Yuxi Wang, Yaping Tao, Yi Wang, and Yingmin Hou. "Theoretical Investigation of Excited-State Intramolecular Double-Proton Transfer Mechanism of Substituent Modified 1, 3-Bis (2-Pyridylimino)-4,7-Dihydroxyisoindole in Dichloromethane Solution." Journal of Computational Biophysics and Chemistry 20, no. 07 (October 13, 2021): 707–18. http://dx.doi.org/10.1142/s2737416521500423.
Повний текст джерелаPadalkar, Vikas S., and Shu Seki. "Excited-state intramolecular proton-transfer (ESIPT)-inspired solid state emitters." Chemical Society Reviews 45, no. 1 (2016): 169–202. http://dx.doi.org/10.1039/c5cs00543d.
Повний текст джерелаDommett, Michael, and Rachel Crespo-Otero. "Excited state proton transfer in 2′-hydroxychalcone derivatives." Physical Chemistry Chemical Physics 19, no. 3 (2017): 2409–16. http://dx.doi.org/10.1039/c6cp07541j.
Повний текст джерелаConsuelo Jiménez, M., Miguel A. Miranda, and Rosa Tormos. "Photocyclization of 2-cinnamylphenols via excited state proton transfer (ESPT) involving the lowest-lying styrenic singlet." Tetrahedron 53, no. 43 (October 1997): 14729–36. http://dx.doi.org/10.1016/s0040-4020(97)00942-3.
Повний текст джерелаPuente-Muñoz, Virginia, Jose M. Paredes, Sandra Resa, Ana M. Ortuño, Eva M. Talavera, Delia Miguel, Juan M. Cuerva, and Luis Crovetto. "Efficient acetate sensor in biological media based on a selective Excited State Proton Transfer (ESPT) reaction." Sensors and Actuators B: Chemical 250 (October 2017): 623–28. http://dx.doi.org/10.1016/j.snb.2017.04.191.
Повний текст джерелаLiu, Zong-Ying, Jiun-Wei Hu, Teng-Hsing Huang, Kew-Yu Chen, and Pi-Tai Chou. "Excited-state intramolecular proton transfer in the kinetic-control regime." Physical Chemistry Chemical Physics 22, no. 39 (2020): 22271–78. http://dx.doi.org/10.1039/d0cp03408h.
Повний текст джерелаGajst, Oren, Georgi Gary Rozenman, and Dan Huppert. "Anomalous Rate of H+ and D+ Excited-State Proton Transfer (ESPT) in H2O/D2O Mixtures: Irreversible ESPT in 1-Naphthol-4-sulfonate." Journal of Physical Chemistry A 122, no. 1 (December 19, 2017): 209–16. http://dx.doi.org/10.1021/acs.jpca.7b10684.
Повний текст джерелаYuan, Huijuan, Xugeng Guo, and Jinglai Zhang. "Ab initio insights into the mechanism of excited-state intramolecular proton transfer triggered by the second excited singlet state of a fluorescent dye: an anti-Kasha behavior." Materials Chemistry Frontiers 3, no. 6 (2019): 1225–30. http://dx.doi.org/10.1039/c9qm00179d.
Повний текст джерелаWang, Yu-Hsuan, and Peter Wan. "Excited state intramolecular proton transfer (ESIPT) in dihydroxyphenyl anthracenes." Photochemical & Photobiological Sciences 10, no. 12 (2011): 1934. http://dx.doi.org/10.1039/c1pp05187c.
Повний текст джерелаFan, Ka Wa, Hoi Ling Luk, and David Lee Phillips. "Anti-Kasha Behavior of 3-Hydroxyflavone and Its Derivatives." International Journal of Molecular Sciences 22, no. 20 (October 14, 2021): 11103. http://dx.doi.org/10.3390/ijms222011103.
Повний текст джерелаWang, Ye, Hui Li, and Ying Shi. "Evidence for hydrogen-bonded ammonia wire influencing the ESMPT process of the 7-hydroxy-4-methylcoumarin·(NH3)3 cluster." New Journal of Chemistry 39, no. 9 (2015): 7026–32. http://dx.doi.org/10.1039/c5nj01079a.
Повний текст джерелаGöbel, Dominik, Daniel Duvinage, Tim Stauch, and Boris J. Nachtsheim. "Nitrile-substituted 2-(oxazolinyl)-phenols: minimalistic excited-state intramolecular proton transfer (ESIPT)-based fluorophores." Journal of Materials Chemistry C 8, no. 27 (2020): 9213–25. http://dx.doi.org/10.1039/d0tc00776e.
Повний текст джерелаBursulaya, B. D., S. I. Druzhinin, and B. M. Uzhinov. "Fast dynamic excited state proton transfer (ESPT) reaction of weak oxoaromatic bases. Aminocoumarins with fixed amino group." Journal of Photochemistry and Photobiology A: Chemistry 92, no. 3 (December 1995): 163–72. http://dx.doi.org/10.1016/1010-6030(95)04130-x.
