ライフサイエンスコーパス: optical activity

1 matter including absorption, dispersion and optical activity.

2 by vibrational circular dichroism and Raman optical activity.

3 ons, aromaticity is correlated to diminished optical activity.

4 hs are sufficient to account for nonresonant optical activity.

5 nanostructures with chiral shapes and large optical activity.

6 The organic phase, however, still displays optical activity.

7 ctations of the magnitudes and etiologies of optical activity.

8 n the tactoids as manifested by the observed optical activity.

9 e acceptor strength to chromophore nonlinear optical activity.

10 conditions results in significant erosion of optical activity.

11 ires have high aspect ratio, uniformity, and optical activity.

12 responding gamma-butanolides without loss of optical activity.

13 The solid VC did not lose optical activity after several mounts at room temperatur

14 Optical activity, although direct and simple, lacks sens

15 Optical activity and circular dichroism are fascinating

16 oretical analysis of the interaction between optical activity and electro-optic property, the optical

17 ly, the broadband behaviors of nondispersive optical activity and high transmission are insensitive t

18 and birefringent properties, yet its lack of optical activity and semiconducting transport hamper app

19 es, yield a new kind of relationship between optical activity and temperature, and also reveal unusua

20 s connected to the chromophore ring in their optical activity and the important role of pyridyl group

21 superimposable molecules that differ only in optical activity and their interaction with other chiral

22 warf LP944-20, whereas previous searches for optical activity (and one X-ray search) yielded negative

23 ion, thermal and/or electrical conductivity, optical activity, and capability to direct cell growth.

24 parallel fibers evoked a transverse beam of optical activity, and stimulation of the contralateral i

25 ls (LCs), which can impart optical isotropy, optical activity, and sub-millisecond EO response of BPI

26 finds no difference, aside from the expected optical activity, arising from the difference in stereoc

27 dichroism signal confirm the origin of this optical activity as the chiral supramolecular organizati

28 Optical activity associated with retinal binding to TL w

29 overlapping anisotropic lamellae, a kind of optical activity associated with the mesoscale stereoche

30 ble, but the resolved enantiomers exhibit no optical activity at the alphaD-line.

31 p the possibility of controlled induction of optical activity at the nanosecond time scale for exploi

32 There are no Raman optical activity bands characteristic of extended second

33 rossing zero at the nematic temperature, the optical activity becomes so large that it may be observe

34 A marked difference in optical activity between the former 1a and 1b) and latte

35 y Mueller matrix microscopy shows that their optical activity can be individually measured and that t

36 loids, whose nanoscale geometry and rotatory optical activity can be reversibly reconfigured and cycl

37 ions form a basis for making broad structure-optical activity correlations from inspection of molecul

38 of such materials should lead to interesting optical activity effects.

39 Two of the aggregates show very high optical activity even though the isolated chromophores b

40 optically active substrate with its loss of optical activity, F, the fraction of the initially forme

41 The loss in optical activity for these reactions was shown to occur

42 We demonstrate that optical activity in amorphous isotropic thin films of pu

43 CD spectroscopy did not detect any optical activity in the seed polymer.

44 The carotenoid in ethanol has very weak optical activity in the visible region of the spectrum.

45 gnetic dipole polarizability contribution to optical activity in which the sense of electric dipoles

46 Incorporating optical activity into time-resolved spectroscopies has p

47 tive understanding of the vexing property of optical activity is forthcoming for the following reason

48 The relationship between aromaticity and optical activity is investigated in comparisons of heter

49 optical manifestations of birefringence and optical activity (linear and circular birefringence and

50 These films exhibited optical activity (OA) at 380 nm and in the range of 200-

51 of the strong inherent resonances, the giant optical activity obtained via chiral metamaterials gener

52 ter (2, 3, 4a,b) dendrons is mirrored in the optical activities of model compounds 12a, 12b, 19a, and

53 Also in S1 in solution, the induced optical activity of a fluorescein probe linked to SH1 sh

54 nd binding was monitored using the intrinsic optical activity of bound retinol.

