Relevant bibliographies by topics / IR and UV-visible spectroscopy

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'IR and UV-visible spectroscopy'

Author: Grafiati
Published: 4 June 2021
Last updated: 11 February 2022

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Journal articles on the topic "IR and UV-visible spectroscopy"

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A.J.B. "Computer methods in UV, visible and IR spectroscopy." Journal of Molecular Structure 248, no. 1-2 (August 1991): 211–12. http://dx.doi.org/10.1016/0022-2860(91)85016-v.

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Zettler, J. Th, Th Trepk, L. Spanos, Y. Z. Hu, and W. Richter. "High precision UV-visible-near-IR Stokes vector spectroscopy." Thin Solid Films 234, no. 1-2 (October 1993): 402–7. http://dx.doi.org/10.1016/0040-6090(93)90295-z.

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Alam, M. M., S. M. S. Islam, S. M. M. Rahman, and M. M. Rahman. "Simultaneous Preparation of Facial and Meridional Isomer of Cobalt-Amino Acid Complexes and their Characterization." Journal of Scientific Research 2, no. 1 (December 29, 2009): 91–98. http://dx.doi.org/10.3329/jsr.v2i1.2032.

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Preparation and characterization of various complexes of cobalt (III)-amino acid system, especially cobalt (III) glycinato and cobalt (III) alaninato complexes are reported. The identification of the various isomers of these complexes is also reported. The various isomers are separated from their mixture by fractional crystallization. Each of these complexes has been characterized by observing physical characteristics, chemical analysis, UV-visible spectroscopy and IR-spectroscopy. The direct impact of geometry of the complexes to IR stretching frequencies and UV-visible spectral data of amino and carboxyl group in the complexes provided sufficient information about the geometry. A prediction about the geometries of the synthesized has also been focused. Keywords: Cobalt; Amino acid; Isomers; UV-visible; IR. © 2010 JSR Publications. ISSN: 2070-0237 (Print); 2070-0245 (Online). All rights reserved. DOI: 10.3329/jsr.v2i1.2032 J. Sci. Res. 2 (1), 91-98 (2010)
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Kaczmarek, Katarzyna, Andrzej Leniart, Barbara Lapinska, Slawomira Skrzypek, and Monika Lukomska-Szymanska. "Selected Spectroscopic Techniques for Surface Analysis of Dental Materials: A Narrative Review." Materials 14, no. 10 (May 17, 2021): 2624. http://dx.doi.org/10.3390/ma14102624.

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The presented work focuses on the application of spectroscopic methods, such as Infrared Spectroscopy (IR), Fourier Transform Infrared Spectroscopy (FT-IR), Raman spectroscopy, Ultraviolet and Visible Spectroscopy (UV-Vis), X-ray spectroscopy, and Mass Spectrometry (MS), which are widely employed in the investigation of the surface properties of dental materials. Examples of the research of materials used as tooth fillings, surface preparation in dental prosthetics, cavity preparation methods and fractographic studies of dental implants are also presented. The cited studies show that the above techniques can be valuable tools as they are expanding the research capabilities of materials used in dentistry.
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Rajeswari, R., and K. Jeyaprakash. "Bioactive potential analysis of brown seaweed Sargassum wightii using UV-VIS and FT-IR." Journal of Drug Delivery and Therapeutics 9, no. 1 (January 15, 2019): 150–53. http://dx.doi.org/10.22270/jddt.v9i1.2199.

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The current study was investigated to explore the biogenic molecules of Sargassum wightii collected from the south east of Tamil Nadu, India. The biogenic molecules extracted from Sargassum wightii by using methanol as a solvent and the analysis was carried out by using UV-Visible spectroscopy and FT-IR. The UV-Visible spectrum of the methanolic extract of Sargassum wightii exposed the existence of the biogenic molecules separated from 200 - 1100 nm among the absorption. The incidence of peaks from 234-676 nm discovered the presence of flavonoids and its derivatives. The unprocessed methanolic extract of Sargassum wightii was travelled in to FT-IR and it indicated the being of phenols and flavonoids their functional groups such as alcohol, alkane, carboxylic acids, esters, ethers, alkynes and aromatics. From the results, the future aim of this study is necessary to develop the target site to treat dreadful diseases. Keywords: Sargassum Wightii, FT-IR, UV-Visible Spectroscopy, Phytochemical analysis.
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Huang, Sung-Chou, and Ching-Yao Lin. "Reductive electropolymerization of N-methyl-3-pyridylethynyl-porphyrins." Chemical Communications 51, no. 3 (2015): 519–21. http://dx.doi.org/10.1039/c4cc08157a.

