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Relevant bibliographies by topics / UV resonant Raman spectroscopy

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Academic literature on the topic 'UV resonant Raman spectroscopy'

Author: Grafiati

Published: 4 June 2021

Last updated: 14 February 2022

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Journal articles on the topic "UV resonant Raman spectroscopy"

1

Mayorkas, Nitzan, Hanan Sachs, Markus Schütz, et al. "Structural motifs of 2-(2-fluoro-phenyl)-ethylamine conformers." Physical Chemistry Chemical Physics 18, no. 2 (2016): 1191–201. http://dx.doi.org/10.1039/c5cp06131h.

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Vibronic and vibrational spectra of 2-(2-fluoro-phenyl)-ethylamine (2-FPEA) conformers were measured in a molecular beam by resonant two-photon ionization (R2PI), ultraviolet–ultraviolet hole burning (UV–UV HB) spectroscopy, and ionization-loss stimulated Raman spectroscopy (ILSRS).

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Signorile, Matteo, Francesca Bonino, Alessandro Damin, and Silvia Bordiga. "In Situ Resonant UV-Raman Spectroscopy of Polycyclic Aromatic Hydrocarbons." Journal of Physical Chemistry C 119, no. 21 (2015): 11694–98. http://dx.doi.org/10.1021/acs.jpcc.5b02209.

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Kumamoto, Yasuaki, Atsushi Taguchi, Nicholas Isaac Smith, and Satoshi Kawata. "Deep UV resonant Raman spectroscopy for photodamage characterization in cells." Biomedical Optics Express 2, no. 4 (2011): 927. http://dx.doi.org/10.1364/boe.2.000927.

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Dimitrievska, Mirjana, Florian Oliva, Maxim Guc, et al. "Defect characterisation in Cu2ZnSnSe4 kesterites via resonance Raman spectroscopy and the impact on optoelectronic solar cell properties." Journal of Materials Chemistry A 7, no. 21 (2019): 13293–304. http://dx.doi.org/10.1039/c9ta03625c.

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D'Amico, Francesco, Francesca Cammisuli, Riccardo Addobbati, et al. "Oxidative damage in DNA bases revealed by UV resonant Raman spectroscopy." Analyst 140, no. 5 (2015): 1477–85. http://dx.doi.org/10.1039/c4an02364a.

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Kleimeyer, James A., Julius C. Fister, John Zimmerman, and Joel M. Harris. "Liquid Filters for UV Resonance Raman Spectroscopy." Applied Spectroscopy 50, no. 12 (1996): 1597–602. http://dx.doi.org/10.1366/0003702963904502.

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Solutions of organic compounds are proposed as viable high-pass, Rayleigh rejection filters for ultraviolet resonance Raman spectroscopy. The steep transmittance curves of these solutions effectively reject elastically scattered light in this region while passing Raman-shifted frequencies. The materials used in the filters are readily available and inexpensive, and the solutions are easily prepared. Filters for four lines in the range of 288 nm to 342 nm from a Raman-shifted 3rd and 4th harmonic of a Nd:YAG laser are presented, although the principle of preparing similar liquid filters can be applied to virtually any near-UV wavelength. The use of these filter solutions in conjunction with a single monochromator was found to significantly reduce levels of elastically scattered light without sacrifice of optical throughput; Raman scattering at frequency shifts within 200 cm−1 of the Rayleigh line could be observed, and the transmittance at shifts >1000 cm−1 was ≥80%. The Rayleighline rejection efficiencies for the filters in this study are modest (102–103) compared with those for filters employed in the visible region; but they can be easily boosted by increasing the chromophore concentration or filter pathlength with a trade-off of throughput for Raman scattering at small wavenumber shifts.

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Wu, Qiang, Gurusamy Balakrishnan, Alex Pevsner, and Thomas G. Spiro. "Histidine Photodegradation during UV Resonance Raman Spectroscopy†." Journal of Physical Chemistry A 107, no. 40 (2003): 8047–51. http://dx.doi.org/10.1021/jp027190f.

