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Optical rotation

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3068:. However, this is a distinct phenomenon that is not classified as "optical activity." Optical activity is reciprocal, i.e. it is the same for opposite directions of wave propagation through an optically active medium, for example clockwise polarization rotation from the point of view of an observer. In case of optically active isotropic media, the rotation is the same for any direction of wave propagation. In contrast, the Faraday effect is non-reciprocal, i.e opposite directions of wave propagation through a Faraday medium will result in clockwise and anti-clockwise polarization rotation from the point of view of an observer. Faraday rotation depends on the propagation direction relative to that of the applied magnetic field. All compounds can exhibit polarization rotation in the presence of an applied magnetic field, provided that (a component of) the magnetic field is oriented in the direction of light propagation. The Faraday effect is one of the first discoveries of the relationship between light and electromagnetic effects. 739:. Nonlocality means that electric fields in one location of the material drive currents in another location of the material. Light travels at a finite speed, and even though it is much faster than the electrons, it makes a difference whether the charge response naturally wants to travel along with the electromagnetic wavefront, or opposite to it. Spatial dispersion means that light travelling in different directions (different wavevectors) sees a slightly different permittivity tensor. Natural optical rotation requires a special material, but it also relies on the fact that the wavevector of light is nonzero, and a nonzero wavevector bypasses the symmetry restrictions on the local (zero-wavevector) response. However, there is still reversal symmetry, which is why the direction of natural optical rotation must be 'reversed' when the direction of the light is reversed, in contrast to magnetic 714:. Think of one enantiomer in a solution as a large number of little helices (or screws), all right-handed, but in random orientations. Birefringence of this sort is possible even in a fluid because the handedness of the helices is not dependent on their orientation: even when the direction of one helix is reversed, it still appears right handed. And circularly polarized light itself is chiral: as the wave proceeds in one direction the electric (and magnetic) fields composing it are rotating clockwise (or counterclockwise for the opposite circular polarization), tracing out a right (or left) handed screw pattern in space. In addition to the bulk 486: 27: 636:. Since the early 21st century, the development of artificial materials has led to the prediction and realization of chiral metamaterials with optical activity exceeding that of natural media by orders of magnitude in the optical part of the spectrum. Extrinsic chirality associated with oblique illumination of metasurfaces lacking two-fold rotational symmetry has been observed to lead to large linear optical activity in transmission and reflection, as well as nonlinear optical activity exceeding that of lithium iodate by 30 million times. 474: 590:
polarized light clockwise, while the other form rotate light counterclockwise. An equal mix of the two has no polarizing effect on light. Pasteur deduced that the molecule in question is asymmetric and could exist in two different forms that resemble one another as would left- and right-hand gloves, and that the organic form of the compound consists of purely the one type.
3020:. In that case, rotation of the plane of polarization is observed due to the relative rotation between crystal planes, thus making the crystal formally chiral as we have defined it above. The rotation of the crystal planes can be right or left-handed, again producing opposite optical activities. On the other hand, 2514: 601:
independently proposed that this phenomenon of optical activity in carbon compounds could be explained by assuming that the 4 saturated chemical bonds between carbon atoms and their neighbors are directed towards the corners of a regular tetrahedron. If the 4 neighbors are all different, then there
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Optical activity is normally observed for transmitted light. However, in 1988, M. P. Silverman discovered that polarization rotation can also occur for light reflected from chiral substances. Shortly after, it was observed that chiral media can also reflect left-handed and right-handed circularly
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chiral; an ordinary right-handed screw thread, viewed in a mirror, would appear as a left-handed screw (very uncommon) which could not possibly screw into an ordinary (right-handed) nut. A human viewed in a mirror would have their heart on the right side, clear evidence of chirality, whereas the
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has no such effect, even though its reactions are identical and its elemental composition is the same. Pasteur noticed that the crystals come in two asymmetric forms that are mirror images of one another. Sorting the crystals by hand gave two forms of the compound: Solutions of one form rotate
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A. Fresnel, "MĂ©moire sur la double rĂ©fraction que les rayons lumineux Ă©prouvent en traversant les aiguilles de cristal de roche suivant les directions parallĂšles Ă  l'axe", read 9 December 1822; printed in H. de Senarmont, E. Verdet, and L. Fresnel (eds.),
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Biot (1818 & 1819) "Extrait d'un mémoire sur les rotations que certaines substances impriment aux axes de polarisation des rayons lumineux" (Extract from a memoir on the rotations that certain substances impress on the axes of polarization of light rays),
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tensor (i.e., a charge response that only depends on the local electric field vector), as symmetry considerations forbid this. Rather, circular birefringence only appears when considering nonlocality of the material response, a phenomenon known as
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In order to display optical activity, a fluid must contain only one, or a preponderance of one, stereoisomer. If two enantiomers are present in equal proportions, then their effects cancel out and no optical activity is observed; this is termed a
689:, more of one enantiomer than the other, the cancellation is incomplete and optical activity is observed. Many naturally occurring molecules are present as only one enantiomer (such as many sugars). Chiral molecules produced within the fields of 605:
In 1945, Charles William Bunn predicted optical activity of achiral structures, if the wave's propagation direction and the achiral structure form an experimental arrangement that is different from its mirror image. Such optical activity due to
2341: 753:, defined as the speed of light (in free space) divided by its speed in the medium. The difference in the refractive indices between the two circular polarizations quantifies the strength of the circular birefringence (polarization rotation), 526:: whereas previously known cases of birefringence were due to the different speeds of light polarized in two perpendicular planes, optical rotation was due to the different speeds of right-hand and left-hand circularly polarized light. Simple 625:
polarized waves with different efficiencies. These phenomena of specular circular birefringence and specular circular dichroism are jointly known as specular optical activity. Specular optical activity is very weak in natural materials.
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Where their chiralities are the same, there will be a small additional effect on the wave's velocity, but the opposite circular polarization will experience an opposite small effect as its chirality is opposite that of the molecules.
3217: 465:)-enantiomer is the dextrorotary (+) enantiomer, and in other cases it is the levorotary (−) enantiomer. The relationship must be determined on a case-by-case basis with experimental measurements or detailed computer modeling. 185:-rotary. For a given substance, the angle by which the polarization of light of a specified wavelength is rotated is proportional to the path length through the material and (for a solution) proportional to its concentration. 1435: 1346: 3633:
Silverman, M.; Ritchie, N.; Cushman, G.; Fisher, B. (1988). "Experimental configurations using optical phase modulation to measure chiral asymmetries in light specularly reflected from a naturally gyrotropic medium".
2084: 919: 1673: 367:-form by definition. The prefix used to indicate absolute configuration is not directly related to the (+) or (−) prefix used to indicate optical rotation in the same molecule. For example, nine of the nineteen 2856: 509:
discovered that different individual quartz crystals, whose crystalline structures are mirror images of each other (see illustration), rotate linear polarization by equal amounts but in opposite directions.
3205: 1819: 856:(addition) of a left and right circularly polarized wave in equal proportion. The phase difference between these two waves is dependent on the orientation of the linear polarization which we'll call 602:
are two possible orderings of the neighbors around the tetrahedron, which will be mirror images of each other. This led to a better understanding of the three-dimensional nature of molecules.
2525: 3431:, vol. 1 (1866), pp. 731–751; translated as "Memoir on the double refraction that light rays undergo in traversing the needles of quartz in the directions parallel to the axis", 845:
is small in natural materials, examples of giant circular birefringence resulting in a negative refractive index for one circular polarization have been reported for chiral metamaterials.
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Kuwata-Gonokami, M.; Saito, N.; Ino, Y.; Kauranen, M.; Jefimovs, K.; Vallius, T.; Turunen, J.; Svirko, Y. (2005). "Giant Optical Activity in Quasi-Two-Dimensional Planar Nanostructures".
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syrup to a mixture of the component simple sugars, fructose, and glucose, gets its name from the fact that the conversion causes the direction of rotation to "invert" from right to left.
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Stephens, P. J.; Devlin, F. J.; Cheeseman, J. R.; Frisch, M. J.; Bortolini, O.; Besse, P. (2003). "Determination of absolute configuration using calculation of optical rotation".
