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1 rrelate well with Kosower Z values (based on solvatochromism).
2 bility, and sensitivity to solvent polarity (solvatochromism).
3 mechanical displacement, interferometry, and solvatochromism.
4 hat causes a large Stokes shift and positive solvatochromism.
5 nce in polar aprotic solvents accompanied by solvatochromism.
6 ighly fluorescent with a pronounced emission solvatochromism.
7 action effects with respect to quenching and solvatochromism.
8 henolates 3a-d, which revealed a reversal in solvatochromism.
9 rity sensors with a strong positive emission solvatochromism.
10 high quantum yields, and strong fluorescence solvatochromism.
11 narrow and asymmetric and exhibits only weak solvatochromism.
12 ionally, all chromophores exhibited positive solvatochromism.
13 luorescence, large Stokes shifts, and strong solvatochromism.
14 nor and acceptor groups, which show positive solvatochromism.
15 h quantum yields in non-aqueous solvents and solvatochromism.
16 their nonlinear optical (NLO) properties and solvatochromism.
17 sensing tool by coupling it with vibrational solvatochromism.
18 ramolecular charge separation and pronounced solvatochromism.
19 easing solvent polarity and exhibit positive solvatochromism.
20 Stokes shift, high quantum yield, and strong solvatochromism.
21   Additionally, the promising compounds show solvatochromism and acidochromic effects.
22  results in the observed correlation between solvatochromism and an increase of fluorescence intensit
23  this series of molecules, a more pronounced solvatochromism and clear chiroptical behaviors are obse
24                                              Solvatochromism and concentration-dependent emissions of
25 za-7-benzofuran-2'-deoxyxanthosine disclosed solvatochromism and enhanced fluorescence when the pH or
26                                              Solvatochromism and NMR chemical shift studies of 1 and
27 r and -CF(3) substitution displaying notable solvatochromism and polarity-enhanced emission (PEE).
28 thenes, the metastable isomers show negative solvatochromism and red-shifted absorption in apolar sol
29 st fluorogenic alpha-amino acid demonstrated solvatochromism and sensitivity to pH.
30 generation dendrimers (G2 and G3) to exhibit solvatochromism and thermochromism, while their oligomer
31 alibrated by vibrational Stark spectroscopy, solvatochromism, and MD simulations.
32 ) forms, solution-state kinetic experiments, solvatochromism, and NMR studies.
33 ivative exhibit a large Stokes shift, strong solvatochromism, and quantum yield values up to 0.47; th
34      Photophysical properties (fluorescence, solvatochromism, and quantum yields) of azide-alkyne cli
35      Photophysical properties (fluorescence, solvatochromism, and quantum yields) of the new 8-aza-7-
36 nine forms, in conjunction with computation, solvatochromism, and solution NMR studies, we have inves
37 ingly, the compounds exhibited excited-state solvatochromism attributable to the structural reorganiz
38 ion band to shorter wavelengths) to inverted solvatochromism, characterized by the transition from ne
39 nt polarity, leading to substantial negative solvatochromism (Deltalambda approximately 10(2) nm) and
40 hange in the spectral behavior from negative solvatochromism (displacement of the absorption band to
41  by the transition from negative to positive solvatochromism (displacement of the absorption band to
42                    All complexes show strong solvatochromism due to the large dipole moment of the gr
43 avior of the dyes, transforming the negative solvatochromism exhibited by the shorter analogs into a
44 thora of spectral properties, such as strong solvatochromism, high polarizability and hyperpolarizabi
45                             By exploring the solvatochromism in a series of solvents, the conditions
46 uraldehyde) that possesses a strong positive solvatochromism in emission of 119 nm from toluene to me
47 vative 3a is preferred because of its strong solvatochromism in fluorescence where a mechanism of inc
48 s a deep purple solid that exhibits positive solvatochromism in solution.
49  found inadequate for reproducing the strong solvatochromism in the absorption spectra.
50                       All the dyes displayed solvatochromism in the emission spectra characteristic o
51 ne-containing derivatives displayed positive solvatochromism in the fluorescence spectra indicating a
52 ately 1 for the pure acceptors), and notable solvatochromism in the fluorescence suggests emission fr
53  interesting fluorophores that show positive solvatochromism in the range from 404 nm (toluene) to 54
54 s, as well as a remarkable positive emission solvatochromism, indicating charge-transfer character in
55                                       Strong solvatochromism is also displayed.
56 ansfer (CT) excited states, but the emission solvatochromism is not more pronounced.
57 hat the transition from negative to inverted solvatochromism is the result of an enhanced sensitivity
58 -BF2 and p-HOPyDI:Zn (excited state pK(a)'s, solvatochromism, kinetics, and thermodynamics of proton
59                           Differences in the solvatochromism of [Rc(CH)(3)Rc](+) and [Fc(CH)(3)Fc](+)
60  by the measurement of a single probe (e.g., solvatochromism of an iron coordination complex).
61                                          The solvatochromism of each dye was studied in 28 organic so
62  HRS data in methanol show that the stronger solvatochromism of the Fe(II) complexes causes their NLO
63                                              Solvatochromism of the fluorescence spectra confirms thi
64 udies, based on site-directed mutagenesis or solvatochromism of the isolated chromophore, have conclu
65  use of the unexpectedly strong fluorescence solvatochromism of this aromatic hydrocarbon, the validi
66 was controlled by exposure to solvent vapor (solvatochromism) or temperature change (thermochromism),
67                                     Negative solvatochromism, pai-pai interactions, C(sp(2))-H...O hy
68 s, including emission wavelength tunability, solvatochromism, red-edge excitation, chemical stability
69 ng photophysical properties such as negative solvatochromism, solidstate, and aggregation-induced emi
70  series of optical spectroscopy experiments, solvatochromism studies, density functional theory (DFT)
71 c character in the PMC form, as found in the solvatochromism studies.
72                         This strong emission solvatochromism suggests the formation of an intramolecu
73                                     It shows solvatochromism that is similar to five other PRODAN der
74 nearly mirror-like and characterized by weak solvatochromism; the marked hypsochromic shifts are obse
75                  On the basis of chromophore solvatochromism, these results are consistent with a les
76 ispersion interactions control excited-state solvatochromism through two distinct mechanisms.
77 xpanded beyond the theory of their color and solvatochromism toward their electronic structure in the
78  deltaomega(0)(t) is a dynamic analog of the solvatochromism used in interpreting solvent effects on
79 is and fluorescence spectroscopy, as well as solvatochromism, were studied for selected derivatives a
80 und that all compounds exhibit a reversal in solvatochromism, which is interpreted in terms of the ab
81 (2)(4+).(Cl(-))(2).(I(-))(2) show a negative solvatochromism, while their UV-vis acid-base titration