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Relevant bibliographies by topics / IR-UV Double Resonance Spectroscopy

Academic literature on the topic 'IR-UV Double Resonance Spectroscopy'

Author: Grafiati

Published: 10 December 2022

Last updated: 28 January 2023

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Dissertations / Theses
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Journal articles on the topic "IR-UV Double Resonance Spectroscopy"

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Callahan, Michael P., Bridgit Crews, Ali Abo-Riziq, Louis Grace, Mattanjah S. de Vries, Zsolt Gengeliczki, Tiffani M. Holmes, and Glake A. Hill. "IR-UV double resonance spectroscopy of xanthine." Physical Chemistry Chemical Physics 9, no. 32 (2007): 4587. http://dx.doi.org/10.1039/b705042a.

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Crews, Bridgit, Ali Abo-Riziq, Louis Grace, Michael Callahan, Martin Kabeláč, Pavel Hobza, and Mattanjah S. de Vries. "IR-UV double resonance spectroscopy of guanine–H2O clusters." Physical Chemistry Chemical Physics 7, no. 16 (2005): 3015. http://dx.doi.org/10.1039/b506107e.

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Plützer, Chr, E. Nir, M. S. de Vries, and K. Kleinermanns. "IR–UV double-resonance spectroscopy of the nucleobase adenine." Physical Chemistry Chemical Physics 3, no. 24 (December 5, 2001): 5466–69. http://dx.doi.org/10.1039/b107997b.

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Inokuchi, Yoshiya, Yusuke Kobayashi, Takafumi Ito, and Takayuki Ebata. "Conformation ofl-Tyrosine Studied by Fluorescence-Detected UV−UV and IR−UV Double-Resonance Spectroscopy." Journal of Physical Chemistry A 111, no. 17 (May 2007): 3209–15. http://dx.doi.org/10.1021/jp070163a.

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Bouchet, Aude, Johanna Klyne, Shun-ichi Ishiuchi, Otto Dopfer, Masaaki Fujii, and Anne Zehnacker. "Stereochemistry-dependent structure of hydrogen-bonded protonated dimers: the case of 1-amino-2-indanol." Physical Chemistry Chemical Physics 20, no. 18 (2018): 12430–43. http://dx.doi.org/10.1039/c8cp00787j.

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Stereochemistry effects on the structure of molecular aggregates are studied in the prototypical 1-amino-2-indanol. Conformer-selective IR-UV double resonance spectroscopy reveals how stereochemistry shapes its dimers.

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Abo-Riziq, Ali G., Bridgit Crews, John E. Bushnell, Michael P. Callahan, and Mattanjah S. De Vries *. "Conformational analysis of cyclo(Phe-Ser) by UV–UV and IR–UV double resonance spectroscopy andab initiocalculations." Molecular Physics 103, no. 11-12 (June 10, 2005): 1491–95. http://dx.doi.org/10.1080/00268970500095923.

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Chadwick, B. L., A. P. Milce, and B. J. Orr. "Fluorescence-detected infrared– and Raman–ultraviolet double resonance in acetylene gas: studies of spectroscopy and rotational energy transfer." Canadian Journal of Physics 72, no. 11-12 (November 1, 1994): 939–53. http://dx.doi.org/10.1139/p94-124.

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Fluorescence-detected Raman–ultraviolet and infrared–ultraviolet double resonance (DR) spectroscopy enables state-selective studies of rotational and vibrational energy transfer in gas-phase acetylene (C2H2) and its deuterated isotopomers (C2HD, C2D2). The Raman–UV DR approach entails pulsed coherent Raman excitation in the ν2 rovibrational band of C2H2(g), followed by fluorescence-detected rovibronic probing of the resulting rovibrational population distributions. Corresponding IR–UV DR experiments employ a line-tunable, pulsed CO2 laser to excite rovibrational transitions in the 2ν4 band of C2HD(g) and in the (ν4 + ν5) band of C2D2(g), with similar fluorescence-detected rovibronic probing. These time-resolved DR spectroscopic techniques provide rotationally specific information on collision-induced molecular energy transfer in acetylene. This paper extends previous Raman–UV DR spectroscopic studies of C2H2 and presents fresh IR–UV DR spectra of gas-phase C2HD and C2D2, including evidence of a novel two-step excitation sequence in which a single CO2-laser pulse promotes C2D2 by successive transitions in the (ν4 + v5) and (2ν4 + 2ν5−ν4−v5) absorption bands. Kinetic measurements and mechanistic observations are also reported for collision-induced rotational energy transfer in acetylene gas, complementing other investigations of rotationally resolved vibrational energy transfer.

