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1                            Compounds 2-4 are photoluminescent.
2                        In this study we used photoluminescent 11-mercaptoundecanoic acid-bound gold n
3  biosensing platform operates with different photoluminescent agents and different analytes.
4 d the DNA binding resulted in changes to the photoluminescent and absorption properties of the C-dots
5                                         Both photoluminescent and electroluminescent emission from th
6                  In this form, compound 1 is photoluminescent and exhibits a broad emission band with
7 s is synthesized, which is pale-colored, non-photoluminescent and non-mesogenic at a spiro form, but
8 cessfully applied to the preparation of both photoluminescent and non-photoluminescent micro Quick Re
9  of hundreds of nm) is demonstrated for both photoluminescent and non-photoluminescent polymers by ca
10     CitraBoneQMg provides sustained release, photoluminescent and photoacoustic imaging capabilities,
11 roteins) in a single step for converting the photoluminescent and superparamagnetic Janus nanoparticl
12                    The silicon replicas were photoluminescent, and exhibited rapid changes in impedan
13 ures, structural phase transitions, optical, photoluminescent, and magnetic properties of these compo
14 mesogenic at a spiro form, but dark-colored, photoluminescent, and mesogenic at a merocyanine form.
15 that utilizes sandwich hybridization between photoluminescent anionic conjugated polyelectrolyte (CPE
16       No known iron complexes are considered photoluminescent at room temperature, and their rapid ex
17                        Within 10 cycles, red photoluminescent AuNCs@ew with maximum emission waveleng
18                        Zr((Me)PDP)2 exhibits photoluminescent behavior and its excited state can be q
19                       A new series of highly photoluminescent benzobis(imidazolium) salts with tunabl
20 graphene oxide-coated microplates (GOMs) and photoluminescent bioprobes (PLBs).
21                                    Design of photoluminescent bis-heterocycles, aided by density func
22 ng the structure-properties relationships of photoluminescent Carbon dots (C-dots).
23 isted method was used to prepare small-sized photoluminescent carbon dots (CDs) from Chocolate Brown
24                                              Photoluminescent carbon nanoparticles, carbon dots (CDs)
25                                              Photoluminescent carbon nanoparticles, or carbon dots, a
26 or ethyl acetate (1d), demonstrate different photoluminescent characteristics.
27  carbon atoms, are capable of housing stable photoluminescent colour centres, namely the silicon vaca
28 d the relatively long distance between these photoluminescent complexes and the GO-coated surface.
29 d to the identification of an efficient blue photoluminescent composite material, Gd3Ga5O12/SiO2.
30                                              Photoluminescent compounds can undergo various structura
31                                         Four photoluminescent dye crystals, TPB-n (n = 1-3) and TPCH,
32                                              Photoluminescent emission spectra of the layered double
33  was measured by angle-dependent p-polarized photoluminescent emission spectroscopy.
34 buted to electronic transitions, scattering, photoluminescent emission, and Raman scattering in a dis
35 bination was in excess of that stored in the photoluminescent excited state.
36 QD and polymer has potential applications as photoluminescent fibers or films.
37 ove 425 degrees C are critical for realizing photoluminescent GaAs quantum dots, which emphasizes the
38                     The advantage offered by photoluminescent imaging with Gd2O3:Eu(3+) nanorods is t
39                          This complex is not photoluminescent in aqueous solution nor in the presence
40 es are monodisperse, colloidally stable, and photoluminescent in aqueous solution.
41           The resulting complexes are highly photoluminescent in the blue region due to triplet-tripl
42 ly the polymers presented herein become more photoluminescent, in the thin film, under continuous irr
43                                 As such, the photoluminescent intensity of the phosphors increased by
44 w describes recent progress in the design of photoluminescent intensity-independent optical probes fo
45                           For these strongly photoluminescent ions, accumulation of some femto- to pi
46 ns for the rational design of more effective photoluminescent lanthanide complexes are discussed.
