Optical Rotatory Dispersion
Stereoisomerism
Magnetic Resonance Spectroscopy
Molecular Structure
Chemistry
Infrared dichroism of the DNA-caffeine complex. A new method for determination of the ligand orientation. (1/218)
Infrared linear dichroism (LD) measurements on films of the DNA-caffeine complex in terms of the relative humidity (r.h.) show two main effects. Firstly, there is an insertion of caffeine molecules into the DNA double helix (B form), as evidenced by a very strong parallel LD behaviour of the 745 cm-1 band due to the C-H out-of-plane deformation vibration of caffeine. Furthermore, a high r.h. values a modified B form occurs in the complex similar to the B form recently reported by BRAHMS and coworkers for DNA-polypeptide complexes. The reversible B-A transition of the DNA in dependence of the r.h. is not affected in general in the presence of caffeine. (+info)Lactonamycin, a new antimicrobial antibiotic produced by Streptomyces rishiriensis MJ773-88K4. II. Structure determination. (2/218)
The absolute structure of a new antibiotic lactonamycin is described. The NMR studies deduced one of four possible structures for the aglycon attached by a rhodinose through glycosidic bond. The stereochemistry of the sugar obtained by an acid hydrolysis was determined to be L-form by measuring optical rotation. The stereochemistry of the aglycon was determined by X-ray crystallographic analysis. (+info)Structure elucidation of Sch 20562, a glucosidic cyclic dehydropeptide lactone--the major component of W-10 antifungal antibiotic. (3/218)
A novel bacterium designated as Aeromonas sp. W-10 produces the antibiotic W-10 complex which comprises of two major and several minor components. The two major components from this complex, Sch 20562 (1) and Sch 20561 (1a), are of biological interest in view of their potent antifungal activity. The chemical degradation studies utilized for the assignment of structure 1 for Sch 20562 are described here. Some of the noteworthy diversity of structural features in this glucosidic cyclic dehydrononapeptide lactone 1 are: an N-terminal (D)-beta-hydroxymyristyl unit, three D-amino acid units, two (E)-alpha-aminocrotonyl units, and an O-alpha-D-glucosyl-N-methyl-L-allo-threonine unit. The structure determination of 1 utilized the selective cleavage of the dehydropeptide units by ozonolysis to form fragments that were sequenced by mass spectrometry. The stereochemistry of the amino acid units were assigned by isolation of the free amino acids from the hydrolysates of the fragments. The stereochemistry of the alpha-aminocrotonyl units and the glucosidic linkage were assigned by nmr spectroscopy and molecular rotation data. (+info)Structure elucidation of Sch 20561, a cyclic dehydropeptide lactone--a major component of W-10 antifungal antibiotic. (4/218)
Antibiotic W-10 is a fermentation complex produced by the bacterium Aeromonas sp. W-10. The cyclic dehydropeptide lactones Sch 20562 (1) and Sch 20561 (2) are the major components of this fermentation complex and are of biological interest in view of their unique structural features and potent antifungal activity. The chemical degradation studies that were utilized in the assignment of structure 2 for Sch 20561 are described here. The structure determination of 2 made use of the ozonolytic cleavage of the dehydropeptide units to form fragments that were sequenced by mass spectrometry. The cyclic dehydropeptide lactone Sch 20561 (2) was found to be the aglycone of Sch 20562 (1) and these two natural products were correlated by a chemical transformation involving the deglucosidation of 1 to form 2. (+info)Attraction of the oriental fruit fly, Dacus dorsalis, to methyl eugenol and related olfactory stimulants. (5/218)
The attraction of male oriental fruit flies to methyl eugenol and 34 analogues was investigated quantitatively using the characteristic feeding response. Methyl eugenol was the most active compound studied, with a feeding response to 0.01 mug, but saturation of the allyl side chain or replacement of allyl by allyloxy produced compounds almost as effective. Replacement of the methoxy groups by methylenedioxy, methyl, or chloro groups abolished all response. The ring geometry of the methoxy groups was critical, with orthodimethoxy most active and meta-dimethoxy inactive. Replacement of methoxy with hydroxy, methylthio, or amino groups did not abolish the response. The failure of the oriental fruit fly to respond to the methyl and chloro isosteres of methyl eugenol was contrasted with the response of a human odor panel which perceived these compounds as having weak floral odors. (+info)Optimal integration of texture and motion cues to depth. (6/218)
