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1  and stems from an excited complex (i.e., an exciplex).
2 consistent with formation of a quinone-water exciplex.
3 he ion pair occur almost exclusively via the exciplex.
4 ependence, these bands can be assigned to an exciplex.
5 conversion among the encounter pairs and the exciplex.
6  proceeds through spin-mixing in the triplet exciplex.
7 d hyperfine interactions in the spin triplet exciplex.
8 lower energies, indicative of a new emissive exciplex.
9 , the tetracoordinate excited state, and the exciplex.
10 r emission line is assigned to an Irppy.niBr exciplex.
11 ng the ionic polarization to generate SOC in exciplexes.
12 nformations and the participation of triplet exciplexes.
13  (DA) pair leads, in some cases, to emissive exciplexes.
14 ng excited singlets, triplets, excimers, and exciplexes.
15    The charge transfer (CT) character of the exciplexes (88-97%) was calculated from the electronic c
16 conversion among the encounter pairs and the exciplex (A*/D right harpoon over left harpoon exciplex
17 arge-transfer intermediate we call a "bonded exciplex", A- -D+.
18 s the dominant pathway for relaxation, since exciplex and niBr triplet states give either weak or no
19                      We detect that both the exciplex and the radical ion pair are formed during the
20 s have very similar energies for the dopant, exciplex, and niBr triplet states, such that relaxation
21  ZnO impurities, amine-donor charge-transfer exciplexes, and framework decomposition in samples of MO
22 model compounds is investigated and emissive exciplexes are detected in aromatic solvents.
23 idly interconverting encounter pairs with an exciplex as intermediate, A*/D right harpoon over left h
24                         Rather, they involve exciplexes as the dominant, kinetically and spectroscopi
25             The experimental evidence of the exciplex assignment includes the extremely large Stokes
26  quenching, viz., the loose ion pair and the exciplex, based on the time-resolved magnetic field effe
27 e indicative of an excited-state complex or "exciplex" between trans-stilbene and the antibody.
28                                   The bonded exciplex can be formally thought of as resulting from bo
29 e well suited to demonstrating that emissive exciplexes can be formed in water from purely organic co
30 llowed by the formation of an intramolecular exciplex consisting of amine and pyrenyl groups.
31                Beyond this point, additional exciplex deactivation pathways-fluorescence, intersystem
32 stem crossing (RISC) from triplet to singlet exciplex diminishes, a pronounced isotope effect is obse
33 emission and increases the efficiency of the exciplex emission as the e-h separation reduces, is disc
34 lays a charge transfer band at 450 nm and an exciplex emission at 520 nm, indicating the formation of
35                                      Such an exciplex emission, which has also no precedent in TCBD c
36 is polarization (30 degrees) match observed 'exciplex' emission.
37 anic small-molecule, dendrimer, polymer, and exciplex emitters are all discussed within this review,
38 high CT character in a highly polar solvent, exciplex fluorescence quantum yields up to 0.03 and life
39                                         Weak exciplex fluorescence was observed in each case.
40 gnificantly lowers the activation energy for exciplex formation (E(a)) and helps stabilize the highly
41  the reduction of the singlet-triplet gap by exciplex formation and the external heavy atom effect.
42                                   Due to the exciplex formation between covalently bonded electron-do
43                           The intramolecular exciplex formation event (i.e., excited-state FAD residu
44 mation of both static and dynamic complexes (exciplex formation), which is aided by hydrogen bonding.
45 oly(methyl methacrylate) (PMMA), without any exciplex formation, and its OLPL duration reaches more t
46 of host-guest complexes toward fluorescence, exciplex formation, charge separation, room-temperature
47 he folded conformer, which leads directly to exciplex formation.
48 to such things as self-quenching behavior or exciplex formation.
49 ns (yielding radical ion pairs) or by direct exciplex formation.
50 nor-acceptor interactions, and excited state exciplex formation.
