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1 oupling sites, PYF-T-o exhibits stronger and bathochromic absorption to achieve better photon harvest
2            These porphyrins displayed highly bathochromic and broadened absorbance profiles spanning
3 highest using tannic acid; also,the greatest bathochromic and hyperchromic effects were reasonable fo
4 highest using tannic acid; also,the greatest bathochromic and hyperchromic effects were reasonable fo
5  under the influence of pressure, leading to bathochromic and hyperchromic shifts of their UV-vis abs
6            In all pH, anthocyanins exhibited bathochromic and hyperchromic shifts.
7 cal has a distinct spectrum with significant bathochromic and hypsochromic shifts relative to the rem
8 tabilities of anthocyanins, hyperchromic and bathochromic effects in SNs containing all co-pigment so
9                                     The most bathochromic electronic transition of the chromophores e
10 orter the N-cation bond, and the greater the bathochromic emission shift.
11                                          The bathochromic emission shifts due to intramolecular charg
12 he energy difference between the initial and bathochromic intermediates and the normalized difference
13 Photolysis of VCOP-D108A at 70 K generates a bathochromic photostationary state (lambdamax = 380 nm).
14 ome this, we generated variants of RLuc with bathochromic (red) shifts of up to 66 nm (547 nm peak) t
15 nzochlorin analogues exhibited a significant bathochromic shift ( approximately 10 nm) in the electro
16 duced strong hyperchromic (0.26-0.55 nm) and bathochromic shift (6.6-14.2 nm).
17 nd gap (DeltaE = 2.723-2.659 eV) with larger bathochromic shift (lambda(max) = 554.218-543.261 nm in
18 angements, energy storage, and origin of the bathochromic shift accompanying the transformation of rh
19  of a pyrrole hydrogen-bond donor leads to a bathochromic shift allowing for quantitative bidirection
20 M3Q was monitored by UV spectroscopy a 22-nm bathochromic shift and 75% hypochromicity of the porphin
21 red by two ammonium substituents, inducing a bathochromic shift and a significant increase in quantum
22  while absorption and emission data showed a bathochromic shift and increase in quantum efficiency.
23 llent solvatochromic properties with a large bathochromic shift by varying the solvent polarities.
24 ) value (for methanol, this corresponds to a bathochromic shift from 543 to 732 nm).
25 f the fused porphyrins undergo a progressive bathochromic shift in a series of naphthyl (lambda(max)
26 bsorption and fluorescence changes, namely a bathochromic shift in absorption and fluorescence quench
27 on reaction was accompanied by a substantial bathochromic shift in both the absorption and emission s
28 r organic versus inorganic layers leads to a bathochromic shift in emission peak wavelength, a decrea
29  binding leads to either a hypsochromic or a bathochromic shift in emission via interaction of the me
30 ption spectrum of the complex showed a 32-nm bathochromic shift in lambdamax with minor peaks at 460
31  bond was found to give rise to only a 20 nm bathochromic shift in the absorbance and fluorescence sp
32 sful activation strategy would necessitate a bathochromic shift in the absorbance profile, an increas
33 acetyl, 7-formyl) progressively causes (1) a bathochromic shift in the absorption maximum of the B ba
34               The aryl substituents caused a bathochromic shift in the absorption spectra of up to 52
35 hene-bridged bisborole (14) exhibits a large bathochromic shift in the absorption spectrum, demonstra
36 ia click chemistry resulted in a significant bathochromic shift in the fluorescence excitation (15 nm
37 n with a model MsrA (E. coli), it exhibits a bathochromic shift in the fluorescence maximum.
38                       We observe an ~240 meV bathochromic shift in the lowest energy absorption peak
39 is provides a molecular basis to explain the bathochromic shift in the maximal absorbance wavelength
40 t addition of small amounts of HMPA causes a bathochromic shift in the spectrum of 1-Li.
41 pical characteristics of amyloids, such as a bathochromic shift in the wavelength of maximum absorpti
42 pical characteristics of amyloids, such as a bathochromic shift in the wavelength of maximum absorpti
43 mpounds through para-substitution leads to a bathochromic shift in their activation wavelength.
44 d pai-extended porphyrins displayed a modest bathochromic shift in their electronic absorption and em
45 ancing absorption and inducing a significant bathochromic shift into the NIR I and II regions.
