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Relevant bibliographies by topics / Intramolecular excimer

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Academic literature on the topic 'Intramolecular excimer'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Intramolecular excimer"

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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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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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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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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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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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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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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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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Dissertations / Theses on the topic "Intramolecular excimer"

1

Yin, Jie. "Photophysical studies of intramolecular excimer formation." Thesis, Lancaster University, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.332399.

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2

JING, DONG-PING. "Etude de la dynamique locale dans les polymeres en masse par l'analyse de la fluorescence de sondes excimeres." Paris 6, 1988. http://www.theses.fr/1988PA066315.

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Etude par fluorescence de dispersions de sondes excimeres dans des matrices de polymeres amorphes pour comprendre les mouvements impliques dans la transition vitreuse. Etude de l'influence de la temperature et de la pression sur la formation de l'excimere

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3

Holland, Simon Michael. "Highly excited molecules and the interstellar maser." Thesis, University of Bristol, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.265469.

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Weragoda, Geethika K. "Excited state intramolecular proton transfer (ESIPT) and trans-cis isomerization on the triplet excited states." University of Cincinnati / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1439296134.

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Le, Gourrierec Denis. "Excited state intramolecular proton transfer (ESIPT) to nitrogen in heterocyclic compounds." Thesis, University of Central Lancashire, 1996. http://clok.uclan.ac.uk/21906/.

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Excited state intramolecular proton transfer (ESIPT) reactions have aroused considerable interest in the last 10-15 years. The ESIPT reaction is normally extremely rapid and yields excited species of considerably lower energy than the initial Franck-Condon excited state. ESIPT has therefore been used for the rapid dissipation of energy (e. g. for polymer protection against UV degradation) and to produce fluorophores with large Stokes shifts. Approximately half of the compounds studied to date involve ESIPT to nitrogen but there has been no real attempt at a coherent study of ESIPT to nitrogen.

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Green, Alistair Malcolm. "Photoelectron spectroscopy as a probe of intramolecular vibrational dynamics in electronically excited toluene." Thesis, University of Nottingham, 2011. http://eprints.nottingham.ac.uk/12170/.

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Intramolecular vibrational energy redistribution (IVR) is a commonly-observed phenomenon whereby vibrational energy can be transferred between different parts of a polyatomic molecule. This process has profound implications for the understanding of chemical reactivity. In this work, IVR is studied in the S1 electronic state of toluene using time-resolved and frequency-resolved techniques. Both experiments are based upon laser photoelectron spectroscopy in the collision-free environment of a molecular beam. The time-resolved experiments employ laser pulses of ~1 ps duration and ~15 cm^-1 bandwi

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Pham, Van Cang Christian. "Etude de la dynamique locale dans les polymeres en masse par l'analyse de la fluorescence de sondes excimeres." Paris 6, 1987. http://www.theses.fr/1987PA066195.

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Les molecules de meso di(n-carbazolyl)-2,4 pentane et oxyde de bis(phenyl-10 anthryl-9 methyl) servent de sondes fluorescentes pour l'analyse de la mobilite des chaines macromoleculaires de: polyoxydes de propene, polysiloxane, polybutadiene, polyisopropene et polyisobutene. Influence de la nature du polymere sur le mouvement de la sonde

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Chen, Weihua. "Chemical Sensors Based on Fluorescence Turn-On Mechanism by Using Excited State Intramolecular Proton Transfer." University of Akron / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=akron1334772708.

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Ortiz, Sánchez Juan Manuel. "Excited state intramolecular proton transfer reactions coupled with non adiabatic processes: electronic structure and quantum dynamical approaches." Doctoral thesis, Universitat Autònoma de Barcelona, 2009. http://hdl.handle.net/10803/3311.