3032:, like a racemic mixture of chiral molecules, has no net optical activity since one or the other crystal structure does not dominate the substance's internal molecular structure. 2228: 1629: 1594: 1249: 1214: 1171: 1136: 2800: 2274: 2193: 3252: 2903: 2709: 2509:{\displaystyle \mathbf {E} _{out}={\frac {\sqrt {2}}{2}}(e^{-i\Delta \theta }e^{-i\theta _{0}}\mathbf {E} _{RHC}+e^{i\Delta \theta }e^{i\theta _{0}}\mathbf {E} _{LHC})\,\,.} 2297: 1552: 2169:. Now let us assume transmission through an optically active material which induces an additional phase difference between the right and left circularly polarized waves of 911: 2124: 881: 3354:"On the rotation impressed by plates of rock crystal on the planes of polarization of the rays of light, as connected with certain peculiarities in its crystallization," 1496: 1467: 2995: 2933: 2880: 2770: 2167: 843: 3339:(Memoir on a remarkable modification that light rays experience during their passage through certain translucent substances and on some other new optical phenomena), 2248: 2144: 743:. All optical phenomena have some nonlocality/wavevector influence but it is usually negligible; natural optical rotation, rather uniquely, absolutely requires it. 4359: 700:
At the fundamental level, polarization rotation in an optically active medium is caused by circular birefringence, and can best be understood in that way. Whereas
2972: 285:(geometric mirror image) will be laevorotary, and vice versa. Enantiomers rotate plane-polarized light the same number of degrees, but in opposite directions. 4364: 1354: 1265: 730:
Unlike linear birefringence, however, natural optical rotation (in the absence of a magnetic field) cannot be explained in terms of a local material
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of light of two different linear polarizations, circular birefringence implies a small difference in the velocities between right and left-handed
4225: 1998: 1053:{\displaystyle \mathbf {E} _{\theta _{0}}={\frac {\sqrt {2}}{2}}(e^{-i\theta _{0}}\mathbf {E} _{RHC}+e^{i\theta _{0}}\mathbf {E} _{LHC})\,\,,} 1804:{\displaystyle \mathbf {E} _{\theta _{0}}={\frac {\sqrt {2}}{2}}(e^{-i\theta _{0}}\mathbf {E} _{RHC}+e^{i\theta _{0}}\mathbf {E} _{LHC})\,\,} 3833:
Plum, E.; Fedotov, V. A.; Schwanecke, A. S.; Zheludev, N. I.; Chen, Y. (2007). "Giant optical gyrotropy due to electromagnetic coupling".
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Optical activity occurs due to molecules dissolved in a fluid or due to the fluid itself only if the molecules are one of two (or more)
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predicted optical activity that depends on the intensity of light and the effect of nonlinear optical activity was observed in 1979 in
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Akhmanov, S. A.; Zhdanov, B. V.; Zheludev, N. I.; Kovrigin, A. I.; Kuznetsov, V. I. (1979). "Nonlinear optical activity in crystals".
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with the molecule, rather than a property of the molecule as a whole. A molecule having exactly one chiral stereocenter (usually an
3229: 1981:{\displaystyle ={\frac {1}{2}}({\hat {x}}(e^{-i\theta _{0}}+e^{i\theta _{0}})+{\hat {y}}i(e^{-i\theta _{0}}-e^{i\theta _{0}}))\,\,} 607: 3270: 3494:"Sur les relations qui existent entre les formules atomiques des corps organiques et le pouvoir rotatoire de leurs dissolutions" 660:(which would be that of a different stereoisomer, or the "opposite enantiomer"). In mathematics, this property is also known as 4054: 3496:(On the relations that exist between the atomic formulas of organic substances and the rotatory power of their solutions), 453:, and (+)/(−) designations, although some correlations exist. For example, of the naturally occurring amino acids, all are 4120:
Zhang, S.; Park, Y.-S.; Li, J.; Lu, X.; Zhang, W.; Zhang, X. (2009). "Negative Refractive Index in Chiral Metamaterials".
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R. Williams (1969). "Optical-rotary power and linear electro-optic effect in nematic liquid crystals of p-azoxyanisole".
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chiral, since its appearance in a mirror is not distinct from itself. However a screw or light bulb base (or any sort of
2642:{\displaystyle \mathbf {E} _{out}={\hat {x}}\cos(\theta _{0}+\Delta \theta )+{\hat {y}}\sin(\theta _{0}+\Delta \theta )} 4218: 3929: 4175: 3284: 3246: 2950:
So we find that the degree of rotation depends on the color of the light (the yellow sodium D line near 589 nm
398:- prefixes describe the molecule as a whole, as do the (+) and (−) prefixes for optical rotation. In contrast, the ( 4397: 3755:
Svirko, Y.; Zheludev, N. I.; Osipov, M. (2001). "Layered chiral metallic microstructures with inductive coupling".
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Bose, Jagadis Chunder (1898). "On the Rotation of Plane of Polarisation of Electric Waves by a Twisted Structure".
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also observed the rotation of the axis of polarization in certain liquids and vapors of organic substances such as
3016:). Although quartz has a substantial linear birefringence, that effect is cancelled when propagation is along the 2935:
will also be wavelength dependent. The resulting variation in rotation with the wavelength of the light is called
594: 430:), but a molecule having multiple stereocenters needs more than one label. For example, the essential amino acid 119: 2714: 2655: 2302: 1634: 1066: 759: 718:
which substantially lowers the phase velocity of light in any dielectric (transparent) material compared to the
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is the wavelength of the light (in vacuum). This will cause a rotation of the linear axis of polarization by
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of chiral molecules in solution. Modulation of a liquid crystal's optical activity, viewed between two sheet
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We defined above the difference in the refractive indices for right and left circularly polarized waves of
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as the superposition of right and left circularly polarized components with a relative phase difference of
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When looking at the source of light, the rotation of the plane of polarization may be either to the right (
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Silverman, M.; Badoz, J.; Briat, B. (1992). "Chiral reflection from a naturally optically active medium".
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polarization relies on the understanding that a linearly polarized wave can as well be described as the
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there is an additional interaction between the chirality of the wave and the chirality of the molecules.
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to measure the sugar concentration of syrup, and generally in chemistry to measure the concentration or
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direction, as we had intended, justifying the representation of any linearly polarized state at angle
122:. It can also be observed in chiral solids such as certain crystals with a rotation between adjacent 4354: 4070:
Plum, E.; Zhou, J.; Dong, J.; Fedotov, V. A.; Koschny, T.; Soukoulis, C. M.; Zheludev, N. I. (2009).
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to rotate to the left. Fructose is even more strongly levorotatory than glucose is dextrorotatory.
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is known, the observed rotation can be used to calculate the concentration. This usage makes a
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components that we have decomposed each circular polarization into. As usual when dealing with
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Mémoires de la classe des sciences mathématiques et physiques de l'Institut Impérial de France
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R. Williams (1968). "Optical Rotatory Effect in the Nematic Liquid Phase of p-Azoxyanisole".
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molecules and are said to have optical activity. If a chiral molecule is dextrorotary, its
201: 83: 4191: 542:, referring to the fact that it causes linearly polarized light to rotate to the right or 8: 4326: 4203: 2909: 2776:
in such a material, there will be an additional phase difference induced between them of
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Rotation of the plane of linearly polarized light as it travels through a chiral material
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Although optical activity is normally thought of as a property of fluids, particularly
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have been used since this time to measure the concentrations of simple sugars, such as
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described the ability of twisted artificial structures to rotate the polarization of
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is commonly used for measurements), and is directly proportional to the path length
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Sucrose solution concentration measuring experiment, demonstrating optical rotation.
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mirror reflection of a doll might well be indistinguishable from the doll itself.
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For a pure substance in solution, if the color and path length are fixed and the
1430:{\displaystyle \mathbf {E} _{LHC}={\frac {\sqrt {2}}{2}}({\hat {x}}-i{\hat {y}})} 1341:{\displaystyle \mathbf {E} _{RHC}={\frac {\sqrt {2}}{2}}({\hat {x}}+i{\hat {y}})} 26: 313:-" prefix. Likewise, a levorotary compound may be labeled using the "(−)-" or " 106:
which alter a beam's state of polarization, optical activity can be observed in
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through the substance and the amount of circular birefringence of the material
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a tool of great importance to those trading in or using sugar syrups in bulk.
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materials, those lacking microscopic mirror symmetry. Unlike other sources of
4453: 4316: 3093: 701: 574: 570: 523: 506: 478: 103: 4438: 4311: 4254: 4149: 4013: 3819: 3789: 3725: 3698: 3655: 3374:"Phenomene de polarisation successive, observés dans des fluides homogenes" 3322: 3204:. These are used infrequently in English, but sometimes they are, see e.g. 3029: 731: 657: 645: 415: 352: 162: 3151: 2947:. Complete knowledge of one spectrum allows the calculation of the other. 577:. A solution of this compound derived from living things (to be specific, 90:
light as it travels through certain materials. Circular birefringence and
3690: 3632: 3376:(Phenomenon of successive polarization, observed in homogeneous fluids), 3045: 527: 189: 178: 59: 31: 3167: 2079:{\displaystyle ={\hat {x}}\cos(\theta _{0})+{\hat {y}}\sin(\theta _{0})} 1518:
notation, it is understood that such quantities are to be multiplied by
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The phase velocity of light in a medium is commonly expressed using the
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are racemic unless a chiral reagent was employed in the same reaction.