We report the results of a depth-matching experiment in which subjects were asked to adjust the height of an ellipse until it matched the depth of a simulated cylinder defined by texture and motion cues. In one-third of the trials the shape of the cylinder was primarily given by motion information, in another one-third of the trials it was given by texture information, and on the remaining trials it was given by both sources of information. Two optimal cue combination models are described where optimality is defined in terms of Bayesian statistics. The parameter values of the models are set based on subjects' responses on trials when either the motion cue or the texture cue was informative. These models provide predictions of subjects' responses on trials when both cues were informative. The results indicate that one of the optimal models provides a good fit to the subjects' data, and the second model provides an exceptional fit. Because the predictions of the optimal models closely match the experimental data, we conclude that observers' cue-combination strategies are indeed optimal, at least under the conditions studied here. (+info)Stereochemical course of the adenosine triphosphate phosphoribosyltransferase reaction in histidine biosynthesis. (7/218)
The product of the first reaction in histidine biosynthesis is shown by optical rotation measurements on three derivatives to have inverted, beta stereochemistry at the newly formed bond. This is in contrast to alpha linkage expected on the basis of previously observed exchange, specificity, and covalent intermediate phenomena. The postulate double displacement mechanism for adenosine triphosphate phosphoribosyltransferase must be modified to account for the product stereochemistry. (+info)Complex formation between mycobacterial polysaccharides or cyclodextrins and palmitoyl coenzyme A. (8/218)
The mycobacterial polysaccharides MMP (3-O-methyl-mannose-containing polysaccharide), MGLP (lipolysaccharide containing 6-O-methylglucose and glucose), and the cyclodextrins (cyclohexaamylose and cycloheptaamylose) form stoichiometric complexes with palmitoyl-CoA (Machida, Y., Bergeron, R., Flick, P., and Bloch, K. (1973) J. Biol. Chem. 248, 6246-6247). Complex formation is presumed to result from hydrophobic interactions. In order to enhance the hydrophobic character of the cyclodextrins the following derivatives have been synthesized: heptakis (2,di-O-propyl)-, heptakis (2,6-di-O-methyl)-, pentakis (6-O-methyl)-, heptakis (3-O-methyl)-, and permethylated beta-cyclo-dextrin. These compounds stimulate fatty acid synthesis catalyzed by the Mycobacterium smegmatis fatty acid synthetase, the magnitude of the effect decreasing in the order in which the alkylated cyclodextrins are listed above. MMP or MGLP are qualitatively indistinguishable from alkylated cyclodextrins both with respect to palmitoyl-CoA binding and with respect to effects on enzyme systems, suggesting that they form inclusion complexes of the same type. On the basis of model building it is postulated that MMP in solution assumes a helical conformation with a hydrophobic channel about 6 A in diameter and approximately 29 A long, dimensions appropriate for accommodating the paraffinic chain of palmitoyl-CoA in the form of an inclusion complex. Since palmitoyl-CoA binds to polysaccharide much more tightly than free palmitate it is further postulated that ionized groups of the CoA moiety of acyl CoA participate in the binding and do so by hydrogen bonding to the hydrophilic exterior of helical MMP. Palmitoyl-CoA, and to a lesser extent palmitate, affect the optical rotation of MMP and also of the alkylated cyclodextrins indicating that complex formation induces conformational changes in the polysaccharides. (+info)Optical rotation, also known as optical activity, is a property of certain substances to rotate the plane of polarization of linearly polarized light as it passes through the substance. This ability arises from the presence of optically active molecules, most commonly chiral molecules, which have a non-superimposable mirror image.
The angle and direction of rotation (either clockwise or counterclockwise) are specific to each optically active substance and can be used as a characteristic identification property. The measurement of optical rotation is an important tool in the determination of the enantiomeric purity of chiral compounds, such as drugs and natural products, in chemistry and pharmacology.
The optical rotation of a substance can be influenced by factors such as temperature, concentration, wavelength of light, and solvent used. The magnitude of the optical rotation is often reported as the specific rotation, which is the optical rotation per unit length (usually expressed in degrees) and per unit concentration (often given in grams per deciliter or g/dL).
Optical rotatory dispersion (ORD) is a phenomenon in which plane-polarized light is rotated as it passes through an optically active substance. It is a measure of the difference in refractive index between left and right circularly polarized light, and is dependent on the wavelength of the light. ORD is used to determine the optical purity and absolute configuration of chiral molecules, particularly in the field of stereochemistry. The magnitude and sign of the rotation can provide information about the concentration and type of optically active compound present in a sample.
