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1 The mechanism for energetic coupling between phosphorescent and fluorescent molecular species is a lo
2 We chemically depth profile and analyse blue phosphorescent and thermally-activated delayed fluoresce
3          This is possible if the material is phosphorescent, and high efficiencies have been observed
4 nce recovery after photobleaching (FRAP) and phosphorescent anisotropy studies suggested that Fcepsil
5                                 The PAOs are phosphorescent at ambient temperature in solution and in
6               Heavy metal complexes that are phosphorescent at room temperature are becoming increasi
7 thalimides have violet-blue fluorescence and phosphorescent bands between 550 and 650 nm (visible at
8 series of rationally designed butterfly-like phosphorescent binuclear platinum complexes that undergo
9 yer capitalizes on the highly photooxidizing phosphorescent [bis(1,10-phenanthroline)(1,4,5,8-tetraaz
10  thermally activated delayed fluorescent and phosphorescent blue organic light-emitting diodes is dem
11 roducing materials exhibiting time-dependent phosphorescent colors (TDPCs).
12                                 Platinum(II) phosphorescent complexes enable facile control of the mo
13 the quantum yields and lifetimes of the blue-phosphorescent complexes.
14 is an efficient quencher of emission of many phosphorescent compounds, thus oxygen concentration coul
15  is not important for the platinum acetylide phosphorescent conjugated polyelectrolyte.
16 tive use of P-, As-, and Sb-based ligands in phosphorescent coordination compounds is reported toward
17 ) capture and channel excitation energy to a phosphorescent core (metalloporphyrin) via intramolecula
18 n molecular organoboron compounds as well as phosphorescent crystalline materials, are not yet known.
19                                              Phosphorescent cyclometalated iridium tris(2-phenylpyrid
20 to the triplet excited state with subsequent phosphorescent decay.
21                                          The phosphorescent detection allows avoiding the interferenc
22 creased power efficiency compared to a fully phosphorescent device.
23                                          Two phosphorescent dinuclear iridium(III) diastereomers (Lam
24 nic solvents, making them very attractive as phosphorescent dopant emitters for solution-processable
25  blue fluorescent molecule in exchange for a phosphorescent dopant, in combination with green and red
26 nds gave good glassy films when doped with a phosphorescent dopant, only the niBr films remained glas
27 repared with green, yellow, and red emissive phosphorescent dopants (Irppy, btIr, and btpIr, respecti
28 n synthesized, characterized, and applied as phosphorescent dopants in the fabrication of solution-pr
29 nnel nearly all of the triplet energy to the phosphorescent dopants, retaining the singlet energy exc
30   The fibers serve as a polymer host for the phosphorescent dye and are shown to be non-cytotoxic.
31 al dynamics, we labeled actin at C374 with a phosphorescent dye and performed TPA experiments.
32  on the microsecond rotational dynamics of a phosphorescent dye attached to C374 on actin, as detecte
33                               A depot of the phosphorescent dye Pd-uroporphyrin was injected into the
34 bilizing Pt(II) octaethylporphine (PtOEP), a phosphorescent dye readily quenched by molecular oxygen,
35 by measuring the excited-state lifetime of a phosphorescent dye.
36 obtain nonwoven fiber meshes embedded with a phosphorescent dye.
37          Measuring excited-state lifetime of phosphorescent dyes in the anterior chamber provides a u
38            Because Pt and Pd porphyrin-based phosphorescent dyes, traditionally used as phosphors in
39 nvestigated pertaining to their fluorescent, phosphorescent, electrochemiluminescent, optoelectronic,
40 l challenging to obtain efficient and stable phosphorescent emission due to the intense quenching eff
41  and the subsequent measurement of serotonin phosphorescent emission from the solid surface.
42 tem crossing and subsequent switching to the phosphorescent emission of blue light.
43 than a 200-fold increase in the photoexcited phosphorescent emission of PtOEP (2,3,7,8,12,13,17,18-oc
44 n bands in the visible region and strong red phosphorescent emission ranging from 611 to 651 nm, with
45  demonstrated using a doped NaCl film with a phosphorescent emitter as the emissive layer.
46                          Using an archetypal phosphorescent emitter, we achieve a two-fold increase i
47 (PtN3N) is developed as an efficient, stable phosphorescent emitter.
48 ely new class of earth abundant, inexpensive phosphorescent emitters based on metal-halide nanocluste
49 cal properties of a new family of metal-free phosphorescent emitters based on phthalimide derivatives
50 emitting diodes, providing a new platform of phosphorescent emitters for low-cost and high-performanc
51                              The use of blue phosphorescent emitters in organic light-emitting diodes
52 attributed to the development of noble metal phosphorescent emitters that facilitated remarkable gain
53 ctive field of research as an alternative to phosphorescent emitters that usually use heavy metal ato
54 6) s(-1)) are comparable to state of the art phosphorescent emitters with noble metals such as Ir and
55  devices now rival those of state-of-the-art phosphorescent emitters.
56 avenue for designing efficient Ir(III)-based phosphorescent emitters.