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Jordan, Trace, and Thomas G. Spiro. "UV resonance Raman spectroscopy of cis--amides." Journal of Raman Spectroscopy 26, no. 8-9 (1995): 867–76. http://dx.doi.org/10.1002/jrs.1250260838.

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Taniguchi, Takaaki, Tomoaki Watanebe, Satoshi Ichinohe, et al. "Nanoscale heterogeneities in CeO2–ZrO2 nanocrystals highlighted by UV-resonant Raman spectroscopy." Nanoscale 2, no. 8 (2010): 1426. http://dx.doi.org/10.1039/c0nr00040j.

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Gao, Y., Samir El-Mashtoly, Biswajit Pal, K. Harada, T. Nakagawa, and T. Kitagawa. "3P099 Investigation of Conformational Changes of Myoglobin upon Ligand binding by UV Resonance Raman Spectroscopy." Seibutsu Butsuri 45, supplement (2005): S228. http://dx.doi.org/10.2142/biophys.45.s228_3.

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Dissertations / Theses on the topic "UV resonant Raman spectroscopy"

1

Kabagambe, Benjamin. "Spectroscopic investigation of proteins : UV resonance Raman studies of apomyoglobin /." Saarbrücken, Germany : VDM Verlag Dr. Müller, 2008. http://etd.library.pitt.edu/ETD/available/etd-10232007-094038.

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Thesis (M.S.)--University of Pittsburgh, Department of Chemistry, 2007.<br>Thesis advisor: Sanford A. Asher. Also available as an electronic book in PDF on the University of Pittsburgh Library Web site. Bibliography: p. 37-41.

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Addison, Christopher James. "Investigating biomolecular structure using fiber-optic UV resonance Raman spectroscopy." Thesis, University of British Columbia, 2011. http://hdl.handle.net/2429/37016.

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The observation of biomolecular structure is critical for the fundamental understanding of biological function. In this work, Fiber-optic UV Resonance Raman Spectroscopy (FO-UVRRS) was employed to study a number of structure-function relationships. A suite of metal-containing dioxygenase enzymes were studied in order to determine the substrate protonation state in the enzyme-substrate complex. Two enzymes with a high degree of sequence identity were studied, where one naturally incorporates a Fe²⁺ metal and the other uses Mn²⁺. Both enzymes react with the same substrate to form an equivalent muconic semialdehyde product. The enzymes are capable of incorporating the non-native metal into the enzymes with no effect on the kinetic properties. The Raman results show that the nature of the metal has no effect on the substrate protonation state. The degradation of 2-hydroxy-6-oxo-6-phenylhexa-2,4-dienoic acid (HOPDA) by BphD in the biphenyl catabolic pathway was studied using FO-UVRRS. Previous reports suggest that enol-keto tautomerization was a critical step in the mechanism of the carbon-carbon bond hydrolase. Hydrolytically impaired variants of BphD were used to study the binding mode of HOPDA. The results show that HOPDA binds to these variants in a strained-enolate geometry and does not undergo an enol-keto tautomerization upon enzyme binding. A fundamental FO-UVRRS study of locked nucleic acid (LNA) olgiomers was performed. LNA bases contain a C4’ to O2’ methylene bridge within the furanose ring of the nucleotide. The research results show that incorporation of a LNA induces a conformational change in the glycosyl bond between the backbone and the base. The results also show that incorporation of an LNA base induces changes in the secondary structure of the nucleic acid. In another study, chemical contamination of synthetic DNA oligomers was observed using FO-UVRRS. The data showed that commercially-available oligomers purified using standard desalting conditions are contaminated with residual benzamide. The results show that a previously assigned –NH₂ scissors vibration in the Raman study of oligomers overlaps with a prominent benzamide vibrational band, calling into question these previous assignments. The results also demonstrate that the extent of benzamide contamination varies from sample-to-sample and between different commercial sources.

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Yazdi, Youseph. "Application of fluorescence and UV resonance Raman spectroscopy to the diagnosis of neoplastic changes in cytological specimens /." Digital version accessible at:, 1997. http://wwwlib.umi.com/cr/utexas/main.

