Relevant bibliographies by topics / Linear dichroism

Contents

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

Academic literature on the topic 'Linear dichroism'

Author: Grafiati
Published: 4 June 2021
Last updated: 30 July 2024

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Journal articles on the topic "Linear dichroism"

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Chang, Huibin, Matthew A. Marcus, and Stefano Marchesini. "Analyzer-free linear dichroic ptychography." Journal of Applied Crystallography 53, no. 5 (September 23, 2020): 1283–92. http://dx.doi.org/10.1107/s160057672001002x.

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Linear dichroism is an important tool to characterize the transmission matrix and determine the crystal or orbital orientation in a material. In order to achieve high-resolution mapping of transmission properties, the linear-dichroism scattering model in ptychographic imaging is introduced, and an efficient two-stage reconstruction algorithm is developed. Using the proposed algorithm on a uniaxial material, the dichroic transmission matrix can be recovered without an analyzer by using ptychography measurements with as few as three different polarization angles, with the help of an empty region to remove phase ambiguities.
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Kuball, Hans-Georg. "Circular Dichroism and Linear Dichroism." Zeitschrift für Physikalische Chemie 212, Part_1 (January 1999): 118–19. http://dx.doi.org/10.1524/zpch.1999.212.part_1.118.

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Polavarapu, Prasad L., and Gang-Chi Chen. "Polarization-Division Interferometry: Far-Infrared Dichroism." Applied Spectroscopy 48, no. 11 (November 1994): 1410–18. http://dx.doi.org/10.1366/0003702944028119.

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We report the first far-infrared dichroism measurements using a polarization-division interferometer (PDI) developed in our laboratory. This interferometer uses a free-standing wire-grid beamsplitter made of tungsten wires. In conjunction with a linear polarizer in front of the source and two roof-top mirrors (one in each arm of the interferometer), the PDI divides the input beam into two orthogonal linear polarization components, recombines them for interference at the beamsplitter, and directs the output beam at 90° to the direction of the input beam. Light exiting the interferometer is manipulated with far-infrared lenses, to avoid polarization distortions that are inherent to the reflecting surfaces of the mirrors. The performance of the PDI is evaluated by measuring the linear dichroism of oriented PVF2 [poly(vinylidenefluoride) and circular dichroism of α-pinene, camphor, and 3-methylcyclohexanone. The dichroic multiplex advantage (ability to measure dichroism in the entire far-infrared region from a single measurement) and throughput advantage are demonstrated. These measurements establish the utility of the PDI in measuring transmission and linear dichroism spectra simultaneously without the need for any additional components. Additional developments appear necessary to establish the circular dichroism measurements when the magnitudes are less than one part in one thousand.
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Polavarapu, Prasad L., Gang-Chi Chen, and Stephen Weibel. "Development, Justification, and Applications of a Mid-Infrared Polarization-Division Interferometer." Applied Spectroscopy 48, no. 10 (October 1994): 1224–35. http://dx.doi.org/10.1366/0003702944027381.

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We report the development of a polarization-division interferometer (PDI) for the mid-infrared region. This interferometer uses a self-designed beamsplitter constructed in-house from a BaF2 polarizer and a matching substrate. In conjunction with a linear polarizer in front of the source and two roof-top mirrors, one in each arm of the interferometer, the PDI divides the input beam into two orthogonal linear polarization components, recombines them for interference at the beamsplitter, and directs the output beam at 90° to the direction of the input beam. Light exiting the interferometer is manipulated entirely with lenses, to avoid polarization distortions that are inherent to the reflecting surfaces of the mirrors. Details of the instrumental design for this mid-infrared PDI are presented. The performance of the PDI is evaluated by measuring the circular dichroism of α-pinene and camphor and the linear dichroism of oriented polypropylene and polystyrene. These measurements establish the utility of the PDI to measure transmission, circular dichroism, and linear dichroism spectra simultaneously without need for any additional components. The dichroic multiplex advantage (ability to measure dichroism in the entire mid-infrared region from a single measurement) and throughput advantage are demonstrated.
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Garab, Győző, and Herbert van Amerongen. "Linear dichroism and circular dichroism in photosynthesis research." Photosynthesis Research 101, no. 2-3 (May 6, 2009): 135–46. http://dx.doi.org/10.1007/s11120-009-9424-4.