Stereoisomerism is a type of isomerism (structural arrangement of atoms) in which molecules have the same molecular formula and sequence of bonded atoms, but differ in the three-dimensional orientation of their atoms in space. This occurs when the molecule contains asymmetric carbon atoms or other rigid structures that prevent free rotation, leading to distinct spatial arrangements of groups of atoms around a central point. Stereoisomers can have different chemical and physical properties, such as optical activity, boiling points, and reactivities, due to differences in their shape and the way they interact with other molecules.
There are two main types of stereoisomerism: enantiomers (mirror-image isomers) and diastereomers (non-mirror-image isomers). Enantiomers are pairs of stereoisomers that are mirror images of each other, but cannot be superimposed on one another. Diastereomers, on the other hand, are non-mirror-image stereoisomers that have different physical and chemical properties.
Stereoisomerism is an important concept in chemistry and biology, as it can affect the biological activity of molecules, such as drugs and natural products. For example, some enantiomers of a drug may be active, while others are inactive or even toxic. Therefore, understanding stereoisomerism is crucial for designing and synthesizing effective and safe drugs.
Molecular conformation, also known as spatial arrangement or configuration, refers to the specific three-dimensional shape and orientation of atoms that make up a molecule. It describes the precise manner in which bonds between atoms are arranged around a molecular framework, taking into account factors such as bond lengths, bond angles, and torsional angles.
Conformational isomers, or conformers, are different spatial arrangements of the same molecule that can interconvert without breaking chemical bonds. These isomers may have varying energies, stability, and reactivity, which can significantly impact a molecule's biological activity and function. Understanding molecular conformation is crucial in fields such as drug design, where small changes in conformation can lead to substantial differences in how a drug interacts with its target.
Magnetic Resonance Spectroscopy (MRS) is a non-invasive diagnostic technique that provides information about the biochemical composition of tissues, including their metabolic state. It is often used in conjunction with Magnetic Resonance Imaging (MRI) to analyze various metabolites within body tissues, such as the brain, heart, liver, and muscles.
During MRS, a strong magnetic field, radio waves, and a computer are used to produce detailed images and data about the concentration of specific metabolites in the targeted tissue or organ. This technique can help detect abnormalities related to energy metabolism, neurotransmitter levels, pH balance, and other biochemical processes, which can be useful for diagnosing and monitoring various medical conditions, including cancer, neurological disorders, and metabolic diseases.
There are different types of MRS, such as Proton (^1^H) MRS, Phosphorus-31 (^31^P) MRS, and Carbon-13 (^13^C) MRS, each focusing on specific elements or metabolites within the body. The choice of MRS technique depends on the clinical question being addressed and the type of information needed for diagnosis or monitoring purposes.
Molecular structure, in the context of biochemistry and molecular biology, refers to the arrangement and organization of atoms and chemical bonds within a molecule. It describes the three-dimensional layout of the constituent elements, including their spatial relationships, bond lengths, and angles. Understanding molecular structure is crucial for elucidating the functions and reactivities of biological macromolecules such as proteins, nucleic acids, lipids, and carbohydrates. Various experimental techniques, like X-ray crystallography, nuclear magnetic resonance (NMR) spectroscopy, and cryo-electron microscopy (cryo-EM), are employed to determine molecular structures at atomic resolution, providing valuable insights into their biological roles and potential therapeutic targets.
In the context of medicine, "chemistry" often refers to the field of study concerned with the properties, composition, and structure of elements and compounds, as well as their reactions with one another. It is a fundamental science that underlies much of modern medicine, including pharmacology (the study of drugs), toxicology (the study of poisons), and biochemistry (the study of the chemical processes that occur within living organisms).
In addition to its role as a basic science, chemistry is also used in medical testing and diagnosis. For example, clinical chemistry involves the analysis of bodily fluids such as blood and urine to detect and measure various substances, such as glucose, cholesterol, and electrolytes, that can provide important information about a person's health status.
Overall, chemistry plays a critical role in understanding the mechanisms of diseases, developing new treatments, and improving diagnostic tests and techniques.
Chemical phenomena refer to the changes and interactions that occur at the molecular or atomic level when chemicals are involved. These phenomena can include chemical reactions, in which one or more substances (reactants) are converted into different substances (products), as well as physical properties that change as a result of chemical interactions, such as color, state of matter, and solubility. Chemical phenomena can be studied through various scientific disciplines, including chemistry, biochemistry, and physics.
