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1 Compounds 2-4 are photoluminescent.
3 d the DNA binding resulted in changes to the photoluminescent and absorption properties of the C-dots
6 cessfully applied to the preparation of both photoluminescent and non-photoluminescent micro Quick Re
7 of hundreds of nm) is demonstrated for both photoluminescent and non-photoluminescent polymers by ca
8 roteins) in a single step for converting the photoluminescent and superparamagnetic Janus nanoparticl
10 that utilizes sandwich hybridization between photoluminescent anionic conjugated polyelectrolyte (CPE
17 carbon atoms, are capable of housing stable photoluminescent colour centres, namely the silicon vaca
18 d to the identification of an efficient blue photoluminescent composite material, Gd3Ga5O12/SiO2.
21 buted to electronic transitions, scattering, photoluminescent emission, and Raman scattering in a dis
27 ly the polymers presented herein become more photoluminescent, in the thin film, under continuous irr
30 most fundamental and important properties of photoluminescent materials and eventually determines the
31 heterogeneous catalysis and as magnetic and photoluminescent materials capable of both metal- and li
32 corporation of polyhedral boranes into novel photoluminescent materials is an area with increasing in
35 omethylphenyl))borate, in toluene produces a photoluminescent, metal-to-ligand charge-transfer (MLCT)
36 preparation of both photoluminescent and non-photoluminescent micro Quick Response (muQR) codes using
39 A novel white light-promoted reaction using photoluminescent nanocrystalline silicon enables the hyd
40 cking but also show that highly photostable, photoluminescent nanoprobes of 10 nm size can be employe
41 al method to relate the optical density of a photoluminescent nanotube sample to the number of indivi
45 xemplified by the synthesis of intrinsically photoluminescent polylactones that enable non-invasive m
46 study was to develop aliphatic biodegradable photoluminescent polymers (BPLPs) and their associated c
47 monstrated for both photoluminescent and non-photoluminescent polymers by capillarity-driven solvent
51 usually long emission lifetime (5-13 mus) of photoluminescent porous silicon nanoparticles can allow
52 is study presents photolytically stable, NIR photoluminescent, porous silicon nanoparticles with a re
55 t of effort has been devoted to the study of photoluminescent probes in combination with time-resolve
56 s (PLNPs) offer advantages over conventional photoluminescent probes, including the potential for enh
57 om approximately 540 to 900 nm, the ERE is a photoluminescent process associated with a wide variety
58 The film retains the photoconductive and photoluminescent properties of ZnO QDs and is applied to
59 se one-dimensional metal wire compounds have photoluminescent properties that are tunable by changing
60 iameter congruent with 2-3 nm) which display photoluminescent properties that can be tuned by changin
61 d possibilities for tailoring and optimizing photoluminescent properties, as demonstrated by these sc
65 In addition, they show extremely different photoluminescent quantum yields in solution and in the s
66 orm a comprehensive analysis of the prepared photoluminescent scaffolds, (13)C cross-polarization mag
67 omoted hydrosilylation reaction is unique to photoluminescent silicon, and does not function on nonem
68 n/Ab-QDs will not be quenched, whereas those photoluminescent sites directly exposed are expected to
71 e 'reservoir' that thermally repopulates the photoluminescent state of CdSe through endothermic rever
72 siently formed five-coordinate MLCT state is photoluminescent under the condition studied, indicating
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