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1 and stems from an excited complex (i.e., an exciplex).
2 conversion among the encounter pairs and the exciplex.
3 lower energies, indicative of a new emissive exciplex.
4 , the tetracoordinate excited state, and the exciplex.
5 r emission line is assigned to an Irppy.niBr exciplex.
6 consistent with formation of a quinone-water exciplex.
7 he ion pair occur almost exclusively via the exciplex.
8 ependence, these bands can be assigned to an exciplex.
9 (DA) pair leads, in some cases, to emissive exciplexes.
10 ng excited singlets, triplets, excimers, and exciplexes.
11 conversion among the encounter pairs and the exciplex (A*/D right harpoon over left harpoon exciplex
13 s the dominant pathway for relaxation, since exciplex and niBr triplet states give either weak or no
15 s have very similar energies for the dopant, exciplex, and niBr triplet states, such that relaxation
16 ZnO impurities, amine-donor charge-transfer exciplexes, and framework decomposition in samples of MO
17 idly interconverting encounter pairs with an exciplex as intermediate, A*/D right harpoon over left h
20 quenching, viz., the loose ion pair and the exciplex, based on the time-resolved magnetic field effe
25 emission and increases the efficiency of the exciplex emission as the e-h separation reduces, is disc
28 anic small-molecule, dendrimer, polymer, and exciplex emitters are all discussed within this review,
30 gnificantly lowers the activation energy for exciplex formation (E(a)) and helps stabilize the highly
32 mation of both static and dynamic complexes (exciplex formation), which is aided by hydrogen bonding.
36 relative intensity of the anthracene-related exciplex, formed from the encounter complex, was 8 times
39 omophore leads to formation of a fluorescent exciplex in polar solvents but pyrene-like fluorescence
40 rmation of the aforementioned intramolecular exciplex in terms of a radical ion pair stabilized throu
41 ion to recent findings on the involvement of exciplexes in photoinduced electron transfer reactions.
45 ne-based pi-pi* fluorescence) a lower-energy exciplex-like emission feature associated with a naphthy
47 the excited-state charge-transfer complexes (exciplexes) of the PPEs with analytes were observed.
51 ciplex (A*/D right harpoon over left harpoon exciplex right harpoon over left harpoon A(*-)/D(*+)).
52 ediate, A*/D right harpoon over left harpoon exciplex right harpoon over left harpoon A(*-)/D(*+).
53 the first time to Au-Au bonded excimers and exciplexes similar to those reported earlier for Ag(I) c
55 designed to study the characteristics of the exciplex state pinned at a donor-acceptor abrupt interfa
57 initial excitations that decay to long-lived exciplex states is approximately equal to the fraction o
58 ons to low-energy states such as triplet and exciplex states that are nonemissive or weakly emissive.
59 s associated with two stacked bases decay to exciplex states, whereas excitations in unstacked bases
63 The results confirm the previously proposed "exciplex" structure of the MLCT state in Lewis basic sol
65 or the reversible formation and decay of the exciplexes were determined using time-correlated single-
66 nd excited-state energies (dopant, niBr, and exciplex) were used to explain the observed spectral pro
67 an unit creates a new route for decay of the exciplex whereby the triplet state of the spiropyran is
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