Optical rotation
John Anthony Schellman
Igor Dzyaloshinskii
Cannabidiol
Polarimeter
Francis G. Slack
H. Stanley Allen
Samuel Francis Boys
Arborane
Magnetometer
Specific rotation
Crystal optics
Joseph Achille Le Bel
Aerobeacon
Shortolide A
Pressure jump
Faraday rotator
Anomer
Lighthouse of Ponta de Sagres
Chromatography detector
Eligio Perucca
Two-photon circular dichroism
Augustin-Jean Fresnel
Henri Bénard
PVLAS
Enantiomeric excess
Hernandaline
Axion
Optical rotatory dispersion
Eskimo yo-yo
Optical rotation - Wikipedia
Self-Oscillating Rubidium Magnetometer using Nonlinear Magneto-Optical Rotation | NIST
A scientific note on the specific optical rotation of three honey types from Bulgaria | Apidologie
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3-Carboxy-2,3-dideoxy-L-threo-pentaric acid | C6H8O7 | ChemSpider
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Structure Databases | Wiley Antibase | ACD/Labs
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High Quality Lemon oil/ lemon essential oil
ISO 3054:1987 - Oil of lavandin abrialis (Lavandula angustifolia P. Miller x Lavandula latifolia (Linnaeus f.) Medikus), France
Magneto-optical2
- The detection of nonlinear magneto-optical rotation (NMOR) of polarized light through alkali atomic vapor is a highly sensitive technique for measuring magnetic fields. (nist.gov)
- Theory of colliding-probe atomic magnetometry: breaking the symmetry-enforced magneto-optical rotation blockade. (bvsalud.org)
Faraday4
- The Faraday rotation angle and the magneto-optical transmission of light through the monolayer graphene with a magnetic field perpendicular to the plane of graphene are calculated within the framework of the low-energy effective quantum field theory of Dirac quasiparticles. (elsevierpure.com)
- Shovkovy, I & Wang, X 2014, ' Analysis of faraday rotation and magneto-optical transmission in monolayer graphene ', International Journal of Modern Physics B , vol. 28, no. 8, 1450061. (elsevierpure.com)
- Another venue to spin-photon interfacing is to make use of the rotation of optical polarization (so-called Faraday or Kerr rotation) induced by a single spin placed at the centre of a cavity-quantum electrodynamics (QED) device. (nature.com)
- Coherent and incoherent effects in ultrafast optical excitation, nonlinear Faraday rotation in magnetic semiconductors. (ufl.edu)
Measurements2
- Illustration of the reference and current position measurements of a set of optical targets (or landmarks) attached to a rigid body. (berkeley.edu)
- The Total Absolute Measurement System (TAMS) unit allows you to choose the right detector for angular-dependent measurements of optical properties of thin and thick samples. (azooptics.com)
Concentration4
- The specific rotation is a measure of the rotation of the said plane of polarization of incident light by a tube of material 1 decimeter long and of concentration 1 g/cc . (geoscience.blog)
- An optical particle counter (OPC), a condensation nucleus counter (CNC), and an electrical low-pressure impactor (ELPI) were used to measure the number concentration of particles and microorganisms aerosolized from MWF. (cdc.gov)
- As was anticipated, the results showed that the concentration of particles aerosolized from pure MWF increased with the increase in the tool rotation speed and the fluid application rate. (cdc.gov)
- For example, at the tool rotation speed of 8000 rpm, the fine particle concentration (0.02-1.0 um) aerosolized from the P. fluorescens suspension in was 50-fold higher than that from pure MWF and 5-fold higher than that from pure P. fluorescens suspension in water. (cdc.gov)
Angle6
- Optical rotation of a substance is the angle through which the change or rotation in plane of polarisation occurs when polarised light passes through optically active substances . (geoscience.blog)
- Specific rotation gives the angle of rotation of plane-polarized light by a certain compound at a certain temperature. (geoscience.blog)
- The angle by which the polarization plane is rotated is called optical rotation. (geoscience.blog)
- The measurement results are availale in only 1 second, independently of the angle of rotation. (azooptics.com)
- Also a high angle of rotation is measured within 1 second. (azooptics.com)
- On the importance of vibrational contributions to small-angle optical rotation: Fluoro-oxirane in gas phase and solution. (lu.se)
Nonlinear1
- Phonon Staircase, Nonlinear Farday Rotation in magnetic semiconductors, Differential Reflection and Transmission Spectroscopy. (ufl.edu)
Clockwise3
- When looking at the source of light, the rotation of the plane of polarization may be either to the right (dextrorotatory or dextrorotary - d-rotary, represented by (+), clockwise), or to the left (levorotatory or levorotary - l-rotary, represented by (−), counter-clockwise) depending on which stereoisomer is dominant. (wikipedia.org)