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GHAMMAMY, SHAHRIAR, and SAJJAD SEDAGHAT. "Preparation and Characterization of the Schiff Base Ligand (E)- N-(3-nitrobenzylidene) isonicotinohydrazide and its Silver (I) Complex [Ag(NNBIH)2]+." Material Science Research India 9, no. 2 (December 25, 2012): 191–95. http://dx.doi.org/10.13005/msri/090203.

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We describe the synthesis and characterization of a new silver (I) complex of the Schiff base ligand (E) - N-(3-nitrobenzylidene) is onicotinohydrazide that abbreviated as NNBIH was synthesized and characterized. Ag (I) Metal complex of this Schiff base ligand prepared by reaction of nitrate salt of Ag (I) with NNBIH. Characterization of the ligand was made by microanalyses, FT-IR, UV–Visible spectroscopy and its complex was made by microanalyses, FT-IR and UV–Visible spectroscopy. TG- DTA and other analytical methods have been applied to the investigation of the thermal behavior and Structure of the compound [Ag(NNBIH)2]+. Thermal decomposition of these compounds is multistage processes.
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Khan, Raihana Imran, and Kasi Pitchumani. "A pyridinium modified β-cyclodextrin: an ionic supramolecular ligand for palladium acetate in C–C coupling reactions in water." Green Chemistry 18, no. 20 (2016): 5518–28. http://dx.doi.org/10.1039/c6gc01326k.

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An ionic Pd(ii) complex stabilized by a water soluble pyridinium modified β-cyclodextrin was prepared and characterized by NMR, mass spectrometry, FT-IR spectroscopy, UV-visible spectroscopy and DLS (dynamic light scattering).
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Jadhav, Ankita S., Ashvini U. Chaudhari, Kisan M. Kodam, and Dipalee D. Malkhede. "Photophysical and NMR studies of encapsulation of 2-cyano-6-hydroxy benzothiazole in p-sulfonatocalix[6]arene and its biological applications." Analyst 146, no. 17 (2021): 5294–306. http://dx.doi.org/10.1039/d1an00770j.

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Study of inclusion complexation of 2-cyano-6-hydroxy benzothiazole and p-sulfonatocalix[6]arene by UV-visible absorption spectroscopy, steady-state fluorescence spectroscopy, HR-MS, FT-IR, NMR, 2D NMR, and FESEM analysis and its biological activity.
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Gautam, Chandkiram. "Synthesis, Structural and Optical Investigations of (Pb, Bi)TiO3 Borosilicate Glasses." Physics Research International 2014 (July 13, 2014): 1–7. http://dx.doi.org/10.1155/2014/606709.

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A new series of lead bismuth titanate borosilicate glasses with addition of one percent lanthanum oxide have been synthesized using melt-quench technique. X-ray diffraction patterns have been recorded to confirm the amorphous nature of the prepared glass samples. The synthesized glasses have been characterized by using various spectroscopic techniques such as UV-visible, infrared, and Raman spectroscopy. UV-visible measurements were recorded in the wavelength range from 200 to 1100 nm whereas IR and Raman spectroscopic measurements were recorded over a continuous wavenumber range from 400 to 5000 cm−1 and 1000 to 2000 cm−1 respectively. The different absorption peaks/bands were formed in IR spectral patterns. The spectral bands appear towards the lower wavenumber sides due to the Bi and Pb, content while the bands appear towards the higher wavenumber sides due to the formation of diborate and triborate network units.
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Dissertations / Theses on the topic "IR and UV-visible spectroscopy"

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Butz, André. "Case studies of stratospheric nitrogen, chlorine and iodine photochemistry based on balloon borne UV / visible and IR absorption spectroscopy." Paris 6, 2006. http://www.theses.fr/2006PA066243.

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Kilic, Ilker. "Optical Characterization Of Silicon Based Hydrogenated Amorphous Thin Films By Uv-visible And Infrared Measurements." Master's thesis, METU, 2006. http://etd.lib.metu.edu.tr/upload/2/12607013/index.pdf.

