ライフサイエンスコーパス: photoexcited

1 n to yield the sensitizer that was initially photoexcited.

2 ized and the attached free base porphyrin is photoexcited.

3 of 300 ps lived charge separated states once photoexcited.

4 rature dependence of the yield of CT between photoexcited 2-aminopurine (Ap) and G through DNA bridge

5 DNA duplexes and DNA:RNA hybrids containing photoexcited 2-aminopurine (Ap).

6 In these systems, the photoexcited acceptor state is predominantly deactivated

7 netostrictive, and photostrictive actuators; photoexcited actuators; electrostatic actuators; and pne

8 tor states, localized in the vicinity of the photoexcited adsorbate, and delocalized states extended

9 We demonstrated that photoexcited aliphatic ketones, such as acetone and diac

10 quential hydride and proton transfers in the photoexcited and ground states, respectively, and is an

11 intermediate, formed by the collision of one photoexcited and one ground-state TIPS-pentacene molecul

12 Electron solvation dynamics in photoexcited anion clusters of I-(D2O)n=4-6 and I-(H2O)4

13 Photoexcited Ap is used as a dual reporter of variations

14 ce, and with the same driving force, HT from photoexcited Ap to G in the 5' to 3' direction is more e

15 Here we show that photoexcited Arabidopsis cryptochrome 2 (CRY2) is phosph

16 Plasmons are launched from a photoexcited array of nanocavities and their propagation

17 cattering to measure the lattice dynamics of photoexcited BaFe2As2.

18 long debated pathway for the deactivation of photoexcited base pairs, with possible implications for

19 uents like these have electrons to feed into photoexcited BODIPYs, quenching their fluorescence, ther

20 and vibrational spectroscopic signatures of photoexcited breathers are predicted, and generalization

21 light can cause phosphorylation of not only photoexcited but also non-excited rhodopsin in rod photo

22 er between CdS and TiO2 when the CdS QDs are photoexcited by wavelengths shorter than 525 nm.

23 copy was used for temporal resolution of the photoexcited carrier dynamics between the QDs and ligand

24 We find evidence that photoexcited carriers acquire spin-polarization from the

25 is responsible for the ultrafast trapping of photoexcited carriers in haematite (alpha-Fe2O3).

26 show a coverage-dependent energy transfer of photoexcited carriers in hydrogenated graphene, giving r

27 Recombination of photoexcited carriers in most two-dimensional metal dich

28 numerical model based on charge transport of photoexcited carriers in the substrate.

29 graphene is a promising detection mechanism; photoexcited carriers rapidly thermalize due to strong e

30 from the escape of either one or both of the photoexcited carriers to the nanocrystal surface.

31 ractions lead to ultrafast relaxation of the photoexcited carriers, and the energy of the incident in

32 aphene layers enhances the collection of the photoexcited carriers.

33 section and ultrafast recombination rates of photoexcited carriers.

34 ed to determine the lifetime and activity of photoexcited catalysts.

35 ibe the charge transfer interactions between photoexcited CdS nanorods and mononuclear water oxidatio

36 g the rate and quantum efficiency of ET from photoexcited CdS NRs to CaI using transient absorption s

37 Electron and energy transfer rates from photoexcited CdSe colloidal quantum dots (QDs) to graphe

38 he relative hole transfer rate constant from photoexcited CdSe/CdS core/shell QDs to tethered ferroce

39 the monolayer MoS2 in the process of ET from photoexcited CdSe/ZnS nanocrystals.

40 Computational modelling indicates that photoexcited charge carriers accumulated at the surface

41 lts help to explain the robust separation of photoexcited charge carriers between the two phases and

42 nement of sp(2) domains, and the trapping of photoexcited charge carriers in the localized states in

43 rimarily due to an energy gain involving the photoexcited charge carriers that are transiently popula

44 force microscopy (EFM) as a means to measure photoexcited charge in polymer films with a resolution o

45 lfide (MoS2 ) monolayers induce an effective photoexcited charge transfer at the interface.

