ライフサイエンスコーパス: bathochromic shift

1 Patterns were similar regarding bathochromic shifts.

2 There were bathochromic shifts (81-105 nm) from pH 1 to 8 and hypso

3 angements, energy storage, and origin of the bathochromic shift accompanying the transformation of rh

4 of a pyrrole hydrogen-bond donor leads to a bathochromic shift allowing for quantitative bidirection

5 M3Q was monitored by UV spectroscopy a 22-nm bathochromic shift and 75% hypochromicity of the porphin

6 while absorption and emission data showed a bathochromic shift and increase in quantum efficiency.

7 anin color while trivalent metal ions caused bathochromic shifts and hue changes.

8 Highest bathochromic shifts and most intense blue colours were o

9 ron-deficiency and LUMO energies of -4.8 eV, bathochromic shifts, and a strong intensity increase of

10 nzochlorin analogues exhibited a significant bathochromic shift ( approximately 10 nm) in the electro

11 rms' protonation results in hypsochromic and bathochromic shifts consistent with the preferential sta

12 ) value (for methanol, this corresponds to a bathochromic shift from 543 to 732 nm).

13 f the fused porphyrins undergo a progressive bathochromic shift in a series of naphthyl (lambda(max)

14 bsorption and fluorescence changes, namely a bathochromic shift in absorption and fluorescence quench

15 binding leads to either a hypsochromic or a bathochromic shift in emission via interaction of the me

16 ption spectrum of the complex showed a 32-nm bathochromic shift in lambdamax with minor peaks at 460

17 bond was found to give rise to only a 20 nm bathochromic shift in the absorbance and fluorescence sp

18 acetyl, 7-formyl) progressively causes (1) a bathochromic shift in the absorption maximum of the B ba

19 hene-bridged bisborole (14) exhibits a large bathochromic shift in the absorption spectrum, demonstra

20 ia click chemistry resulted in a significant bathochromic shift in the fluorescence excitation (15 nm

21 n with a model MsrA (E. coli), it exhibits a bathochromic shift in the fluorescence maximum.

22 t addition of small amounts of HMPA causes a bathochromic shift in the spectrum of 1-Li.

23 mpounds through para-substitution leads to a bathochromic shift in their activation wavelength.

24 ng aryl substituent, consequently results in bathochromic shifts in both absorption and emission.

25 nt changes in Stokes shift, as well as large bathochromic shifts in both excitation maximum (from 521

26 Coproporphyrin exhibits bathochromic shifts in both the Soret and visible absorp

27 polycyclic aromatic hydrocarbons show large bathochromic shifts in the absorption and emission relat

28 wering of the band gap and the corresponding bathochromic shifts in the absorption and emission spect

29 d the substituents, as demonstrated by large bathochromic shifts in the absorption spectra as well as

30 These substituents result in large bathochromic shifts in the chrysene absorption and emiss

31 Significant bathochromic shifts in the electronic spectra, witnessed

32 nomenon manifested by either hypsochromic or bathochromic shifts in the fluorescence lambda max.

33 shifts of the free ligands, lead to similar bathochromic shifts in the Ir complexes of the same liga

34 Bathochromic shifts in the phosphorescence emission upon

35 the former demonstrated significantly larger bathochromic shifts in UV-vis spectroscopy that parallel

36 ts long-range delocalization, as measured by bathochromic shifts in UV/vis spectra.

37 protonation was observed, wherein an initial bathochromic shift is followed by a hypsochromic one wit

38 Largest bathochromic shifts most often occurred in pH 6; while l

39 both of which prevent the typically observed bathochromic shift observed upon transitioning PEs from

40 rizontal lineO) at the 8-position produces a bathochromic shift of all absorption bands and makes alp

41 HR-LBP, this protein exhibited a significant bathochromic shift of approximately 90 nm in association

42 iments, significant induced CD signals and a bathochromic shift of fluorescence emission for the achi

43 this structural feature causes a significant bathochromic shift of lambdamax to higher wavelength.

44 gation in the dyads results in a significant bathochromic shift of longest-wavelength (Qy-like) band,

45 eciable lowering of the oxidation potential, bathochromic shift of the absorption band, and minimizat

46 wering of the energy gap, which leads to the bathochromic shift of the absorption spectrum.

47 spectrum for the P(V)-seleno compounds and a bathochromic shift of the NH absorption in the infrared

48 A bathochromic shift of the nuCO stretching vibration was

49 31mer(-14Cys)X/BChl](n) are accompanied by a bathochromic shift of the Q(y) absorption of the BChl-a

50 bsorption spectroscopy reveals a concomitant bathochromic shift of the surface plasmon resonance band

51 mide cyclic rings demonstrated a significant bathochromic shift of their Q bands in their electronic

52 These new materials display a characteristic bathochromic shift of their visible absorption and emiss

53 osition on ice grains, exhibited unequivocal bathochromic shifts of 10-15 nm of the absorption maxima

54 nitroaniline and N,N-dimethyl-4-nitroaniline bathochromic shifts of 51.3 and 62.0 nm, respectively, w

55 Bathochromic shifts of absorption spectra ( approximatel

56 the series varied from 1.5 to 4.5 A, causing bathochromic shifts of both the absorption and fluoresce

57 changes in the C(**)N ligands, which lead to bathochromic shifts of the free ligands, lead to similar

58 -withdrawing groups display more significant bathochromic shifts of the Soret bands.

59 This paper reports large bathochromic shifts of up to 260 meV in both the exciton

60 at is supported by optical spectroscopy with bathochromic shifts of up to 8-10 nm per ferrocene unit.

61 Thionated NDIs exhibit bathochromic shifts of up to approximately 100 nm in loc

62 by using amino groups as auxochromes to give bathochromic shifts of wavelengths.

63 The ultraviolet spectrum showed a large bathochromic shift on ionization (lambda(max) 244 --> 28

64 Generally, bathochromic shifts on anthocyanins were greatest with m

65 , the emission of which undergoes sequential bathochromic shifts over an increasing concentration gra

66 pectrum of each compound shows a significant bathochromic shift relative to that of the corresponding

67 57 nm, while at 70 K, the pigment exhibits a bathochromic shift to 403 nm with distinct vibronic stru

68 Planarization of 1 results in bathochromic shift to the near-IR region, greater spin d

69 r phenanthrene generally only produces minor bathochromic shifts to this diagnostic absorption band.

70 ith those of the oligomers revealed dramatic bathochromic shifts upon chain elongation, thus suggesti

71 By contrast, the bathochromic shifts upon inhibitor binding seen for acry

72 Bathochromic shifts were observed for both absorbance (u