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Various carbon content hydrogenated amorphous silicon carbide (a-Si1¡
xCx:H) and hydrogenated amorphous silicon (a-Si:H) thin films have been deposited on various substrates by using plasma enhanced chemical vapour deposition (PECVD) technique. Transmission spectra of these films have been determined within UV-Visible region and the obtained data were analysed to find related physical constants such as
refractive indices, thicknesses, etc. Fourier transform infrared (FT-IR) spectrometry technique has been used to determine transmission &
reflection type spectra of these films. Obtained data were analysed to determine bond structures of the films. E®
ects of relative concentration of ethylene (C2H4) gas on thin film bond structure and on optical constants have been questioned.
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Quinebeche, Sébastien. "Suivi cinétique des polymérisations et copolymérisations anioniques de monomères éthyléniques par spectroscopie IR et UV-visible in situ." Bordeaux 1, 2007. http://www.theses.fr/2007BOR13359.

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Les travaux présentés dans ce texte concernent la mise au point d'une nouvelle technique de suivi cinétique des polymérisations et copolymérisations anioniques du styrène (S), de l'isoprène (l), du 1,1-diphényléthythylène (DPE) et du méthacrylate de méthyle (MMA), au moyen du couplage des spectroscopies IR et UV-visible in situ. L'objectif de l'étude est de mieux comprendre l'influence de certains paramètres expérimentaux sur les différentes étapes qui interviennent dans la préparation des copolymères triblocs poly(styrène-b-butadiène-b-méthacrylate de méthyle) (SBM) dans les solvants non polaires. Pour des raisons d'opportunité expérimentale, l'isoprène a été pris comme modèle du butadiène. La technique de suivi des polymérisations utilise des sondes lesquelles, plongées dans le milieu réactionnel, permettent de mesurer simultanément et en temps réel les concentrations en monomères et en espèces activesau cours de la polymérisation. Bien qu'elle ne fasse pas appel aux techniques sous haut vide qui permettent l'accès aux conditions de grande pureté du milieu réactionnel, notre méthode a cependant permis des mesures rapides, précises et reproductibles des constantes de vitesse des différentes homo- et copolymérisations étudiées. Les résultats de l'étude cinétique ont ainsi pu être utilisés pour une meilleure connaissance du comportement réactionnel de ces systèmes. Ainsi, par exemple, il a été montré que, lors de la copolymérisation à blocs du styrène et de l'isoprène amorcée par le n-butyllithium, la nature du solvant aromatique influence seulement la cinétique d'homopolymérisation du styrène (Kss toluène > Kss éthylbenzène). Il a aussi été montré que l'ajout du 2-méthoxyéthanolate de lithium lors de l'étape d'addition du DPE sur le S-b-Ili accélère non seulement la réaction d'addition du DPE mais améliore également l'efficacité de l'amorçage de la polymérisation du MMA, ce qui est essentiel pour la qualité des produits obtenus. Ce ligand, initialement utilisé pour contrôler la polymérisation du MMA, joue donc un rôle triple dans la préparation des SBM.
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Esteves, López Natalia. "Etude du transfert de protons dans les systèmes moléculaires." Thesis, Aix-Marseille, 2017. http://www.theses.fr/2017AIXM0178/document.

