ライフサイエンスコーパス: absorption maxima

1 d-shifted (low pH) or blue-shifted (high pH) absorption maxima.

2 blue shifts in the fluorescence emission and absorption maxima.

3 some acylations also affect the anthocyanin absorption maxima.

4 5R(D)), there is no shift in the two-photon absorption maxima.

5 he meso substituents had a greater impact on absorption maxima.

6 LWS cone pigment results in a blue shift in absorption maxima.

7 are responsible for the 10 nm blue shift in absorption maxima.

8 pectively), on the basis of both the visible absorption maxima (530 versus 490 nm) and photocycle kin

9 All flavonols except kaempferol have absorption maxima above 440nm and so readings at 420nm a

10 c addition, resulting in a blue shift of the absorption maxima and a dramatic decrease in fluorescenc

11 aining 9- or 11-cis-retinal had blue-shifted absorption maxima and altered photo-bleaching properties

12 s of up to approximately 100 nm in localized absorption maxima and increased electron affinities.

13 eveal a Barlow-type relationship between the absorption maxima and the thermal isomerization rate sug

14 ith smaller side chains, (c) blue-shifted Qy absorption maxima, and (d) a sigmoid-shaped circular dic

15 he isomers have different thermal stability, absorption maxima, and quantum yields.

16 tical properties with the longest wavelength absorption maxima around 500-800 nm, which gradually rea

17 ase domain thus prepared exhibits UV-visible absorption (maxima at 419 and 553 nm, shoulder at approx

18 opsin on the basis of the shift in the batho absorption maxima at 10 K [lambda(max) band (native) = 5

19 Copper-free CBCs showed absorption maxima at 204, 275, 333, and 356 with shoulde

20 the formation of reaction intermediates with absorption maxima at 227 and 280 nm are diminished and d

21 obic conditions, reconstituted FNR exhibited absorption maxima at 315 nm and 420 nm, which were repla

22 The cysteine adducts have absorption maxima at 323 and 326 nm, with molar extincti

23 In methanol compounds 1 and 2 had absorption maxima at 360 and 370 nm, respectively, and e

24 l was clearly observed and identified by the absorption maxima at 370, 610, and 690 nm.

25 l-protein intermediate states, with apparent absorption maxima at 380 nm and 440 nm, respectively.

26 The S-bonded complexes feature (3)MLCT absorption maxima at 388 nm (R = BnF(5)), 396 nm (R = Bn

27 T were detected by LFP with strong transient absorption maxima at 390 nm.

28 Purified ferric Hmx1 and CaHmx1 have Soret absorption maxima at 404 and 410 nm, respectively.

29 ed buffer generated a transient species with absorption maxima at 427 and approximately 560 nm.

30 of both the wild-type and F190I MnP exhibit absorption maxima at 429, 529, and 558 nm, resembling th

31 pectral shift of about 38 nm, giving rise to absorption maxima at 432, 462, and 492 nm in 20 mM Tris-

32 tion was supported by H2O2 and exhibited the absorption maxima at 435 and 930 nm characteristic of an

33 g both chromophores) exhibits characteristic absorption maxima at 435 nm due to the PYP domain and at

34 different conformations, having their (0,0) absorption maxima at 489 and 522 nm, respectively.

35 yl)ethenyl], which leads to derivatives with absorption maxima at 503, 587, and 668 nm, respectively.

36 photointerconvertible Pr and Pfr states with absorption maxima at 630 and 704 nm, respectively.

37 ith PCB and apophycocyanin, the products had absorption maxima at 635 nm and very low fluorescence yi

38 chromophore have been synthesized; both have absorption maxima at 650 nm, where all the shellfish ext

39 bsence of dioxygen, indicated a species with absorption maxima at approximately 330 and approximately

40 WMG1 and WMG2 show absorption maxima at around 800 nm, which favors tissue

41 cupredoxins before, with intense electronic absorption maxima at ~410 and 760 nm.

42 , all except for luteolin and orientin, have absorption maxima below 400nm.

43 ed samples revealed the formation of two new absorption maxima characteristic of Cob(I)alamin.