- From the point of view of the observer, dextrorotation refers to clockwise or right-handed rotation, and laevorotation refers to counterclockwise or left-handed rotation. (wikipedia.org)
- Optical activity: Optical activity is the property of certain organic substances to rotate the plane of plane polarised light towards the right (clockwise) or towards the left (anticlockwise) . (geoscience.blog)
Crystals1
- It can also be observed in chiral solids such as certain crystals with a rotation between adjacent crystal planes (such as quartz) or metamaterials. (wikipedia.org)
Polarimetry1
- By polarimetry the optical activity of a substance is determined. (azooptics.com)
Beam2
- Optical rotation is the rotation of plane-polarized light when a light beam is directed through certain materials. (geoscience.blog)
- To measure optical rotation, a Light Emitting Diode (LED) produces a beam of ordinary light. (geoscience.blog)
Illusion2
- Under the principle of minimally invasive dentistry, cosmetic contouring appeared as a technique for dental remodeling by an optical illusion, by reduction of dental angles, or by the addition of resin. (bvsalud.org)
- This study aimed to discuss the advantages and limitations of using the technique of cosmetic contouring and to describe the case of a patient with tooth rotation, inverted smile, and changes in color and in the mesiodistal distance of the upper incisor battery who underwent cosmetic remodeling of the smile based on principles of optical illusion, with minimal tooth abrasion and the addition of composite resin. (bvsalud.org)
Molecule3
- The prefix used to indicate absolute configuration is not directly related to the (+) or (−) prefix used to indicate optical rotation in the same molecule. (wikipedia.org)
- The D- and L- prefixes describe the molecule as a whole, as do the (+) and (−) prefixes for optical rotation. (wikipedia.org)
- The cause of optical activity for a molecule is when the molecule is chiral . (geoscience.blog)
Physics2
- Dextrorotation and laevorotation (also spelled levorotation) are terms used in chemistry and physics to describe the optical rotation of plane-polarized light. (wikipedia.org)
- We discuss the possibility of detecting PNC optical rotation in accessible transitions in metastable Xe and Hg, and ground state I. In particular, the physics of the PNC optical rotation is presented, and we explore the lineshape effects on the expected PNC optical rotation signals. (bec.gr)
Chiral3
- Optical activity occurs only in chiral materials, those lacking microscopic mirror symmetry. (wikipedia.org)
- Compounds with these properties consist of chiral molecules and are said to have optical activity. (wikipedia.org)
- Molecules or ions that are present in optical isomers are called chiral. (geoscience.blog)
Polarization8
- Optical rotation, also known as polarization rotation or circular birefringence, is the rotation of the orientation of the plane of polarization about the optical axis of linearly polarized light as it travels through certain materials. (wikipedia.org)
- Unlike other sources of birefringence which alter a beam's state of polarization, optical activity can be observed in fluids. (wikipedia.org)
- Optical activity is defined as the property shown by the compounds in which the plane of polarization is rotated for a plane-polarized light. (geoscience.blog)
- These perspectives rely on the possibility that a single spin induces a macroscopic rotation of a photon polarization. (nature.com)
- Such polarization rotations induced by single spins were recently observed, yet limited to a few 10 −3 degrees due to poor spin-photon coupling. (nature.com)
- The cavity-enhanced coupling between the incoming photons and the solid-state spin results in a polarization rotation by ±6° when the spin is optically initialized in the up or down state. (nature.com)
- In this work, we technologically implement a cavity-QED device coupled to a stationary spin qubit, allowing the enhancement by three orders of magnitude of the polarization rotation. (nature.com)
- The fabricated device presents an optimal QD-cavity coupling strength, nearly polarization-degenerate optical modes and an efficient coupling with external beams 25 , 26 . (nature.com)
Magnetic1
- Electronic and optical properties of quantum confined Dilute Magnetic Semiconductors. (ufl.edu)
Polarizers1
- Modulation of a liquid crystal's optical activity, viewed between two sheet polarizers, is the principle of operation of liquid-crystal displays (used in most modern televisions and computer monitors). (wikipedia.org)
Polarimeter4
- Optical activity is measured using a polarized source and polarimeter. (wikipedia.org)
- What is optical rotation in polarimeter? (geoscience.blog)
- What is optical rotation in optics and how it is measured through polarimeter? (geoscience.blog)
- [α] λ T ) of an optically active compound is defined as follows: α = observed rotation measured using a polarimeter. (geoscience.blog)