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Une des meilleures sources d’énergie verte serait d’être capable de casser une molécule d’eau à partir du rayonnement visible fourni par le soleil, afin de générer du H$_2$. L’eau présente le don d’ubiquité sur terre puisqu’elle est présente, sous ses trois phases, dans les océans, la terre et l’atmosphère. Cependant, une énergie de 6.66 eV (VUV) est nécessaire pour rompre directement une des liaisons covalentes de l’eau. Dans ce travail, nous montrons qu’il est possible de dissocier l’eau si celle-ci est associée à un catalyseur photosensible de nature organique, dont les prototypes absorbent dans l’UV, comme la Pyridine (Py). Un récent travail théorique prédit que la Py peut jouer le rôle de ce photocatalyseur, suivant la réaction : Py-H$_2$O + h$\nu_1 \to$ Py*-H$_2$O $\to$ PyH$\bullet$ + OH$\bullet$Pour tester ce modèle théorique nous avons étudié le complexe Py-eau isolé dans un cluster moléculaire froid. Nous avons caractérisé la spectroscopie électronique du PyH$\bullet$ en phase gazeuse et nous avons mis en évidence cette réaction de photodissociation par irradiation UV de clusters Py-(H$_2$O)$_n$. Nous avons aussi testé ce système en matrices cryogéniques pour évaluer l’effet de la solvatation solide. La dernière étape du processus, la régénération du photocatalyseur par absorption d’un deuxième photon UV (PyH$\bullet$ + h$\nu \to$ Py + H$\bullet$) à été aussi prouvé. Il semblerait que seuls les radicaux PyH$\bullet$ chauds soient capables d’engendrer cette dernière réaction.A l’heure actuelle, nous explorons de nouveaux systèmes moléculaires prototypes susceptibles de conduire au même phénomène
A major challenge to generate green energy from sunlight would be to split water which is a ubiquitous molecule to produce H$_2$. However VUV light (6.66 eV) is needed to dissociate the H-OH covalent bond. In this work we will show that it is possible to dissociate water via photo-sensitisation with UVC light, using a simple organic catalyst.Recently, ab-initio calculations predict that pyridine (Py) can act as a photo-catalyst to split water by absorption of a UV photon, following the reaction:Py-H$_2$O + h$\nu_1 \to$ Py*-H$_2$O $\to$ PyH$\bullet$ + OH$\bullet$ To test this prediction, we studied the Py-H$_2$O complex in isolated cold molecular cluster and the system trapped in cryogenic matrices. We characterized the electronic spectroscopy of the PyH$\bullet$ in the gas phase and we evidenced the reaction through UV excitation of Py-(H$_2$O) $_n$ clusters. We have evidenced that the reaction leads PyH$\bullet$ as photoproduct of the reaction. We also evidenced that the surrounding conditions play an important role in the reaction.We have demonstrated that the UV excitation of Py-water clusters leads to the formation of PyH$\bullet$, thus we have evidenced the water splitting reaction. The last step of the process, that is the regeneration of the catalyst by absorption of a second UV photon (PyH$\bullet$ + h$\nu \to$ Py + H$\bullet$) has been studied and it seems that only hot PyH$\bullet$ molecules are able to follow this channel. In the present, we are studying other aromatic molecules which are expected to lead the photochemical dissociation of water
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Yang, Jingchen. "Using the Transient IR Spectroscopy to Elucidate Reaction Mechanisms in Visible Light Photoredox Catalysis:." Thesis, Boston College, 2020. http://hdl.handle.net/2345/bc-ir:108934.

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Thesis advisor: Matthias M. Waegele
Studying the visible light-driven photoredox catalysis coupled with transition-metal complexes is of overriding importance in the development of synthetic strategy. Comparing to conventional thermal catalysis, reactions catalyzed and/ or initiated by photon energy are not only attractive for establishing a more sustainable system, but also for their unique reactivity that has previously been inaccessible. However, one issue draws our attention is that such photoredox catalytic schemes often suffer from a limited substrate scope. To develop more efficient and effective synthetic strategies applicable to broader range of substrates, it is of our interest to construct an functional and reliable instrument to identify the critical mechanistic steps that lead to low product yield. To this end, we designed a time-resolved visible-pump/ infrared-probe spectroscopic measurement technique to monitor reaction dynamics in-situ. Using our transmission infrared setup, we effectively demonstrated in-situ photoexcitation and decay process of Tris(2,2′-bipyridyl)dichlororuthenium(II) hexahydrate in deuterated acetonitrile. In addition, to optimize signal resolution, an electronic filter was installed in one of the data-collecting channels to allow for concurrent AC-coupled and DC-coupled signal recording. A series of chopper wheel experiments was conducted to assure the functionality of the system and reliability of obtained data
Thesis (MS) — Boston College, 2020
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
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Mavadat, Maryam. "Characterization of biomedical used plasmas by IR and UV-VIS emission spectroscopy." Thesis, Université Laval, 2014. http://www.theses.ulaval.ca/2014/30780/30780.pdf.