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The two asymmetric crystal forms, dextrorotatory and levorotatory, of
379:- prefix, actually dextrorotary (at a wavelength of 589 nm), and 3021: 661: 633: 431: 235: 3437: 2230:
the result of passing the original wave linearly polarized at angle
547: 384: 161:-rotary, represented by (−), counter-clockwise) depending on which 4069: 3889: 2851:{\displaystyle 2\Delta \theta ={\frac {\Delta nL2\pi }{\lambda }}} 1554:
and then the actual electric field at any instant is given by the
1506:, in this case representing the 90 degree phase shift between the 473: 445:)-threonine. There is no strict relationship between the R/S, the 309:
A compound may be labeled as dextrorotary by using the "(+)-" or "
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through this medium. This will apply additional phase factors of
682: 563: 531: 239: 170: 166: 123: 3977: 883:, and their electric fields have a relative phase difference of 3754: 3432: 3025: 3009: 1515: 522:
found that optical rotation could be explained as a species of
498: 304: 127: 99: 3980:"Giant nonlinear optical activity in a plasmonic metamaterial" 3300: 3236: 2997:
which, for a solution, may be computed from the substance's
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In general, the refractive index depends on wavelength (see
1177:(having zero phase difference). Assuming propagation in the 546:
side. In a similar manner, levulose, more commonly known as
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Bulletin des Sciences, par la Société Philomatique de Paris
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The last equation shows that the resulting vector has the
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of light passing through it, but tartaric acid derived by
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Optical activity is measured using a polarized source and
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Archives NĂ©erlandaises des Sciences Exactes et Naturelles
3262: 3230:"Determination of optical rotation and specific rotation" 2299:
to the right and left circularly polarized components of
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is sometimes called "levulose" because it is levorotary.
347:-" prefixes are used to specify the enantiomer of chiral 208:(used in most modern televisions and computer monitors). 149:-rotary, represented by (+), clockwise), or to the left ( 3870:"Optical activity in extrinsically chiral metamaterial" 652:. The structure of such a molecule is such that it is 2980: 2960: 2918: 2888: 2868: 2811: 2782: 2755: 2717: 2694: 2658: 2528: 2344: 2305: 2282: 2256: 2236: 2201: 2175: 2152: 2132: 2105: 2001: 1822: 1676: 1637: 1602: 1567: 1524: 1475: 1446: 1357: 1268: 1222: 1187: 1144: 1109: 1069: 922: 889: 862: 828: 762: 82:, is the rotation of the orientation of the plane of 325:-" prefixes are obsolete, and are distinct from the 254:
refers to counterclockwise or left-handed rotation.
4072:"Metamaterial with negative index due to chirality" 3978:Ren, M.; Plum, E.; Xu, J.; Zheludev, N. I. (2012). 3930:"Specular optical activity of achiral metasurfaces" 3357:
Transactions of the Cambridge Philosophical Society
3051: 2652:thus describing a wave linearly polarized at angle 437:
contains two chiral stereocenters and is written (2
3928:Plum, E.; Fedotov, V. A.; Zheludev, N. I. (2016). 3868:Plum, E.; Fedotov, V. A.; Zheludev, N. I. (2008). 2989: 2966: 2927: 2897: 2874: 2850: 2794: 2764: 2739: 2703: 2680: 2641: 2508: 2327: 2291: 2268: 2242: 2222: 2187: 2161: 2138: 2118: 2078: 1980: 1803: 1659: 1623: 1588: 1546: 1490: 1461: 1429: 1340: 1243: 1208: 1165: 1130: 1091: 1052: 905: 875: 837: 810: 250:refers to clockwise or right-handed rotation, and 4365:Ultraviolet–visible spectroscopy of stereoisomers 3008:, it has also been observed in crystals such as 375:naturally occurring in proteins are, despite the 4451: 3518:. New York: Oxford University Press. p. 88. 3422: 3420: 3410:; for Biot's experiments with turpentine vapor ( 3269:Solomons, T.W. Graham; Fryhle, Graig B. (2008). 2099:components in phase and oriented exactly in the 704:in a crystal involves a small difference in the 269:, while a compound that causes laevorotation is 913:which then add to produce linear polarization: 3603:. Moscow: USSR Academy of Sciences Publishing. 3601:Mikrostruktura Sveta (Microstructure of Light) 3462: : 56–99; see also appendix, pp. 99–117. 3268: 610:was observed in the 1960s in liquid crystals. 4219: 3473:"Sur les formules de structure dans l'espace" 3417: 277:. Compounds with these properties consist of 573:resolved a problem concerning the nature of 216:"Levo" redirects here. For the company, see 52:Sample tube containing molecules under study 3636:Journal of the Optical Society of America A 3563: 3528: 2772:. Considering propagation through a length 4226: 4212: 4196:Morrison. Robert. T, and Boyd. Robert. N, 3441:, 2021 (open access); especially §13. 3124:Hyper Rayleigh Scattering Optical Activity 2740:{\displaystyle \mathbf {E} _{\theta _{0}}} 2681:{\displaystyle \theta _{0}+\Delta \theta } 2328:{\displaystyle \mathbf {E} _{\theta _{0}}} 1660:{\displaystyle \mathbf {E} _{\theta _{0}}} 1092:{\displaystyle \mathbf {E} _{\theta _{0}}} 811:{\displaystyle \Delta n=n_{RHC}-n_{LHC}\,} 246:. From the point of view of the observer, 192:. This is a tool particularly used in the 4025: 4023: 4003: 3888: 3436: 2502: 2501: 1977: 1976: 1800: 1799: 1046: 1045: 807: 110:. This can include gases or solutions of 3498:Bulletin de la SociĂ©tĂ© Chimique de Paris 3165:, meaning "right" (as opposed to left). 2912:) and the differential refractive index 484: 472: 25: 3598: 3293: 114:such as sugars, molecules with helical 4452: 4020: 4207: 2519:Using similar math as above we find: 848:The familiar rotation of the axis of 538:-glucose (the biological isomer), is 288: 4200:(6th ed.), Prentice-Hall Inc (1992). 3711: 3513: 3475:(On structural formulas in space), 3429:Oeuvres complĂštes d'Augustin Fresnel 534:, in solution. In fact one name for 497:light was first observed in 1811 in 4187:, World Scientific, Singapore, 1994 4043:Electrodynamics of Continuous Media 3241:. World Health Organization. 