46 protonation was observed, wherein an initial bathochromic shift is followed by a hypsochromic one wit
47        On the other hand, an unusually large bathochromic shift is observed in CT band upon addition
48 both of which prevent the typically observed bathochromic shift observed upon transitioning PEs from
49  highly sensitive to solvent polarity with a bathochromic shift of 115 nm on changing from THF to pho
50  color NPs to reddish-yellow with associated bathochromic shift of absorption peak when pesticide int
51 rizontal lineO) at the 8-position produces a bathochromic shift of all absorption bands and makes alp
52 HR-LBP, this protein exhibited a significant bathochromic shift of approximately 90 nm in association
53 iments, significant induced CD signals and a bathochromic shift of fluorescence emission for the achi
54 this structural feature causes a significant bathochromic shift of lambdamax to higher wavelength.
55 gation in the dyads results in a significant bathochromic shift of longest-wavelength (Qy-like) band,
56 eciable lowering of the oxidation potential, bathochromic shift of the absorption band, and minimizat
57 e motors result in improved solubility and a bathochromic shift of the absorption maxima.
58 wering of the energy gap, which leads to the bathochromic shift of the absorption spectrum.
59                     Especially, gBBB shows a bathochromic shift of the electronic spectra upon bindin
60 m colourless to yellowish green along with a bathochromic shift of the emission peak.
61 spectrum for the P(V)-seleno compounds and a bathochromic shift of the NH absorption in the infrared
62                                            A bathochromic shift of the nuCO stretching vibration was
63 oleate capping ligands for NHCs results in a bathochromic shift of the optical band gap of CdSe QDs (
64 31mer(-14Cys)X/BChl](n) are accompanied by a bathochromic shift of the Q(y) absorption of the BChl-a
65 groups not only induces significant emission bathochromic shift of the resultant MOFs, but also endow
66 bsorption spectroscopy reveals a concomitant bathochromic shift of the surface plasmon resonance band
67 ions at room temperature showed a systematic bathochromic shift of the UV-vis absorption and emission
68 mide cyclic rings demonstrated a significant bathochromic shift of their Q bands in their electronic
69 These new materials display a characteristic bathochromic shift of their visible absorption and emiss
70   The ICT was observed in both series by the bathochromic shift on increasing the polarity of the sol
71      The ultraviolet spectrum showed a large bathochromic shift on ionization (lambda(max) 244 --> 28
72 pectrum of each compound shows a significant bathochromic shift relative to that of the corresponding
73 57 nm, while at 70 K, the pigment exhibits a bathochromic shift to 403 nm with distinct vibronic stru
74                Planarization of 1 results in bathochromic shift to the near-IR region, greater spin d
75  We leverage the fact that SCR-1 undergoes a bathochromic shift when aggregated for in vivo studies b
76 assembles into nanofibers, affording another bathochromic shift with an absorption maximum at 1095 nm
77 hydroxyl group, which also leads to emission bathochromic shift, increased Stokes shift, enhanced pho
78 ce (including increased oscillator strength, bathochromic shift, reduced linewidth and lifetime) at r
79  acid coordinates to the enone and induces a bathochromic shift, which allows for selective excitatio
80 eractions that are critical for the atypical bathochromic shift.
81 tone, hyperchromic effect, and a significant bathochromic shift.
82 to those in Bk1 and Cf1 and show substantial bathochromic shifting of several 5f -> 5f transitions.
83 to the 3-4 or 4-5 site instantly resulted in bathochromic shifting of the n n* transition bands, and
84 to the 3-4 or 4-5 site instantly resulted in bathochromic shifting of the pai -> pai* transition band
85                                   There were bathochromic shifts (81-105 nm) from pH 1 to 8 and hypso
86 nce of a fused anthracene unit induced minor bathochromic shifts and did not significantly affect the
87 anin color while trivalent metal ions caused bathochromic shifts and hue changes.
88                                      Highest bathochromic shifts and most intense blue colours were o
89 ion or blue shift of the SubPz Q-band, while bathochromic shifts are always observed for the emission
90  (pai,pai* electronic transitions) displayed bathochromic shifts as the solvent polarity is increased
91 rms' protonation results in hypsochromic and bathochromic shifts consistent with the preferential sta
92                       The extensions lead to bathochromic shifts in absorption and fluorescence while
93  distinct color change in solution and large bathochromic shifts in absorption bands with an absorpti
94                    Protonation induces large bathochromic shifts in absorption of up to 500 nm, with
95 ng aryl substituent, consequently results in bathochromic shifts in both absorption and emission.