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La modification de surface par plasma est une technique largement utilisée pour améliorer les propriétés de surface de polymères par le greffage de différents groupes fonctionnels. Dans ce projet de recherche, différentes méthodes pour améliorer les techniques de caractérisation de décharge micro-ondes de N2 et N2-H2 ont été étudiées dans le but d’optimiser le procédé de traitement de surface par plasma. Tout d'abord, un certain nombre de paramètres du plasma ont été mesurés à différentes conditions de traitement. Pour déterminer les paramètres du plasma, la spectroscopie d'émission optique a été utilisée dans la région l’ultraviolet, du visible et l’infrarouge (rarement utilisée dans la littérature scientifique). L’utilisation de la spectroscopie d'émission dans cette dernière région spectrale est avantageuse car elle permet d'éliminer les forts chevauchements entre les transitions atomiques et moléculaires et de pallier la faible intensité du signal observée dans la région de l’ultraviolet et du visible. Par la suite, la composition chimique de surface du PTFE a été analysée par XPS pour déterminer les concentrations en carbone, fluor, azote et des groupements amine suite à un traitement par plasma. Les résultats mentionnés ci-dessus ont été utilisés pour corréler les conditions de traitement et les paramètres de décharge micro-ondes à la composition chimique du PTFE modifié, dans l’objectif de mettre en évidence les paramètres expérimentaux du plasma et les espèces présentes dans le plasma qui jouent un rôle clé pour maximiser la fonctionnalisation de surface du polymère avec des groupements amine. En outre, un modèle mathématique a été développé en utilisant la technique de régression PLS. Pour construire ce modèle, un ensemble de données de variables d'entrée contenant les conditions de traitement et les paramètres spectroscopiques du plasma et une matrice de réponse contenant les propriétés de surface du polymère ont été générées. La base de données obtenue a été utilisée pour établir la relation entre les paramètres du plasma, les conditions de traitement et la chimie de surface du film. Cela a finalement permis de prédire la composition chimique de la surface à partir d’informations relatives au plasma, sans avoir à effectuer des analyses de surface après le traitement.
Plasma surface modification is a widely used technique for improving the surface properties ‎of ‎polymers through the introduction of different functional groups. In ‎the current research project, ‎different methods to improve the characterization techniques of ‎N2 and N2-H2 microwave discharge ‎were investigated with the aim of optimizing the ‎plasma surface process. First of all, a number of plasma parameters were measured at ‎different process conditions. To determine the plasma ‎parameters, optical emission spectroscopy was used ‎not only within the well-documented ‎UV-Visible region but also within the rarely ‎studied infrared zone. Using infrared optical emission ‎spectroscopy is advantageous as it ‎eliminates the strong overlap between atomic and molecular ‎transitions as well as the low ‎intensity UV-Visible emission spectroscopy limitations. In the next step, the PTFE surface chemical composition was analyzed via XPS to quantify the ‎concentrations of carbon, fluorine, and nitrogen after a plasma treatment in a N2-H2 gaseous ‎environment. The XPS analyses were also performed after chemical derivatization to quantify the ‎surface concentration of amino groups (%NH2) at different process conditions. The above-mentioned results were used to correlate process conditions and microwave N2-‎H2 ‎discharge‏ ‏parameters‏ ‏to the chemical composition of the modified ‎PTFE. The purpose was ‎to ‎determine the external plasma parameters and species present within the plasma ‎which ‎‎play a key ‎role in the introduction of amino groups to the polymer surface. ‎Furthermore, a mathematical model was developed using ‎the Partial Least Squares ‎Regression, ‎‎(PLSR) ‎using custom scripts written in MATLAB. A data set of ‎input variables including the process conditions ‎and plasma ‎parameters for each experiment ‎were generated along with the corresponding response ‎matrix which in turn contained the ‎surface ‎properties of the film.‎ ‎The resulting database was used to ‎build the relationship ‎between the plasma parameters, ‎process condition and the resulting film ‎surface chemistry. ‎This ultimately enabled to predict the PTFE surface chemistry from data originating ‎from the plasma, without having to proceed to post-plasma surface characterization.
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Kyriaki, Kosma. "UV-pump IR-probe Spectroscopy of Molecules with Time-Resolution reaching the 10-fs Range." Diss., lmu, 2008. http://nbn-resolving.de/urn:nbn:de:bvb:19-92803.

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Godard, Marie. "Les carbones amorphes hydrogénés : observations, synthèse et caractérisation en laboratoire de poussières interstellaires." Phd thesis, Université Paris Sud - Paris XI, 2011. http://tel.archives-ouvertes.fr/tel-00635907.