46 The photoexcited charge transfer state of DMJ-An acts as a h

47 tion, the photoresponse due to the different photoexcited-charge-carrier trapping times in sp(2) and

48 Imaging the microchannel flows carrying thus photoexcited chelates of lanthanide ions allowed us to e

49 upled electronic states corresponding to the photoexcited chlorophyll special pair (donor), the reduc

50 namics of a three-spin system representing a photoexcited chromophore coupled to a stable radical spe

51 d structural rearrangement at the level of a photoexcited chromophore is known to occur in the femtos

52 ization of the molecular choreography of the photoexcited chromophore requires a spectroscopic techni

53 s studies have shown that the collision of a photoexcited chromophore with a ground-state chromophore

54 Relaxation of photoexcited chromophores is a key factor determining di

55 As a result, the photoexcited coumarin did not show any of the typical re

56 ults are consistent with the hypothesis that photoexcited CRY2 disengages its C-terminal domain from

57 clear bodies may result from accumulation of photoexcited CRY2-GFP waiting to be degraded.

58 ike kinases) interact with and phosphorylate photoexcited CRY2.

59 We have determined the steady state, photoexcited crystal structure of a flavin-bound LOV dom

60 The singlet fluorescence dynamics of photoexcited [Cu(I)(dmp)(2)](+) were measured in the coo

61 onal energy relaxation and redistribution in photoexcited cycloparaphenylene carbon nanorings with in

62 ergy transfer phenomenon that occurs between photoexcited D-/L-Trp enantiomers and rGO/gamma-CD givin

63 , demonstrating that both hole transfer from photoexcited DBFI-T to PSEHTT and electron transfer from

64 According to our analysis, 30% of the photoexcited diazo precursor molecules are eventually pr

65 ch liberates only trace hydrogen levels when photoexcited directly, does not appear to independently

66 One major decay channel of photoexcited DNA leads to reactive charge transfer state

67 ium(III) acceptor, a substantial fraction of photoexcited donor exhibits fast oxidative quenching (>3

68 xcited-state relaxation and injection as the photoexcited dye relaxes through the (3)MLCT manifold to

69 adsorbed O2 for receiving electrons from the photoexcited dyes.

70 Here we explore the photoexcited dynamics of molecules by an interaction wit

71 Evolution of the time-dependent photoexcited electron during the initial 5 fs after inst

72 photo-induced resonant tunneling in which a photoexcited electron in the STM tip is transferred to t

73 and short-circuit the cell by accepting the photoexcited electron on a subpicosecond time scale.

74 t absorption (TA) spectroscopy revealed that photoexcited electron transfer rates increase with incre

75 tite (alpha-Fe2 O3) is engineered to improve photoexcited electron-hole pair separation by synthesizi

76 nce time-domain simulations, suggesting that photoexcited electron-hole pairs in the silicon waveguid

77 Together this nano-architecture lets photoexcited electrons and holes dissociate instantaneou

78 results imply that the recombination of the photoexcited electrons and holes is suppressed by the sc

79 pathways for rapid and balanced transport of photoexcited electrons and holes, respectively, while mi

80 Photoexcited electrons are transferred to the metal and

81 HMe2(+)), which were capable of transferring photoexcited electrons directly to the negatively charge

82 he device is based on thermionic emission of photoexcited electrons from a semiconductor cathode at h

83 electron microscopy, we imaged the motion of photoexcited electrons from high-energy to low-energy st

84 a reduction step could occur by transfer of photoexcited electrons from the p-GaP photocathode and w

85 takes advantage of the reducing potential of photoexcited electrons in the conduction band of CdS and

86 (-) species is generated by the reaction of photoexcited electrons in the perovskite and molecular o

87 The photoexcited electrons of CZTS can be readily transporte

88 mechanism involving the coupling between the photoexcited electrons of the nanoparticles and the gold

89 mionic emission relies on vacuum emission of photoexcited electrons that are in thermal equilibrium w

90 It is found that both the transfer of photoexcited electrons to pyridinium and pyridinium adso

91 electrodes that can reduce water to H2 using photoexcited electrons.

92 Hole injection by photoexcited ethidium followed by radical migration to o

93 Absorption of X-ray photons generates photoexcited Fe(II)(LS) domains whose size rapidly grows

94 tion triggered by electron transfer from the photoexcited flavin cofactor to the dimer.

95 rface, without changes in the others, as the photoexcited fraction is increased.

96 The evolution from the photoexcited Franck-Condon MLCT state to the thermally e

97 y act as electron acceptors, whereas for the photoexcited fullerenes, SWCNTs act as electron donors.

