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Journal articles on the topic 'Intramolecular excimer'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Lewis, Frederick D., and Todd L. Kurth. "Intramolecular excimer fluorescence from folded ground state rotamers of N,N'dimethyl-N,N'-dipyrenylurea protophanes." Canadian Journal of Chemistry 81, no. 6 (2003): 770–76. http://dx.doi.org/10.1139/v03-059.

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The molecular structure, absorption, and fluorescence spectra of N,N'-dimethyl-N,N'-di-1-pyrenylurea and N,N'-dimethyl-N,N'-di-2-pyrenylurea have been investigated and compared to the properties of N,N,N'-trimethyl-N'-pyrenylurea model compounds. Di-1-pyrenylurea exists as a mixture of folded (E,E) syn- and anti-rotamers that interconvert via flipping of one of the pyrene rings to an unfolded (E,Z) rotamer geometry. The symmetric di-2-pyrenylurea exists as a single folded (E,E) conformation which is in equilibrium with a less-stable, unfolded (E,Z) rotamer. The absorption and fluorescence spec

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2

Lee, Sam, and Mitchell A. Winnik. "Photophysical behavior of oligoethylene glycols labeled with naphthalene carboxylate and phosphate esters." Canadian Journal of Chemistry 72, no. 6 (1994): 1587–95. http://dx.doi.org/10.1139/v94-198.

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The fluorescence spectra of tri- and tetraethylene glycol esterified with 2-(1-naphthyl)ethyl ethyl phosphate and 2-(1-naphthyl)ethyl 2-(ethoxy)ethyl phosphate were studied in dilute solutions of tetrahydrofuran (THF) and diethyl ether. They were compared with the fluorescence from tri- and tetraethylene glycol esterified with 1-naphthyl acetic acid. These compounds form intramolecular excimers. The extent of excimer formation is not extensive, but the relative amount of excimer emission from these compounds varies with the choice of solvent. Three synthetic intermediates to the phosphates, th

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3

Kondo, Shin-ichi, Yuka Taguchi, and Yi Bie. "Solvent dependent intramolecular excimer emission of di(1-pyrenyl)silane and di(1-pyrenyl)methane derivatives." RSC Advances 5, no. 8 (2015): 5846–49. http://dx.doi.org/10.1039/c4ra12153h.

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Di(1-pyrenyl)silane and methane derivatives showed unprecedented intramolecular excimer emission in polar organic solvents such as DMSO and the ratio of excimer/monomer emissions strongly depends on the dielectric constants of the solvents.

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4

Itoh, Takao, Mei-Hui Yang, and Chyuan Chou. "Intramolecular excimer formation in diphenylsiloxane-based copolymers." Journal of the Chemical Society, Faraday Transactions 92, no. 19 (1996): 3593. http://dx.doi.org/10.1039/ft9969203593.

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5

Barros, T. C., P. Berci Filho, V. G. Toscano, and M. J. Politi. "Intramolecular excimer formation from 1,8-N-alkyldinaphthalimides." Journal of Photochemistry and Photobiology A: Chemistry 89, no. 2 (1995): 141–46. http://dx.doi.org/10.1016/1010-6030(95)04040-m.

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6

Deng, Yulin, Samuel Kin-Man Lai, Linghui Kong, and Ho Yu Au-Yeung. "Fine-tuning of the optical output in a dual responsive catenane switch." Chemical Communications 57, no. 23 (2021): 2931–34. http://dx.doi.org/10.1039/d1cc00310k.

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7

Ilharco, L. M., A. M. Santos, M. J. Silva, and J. M. G. Martinho. "Intramolecular Pyrene Excimer Probing the Sol-Gel Process." Langmuir 11, no. 7 (1995): 2419–22. http://dx.doi.org/10.1021/la00007a018.

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8

Chanmungkalakul, Supphachok, Vuthichai Ervithayasuporn, Patcharaporn Boonkitti, et al. "Anion identification using silsesquioxane cages." Chemical Science 9, no. 40 (2018): 7753–65. http://dx.doi.org/10.1039/c8sc02959h.

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9

Cho, Dae Won, and Dae Won Cho. "Excimer and exciplex emissions of 1,8-naphthalimides caused by aggregation in extremely polar or nonpolar solvents." New J. Chem. 38, no. 6 (2014): 2233–36. http://dx.doi.org/10.1039/c3nj01473h.

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10

Mikata, Yuji, Risa Ohnishi, Anna Ugai, et al. "OFF–ON–OFF fluorescent response of N,N,N′,N′-tetrakis(1-isoquinolylmethyl)-2-hydroxy-1,3-propanediamine (1-isoHTQHPN) toward Zn2+." Dalton Transactions 45, no. 17 (2016): 7250–57. http://dx.doi.org/10.1039/c6dt00506c.

