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1 )cellulose was functionalized with Brooker's merocyanine.
2 the cyanine family whereas rhodols belong to merocyanines.
3 is isomerization of the thiocarbocyanine dye Merocyanine 540 (MC540), were first analyzed by fluoresc
4                                              Merocyanine 540 (MC540)-mediated photodynamic action is
5 w cytometry analysis using dual stainings of merocyanine 540 and Hoechst 33342.
6 luorescence spectroscopy were used to assess merocyanine 540 emission, laurdan generalized polarizati
7                      First, intercalation of merocyanine 540 into the membrane was improved, suggesti
8  that the development of oligonucleotide and merocyanine 540 permeability in differentiated granular
9             In contrast, the fluorescence of merocyanine 540, a probe sensitive to lipid packing, was
10                                              Merocyanine 540, a probe whose fluorescence is sensitive
11 ential scanning calorimetry, fluorescence of merocyanine 540, fluorescence polarization of 1,6-diphen
12 eriments with phenylhydrazine, KCl, quinine, merocyanine 540, the calpain inhibitor E-64d, and the sc
13 totic cells with altered membrane potential, merocyanine 540, was found elevated in the cytoplasm of
14 , a novel multifunctional nanoagent based on Merocyanine 540-coupled Gd(2) (WO(4) )(3) :Tb nanoscinti
15 mation between spiropyran (a ring-close) and merocyanine (a ring-open) states, simple exposure of the
16  null and wild-type littermates, but agents (merocyanine and annexin) that measure phospholipid packi
17 ore stacks is obtained upon self-assembly of merocyanine and bis(merocyanine) dyes in nonpolar solven
18  easily performed using protonated sulfonato-merocyanine and chitosan based molecular and macromolecu
19 h orthogonal optical control of the colorful merocyanine and colorless spiro states of the NitroBIPS
20 rate modified photoisomerization kinetics of merocyanine and diarylethene by coupling the reactant's
21  interconversions that includes H-aggregated merocyanine and its light-triggered disaggregation under
22 ethenes effectively bridge the properties of merocyanines and diarylethenes.
23 h are a colorless spiropyran, a purple trans-merocyanine, and its yellow-green protonated form.
24 anine state and lipophilicity (ClogP) of the merocyanine architecture, making this class of dyes a si
25 lowered transmembrane diffusion rates of the merocyanine-containing redox carriers.
26 y toward a red-shifted environment-sensitive merocyanine derivative, termed sI-Pht.
27  we have studied excited state dynamics of a merocyanine dye known as HB194, which has shown commenda
28 pyran mechanophore that produces a permanent merocyanine dye upon mechanochemical activation, in cont
29 -red (650-700 nm) to near-infrared flavylium merocyanine dyes and demonstrate that, unlike convention
30                                              Merocyanine dyes are a versatile class of donor-acceptor
31                                              Merocyanine dyes are of great interest amongst researche
32                     A series of nine dipolar merocyanine dyes has been studied as organic semiconduct
33 ticles of 40-400 nm diameter with spiropyran-merocyanine dyes incorporated into their hydrophobic cav
34                                              Merocyanine dyes that convert to spiropyran moieties upo
35                           We report here new merocyanine dyes that make possible the quantitation of
36  Trapping with boron trifluoride renders the merocyanine dyes thermally persistent and reveals appare
37 o-/naphthopyrans into highly colored anionic merocyanine dyes with high molar absorptivities to permi
38     Phenothiazinyl rhodanylidene acetic acid merocyanine dyes with variable substitution pattern on t
39 king the dipolar chromophores within the bis(merocyanine) dyes allows one to direct the dipole-dipole
40 ed upon self-assembly of merocyanine and bis(merocyanine) dyes in nonpolar solvents.
41                                          The merocyanine efficiently quenched the fluorescence of PFB
42 ternal stimuli that influence the spiropyran-merocyanine equilibrium.
43                                          The merocyanine-equipped COFs are extremely stable and posse
44 ogen in the closed spiropyran (4.8) and open merocyanine form (6.8) leads to a reversible proton rele
45 l surface-bound spiropyran to its protonated merocyanine form (MEH+).
46  near-UV region results in ring opening to a merocyanine form (P-Sp(o)) that absorbs at 600 nm.
47 itching off the light yields the deactivated merocyanine form and a creep-resistant polymer network.
48 nt reversible photoswitching behavior to its merocyanine form in the solid state in response to UV/Vi
49 citation of the zinc porphyrin moiety in the merocyanine form of the dyad yields 1PZn-Sp(o).
50        Under visible light illumination, the merocyanine form reverts to the original spiropyran geom
51         UV-induced isomerization to the open merocyanine form shuts down the FRET process by efficien
52 mal isomerization of spiropyran to its open, merocyanine form, and exposure to visible light triggers
53 ility of the photoswitch, the acidity of the merocyanine form, the thermal equilibrium position betwe
54 verted spiropyran into its visible-absorbing merocyanine form.
55 olored, photoluminescent, and mesogenic at a merocyanine form.
56 orescent character in most environments, the merocyanine forms of the encapsulated dyes are highly fl
57  of UV light to switch between the spiro and merocyanine forms, with locking and unlocking of each st
58 ng solution-phase ultrasonication, permanent merocyanine generation is also achieved in solid polymer
59 f fluorescence quenching of 1ZnTPPS4- by the merocyanine group and lowered transmembrane diffusion ra
60  research on the structure and properties of merocyanines in different media is reviewed in the conte
61 licated by either the established spiropyran-merocyanine interconversion model or hydrolysis.