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Els enllaços d'hidrogen són d'importància universal en química i bioquímica. Les propietats dels enllaços d'hidrogen en l'estat electrònic fonamental han estat estudiades durant molt anys. Malgrat tot, molt poc es coneix sobre les reaccions químiques on intervenen enllaços d'hidrogen en els estats electrònics excitats. Una de les reaccions més interessants són les transferències protòniques intramoleculars en estat excitat (ESIPT de les seves sigles en anglès), ja que juguen un paper crucial en una gran varietat de reaccions químiques fotoquímiques de gran rellevància.<br/>Les tècniques més m

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Zhang, Wanying. "Comprehensive Study on Fluorescent ESIPT Liquid Crystal Materials and the Potential for Optoelectronic Applications." Doctoral thesis, Kyoto University, 2021. http://hdl.handle.net/2433/263621.

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Books on the topic "Intramolecular excimer"

1

NATO Advanced Research Workshop on Stochasticity and Intramolecular Redistribution of Energy (1986 Orsay, France). Stochasticity and intramolecular redistribution of energy. D. Reidel, 1987.

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2

Baer, Tomas, and William L. Hase. Unimolecular Reaction Dynamics. Oxford University Press, 1996. http://dx.doi.org/10.1093/oso/9780195074949.001.0001.

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This book provides a penetrating and comprehensive description of energy selected reactions from a theoretical as well as experimental view. Three major aspects of unimolecular reactions involving the preparation of the reactants in selected energy states, the rate of dissociation of the activated molecule, and the partitioning of the excess energy among the final products, are fully discussed with the aid of 175 illustrations and over 1,000 references, most from the recent literature. Examples of both neutral and ionic reactions are presented. Many of the difficult topics are discussed at sev

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Book chapters on the topic "Intramolecular excimer"

1

De Schryver, F. C., P. Collart, R. Goedeweeck, F. Ruttens, F. Lopez Arbelao, and M. VanderAuweraer. "Configurational and Conformational Aspects of Intramolecular Excimer Formation." In ACS Symposium Series. American Chemical Society, 1987. http://dx.doi.org/10.1021/bk-1987-0358.ch016.

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Lehrer, S. S., and Y. Ishii. "Intramolecular Excimer Fluorescence of Pyrene Maleimide-Labeled Dithiothreitol (Pyrene-DTT)." In Fluorescent Biomolecules. Springer US, 1989. http://dx.doi.org/10.1007/978-1-4684-5619-6_40.

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3

Zinna, Francesco, Elodie Brun, Alexandre Homberg, and Jérôme Lacour. "Circularly Polarized Luminescence from Intramolecular Excimers." In Circularly Polarized Luminescence of Isolated Small Organic Molecules. Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-2309-0_12.

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4

Ratner, Mark A., R. B. Gerber, and V. Buch. "Excited Vibrational States: Semiclassical Self-Consistent-Field and Statistical Considerations." In Stochasticity and Intramolecular Redistribution of Energy. Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3837-3_5.

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5

Breckenridge, W. H., O. Benoist d’Azy, M. C. Duval, C. Jouvet, and B. Soep. "Excited Van Der Waals Complexes as a Probe for Intermediate States in Collisions." In Stochasticity and Intramolecular Redistribution of Energy. Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3837-3_11.

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6

Krishnamoorthy, Govindarajan. "Hydrogen-Bonding Effects on Intramolecular Charge Transfer." In Hydrogen Bonding and Transfer in the Excited State. John Wiley & Sons, Ltd, 2010. http://dx.doi.org/10.1002/9780470669143.ch14.

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7

Kuzmin, M. V., and A. A. Stuchebrukhov. "Dynamical Chaos and Intramolecular Vibrational Relaxation in Polyatomic Molecules." In Laser Spectroscopy of Highly Vibrationally Excited Molecules. CRC Press, 2021. http://dx.doi.org/10.1201/9781003208921-4.

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8

Klöpffer, Walter. "Intramolecular Proton Transfer in Electronically Excited Molecules." In Advances in Photochemistry. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470133408.ch5.