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Mahé, Jérôme, Sander Jaeqx, Anouk M. Rijs, and Marie-Pierre Gaigeot. "Can far-IR action spectroscopy combined with BOMD simulations be conformation selective?" Physical Chemistry Chemical Physics 17, no. 39 (2015): 25905–14. http://dx.doi.org/10.1039/c5cp01518a.

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The combination of conformation selective far-IR/UV double resonance spectroscopy with Born–Oppenheimer molecular dynamics (BOMD) simulations is presented here for the structural characterization of the Ac-Phe-Pro-NH₂ peptide in the far-infrared spectral domain, i.e. for radiation below 800 cm⁻¹.

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Asami, Hiroya, Shu-hei Urashima, and Hiroyuki Saigusa. "Structural identification of uric acid and its monohydrates by IR-UV double resonance spectroscopy." Physical Chemistry Chemical Physics 13, no. 45 (2011): 20476. http://dx.doi.org/10.1039/c1cp22540e.

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Lettenberger, M., F. Emmerling, N. H. Gottfried, and A. Laubereau. "Orientational motion of anthracene in liquid solution studied by IR/UV double-resonance spectroscopy." Chemical Physics Letters 240, no. 4 (June 1995): 324–29. http://dx.doi.org/10.1016/0009-2614(95)00528-c.

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More sources

Dissertations / Theses on the topic "IR-UV Double Resonance Spectroscopy"

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McNaghten, Edward Dennison. "Some studies of gas phase vibrational energy transfer processes using the IR-UV double resonance technique." Thesis, Queen's University Belfast, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.329391.

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Offenbacher, Adam R. "Protein structural changes and tyrosyl radical-mediated electron transfer reactions in ribonucleotide reductase and model compounds." Diss., Georgia Institute of Technology, 2011. http://hdl.handle.net/1853/39473.

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Tyrosyl radicals can facilitate proton-coupled electron transfer (PCET) reactions that are linked to catalysis in many biological systems. One such protein system is ribonucleotide reductase (RNR). This enzyme is responsible for the conversion of ribonucleotides to deoxyribonucleotides. The beta2 subunit of class Ia RNRs contains a diiron cluster and a stable tyrosyl radical (Y122*). Reduction of ribonucleotides is dependent on reversible, long-distance PCET reactions involving Y122* located 35 Å from the active site. Protein conformational dynamics are postulated to precede diiron cluster assembly and PCET reactions in RNR. Using UV resonance Raman spectroscopy, we identified structural changes to histidine, tyrosine, and tryptophan residues with metal cluster assembly in beta2. With a reaction-induced infrared spectroscopic technique, local amide bond structural changes, which are associated with the reduction of Y122*, were observed. Moreover, infrared spectroscopy of tyrosine-containing pentapeptide model compounds supported the hypothesis that local amide bonds are perturbed with tyrosyl radical formation. These findings demonstrate the importance of the amino acid primary sequence and amide bonds on tyrosyl radical redox changes. We also investigated the function of a unique tyrosine-histidine cross-link, which is found in the active site of cytochrome c oxidase (CcO). Spectrophotometric titrations of model compounds that mimic the cross-link were consistent with a proton transfer role in CcO. Infrared spectroscopic data support the formation of tyrosyl radicals in these model compounds. Collectively, the effect of the local structure and the corresponding protein dynamics involved in tyrosyl radical-mediated PCET reactions are illustrated in this work.

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Luck, Meike. "Erstcharakterisierung von Histidinkinase-Rhodopsinen aus einzelligen Grünalgen." Doctoral thesis, Humboldt-Universität zu Berlin, 2018. http://dx.doi.org/10.18452/19607.