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Pellow, Robert, and Martin Vala. "Magnetic circular dichroism and magnetic linear dichroism of randomly oriented linear molecules." Molecular Physics 68, no. 4 (November 1989): 893–901. http://dx.doi.org/10.1080/00268978900102611.

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Lippitsch, M. E., M. Riegler, F. R. Aussenegg, N. Friedman, M. Sheves, Y. Mazur, and L. Margulies. "Linear Dichroism Spectroscopy of Retinal with Picosecond Time Resolution." Zeitschrift für Naturforschung C 40, no. 11-12 (October 1, 1985): 880–85. http://dx.doi.org/10.1515/znc-1985-11-1222.

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Abstract For the first time linear dichroism spectroscopy has been extended to the picosecond time regime. 11-cis retinal, all-trans retinal and 1,8-diphenyl-1,3,5,7-octatetraene (DPOT) are incorporated into polyethylene films and oriented by stretching the films. By measuring picosecond transient absorption spectra polarized parallel and perpendicular to the stretching direction and calculating the dichroic ratio we get informations about the molecular geometry in excited singlet and triplet states. The results may have relevance to vision.
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Pagni, R. M. "Circular Dichroism and Linear Dichroism (Rodger, Alison; Norden, Bengt)." Journal of Chemical Education 75, no. 9 (September 1998): 1095. http://dx.doi.org/10.1021/ed075p1095.

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LYLE, PAUL A., and WALTER S. STRUVE. "DYNAMIC LINEAR DICHROISM IN CHROMOPROTEINS." Photochemistry and Photobiology 53, no. 3 (March 1991): 359–65. http://dx.doi.org/10.1111/j.1751-1097.1991.tb03641.x.

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Ade, H., and B. Hsiao. "X-ray Linear Dichroism Microscopy." Science 262, no. 5138 (November 26, 1993): 1427–29. http://dx.doi.org/10.1126/science.262.5138.1427.

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Dissertations / Theses on the topic "Linear dichroism"

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Bulheller, Benjamin M. "Circular and linear dichroism spectroscopy of proteins." Thesis, University of Nottingham, 2009. http://eprints.nottingham.ac.uk/10866/.

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Circular dichroism (CD) is an important technique in the structural characterization of proteins, and especially for secondary structure determination. The CD of proteins can be calculated from first principles using the matrix method, with an accuracy that is almost quantitative for helical proteins. Thus, for proteins of unknown structure, CD calculations and experimental data can be used in conjunction to aid structure analysis. The vacuum-UV region (below 190 nm), where charge-transfer transitions have an influence on the CD spectra, can be accessed using synchrotron radiation circular dichroism (SRCD) spectroscopy. Calculations of the vacuum-UV CD spectra have been performed for 71 proteins, for which experimental SRCD spectra and X-ray crystal structures are available. The theoretical spectra are calculated considering charge-transfer and side chain transitions, which significantly improves the agreement with experiment, raising the Spearman correlation coefficient between the calculated and experimental intensity at 175 nm from 0.12 to 0.79. The influence of the different conformations used for the calculation of charge-transfer transitions is discussed in detail, focussing on the effect in the vacuum-UV. Linear dichroism (LD) provides information on the orientation of molecules but is more challenging to analyze than CD. To aid the interpretation of LD spectra, the calculation of protein LD using the matrix method is established and the results compared to experimental data. The orientations of five prototypical proteins are correctly reproduced by the calculations. Using a simplified approach, matrix method parameter sets for the nucleic bases and naphthalenediimide (NDI) have been created and are used to determine DNA/RNA conformations and to study NDI nanotubes. Finally, to make CD and LD calculations available for the scientific community in an easy-to-use fashion, the web interface DichroCalc is introduced.
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Sandhu, Sandeep Kaur. "Development of a biosensor based on linear dichroism spectroscopy." Thesis, University of Birmingham, 2015. http://etheses.bham.ac.uk//id/eprint/5737/.