98 The photoexcited GNRs enhanced the spin-spin and spin-lattic

99 s of the dynamics of hot electron cooling in photoexcited gold nanoparticles (Au NPs) with diameters

100 Our result suggests that photoexcited graphene transfers a hot electron to benzoy

101 y to accept an electron through space from a photoexcited guest.

102 ure change leading to proton transfer on the photoexcited half of the 7-azaindole dimer.

103 Photoexcited heptanal is believed to undergo rapid inter

104 we use a metallointercalator to introduce a photoexcited hole into the DNA pi-stack at a specific si

105 tion-band electron following transfer of the photoexcited hole to Ag(+).

106 It is not the presence of photoexcited holes and electrons, but a rise in temperat

107 In CdS nanocrystals, photoexcited holes rapidly become trapped at the particl

108 Under optical illumination, photoexcited hot carriers generated in the top layer tun

109 s owing to differences in decay channels for photoexcited hybrid plasmon-phonons and electrons.

110 The relaxation dynamics of the photoexcited hydrated electron have been subject to conf

111 In a spin: the dynamics of photoexcited ICN(-) (Ar)(0-5) are presented.

112 Photoexcited intramolecular charge transfer (CT) states

113 G and CPC is promoted efficiently by HT from photoexcited Ir(III) when the modified bases are positio

114 Mechanistic investigations suggest that the photoexcited iridium catalyst facilitated the nickel act

115 The dynamics of photoexcited lead-free perovskite films, CH3NH3SnI3, wer

116 ill significantly lower than that induced by photoexcited lipofuscin.

117 ging by detecting the acoustic response of a photoexcited material.

118 In contrast to lipofuscin, photoexcited melanosomes did not substantially increase

119 The molecular structure and dynamics of the photoexcited metal-to-ligand-charge-transfer (MLCT) stat

120 The photoexcited metastable triplet state of Mg(2+)-mesoporp

121 ET quenching of both the singlet and triplet photoexcited MMb states, the direction of flow being det

122 rafast motion of electrons and nuclei of the photoexcited molecule presents a challenge to current sp

123 For photoexcited molecules, the nuclear dynamics determine t

124 observation of ultrafast charge transfer in photoexcited MoS2/WS2 heterostructures using both photol

125 Energy transfer from photoexcited nanoparticles to their surroundings was stu

126 ansfer (ET) contributed to the relaxation of photoexcited nc-CdTe relative to the intrinsic radiative

127 Photoexcited (NCN)CNx in the presence of an organic subs

128 ate of hole-capture by the host polymer from photoexcited NCs.

129 diminishes, and blue emission from a trapped photoexcited neutral chromophore dominates because ESPT

130 Photoexcited Nickel(II) tetramesitylporphyrin (NiTMP), l

131 ithin approximately 10 ps, ligand binding to photoexcited NiDPP is progressively longer in pyridine,

132 ibited intramolecular charge-transfer within photoexcited NOM, leading to substantially increased rem

133 IR detection shows that photoexcited o-phenylene thioxocarbonate (2) and 2-chlor

134 ited-state energy transfer prevails from the photoexcited oligofluorene to the energy accepting fulle

135 n data indicate that electron injection from photoexcited PbS QDs to PCBM occurs within our temporal

136 dence is given for an electron transfer from photoexcited Pc1 to the electron-accepting C60A that aff

137 rom photoexcited polymer, hole transfer from photoexcited PCBM, prompt (<100 fs) charge generation in

138 for simulating the nonadiabatic dynamics of photoexcited PCET are discussed.

139 derstanding the fundamental spin dynamics of photoexcited pentacene derivatives is important in order

140 The electron injection dynamics from the photoexcited perovskite layers to the neighboring film s

141 ight perylenes per porphyrin in toluene, the photoexcited perylene-monoimide dye (PMI) decays rapidly

142 observe more than a 200-fold increase in the photoexcited phosphorescent emission of PtOEP (2,3,7,8,1

143 en shown to quench the catalytic activity of photoexcited, phosphorylated rhodopsin in a reconstitute

144 nhancing electron transfer rates between the photoexcited photoredox catalyst and the substrate.

145 g at two well-separated energies in a highly photoexcited planar microcavity at room temperature.