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Kranert, Christian. "Investigation of wide-bandgap semiconductors by UV Raman spectroscopy: resonance effects and material characterization." Doctoral thesis, Universitätsbibliothek Leipzig, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-160062.

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Die vorliegende Arbeit befasst sich mit der Untersuchung von weitbandlückigen Halbleitern mittels Raman-Spektroskopie. Diese wurde vorwiegend unter Verwendung von Licht einer Wellenlänge von 325 nm im ultravioletten Spektralbereich angeregt. Damit konnten zum einen aufgrund eines erhöhten Streuquerschnittes Messungen zur Probencharakterisierung durchgeführt werden, die mit Anregung im sichtbaren Spektralbereich nicht möglich gewesen wären. Zum anderen wurden bei dieser Anregungswellenlänge auftretende Resonanzeffekte untersucht. Dabei werden zwei verschiedene Materialsysteme behandelt: zum einen Kristalle mit Wurtzitstruktur und zum anderen binäre und ternäre Sesquioxide mit Metallionen der III. Hauptgruppe. An den Kristallen mit Wurtzitstruktur wurde die Streuung des Anregungslichts mit Energie oberhalb der Bandlücke an longitudinal-optischen (LO) Phononen untersucht. Die Streuung an einzelnen LO-Phononen wird unter diesen Anregungsbedingungen von einem Prozess dominiert, der eine elastische Streuung beinhaltet, durch die die Impulserhaltung verletzt wird. Es wurde ein Modell aufgestellt, dass zwischen einer elastischen Streuung an der Oberfläche und an Punktdefekten unterscheidet, und mit Hilfe von Experimenten verifiziert. Weiterhin wurde der Einfluss von Ladungsträgern auf die Energie der LO-Phononen untersucht und es wird eine Anwendung dieser Erkenntnisse zur Charakterisierung der Oberfläche von Zinkoxid vorgestellt. An den binären Oxiden des Galliums und Indiums wurden die Energien der Phononenmoden ermittelt und die resonante Verstärkung bei der verwendeten Anregungswellenlänge untersucht. Für das Galliumoxid wurde dabei insbesondere die Anisotropie des Materials berücksichtigt. Für das Indiumoxid wird dargestellt, dass durch die resonante Anregung alle Phononenmoden beobachtet werden können, was insbesondere auch die Bestimmung der Phononenmoden von Dünnschichtproben ermöglicht. Weiterhin waren Mischkristalle des Galliumoxids Untersuchungsgegenstand, in denen das Gallium teilweise durch Indium oder Aluminium ersetzt wurde. Die Phononenenergien wurden in Abhängigkeit der Zusammensetzung ermittelt und der Einfluss von strukturellen Eigenschaften darauf sowie das Auftreten von Phasenübergängen untersucht.

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Westley, Chloe. "Raman spectroscopy and its enhancement techniques for the direct monitoring of biotransformations." Thesis, University of Manchester, 2017. https://www.research.manchester.ac.uk/portal/en/theses/raman-spectroscopy-and-its-enhancement-techniques-for-the-direct-monitoring-of-biotransformations(4ff7ebac-048b-4d81-b13c-7087a2028464).html.