Повний текст джерелаHuang, Fuhua, Beibei An, Yumiao Jiang, Shuopan Dun, Jinglai Zhang, and Xugeng Guo. "Theoretical investigation of excited-state proton transfer (ESPT) for 2,5-bis(2-benzothiazolyl)hydroquinone: single or double?" Molecular Physics 118, no. 14 (December 22, 2019): e1705413. http://dx.doi.org/10.1080/00268976.2019.1705413.
Повний текст джерелаSolaris, Janak, Taylor D. Krueger, Cheng Chen, and Chong Fang. "Photogrammetry of Ultrafast Excited-State Intramolecular Proton Transfer Pathways in the Fungal Pigment Draconin Red." Molecules 28, no. 8 (April 16, 2023): 3506. http://dx.doi.org/10.3390/molecules28083506.
Повний текст джерелаReszka, Milena, Illia E. Serdiuk, Karol Kozakiewicz, Andrzej Nowacki, Henryk Myszka, Piotr Bojarski та Beata Liberek. "Influence of a 4′-substituent on the efficiency of flavonol-based fluorescent indicators of β-glycosidase activity". Organic & Biomolecular Chemistry 18, № 38 (2020): 7635–48. http://dx.doi.org/10.1039/d0ob01505a.
Повний текст джерелаZhu, Hanming, Pan Ma, You Qian, Jiaoyun Xia, Fuchun Gong, Lusen Chen, and Lujie Xu. "Spectral Properties Echoing the Tautomerism of Milrinone and Its Application to Fe3+ Ion Sensing and Protein Staining." Biosensors 12, no. 10 (September 20, 2022): 777. http://dx.doi.org/10.3390/bios12100777.
Повний текст джерелаSreedevi, K. C. Gowri, Ajesh P. Thomas, K. H. Aparna, Renuka Pradhan, M. L. P. Reddy, U. Lourderaj, and A. Srinivasan. "Photoenolization via excited state double proton transfer induces “turn on” fluorescence in diformyl diaryl dipyrromethane." Chem. Commun. 50, no. 63 (2014): 8667–69. http://dx.doi.org/10.1039/c4cc03668a.
Повний текст джерелаGöbel, Dominik, Pascal Rusch, Daniel Duvinage, Nadja C. Bigall, and Boris J. Nachtsheim. "Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores." Chemical Communications 56, no. 98 (2020): 15430–33. http://dx.doi.org/10.1039/d0cc05780k.
Повний текст джерелаBudzák, Šimon, and Denis Jacquemin. "Excited state intramolecular proton transfer in julolidine derivatives: an ab initio study." Physical Chemistry Chemical Physics 20, no. 38 (2018): 25031–38. http://dx.doi.org/10.1039/c8cp04356f.
Повний текст джерелаHan, Jianhui, Xiaochun Liu, Chaofan Sun, You Li, Hang Yin, and Ying Shi. "Ingenious modification of molecular structure effectively regulates excited-state intramolecular proton and charge transfer: a theoretical study based on 3-hydroxyflavone." RSC Advances 8, no. 52 (2018): 29589–97. http://dx.doi.org/10.1039/c8ra05812a.
Повний текст джерелаJiang, Guanyu, Feiyan Li, Jianzhong Fan, Yuzhi Song, Chuan-Kui Wang, and Lili Lin. "Theoretical perspective for luminescent mechanism of thermally activated delayed fluorescence emitter with excited-state intramolecular proton transfer." Journal of Materials Chemistry C 8, no. 1 (2020): 98–108. http://dx.doi.org/10.1039/c9tc05299b.
Повний текст джерелаMatsumoto, Hisato, Yoshinobu Nishimura, and Tatsuo Arai. "Excited-state intermolecular proton transfer dependent on the substitution pattern of anthracene–diurea compounds involved in fluorescent ON1–OFF–ON2 response by the addition of acetate ions." Organic & Biomolecular Chemistry 15, no. 31 (2017): 6575–83. http://dx.doi.org/10.1039/c7ob01376k.
Повний текст джерелаQin, Xiaoling, Guoqiang Zhou, Pan Ma, Jiaoyun Xia, Fuchun Gong, Lusen Chen, and Lujie Xu. "A polystyrene-based ESIPT fluorescent polymeric probe for highly sensitive detection of chromium(vi) ions and protein staining." RSC Advances 13, no. 36 (2023): 25350–59. http://dx.doi.org/10.1039/d3ra02698a.
Повний текст джерелаZou, Wu, Qinge Wang, Fuchun Gong, Yinjie Kuang, Jiaoyun Xia, and Zhong Cao. "Polymer nanoparticles integrated with ESIPT modules for sensing cysteine based on modulation of their tautomeric emission." Analytical Methods 11, no. 29 (2019): 3714–20. http://dx.doi.org/10.1039/c9ay00888h.
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