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1 e the research impact of ECL studies for any luminophore.
2 e intramolecular motions of the incorporated luminophore.
3 one thermally activated delayed fluorescence luminophore.
4 ength than the singlet emission from the ECL luminophore.
5 er of magnitude higher than that of the free luminophore.
6 PrA) as a coreactant and Ru(bpy)(3)(2+) as a luminophore.
7  simplifies the synthesis of known dioxetane luminophores.
8 of yet unexplored dioxetane chemiluminescent luminophores.
9 as precursors for dioxetane chemiluminescent luminophores.
10 ment of chemiluminescence in the presence of luminophores.
11 g patterned ion gels containing redox-active luminophores.
12 d for the development of boron-doped organic luminophores.
13 recursors, Lewis acid catalysts, and certain luminophores.
14 solar cells in thin matrix layers doped with luminophores.
15 ferins that were predicted to be red-shifted luminophores.
16 y as well as analytes of interest and common luminophores.
17 le can, thus, be associated with photostable luminophores.
18 es have not yet been considered as effective luminophores.
19 phobic and/or hydrophilic stimuli-responsive luminophores.
20 norganic (upconversion nanoparticles, UCNPs) luminophores.
21 o complement well-known isoelectronic Pt(II) luminophores.
22 + 3 (composed of hexacyclen 1, nanoswitch 2, luminophore 3) was treated with 2-cyano-2-phenylpropanoi
23 ica nanobeads doped with a ruthenium-complex luminophore and functionalized with antihuman CD3, antih
24 en = 4,7-diphenyl-1,10-phenanthroline) asthe luminophore and polystyrene, poly(trimethylsilylmethyl m
25 t on overlap in the emission spectrum of the luminophore and the absorption spectra of acceptors, sug
26 dyl)-ruthenium(II) ([Ru(bpy)(3)](2+)) as the luminophore and tri-n-propylamine (TPrA) as the co-react
27 carbon particles using [Ru(bpy)3](2+) as the luminophore and tripropylamine as the coreactant, at an
28 ven to be a useful tool to construct organic luminophores and a deuterated trisubstituted alkene.
29 phobic polycyclic aromatic hydrocarbon (PAH) luminophores and boron dipyrromethene (BODIPY).
30            Substituting precious elements in luminophores and photocatalysts by abundant first-row tr
31 ant in the greater contexts of designing new luminophores and photosensitizers for use in red-light-d
32 e chelate ligands constitute a new family of luminophores and photosensitizers, which is complementar
33 chemiluminescence beyond classical molecular luminophores and toward dynamic, structure-responsive ma
34 nt of the salt acts as the photoactive unit (luminophore) and its nonemissive counterion is selected
35 roles as redox mediators, battery materials, luminophores, and photoredox catalysts.
36        Importantly, the quantum yield of the luminophores approaches that of the higher quantum yield
37                          Adamantyl-dioxetane luminophores are an important class of chemiluminescent
38                                        These luminophores are based on resonance energy transfer (RET
39                             Chemiluminescent luminophores are considered as one of the most sensitive
40                                        These luminophores are covalently linked pairs with a long-lif
41                                          The luminophores are doped inside the nanoparticles, and the
42                                              Luminophores are frequently utilized probe labels for de
43                  Even although the very same luminophores are known to sensitize intermolecularly the
44           Aggregation-induced emitting (AIE) luminophores are sensitive and easy-to-handle types of p
45         In this initial study, ruthenium(II) luminophores are used as phosphorescent lifetime imaging
46                                          The luminophores are well-protected from the environmental o
47  These findings establish stimuli-responsive luminophores as a groundbreaking class of ECL labels, pr
48 ed by the formation of an adduct between the luminophore - at the ground state - and the quencher.
49 ht-emission pathway of phenoxy-1,2-dioxetane luminophores attracts growing interest within the scient
50             Thus, we can envisage the use of luminophores based on more abundant transition metal com
51 mission maxima and decay time of such tandem luminophores can be readily adjusted by selection of the
52            The local environment surrounding luminophores can significantly influence their photophys
53 tituted styryl- and bistyryl-2,2'-bipyridine luminophores (compounds 16-23) have been synthesized via
54                    A series of novel Ir(III) luminophores containing pendant pyridyl moieties that al
55 block used in the self-assembly process, the luminophore-containing building block adopts a highly tw
56 The immunosensor incorporating the cleavable luminophore demonstrated a 40% lower detection limit and
57 s represent rare examples of monoboron-doped luminophores displaying deep-red-to-NIR emission.
58  The antibody was first immobilized onto the luminophore-doped nanoparticle through silica chemistry
59       The advantages of using small, uniform luminophore-doped nanoparticles are discussed.
60   The conjugation method is based on uniform luminophore-doped silica (LDS) nanoparticles (63 +/- 4 n
61 issive species is formed from the bpy-BODIPY luminophores during the annihilation process.
62 ibria could be improved significantly if the luminophore emission is shifted toward the near-infrared
63 lightly red-shifted with respect to the main luminophore emission; a possible explanation for this ph
64 ruthenium(II) ([Ru(bpy)(3)](2+)) is a common luminophore for photoluminescence and electrochemilumine
65 isible upconversion mechanism with optimized luminophore geometries and fabrication designs.