2017. 3143: 3001:and its concentration in solution. 1561:Substituting these expressions for 493:The rotation of the orientation of 204:, is the principle of operation of 13: 4160: 3218:LibreTexts Chemistry – Polarimetry 2981: 2919: 2889: 2827: 2815: 2786: 2756: 2695: 2672: 2630: 2584: 2452: 2392: 2283: 2260: 2223:{\displaystyle \mathbf {E} _{out}} 2179: 1624:{\displaystyle \mathbf {E} _{LHC}} 1589:{\displaystyle \mathbf {E} _{RHC}} 1244:{\displaystyle \mathbf {E} _{LHC}} 1209:{\displaystyle \mathbf {E} _{RHC}} 1166:{\displaystyle \mathbf {E} _{LHC}} 1131:{\displaystyle \mathbf {E} _{RHC}} 829: 763: 505:. In 1820, the English astronomer 98:. Optical activity occurs only in 14: 4476: 4360:NMR spectroscopy of stereoisomers 4170:, 3rd ed., Addison-Wesley, 1998, 1173:are the two circularly polarized 408:Cahn–Ingold–Prelog priority rules 55:Optical rotation due to molecules 4398:Diastereomeric recrystallization 3714:Proceedings of the Royal Society 3456:Annales de chimie et de physique 3412:vapeur d'essence de tĂ©rĂ©benthine 3392:Annales de Chimie et de Physique 3258:from the original on 2022-10-09. 3192:The equivalent French terms are 3052:Comparison to the Faraday effect 2943:spectra are related through the 2720: 2531: 2482: 2425: 2347: 2308: 2204: 1780: 1739: 1679: 1640: 1605: 1570: 1360: 1271: 1225: 1190: 1147: 1112: 1072: 1026: 985: 925: 355:and are based on the compound's 118:such as some proteins, and also 34:for measuring optical rotation. 4185:Beltrami Fields in Chiral Media 4113: 4063: 3971: 3921: 3861: 3826: 3783: 3748: 3705: 3662: 3626: 3607: 3592: 3557: 3522: 3507: 3486: 3465: 3444: 3383: 3238:The International Pharmacopoeia 3035: 2795:{\displaystyle 2\Delta \theta } 2711:relative to the incoming wave: 2269:{\displaystyle -\Delta \theta } 2188:{\displaystyle 2\Delta \theta } 664:. For instance, a metal rod is 4142:10.1103/PhysRevLett.102.023901 4045:. Vol. 8 (2nd ed.). 3366: 3346: 3329: 3222: 3211: 3186: 2898:{\displaystyle \Delta \theta } 2704:{\displaystyle \Delta \theta } 2636: 2614: 2602: 2590: 2568: 2556: 2498: 2378: 2292:{\displaystyle \Delta \theta } 2073: 2060: 2048: 2036: 2023: 2011: 1973: 1970: 1921: 1912: 1900: 1851: 1845: 1836: 1796: 1711: 1547:{\displaystyle e^{-i\omega t}} 1482: 1453: 1424: 1418: 1400: 1391: 1335: 1329: 1311: 1302: 1042: 957: 685:mixture. But when there is an 261:that causes dextrorotation is 1: 3812:10.1103/PhysRevLett.95.227401 3136: 2802:(as we used above) given by: 558:, commercially formed by the 4393:Chiral column chromatography 3114:Chirality (electromagnetism) 906:{\displaystyle 2\theta _{0}} 595:Jacobus Henricus van 't Hoff 242:are the optical rotation of 7: 4190:A step by step tutorial on 3566:Journal of Chemical Physics 3277:John Wiley & Sons, Inc. 3071: 3060:may also occur through the 2937:optical rotatory dispersion 2119:{\displaystyle \theta _{0}} 876:{\displaystyle \theta _{0}} 461:). For some molecules the ( 165:is dominant. For instance, 10: 4481: 4355:Chiral derivatizing agents 4236:enantioselective synthesis 4099:10.1103/PhysRevB.79.035407 3551:10.1103/PhysRevLett.21.342 1491:{\displaystyle {\hat {y}}} 1462:{\displaystyle {\hat {x}}} 1181:direction, we could write 468: 317:-" prefix. The lowercase " 298: 292: 215: 94:are the manifestations of 86:about the optical axis of 21:circularly polarized light 18: 4406: 4373: 4342: 4294: 4242: 3471:van 't Hoff, J.H. (1874) 3343:, 1st part : 93–134. 3275:(9th ed.). Hoboken: 3149:The first word component 639: 30:Operating principle of a 4281:Supramolecular chirality 3516:Chemical Crystallography 3352:Herschel, J.F.W. (1820) 3064:which involves a static 2990:{\displaystyle \Delta n} 2945:Kramers–Kronig relations 2928:{\displaystyle \Delta n} 2875:{\displaystyle \lambda } 2765:{\displaystyle \Delta n} 2162:{\displaystyle 2\theta } 838:{\displaystyle \Delta n} 414:of each specific chiral 211: 49:Linearly polarized light 19:Not to be confused with 4122:Physical Review Letters 3937:Applied Physics Letters 3877:Applied Physics Letters 3835:Applied Physics Letters 3792:Physical Review Letters 3757:Applied Physics Letters 3599:Vavilov, S. I. (1950). 3531:Physical Review Letters 3206:Patrick Mailliet et al. 2939:(ORD). ORD spectra and 2243:{\displaystyle \theta } 2139:{\displaystyle \theta } 1631:into the equation for 1259:components as follows: 1103:of the net wave, while 581:) rotates the plane of 206:liquid-crystal displays 3726:10.1098/rspl.1898.0019 3656:10.1364/JOSAA.5.001852 3183:, meaning "left side". 3129:Raman optical activity 2991: 2968: 2929: 2899: 2876: 2852: 2796: 2766: 2741: 2705: 2682: 2643: 2510: 2329: 2293: 2270: 2244: 2224: 2189: 2163: 2140: 2120: 2080: 1982: 1805: 1661: 1625: 1590: 1548: 1498:are unit vectors, and 1492: 1463: 1431: 1342: 1245: 1210: 1167: 1132: 1093: 1054: 907: 877: 839: 812: 711:circular polarizations 648:; this is known as an 507:Sir John F.W. Herschel 490: 482: 422:atom) can be labeled ( 412:absolute configuration 357:absolute configuration 301:Absolute configuration 120:chiral liquid crystals 80:circular birefringence 68: 4419:Chiral pool synthesis 4333:Diastereomeric excess 4047:Butterworth-Heinemann 3984:Nature Communications 3492:Le Bel, J.-A. (1874) 3177:comes from the Latin 3109:Chirality (chemistry) 3058:plane of polarization 2992: 2969: 2930: 2900: 2877: 2853: 2797: 2767: 2742: 2706: 2683: 2644: 2511: 2330: 2294: 2271: 2245: 2225: 2190: 2164: 2141: 2121: 2081: 1983: 1806: 1662: 1626: 1591: 1549: 1493: 1464: 1432: 1343: 1246: 1211: 1168: 1133: 1094: 1055: 908: 878: 840: 813: 630:Jagadish Chandra Bose 599:Joseph Achille Le Bel 552:plane of polarization 520:Augustin-Jean Fresnel 488: 476: 406:)- prefixes from the 295:Chirality (chemistry) 244:plane-polarized light 76:polarization rotation 29: 4460:Polarization (waves) 4429:Asymmetric catalysis 4414:Asymmetric induction 4049:. pp. 362–365. 3720:(389–400): 146–152. 3691:10.1364/OL.17.000886 3514:Bunn, C. W. (1945). 