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Existing methodologies for biomolecular detection are limited in several key areas. Heterogeneous assays struggle with various wash steps which can prolong assay time, while other assays require costly reagents, lack mobility and can be highly complex in nature. This project demonstrates how a bio-nano particle in the form of M13 bacteriophage (M13) can be used for the basis of a novel homogeneous immunoassay which incorporates the use of linear dichroism spectroscopy (LD). M13 has a high aspect ratio which allows it to align easily in shear flow, this in turn generates a large LD signal. This property of M13 has been manipulated for use in a new in-vitro diagnostic technique. Existing M13 production yields are much lower than those required for this assay. A new method was developed which increased the yield 10 fold. Chemical modifications were made by covalently attaching chromophores, this enabled the M13 LD signal to be visualised in the visible region and develops the potential for multiplexing. By chemically modifying M13 with chromophores and antibodies it was possible to create an assay capable of detecting 10⁵ cells/mL of Escherichia coli O157. This is 100 times more sensitive than the M13 based assay developed by Pacheco-Gomez et al. (2012). The assay was reassembled to detect small molecules and was found to have a sensitivity of 0.01 mM. The assays presented form a sensitive, specific, fast diagnostic tool capable of detecting pathogens and small molecules. It offers significant improvements over existing methods, and could act as a platform in developing a multimodal detection system.
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Norton, Stephen R. "Linear dichroism spectroscopy and biophysics of an amyloid protein." Thesis, University of Warwick, 2015. http://wrap.warwick.ac.uk/79946/.

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Though Parkinson’s Disease is known to be caused by cell death in one region of the brain, and though the protein α-synuclein is known to be associated with it, the causes are still poorly understood. It has not yet been shown how α-synuclein may cause cells to die, with research focusing on the range of structures the protein is able to adopt. The classic amyloid fibrils are currently believed to be non-toxic, but smaller, soluble oligomers appear to be the toxic species. Key to toxicity and to the normal function of α-synucein (also unknown to-date) appear to be the ability of the protein to bind to lipids, as toxicity may be due to oligomers forming pores in cells, and the normal function of the protein may be in vesicle transport. The work presented in this thesis represents a collection of studies, across several disciplines, that test aspects of the behaviour of α-synuclein. Circular dichroism and fluorescence data presented here show that the protein interacts with the lipid POPS in a concentration-dependent manner. Linear dichroism was an important and complementary technique to these, but required some method refinement and sample preparation improvement. This work is presented in this thesis, alongside experimental and theoretical studies into the behaviour of lipid vesicles in Couette flow. It was shown that certain lipids perform better in Couette flow, particularly the mixture of POPC and POPS. This informed the linear dichroism studies, and enabled experiments suggesting that oligomers of α-synuclein may insert across the membrane of vesicles. If confirmed, this would support the amyloid pore theory of α-synuclein toxicity.
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Wang, Xiao. "Confocal angle resolved linear dichroism microscopy for structural fluorescence imaging." Ecole centrale de Marseille, 2013. http://tel.archives-ouvertes.fr/docs/00/87/10/10/PDF/Wang-Thesis.pdf.