66       Here, we report that a single cationic luminophore gives rise to either monomer, dimer, excimer
67 the much more sensitive chemically initiated luminophores have been limited.
68 mparable quantum efficiency of 13% to strong luminophores in aqueous media, suggested a mechanism tha
69 f the most prominent and extensively studied luminophores in ECL studies, only H(2)O(2) has been wide
70  via click chemistry that could be potential luminophores in metal complexes.
71 eneration of light from electrically excited luminophores in sample droplets.
72 ally those based on photostable metalorganic luminophores, in biochemical analysis and biomolecular i
73  originate from the asymmetric [MnCl(6)](4-) luminophores induced by N-H...Cl hydrogen bonding with R
74 NIR Nd((4)F(3/2) -> (4)I(J)) emission of the luminophore is amplified and linearly correlated with th
75 IR-II emission, the PL performance of NIR-II luminophores is largely limited by nonradiative processe
76 tally alter the electronic properties of the luminophore itself.
77 oncept/strategy is not limited to a specific luminophore or a co-reactant and is thus generalizable.
78 ed on the investigation of materials, either luminophores or coreactants, while fundamental mechanist
79                         Multiple fluorescent luminophores, or fluorophores, can be readily distinguis
80 nitrospiropyrans, the transition to covalent luminophore-photochrome assemblies tends to promote degr
81 ransformations occur upon irradiation of the luminophore-photochrome assemblies.
82                                      Two new luminophore polymorphs of 4-bromo-7-(4-nonylphenyl)benzo
83     Herein we describe a new class of hybrid luminophore probes that emit light of distinct wavelengt
84 using the mechanical bond to refine existing luminophores, providing a new avenue for emitter optimiz
85 ECL signal generation on the nanoscale using luminophore-reporter-modified DNA-based nanoswitches (i.
86 esults demonstrate that de-excitation of the luminophore results in a complex cascade of photoinduced
87 oreactants for the ECL emission of different luminophores ([Ru(bpy)3](2+) at lambda = 620 nm and lumi
88 articles (Si NP) functionalized with the ECL luminophore [Ru(bpy)(2)PICH(2)](2+)], and IgG labelled G
89 i(f) measurements, which are for transparent luminophore solutions commonly done relative to a refere
90 uthenium(II) tris(bipyridine) (Ru(bpy)3(2+)) luminophore species, which showed a half-wave potential
91                                  When an ECL luminophore, such as rubrene, is added to the emulsion d
92 molecules with optically stable metalorganic luminophores, such as tris(2,2'-bipyridyl)dichlororuthen
93                     Moreover, when a blended luminophore system containing a 60:40 mixture of Ru(bpy)
94         We describe a new approach to making luminophores that display long emission wavelengths, lon
95  H to Me and Ph, we have yielded a series of luminophores that exhibit poor-to-excellent performance,
96    A palladium porphyrin was used as a model luminophore to quantitatively evaluate the algorithm in
97 ganically modified silicates) doped with the luminophore tris(4,7'-diphenyl-1,10'-phenanthroline) rut
98 Ru(bpy)3Cl2 (relative to [EMI][TFSI]) as the luminophore turned on at an AC peak-to-peak voltage as l
99 thod for accelerating the discovery of ionic luminophores using combinatorial techniques is reported.
100 n sp(3) linker, six TPA-based AIE-active RTP luminophores were obtained.
101 ar emitters featuring dynamic propeller-like luminophores were prepared in one step from cyclic(alkyl
102 cribe an approach to creating a new class of luminophores which display both long wavelength emission
103 uorescence of the built-in binding sensitive luminophores which served as a sensor for affinity deter
104  the pyridyl groups, in contrast to the free luminophore, which involves the diphenyl sulfone moiety.
105  (MeQn(+)) as a permanently charged cationic luminophore, which we pair with a series of monovalent a
106 on constitute a new class of blue and NIR-II luminophores, which complement the classical established
107 tly developed technology of chemiluminescent luminophores, which emit light under physiological condi
108    Here, we report two naphthalene-based RTP luminophores whose phosphorescence emission is enabled b
109 ticipate that our strategy for obtaining NIR luminophores will open new doors for further exploration
110 s, giving rise to a robust narrow-band green luminophore with a photoluminescent (PL) efficiency up t
111 nsemble consisting of a double ion-selective luminophore with two distinct receptor sites, hexacyclen
112 he development of the first chemiluminescent luminophores with a direct mode of NIR light emission th
113                               Masking of the luminophores with analyte-responsive groups has resulted
114  manner, we designed and synthesized two new luminophores with direct light emission wavelength in th
115 tramolecular proton transfer (ESIPT) organic luminophores with excitation wavelength-dependent color
116 is observation may help design new pCp-based luminophores with finely tuned photophysical properties.
117  Difluoroboron B-diketonates are a family of luminophores with high quantum yields and tunable fluore
118                                              Luminophores with long-wavelength emission and long life
119    Due to their high signal-to-noise ratios, luminophores with near-infrared (NIR) emission are parti
120                                              Luminophores with these useful spectral properties can a
121             Here, we report on a new Ir(III) luminophore, with an unusually high triplet energy near
122                         The sequestration of luminophores within supramolecular polyhedral compartmen
123 he blue light excites the analyte-responsive luminophores within the CRSA.

 
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