3119:Polarization rotator 3056:Rotation of light's 2978: 2958: 2916: 2886: 2866: 2809: 2780: 2753: 2715: 2692: 2656: 2526: 2342: 2303: 2280: 2254: 2234: 2199: 2173: 2150: 2130: 2103: 1999: 1820: 1674: 1635: 1600: 1565: 1522: 1473: 1444: 1355: 1266: 1220: 1185: 1142: 1107: 1067: 920: 887: 860: 826: 760: 702:linear birefringence 501:by French physicist 4327:Enantiomeric excess 4134:2009PhRvL.102b3901Z 4091:2009PhRvB..79c5407P 3996:2012NatCo...3..833R 3949:2016ApPhL.108n1905P 3899:2008ApPhL..93s1911P 3847:2007ApPhL..90v3113P 3804:2005PhRvL..95v7401K 3769:2001ApPhL..78..498S 3683:1992OptL...17..886S 3648:1988JOSAA...5.1852S 3578:1969JChPh..50.1324W 3543:1968PhRvL..21..342W 3450:Pasteur, L. (1850) 3372:Biot, J. B. (1815) 2688:, thus rotated by 748:index of refraction 695:inorganic chemistry 687:enantiomeric excess 608:extrinsic chirality 116:secondary structure 4424:Chiral auxiliaries 4388:Kinetic resolution 4286:Inherent chirality 4271:-symmetric ligands 4005:10.1038/ncomms1805 3315:10.1002/chir.10270 3299:See, for example, 3089:Circular dichroism 2987: 2964: 2941:circular dichroism 2925: 2905:as we have shown. 2895: 2872: 2848: 2792: 2762: 2737: 2701: 2678: 2639: 2506: 2325: 2289: 2266: 2240: 2220: 2185: 2159: 2136: 2116: 2076: 1978: 1801: 1657: 1621: 1586: 1544: 1488: 1459: 1427: 1338: 1251:in terms of their 1241: 1206: 1163: 1128: 1089: 1050: 903: 873: 835: 808: 737:spatial dispersion 587:chemical synthesis 556:Invert sugar syrup 512:Jean Baptiste Biot 495:linearly polarized 491: 483: 339:-" prefixes. The " 289:Chirality prefixes 198:enantiomeric ratio 92:circular dichroism 88:linearly polarized 69: 4447: 4446: 4383:Recrystallization 4375:Chiral resolution 4198:Organic Chemistry 4181:Akhlesh Lakhtakia 4079:Physical Review B 4056:978-0-7506-2634-7 3957:10.1063/1.4944775 3907:10.1063/1.3021082 3855:10.1063/1.2745203 3777:10.1063/1.1342210 3586:10.1063/1.1671194 3483: : 445–454. 3414:), see pp. 72–81. 3272:Organic Chemistry 3208:, page 12 and 15. 3084:Specific rotation 3042:specific rotation 3006:aqueous solutions 2999:specific rotation 2967:{\displaystyle L} 2846: 2605: 2559: 2376: 2372: 2051: 2014: 1915: 1848: 1834: 1709: 1705: 1558:of that product. 1485: 1456: 1421: 1403: 1389: 1385: 1332: 1314: 1300: 1296: 955: 951: 691:organic chemistry 656:identical to its 537: 456: 452: 448: 434: 420:asymmetric carbon 410:characterize the 397: 393: 382: 378: 370: 366: 349:organic compounds 346: 342: 338: 334: 330: 259:chemical compound 41:Unpolarized light 4472: 4350:Optical rotation 4295:Chiral molecules 4260:Planar chirality 4228: 4221: 4214: 4205: 4204: 4192:Optical Rotation 4154: 4153: 4117: 4111: 4110: 4076: 4067: 4061: 4060: 4027: 4018: 4017: 4007: 3975: 3969: 3968: 3934: 3925: 3919: 3918: 3892: 3874: 3865: 3859: 3858: 3830: 3824: 3823: 3787: 3781: 3780: 3752: 3746: 3745: 3709: 3703: 3702: 3666: 3660: 3659: 3630: 3624: 3623: 3611: 3605: 3604: 3596: 3590: 3589: 3561: 3555: 3554: 3526: 3520: 3519: 3511: 3505: 3504: : 337–347. 3490: 3484: 3469: 3463: 3448: 3442: 3440: 3424: 3415: 3387: 3381: 3370: 3364: 3350: 3344: 3333: 3327: 3326: 3297: 3291: 3290: 3266: 3260: 3259: 3257: 3234: 3226: 3220: 3215: 3209: 3190: 3184: 3147: 2996: 2994: 2993: 2988: 2973: 2971: 2970: 2965: 2934: 2932: 2931: 2926: 2904: 2902: 2901: 2896: 2881: 2879: 2878: 2873: 2857: 2855: 2854: 2849: 2847: 2842: 2825: 2801: 2799: 2798: 2793: 2771: 2769: 2768: 2763: 2746: 2744: 2743: 2738: 2736: 2735: 2734: 2733: 2723: 2710: 2708: 2707: 2702: 2687: 2685: 2684: 2679: 2668: 2667: 2648: 2646: 2645: 2640: 2626: 2625: 2607: 2606: 2598: 2580: 2579: 2561: 2560: 2552: 2546: 2545: 2534: 2515: 2513: 2512: 2507: 2497: 2496: 2485: 2479: 2478: 2477: 2476: 2459: 2458: 2440: 2439: 2428: 2422: 2421: 2420: 2419: 2399: 2398: 2377: 2368: 2367: 2362: 2361: 2350: 2334: 2332: 2331: 2326: 2324: 2323: 2322: 2321: 2311: 2298: 2296: 2295: 2290: 2275: 2273: 2272: 2267: 2249: 2247: 2246: 2241: 2229: 2227: 2226: 2221: 2219: 2218: 2207: 2194: 2192: 2191: 2186: 2168: 2166: 2165: 2160: 2145: 2143: 2142: 2137: 2125: 2123: 2122: 2117: 2115: 2114: 2085: 2083: 2082: 2077: 2072: 2071: 2053: 2052: 2044: 2035: 2034: 2016: 2015: 2007: 1987: 1985: 1984: 1979: 1969: 1968: 1967: 1966: 1946: 1945: 1944: 1943: 1917: 1916: 1908: 1899: 1898: 1897: 1896: 1876: 1875: 1874: 1873: 1850: 1849: 1841: 1835: 1827: 1810: 1808: 1807: 1802: 1795: 1794: 1783: 1777: 1776: 1775: 1774: 1754: 1753: 1742: 1736: 1735: 1734: 1733: 1710: 1701: 1700: 1695: 1694: 1693: 1692: 1682: 1666: 1664: 1663: 1658: 1656: 1655: 1654: 1653: 1643: 1630: 1628: 1627: 1622: 1620: 1619: 1608: 1595: 1593: 1592: 1587: 1585: 1584: 1573: 1553: 1551: 1550: 1545: 1543: 1542: 1497: 1495: 1494: 1489: 1487: 1486: 1478: 1468: 1466: 1465: 1460: 1458: 1457: 1449: 1436: 1434: 1433: 1428: 1423: 1422: 1414: 1405: 1404: 1396: 1390: 1381: 1380: 1375: 1374: 1363: 1347: 1345: 1344: 1339: 1334: 1333: 1325: 1316: 1315: 1307: 1301: 1292: 1291: 1286: 1285: 1274: 1250: 1248: 1247: 1242: 1240: 1239: 1228: 1215: 1213: 1212: 1207: 1205: 1204: 1193: 1172: 1170: 1169: 1164: 1162: 1161: 1150: 1137: 1135: 1134: 1129: 1127: 1126: 1115: 1098: 1096: 1095: 1090: 1088: 1087: 1086: 1085: 1075: 1059: 1057: 1056: 1051: 1041: 1040: 1029: 1023: 1022: 1021: 1020: 1000: 999: 988: 982: 981: 980: 979: 956: 947: 946: 941: 940: 939: 938: 928: 912: 910: 909: 904: 902: 901: 882: 880: 879: 874: 872: 871: 844: 842: 841: 836: 817: 815: 814: 809: 806: 805: 787: 786: 741:Faraday rotation 716:refractive index 535: 457:, and most are ( 454: 450: 446: 432: 395: 391: 380: 376: 368: 364: 359:relative to (+)- 344: 340: 336: 332: 326: 177:-rotary whereas 126:planes (such as 112:chiral molecules 96:optical activity 74:, also known as 72:Optical rotation 45:Linear polarizer 4480: 4479: 4475: 4474: 4473: 4471: 4470: 4469: 4465:Stereochemistry 4450: 4449: 4448: 4443: 4434:Organocatalysis 4402: 4369: 4338: 4322:Racemic mixture 4290: 4276:Axial chirality 4270: 4243:Chirality types 4238: 4232: 4163: 4161:Further reading 4158: 4157: 4118: 4114: 4074: 4068: 4064: 4057: 4039:L.P. Pitaevskii 4028: 4021: 3976: 3972: 3932: 3926: 3922: 3872: 3866: 3862: 3831: 3827: 3788: 3784: 3753: 3749: 3710: 3706: 3667: 3663: 3631: 3627: 3612: 3608: 3597: 3593: 3562: 3558: 3527: 3523: 3512: 3508: 3491: 3487: 3470: 3466: 3449: 3445: 3425: 3418: 3388: 3384: 3371: 3367: 3363: : 43–51. 