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Histidinkinase-Rhodopsine (HKRs) können als besondere Gruppe der Hybrid-Histidinkinasen beschrieben werden, deren N-terminale sensorische Domäne ein mikrobielles Rhodopsin ist. HKR-codierende Sequenzen konnten in den Genomen verschiedener Algen, Pilze und Amoeben gefunden werden doch ihre Aufgaben und Wirkungsweisen sind bisher ungeklärt. Im Rahmen dieser Arbeit wurden die rekombinanten Rhodopsin-Domänen von zwei HKRs mit verschiedenen spektroskopischen Techniken charakterisiert. Sie zeigten mehrere Besonderheiten. Das Rhodopsin-Fragment von Cr-HKR1 aus Chlamydomonas reinhardtii kann durch alternierende kurzwellige und langwellige Belichtung zwischen zwei stabilen Absorptionsformen konvertiert werden: einer Blaulicht-absorbierenden (Rh-Bl) und einer UVA-Licht-absorbierenden Form (Rh-UV). Dies resultiert aus der ungewöhnlichen thermischen Stabilität des Zustandes mit deprotonierter Schiff’scher Base. Das zweite charakterisierte HKR, die Os-HKR-Rhodopsin-Domäne aus der marinen Picoalge Ostreococcus tauri, zeigt eine Dunkelabsorption von 505 nm. Auch Os-HKR ist photochrom und die deprotonierte Spezies kann effizient akkumuliert werden. Diese P400-Absorptionsform ist jedoch nicht völlig stabil sondern es kommt nach Belichtungsende zur langsamen Dunkelzustands-Regeneration. Überraschenderweise konnte die Bindung sowie die transiente Abgabe eines Anions während des Os-HKR-Photozyklus festgestellt werden. Somit beeinflusst nicht nur das Licht, sondern auch das Salz in der Umgebung die Os-HKR-Reaktionen. Aufgrund ihrer photochromen Eigenschaften werden die HKRs als wirksame lichtinduzierte Schalter für die C-terminalen Signaltransduktionsdomänen postuliert. Schwingungsspektroskopische Analysen deckten eine Heterogenität hinsichtlich der im Protein gebundenen Retinal‐Konfiguration sowie die Existenz von zwei parallelen Photozyklen auf. Jeder dieser Photozyklen geht aus einer der beiden Retinal-Isomere hervor.
Histidine kinase rhodopsins (HKRs) can be described as hybrid histidine kinases with a microbial rhodopsin as N-terminal sensory domain. HKR-encoding sequences were found in the genomes of various unicellular organisms such as algae, fungi and amoeba but their mechanistic and physiologic function is unknown. During this work the absorptive properties of the recombinant rhodopsin domains of two HKRs were studied by the usage of different spectroscopic techniques. Both HKRs showed unusual characteristics. The rhodopsin fragment of Cr‐HKR1 from Chlamydomonas reinhardtii can be interconverted between two stable absorbance forms by the alternate application of short‐ and long‐wavelength light: a blue light-absorbing dark form (Rh-Bl) and a UVA light-absorbing form (Rh-UV). This unusual photocycle results from the uncommon thermal stability of the absorbance state with a deprotonated retinal Schiff base. The second studied HKR, the Os‐HKR rhodopsin domain from the marine picoalga Ostreococcus tauri, shows an absorbance maximum at 505 nm in darkness. Likewise Cr‐HKR1 the Os‐HKR is photochromic and the deprotonated form P400 can be efficiently accumulated. But the Os-HKR P400-form is not completely stable. A slow dark state recovery occurs. Surprisingly the dark state absorbance of Os‐HKR was found to be dependent on anion binding in the protein. Furthermore during the photocycle the transient anion release occurs and therefore not only light but also salt impacts the Os-HKR-reactions. Due to their pronounced photochromic properties, the HKRs are postulated to act as effective molecular switches for the C-terminal signal transduction domains in response to the light conditions. Vibrational spectroscopy revealed the heterogeneity with regard to the retinal configuration bound in the HKRs suggesting the existence of two parallel photocycles. Either of these photocycles originates from one of the two retinal isoforms.

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Michaille, Laurent. "Étude des états vibrationnels très excités de la molécule CS2 : dynamique non linéaire et corrélations spectrales." Université Joseph Fourier (Grenoble ; 1971-2015), 1998. http://www.theses.fr/1998GRE10009.