51 relative intensity of the anthracene-related exciplex, formed from the encounter complex, was 8 times
52                     Using the newly designed exciplex-forming 1,2,3-triazole-based acceptors with fas
53                                 Usage of the exciplex-forming host allowed us to achieve a low turn-o
54 n of time-resolved magnetic field effects in exciplex-forming organic donor-acceptor systems.
55                                          The exciplex has a lifetime of a few nanoseconds and undergo
56 omophore leads to formation of a fluorescent exciplex in polar solvents but pyrene-like fluorescence
57 rmation of the aforementioned intramolecular exciplex in terms of a radical ion pair stabilized throu
58 ion to recent findings on the involvement of exciplexes in photoinduced electron transfer reactions.
59                      Evidence for the bonded exciplex intermediate comes from studies of steric and C
60                No long-lived radical ions or exciplex intermediates can be detected on the picosecond
61 al that the triplet-to-singlet conversion in exciplexes involves an artificially generated spin-orbit
62      The delayed fluorescence emitted by the exciplex is magnetosensitive if the reaction pathway inv
63 adiative triplets into radiative singlets in exciplex light-emitting diodes are reported.
64 ne-based pi-pi* fluorescence) a lower-energy exciplex-like emission feature associated with a naphthy
65             By monitoring the changes in the exciplex luminescence intensity when applying external m
66 the excited-state charge-transfer complexes (exciplexes) of the PPEs with analytes were observed.
67      Simple trilayer, deep blue, fluorescent exciplex organic light-emitting diodes (OLEDs) are repor
68 inescence in the same solution with 100-fold exciplex partner added.
69 However, even in comparably polar media, the exciplex pathway remains remarkably significant.
70            Unlike numerous known examples of exciplexes (products of charge formation reactions), we
71 actions), we reported recently that cationic exciplexes (products of charge shift reactions) can be f
72 ing" aliphatic amine forms an intramolecular exciplex, providing alternative nonradiative deactivatio
73 ciplex (A*/D right harpoon over left harpoon exciplex right harpoon over left harpoon A(*-)/D(*+)).
74 ediate, A*/D right harpoon over left harpoon exciplex right harpoon over left harpoon A(*-)/D(*+).
75  the first time to Au-Au bonded excimers and exciplexes similar to those reported earlier for Ag(I) c
76                     These OLEDs emit from an exciplex state formed between the highest occupied molec
77 designed to study the characteristics of the exciplex state pinned at a donor-acceptor abrupt interfa
78 n the ground state and the low-energy bonded exciplex state.
79 initial excitations that decay to long-lived exciplex states is approximately equal to the fraction o
80 ons to low-energy states such as triplet and exciplex states that are nonemissive or weakly emissive.
81 s associated with two stacked bases decay to exciplex states, whereas excitations in unstacked bases
82           Irppy-based devices emit only from exciplex states, with low efficiency (external efficienc
83 tates decay rapidly and irreversibly to dark exciplex states.
84 ysis supports their assignment to excimer or exciplex states.
85 The results confirm the previously proposed "exciplex" structure of the MLCT state in Lewis basic sol
86 L emitters are mainly based on a bimolecular exciplex system which usually needs an expensive small m
87 th high mobility, combined with an interface exciplex that confines excitons at the emissive layer/el
88 ayed fluorescence (TADF) from donor-acceptor exciplexes that are either protonated (H) or deuterated
89 )(-)](n) and *[Ag(CN)(2)(-)](n) excimers and exciplexes that differ in "n" and geometry.
90 -pyrimidine (B3PYMPM) (DeltaE(ST) = 130 meV) exciplexes, the SOC generated by the intermolecular char
91                           The most efficient exciplex-type thermally activated delayed fluorescence w
92 or the reversible formation and decay of the exciplexes were determined using time-correlated single-
93 nd excited-state energies (dopant, niBr, and exciplex) were used to explain the observed spectral pro
94 an unit creates a new route for decay of the exciplex whereby the triplet state of the spiropyran is
95            ECL from this system exhibited an exciplex whose energy and intensity relative to the emis