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11

Maeda, Hajime, Masato Hironishi, Rikiya Ishibashi, Kazuhiko Mizuno, and Masahito Segi. "Synthesis and fluorescence properties of dioxa-, dithia-, and diselena-[3.3](1,3)pyrenophanes." Photochemical & Photobiological Sciences 16, no. 2 (2017): 228–37. http://dx.doi.org/10.1039/c6pp00402d.

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The fluorescence spectra of [3.3](1,3)pyrenophanes in solution contain both monomer and intramolecular excimer emission bands. The ratio of the intensities is controlled by solvent polarity and temperature.

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12

Karmakar, Rana, and Anunay Samanta. "Intramolecular excimer formation kinetics in room temperature ionic liquids." Chemical Physics Letters 376, no. 5-6 (2003): 638–45. http://dx.doi.org/10.1016/s0009-2614(03)01040-6.

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13

Alamiry, Mohammed A. H., Andrew C. Benniston, Graeme Copley, Anthony Harriman, and David Howgego. "Intramolecular Excimer Formation for Covalently Linked Boron Dipyrromethene Dyes." Journal of Physical Chemistry A 115, no. 44 (2011): 12111–19. http://dx.doi.org/10.1021/jp2070419.

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14

Esteban, M. Isabel, M. Reyes Vigil, Valent�n Moreno-Montes, and Carmen S. Renamayor. "Intramolecular excimer formation in copolymers of methylmethacrylate and indene." Polymer International 49, no. 7 (2000): 663–68. http://dx.doi.org/10.1002/1097-0126(200007)49:7<663::aid-pi428>3.0.co;2-l.

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15

Boong Chung, Young, Du-Jeon Jang, Dongho Kim, Minyung Lee, Hyun Sook Kim, and Bong Hyun Boo. "Intramolecular excimer formation dynamics of bis (9-fluorenyl) methane." Chemical Physics Letters 176, no. 5 (1991): 453–58. http://dx.doi.org/10.1016/0009-2614(91)90236-3.

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16

Hashimoto, Yuichiro, Takuya Nakashima, Daiya Shimizu, and Tsuyoshi Kawai. "Photoswitching of an intramolecular chiral stack in a helical tetrathiazole." Chemical Communications 52, no. 29 (2016): 5171–74. http://dx.doi.org/10.1039/c6cc01277a.

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17

YOSHIDA, Hideyuki, Hitoshi NOHTA, and Masatoshi YAMAGUCHI. "Highly Selective Derivatization Method Based on Intramolecular Excimer-Forming Fluorescence." BUNSEKI KAGAKU 55, no. 4 (2006): 213–21. http://dx.doi.org/10.2116/bunsekikagaku.55.213.

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18

Lin, Z., S. Priyadarshy, A. Bartko, and D. H. Waldeck. "Photophysics and intramolecular excimer formation in a constrained anthracenyl diadduct." Journal of Photochemistry and Photobiology A: Chemistry 110, no. 2 (1997): 131–39. http://dx.doi.org/10.1016/s1010-6030(97)00193-7.

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19

Chakraborty, Tapas, and Edward C. Lim. "Conformation-Dependent Intramolecular Excimer Formation in Jet-Cooled 1,3-Diphenylpropane." Journal of Physical Chemistry 99, no. 49 (1995): 17505–8. http://dx.doi.org/10.1021/j100049a007.

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20

van Walree, Cornelis A., Veronica E. M. Kaats-Richters, Leonardus W. Jenneskens, René M. Williams, and Ivo H. M. van Stokkum. "Intramolecular excimer and exciplex emission of 1,4-dipyrenyl substituted cyclohexasilane." Chemical Physics Letters 355, no. 1-2 (2002): 65–70. http://dx.doi.org/10.1016/s0009-2614(02)00183-5.

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21

Itoh, Yoshihiro, Masakazu Nakada, Hideto Satoh, Akira Hachimori, and Stephen E. Webber. "Intramolecular excimer formation and energy transfer in alternating carbazole copolymers." Macromolecules 26, no. 8 (1993): 1941–46. http://dx.doi.org/10.1021/ma00060a022.

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22

Ohkita, Hideo, Shinzaburo Ito, Masahide Yamamoto, Yasuo Tohda, and Keita Tani. "Intramolecular Excimer Emissions ofsyn-andanti-[3.3](3,9)Carbazolophanes in Solutions†." Journal of Physical Chemistry A 106, no. 10 (2002): 2140–45. http://dx.doi.org/10.1021/jp0125146.

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23

Itagaki, Hideyuki, Kouji Sugiura та Hiyori Sato. "Intramolecular Excimer Formation of Poly(γ-(1-naphthylmethyl)-L-glutamate)". Macromolecular Chemistry and Physics 202, № 1 (2001): 90–96. http://dx.doi.org/10.1002/1521-3935(20010101)202:1<90::aid-macp90>3.0.co;2-h.