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Lukashov, Sergey, Alexander Petrov, and Anatoly Pravilov. "Intramolecular Perturbations in the Electronically Excited States." In The Iodine Molecule. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-70072-4_4.

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Barbara, Paul F., and Włodzimierz Jarzeba. "Ultrafast Photochemical Intramolecular Charge and Excited State Solvation." In Advances in Photochemistry. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470133453.ch1.

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Conference papers on the topic "Intramolecular excimer"

1

Hattori, Takashi, Yuko Tsuchiya, Yoshiyuki Yokoyama, et al. "Microswelling-free negative resists for ArF excimer laser lithography utilizing acid-catalyzed intramolecular esterification." In Microlithography '99, edited by Will Conley. SPIE, 1999. http://dx.doi.org/10.1117/12.350223.

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2

Riedle, Eberhard, Stefan Lochbrunner, Alexander J. Wurzer, Vincent de Waele, and Regina de Vivie-Riedle. "Does the proton move during ultrafast excited state intramolecular proton transfer?" In International Conference on Ultrafast Phenomena. OSA, 2000. http://dx.doi.org/10.1364/up.2000.me3.

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Lochbrunner, Stefan, Michael Schmitt, James P. Shaffer, Thomas Schultz, and Albert Stolow. "Time-Resolved Photoelectron Spectroscopy of Excited State Intramolecular Proton Transfer Dynamics." In International Conference on Ultrafast Phenomena. OSA, 2000. http://dx.doi.org/10.1364/up.2000.tuf37.

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4

Park, Soo Young, and Sehoon Kim. "Molecular photonics materials with excited-state intramolecular proton transfer (ESIPT) activity." In Integrated Optoelectronics Devices, edited by James G. Grote and Toshikuni Kaino. SPIE, 2003. http://dx.doi.org/10.1117/12.485821.

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Rini, M., A. Kummrow, J. Dreyer, E. T. J. Nibbering, and T. Elsaesser. "Ultrafast site-specific mid-infrared spectroscopy of excited-state intramolecular proton transfer." In International Conference on Ultrafast Phenomena. OSA, 2002. http://dx.doi.org/10.1364/up.2002.thb5.

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Skilitsi, Anastasia I., Damianos Agathangelou, Andrey Klymchenko, Yves Mély, Stefan Haacke, and Jeremie Leonard. "Ultrafast, Solvation-Controlled Excited-State Intramolecular Proton Transfer in 4’-Methoxy-3-Hydroxyflavone." In International Conference on Ultrafast Phenomena. OSA, 2016. http://dx.doi.org/10.1364/up.2016.uw4a.31.

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Lee, Junghwa, Chul Hoon Kim, and Taiha Joo. "Molecular Reaction Dynamics of Excited-State Intramolecular Proton Transfer Revealed by Isotope Dependence." In International Conference on Ultrafast Phenomena. OSA, 2010. http://dx.doi.org/10.1364/up.2010.tud6.

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Klymchenko, Andriy S., and Alexander P. Demchenko. "Internal Stark effect mediates intramolecular excited-state proton transfer in 3-hydroxyflavone derivatives." In XV International School on Spectroscopy of Molecules and Crystals, edited by Galina A. Puchkovska and Sergey A. Kostyukevych. SPIE, 2002. http://dx.doi.org/10.1117/12.486637.

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Jen, Myungsam, Sebok Lee, and Yoonsoo Pang. "Ultrafast solvation dynamics of dimethyl sulfoxide induced by excited-state intramolecular proton transfers." In International Conference on Ultrafast Phenomena. OSA, 2020. http://dx.doi.org/10.1364/up.2020.m4b.27.

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Kim, Chul Hoon, and Taiha Joo. "Effects of conformational diversity on the excited state intramolecular reaction dynamics in condensed phases." In 2007 Conference on Lasers and Electro-Optics - Pacific Rim. IEEE, 2007. http://dx.doi.org/10.1109/cleopr.2007.4391608.

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