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Les carbones amorphes hydrogénés (a-C:H ou HAC) constituent une composante importante de la poussière interstellaire. Ces grains hydrocarbonés sont observés au travers de bandes d'absorption IR à 3.4, 6.9 et 7.3 microns, caractéristiques des vibrations des liaisons C-H aliphatiques. Leurs signatures spectrales sont détectées dans le milieu interstellaire diffus de différentes lignes de visée de la Voie Lactée, mais aussi de nombreuses autres galaxies. Cette thèse porte sur l'étude de ces a-C:H interstellaires, à la fois au travers d'observations de ces poussières, et grâce à la synthèse et la caractérisation d'analogues de laboratoire.Une première partie de mon travail de thèse est consacrée à l'observation de la bande à 3.4 microns des a-C:H du milieu interstellaire diffus galactique en direction de la source IRAS 18511+0146. La bande d'absorption des modes d'élongation C-H détectée dans cette direction, vers différentes lignes de visée proches les unes des autres, présente des profondeurs optiques similaires et les plus fortes observées dans la Voie Lactée en dehors du centre galactique. Différentes interprétations de la profonde bande dans cette direction sont discutées.Des analogues de ces poussières carbonées aliphatiques ont été synthétisés en laboratoire, sous forme de films, grâce à un plasma, et reproduisent bien les bandes IR observées dans le milieu interstellaire diffus. Ces échantillons ont été caractérisés par spectroscopie d'absorption dans l'UV-visible et l'IR.Puisque les a-C:H émettent un rayonnement visible après absorption de photons UV ou visibles, une partie de la thèse est consacrée à une étude systématique de cette photoluminescence. Pour la première fois, les rendements absolus et intrinsèques de photoluminescence d'a-C:H sont déterminés pour une large gamme de longueurs d'onde d'excitation. Les propriétés de la photoluminescence des a-C:H sont confrontées aux observations de l'Emission Rouge Etendue, une large bande d'émission interstellaire dont les porteurs ne sont pas identifiés.Afin de déduire l'influence des rayons cosmiques sur ces poussières carbonées, les analogues produits ont été irradiés par différents ions énergétiques dont le dépôt d'énergie est similaire à celui du rayonnement cosmique interstellaire. Les effets induits ont été suivies par IR. L'analyse de la déshydrogénation des a-C:H observée au travers de la disparition progressive des bandes des C-H aliphatiques permet de déduire l'évolution de ces poussières interstellaires et de leurs signatures spectrales sous l'effet des rayons cosmiques. La destruction induite par les rayons cosmiques est comparée aux effets de l'exposition aux photons UV et aux atomes d'hydrogène afin d'interpréter l'évolution de la bande d'absorption à 3.4 microns observée dans le milieu interstellaire diffus, mais pas dans les nuages denses.
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Holland, Torrey. "VIBRATIONAL SPECTROSCOPY ANALYSES OF THE DEGRADATION AND CONTAMINATION OF ENGINE OIL LUBRICANTS COUPLED WITH MULTIPLE SPECTROSCOPIC TECHNIQUES." OpenSIUC, 2018. https://opensiuc.lib.siu.edu/theses/2399.

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The spectral analysis techniques afforded us from the field of physics has enabled us to explore the spectral signatures of trace contaminants and degradation products in used or in service engine oil through atomic and molecular spectroscopy. Here we have examined the need to address proper preparation of calibrating samples for infrared spectroscopy analysis by inducing emulsification and have evaluated multiple procedures for proper emulsification of samples with the intent to help establish the protocols that are not explicitly set forth in the ASTM International standard. We have also explored the use of Fourier-transform infrared spectroscopy techniques to examine the suppression of the O–H stretching mode of water due to the influence of ethylene glycol, which may help in the quantification of water when both are present in oil. This was done in conjunction with exploring alternative methods for direct and indirect measurement of the glycol contamination by use of UV/Vis spectroscopy, Raman, and laser-induced breakdown spectroscopy. An exploration of FT-IR and UV/Vis data on the oxidation of oil by means of ANOVA calculations has led to the reporting of highly significant differences in the data of differing oxidation times and in regions of the spectrum not known to have been previously reported.
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Nickum, Elisa A. "Analysis of Regulated Drugs Using Chromatographic and Spectrophotometric Techniques Coupled with Spectroscopy An Orthogonal Approach to Protecting Public Health." University of Cincinnati / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1504799568245931.