55 Because of the optical activity of chiral molecules, it has been hypoth

56 The optical activity of chitin was found to be levorotatory.

57 ence that cannot be explained by the natural optical activity of corresponding compounds, some of whi

58 And the optical activity of multi-layer chiral metamaterials is

59 Both the aqueous and organic phases show optical activity of near mirror image relationship.

60 cal activity and electro-optic property, the optical activity of the crystal has no influence on the

61 Agreement between the optical activity of the model compounds and that of the

62 state is obtained at high temperatures, the optical activity of the supramolecular stack self-assemb

63 the anisotropic absorption property and the optical activity of the twist alignment nematic cell, sp

64 The optical activity of these chiral dendritic structures is

65 The optical activity of these chiral dendritic structures wa

66 Environmentally induced optical activity of Trp/Tyr/Phe (2:4:12) detected by nea

67 The changes in the optical activity of Trp510 and SH1 bound fluorescein in

68 In myosin S1 in solution, the optical activity of Trp510 senses conformation change in

69 of VC was related to isomerization (loss of optical activity) of the l-enantiomer either to d-enanti

70 Surface-enhanced Raman optical activity offers potential capabilities for sensi

71 yet unexpected, dependence of the dispersive optical activity on the nature (phase) of the surroundin

72 for obtaining either highly confined modes, optical activity, or a low-scattering signature, but at

73 aveguide with a low-visibility and broadband optical activity represents a transformative wave manipu

74 nd can therefore avoid the highly dispersive optical activity resulting from resonances.

75 ), have been studied using vibrational Raman optical activity (ROA) and ultraviolet circular dichrois

76 o conformational mobility, vibrational Raman optical activity (ROA) has provided new insights into th

77 , and Er) complexes were recorded on a Raman optical activity (ROA) instrument.

78 Raman optical activity (ROA) is an advanced technique capable

79 the first observations of vibrational Raman optical activity (ROA) on intact viruses.

80 We report the collection of Raman optical activity (ROA) spectra of adenine in silver coll

81 e report calculations of the Raman and Raman optical activity (ROA) spectra of methyl-beta-D-glucose

82 Here we analyze Raman optical activity (ROA) spectra of N-acetylalanine-N'-met

83 Vibrational Raman optical activity (ROA) spectra of the wheat proteins alp

84 Raman and Raman optical activity (ROA) spectra were collected for four R

85 The CPL spectra were measured on a Raman optical activity (ROA) spectrometer, which ensured high

86 The Raman optical activity (ROA) spectroscopic technique has been

87 Here, we utilized Raman spectroscopy, Raman optical activity (ROA), circular dichroism (CD), and tip

88 Vibrational Raman optical activity (ROA), measured as a small difference i

89 uch higher order structure, we applied Raman optical activity (ROA)-a spectroscopic technique that is

90 a combination of Raman scattering and Raman optical activity (ROA).

91 degrees C at pH 2.0, was studied using Raman optical activity (ROA).

92 brational circular dichroism, VCD, and Raman optical activity, ROA) provide more reliable assignments

93 al solution, that is, surface-enhanced Raman optical activity (SEROA) using considerably shorter data

94 The optical activity spans 2 orders of magnitude depending o

95 irror image surface enhanced resonance Raman optical activity spectra for the two enantiomers of both

96 The Raman optical activity spectra of all these proteins are very

97 We report Raman and Raman optical activity spectra of hyaluronan polymer, the hyal

98 these proteins has been provided by a Raman optical activity study, supplemented with differential s

99 ervations using the novel technique of Raman optical activity suggest that individual residues in unf

100 Optical activity, used here for the first time to gain i

101 Optical activity was fully preserved throughout.

102 The optical activity was reduced (100%) to zero after 6 and

103 The structure and optical activity was sensitive to imidazole concentratio

104 irst proposed by Hohn and Weigang for linear optical activity, we presented a dynamic coupling model

105 derivatives can exhibit excellent nonlinear optical activity when extended through pi-bridges.

106 hat one of the diastereomers has very strong optical activity, which overrules the cancelation of the

107 amaterial can achieve nondispersive and pure optical activity with high transmittance in a broadband

108 synthetic material are identical (except for optical activity) with respect to structure and biologic