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La microscopie de fluorescence a récemment été complétée par une technique appelée dichroïsme linéaire résolu angulairement, basé sur le fait que l'absorption de la lumière est un processus sensible à l'orientation moléculaire. En analysant la réponse d'émission de fluorescence en fonction de l'orientation de la polarisation de la lumière excitatrice, cette technique permet de remonter à l'information d'orientation sur un ensemble de molécules fluorescentes, plus précisément son angle d'orientation moyenne et l'amplitude de ses fluctuations angulaires autour de cette moyenne. Dans cette thèse, nous mettons en oeuvre de nouvelle méthodes et instrumentations capables d'améliorer la robustesse et la rapidité de l'analyse de données de réponses résolues en polarisation, la vitesse de l'acquisition de données, et d'explorer la possibilité de mesurer l'orientation 3D de molécules. Nous proposons une méthode capable de mesurer les propriétés d'orientation de sondes lipidiques fluorescentes par l'utilisation d'un disque de Nipkow couplé à une imagerie par caméra, et combiné avec la modulation rapide de la polarisation par modulateur électro-optique. Une nouvelle méthode de traitement de données est développée pour considérablement améliorer la rapidité et la précision de l'information par une étude des sources de bruit et d'incertitude, dues au bruit et aux facteurs instrumentaux. Cette technique a été testée avec succés sur des vésicules géantes uni-lamellaires et sur cellules vivantes, marquées par les sondes lipidiques DiIC18 et di-8-ANEPPQ. Cette méthode est capable d'acquérir une information précise sur l'orientation moléculaire à une cadence d'une image par seconde. Enfin, afin de sonder de manière non ambiguë l'orientation 3D d'un ensemble de molécules, une nouvelle méthode est proposée, supportée par des simulations numériques, basée sur la variation hors plan de la polarisation d'excitation dans le volume focal par une somme cohérente de champs polarisés linéairement et radialement
Based on the fact that the absorption of light is a molecular-orientation sensitive process, fluorescence microscopy has been recently completed by a technique called angle-resolved linear dichroism. By analyzing the fluorescence emission response with respect to the polarization orientation of the exciting light, this technique allows retrieving orientation information of an ensemble of fluorescent molecules, namely the average orientation angle and the amplitude of the angular fluctuations around this average. In this PhD thesis, we implement new methods and instrumentation tools able to improve the robustness and speed of the polarization resolved data analysis, the rate of the data acquisition, and at last to explore the possibility to record molecular 3D orientation information. A scheme able to monitor the real-time orientation properties of fluorescent lipid probes is proposed using a high-speed spinning disk coupled to camera imaging, combined with fast switching of the polarization state by an electro optical modulator. A new data processing method is developed which considerably improves the speed and the precision of the retrieved information by investigating the sources of bias and uncertainty due to noise and instrumentation factors. The technique has been successfully tested on giant unilamellar vesicles and on living cells labeled with different fluorescent lipid probes, DiIC18 and di-8-ANEPPQ. It was able to acquire precise molecular orientation images at full frame rates in the range of one frame per second. At last in order to probe unambiguously the 3D orientation information of an ensemble of molecules, a new method is proposed and supported by simulations, based on the out-of-plane tuning of the excitation polarization realized in the focusing volume by coherently summing linearly and radially polarized fields
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Little, Haydn Andrew. "The development of novel diagnostic sensors based on linear dichroism spectroscopy." Thesis, University of Birmingham, 2017. http://etheses.bham.ac.uk//id/eprint/7421/.

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Within this thesis the use of linear dichroism (LD) spectroscopy was utilised as a new platform for the development of diagnostic sensors. To develop a novel diagnostic sensor in combination with LD spectroscopy a particle with a high aspect ratio is need. Such a particle is M13 bacteriophage, this micron long molecular scaffold is easily alignable in shear flow generating a large LD signal. Using LD spectroscopy, it was possible to demonstrate the successful detection of multiple DNA targets, and that the sensor can also discriminate between DNA sequences differing in length, with a limit of detection (LOD) of 2 M, competitive with the current non amplification methods of DNA detection. The reversibility and regeneration of the sensor were also investigated. Finally, the development of an M13 bacteriophage sensor for the detection of proteins was designed in an unprecedented plug-and-play format. The assay was designed to detect thrombin, which is important in the monitoring of blood clotting disorders. LD spectroscopy enabled the detection of thrombin with a LOD of 10 pM and with a dynamic range from 10 pM to 47 nM.
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Rittman, Martyn. "Charaterisation of polymeric biomacromolecules using linear dichroism and Markov chain Monte Carlo." Thesis, University of Warwick, 2008. http://wrap.warwick.ac.uk/2237/.

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Riffel, Richard W. "Characterization of dichroism and linear polarization effects on colorimetric properties of plastic transmitting materials /." Online version of thesis, 1992. http://hdl.handle.net/1850/11650.

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Amarasinghe, Don Praveen. "A study of the alignment of polymeric molecules and vesicles in fluid flows for linear dichroism experiments." Thesis, University of Warwick, 2018. http://wrap.warwick.ac.uk/105768/.