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Pour les etats de vibration tres excites de certaines molecules, l'attribution en termes des nombres quantiques usuels n'est plus valable. Dans cs#2, les modes d'elongation symetrique et de pliage sont fortement couples par une resonance non lineaire de fermi. Au moins a basse energie le mode d'elongation antisymetrique reste faiblement couple par des anharmonicites. La dynamique quantique, classique et semiclassique de ce modele tres important en physique moleculaire est etudie en detail. Il est montre comment les bifurcations successives des orbites periodiques permettent de rendre compte de l'evolution de la dynamique quantique en fonction de l'energie. L'etude du vibrogramme permet egalement d'evaluer la validite du modele de fermi entre 12000 et 19000 cm##1 dans un domaine ou elle n'etait pas connue. Nous avons ensuite effectue des experiences de fluorescence resolue a plus de 19000 cm##1 au-dessus du fondamental afin de pratiquer les statistiques spectrales permettant de caracteriser le chaos quantique. Pres de 400 raies experimentales ont ete obtenues. L'analyse demontre plusieurs points importants. En premier lieu, la transition vers le chaos quantique de la molecule vers 13000 cm##1 est remise en question a cause d'une excitation impure. D'autre part, nous avons montre le role de la resolution sur les statistiques spectrales. Des spectres mal resolus peuvent presenter des correlations qui sont des artefacts. Ceci nous a conduit a remettre en question toutes les preuves experimentales existantes de l'existence de chaos quantique vibrationnel dans les molecules. Afin d'obtenir des spectres vibrationnels purs, nous avons developpe deux nouvelles experiences pour la spectroscopie de cs#2 : la double resonance i-r u-v et un jet supersonique. Si les transferts rotationnels observes en double resonance rendent difficiles l'utilisation de cette technique, le jet supersonique permet d'exciter veritablement une raie unique.

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Tarabek, Jan. "Elektropolymerisation, Spektroelektrochemie und Potentiometrie von funktionalisierten leitfähigen Polymeren." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2004. http://nbn-resolving.de/urn:nbn:de:swb:14-1103635385062-58674.

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Die vorliegende Arbeit behandelt die elektrochemische Synthese (elektrochemische Polymerisation und Copolymerisation) und die Charakterisierung der Redox- und sensorischen Eigenschaften neuer funktionalisierter Polymere für die Ionensensorik. Die Funktionalisierung wird sowohl in der Polymer-Hauptkette (Polysalene) als auch in der Polymer-Seitenkette (ein Thiophen-Copolymer: 3-Methylthiophen/6-Hydroxy-2-(2-(3-thienyl)-ethoxy)-acetophenon) dargestellt. Die Redox-Prozesse der funktionalisierten Polymere wurden mit spektroelektrochemischen Methoden: ESR-, UV-Vis-NIR- und FTIR-Spektroelektrochemie charakterisiert. Durch diese Methoden konnten während der elektrochemischen Oxidation von funktionalisierten leitfähigen Polymeren verschiedene Polymer- bzw. Copolymer-Ladungsträger nachgewiesen werden: Polaronen, Bipolaronen beim Thiophen-Copolymer, zwei Polaronen auf einer Polymerkette im Singulettezustand beim Poly(3-methylthiophen) und eine diamagnetische Spin-Spin-Wechselwirkung zwischen ungepaarten Elektronen der Cu(II)-Ionen und der ungepaarten Elektronen von bisphenolischen Ligand-Kationradikalen beim Poly[Cu(II)-salen]. Sensorische Eigenschaften gegenüber Ni(II)-Ionen wurden durch Potentiometrie an einem Poly[Ni(II)-salen]-Derivat getestet. Es zeigt eine gute potentiometrische Ni(II)-Ionenselektivität (der Logarithmus des potentiometrischen Selektivitätskoeffizienten liegt im Bereich von -0.5 bis -1.5) in Anwesenheit von Cd(II), Mn(II), Zn(II) und Na(I).

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Fritz, Mark David. "The characterization of highly excited rovibrational states two-dimensional IR-UV double resonance and photoacoustic spectroscopy of acetylene and formaldehyde /." 1993. http://catalog.hathitrust.org/api/volumes/oclc/31370853.html.

