ライフサイエンスコーパス: phosphorescent

1 The mechanism for energetic coupling between phosphorescent and fluorescent molecular species is a lo

2 This is possible if the material is phosphorescent, and high efficiencies have been observed

3 nce recovery after photobleaching (FRAP) and phosphorescent anisotropy studies suggested that Fcepsil

4 The PAOs are phosphorescent at ambient temperature in solution and in

5 Heavy metal complexes that are phosphorescent at room temperature are becoming increasi

6 thalimides have violet-blue fluorescence and phosphorescent bands between 550 and 650 nm (visible at

7 series of rationally designed butterfly-like phosphorescent binuclear platinum complexes that undergo

8 is an efficient quencher of emission of many phosphorescent compounds, thus oxygen concentration coul

9 is not important for the platinum acetylide phosphorescent conjugated polyelectrolyte.

10 ) capture and channel excitation energy to a phosphorescent core (metalloporphyrin) via intramolecula

11 Phosphorescent cyclometalated iridium tris(2-phenylpyrid

12 The phosphorescent detection allows avoiding the interferenc

13 creased power efficiency compared to a fully phosphorescent device.

14 Two phosphorescent dinuclear iridium(III) diastereomers (Lam

15 nic solvents, making them very attractive as phosphorescent dopant emitters for solution-processable

16 blue fluorescent molecule in exchange for a phosphorescent dopant, in combination with green and red

17 nds gave good glassy films when doped with a phosphorescent dopant, only the niBr films remained glas

18 repared with green, yellow, and red emissive phosphorescent dopants (Irppy, btIr, and btpIr, respecti

19 n synthesized, characterized, and applied as phosphorescent dopants in the fabrication of solution-pr

20 nnel nearly all of the triplet energy to the phosphorescent dopants, retaining the singlet energy exc

21 al dynamics, we labeled actin at C374 with a phosphorescent dye and performed TPA experiments.

22 on the microsecond rotational dynamics of a phosphorescent dye attached to C374 on actin, as detecte

23 A depot of the phosphorescent dye Pd-uroporphyrin was injected into the

24 bilizing Pt(II) octaethylporphine (PtOEP), a phosphorescent dye readily quenched by molecular oxygen,

25 by measuring the excited-state lifetime of a phosphorescent dye.

26 Measuring excited-state lifetime of phosphorescent dyes in the anterior chamber provides a u

27 Because Pt and Pd porphyrin-based phosphorescent dyes, traditionally used as phosphors in

28 and the subsequent measurement of serotonin phosphorescent emission from the solid surface.

29 tem crossing and subsequent switching to the phosphorescent emission of blue light.

30 than a 200-fold increase in the photoexcited phosphorescent emission of PtOEP (2,3,7,8,12,13,17,18-oc

31 n bands in the visible region and strong red phosphorescent emission ranging from 611 to 651 nm, with

32 demonstrated using a doped NaCl film with a phosphorescent emitter as the emissive layer.

33 (PtN3N) is developed as an efficient, stable phosphorescent emitter.

34 ely new class of earth abundant, inexpensive phosphorescent emitters based on metal-halide nanocluste

35 emitting diodes, providing a new platform of phosphorescent emitters for low-cost and high-performanc

36 The use of blue phosphorescent emitters in organic light-emitting diodes

37 avenue for designing efficient Ir(III)-based phosphorescent emitters.

38 ions provide insight about the nature of the phosphorescent emitting states, which involves a strong

39 a model of the photophysics to decompose the phosphorescent enhancement into contributions from incre

40 containing an even dispersion of the pendant phosphorescent fragments.

41 Brightly phosphorescent gold-based metallopolymers have been synt

42 Thin film phosphorescent green OLEDs fabricated on plastic substra

43 By employing a light out-coupling structure, phosphorescent green organic light-emitting diodes exhib

44 H(2))(8)- chain between the polymer host and phosphorescent guest is thus an important design princip

45 ctivated delayed fluorescence(TADF) host and phosphorescent guests were fabricated using solution pro

46 Inclusion of highly phosphorescent heavy-metal organic complexes as dopants

47 metalated onto an iridium core to form three phosphorescent heteroleptic molecules, (bppo)2Ir(acac),

48 The oxygen sensor nanoparticles consist of phosphorescent indicator dye embedded in poly(styrene-bl

49 rgy transfer between bonded systems of a red phosphorescent iridium complex 13 and a conjugated polym

50 f the back transfer of triplets from the red phosphorescent iridium complex to the polyfluorene backb

51 Red-emitting phosphorescent iridium complexes based on the [Ir(btp)(2

52 tudy, ruthenium(II) luminophores are used as phosphorescent lifetime imaging microscopy (PLIM) probes

53 This method takes advantage of the long phosphorescent lifetime of terbium chelates, a property

54 n this study, we extend our previous work on phosphorescent, low molecular weight platinum(II) comple

55 ve, near-infrared emitting and water-soluble phosphorescent macromolecular probe can not only report

56 Metal-free organic phosphorescent materials are attractive alternatives to

57 Inorganic phosphorescent materials exhibiting persistent luminesce

58 se-change materials can transform widespread phosphorescent materials into high-speed optical sources

59 Developing metal-free organic phosphorescent materials is promising but challenging be

60 he decay process of typical fluorescence and phosphorescent materials with a recombination lifetime f

61 numerous possibilities for the synthesis of phosphorescent materials, with emission colours over the

62 The replacement of phosphorescent metal complexes with inexpensive organic

63 rate electroluminescence from earth-abundant phosphorescent metal halide nanoclusters.