Degrees3
- Values for specific rotation are reported in units of deg·mL·g − 1 ·dm − 1 , which are typically shortened to just degrees, wherein the other components of the unit are tacitly assumed. (geoscience.blog)
- Tartaric acid has a specific rotation of +12.0 degrees . (geoscience.blog)
- A resident hole spin, in a semiconductor QD-pillar cavity device, is initialized 23 and measured using resonant pump and probe beams: a Kerr rotation of several degrees is obtained. (nature.com)
Consist1
- Rotation trainers consist of a disk - with various designs - that is attached to a rod-like base. (mchenryoptical.com)
Equations1
- Matrix Methods for Solution of Boltzmann Transport Equations in Ultrafast Optical Excitation. (ufl.edu)
Optically2
- Optical activity of an organic compound refers to the property of an organic compound by the virtue of which, it rotates the plane polarized light (produced by passing ordinary light through Nicol prism) when it is passed through their solutions and the compounds are known as optically active compounds. (geoscience.blog)
- Therefore, those compounds are called optically active and their property is referred to as optical rotation. (geoscience.blog)
Coherent1
- Coherent Optical Phonons in Thin Films. (ufl.edu)
Atomic1
- Using recent atomic structure theoretical calculations, we present simulations of the PNC optical rotation signals for all proposed transitions, assuming a range of experimentally feasible parameters. (bec.gr)
Content1
- Each compound was characterized for carbon and hydrogen content, optical rotation, UV-visible light absorption, and melting point. (usda.gov)
Principle1
- The present invention relates to chemical experiment teaching technical field, and in particular to a kind of university chemistry based on counter-rotation principle Test tube cleaning equipment is used in teaching. (google.com)
Specific7
- What is optical and specific rotation? (geoscience.blog)
- This is the key difference between optical rotation and specific rotation. (geoscience.blog)
- In the circumstance of 20 °C, the specific optical rotation of sucrose is known to be 66.6° , whereas that of glucose and fructose is 52.2° and −92.4°, respectively. (geoscience.blog)
- What is specific rotation sugar? (geoscience.blog)
- What do you understand from the specific rotation of sugar solution? (geoscience.blog)
- What is the formula of specific rotation? (geoscience.blog)
- What is the specific rotation of tartaric acid? (geoscience.blog)
Applications1
- In many applications, the targets are optical and the data are recorded with a computer vision system. (berkeley.edu)
Polarized light1
- The rotation of the orientation of linearly polarized light was first observed in 1811 in quartz by French physicist François Arago. (wikipedia.org)
Data1
- Unlike traditional optical profiling systems that are hard to use and have material restrictions due to low dynamic range, the VR-6000 offers a simple place-and-press interface partnered with HDR scanning to capture highly-accurate data, even on glossy or matte surfaces,' said a company spokesperson. (mfgnewsweb.com)
Components1
- The directional sensitivity of the existing real space imaging methods is limited to a few directions on the imaging plane and requires scanning of the optical components, or the rotation of either the sample or the imaging setup, in order to cover the full range of possible scattering directions. (lu.se)
Unit1
- What is the unit of optical rotation? (geoscience.blog)
Activity3
- Circular birefringence and circular dichroism are the manifestations of optical activity. (wikipedia.org)
- What is optical activity Class 12? (geoscience.blog)
- What is optical activity Class 11? (geoscience.blog)
Properties1
- 3 In this regard, one should mention nanoparticle-reinforced resins, which have excellent physical, mechanical, and optical properties and, therefore, conclude that the evolution of available materials and the improvement of surgical techniques have given highly significant and favorable results in the quest for self-image. (bvsalud.org)
Measure1
- How do you measure optical rotation? (geoscience.blog)
Application1
- The tool rotation speed varied from 800 to 8000 rpm and the fluid application rate varied from 0.4 to 1.6 l min-1. (cdc.gov)
Physical1
- What is optical rotation in physical pharmaceutics? (geoscience.blog)
Left2
- Case Report: Cosmetic contouring was applied to a female patient who presented with rotation of maxillary left lateral incisor, and concave and fractured edges of the upper central incisors, creating an impression of an "inverted smile. (bvsalud.org)
- On clinical examination, rotation of tooth left lateral superior incisor was observed, as well as a concave edge of the central incisors in relation to the lower lip, creating an impression of an "inverted smile. (bvsalud.org)