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Books on the topic "IR and UV-visible spectroscopy"

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A Handbook of spectroscopic data chemistry (UV, IR, PMR, 13CNMR and mass spectroscopy). Jaipur: Oxford Book Co., 2009.

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Räty, Jukka. UV-Visible Reflection Spectroscopy of Liquids. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004.

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Räty, Jukka, Kai-Erik Peiponen, and Toshimitsu Asakura. UV-Visible Reflection Spectroscopy of Liquids. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-540-45093-1.

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Lützen, Jan Winther. In-line UV-visible spectroscopy of additive concentrations in polymer melts during extrusion. Ottawa: National Library of Canada, 2002.

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North Atlantic Treaty Organization. Advisory Group for Aerospace Research and Development. Atmospheric propagation in the UV, visible, IR and MM-wave region and related systems aspects. Neuilly sur Seine, France: AGARD, 1990.

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(Editor), H. A. Willis, ed. Computer Methods in Uv, Visible, and Ir Spectroscopy. Royal Society of Chemistry, 1991.

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O, George W., Willis H. A, Royal Society of Chemistry (Great Britain), and Polytechnic of Wales, eds. Computer methods in UV, visible, and IR spectroscopy. Cambridge [England]: Royal Society of Chemistry, 1990.

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O, George W., and Willis H. A, eds. Computer methods in UV, visible, and IR spectroscopy. Cambridge: Royal Society of Chemistry, 1990.

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(Editor), I. I. Sobelman, and Vladimir A. Slemzin (Editor), eds. Current Russian Research in Optics & Photonics: New Methods & Instruments for Space & Earth Based Spectroscopy in Xuv, Uv, Ir< & Millimeter Waves (Proceedings ... Russian Research in Optics & Photonics). SPIE-International Society for Optical Engine, 1998.

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Peiponen, Kai-Erik, Toshimitsu Asakura, and Jukka A. Räty. UV-Visible Reflection Spectroscopy of Liquids. Springer, 2014.

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Book chapters on the topic "IR and UV-visible spectroscopy"

1

Michl, Josef, and Erik W. Thulstrup. "Applications of IR and UV-Visible Linear Dichroism." In Polarized Spectroscopy of Ordered Systems, 25–55. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-3039-1_2.

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Glownia, J. H., J. Misewich, and P. P. Sorokin. "Subpicosecond UV/IR Absorption Spectroscopy." In Atomic and Molecular Processes with Short Intense Laser Pulses, 359–66. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4613-0967-3_43.

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Jentoft, Friederike C. "Electronic Spectroscopy: Ultra Violet-Visible and near IR Spectroscopies." In Characterization of Solid Materials and Heterogeneous Catalysts, 89–147. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527645329.ch3.

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Hoffmann, Christian, and Werner Mäntele. "Optically Transparent Electrodes (Ote) for Spectro- Electrochemical Cells for Investigations on Redox Reactions of Proteins in the UV-, Visible and IR-Region." In Spectroscopy of Biological Molecules: Modern Trends, 595–96. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5622-6_269.

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Glownia, J. H., J. Misewich, and P. P. Sorokin. "Utilization of UV and IR Supercontinua in Gas-Phase Subpicosecond Kinetic Spectroscopy." In The Supercontinuum Laser Source, 299–336. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3326-6_8.

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Clownia, J. H., J. Misewich, and P. P. Sorokin. "Utilization of UV and IR Supercontinua in Gas-Phase Subpicosecond Kinetic Spectroscopy." In The Supercontinuum Laser Source, 337–76. New York, NY: Springer New York, 1989. http://dx.doi.org/10.1007/978-1-4757-2070-9_8.

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Nakamura, Ryosuke, and Norio Hamada. "Vibrational Dynamics in Photoactive Yellow Protein Revealed by Mid-IR Pump/Visible Probe Spectroscopy." In Springer Proceedings in Physics, 524–27. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-13242-6_128.

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Krätschmer, W., and K. Nachtigall. "Spectroscopy of Matrix-Isolated Carbon Molecules in the UV, Vis, and IR Spectral Range." In Polycyclic Aromatic Hydrocarbons and Astrophysics, 75–83. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-4776-4_7.