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Protein engineering strategies, such as directed evolution, generate large libraries of enzyme variants, typically in the range of 106-108 variants. However, the availability of rapid, robust high-throughput screening methods has often limited the impact of directed evolution in discovering enzymes with enhanced catalyst performance. Raman spectroscopy is an established analytical technique, providing molecular specific information, permitting analysis in aqueous solutions and as such is an attractive, alternative screening method for biological systems. Although an inherently weak physical phenomenon, enhanced Raman scattering techniques, such as surface enhanced Raman scattering (SERS) and ultraviolet resonance Raman (UVRR) spectroscopy, can be used to overcome the associated sensitivity issues. Herein, we successfully monitored xanthine oxidase (XO) catalysed conversions of xanthine to uric acid, before extending to hypoxanthine, using two contrasting Raman scattering enhanced approaches. Firstly, a SERS-based assay was developed utilising silver nanoparticles to measure analytes directly and quantitatively on micromolar scale, in the absence of chromogenic substrates or lengthy chromatography. Secondly, a UVRR approach was developed enabling monitoring of the XO-mediated reaction in real-time and without the need to quench the system. Significantly, both methods demonstrated over >30 fold reduction in acquisition times (when compared to conventional HPLC analysis), and offered excellent medium-term reproducibility and accuracy of results over significant time periods. Furthermore, investigations were made into developing this SERS-based assay into an enantiomeric screen using another vibrational spectroscopy approach, Raman optical activity (ROA), along with circular dichroism (CD). Successful chiral reduced nanoparticles were synthesised, with multiple characterisation techniques employed, affording enantiopure Au-cysteine and Ag-tyrosine colloids. However, it was not possible to generate consistent and reproducible SEROA responses, with these techniques ultimately being unsuccessful in analysing these chiral sensitive nanoprobes, and thus differentiating between the D- and L- forms. Finally, a novel SERS-based approach, in combination with the standard addition method (SAM), was developed for the routine analysis of uric acid (end product in XO catalysed reaction(s) and biomarker for various diseases), at clinically relevant levels in urine samples from patients. Results were highly comparable and in very good agreement with HPLC analyses, with an average < 9% difference in predictions between the two analytical approaches across all samples analysed, and a 60-fold reduction in acquisition time (when compared with HPLC). Together, the research presented in this thesis demonstrates the suitability of Raman enhanced techniques for quantitative analysis, measuring the analytes directly using a portable Raman instrument and, most importantly, offering significant reductions in acquisition times when compared to established analytical techniques.

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Montagnac, Gilles. "Spectroscopie Raman résonnante UV in situ à haute température ou à haute pression." Thesis, Lyon, École normale supérieure, 2012. http://www.theses.fr/2012ENSL0784/document.

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Dans cette thèse, la spectroscopie Raman résonante UV (SRRUV) est appliquée pour la première fois à l'étude ‘in situ’ de matériaux carbonés à très haute température (> 2000 K) ou à haute pression (< 1 GPa).La thèse est constituée de trois parties. La première aborde notre travail de caractérisation en SRRUV (1) de films semi conducteurs de diamants ultra-nano-cristalins, (2) des kérogènes issues de météorites chondritiques et de charbons, et (3) des tholins, échantillons de carbone-hydrogène-azote, synthétisés comme analogues de l'atmosphère de Titan.L’intérêt pour ces phases du carbone en planétologie et en science des matériaux nous a poussé à mettre en œuvre leur étude ‘in situ’ en SRRUV. La seconde partie de la thèse est consacrée au développement d'une platine chauffante, grâce à laquelle les spectres Raman du graphite sous sa forme pyrolitique et HOPG ont été mesurés jusqu'à 2700 K. Ces données valident les modèles anharmoniques théoriques d’interaction électron-phonon et phonon-phonon. Le spectre Raman du graphite a été étalonné en fonction de la température et devient un « thermomètre » à très haute température.Dans la troisième partie de cette thèse, une presse à enclumes opposées a été modifiée pour suivre en SRRUV les changements structuraux de cristaux moléculaires très luminescents. Les vibrations intramoléculaires du cristal de pérylène sont étudiées sous pression par SRRUV. Ce composé est un cristal formé de molécules organiques polyaromatiques, avec des propriétés de semi-conducteur. Les effets de la pression sur certains modes de vibrations sont non linéaires et mettent en évidence des changement structuraux et de planéité de la molécule<br>I applied UV resonant Raman spectroscopy (UVRRS) to an ‘in situ’ study of carbon materials at very hight temperature (> 2000 K) or at high pressure (< 1 GPa).The advantages of UVRRS are presented in the first part of this PHD thesis, and used to investigate details of the composition and structure of disordered carbon materials such as: (1) n-type nanocrystalline films, (2) carbonaceous matter in chondrites and (3) tholins, HCN synthetic samples of Titan 's atmosphere.‘In situ’ Raman studies are limited to 2000 K by the visible black-body emission. I designed a high temperature cell to perform UVRRS above this limit. The second part of the manuscript presents Raman spectra of pyrolitic graphite and HOPG up to 2700 K. This data are consistent with anharmonic models up to 900 K, and show the coupling effects of electron-phonon and phonon-phonon. The last one dominates the anharmonicity above 1000 K. The Raman spectra was calibrated as a function of temperature and became a “thermometer” up to 2700 K.For high pressure measurements in the third part, I modified an anvil cell to study by UVRRS, the vibrational changes induced by pressure on very luminescent molecular organic crystals. I present an analysis at 244 nm of resonant Raman modes of perylene crystal under hydrostatic pressure up to 0.8 GPa. Some of them have a non linear feature under pressure, revealing structural and planar modifications of the molecules