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Roudná, Štěpánka. "Stavební bloky supramolekulárních polymerů založených na vodíkové vazbě." Master's thesis, 2011. http://www.nusl.cz/ntk/nusl-297585.

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The connection of molecular monomers through non-covalent interaction (e.g. hydrogen bonding, π-π interaction, coordination bonding) enables the formation of supramolecular polymers. The major advantage of these bonds is their reversibility and consequently their ability to self-assembly or to disconnect depending on given conditions. This thesis examines the self-assembly through quadruple hydrogen bonding, which is strong and the resulting structures stable. Ureidopyrimidinon A and aromatic amines were always used as the starting compound for the preparation of monofunctional and bifunctional ureidopyrimidinones.

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Dionne, Éric. "Cage de résonance à base de films minces transparents et conducteurs de nanotubes de carbone." Thèse, 2008. http://hdl.handle.net/1866/7812.

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Dionne, Éric R. "Cage de résonance à base de films minces transparents et conducteurs de nanotubes de carbone." Thesis, 2008. http://hdl.handle.net/1866/7812.

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Book chapters on the topic "IR-UV Double Resonance Spectroscopy"

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Wang, X. M., G. Y. Wu, P. X. Ding, J. D. Chen, W. B. Gao, H. T. Ji, and S. H. Liu. "Vibrational Energy Transfer Study of Benzene by IR-UV Double Resonance." In Springer Series in Optical Sciences, 159–60. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-540-39664-2_47.

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Ebata, Takayuki. "DYNAMICS OF THE VIBRATIONALLY EXCITED MOLECULES AND CLUSTERS STUDIED BY IR-UV AND UV-IR DOUBLE RESONANCE SPECTROSCOPY." In Advances in Multi-Photon Processes and Spectroscopy, 1–29. WORLD SCIENTIFIC, 2010. http://dx.doi.org/10.1142/9789814293594_0001.

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Bortiatynski, Jacqueline M., and Patrick G. Hatcher. "The Development of 13C Labeling and 13C NMR Spectroscopy Techniques to Study the Interaction of Pollutants with Humic Substances." In Nuclear Magnetic Resonance Spectroscopy in Environment Chemistry. Oxford University Press, 1997. http://dx.doi.org/10.1093/oso/9780195097511.003.0007.

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Modern agricultural practices have contributed to the accumulation of herbicides, pesticides and their decomposition products in the soil. These pollutants are known to interact with soil organic matter to form covalent and/or noncovalent bonding associations. The covalent bonds are thought to result from addition or oxidative coupling reactions, some of which may be catalyzed by oxidoreductive enzymes. Noncovalent associations include such interactions as ion exchange, hydrogen bonding, protonation, charge transfer, ligand exchange, coordination through metal ions, van der Waals forces, and hydrophobic bonding. The association of pollutants with soil organic matter is an area of study that is of extreme interest for two reasons. First, dissolved organic matter present in lakes and streams is known to enhance the solubility of pollutants, which poses a real threat to the quality of fresh water supplies. Therefore, if we are to predict the movement of pollutants in the water table we need to have a mechanistic understanding of their interactions with dissolved humic materials. Second, early studies had indicated that some pollutants chemically bind to humic materials, thus reducing the risk of further transport and dispersion. If this chemical binding of the pollutants is irreversible, then this process may serve as a natural means for their detoxification. Regardless of the type of association, the first task in any mechanistic study is to characterize the reaction products structurally. In the case of noncovalent binding mechanisms, studies have focused on the physical characteristics of the process and not on the structure of the associated pollutant. Association studies are used to determine the sorption kinetics and transport of pollutants as well as their association constants. These types of studies utilize various techniques such as batch sorption, gas-purge desorption, column adsorption, and miscible displacement. All of these techniques are only capable of providing quantitative information on the amount of pollutant sorbed by a substrate. The study of the covalent binding of pollutants to humic substances has utilized 14C labeling in addition to various spectrometric techniques such as ultraviolet (UV) difference, fluorescence polarization and infrared (IR) spectroscopy.

