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1 is assigned computationally according to its optical rotation.
2  crystals allowed for a measurement of their optical rotation.
3 lysis to aglycones, antioxidant capacity and optical rotation.
4 ntitative correlations between structure and optical rotation.
5 ass losses, amorphous in nature and negative optical rotations.
6 resultant chiral polymers exhibit very large optical rotations.
7 S,19S,20S,21R configuration by comparison of optical rotations.
8 rcular dichroism spectra and of the specific optical rotations.
9                                              Optical rotation, a form of optical activity, is a pheno
10 tamaterials that provide near dispersionless optical rotation across a broad band of frequencies from
11                                          The optical rotation [[alpha]D +22.8 (c 0.50, CHCl3)] obtain
12 on this material confirmed that the reported optical rotation [[alpha]D 0 (c 0.50, CHCl3)]47 was biog
13                       A combination of HPLC, optical rotation and CD spectroscopy was employed to dis
14 concerted use of transparent spectral region optical rotation and circular dichroism in determining t
15 hiral HPLC enabled their characterization by optical rotation and circular dichroism spectroscopy.
16 king but represents the long-sought specular optical rotation and indicates a new intertwined order.
17  calculations of transparent spectral region optical rotation and of circular dichroism has recently
18                               Here we report optical rotation and polar Kerr measurements in CsV(3)Sb
19 making the OV with large TC not suitable for optical rotation and short-distance communication.
20        These methods were used to assign the optical rotation and to prepare milligram quantities of
21        This enabled the measurement of their optical rotations and CD spectra.
22                                              Optical rotations and characteristic (1)H NMR data for t
23 culation of both transparent spectral region optical rotations and electronic circular dichroism (CD)
24                                              Optical rotations and rotatory strengths are calculated
25 sicochemical studies (UV-vis absorption, CD, optical rotation, and cyclic voltammetry) of the [7]heli
26 concentration, aggregation number, polarity, optical rotation, and partial specific volume.
27 concentration, aggregation number, polarity, optical rotation, and partial specific volume.
28  This approach links chemical structure with optical rotation angle and provides a quantitative measu
29 that atoms and functional groups make to the optical rotation angle and, more generally, to the molec
30                                          The optical rotation angle is determined by measuring the ph
31 to determine the atomic contributions to the optical rotation angle is reported.
32 pound, polygonapholine should not exhibit an optical rotation as reported.
33                  Remarkably, the sign of the optical rotation at 1.54 microm (that is, at wavelengths
34 n of trichoflectin and deflectin-1a based on optical rotation, CD spectra, and X-ray crystallography.
35 hed by comprehensive spectroscopic analyses, optical rotations, chemical correlations with known sesq
36  on a combination of 1D and 2D NMR analysis, optical rotation, circular dichroism, and preparation of
37 A comparison of experimental and theoretical optical rotation, circular dichroism, and two-dimensiona
38 asis is on the evaluation of long wavelength optical rotation, consistent with quantum chemical compu
39 n of electronic circular dichroism (ECD) and optical rotation data of all possible stereoisomers, the
40         Comparison of the 1H and 13C NMR and optical rotation data of the resulting isomers with the
41 X-ray experiment in conjunction with NMR and optical rotation data, whereas the depside molecular str
42 on mechanism were further studied by NMR and optical rotation demonstrating that the reaction product
43 ts" from nanohelicoids should provide strong optical rotation due to alignment of helical axis with p
44 n certain physicochemical properties such as optical rotation, electrostatic potentials, and intermol
45 20) and for the first time gives the ECD and optical rotation for eusiderins B (2), G (25), L (23), a
46 rted by the ab initio prediction of positive optical rotation for the most stable conformer with an (
47 s to study the correspondence between CD and optical rotation for zwitterionic and protonated l-amino
48                        Thus, the sign of the optical rotation had to be revised.
49    An isotropic component in the spontaneous optical rotation has also been reported and was interpre
50      The 5S,6R,9S isomer has NMR spectra and optical rotation identical with those of the natural com
51                 Here we show that mechanical-optical rotation in the pulsar magnetosphere affects pol
52 ircular dichroism (CD) can be applied to the optical rotation in this case, but with some restriction
53                       Hence the bandwidth of optical rotation is found to be relatively independent o
54                             Strong nonlinear optical rotation is observed at key spectral locations,
55                                              Optical rotation measurements and chiral HPLC analysis d
56 ion with chiral compounds has been probed by optical rotation measurements during exposure to enantio
57 MR of the underivatised natural product, and optical rotation measurements of the hydrolysed sugar mo
58 e set of NMR data along with ECD spectra and optical rotation measurements of the synthesized natural
59                                      Precise optical rotation measurements play an important role in
60 al studies using circular dichroism (CD) and optical rotation measurements show that these collagen a
61                                 Nuclear spin optical rotation (NSOR) has been investigated as a magne
62                                In both, pure optical rotation occurs in a frequency band between two
63                         A calculation of the optical rotation of (R)-(-)-3-chloro-1-butene found a re
64 ecular weight of 1.35x10(6)Da and a specific optical rotation of +64 degrees (c 1.0, H2O), was isolat
65 neously acquired signals associated with the optical rotation of a laser beam traversing the atomic s
66 eport stable optical trapping and switchable optical rotation of nanoparticle (NP)-assembled micromot
67 r the odd-parity phonon mode and the magneto-optical rotation of scattered light from the even-parity
68 ergy conformers as 1315 cal/mol and gave the optical rotation of the low-energy conformer and the ave
69                                  We observed optical rotation of the plane of polarization of the sec
70                Lastly, we performed coherent optical rotations of a single collective nuclear spin ex
71 e calculation of transparent spectral region optical rotations of chiral molecules provides a new app
72                 A comparison of the specific optical rotations of synthetic seimatopolides with those
73 ed fashion with large deviations in specific optical rotation (OR) and CD Cotton effect as a conseque
74 of a chiral molecule can be deduced from its optical rotation (OR) and/or its electronic circular dic
75 roism (ECD), and transparent spectral region optical rotation (OR) has revolutionized the determinati
76 ronic circular dichroism (ECD) spectrum, and optical rotation (OR) to experimental VCD, ECD, and OR d
77                           The calculation of optical rotation (OR, [a](D)) for nonrigid molecules was
78 s and in particular electrical conductivity, optical rotation, pH and sugar composition revealed some
79  CHCl3/acetonitrile, and CD spectroscopy and optical rotation show that the resolved, crystalline mat
80                                              Optical rotation techniques are especially attractive be
81       Comparisons are made of the calculated optical rotation tensors of C(2v)-symmetric, polyaromati
82 isotropic components of 1 milliradian in the optical rotation that do not respond to applied magnetic
83  of the natural product, as well as matching optical rotations, the two compounds are believed to be
84                               The ability of optical rotation to detect enantiospecific adsorption ar
85 rations were determined by comparison of the optical rotation value of the products with literature d
86 al studies comparing experimentally obtained optical rotation values, electronic circular dichroism s
87 nerating a new class of materials with large optical rotations, various arylamines were condensed wit
88            The effect of conformation on the optical rotation was confirmed by a study of the tempera
89                             By comparison of optical rotation, we assign naturally occurring 3-amino-
90 erometric detection and in-line detection of optical rotation with an in-line laser polarimeter for a
91 tural material is evaluated by comparing its optical rotation with that of synthetic material.
92 )-12 were confirmed by a comparison of their optical rotations with those of the compounds synthesize