3351: 3347: 3334: 3330: 3298: 3294: 3287: 3267: 3263: 3255: 3249: 3232: 3228: 3227: 3223: 3216: 3212: 3191: 3187: 3155:comes from the 3148: 3144: 3139: 3134: 3099:Geometric phase 3079:Cryptochirality 3074: 3054: 3038: 3015: 2979: 2976: 2975: 2959: 2956: 2955: 2917: 2914: 2913: 2887: 2884: 2883: 2867: 2864: 2863: 2826: 2824: 2810: 2807: 2806: 2781: 2778: 2777: 2754: 2751: 2750: 2729: 2725: 2724: 2719: 2718: 2716: 2713: 2712: 2693: 2690: 2689: 2663: 2659: 2657: 2654: 2653: 2621: 2617: 2597: 2596: 2575: 2571: 2551: 2550: 2535: 2530: 2529: 2527: 2524: 2523: 2486: 2481: 2480: 2472: 2468: 2464: 2460: 2448: 2444: 2429: 2424: 2423: 2415: 2411: 2404: 2400: 2385: 2381: 2366: 2351: 2346: 2345: 2343: 2340: 2339: 2317: 2313: 2312: 2307: 2306: 2304: 2301: 2300: 2281: 2278: 2277: 2255: 2252: 2251: 2235: 2232: 2231: 2208: 2203: 2202: 2200: 2197: 2196: 2174: 2171: 2170: 2151: 2148: 2147: 2131: 2128: 2127: 2110: 2106: 2104: 2101: 2100: 2067: 2063: 2043: 2042: 2030: 2026: 2006: 2005: 2000: 1997: 1996: 1962: 1958: 1954: 1950: 1939: 1935: 1928: 1924: 1907: 1906: 1892: 1888: 1884: 1880: 1869: 1865: 1858: 1854: 1840: 1839: 1826: 1821: 1818: 1817: 1784: 1779: 1778: 1770: 1766: 1762: 1758: 1743: 1738: 1737: 1729: 1725: 1718: 1714: 1699: 1688: 1684: 1683: 1678: 1677: 1675: 1672: 1671: 1649: 1645: 1644: 1639: 1638: 1636: 1633: 1632: 1609: 1604: 1603: 1601: 1598: 1597: 1574: 1569: 1568: 1566: 1563: 1562: 1529: 1525: 1523: 1520: 1519: 1477: 1476: 1474: 1471: 1470: 1448: 1447: 1445: 1442: 1441: 1413: 1412: 1395: 1394: 1379: 1364: 1359: 1358: 1356: 1353: 1352: 1324: 1323: 1306: 1305: 1290: 1275: 1270: 1269: 1267: 1264: 1263: 1229: 1224: 1223: 1221: 1218: 1217: 1194: 1189: 1188: 1186: 1183: 1182: 1175:basis functions 1151: 1146: 1145: 1143: 1140: 1139: 1116: 1111: 1110: 1108: 1105: 1104: 1081: 1077: 1076: 1071: 1070: 1068: 1065: 1064: 1030: 1025: 1024: 1016: 1012: 1008: 1004: 989: 984: 983: 975: 971: 964: 960: 945: 934: 930: 929: 924: 923: 921: 918: 917: 897: 893: 888: 885: 884: 867: 863: 861: 858: 857: 827: 824: 823: 795: 791: 776: 772: 761: 758: 757: 642: 471: 363:, which is the 307: 297: 291: 221: 214: 67: 60:linear analyzer 24: 17: 12: 11: 5: 4478: 4468: 4467: 4462: 4445: 4444: 4442: 4441: 4436: 4431: 4426: 4421: 4416: 4410: 4408: 4404: 4403: 4401: 4400: 4395: 4390: 4385: 4379: 4377: 4371: 4370: 4368: 4367: 4362: 4357: 4352: 4346: 4344: 4340: 4339: 4337: 4336: 4330: 4324: 4319: 4314: 4309: 4304: 4298: 4296: 4292: 4291: 4289: 4288: 4283: 4278: 4273: 4268: 4262: 4257: 4252: 4246: 4244: 4240: 4239: 4231: 4230: 4223: 4216: 4208: 4202: 4201: 4194: 4188: 4178: 4166:Eugene Hecht, 4162: 4159: 4156: 4155: 4112: 4062: 4055: 4019: 3970: 3943:(14): 141905. 3920: 3883:(19): 191911. 3860: 3841:(22): 223113. 3825: 3798:(22): 227401. 3782: 3747: 3704: 3671:Optics Letters 3661: 3625: 3606: 3591: 3556: 3521: 3506: 3485: 3464: 3458:, 3rd series, 3443: 3416: 3394:, 2nd series, 3382: 3365: 3345: 3328: 3292: 3285: 3261: 3247: 3221: 3210: 3185: 3141: 3140: 3138: 3135: 3133: 3132: 3126: 3121: 3116: 3111: 3106: 3101: 3096: 3091: 3086: 3081: 3075: 3073: 3070: 3066:magnetic field 3062:Faraday effect 3053: 3050: 3037: 3034: 3013: 2986: 2983: 2963: 2924: 2921: 2894: 2891: 2871: 2860: 2859: 2845: 2841: 2838: 2835: 2832: 2829: 2823: 2820: 2817: 2814: 2791: 2788: 2785: 2761: 2758: 2732: 2728: 2722: 2700: 2697: 2677: 2674: 2671: 2666: 2662: 2650: 2649: 2638: 2635: 2632: 2629: 2624: 2620: 2616: 2613: 2610: 2604: 2601: 2595: 2592: 2589: 2586: 2583: 2578: 2574: 2570: 2567: 2564: 2558: 2555: 2549: 2544: 2541: 2538: 2533: 2517: 2516: 2505: 2500: 2495: 2492: 2489: 2484: 2475: 2471: 2467: 2463: 2457: 2454: 2451: 2447: 2443: 2438: 2435: 2432: 2427: 2418: 2414: 2410: 2407: 2403: 2397: 2394: 2391: 2388: 2384: 2380: 2375: 2371: 2365: 2360: 2357: 2354: 2349: 2320: 2316: 2310: 2288: 2285: 2265: 2262: 2259: 2239: 2217: 2214: 2211: 2206: 2195:. Let us call 2184: 2181: 2178: 2158: 2155: 2135: 2113: 2109: 2089: 2088: 2087: 2086: 2075: 2070: 2066: 2062: 2059: 2056: 2050: 2047: 2041: 2038: 2033: 2029: 2025: 2022: 2019: 2013: 2010: 2004: 1991: 1990: 1989: 1988: 1975: 1972: 1965: 1961: 1957: 1953: 1949: 1942: 1938: 1934: 1931: 1927: 1923: 1920: 1914: 1911: 1905: 1902: 1895: 1891: 1887: 1883: 1879: 1872: 1868: 1864: 1861: 1857: 1853: 1847: 1844: 1838: 1833: 1830: 1825: 1812: 1811: 1798: 1793: 1790: 1787: 1782: 1773: 1769: 1765: 1761: 1757: 1752: 1749: 1746: 1741: 1732: 1728: 1724: 1721: 1717: 1713: 1708: 1704: 1698: 1691: 1687: 1681: 1652: 1648: 1642: 1618: 1615: 1612: 1607: 1583: 1580: 1577: 1572: 1541: 1538: 1535: 1532: 1528: 1504:imaginary unit 1484: 1481: 1455: 1452: 1438: 1437: 1426: 1420: 1417: 1411: 1408: 1402: 1399: 1393: 1388: 1384: 1378: 1373: 1370: 1367: 1362: 1349: 1348: 1337: 1331: 1328: 1322: 1319: 1313: 1310: 1304: 1299: 1295: 1289: 1284: 1281: 1278: 1273: 1238: 1235: 1232: 1227: 1203: 1200: 1197: 1192: 1160: 1157: 1154: 1149: 1125: 1122: 1119: 1114: 1101:electric field 1084: 1080: 1074: 1061: 1060: 1049: 1044: 1039: 1036: 1033: 1028: 1019: 1015: 1011: 1007: 1003: 998: 995: 992: 987: 978: 974: 970: 967: 963: 959: 954: 950: 944: 937: 933: 927: 900: 896: 892: 870: 866: 834: 831: 820: 819: 804: 801: 798: 794: 790: 785: 782: 779: 775: 771: 768: 765: 720:speed of light 706:phase velocity 641: 638: 619:lithium iodate 615:Sergey Vavilov 503:François Arago 470: 467: 361:glyceraldehyde 293:Main article: 290: 287: 263:dextrorotatory 248:dextrorotation 230:(also spelled 224:Dextrorotation 218:Levo (company) 213: 210: 194:sugar industry 139:dextrorotatory 66: 65: 62: 56: 53: 50: 47: 42: 39: 35: 15: 9: 6: 4: 3: 2: 4477: 4466: 4463: 4461: 4458: 4457: 4455: 4440: 4437: 4435: 4432: 4430: 4427: 4425: 4422: 4420: 4417: 4415: 4412: 4411: 4409: 4405: 4399: 4396: 4394: 4391: 4389: 4386: 4384: 4381: 4380: 4378: 4376: 4372: 4366: 4363: 4361: 4358: 4356: 4353: 4351: 4348: 4347: 4345: 4341: 4334: 4331: 4328: 4325: 4323: 4320: 4318: 4317:Meso compound 4315: 4313: 4310: 4308: 4305: 4303: 4300: 4299: 4297: 4293: 4287: 4284: 4282: 4279: 4277: 4274: 4272: 4267: 4263: 4261: 4258: 4256: 4253: 4251: 4248: 4247: 4245: 4241: 4237: 4229: 4224: 4222: 4217: 4215: 4210: 4209: 4206: 4199: 4195: 4193: 4189: 4186: 4182: 4179: 4177: 4176:0-201-30425-2 4173: 4169: 4165: 4164: 4151: 4147: 4143: 4139: 4135: 4131: 4128:(2): 023901. 