62 rreversibility of the mechanically generated merocyanine is due to a unique reaction in which the sci
63                       Zwitterionic sulfonato-merocyanine is employed as a light-induced amphiphile to
64 ound that the lifetimes of the transient cis-merocyanine isomers ranged from 30 to 550 ns.
65 rium position between the spiropyran and the merocyanine isomers, and the increased acidity under vis
66 xamine isomerization between the two product merocyanine isomers, as well as their ring-closure react
67  reveals the cis-trans photoisomerization of merocyanine isomers.
68      Under neutral conditions, the open-ring merocyanine (MC(-)) exists to 48% and closes quantitativ
69 ble conformational change of spiropyran (SP)-merocyanine (MC) covalently attached to gold triangular
70                                              Merocyanine (MC) dyes containing an aromatic donor vinyl
71 ring spiropyran (SP) moiety to the open-ring merocyanine (MC) form caused the quantum yield to decrea
72 radiation, the SP was isomerized to the open merocyanine (MC) form, causing the fluid viscosity to de
73 rmation of H-type pi-pi interactions between merocyanine (MC) isomers within the sterically crowded e
74 coupled to a light-sensitive spiropyran (SP)/merocyanine (MC) motif was synthesized and characterized
75 Here we report a synthetic protocol toward a merocyanine (MC) pentamer 1 which represents the first m
76 less spiro (SP) state and a brightly colored merocyanine (MC) state.
77 optical switching between the spiro (SP) and merocyanine (MC) states of different photochromes specif
78 ons between their spiro (SP) and fluorescent merocyanine (MC) states.
79  the photoinduced conversion, as well as the merocyanine-metal ion (MC-M(2+)) interaction.
80 ps by singlet-singlet energy transfer to the merocyanine moiety to give PZn-1Sp(o).
81 e shuttling motion, from the viologen to the merocyanine moiety.
82 erves to convert the SP to the corresponding merocyanine (MR) form.
83 e (MC) pentamer 1 which represents the first merocyanine oligomer longer than a dimer.
84                                              Merocyanines, owing to their readily tunable electronic
85                       This work introduces a merocyanine photoacid for precise and reversible spatiot
86  a sensing membrane consisting of a modified merocyanine photoacid polymer and a calcium ionophore in
87 issipative assemblies built from DNA using a merocyanine photoacid that responds to visible light.
88 ct the change in pH obtained for any related merocyanine photoacid.
89 d by physicochemical changes of a spiropyran-merocyanine photochromic dyad, while drug quantification
90 or experiments, photoswitching of spiropyran/merocyanine photoswitches is decelerated in a cavity.
91                 We introduce a series of new merocyanine photoswitches, which deliver reversible bulk
92 and TTT cis-trans isomers, for the open-ring merocyanine product, and discover a strong solvent polar
93 haracter on going from SP to the ring-opened merocyanine product.
94 ative distribution of two distinctly colored merocyanine products is altered predictably with differe
95              The transient phenolate form of merocyanine promotes rapid Z-to-E isomerization of the T
96 -opening reaction of spiropyran to a colored merocyanine provides a useful method by which to image t
97                                              Merocyanine's behavior was more complex.
98 e photochromic fluorescent system spiropyran-merocyanine (SP <--> MC) interacting with gold nanoparti
99 d addition induces guest transformation to a merocyanine species activating a second recognition site
100 ransformation of naphthopyran into a colored merocyanine species in polymeric materials is achieved u
101 ts in ring opening to form the corresponding merocyanine species.
102 t and complete conversion of the hydrophilic merocyanine speciesto the hydrophobic spiropyran form, w
103                                  Because the merocyanine-spirooxazine is an unusual reverse photochro
104 longer-wavelength irradiation of an attached merocyanine-spirooxazine reverse photochromic moiety hav
105                      Our results showed that merocyanine states, with a larger dipole moment, interac
106                               While modified merocyanine switching can be explained by changes in rad
107 itio calculations, the ability of spiropyran/merocyanine systems to selectively detect alkali, alkali
108 rsion from the closed spiropyran to the open merocyanine takes 1.6 ps whereas the reversed photoreact
109                 One of them is a photoactive merocyanine that switches to a spiropyran, releasing a p
110 eir pyranylidene analogues, and, unlike most merocyanines, the degree of charge transfer does not dec
111 -determining step involving the formation of merocyanine-the ring-opened form of spiropyran.
112                                          For merocyanines, these regularities have been explored for
113 nd reveals a B-hydroxy ketone that locks the merocyanine through an intramolecular H-bonding interact
114  the phototriggered reversible spiropyran to merocyanine transition in the cross-linking layer is key
115 ted with the probes, optically induced spiro-merocyanine transition positively shifted nonlinear capa
116  transfer from the pyrene chromophore to the merocyanine unit leads to an increased rate of ring clos
117 obes used (bis-pyrene, nystatin, prodan, and merocyanine) were chosen because they differ in the loca
118 le force-sensitive isomerization of STP to a merocyanine, which reacts rapidly with activated C=C bon
119  for comprehension of the variable nature of merocyanines, with the main emphasis on understanding th

 
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