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1 tone, hyperchromic effect, and a significant bathochromic shift.
2 eractions that are critical for the atypical bathochromic shift.
3 Patterns were similar regarding bathochromic shifts.
6 angements, energy storage, and origin of the bathochromic shift accompanying the transformation of rh
7 of a pyrrole hydrogen-bond donor leads to a bathochromic shift allowing for quantitative bidirection
8 M3Q was monitored by UV spectroscopy a 22-nm bathochromic shift and 75% hypochromicity of the porphin
9 red by two ammonium substituents, inducing a bathochromic shift and a significant increase in quantum
10 while absorption and emission data showed a bathochromic shift and increase in quantum efficiency.
11 nce of a fused anthracene unit induced minor bathochromic shifts and did not significantly affect the
14 ron-deficiency and LUMO energies of -4.8 eV, bathochromic shifts, and a strong intensity increase of
15 nzochlorin analogues exhibited a significant bathochromic shift ( approximately 10 nm) in the electro
16 ion or blue shift of the SubPz Q-band, while bathochromic shifts are always observed for the emission
17 (pai,pai* electronic transitions) displayed bathochromic shifts as the solvent polarity is increased
18 llent solvatochromic properties with a large bathochromic shift by varying the solvent polarities.
19 rms' protonation results in hypsochromic and bathochromic shifts consistent with the preferential sta
21 f the fused porphyrins undergo a progressive bathochromic shift in a series of naphthyl (lambda(max)
22 bsorption and fluorescence changes, namely a bathochromic shift in absorption and fluorescence quench
23 on reaction was accompanied by a substantial bathochromic shift in both the absorption and emission s
24 r organic versus inorganic layers leads to a bathochromic shift in emission peak wavelength, a decrea
25 binding leads to either a hypsochromic or a bathochromic shift in emission via interaction of the me
26 ption spectrum of the complex showed a 32-nm bathochromic shift in lambdamax with minor peaks at 460
27 bond was found to give rise to only a 20 nm bathochromic shift in the absorbance and fluorescence sp
28 sful activation strategy would necessitate a bathochromic shift in the absorbance profile, an increas
29 acetyl, 7-formyl) progressively causes (1) a bathochromic shift in the absorption maximum of the B ba
31 hene-bridged bisborole (14) exhibits a large bathochromic shift in the absorption spectrum, demonstra
32 ia click chemistry resulted in a significant bathochromic shift in the fluorescence excitation (15 nm
35 is provides a molecular basis to explain the bathochromic shift in the maximal absorbance wavelength
37 pical characteristics of amyloids, such as a bathochromic shift in the wavelength of maximum absorpti
38 pical characteristics of amyloids, such as a bathochromic shift in the wavelength of maximum absorpti
40 d pai-extended porphyrins displayed a modest bathochromic shift in their electronic absorption and em
42 distinct color change in solution and large bathochromic shifts in absorption bands with an absorpti
44 ng aryl substituent, consequently results in bathochromic shifts in both absorption and emission.
45 nt changes in Stokes shift, as well as large bathochromic shifts in both excitation maximum (from 521
49 henylcycloheptatriene (Ph(7)C(7)H), displays bathochromic shifts in its absorption and emission spect
50 polycyclic aromatic hydrocarbons show large bathochromic shifts in the absorption and emission relat
51 wering of the band gap and the corresponding bathochromic shifts in the absorption and emission spect
52 ed dithia-bis(calix)-sapphyrins showed large bathochromic shifts in the absorption bands, indicating
53 d the substituents, as demonstrated by large bathochromic shifts in the absorption spectra as well as
58 shifts of the free ligands, lead to similar bathochromic shifts in the Ir complexes of the same liga
60 rity in the excited state, displaying >50 nm bathochromic shifts in the photoluminescence spectra.