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Linear dichroism (LD) spectroscopy is a technique which uses polarised light to make inferences on the relative orientations of chemical groups within a molecule. A requirement for experiments using this technique is the alignment of molecules in the analyte. This thesis considers the use of fluid flows to align molecules. The use of bead-spring and bead-rod models to simulate the behaviour of polymers and particles in fluid flows has been extensively discussed in the literature. In this work, the FENE-Fraenkel spring force law is implemented in bead-spring chain simulations, to assess the alignment behaviour of molecules in flow. Analytical properties of FENE-Fraenkel springs are derived and used to inform the coding of the simulation programme and to assess its outputs. The results of these simulations were comparable to both analytical results in zero-shear conditions and to data previously published by Hsieh et al. [48] on bead-spring chains in extensional flow, albeit with a reduced signal-to-noise ratio. Simulations of the alignment of FENE-Fraenkel spring dumbbells in shear flows show increased alignment with high shear rates, similar to modelling data published by McLachlan et al. [89]. This work also considers the use of microfluidic devices manufactured from polydimethylsiloxane to perform linear dichroism studies on DNA and vesicles in solution. A wide channel and cross-slot device are developed to provide conditions for pressure-driven and extensional flow to align molecules. Both devices are shown to align DNA molecules to measure an LD signal, with the cross-slot performing better than the wide channel device. With solutions of vesicles containing 1,6-Diphenylhexa-1,3,5-triene, a membrane probe, the wide channel device is shown to provide weak vesicle alignment to measure an LD signal. However, both microfluidic devices are unable to align molecules as well as Couette flow, the method normally used to align molecules for LD experiments.
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Rodger, Alison. "Molecular aspects of biomolecule structure and function." Thesis, The University of Sydney, 2002. http://hdl.handle.net/2123/516.

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All biological processes are fundamentally inter-molecular interactions. In order to understand, and hence control, biomolecular structure and function, methods are required that probe biological systems at the molecular level, ideally with those molecules being in their native environment. The research summarized herein has at its core the development and application of ultra violet (UV)-visible spectrophotometric techniquies for this prupose, in particular circular dichrosim (CD) and linear dichrosim (LD) but also absorbance, fluorescence and resonance light scattering. The spectroscopy is complemented by fundamental theoretical work on molecular structure and reactivity that forms the basis for designing molecules to bind to biomolecules for a particular structural or functional effect. A brief summary of the contributions of the listed publications to our understanding of 'Molecular aspects of biololecule structure and function' is given below under five headings: Circular dichroism theory Molecular geometry and reactivity Small molecule-macromolecule interactions: spectroscopic probes of inter-molecular geometries Molecular design for nucleic acid structure and control Spectroscopic probes of biomolecule structure: instrumentation and application In general terms these correspond to successive phases of the research programme, however, all areas have been present since the first publications in 1983 and can be traced weaving through all subsequent activity.
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Rodger, Alison. "Molecular aspects of biomolecule structure and function." University of Sydney. Chemistry, 2002. http://hdl.handle.net/2123/516.

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All biological processes are fundamentally inter-molecular interactions. In order to understand, and hence control, biomolecular structure and function, methods are required that probe biological systems at the molecular level, ideally with those molecules being in their native environment. The research summarized herein has at its core the development and application of ultra violet (UV)-visible spectrophotometric techniquies for this prupose, in particular circular dichrosim (CD) and linear dichrosim (LD) but also absorbance, fluorescence and resonance light scattering. The spectroscopy is complemented by fundamental theoretical work on molecular structure and reactivity that forms the basis for designing molecules to bind to biomolecules for a particular structural or functional effect. A brief summary of the contributions of the listed publications to our understanding of 'Molecular aspects of biololecule structure and function' is given below under five headings: Circular dichroism theory Molecular geometry and reactivity Small molecule-macromolecule interactions: spectroscopic probes of inter-molecular geometries Molecular design for nucleic acid structure and control Spectroscopic probes of biomolecule structure: instrumentation and application In general terms these correspond to successive phases of the research programme, however, all areas have been present since the first publications in 1983 and can be traced weaving through all subsequent activity.
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Books on the topic "Linear dichroism"

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Rodger, Alison. Circular dichroism and linear dichroism. Oxford: Oxford University Press, 1997.

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Nordén, Bengt. Linear dichroism and circular dichroism: A textbook on polarized-light spectroscopy. Cambridge: Royal Society of Chemistry, 2010.