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24

Okamoto, Yoshiki, Mitsunobu Nakamura, Min Shi and, and Setsuo Takamuku. "FORMATION OF INTRAMOLECULAR EXCIMER IN ARYL PHOSPHATES AND THEIR REACTIVITIES." Photochemistry and Photobiology 56, no. 3 (1992): 403–7. http://dx.doi.org/10.1111/j.1751-1097.1992.tb02178.x.

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25

Benten, Hiroaki, Hideo Ohkita, Shinzaburo Ito, et al. "Intramolecular Excimer Emission of Triply Bridged [3.3.n](3,6,9)Carbazolophanes." Journal of Physical Chemistry B 109, no. 42 (2005): 19681–87. http://dx.doi.org/10.1021/jp051539s.

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26

Cheng, Liusheng, Guochang Wang, and Mitchell A. Winnik. "Intramolecular excimer formation in 1-naphthylmethyl methacrylate/methyl methacrylate copolymers." Polymer 31, no. 9 (1990): 1611–14. http://dx.doi.org/10.1016/0032-3861(90)90176-y.

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27

Locke, R. J., and E. C. Lim. "Orientational effect on intramolecular triplet excimer formation in (1,n)-dinaphthylalkanes." Journal of Physical Chemistry 93, no. 16 (1989): 6017–19. http://dx.doi.org/10.1021/j100353a017.

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28

Goedeweeck, M., M. Van der Auweraer, and F. C. De Schryver. "Molecular dynamics of a peptide chain, studied by intramolecular excimer formation." Journal of the American Chemical Society 107, no. 8 (1985): 2334–41. http://dx.doi.org/10.1021/ja00294a024.

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29

Cheng, K. H., L. Ruymgaart, L. I. Liu, P. Somerharju, and I. P. Sugar. "Intramolecular excimer kinetics of fluorescent dipyrenyl lipids: 1. DMPC/cholesterol membranes." Biophysical Journal 67, no. 2 (1994): 902–13. http://dx.doi.org/10.1016/s0006-3495(94)80552-1.

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30

Cheng, K. H., L. Ruymgaart, L. I. Liu, P. Somerharju, and I. P. Sugar. "Intramolecular excimer kinetics of fluorescent dipyrenyl lipids: 2. DOPE/DOPC membranes." Biophysical Journal 67, no. 2 (1994): 914–21. http://dx.doi.org/10.1016/s0006-3495(94)80553-3.

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31

Picraux, Laura B., Brandon T. Weldon, and James K. McCusker. "Intramolecular Excimer Formation in a Naphthalene-Appended Dinuclear Iron−Oxo Complex." Inorganic Chemistry 42, no. 2 (2003): 273–82. http://dx.doi.org/10.1021/ic026054m.

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32

Deng, Min, Nathan D. Schley, and Gaël Ung. "Solvent-Dependent Sensitization of Ytterbium and Neodymium via an Intramolecular Excimer." Inorganic Chemistry 57, no. 24 (2018): 15399–405. http://dx.doi.org/10.1021/acs.inorgchem.8b02709.

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33

Liu, Guojun, and J. E. Guillet. "A kinetic description of diffusion-controlled intramolecular excimer and exciplex formation." Macromolecules 23, no. 19 (1990): 4292–98. http://dx.doi.org/10.1021/ma00221a016.

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34

Hamada, Fumio, Koichi Murai, Akihiko Ueno, Iwao Suzuki та Tetsuo Osa. "Excimer Formation and Intramolecular Self-Complexation of Double-Armed γ-Cyclodextrin". Bulletin of the Chemical Society of Japan 61, № 10 (1988): 3758–60. http://dx.doi.org/10.1246/bcsj.61.3758.

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35

Benniston, Andrew C, Anthony Harriman, Sarah L Howell, Craig A Sams, and Yong-Gang Zhi. "Intramolecular Excimer Formation and Delayed Fluorescence in Sterically Constrained Pyrene Dimers." Chemistry - A European Journal 13, no. 16 (2007): 4665–74. http://dx.doi.org/10.1002/chem.200601498.

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36

Cai, Jianjian, and Edward C. Lim. "Intramolecular photoassociation and photoinduced charge transfer in bridged diaryl compound. 5. Intramolecular triplet excimer of 1,1'-dinaphthylamine." Journal of Physical Chemistry 97, no. 23 (1993): 6203–7. http://dx.doi.org/10.1021/j100125a019.

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37

Yeşilot, Serkan, Bünyemin Çoşut, Hüsnüye Ardıç Alidağı, Ferda Hacıvelioğlu, Gül Altınbaş Özpınar, and Adem Kılıç. "Intramolecular excimer formation in hexakis(pyrenyloxy)cyclotriphosphazene: photophysical properties, crystal structure, and theoretical investigation." Dalton Trans. 43, no. 9 (2014): 3428–33. http://dx.doi.org/10.1039/c3dt52957f.