62 the former demonstrated significantly larger bathochromic shifts in UV-vis spectroscopy that parallel
64 hydroxyl group, which also leads to emission bathochromic shift, increased Stokes shift, enhanced pho
66 protonation was observed, wherein an initial bathochromic shift is followed by a hypsochromic one wit
68 nd gap (DeltaE = 2.723-2.659 eV) with larger bathochromic shift (lambda(max) = 554.218-543.261 nm in
70 both of which prevent the typically observed bathochromic shift observed upon transitioning PEs from
71 The DFT studies also support the significant bathochromic shifts observed for protonated dithia-bis(c
72 highly sensitive to solvent polarity with a bathochromic shift of 115 nm on changing from THF to pho
73 color NPs to reddish-yellow with associated bathochromic shift of absorption peak when pesticide int
74 rizontal lineO) at the 8-position produces a bathochromic shift of all absorption bands and makes alp
75 HR-LBP, this protein exhibited a significant bathochromic shift of approximately 90 nm in association
76 iments, significant induced CD signals and a bathochromic shift of fluorescence emission for the achi
77 this structural feature causes a significant bathochromic shift of lambdamax to higher wavelength.
78 gation in the dyads results in a significant bathochromic shift of longest-wavelength (Qy-like) band,
79 eciable lowering of the oxidation potential, bathochromic shift of the absorption band, and minimizat
84 spectrum for the P(V)-seleno compounds and a bathochromic shift of the NH absorption in the infrared
86 oleate capping ligands for NHCs results in a bathochromic shift of the optical band gap of CdSe QDs (
87 31mer(-14Cys)X/BChl](n) are accompanied by a bathochromic shift of the Q(y) absorption of the BChl-a
88 groups not only induces significant emission bathochromic shift of the resultant MOFs, but also endow
89 bsorption spectroscopy reveals a concomitant bathochromic shift of the surface plasmon resonance band
90 ions at room temperature showed a systematic bathochromic shift of the UV-vis absorption and emission
91 mide cyclic rings demonstrated a significant bathochromic shift of their Q bands in their electronic
92 These new materials display a characteristic bathochromic shift of their visible absorption and emiss
93 to those in Bk1 and Cf1 and show substantial bathochromic shifting of several 5f -> 5f transitions.
94 to the 3-4 or 4-5 site instantly resulted in bathochromic shifting of the n n* transition bands, and
95 to the 3-4 or 4-5 site instantly resulted in bathochromic shifting of the pai -> pai* transition band
96 osition on ice grains, exhibited unequivocal bathochromic shifts of 10-15 nm of the absorption maxima
97 nitroaniline and N,N-dimethyl-4-nitroaniline bathochromic shifts of 51.3 and 62.0 nm, respectively, w
98 ole carbons of triphyrin(2.1.1) resulting in bathochromic shifts of absorption bands relative to trip
100 the series varied from 1.5 to 4.5 A, causing bathochromic shifts of both the absorption and fluoresce
101 changes in the C(**)N ligands, which lead to bathochromic shifts of the free ligands, lead to similar
102 toelectronic properties of the compounds and bathochromic shifts of the longest wavelength absorption
104 ols, 3-hydroxyflavothiones, show substantial bathochromic shifts of their absorption maxima and enhan
107 at is supported by optical spectroscopy with bathochromic shifts of up to 8-10 nm per ferrocene unit.
110 The ICT was observed in both series by the bathochromic shift on increasing the polarity of the sol
111 The ultraviolet spectrum showed a large bathochromic shift on ionization (lambda(max) 244 --> 28
113 , the emission of which undergoes sequential bathochromic shifts over an increasing concentration gra
114 ce (including increased oscillator strength, bathochromic shift, reduced linewidth and lifetime) at r
115 pectrum of each compound shows a significant bathochromic shift relative to that of the corresponding
116 nd identified several examples with stronger bathochromic shifts than the dfdc azobenzene lead struct
117 57 nm, while at 70 K, the pigment exhibits a bathochromic shift to 403 nm with distinct vibronic stru
119 r phenanthrene generally only produces minor bathochromic shifts to this diagnostic absorption band.
120 ith those of the oligomers revealed dramatic bathochromic shifts upon chain elongation, thus suggesti
121 spectra displayed pronounced hypochromic and bathochromic shifts upon DNA titration, indicating stron
124 We leverage the fact that SCR-1 undergoes a bathochromic shift when aggregated for in vivo studies b
125 acid coordinates to the enone and induces a bathochromic shift, which allows for selective excitatio
126 assembles into nanofibers, affording another bathochromic shift with an absorption maximum at 1095 nm