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Litvin, Feliks, Lyudmila Satina, Ravil' Hatypov, Galina Mikulinskaya, Nikita Pen'kov, and Konstantin Neverov. Molecular spectroscopy. Fundamentals of theory and practice. ru: INFRA-M Academic Publishing LLC., 2022. http://dx.doi.org/10.12737/1870280.

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The textbook is an introduction to the theory and practice of spectroscopy in the ultraviolet, visible and infrared regions. The presentation of the theoretical foundations is accompanied by a detailed guide on the practical use of spectroscopy for quantitative and qualitative analysis of substances and reactions in simple and complex systems. Attention is paid to modern methods of infrared spectroscopy with Fourier transform (FTIR), intermolecular energy transfer (FRET), linear dichroism of complex objects. It is intended for a wide range of biologists, chemists, students and postgraduates of natural science specialties.
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B, Samori', and Thulstrup Erik Waaben 1941-, eds. Polarized spectroscopy of ordered systems. Dordrecht: Kluwer Academic Publishers, 1988.

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Circular and Linear Dichroism. Nova Science Publishers, Incorporated, 2015.

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Dafforn, Tim, Alison Rodger, and Bengt Nordén. Linear Dichroism and Circular Dichroism: A Textbook on Polarized-Light Spectroscopy. Royal Society of Chemistry, The, 2023.

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Dafforn, Tim, Alison Rodger, and Bengt Nordén. Linear Dichroism and Circular Dichroism: A Textbook on Polarized-Light Spectroscopy. Royal Society of Chemistry, The, 2019.

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Pellow, Robert C. Matrix isolation spectroscopy: Magnetic circular and linear dichroism. 1990.

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Schattschneider, Peter. Linear and Chiral Dichroism in the Electron Microscope. Jenny Stanford Publishing, 2012.

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Schattschneider, Peter. Linear and Chiral Dichroism in the Electron Microscope. Jenny Stanford Publishing, 2012.

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Book chapters on the topic "Linear dichroism"

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Rodger, Alison. "Linear Dichroism." In Encyclopedia of Biophysics, 1–3. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-642-35943-9_640-1.

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Rodger, Alison. "Linear Dichroism." In Encyclopedia of Biophysics, 1237–39. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-16712-6_640.

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Rodger, Alison. "Linear Dichroism." In Comprehensive Chiroptical Spectroscopy, 493–523. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118120187.ch18.

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Rodger, Alison. "Polarized Light, Linear Dichroism, and Circular Dichroism." In Encyclopedia of Biophysics, 1–3. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-642-35943-9_637-1.

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Rodger, Alison. "Polarized Light, Linear Dichroism, and Circular Dichroism." In Encyclopedia of Biophysics, 1891–93. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-16712-6_637.

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Rodger, Alison. "Nucleic Acid Linear Dichroism." In Encyclopedia of Biophysics, 1–3. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-642-35943-9_631-1.

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Rodger, Alison. "Linear Dichroism Spectroscopy: Theory." In Encyclopedia of Biophysics, 1–5. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-642-35943-9_641-1.

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Rodger, Alison. "Linear Dichroism Spectra: Measurement." In Encyclopedia of Biophysics, 1–6. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-642-35943-9_642-1.

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Rodger, Alison. "Nucleic Acid Linear Dichroism." In Encyclopedia of Biophysics, 1761–63. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-16712-6_631.

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Rodger, Alison. "Linear Dichroism Spectroscopy: Theory." In Encyclopedia of Biophysics, 1244–48. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-16712-6_641.

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Conference papers on the topic "Linear dichroism"

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Galgano, G. D., A. B. Henriques, E. Abramof, Marília Caldas, and Nelson Studart. "Magnetic Linear Dichroism Effects in EuTe." In PHYSICS OF SEMICONDUCTORS: 29th International Conference on the Physics of Semiconductors. AIP, 2010. http://dx.doi.org/10.1063/1.3295493.

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Kilchoer, C., J. A. Dolan, M. Saba, N. Abdollahi, K. Korzeb, U. Wiesner, U. Steiner, I. Gunkel, and B. D. Wilts. "Linear and Circular Dichroism in Gyroid Optical Metamaterials." In 2018 12th International Congress on Artificial Materials for Novel Wave Phenomena (Metamaterials). IEEE, 2018. http://dx.doi.org/10.1109/metamaterials.2018.8534182.