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38

Hara, Kimihiko, and Hideo Suzuki. "High-pressure studies of intramicellar viscosity determined by intramolecular excimer forming probe." Journal of Physical Chemistry 94, no. 3 (1990): 1079–81. http://dx.doi.org/10.1021/j100366a010.

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39

Yoshida, Hideyuki, Hajime Harada, Hitoshi Nohta, and Masatoshi Yamaguchi. "Liquid chromatographic determination of bisphenols based on intramolecular excimer-forming fluorescence derivatization." Analytica Chimica Acta 488, no. 2 (2003): 211–21. http://dx.doi.org/10.1016/s0003-2670(03)00700-1.

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40

Liu, Lin-I., Kwan Hon Cheng, and Pentti Somerharju. "Frequency-resolved intramolecular excimer fluorescence study of lipid bilayer and nonbilayer phases." Biophysical Journal 64, no. 6 (1993): 1869–77. http://dx.doi.org/10.1016/s0006-3495(93)81558-3.

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41

Cho, Dae Won, Mamoru Fujitsuka, Kyung Hwa Choi, Man Jae Park, Ung Chan Yoon, and Tetsuro Majima. "Intramolecular Exciplex and Intermolecular Excimer Formation of 1,8-Naphthalimide−Linker−Phenothiazine Dyads." Journal of Physical Chemistry B 110, no. 10 (2006): 4576–82. http://dx.doi.org/10.1021/jp056078p.

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42

Piryatinski, Andrei, and Robert T. Deck. "Excimer states and enhanced two-photon absorption in intramolecular charge-transfer crystals." Chemical Physics Letters 269, no. 1-2 (1997): 156–60. http://dx.doi.org/10.1016/s0009-2614(97)00264-9.

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43

De Schryver, Frans C., Pol Collart, Jan Vandendriessche, Rudy Goedeweeck, Anne Mie Swinnen, and Marc Van der Auweraer. "Intramolecular excimer formation in bichromophoric molecules linked by a short flexible chain." Accounts of Chemical Research 20, no. 5 (1987): 159–66. http://dx.doi.org/10.1021/ar00137a001.

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44

Smith, T. A., G. D. Scholes, G. O. Turner, and K. P. Ghiggino. "Faraday communications. Intramolecular excimer formation in 1,5-di(9-anthryl)-n-pentane." Journal of the Chemical Society, Faraday Transactions 90, no. 18 (1994): 2845. http://dx.doi.org/10.1039/ft9949002845.

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45

YOSHIDA, Hideyuki. "Analyses of Biogenic Related Compounds Based on Intramolecular Excimer-forming Fluorescence Derivatization." YAKUGAKU ZASSHI 123, no. 8 (2003): 691–96. http://dx.doi.org/10.1248/yakushi.123.691.

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46

Vandendriessche, J., M. van Der Auwerser, and F. C. De Schryvar. "Viscosity Dependency of Intramolecular Excimer Formation in Modelsystems for Poly (N-Vinylcarbazole)." Bulletin des Sociétés Chimiques Belges 94, no. 11-12 (2010): 991–1007. http://dx.doi.org/10.1002/bscb.19850941121.

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47

Albelda, M. Teresa, Enrique García-España, Laura Gil, et al. "Intramolecular Excimer Formation in a Tripodal Polyamine Receptor Containing Three Naphthalene Fluorophores." Journal of Physical Chemistry B 107, no. 27 (2003): 6573–78. http://dx.doi.org/10.1021/jp0343032.

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48

ITAGAKI, Hideyuki, Kazuyuki HORIE, Itaru MITA, et al. "Intramolecular excimer formation of diastereomeric styrene trimers measued by picosecond pulse radiolysis." NIPPON KAGAKU KAISHI, no. 8 (1989): 1299–303. http://dx.doi.org/10.1246/nikkashi.1989.1299.

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49

Goedeweeck, R., and F. C. De Schryver. "SOLVENT EFFECTS ON INTRAMOLECULAR EXCIMER FORMATION IN N-ACETYL-BIS(PYRENYLALANINE)-METHYLESTER." Photochemistry and Photobiology 39, no. 4 (2008): 515–20. http://dx.doi.org/10.1111/j.1751-1097.1984.tb03885.x.

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50

Boileau, Sylvie, Françoise Méchin, Krzysztof Sienicki, and Mitchell A. Winnik. "Cyclization of poly(bisphenol A-diethylene glycol carbonate)—Intramolecular pyrene excimer formation." European Polymer Journal 24, no. 4 (1988): 307–11. http://dx.doi.org/10.1016/0014-3057(88)90192-9.

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