96 nt changes in Stokes shift, as well as large bathochromic shifts in both excitation maximum (from 521
97        Herein, we show that pressure-induced bathochromic shifts in both fluorescence emission and UV
98                      Coproporphyrin exhibits bathochromic shifts in both the Soret and visible absorp
99 Flavone copigments produced hyperchromic and bathochromic shifts in both.
100 henylcycloheptatriene (Ph(7)C(7)H), displays bathochromic shifts in its absorption and emission spect
101  polycyclic aromatic hydrocarbons show large bathochromic shifts in the absorption and emission relat
102 wering of the band gap and the corresponding bathochromic shifts in the absorption and emission spect
103 ed dithia-bis(calix)-sapphyrins showed large bathochromic shifts in the absorption bands, indicating
104 d the substituents, as demonstrated by large bathochromic shifts in the absorption spectra as well as
105           These substituents result in large bathochromic shifts in the chrysene absorption and emiss
106                                  Significant bathochromic shifts in the electronic spectra, witnessed
107 ed molecular orbital) energies and engenders bathochromic shifts in the emission.
108 nomenon manifested by either hypsochromic or bathochromic shifts in the fluorescence lambda max.
109  shifts of the free ligands, lead to similar bathochromic shifts in the Ir complexes of the same liga
110                                              Bathochromic shifts in the phosphorescence emission upon
111 rity in the excited state, displaying >50 nm bathochromic shifts in the photoluminescence spectra.
112                             They also showed bathochromic shifts in the visible region in chloroform
113 the former demonstrated significantly larger bathochromic shifts in UV-vis spectroscopy that parallel
114 ts long-range delocalization, as measured by bathochromic shifts in UV/vis spectra.
115                                      Largest bathochromic shifts most often occurred in pH 6; while l
116 The DFT studies also support the significant bathochromic shifts observed for protonated dithia-bis(c
117 osition on ice grains, exhibited unequivocal bathochromic shifts of 10-15 nm of the absorption maxima
118 nitroaniline and N,N-dimethyl-4-nitroaniline bathochromic shifts of 51.3 and 62.0 nm, respectively, w
119 ole carbons of triphyrin(2.1.1) resulting in bathochromic shifts of absorption bands relative to trip
120                                              Bathochromic shifts of absorption spectra ( approximatel
121 the series varied from 1.5 to 4.5 A, causing bathochromic shifts of both the absorption and fluoresce
122 changes in the C(**)N ligands, which lead to bathochromic shifts of the free ligands, lead to similar
123 toelectronic properties of the compounds and bathochromic shifts of the longest wavelength absorption
124 -withdrawing groups display more significant bathochromic shifts of the Soret bands.
125 ols, 3-hydroxyflavothiones, show substantial bathochromic shifts of their absorption maxima and enhan
126                                          The bathochromic shifts of these dyes are driven by the exte
127                     This paper reports large bathochromic shifts of up to 260 meV in both the exciton
128 at is supported by optical spectroscopy with bathochromic shifts of up to 8-10 nm per ferrocene unit.
129                       Thionated NDIs exhibit bathochromic shifts of up to approximately 100 nm in loc
130 by using amino groups as auxochromes to give bathochromic shifts of wavelengths.
131                                   Generally, bathochromic shifts on anthocyanins were greatest with m
132 , the emission of which undergoes sequential bathochromic shifts over an increasing concentration gra
133 nd identified several examples with stronger bathochromic shifts than the dfdc azobenzene lead struct
134 r phenanthrene generally only produces minor bathochromic shifts to this diagnostic absorption band.
135 ith those of the oligomers revealed dramatic bathochromic shifts upon chain elongation, thus suggesti
136 spectra displayed pronounced hypochromic and bathochromic shifts upon DNA titration, indicating stron
137                             By contrast, the bathochromic shifts upon inhibitor binding seen for acry
138                                              Bathochromic shifts were observed for both absorbance (u
139 ron-deficiency and LUMO energies of -4.8 eV, bathochromic shifts, and a strong intensity increase of
140              Patterns were similar regarding bathochromic shifts.
141 rry exerted significantly greater hyper- and bathochromic spectral shifts than their acylated counter

 
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