64 usion-controlled luminescence quenching of a phosphorescent metal-organic framework built from the Ru

65 iameter were loaded into stable, porous, and phosphorescent metal-organic frameworks (MOFs 1 and 2) b

66 requency phase modulation of tissue-embedded phosphorescent microprobes.

67 (Ni4 P2 ) into two highly stable and porous phosphorescent MOFs.

68 00 per cent internal quantum efficiency: the phosphorescent molecules harness the triplet excitons th

69 For the phosphorescent molecules, the electron spins are localiz

70 The phosphorescent nanoparticles exhibit strong phosphoresce

71 matrixes for making bright and monodispersed phosphorescent nanoparticles.

72 o-photon microscopy method, based on a novel phosphorescent nanoprobe, to image tissue oxygenation in

73 ed imaging system with a two-photon-enhanced phosphorescent nanoprobe.

74 In contrast, phosphorescent OLEDs (PHOLEDs) can emit light from tripl

75 (eta(P,max) = 118 lm W(-1) ) ITO-free green phosphorescent OLEDs (PHOLEDs) with multilayered, highly

76 h of the academic and commercial pursuits in phosphorescent OLEDs have been dominated by Ir(III) comp

77 king (EBL) and hole-blocking layers (HBL) in phosphorescent OLEDs is explored.

78 8-naphthalimide derivatives were examined in phosphorescent organic light emitting diodes (OLEDs), i.

79 s chemistry, principally due to their use in phosphorescent organic light-emitting devices (OLEDs).

80 and high efficiencies have been observed in phosphorescent organic light-emitting devices.

81 A non-doped phosphorescent organic light-emitting diode (PhOLED) bas

82 Phosphorescent organic light-emitting diodes (OLEDs) are

83 high brightness and deep blue emission from phosphorescent organic light-emitting diodes (PHOLED) is

84 years ago, the operational lifetime of blue phosphorescent organic light-emitting diodes (PHOLEDs) h

85 2.9 candela per ampere, similar to the CE of phosphorescent organic light-emitting diodes, with two m

86 lyzed by the MOFs using UV-vis spectroscopy, phosphorescent oxygen detection, and gas chromatographic

87 sing platform based on diamine oxidase and a phosphorescent oxygen nanosensor.

88 Discrete solid-state phosphorescent oxygen sensors produced by local solvent-

89 of mitochondrial oxygen consumption using a phosphorescent oxygen-sensitive probe, standard microtit

90 The cross-linked phosphorescent particles using halogen-containing copoly

91 n the square plane) were strongly orange-red phosphorescent (Phi = 0.2-0.3) in a room-temperature oxy

92 structure and the optical properties of the phosphorescent platinum compounds: Pt(II) (2-(4',6'-difl

93 n between singlet and triplet is observed in phosphorescent platinum octaethylporphyrin (PtOEP), on a

94 A butterfly-like phosphorescent platinum(II) binuclear complex can underg

95 ies of Ir(III) corroles differ from those of phosphorescent porphyrin complexes, cyclometalated and p

96 Both sensors rely on near infrared (NIR) phosphorescent porphyrin dyes, wherefore the signals can

97 The changes in actin were reported by (a) a phosphorescent probe (ErIA) attached to Cys 374 and (b)

98 Actin was labeled with a phosphorescent probe at C374, and the myosin head (S1) w

99 KA), we have covalently bound the long-lived phosphorescent probe erythrosin isothiocyanate (Er-ITC)

100 The so far developed two-photon-enhanced phosphorescent probes comprise antenna-core constructs,

101 on absorption cross-sections of conventional phosphorescent probes.

102 photon (2P) absorption properties of several phosphorescent Pt (II) porphyrins, focusing on the effec

103 s in cultures of adherent cells, using three phosphorescent Pt-porphyrin based probes with different

104 Considered to be practically non-phosphorescent, purely organic compounds (metal-free) ar

105 -halogenated, non-carbonyl analogue, ambient phosphorescent quantum yields reach 55%.

106 Hemoprotein-based scaffolds containing phosphorescent ruthenium(II) CO mesoporphyrin IX (RuMP)

107 t this deficiency can be overcome by using a phosphorescent sensitizer to excite a fluorescent dye.

108 A phosphorescent sensor based on a multichromophoric iridi

109 gnetic particle, elicits a rapid, long-lived phosphorescent signal.

110 a PEDOT:PSS HIL/HTL, and solution-processed, phosphorescent, small-molecule, green OLEDs with maximum

111 Cu interactions that are strengthened in the phosphorescent state.

112 ion energy for exchange in proteins having a phosphorescent Trp and, for example, for studying the ef

113 ibit external quantum efficiency >60%, while phosphorescent white organic light-emitting diodes exhib

114 We report the development of a new class of phosphorescent zwitterionic bis(heteroleptic) Ir(III) co