ライフサイエンスコーパス: absorption maxima

1 lysis as yields are maximized near the COF's absorption maxima.

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

3 d solubility and a bathochromic shift of the absorption maxima.

4 blue shifts in the fluorescence emission and absorption maxima.

5 some acylations also affect the anthocyanin absorption maxima.

6 5R(D)), there is no shift in the two-photon absorption maxima.

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

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

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

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

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

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

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

14 drawing groups show bathochromically shifted absorption maxima and considerably enhanced CO release y

15 how substantial bathochromic shifts of their absorption maxima and enhanced photosensitivity but prov

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

38 n A. limacinum we identified three ACRs with absorption maxima at 485, 545, and 590 nm, indicating co

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

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

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

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

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

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

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

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

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

48 of the CAArC leads to relatively low energy absorption maxima between 350 and 550 nm in THF with hig

49 rolled ATRP at wavelengths longer than their absorption maxima but required higher loadings.

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

51 These reactive dyes exhibit absorption maxima close to 450 nm and emission above 600

52 UV-vis absorption maxima difference (Deltalambda(avg)) correlat

53 e these photophysical properties, namely the absorption maxima, emission maxima, Stokes shifts, vibro

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

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

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

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

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

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

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

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

62 t localized in glioblastoma tumor cells, has absorption maxima in NIR region, and showed similar ther

63 -738 nm) upon irradiation of either of their absorption maxima in the blue and red regions.

64 The Aza-COFs exhibit light absorption maxima in the blue spectral region, and each

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

66 ngle substitution allows modulation of their absorption maxima in the range of 693-805 nm and photoph

67 lent photoluminescence properties having two absorption maxima in the region between 270-280 and 338-

68 The selenophene derivatives present absorption maxima in the UV-A region and fluorescence em

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

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

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

72 arameters such as (19)F NMR chemical shifts, absorption maxima (lambda(max)(abs)), and emission maxim

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

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

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

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

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

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

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

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

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

82 The absorption maxima of Az48W* display an approximately 23

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

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

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

86 The absorption maxima of naphthoporphyrins substituted with

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

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

89 tic red-shift in the absorption spectra: the absorption maxima of the fused dimer and trimer appear a

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

91 The absorption maxima of these chromophores shift predominan

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

93 ricyanofuran photoacids are synthesized with absorption maxima of varying wavelengths across the whol

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

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

96 With absorption maxima overlapping with the wavelengths of co

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

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

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

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

101 Absorption maxima saturate for n = 4 in vacuum and for n

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

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

104 spectra suggested by the shift in UV-visible absorption maxima that correspond with a rise in L-Citru

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

106 in naphthoylquinoline hydrazones pushes the absorption maxima toward the visible spectral region.

107 ts by using pigment-containing proteins with absorption maxima tuned to each ecological niche.

108 ost red-shifted channelrhodopsins known with absorption maxima up to 610 nm.

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

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

111 The absorption maxima were 665 and 704 nm, while the emissio

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

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

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

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

116 ,23-core-modified porphyrins 1-5 gave band I absorption maxima with lambda(max) of 695-701 nm.

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