57 ions provide insight about the nature of the phosphorescent emitting states, which involves a strong
58 a model of the photophysics to decompose the phosphorescent enhancement into contributions from incre
59 oscopy allows us to observe the evolution of phosphorescent excited states within the doublet manifol
60 containing an even dispersion of the pendant phosphorescent fragments.
61                                     Brightly phosphorescent gold-based metallopolymers have been synt
62                                    Thin film phosphorescent green OLEDs fabricated on plastic substra
63 By employing a light out-coupling structure, phosphorescent green organic light-emitting diodes exhib
64 H(2))(8)- chain between the polymer host and phosphorescent guest is thus an important design princip
65 ctivated delayed fluorescence(TADF) host and phosphorescent guests were fabricated using solution pro
66                          Inclusion of highly phosphorescent heavy-metal organic complexes as dopants
67 metalated onto an iridium core to form three phosphorescent heteroleptic molecules, (bppo)2Ir(acac),
68   The oxygen sensor nanoparticles consist of phosphorescent indicator dye embedded in poly(styrene-bl
69 rgy transfer between bonded systems of a red phosphorescent iridium complex 13 and a conjugated polym
70 f the back transfer of triplets from the red phosphorescent iridium complex to the polyfluorene backb
71                                 Red-emitting phosphorescent iridium complexes based on the [Ir(btp)(2
72 focusses on the significance of fluorescent, phosphorescent labelling and tracking of extracellular v
73 tudy, ruthenium(II) luminophores are used as phosphorescent lifetime imaging microscopy (PLIM) probes
74      This method takes advantage of the long phosphorescent lifetime of terbium chelates, a property
75 n this study, we extend our previous work on phosphorescent, low molecular weight platinum(II) comple
76 ve, near-infrared emitting and water-soluble phosphorescent macromolecular probe can not only report
77                           Metal-free organic phosphorescent materials are attractive alternatives to
78 , we develop photoactivated room temperature phosphorescent materials by covalently attaching lignin
79      The crystal structures of the efficient phosphorescent materials establish the existence of an u
80  Sustainable photoactivated room temperature phosphorescent materials exhibit great potential but are
81                                    Inorganic phosphorescent materials exhibiting persistent luminesce
82 se-change materials can transform widespread phosphorescent materials into high-speed optical sources
83                Developing metal-free organic phosphorescent materials is promising but challenging be
84 he decay process of typical fluorescence and phosphorescent materials with a recombination lifetime f
85  numerous possibilities for the synthesis of phosphorescent materials, with emission colours over the
86                Time-gated measurements using phosphorescent metal complexes can improve imaging, at t
87                           The replacement of phosphorescent metal complexes with inexpensive organic
88 rate electroluminescence from earth-abundant phosphorescent metal halide nanoclusters.
89 usion-controlled luminescence quenching of a phosphorescent metal-organic framework built from the Ru
90 iameter were loaded into stable, porous, and phosphorescent metal-organic frameworks (MOFs 1 and 2) b
91 vative technology based on oxygen-sensitive, phosphorescent metalloporphyrin allowing continuous and
92 requency phase modulation of tissue-embedded phosphorescent microprobes.
93  (Ni4 P2 ) into two highly stable and porous phosphorescent MOFs.
94 00 per cent internal quantum efficiency: the phosphorescent molecules harness the triplet excitons th
95                                      For the phosphorescent molecules, the electron spins are localiz
96                                          The phosphorescent nanoparticles exhibit strong phosphoresce
97 matrixes for making bright and monodispersed phosphorescent nanoparticles.
98 o-photon microscopy method, based on a novel phosphorescent nanoprobe, to image tissue oxygenation in
99 ed imaging system with a two-photon-enhanced phosphorescent nanoprobe.
100 nt using a commercially available multimodal phosphorescent nanosensor (MM2).
101                                 In contrast, phosphorescent OLEDs (PHOLEDs) can emit light from tripl
102  (eta(P,max) = 118 lm W(-1) ) ITO-free green phosphorescent OLEDs (PHOLEDs) with multilayered, highly
103 h of the academic and commercial pursuits in phosphorescent OLEDs have been dominated by Ir(III) comp
104 king (EBL) and hole-blocking layers (HBL) in phosphorescent OLEDs is explored.
105  the recent first incorporation as a host in phosphorescent OLEDs or as charge transporter in organic
106 e validate this approach for fluorescent and phosphorescent OLEDs, demonstrating good thickness unifo
107 amely organic light emitting diodes (OLEDs), phosphorescent OLEDs, organic field-effect transistors (
108 8-naphthalimide derivatives were examined in phosphorescent organic light emitting diodes (OLEDs), i.
109 s chemistry, principally due to their use in phosphorescent organic light-emitting devices (OLEDs).
110  and high efficiencies have been observed in phosphorescent organic light-emitting devices.