47 in near-infrared dual emission with extended photoluminescent lifetime.
48 most fundamental and important properties of photoluminescent materials and eventually determines the
49  heterogeneous catalysis and as magnetic and photoluminescent materials capable of both metal- and li
50                           Stimuli-responsive photoluminescent materials have attracted considerable a
51 tration), leads to four distinct families of photoluminescent materials in which the emissive signal
52 corporation of polyhedral boranes into novel photoluminescent materials is an area with increasing in
53                           Developing organic photoluminescent materials with high emission efficienci
54                                              Photoluminescent materials, that are now ubiquitous in o
55 limiting the rational design of well-defined photoluminescent materials.
56 ocks for polyfunctional heterocycles, and in photoluminescent materials.
57 n establish them as an important category of photoluminescent materials.
58  boosting the performance and versatility of photoluminescent materials.
59 omethylphenyl))borate, in toluene produces a photoluminescent, metal-to-ligand charge-transfer (MLCT)
60 preparation of both photoluminescent and non-photoluminescent micro Quick Response (muQR) codes using
61           This work shows a highly efficient photoluminescent Mn-based halide and offers a strategy f
62           Therefore, this new mode of highly photoluminescent MOF materials is studied for the first
63                                              Photoluminescent molecular crystals integrated with the
64                                              Photoluminescent molecules are widely used for real-time
65 approach for the production of biocompatible photoluminescent nanocrystal probes.
66  A novel white light-promoted reaction using photoluminescent nanocrystalline silicon enables the hyd
67 birefringent nanostructures, and emission of photoluminescent nanomaterials and molecules.
68 cking but also show that highly photostable, photoluminescent nanoprobes of 10 nm size can be employe
69 al method to relate the optical density of a photoluminescent nanotube sample to the number of indivi
70                                              Photoluminescent nitrogen-doped carbon nanodots (N-doped
71 ng approach favorably compares with strictly photoluminescent or electrochemical techniques and appea
72         With intrinsically ultra-stretchable photoluminescent organogels, flexible phosphorous layers
73 (reduction of Os(bpy)3(3+) by analyte to the photoluminescent Os(bpy)3(2+)) in a CTR.
74 /or charges an integrated battery, and (iii) photoluminescent packaging, where ambient light activate
75                                       A L-Al Photoluminescent Paper-based Platform (L-Al(3xP)) with a
76                It has been demonstrated that photoluminescent Pdots provide selective nuclear translo
77 n nanoliposome/zero-valent iron nanoparticle/photoluminescent pigment).
78  robust narrow-band green luminophore with a photoluminescent (PL) efficiency up to 93%.
79                                        Local photoluminescent (PL) images obtained with an immersion
80 passivated Lewis basic sites to preserve the photoluminescent (PL) properties of the NCs.
81                                              Photoluminescent (PL) spectra of synthetic diamond powde
82 agent mimic diethyl chlorophosphate (DCP) in photoluminescent (PL) spectroscopic channels.
83 xemplified by the synthesis of intrinsically photoluminescent polylactones that enable non-invasive m
84 study was to develop aliphatic biodegradable photoluminescent polymers (BPLPs) and their associated c
85 monstrated for both photoluminescent and non-photoluminescent polymers by capillarity-driven solvent
86 s, resins, insulators, optical coatings, and photoluminescent polymers.