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Kranert, Christian [Verfasser], Marius [Akademischer Betreuer] Grundmann, Marius [Gutachter] Grundmann, and Dietrich [Gutachter] Zahn. "Investigation of wide-bandgap semiconductors by UV Raman spectroscopy: resonance effects and material characterization / Christian Kranert ; Gutachter: Marius Grundmann, Dietrich Zahn ; Betreuer: Marius Grundmann." Leipzig : Universitätsbibliothek Leipzig, 2015. http://d-nb.info/1239423187/34.

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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.<br>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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Patil, Raj. "Deep UV Raman Spectroscopy." Thesis, The University of Arizona, 2016. http://hdl.handle.net/10150/613378.

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This thesis examines the performance of a custom built deep UV laser (257.5nm) for Raman spectroscopy and the advantages of Raman spectroscopy with a laser in the deep UV over a laser in the visible range (532 nm). It describes the theory of resonance Raman scattering, the experimental setup for Raman spectroscopy and a few Raman spectroscopy measurements. The measurements were performed on biological samples oak tree leaf and lactobacillus acidophilus and bifidobacteria from probotioc medicinal capsules. Fluorescence free Raman spectra were acquired for the two samples with 257.5 nm laser. The Raman spectra for the two samples with a 532nm laser was masked with fluorescence. Raman measurements for an inorganic salt sodium nitrate showed a resonance Raman effect with 257.5 nm laser which led to enhancement in the Raman intensity as compared to that with 532 nm laser. Therefore we were able to demonstrate two advantages of deep UV Raman spectroscopy. First one is the possibility of acquiring fluorescence free spectra for biological samples. Second is the possibility of gaining enhancement in Raman intensity due to resonance Raman effect. It was observed that 257.5 nm laser requires optimization to reduce the bandwidth of the laser to get better resolution. The 257.5 nm laser also needs to be optimized to obtain higher power to get better signal to noise ratio. The experimental setup can also be further improved to obtain better resolution. If the improvements required in the setup are implemented, the deep UV Raman setup will become an important tool for spectroscopy.

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Books on the topic "UV resonant Raman spectroscopy"

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L, McKenzie Robert, and Ames Research Center, eds. Measurements of density,temperature, and their fluctuations in turbulent supersonic flow using UV laser spectroscopy. National Aeronautics and Space Administration, Ames Research Center, 1992.

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Measurements of density,temperature, and their fluctuations in turbulent supersonic flow using UV laser spectroscopy. National Aeronautics and Space Administration, Ames Research Center, 1992.

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L, McKenzie R., and Ames Research Center, eds. Measurements of density,temperature, and their fluctuations in turbulent supersonic flow using UV laser spectroscopy. National Aeronautics and Space Administration, Ames Research Center, 1992.

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L, McKenzie Robert, and Ames Research Center, eds. Measurements of density,temperature, and their fluctuations in turbulent supersonic flow using UV laser spectroscopy. National Aeronautics and Space Administration, Ames Research Center, 1992.

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Graupner, R., and F. Hauke. Functionalization of single-walled carbon nanotubes: Chemistry and characterization. Edited by A. V. Narlikar and Y. Y. Fu. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199533046.013.16.