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Conference papers on the topic "IR-UV Double Resonance Spectroscopy"

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DeBlase, Andrew, Timothy Zwier, Scott McLuckey, Patrick Walsh, and Christopher Harrilal. "IR-UV DOUBLE RESONANCE SPECTROSCOPY OF A COLD PROTONATED FIBRIL-FORMING PEPTIDE: NNQQNY·H+." In 71st International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2016. http://dx.doi.org/10.15278/isms.2016.wi02.

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Obenchain, Daniel, Joseph Knee, Stewart Novick, E. Arsenault, Cara Rivera, and Caitlin Bray. "HYDROGEN BONDING IN 4-AMINOPHENYL ETHANOL: A COMBINED IR-UV DOUBLE RESONANCE AND MICROWAVE STUDY." In 70th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2015. http://dx.doi.org/10.15278/isms.2015.rh13.

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Harrilal, Christopher, Timothy Zwier, Scott McLuckey, John Lawler, Joshua Fischer, and Andrew DeBlase. "PROBING IR-INDUCED ISOMERIZATION OF A MODEL PENTAPEPTIDE IN A CRYO-COOLED ION TRAP USING IR-UV DOUBLE RESONANCE." In 72nd International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2017. http://dx.doi.org/10.15278/isms.2017.fe05.

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Mahjoub, A., K. Le Barbu-Debus, A. Zehnacker-Rentien, Mourad Telmini, Najeh Thabet Mliki, and Ezeddine Sediki. "Double resonance IR∕UV study of the complexes of methyl mandelate with methyl glycolate and methyl lactate." In FUNDAMENTAL AND APPLIED SPECTROSCOPY: Second International Spectroscopy Conference, ISC 2007. AIP, 2007. http://dx.doi.org/10.1063/1.2795416.

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Yang, Shaoyue, Kevin Lehmann, and George Schwartz. "CH3D NEAR INFRARED CAVITY RING-DOWN SPECTRUM REANALYSIS AND IR-IR DOUBLE RESONANCE." In 70th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2015. http://dx.doi.org/10.15278/isms.2015.mh12.

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Harrilal, Christopher, Timothy Zwier, Scott McLuckey, and Anthony Pitts-McCoy. "THE ROLE OF TYROSINE IN STABILIZING GAS PHASE ZWITTERIONIC CONFIGURATIONS OF PEPTIDE IONS REVEALED BY IR-UV DOUBLE RESONANCE SPECTROSCOPY." In 74th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2019. http://dx.doi.org/10.15278/isms.2019.tj09.

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Schneiderman, Max, Danielle Reyes, Robert Bernath, Henry O. Everitt, and Martin Richardson. "Transient Coherence in IR/THz Double Resonance Spectroscopy for Remote Sensing." In Frontiers in Optics. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/fio.2022.ftu6e.5.

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Infrared/Terahertz double resonance spectroscopy is explored for remote identification of trace molecular gases at atmospheric pressures. Free induction decay of low pressure hyperfine-resolved transitions in CH335Cl inform a roadmap for future atmospheric pressure studies.

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Vodopyanov, Konstantin L. "Two-dimensional electrons studied by double-resonance mid-IR laser spectroscopy." In Eleventh International Vavilov Conference on Nonlinear Optics, edited by Sergei G. Rautian. SPIE, 1998. http://dx.doi.org/10.1117/12.328298.

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Johnson, Mark, and Conrad Wolke. "ISOLATING SITE-SPECIFIC SPECTRAL SIGNATURES OF INDIVIDUAL WATER MOLECULES IN H-BONDED NETWORKS WITH ISOTOPOMER-SELECTIVE, IR-IR DOUBLE RESONANCE VIBRATIONAL PREDISSOCIATION SPECTROSCOPY." In 71st International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2016. http://dx.doi.org/10.15278/isms.2016.wi01.

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Harrilal, Christopher, Timothy Zwier, Scott McLuckey, and Anthony Pitts-McCoy. "INVESTIGATING ELECTRONIC AND STRUCTURAL CHANGES IMPOSED BY ZWITTERIONIC PARING IN MODEL PEPTIDE SYSTEMS USING IR-UV-IR TRIPLE RESONANCE SPECTROSCOPY." In 73rd International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2018. http://dx.doi.org/10.15278/isms.2018.fe02.

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