87                           When intrinsically photoluminescent porous Si films or nanoparticles are us
88                                              Photoluminescent porous silicon (PSi) was produced by Pt
89 usually long emission lifetime (5-13 mus) of photoluminescent porous silicon nanoparticles can allow
90 is study presents photolytically stable, NIR photoluminescent, porous silicon nanoparticles with a re
91                                              Photoluminescent, porous silicon pixel arrays were fabri
92                                          The photoluminescent potential of 1,5-benzodiazepin-2-ones,
93 t of effort has been devoted to the study of photoluminescent probes in combination with time-resolve
94 s (PLNPs) offer advantages over conventional photoluminescent probes, including the potential for enh
95 om approximately 540 to 900 nm, the ERE is a photoluminescent process associated with a wide variety
96 hip between void fraction and the structure, photoluminescent properties and humidity stability was e
97 ogeneous thin films of [5]HeliCOFs disclosed photoluminescent properties arising from the controlled
98 le, facilitating dynamic modulation of their photoluminescent properties in response to environmental
99 gnificant attention due to their exceptional photoluminescent properties in solution and solid state.
100 of the pyrimidine ring allowed tuning of the photoluminescent properties of the alpha-amino acids.
101 nship between dielectric confinement and the photoluminescent properties of tin iodide perovskite nan
102     The film retains the photoconductive and photoluminescent properties of ZnO QDs and is applied to
103 erve as edible photonic biomaterials and the photoluminescent properties provide parametric support o
104 regation of the complexes leads to different photoluminescent properties that allow visualization of
105 se one-dimensional metal wire compounds have photoluminescent properties that are tunable by changing
106 iameter congruent with 2-3 nm) which display photoluminescent properties that can be tuned by changin
107 d possibilities for tailoring and optimizing photoluminescent properties, as demonstrated by these sc
108 olid nonconjugated molecules exhibit curious photoluminescent properties, which can be attributed to
109 L-Al) that were characterized, demonstrating photoluminescent properties.
110 ap, and it will be possible to control their photoluminescent properties.
111  (PNA) conjugate with diverse morphology and photoluminescent properties.
112 shown that copper NCs (CuNCs) possess unique photoluminescent properties.
113 of (dis)assembly due to their characteristic photoluminescent properties.
114  CsPbX(3) , X = Cl, Br, or I, have excellent photoluminescent properties: high quantum yield, tunable
115 on the size and superior photo-properties of photoluminescent quantum dots (Qdots).
116                        The compounds exhibit photoluminescent quantum efficiencies up to 100% in flui
117 onstrate an inverse relationship between the photoluminescent quantum yield and V in 0-D VDPDs.
118  Most notably, the compound with the highest photoluminescent quantum yield in this series showed an
119 uted to high ambipolar charge mobilities and photoluminescent quantum yield.
120 o control the exciton relaxation pathway and photoluminescent quantum yield.
121                                              Photoluminescent quantum yields (Phi) for the 10 compoun
122  the furan-phenylene-furan core possess high photoluminescent quantum yields in solution (83-98%), wh
123   In addition, they show extremely different photoluminescent quantum yields in solution and in the s
124                                          The photoluminescent response of BHN towards various biogeni
125 how modified inorganic layer band gaps and a photoluminescent reversed type I nanoheterostructure wit
126 orm a comprehensive analysis of the prepared photoluminescent scaffolds, (13)C cross-polarization mag
127 omoted hydrosilylation reaction is unique to photoluminescent silicon, and does not function on nonem
128 n/Ab-QDs will not be quenched, whereas those photoluminescent sites directly exposed are expected to
129 nd they dissolve in polar solvent to produce photoluminescent solutions.
130  a striking red-shift of up to 100 nm in the photoluminescent spectra, a highly unusual and visually
131 ining time-resolved transient absorption and photoluminescent spectroscopic methods.
132                           Two series of new, photoluminescent star-shaped discotic liquid crystals, r
133 e 'reservoir' that thermally repopulates the photoluminescent state of CdSe through endothermic rever
134  dominant energy transfer mechanism in these photoluminescent systems.
135               Despite remarkable advances in photoluminescent temperature indicators, existing optica
136 siently formed five-coordinate MLCT state is photoluminescent under the condition studied, indicating
137                             We report here a photoluminescent uranium organic framework, whose photol
138       During the development of immunosensor photoluminescent ZnO nanorods (ZnO-NRs) were deposited o

 
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