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Baumruk, V., M. Abdelkafi, N. Leulliot, L. Bednárová, C. Hervé Du Penhoat, P. Y. Turpin, A. Namane, C. Gouyette, T. Huynh-Dinh, and M. Ghomi. "Common Structural Features of UNCG Tetraloops in Very Short Hairpins Determined by UV Absorption, Raman, IR and NMR Spectroscopies." In Spectroscopy of Biological Molecules: Modern Trends, 241–42. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5622-6_107.

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Fogel, Christian, Fabienne Petry, Andreas Barth, and Werner Mäntele. "Titration of Protonable Residues in Proteins by Flash Induced H+-Release from “Caged Proton” — UV/VIS and IR Studies." In Fifth International Conference on the Spectroscopy of Biological Molecules, 113–14. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1934-4_39.

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Conference papers on the topic "IR and UV-visible spectroscopy"

1

Lu, Grant, Gerhard F. Schoetz, Jan Vydra, and Daniel G. Fabricant. "Optical fiber for UV-IR broadband spectroscopy." In Astronomical Telescopes & Instrumentation, edited by Sandro D'Odorico. SPIE, 1998. http://dx.doi.org/10.1117/12.316759.

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Tcibulnikova, Anna V., Rodion R. Y. Borkunov, Valery V. Bryukhanov, Vasiliy A. Slezhkin, Ilya I. G. Samusev, and Andrey Y. Zyubin. "Visible and IR spectroscopy of ablative ytterbium nanoparticles." In SPIE Nanophotonics Australasia 2017, edited by James W. M. Chon and Baohua Jia. SPIE, 2018. http://dx.doi.org/10.1117/12.2282558.

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Habka, Sana, Eric Gloaguen, Michel Mons, and Valerie Brenner. "GAZ PHASE IR AND UV SPECTROSCOPY OF NEUTRAL CONTACT ION PAIRS." In 71st International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2016. http://dx.doi.org/10.15278/isms.2016.ti11.

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Barnett, Steven M., Richard W. Bormett, and Andrew Whitley. "Multidimensional Raman spectroscopy: from the UV to the near IR." In BiOS '99 International Biomedical Optics Symposium, edited by Dario Cabib, Carol J. Cogswell, Jose-Angel Conchello, Jeremy M. Lerner, and Tony Wilson. SPIE, 1999. http://dx.doi.org/10.1117/12.347577.

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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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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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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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Huston, Alan L., Vasanthi Sivaprakasam, Cathy S. Scotto, Horn-Bond Lin, Jay D. Eversole, Abraham Schultz, and Jeff M. Willey. "Optical classification of bioaerosols using UV fluorescence and IR absorption spectroscopy." In European Symposium on Optics and Photonics for Defence and Security, edited by John C. Carrano and Arturas Zukauskas. SPIE, 2004. http://dx.doi.org/10.1117/12.578062.

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Sun, Dewei, Timothy Zwier, Karl Blodgett, and Joshua Fischer. "CONFORMATION-SPECIFIC IR AND UV SPECTROSCOPY OF A MODEL SYNTHETIC FOLDAMER: β3-ALA TRIPEPTIDE." In 73rd International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2018. http://dx.doi.org/10.15278/isms.2018.ml09.

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Zwier, Timothy, Scott McLuckey, Jacob Dean, James Redwine, and Nicole Burke. "COLD, GAS-PHASE UV AND IR SPECTROSCOPY OF PROTONATED LEUCINE ENKEPHALIN AND ITS ANALOGUES." In 69th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2014. http://dx.doi.org/10.15278/isms.2014.tg11.

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Reports on the topic "IR and UV-visible spectroscopy"

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Dickens, Brian, and Eric Byrd. Programs to Estimate UV Dosage and Damage. National Institute of Standards and Technology, September 1999. http://dx.doi.org/10.6028/nist.ir.7500.

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Abstract:
The system of programs described in this paper is concerned with estimating the damage ensuing from exposure of specimens in dry and humid atmospheres to UV and visible radiation covering the solar range. Damage is monitored quantitatively by changes in IR spectra. The dose is estimated from UV spectra of the lamps and the interference filters (used to isolate a particular wavelength range). The dosage is estimated from the dose and the UV absorption of the specimens themselves. These programs allow rapid estimation of dosage and damage from regions of data, and manipulation and processing of the massive amounts of data required to carry out such comprehensive tests in a complete yet user-friendly manner.
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