ライフサイエンスコーパス: luminophore

1 ength than the singlet emission from the ECL luminophore.

2 g patterned ion gels containing redox-active luminophores.

3 d for the development of boron-doped organic luminophores.

4 recursors, Lewis acid catalysts, and certain luminophores.

5 ment of chemiluminescence in the presence of luminophores.

6 solar cells in thin matrix layers doped with luminophores.

7 le can, thus, be associated with photostable luminophores.

8 ica nanobeads doped with a ruthenium-complex luminophore and functionalized with antihuman CD3, antih

9 en = 4,7-diphenyl-1,10-phenanthroline) asthe luminophore and polystyrene, poly(trimethylsilylmethyl m

10 t on overlap in the emission spectrum of the luminophore and the absorption spectra of acceptors, sug

11 carbon particles using [Ru(bpy)3](2+) as the luminophore and tripropylamine as the coreactant, at an

12 phobic polycyclic aromatic hydrocarbon (PAH) luminophores and boron dipyrromethene (BODIPY).

13 Importantly, the quantum yield of the luminophores approaches that of the higher quantum yield

14 These luminophores are based on resonance energy transfer (RET

15 Chemiluminescent luminophores are considered as one of the most sensitive

16 These luminophores are covalently linked pairs with a long-lif

17 The luminophores are doped inside the nanoparticles, and the

18 Luminophores are frequently utilized probe labels for de

19 Even although the very same luminophores are known to sensitize intermolecularly the

20 In this initial study, ruthenium(II) luminophores are used as phosphorescent lifetime imaging

21 The luminophores are well-protected from the environmental o

22 mission maxima and decay time of such tandem luminophores can be readily adjusted by selection of the

23 tituted styryl- and bistyryl-2,2'-bipyridine luminophores (compounds 16-23) have been synthesized via

24 A series of novel Ir(III) luminophores containing pendant pyridyl moieties that al

25 The antibody was first immobilized onto the luminophore-doped nanoparticle through silica chemistry

26 The advantages of using small, uniform luminophore-doped nanoparticles are discussed.

27 The conjugation method is based on uniform luminophore-doped silica (LDS) nanoparticles (63 +/- 4 n

28 issive species is formed from the bpy-BODIPY luminophores during the annihilation process.

29 lightly red-shifted with respect to the main luminophore emission; a possible explanation for this ph

30 the much more sensitive chemically initiated luminophores have been limited.

31 via click chemistry that could be potential luminophores in metal complexes.

32 eneration of light from electrically excited luminophores in sample droplets.

33 ally those based on photostable metalorganic luminophores, in biochemical analysis and biomolecular i

34 tally alter the electronic properties of the luminophore itself.

35 Multiple fluorescent luminophores, or fluorophores, can be readily distinguis

36 nitrospiropyrans, the transition to covalent luminophore-photochrome assemblies tends to promote degr

37 ransformations occur upon irradiation of the luminophore-photochrome assemblies.

38 Herein we describe a new class of hybrid luminophore probes that emit light of distinct wavelengt

39 esults demonstrate that de-excitation of the luminophore results in a complex cascade of photoinduced

40 oreactants for the ECL emission of different luminophores ([Ru(bpy)3](2+) at lambda = 620 nm and lumi

41 articles (Si NP) functionalized with the ECL luminophore [Ru(bpy)(2)PICH(2)](2+)], and IgG labelled G

42 uthenium(II) tris(bipyridine) (Ru(bpy)3(2+)) luminophore species, which showed a half-wave potential

43 When an ECL luminophore, such as rubrene, is added to the emulsion d

44 molecules with optically stable metalorganic luminophores, such as tris(2,2'-bipyridyl)dichlororuthen

45 Moreover, when a blended luminophore system containing a 60:40 mixture of Ru(bpy)

46 We describe a new approach to making luminophores that display long emission wavelengths, lon

47 A palladium porphyrin was used as a model luminophore to quantitatively evaluate the algorithm in

48 ganically modified silicates) doped with the luminophore tris(4,7'-diphenyl-1,10'-phenanthroline) rut

49 Ru(bpy)3Cl2 (relative to [EMI][TFSI]) as the luminophore turned on at an AC peak-to-peak voltage as l

50 thod for accelerating the discovery of ionic luminophores using combinatorial techniques is reported.

51 cribe an approach to creating a new class of luminophores which display both long wavelength emission

52 ticipate that our strategy for obtaining NIR luminophores will open new doors for further exploration

53 he development of the first chemiluminescent luminophores with a direct mode of NIR light emission th

54 Masking of the luminophores with analyte-responsive groups has resulted

55 manner, we designed and synthesized two new luminophores with direct light emission wavelength in th

56 Luminophores with long-wavelength emission and long life

57 Due to their high signal-to-noise ratios, luminophores with near-infrared (NIR) emission are parti

58 Luminophores with these useful spectral properties can a

59 The sequestration of luminophores within supramolecular polyhedral compartmen

60 he blue light excites the analyte-responsive luminophores within the CRSA.