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This article examines the chemical functionalization and structural alteration of single-walled carbon nanotubes (SWCNTs). It describes the covalent functionalization of the SWCNT framework that is the covalent attachment of functional entities onto the CNT scaffold. In particular, it considers the chemical modification and reactivity of SWCNTs in the context of the reactivity of graphite and fullerenes. It also discusses the defect and sidewall functionalization of SWCNTs, along with various techniques used in the characterization ofSWCNTs upon functionalization, namely: thermogravimetric analysis, spectroscopic techniques such as UV-Vis-NIR spectroscopy and Raman spectroscopy, and microscopic techniques like transmission electron microscopy, atomic force microscopy and scanning tunnelling microscopy.

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Book chapters on the topic "UV resonant Raman spectroscopy"

1

Spiro, T. G., K. Rodgers, and C. Su. "Protein Dynamics From UV Resonance Raman Spectroscopy." In Springer Proceedings in Physics. Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-84771-4_1.

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Aubard, J., J. P. Marsault, G. Levi, L. Chinsky, F. Sureau, and P. Y. Turpin. "UV Resonance Raman Study of Ellipticine and Derivatives." In Fifth International Conference on the Spectroscopy of Biological Molecules. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1934-4_94.

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Handen, Joseph D., and Igor K. Lednev. "Deep UV Resonance Raman Spectroscopy for Characterizing Amyloid Aggregation." In Methods in Molecular Biology. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-2978-8_6.

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Kitagawa, T., S. Kaminaka, Y. Mizutani, K. Imai, and M. Nagai. "UV Resonance Raman Studies of Quaternary Structures of Hemoglobin Using Several Mutants." In Spectroscopy of Biological Molecules. Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0371-8_105.

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Li, P., X. G. Chen, and S. A. Asher. "UV Resonance Raman Studies of the Photochemical Dynamics of N-Methylacetamide Isomerization." In Spectroscopy of Biological Molecules. Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0371-8_19.

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Wheeler, G. V., A. Laigle, B. Jolles, P. Y. Turpin, and L. Chinsky. "The Quadruplex Form of Polyriboinosinic Acid as Studied by UV Resonance Raman Spectroscopy." In Spectroscopy of Biological Molecules. Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0371-8_146.

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Leigh, Brian S., Diana E. Schlamadinger, and Judy E. Kim. "Structures and Dynamics of Proteins Probed by UV Resonance Raman Spectroscopy." In Biophysical Methods for Biotherapeutics. John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118354698.ch9.

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Lednev, Igor K., Anton S. Karnoup, Mark C. Sparrow, and Sanford A. Asher. "Nanosecond UV resonance Raman examination of initial steps in α-helix secondary structure evolution." In Spectroscopy of Biological Molecules: New Directions. Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4479-7_3.

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Asamoto, DeeAnn K., and Judy E. Kim. "UV Resonance Raman Spectroscopy as a Tool to Probe Membrane Protein Structure and Dynamics." In Methods in Molecular Biology. Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9512-7_14.

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Efremov, R. G., D. I. Gulyaev, A. V. Feofanov, G. Vergoten, and A. J. P. Alix. "Environmental Characteristics of Residues in Proteins UV Resonance Raman Spectroscopy and 3d Molecular Hydrophobicity Potential Approach." In Fifth International Conference on the Spectroscopy of Biological Molecules. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1934-4_47.

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Conference papers on the topic "UV resonant Raman spectroscopy"

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Wert, Jonathan, Sanford A. Asher, P. M. Champion, and L. D. Ziegler. "UV Resonance Raman Spectroscopy Of Ethylguanidine." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482881.

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Lacey, Richard J., Ian P. Hayward, H. S. Sands, and David N. Batchelder. "Characterization and identification of contraband using UV resonant Raman spectroscopy." In Enabling Technologies for Law Enforcement and Security, edited by Pierre Pilon and Steve Burmeister. SPIE, 1997. http://dx.doi.org/10.1117/12.266763.