111                                  A non-doped phosphorescent organic light-emitting diode (PhOLED) bas
112                                              Phosphorescent organic light-emitting diodes (OLEDs) are
113  high brightness and deep blue emission from phosphorescent organic light-emitting diodes (PHOLED) is
114                                              Phosphorescent organic light-emitting diodes (PHOLEDs) f
115  years ago, the operational lifetime of blue phosphorescent organic light-emitting diodes (PHOLEDs) h
116 2.9 candela per ampere, similar to the CE of phosphorescent organic light-emitting diodes, with two m
117                                   Unlike the phosphorescent organic materials and organometallic comp
118  for potential eco-friendly applications in (phosphorescent) organic light emitting diodes, in imagin
119 lyzed by the MOFs using UV-vis spectroscopy, phosphorescent oxygen detection, and gas chromatographic
120 sing platform based on diamine oxidase and a phosphorescent oxygen nanosensor.
121   The system uses disposable swab vials with phosphorescent oxygen sensors integrated in the bottom p
122                         Discrete solid-state phosphorescent oxygen sensors produced by local solvent-
123  of mitochondrial oxygen consumption using a phosphorescent oxygen-sensitive probe, standard microtit
124                             The cross-linked phosphorescent particles using halogen-containing copoly
125 n the square plane) were strongly orange-red phosphorescent (Phi = 0.2-0.3) in a room-temperature oxy
126  structure and the optical properties of the phosphorescent platinum compounds: Pt(II) (2-(4',6'-difl
127 n between singlet and triplet is observed in phosphorescent platinum octaethylporphyrin (PtOEP), on a
128                             A butterfly-like phosphorescent platinum(II) binuclear complex can underg
129 ies of Ir(III) corroles differ from those of phosphorescent porphyrin complexes, cyclometalated and p
130     Both sensors rely on near infrared (NIR) phosphorescent porphyrin dyes, wherefore the signals can
131  The changes in actin were reported by (a) a phosphorescent probe (ErIA) attached to Cys 374 and (b)
132                     Actin was labeled with a phosphorescent probe at C374, and the myosin head (S1) w
133 KA), we have covalently bound the long-lived phosphorescent probe erythrosin isothiocyanate (Er-ITC)
134 oflavin has excellent potential as an edible phosphorescent probe for molecular mobility in food and
135 ity and limitations of using riboflavin as a phosphorescent probe for monitoring matrix molecular mob
136 t introduces a cucurbituril[8] (CB[8])-based phosphorescent probe for their detection.
137 elopment and in vivo application of a NIR-II phosphorescent probe that has lifetimes of hundreds of m
138 l dynamics of actin filaments, we attached a phosphorescent probe to F-actin at Cys-374 and performed
139     The so far developed two-photon-enhanced phosphorescent probes comprise antenna-core constructs,
140 uclear polypyridylruthenium(II) complexes as phosphorescent probes have strong phosphorescence, selec
141 on absorption cross-sections of conventional phosphorescent probes.
142 oute for generating materials with specific, phosphorescent properties and is an exciting alternative
143 photon (2P) absorption properties of several phosphorescent Pt (II) porphyrins, focusing on the effec
144 s in cultures of adherent cells, using three phosphorescent Pt-porphyrin based probes with different
145             Considered to be practically non-phosphorescent, purely organic compounds (metal-free) ar
146 -halogenated, non-carbonyl analogue, ambient phosphorescent quantum yields reach 55%.
147       Developing recyclable room-temperature phosphorescent (RTP) films using ultrafast fabrication t
148                             Room temperature phosphorescent (RTP) hydrogels exhibit great potential b
149                   Producing room temperature phosphorescent (RTP) materials from biomass resources us
150                             Room-temperature phosphorescent (RTP) materials have enormous potential i
151                  Photocured room temperature phosphorescent (RTP) materials hold great potential for
152 rest in the construction of room-temperature phosphorescent (RTP) materials.
153                        Most room temperature phosphorescent (RTP) organic materials have O- or N-lone
154       Hemoprotein-based scaffolds containing phosphorescent ruthenium(II) CO mesoporphyrin IX (RuMP)
155 t this deficiency can be overcome by using a phosphorescent sensitizer to excite a fluorescent dye.
156                                            A phosphorescent sensor based on a multichromophoric iridi
157 gnetic particle, elicits a rapid, long-lived phosphorescent signal.
158 a PEDOT:PSS HIL/HTL, and solution-processed, phosphorescent, small-molecule, green OLEDs with maximum
159 em crossing (RISC) rival the efficiencies of phosphorescent state-of-the-art organic light-emitting d
160 Cu interactions that are strengthened in the phosphorescent state.
161 thermally activated delayed fluorescence and phosphorescent systems, which would greatly benefit from
162 ion energy for exchange in proteins having a phosphorescent Trp and, for example, for studying the ef
163 H(22) exhibits blue fluorescence and becomes phosphorescent when substituted at various positions on
164 ibit external quantum efficiency >60%, while phosphorescent white organic light-emitting diodes exhib
165  We report the development of a new class of phosphorescent zwitterionic bis(heteroleptic) Ir(III) co

 
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