146 These include electron transfer from photoexcited polymer, hole transfer from photoexcited PC

147 o determine the interspin distance between a photoexcited porphyrin triplet state (S = 1) and a nitro

148 For example, with respect to the photoexcited porphyrins and phthalocyanines, SWCNTs usua

149 In the triple mutant, the decay of the photoexcited primary electron donor (P) occurs with a ti

150 ations are triggered by reorientation of the photoexcited protein.

151 DBFI-T to PSEHTT and electron transfer from photoexcited PSEHTT to DBFI-T contribute substantially t

152 Approximately 10-50% of all photoexcited pyrimidine bases decay via the (1)npi* stat

153 oxidation is initiated by hole transfer from photoexcited QD to surface DTO and that these substrates

154 Photoexcited QDs could be used in the study of the effec

155 this process, in particular, whether or not photoexcited QDs play a direct role in the photoinduced

156 ates in the energy transfer process from the photoexcited QDs to the molecular energy acceptor.

157 ination kinetics of the electron and hole of photoexcited QDs.

158 Here, we show that photoexcited quantum dots (QDs) can kill a wide range of

159 Cu(I) oxidation by a photoexcited Re(I)-diimine at position 124 on a histidin

160 The analysis revealed that 30% of the photoexcited receptor molecules followed Cycle 1 through

161 , while CPG undergoes ring-opening both with photoexcited [Rh(phi)2(bpy)]3+ and with [Ru(phen)(dppz)(

162 A photoexcited rhodium intercalator, Rh(phi)2DMB3+ (phi =

163 mma and, as heterotrimeric proteins, bind to photoexcited rhodopsin (R*).

164 Gbetagamma(t) or activation of transducin by photoexcited rhodopsin (R*).

165 Photoexcited rhodopsin activates an enzymatic cascade in

166 al rod cells, which controls the lifetime of photoexcited rhodopsin by inhibiting rhodopsin kinase.

167 In vertebrate photoreceptors, photoexcited rhodopsin interacts with the G protein tran

168 ydrolysis occurring over the period in which photoexcited rhodopsin is quenched.

169 ansducin and an increased activation rate by photoexcited rhodopsin or more efficient activation of c

170 GDP-bound x-ray structure of Gt reveals that photoexcited rhodopsin promotes the formation of a conti

171 well established that normal inactivation of photoexcited rhodopsin, the GPCR of rod phototransductio

172 restin molecules are available to quench the photoexcited rhodopsin.

173 ial first step in the prompt deactivation of photoexcited rhodopsin.

174 er effect spectroscopy while it was bound to photoexcited rhodopsin.

175 ntermediates are generated upon quenching of photoexcited Ru*(bpz)3(2) with a variety of thiols.

176 The excited-state lifetime of photoexcited [Ru(bpy)(2)(pbnHH)](2+) is found to be abou

177 systems, electron-transfer occurred from the photoexcited ruthenium polypyridyl donor to the pentammi

178 nfrared (TRIR) spectroscopy was performed on photoexcited ruthenium polypyridyl-DNA crystals, the ato

179 odopsin in the native membrane suggested the photoexcited samples were heterogeneous.

180 Photoexcited semiconductor nanoparticles undergo charge

181 c photocurrent results from reduction of the photoexcited sensitizer by free electrons in ITO.

182 sensitizer-acceptor design in which multiple photoexcited sensitizers resonantly and simultaneously t

183 receptor, in particular the lifetime of the photoexcited signaling states.

184 single-junction solar cells by splitting one photoexcited singlet exciton (S1) into two triplets (2T1

185 The reason is that photoexcited singlet oxygen is highly reactive, so the p

186 produces two triplet excited states from one photoexcited singlet state, is a means to circumvent the

187 Correspondingly, charge-separation ET from a photoexcited singlet zinc porphyrin incorporated within

188 neration of two spin triplet states from one photoexcited singlet.

189 experimental constraints on the reaction of photoexcited SO2 with atmospheric hydrocarbons.

190 of an applied external electric field on the photoexcited species of CH3NH3PbI3 thin films, both at r

191 t affects the nonradiative decay rate of the photoexcited species.