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Punihaole, David, Sanford A. Asher, P. M. Champion, and L. D. Ziegler. "Interrogation of Fibril Aggregation Using UV Resonance Raman Spectroscopy." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482856.

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Asher, S., B. Sharma, L. Ma, et al. "UV Resonance Raman Investigations of Peptide∕Protein Conformation and Folding." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482445.

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Höhl, Martin, Merve Meinhardt-Wollweber, Heike Schmitt, Thomas Lenarz, and Uwe Morgner. "UV-resonance Raman spectroscopy of amino acids." In SPIE BiOS, edited by Anita Mahadevan-Jansen and Wolfgang Petrich. SPIE, 2016. http://dx.doi.org/10.1117/12.2212781.

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Arzhantsev, Sergey, Connie M. Ruzicka, John F. Kauffman, P. M. Champion, and L. D. Ziegler. "Comparative Studies of Therapeutic Protein Secondary Structure Using Deep UV Resonance Raman Spectroscopy." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482450.

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Loppnow, Glen R., P. M. Champion, and L. D. Ziegler. "UV Resonance Raman-derived Initial Excited-state Structural Dynamics of Nucleobases, Nucleosides and Dinucleotides." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482557.

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Pieridou, G., C. Avgousti-Menelaou, P. Tamamis, et al. "UV Resonance Raman Study of TTR(105–115) Structural Evolution as a Function of Temperature." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482862.

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Sharma, Bhavya, Sanford A. Asher, P. M. Champion, and L. D. Ziegler. "The Hunt for Underlying Electronic Transitions in Peptides: UV Resonance Raman Excitation Profiles and Depolarization Ratios." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482855.

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Balakrishnan, Gurusamy, Ying Hu, Thomas G. Spiro, P. M. Champion, and L. D. Ziegler. "Early Steps in Cytochrome C Unfolding Probed by Nanosecond Laser Induced T-jump∕UV Resonance Raman Spectroscopy." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482395.

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Reports on the topic "UV resonant Raman spectroscopy"

1

Azuma, Y., T. LeBrun, M. MacDonald, and S. H. Southworth. Auger resonant Raman spectroscopy. Office of Scientific and Technical Information (OSTI), 1995. http://dx.doi.org/10.2172/166503.

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Cowan, P. L., T. LeBrun, and R. D. Deslattes. X-ray resonant Raman spectroscopy. Office of Scientific and Technical Information (OSTI), 1995. http://dx.doi.org/10.2172/166502.

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Whitehead, C. A., B. D. Cannon, and J. F. Wacker. Krypton isotope analysis using near-resonant stimulated Raman spectroscopy. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10106570.

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Lunsford, Robert, David Gillis, Jacob Grun, Pratima Kunapareddy, Charles Manka, and Segei Nikitin. Component Identification in Multi-Chemical Mixtures With Swept-Wavelength Resonant-Raman Spectroscopy. Defense Technical Information Center, 2011. http://dx.doi.org/10.21236/ada539575.

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Nelson, W. H., and J. F. Sperry. The Rapid Detection of Single Bacterial Cells by Deep UV Micro Raman Spectroscopy. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada249811.

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Tewell, Craig Richmond. UV-Raman spectroscopy, X-ray photoelectron spectroscopy, and temperature programmed desorption studies of model and bulk heterogeneous catalysts. Office of Scientific and Technical Information (OSTI), 2002. http://dx.doi.org/10.2172/803863.

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Windisch, Charles F., B. Peter McGrail, and Gary D. Maupin. Soret Effect Study on High-Pressure CO2-Water Solutions Using UV-Raman Spectroscopy and a Concentric-Tube Optical Cell. Office of Scientific and Technical Information (OSTI), 2012. http://dx.doi.org/10.2172/1043128.

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Langer, B., N. Berrah, and A. Farhat. Auger resonant Raman spectroscopy used to study the angular distributions of the Xe 4d{sub 5/2} {yields} 6p decay spectrum. Office of Scientific and Technical Information (OSTI), 1997. http://dx.doi.org/10.2172/604269.

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