4127: 4123: 4116: 4108: 4104: 4100: 4096: 4092: 4088: 4085:(3): 035407. 4084: 4080: 4073: 4066: 4058: 4052: 4048: 4044: 4040: 4036: 4035:E.M. Lifshitz 4032: 4026: 4024: 4015: 4011: 4006: 4001: 3997: 3993: 3989: 3985: 3981: 3974: 3966: 3962: 3958: 3954: 3950: 3946: 3942: 3938: 3931: 3924: 3916: 3912: 3908: 3904: 3900: 3896: 3891: 3886: 3882: 3878: 3871: 3864: 3856: 3852: 3848: 3844: 3840: 3836: 3829: 3821: 3817: 3813: 3809: 3805: 3801: 3797: 3793: 3786: 3778: 3774: 3770: 3766: 3762: 3758: 3751: 3743: 3739: 3735: 3731: 3727: 3723: 3719: 3715: 3708: 3700: 3696: 3692: 3688: 3684: 3680: 3676: 3672: 3665: 3657: 3653: 3649: 3645: 3641: 3637: 3629: 3621: 3617: 3610: 3602: 3595: 3587: 3583: 3579: 3575: 3571: 3567: 3560: 3552: 3548: 3544: 3540: 3536: 3532: 3525: 3517: 3510: 3503: 3499: 3495: 3489: 3482: 3478: 3474: 3468: 3461: 3457: 3453: 3447: 3439: 3434: 3430: 3423: 3421: 3413: 3409: 3405: 3401: 3397: 3393: 3386: 3379: 3375: 3369: 3362: 3358: 3355: 3349: 3342: 3338: 3335:Arago (1811) 3332: 3324: 3320: 3316: 3312: 3308: 3304: 3296: 3288: 3286:9780471684961 3282: 3279:p. 195. 3278: 3274: 3273: 3265: 3254: 3250: 3248:9789241550031 3244: 3240: 3239: 3231: 3225: 3219: 3214: 3207: 3203: 3202: 3197: 3196: 3189: 3182: 3181: 3176: 3175: 3170: 3169: 3164: 3163: 3158: 3154: 3153: 3146: 3142: 3130: 3127: 3125: 3122: 3120: 3117: 3115: 3112: 3110: 3107: 3105: 3102: 3100: 3097: 3095: 3094:Birefringence 3092: 3090: 3087: 3085: 3082: 3080: 3077: 3076: 3069: 3067: 3063: 3059: 3049: 3047: 3043: 3033: 3031: 3027: 3023: 3019: 3011: 3007: 3002: 3000: 2984: 2961: 2953: 2948: 2946: 2942: 2938: 2922: 2911: 2906: 2892: 2869: 2843: 2839: 2836: 2833: 2830: 2821: 2818: 2812: 2805: 2804: 2803: 2789: 2783: 2775: 2759: 2747: 2730: 2726: 2698: 2675: 2669: 2664: 2660: 2633: 2627: 2622: 2618: 2611: 2608: 2599: 2593: 2587: 2581: 2576: 2572: 2565: 2562: 2553: 2547: 2542: 2539: 2536: 2522: 2521: 2520: 2503: 2493: 2490: 2487: 2473: 2469: 2465: 2461: 2455: 2449: 2445: 2441: 2436: 2433: 2430: 2416: 2412: 2408: 2405: 2401: 2395: 2389: 2386: 2382: 2373: 2369: 2363: 2358: 2355: 2352: 2338: 2337: 2336: 2318: 2314: 2286: 2263: 2257: 2237: 2215: 2212: 2209: 2182: 2176: 2156: 2153: 2133: 2111: 2107: 2098: 2094: 2068: 2064: 2057: 2054: 2045: 2039: 2031: 2027: 2020: 2017: 2008: 2002: 1995: 1994: 1993: 1992: 1963: 1959: 1955: 1951: 1947: 1940: 1936: 1932: 1929: 1925: 1918: 1909: 1903: 1893: 1889: 1885: 1881: 1877: 1870: 1866: 1862: 1859: 1855: 1842: 1831: 1828: 1823: 1816: 1815: 1814: 1813: 1791: 1788: 1785: 1771: 1767: 1763: 1759: 1755: 1750: 1747: 1744: 1730: 1726: 1722: 1719: 1715: 1706: 1702: 1696: 1689: 1685: 1670: 1669: 1668: 1650: 1646: 1616: 1613: 1610: 1581: 1578: 1575: 1559: 1557: 1539: 1536: 1533: 1530: 1526: 1517: 1513: 1509: 1505: 1501: 1479: 1450: 1415: 1409: 1406: 1397: 1386: 1382: 1376: 1371: 1368: 1365: 1351: 1350: 1326: 1320: 1317: 1308: 1297: 1293: 1287: 1282: 1279: 1276: 1262: 1261: 1260: 1258: 1254: 1236: 1233: 1230: 1201: 1198: 1195: 1180: 1176: 1158: 1155: 1152: 1123: 1120: 1117: 1102: 1082: 1078: 1047: 1037: 1034: 1031: 1017: 1013: 1009: 1005: 1001: 996: 993: 990: 976: 972: 968: 965: 961: 952: 948: 942: 935: 931: 916: 915: 914: 898: 894: 890: 868: 864: 855: 854:superposition 851: 846: 832: 802: 799: 796: 792: 788: 783: 780: 777: 773: 769: 766: 756: 755: 754: 752: 749: 744: 742: 738: 733: 728: 725: 722:(in vacuum), 721: 717: 713: 712: 707: 703: 698: 696: 692: 688: 684: 678: 675: 671: 667: 663: 659: 655: 651: 647: 646:stereoisomers 637: 635: 631: 626: 622: 620: 616: 611: 609: 603: 600: 596: 591: 588: 584: 580: 576: 575:tartaric acid 572: 571:Louis Pasteur 567: 565: 561: 557: 553: 550:, causes the 549: 545: 541: 533: 529: 525: 524:birefringence 521: 517: 513: 508: 504: 500: 496: 487: 480: 479:tartaric acid 475: 466: 464: 460: 444: 440: 436: 429: 425: 421: 417: 413: 409: 405: 401: 388: 386: 374: 362: 358: 354: 350: 329: 324: 320: 316: 312: 306: 302: 296: 286: 284: 280: 276: 272: 271:laevorotatory 268: 264: 260: 255: 253: 252:laevorotation 249: 245: 241: 237: 233: 229: 228:laevorotation 225: 219: 209: 207: 203: 199: 195: 191: 186: 184: 180: 176: 172: 168: 164: 160: 156: 152: 148: 144: 140: 135: 133: 132:metamaterials 129: 125: 121: 117: 113: 109: 105: 104:birefringence 101: 97: 93: 89: 85: 81: 77: 73: 63: 61: 57: 54: 51: 48: 46: 43: 40: 37: 36: 33: 28: 22: 4439:Biocatalysis 4349: 4312:Diastereomer 4302:Stereoisomer 4265: 4255:Stereocenter 4234:Concepts in 4197: 4167: 4125: 4121: 4115: 4082: 4078: 4065: 4042: 3987: 3983: 3973: 3940: 3936: 3923: 3880: 3876: 3863: 3838: 3834: 3828: 3795: 3791: 3785: 3760: 3756: 3750: 3717: 3713: 3707: 3674: 3670: 3664: 3642:(11): 1852. 3639: 3635: 3628: 3619: 3616:JETP Letters 3615: 3609: 3600: 3594: 3569: 3565: 3559: 3534: 3530: 3524: 3515: 3509: 3501: 3497: 3488: 3480: 3476: 3467: 3459: 3455: 3446: 3428: 3411: 3403: 3395: 3391: 3385: 3377: 3368: 3360: 3356: 3348: 3340: 3331: 3306: 3302: 3295: 3271: 3264: 3237: 3224: 3213: 3200: 3194: 3188: 3178: 3172: 3166: 3160: 3150: 3145: 3104:Polarization 3055: 3039: 3036:Applications 3030:fused quartz 3003: 2949: 2907: 2861: 2773: 2748: 2651: 2518: 2096: 2092: 2090: 1560: 1555: 1511: 1507: 1499: 1439: 1256: 1252: 1178: 1062: 849: 847: 821: 750: 745: 732:permittivity 729: 723: 709: 699: 679: 673: 665: 658:mirror image 653: 643: 627: 623: 612: 604: 592: 583:polarization 568: 539: 528:polarimeters 492: 462: 458: 442: 438: 427: 423: 416:stereocenter 403: 399: 389: 353:biochemistry 322: 318: 314: 310: 308: 274: 270: 267:dextrorotary 266: 262: 256: 251: 247: 232:levorotation 231: 227: 223: 222: 187: 182: 174: 163:stereoisomer 158: 154: 151:levorotatory 150: 146: 143:dextrorotary 142: 138: 136: 95: 84:polarization 79: 75: 71: 70: 38:Light source 4031:L.D. Landau 3965:10220/40854 3677:(12): 886. 3572:(3): 1324. 3046:polarimeter 1667:we obtain: 518:. In 1822, 373:amino acids 275:laevorotary 190:polarimeter 179:cholesterol 32:polarimeter 4454:Categories 4307:Enantiomer 3763:(4): 498. 