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Dipold, J., G. Koeckelberghs, M. G. Vivas, L. De Boni, and C. R. Mendonca. "Two-Photon Circular-Linear Dichroism on a Binaphtalenebased Polymer." In Frontiers in Optics. Washington, D.C.: OSA, 2017. http://dx.doi.org/10.1364/fio.2017.jw4a.91.

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George, D. K., J. Seo, H. Zhang, C. Zhang, T. Kirzhner, G. Koren, J. Y. T. Wei, A. Markelz, and J. Cerne. "Linear Dichroism in High Temperature Superconductors in THz Range." In 2020 45th International Conference on Infrared, Millimeter and Terahertz Waves (IRMMW-THz). IEEE, 2020. http://dx.doi.org/10.1109/irmmw-thz46771.2020.9370370.

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Schwickert, Markus M. "Studies of X-ray magnetic linear dichroism in absorption." In The 11th US national synchrotron radiation instrumentation conference (SRI99). AIP, 2000. http://dx.doi.org/10.1063/1.1291769.

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Mykowska, Ewa, Krzysztof Fiksinski, and Danuta Bauman. "Linear dichroism of dyes used in liquid crystal displays." In XIII International Conference on Liquid Crystals: Chemistry, Physics, and Applications, edited by Stanislaw J. Klosowicz, Jolanta Rutkowska, Jerzy Zielinski, and Jozef Zmija. SPIE, 2000. http://dx.doi.org/10.1117/12.385704.

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"Fluorescence detected linear dichroism and anisotropy imaging using RCM." In European Light Microscopy Initiative 2024. Royal Microscopical Society, 2024. http://dx.doi.org/10.22443/rms.elmi2024.166.

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Simon, John D., Kiaoliang Xie, and Robert Dunn. "Time-resolved circular dichroism studies of biological systems." In OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1990. http://dx.doi.org/10.1364/oam.1990.mbb4.

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Abstract:
This paper examines a new experimental approach for studying ultrafast relaxation processes in biological systems—picosecond time-resolved circular-dichroism spectroscopy. The technical details of the experimental apparatus will be discussed. Optical analysis using Jones matrix calculus shows how complications due to pump induced linear dichroism can be eliminated enabling the isolation and measurement of transient circular dichroism signals. Extension of this approach to femtosecond time resolution will also be examined.
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Bertolotto, J. A., G. B. Roston, G. M. Corral, and M. E. Ascheri. "Reduced Electric Linear Dichroism of DNA Fragments in Aqueous Solutions." In NONEQUILIBRIUM STATISTICAL MECHANICS AND NONLINEAR PHYSICS: XV Conference on Nonequilibrium Statistical Mechanics and Nonlinear Physics. AIP, 2007. http://dx.doi.org/10.1063/1.2746740.

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Dowrey, Anthony E., Greg G. Hillebrand, Isao Noda, and Curtis Marcott. "Dynamic Infrared Linear Dichroism (DIRLD) Spectroscopy Of Human-Hair Keratin." In Intl Conf on Fourier and Computerized Infrared Spectroscopy, edited by David G. Cameron. SPIE, 1989. http://dx.doi.org/10.1117/12.969403.

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Reports on the topic "Linear dichroism"

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Schumann, F. O., R. F. Willis, and K. W. Goodman. Magnetic x-ray linear dichroism of ultrathin Fe-Ni alloy films. Office of Scientific and Technical Information (OSTI), April 1997. http://dx.doi.org/10.2172/603528.

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Mishra, S., W. J. Gammon, and D. P. Pappas. Magnetic x-ray linear dichroism in resonant and non-resonant Gd 4f photoemission. Office of Scientific and Technical Information (OSTI), April 1997. http://dx.doi.org/10.2172/603526.

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Ohta, Taisuke, Taisuke Ohta, Robert Copeland, and Robert Copeland. Testing the possibility of magnetic domain imaging based on circular & linear dichroism using photoemission electron microscopy. Office of Scientific and Technical Information (OSTI), November 2018. http://dx.doi.org/10.2172/1760415.

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