192 y measuring an electromotive force driven by photoexcited spin-polarized electrons drifting through G

193 ith high reactivity with O(2) at the triplet photoexcited state and favorable redox potential and cou

194 , the role of small polaron formation in the photoexcited state and how this affects the photoconvers

195 eds through rapid internal conversion of the photoexcited state into a dark state of multi-exciton ch

196 presents a novel case in which the molecular photoexcited state is at the edge of the conduction band

197 In the system under investigation, the photoexcited state lies close to the bottom of the TiO 2

198 sion of (+)-2 into 14 by binding the triplet photoexcited state of 6 in proximity to (+)-2.

199 chieving catalytic promiscuity that uses the photoexcited state of nicotinamide co-factors (molecules

200 n kinase and to modulate the lifetime of the photoexcited state of rhodopsin (Rh*), the visual pigmen

201 sistent with that of photolyase in which the photoexcited state of the purine donates an electron to

202 ssion occurs directly from the initial 1B(u) photoexcited state on ultrafast time scales.

203 The photoexcited state Ru(II*) of Ru2Z is reduced to Ru(I) b

204 ays the electronic relaxation of the initial photoexcited state within 200 fs.

205 dy configurations within the lifetime of the photoexcited state.

206 m a particular C-O bond stretch in the pipi* photoexcited state.

207 s a result of changes in the distribution of photoexcited-state energies and, hence, in the density o

208 h in generating a nonuniform distribution of photoexcited states and in driving the ET process.

209 the broad emission comes from the transient photoexcited states generated by self-trapped excitons (

210 estigation of the dynamics and relaxation of photoexcited states in conjugated polyfluorenes, which a

211 at, like their dihydrophenazine analogs, the photoexcited states of phenoxazine photoredox catalysts

212 The singlet S(1) and triplet T(1) photoexcited states of the compounds containing MM quadr

213 ntal and computational studies show that the photoexcited states of the two complexes are very differ

214 fer, injection in particular, accelerate for photoexcited states that are delocalized between the two

215 he structure of transient molecules, such as photoexcited states, in disordered media (such as in sol

216 oflavin dimers do not interact in ground and photoexcited states.

217 The study of photoexcited strongly correlated materials is attracting

218 This fundamental insight into the role of photoexcited surface FLPs for catalytic CO2 reduction co

219 Our results also indicate that photoexcited SWCNTs can catalyze lipid peroxidation simi

220 ransfer states due to electron transfer from photoexcited tetracene to the lowest unoccupied molecula

221 e used, while in cage oxygen transfer to the photoexcited (thio)pyrylium derivatives have been charac

222 g on the interfacial charge transfer between photoexcited TiO2 and SWNTs as well as the mechanism of

223 Longer than 1 ns lifetimes for holes photoexcited to the lower valence subband offer a potent

224 ace and bulk transient carrier dynamics in a photoexcited topological insulator can control an essent

225 g the electronic and geometric structures of photoexcited transient species with high accuracy is cru

226 e singlet excited state, but does quench the photoexcited triplet excited state as a function of TEMP

227 The delocalization of the photoexcited triplet state in a linear butadiyne-linked

228 lar oxygen via the presumed quenching of the photoexcited triplet state of 6.

229 temperature dependence and splitting of the photoexcited triplet state of myoglobin in which the iro

230 troscopic probe used in these studies is the photoexcited triplet state of Trp37, which is associated

231 phyrin oligomers lead to localization of the photoexcited triplet state on a single porphyrin unit, w

232 y acquired from the spin polarization of the photoexcited triplet state spectrum.

233 The photoexcited triplet states of a series of linear and cy

234 The transient EPR spectra of the photoexcited triplet states of the porphyrin monomer and

235 obins (Mb) the fluorescence quenching of the photoexcited tryptophan 14 (*Trp(14)) residue is in part

236 cond of the electron-transfer process in the photoexcited type-II heterostructure-a fundamental pheno

237 Photoexcited visual pigment activates the GTP-binding pr

238 anism involves the ultrafast collapse of the photoexcited wave function due to nonadiabatic electroni

239 ibit hole injection into surface states when photoexcited with visible light (lambda = 400-680 nm).

240 s when other bacteriorhodopsin molecules are photoexcited within the two-dimensional lattice of the p

241 Electron transfer from photoexcited zinc porphyrin to C(60) is witnessed in the

242 the vesicle was capable of reacting with the photoexcited zinc porphyrin.