3537:(6): 342. 3380:, 190–192. 3309:: S57–64. 3195:dextrogyre 3137:References 3018:optic axis 2952:wavelength 2910:dispersion 650:enantiomer 634:microwaves 621:crystals. 560:hydrolysis 516:turpentine 435:-threonine 328:SMALL CAPS 299:See also: 283:enantiomer 202:polarizers 155:levorotary 58:Rotatable 4407:Reactions 4250:Chirality 4107:119259753 3915:117891131 3890:0807.0523 3406: : 3398: : 3303:Chirality 3024:forms of 3022:amorphous 2982:Δ 2920:Δ 2893:θ 2890:Δ 2870:λ 2844:λ 2840:π 2828:Δ 2819:θ 2816:Δ 2790:θ 2787:Δ 2757:Δ 2727:θ 2699:θ 2696:Δ 2676:θ 2673:Δ 2661:θ 2634:θ 2631:Δ 2619:θ 2612:⁡ 2603:^ 2588:θ 2585:Δ 2573:θ 2566:⁡ 2557:^ 2470:θ 2456:θ 2453:Δ 2413:θ 2406:− 2396:θ 2393:Δ 2387:− 2315:θ 2287:θ 2284:Δ 2264:θ 2261:Δ 2258:− 2238:θ 2183:θ 2180:Δ 2157:θ 2134:θ 2108:θ 2065:θ 2058:⁡ 2049:^ 2028:θ 2021:⁡ 2012:^ 1960:θ 1948:− 1937:θ 1930:− 1913:^ 1890:θ 1867:θ 1860:− 1846:^ 1768:θ 1727:θ 1720:− 1686:θ 1647:θ 1556:real part 1537:ω 1531:− 1483:^ 1454:^ 1419:^ 1407:− 1401:^ 1330:^ 1312:^ 1079:θ 1014:θ 973:θ 966:− 932:θ 895:θ 865:θ 830:Δ 789:− 764:Δ 662:chirality 613:In 1950, 593:In 1874, 579:wine lees 569:In 1849, 236:chemistry 4343:Analysis 4150:19257274 4041:(1984). 4014:22588295 3820:16384264 3742:89292757 3699:19794663 3323:12884375 3253:Archived 3201:lĂ©vogyre 3072:See also 3028:such as 628:In 1898 548:fructose 540:dextrose 402:)- and ( 385:fructose 343:-" and " 335:-" and " 321:-" and " 64:Detector 4130:Bibcode 4087:Bibcode 3992:Bibcode 3990:: 833. 3945:Bibcode 3895:Bibcode 3843:Bibcode 3800:Bibcode 3765:Bibcode 3679:Bibcode 3644:Bibcode 3574:Bibcode 3539:Bibcode 3438:4745976 3435::  3400:372–389 3152:dextro- 1502:is the 1099:is the 683:racemic 564:sucrose 532:glucose 469:History 240:physics 171:camphor 167:sucrose 124:crystal 4174:  4168:Optics 4148:  4105:  4053:  4012:  3913:  3818:  3740:  3734:115973 3732:  3697:  3622:: 264. 3433:Zenodo 3321:  3283:  3245:  3180:laevus 3168:Laevo- 3162:dexter 3026:silica 3010:quartz 2862:where 1516:phasor 1440:where 1063:where 850:linear 822:While 640:Theory 544:dexter 499:quartz 426:) or ( 394:- and 305:Aldose 279:chiral 128:quartz 108:fluids 100:chiral 4103:S2CID 4075:(PDF) 3933:(PDF) 3911:S2CID 3885:arXiv 3873:(PDF) 3738:S2CID 3730:JSTOR 3408:63–81 3256:(PDF) 3233:(PDF) 3174:levo- 3159:word 3157:Latin 3131:(ROA) 670:helix 234:) in 212:Forms 130:) or 4335:(de) 4329:(ee) 4172:ISBN 4146:PMID 4051:ISBN 4010:PMID 3816:PMID 3695:PMID 3319:PMID 3281:ISBN 3243:ISBN 3198:and 3012:(SiO 2276:and 2095:and 1596:and 1510:and 1469:and 1255:and 1216:and 1138:and 597:and 390:The 303:and 238:and 226:and 173:are 169:and 4138:doi 4126:102 4095:doi 4000:doi 3961:hdl 3953:doi 3941:108 3903:doi 3851:doi 3808:doi 3773:doi 3722:doi 3687:doi 3652:doi 3582:doi 3547:doi 3311:doi 3171:or 2609:sin 2563:cos 2055:sin 2018:cos 693:or 666:not 654:not 562:of 351:in 273:or 265:or 181:is 153:or 141:or 78:or 4456:: 4183:, 4144:. 4136:. 4124:. 4101:. 4093:. 4083:79 4081:. 4077:. 4037:; 4033:; 4022:^ 4008:. 3998:. 3986:. 3982:. 3959:. 3951:. 3939:. 3935:. 3909:. 3901:. 3893:. 3881:93 3879:. 3875:. 3849:. 3839:90 3837:. 3814:. 3806:. 3796:95 3794:. 3771:. 3761:78 3759:. 3736:. 3728:. 3718:63 3716:. 3693:. 3685:. 3675:17 3673:. 3650:. 3638:. 3620:29 3618:. 3580:. 3570:50 3568:. 3545:. 3535:21 3533:. 3502:22 3500:, 3479:, 3460:28 3419:^ 3404:10 3402:; 3359:, 3317:. 3307:15 3305:. 3251:. 3235:. 2335:: 1179:+z 674:is 672:) 441:,3 257:A 157:— 145:— 134:. 4269:2 4266:C 4227:e 4220:t 4213:v 4152:. 4140:: 4132:: 4109:. 4097:: 4089:: 4059:. 4016:. 4002:: 3994:: 3988:3 3967:. 3963:: 3955:: 3947:: 3917:. 3905:: 3897:: 3887:: 3857:. 3853:: 3845:: 3822:. 3810:: 3802:: 3779:. 3775:: 3767:: 3744:. 3724:: 3701:. 3689:: 3681:: 3658:. 3654:: 3646:: 3640:5 3588:. 3584:: 3576:: 3553:. 3549:: 3541:: 3481:9 3396:9 3361:1 3325:. 3313:: 3289:. 3014:2 2985:n 2962:L 2923:n 2858:, 2837:2 2834:L 2831:n 2822:= 2813:2 2784:2 2774:L 2760:n 2731:0 2721:E 2670:+ 2665:0 2637:) 2628:+ 2623:0 2615:( 2600:y 2594:+ 2591:) 2582:+ 2577:0 2569:( 2554:x 2548:= 2543:t 2540:u 2537:o 2532:E 2504:. 2499:) 2494:C 2491:H 2488:L 2483:E 2474:0 2466:i 2462:e 2450:i 2446:e 2442:+ 2437:C 2434:H 2431:R 2426:E 2417:0 2409:i 2402:e 2390:i 2383:e 2379:( 2374:2 2370:2 2364:= 2359:t 2356:u 2353:o 2348:E 2319:0 2309:E 2216:t 2213:u 2210:o 2205:E 2177:2 2154:2 2112:0 2097:y 2093:x 2074:) 2069:0 2061:( 2046:y 2040:+ 2037:) 2032:0 2024:( 2009:x 2003:= 1974:) 1971:) 1964:0 1956:i 1952:e 1941:0 1933:i 1926:e 1922:( 1919:i 1910:y 1904:+ 1901:) 1894:0 1886:i 1882:e 1878:+ 1871:0 1863:i 1856:e 1852:( 1843:x 1837:( 1832:2 1829:1 1824:= 1797:) 1792:C 1789:H 1786:L 1781:E 1772:0 1764:i 1760:e 1756:+ 1751:C 1748:H 1745:R 1740:E 1731:0 1723:i 1716:e 1712:( 1707:2 1703:2 1697:= 1690:0 1680:E 1651:0 1641:E 1617:C 1614:H 1611:L 1606:E 1582:C 1579:H 1576:R 1571:E 1540:t 1534:i 1527:e 1512:y 1508:x 1500:i 1480:y 1451:x 1425:) 1416:y 1410:i 1398:x 1392:( 1387:2 1383:2 1377:= 1372:C 1369:H 1366:L 1361:E 1336:) 1327:y 1321:i 1318:+ 1309:x 1303:( 1298:2 1294:2 1288:= 1283:C 1280:H 1277:R 1272:E 1257:y 1253:x 1237:C 1234:H 1231:L 1226:E 1202:C 1199:H 1196:R 1191:E 1159:C 1156:H 1153:L 1148:E 1124:C 1121:H 1118:R 1113:E 1083:0 1073:E 1048:, 1043:) 1038:C 1035:H 1032:L 1027:E 1018:0 1010:i 1006:e 1002:+ 997:C 994:H 991:R 986:E 977:0 969:i 962:e 958:( 953:2 949:2 943:= 936:0 926:E 899:0 891:2 869:0 833:n 818:. 803:C 800:H 797:L 793:n 784:C 781:H 778:R 774:n 770:= 767:n 751:n 536:D 481:. 463:R 459:S 455:L 451:L 449:/ 447:D 443:S 439:S 433:L 428:S 424:R 404:S 400:R 396:L 392:D 383:- 381:D 377:L 371:- 369:L 365:D 345:L 341:D 337:L 333:D 331:" 323:l 319:d 315:l 311:d 220:. 183:l 175:d 159:l 147:d 23:.

Index

circularly polarized light

polarimeter
Linear polarizer
linear analyzer
polarization
linearly polarized
circular dichroism
chiral
birefringence
fluids
chiral molecules
secondary structure
chiral liquid crystals
crystal
quartz
metamaterials
stereoisomer
sucrose
camphor
cholesterol
polarimeter
sugar industry
enantiomeric ratio
polarizers
liquid-crystal displays
Levo (company)
chemistry
physics
plane-polarized light

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