44 nding, the rate of NO release, and the Soret absorption maxima for nitrophorin I were all pH dependen

45 The absorption maxima for the Soret peaks of the oxidized an

46 h sensitive cone pigments have shifted their absorption maxima from the UV to the visible regions of

47 A = H); these include red-shifted (20-50 nm) absorption maxima, highly solvatochromic emission profil

48 These pigments exhibit absorption maxima in between 532-550 nm and 457-485 nm,

49 were able to reproduce the trend of observed absorption maxima in both A1 and A2 rhodopsins, reveal a

50 from 4-(dimethylamino)phenylethyne (7), have absorption maxima in methanol of 594, 631, and 672 nm, r

51 steps from p-aminophenylacetylene (9), have absorption maxima in methanol of 623, 654, and 680 nm fo

52 -738 nm) upon irradiation of either of their absorption maxima in the blue and red regions.

53 pped in polyurethane hydrogel D4 and feature absorption maxima in the range 660-710 nm and fluorescen

54 sis of 294 A1 and A2 cone pigment literature absorption maxima indicates that the selection of a 6- s

55 e 21,23-core-modified porphyrins gave band I absorption maxima (lambda(max) of 689-717 nm) at longer

56 iaporphyrins 1-4 had little effect on either absorption maxima (lambda(max) of 696-701 nm for band I)

57 ncluding a large separation (70 nm) in their absorption maxima (lambda(max)) and a 2.5-fold increase

58 ynamic properties, including shifted optical absorption maxima (lambdamax) and decreased redox midpoi

59 colorimetric method involving probing of the absorption maxima (lambdamax) on the d-d electronic spec

60 tetramer (9) and pentamer (10) both exhibit absorption maxima matching those of the corresponding si

61 tween GPR and BPR as well as their different absorption maxima may be explained as an adaptation to t

62 , but instead afforded a yellow product with absorption maxima of 257 and 400 nm.

63 V) and bovine blue cone visual pigments have absorption maxima of 358 and 438 nm, respectively, while

64 o long-lived pH-dependent photopigments with absorption maxima of 469 +/- 2.4 and 370 +/- 7.3 nm.

65 vocal bathochromic shifts of 10-15 nm of the absorption maxima of anilines in frozen samples compared

66 The absorption maxima of Az48W* display an approximately 23

67 The absorption maxima of both rod and cone visual pigments o

68 on spectral shifts, i.e., differences in the absorption maxima of colorless and colored forms, observ

69 been examined, revealing that the wavelength absorption maxima of each form increases with increasing

70 The absorption maxima of naphthoporphyrins substituted with

71 ations accurately reproduce the experimental absorption maxima of rhodopsin and the red, green, and b

72 at the two wavelengths corresponding to the absorption maxima of the chromophores, 675 and 750 nm.

73 ch results in a 95 nm difference between the absorption maxima of the two forms, and (ii) induction o

74 The absorption maxima of these chromophores shift predominan

75 Notably, the absorption maxima of these S1 --> S(n) manifolds can be

76 core heteroatoms had little effect on either absorption maxima or quantum yields of singlet oxygen ge

77 hermal stability without affecting the dyes' absorption maxima originates from the twisted geometry o

78 With absorption maxima overlapping with the wavelengths of co

79 ineering gave rise to chimeric variants with absorption maxima ranging from 526 to 545 nm, dovetailin

80 e zinc chlorins exhibit long-wavelength peak absorption maxima ranging from 626 to 667 nm, indicating

81 hytochromobilin adduct displayed red-shifted absorption maxima relative to purified algal phytochrome

82 with red-shifted (D380E, lambdamax = 533 nm) absorption maxima relative to the wild-type protein (lam

83 cted evolution generated 70 GR variants with absorption maxima shifted by up to +/-80nm, extending th

84 ies and the position of its two ground state absorption maxima suggest it as a candidate for controll

85 Two sequential intermediates were found with absorption maxima that exhibit red shifts from the resti

86 te structure is demonstrated by plotting the absorption maxima versus the wavenumber of a Raman band

87 h thermally stability, hypsochromic shift of absorption maxima wavelengths of initial and cyclic form

88 fluorophore emission maxima, and nearly all absorption maxima were significantly red-shifted when co

89 By comparing the shift of the absorption maxima when a visual pigment is converted to

90 significantly affects the position of UV-vis absorption maxima, which can be tuned in a broad range o

91 degrees of blue-shift in the flavin visible absorption maxima while visible CD spectra of the Y93A,

92 ,23-core-modified porphyrins 1-5 gave band I absorption maxima with lambda(max) of 695-701 nm.

93 obtained from the wavelengths of UV/Visible absorption maxima with solute H-bond parameters obtained