ライフサイエンスコーパス: visible light

1 e recovered upon subsequent irradiation with visible light.

2 cyclophanediene (CPD) upon irradiation with visible light.

3 ck/allylic substitution sequence mediated by visible light.

4 ity for hydrogen production from water using visible light.

5 ectron-deficient alkynes is induced by UV or visible light.

6 s(-1)) simply by illuminating the fluid with visible light.

7 Both complexes are highly sensitive to visible light.

8 l system, which can be activated solely with visible light.

9 oxidation state and the presence/absence of visible light.

10 o terminal nitride complexes is triggered by visible light.

11 The stimulant used for HmbRI is visible light.

12 by simply alternating the exposure to UV and visible light.

13 switches between open and closed forms with visible light.

14 on of UV light and anisotropic scattering of visible light.

15 nhanced photoactivated charge transfer under visible light.

16 photopigments with reflected or transmitted visible light.

17 retinol to 11-cis-retinol during exposure to visible light.

18 e photoisomerization upon exposure to UV and visible light.

19 oaromatic compounds has been developed using visible light.

20 etalated rhodium catalyst in the presence of visible light.

21 e fact that these species are able to absorb visible light.

22 e IR transmissive but impenetrable to UV and visible light.

23 f alkenes has been done under irradiation of visible light.

24 exposed to a combination of ultraviolet and visible light.

25 ssible and nondamaging light source, such as visible light.

26 y (99.9%) for the oxidation of benzene under visible light.

27 patible, chemical ligation triggered by mild visible light.

28 cular media (the mainly crystalline lens) in visible light.

29 light-sensing ability after irradiation with visible light.

30 ble hydrogels using different wavelengths of visible light.

31 t, a trithiocarbonate-derived disulfide, and visible light.

32 der cryogenic conditions by using X-rays and visible light.

33 complex 3D structures using high-resolution visible light 3D printing, demonstrating the broad utili

34 This photoinduced system operates with visible light (400 nm) and achieves borylation of a wide

35 46 mg/kg) were exposed in parallel to direct visible light (6000 lx, 24 degrees C, 344 h) and FTIR sp

36 Here we report an air- and moisture-stable, visible light-absorbing Zr(IV) photosensitizer, Zr((Mes)

37 Such reactions are often catalysed by visible-light-absorbing organic molecules or transition-

38 In bulk aqueous solutions, UV- and visible-light-absorbing products are observed at pH 3-4

39 ith Hantzsch ester (HE) anion serving as the visible-light-absorbing reagent and electron and hydroge

40 iented HP nanorods gave rise to the enhanced visible light absorption and the greatly accelerated pho

41 ures endow the carbide network with enhanced visible light absorption, providing high solar energy ha

42 amples were analyzed for spectrally-resolved visible light absorption.

43 form a Kagome (kgm) lattice and show strong visible light absorption.

44 horus is a promising photocatalyst with wide visible-light absorption up to 700 nm, but the fast char

45 uate synthesizability, corrosion resistance, visible-light absorption, and compatibility of the elect

46 By taking advantage of the visible light absorptivity of electron donor-acceptor co

47 transfer has been initiated by utilizing the visible-light absorptivity of Eosin Y for a reductive ge

48 We anticipate that the use of a visible light activated photocatalyst to transform subst

49 We report a visible-light-activated photocatalytic process that intr

50 Visible light activates the photocatalyst, and it acts a

51 dine(III) diacetate in tetrahydrofuran under visible-light activation.

52 this system, we sought to define the role of visible light and a photosensory HWE kinase, LovK, in re

53 ond, and proceeds under mild conditions with visible light and a readily available organic photocatal

54 The process is facilitated by visible light and a silane reducing agent, which trigger

55 Our studies establish a role for visible light and an ensemble of HWE kinases in light-de

56 A promising protocol using visible light and aryl iodides for constructing valuable

57 above and beyond the information provided by visible light and electron microscopy.

58 can benefit from simultaneously controlling visible light and heat.

59 s of magnitude larger than the wavelength of visible light and is readily observed in systems as simp

60 The use of visible light and photoredox catalysis emerged as a powe

61 ivity is exemplified by photoinitiated (with visible light and/or blue LEDs) allylation of perfluoroa

62 xcellent absorption capability in the entire visible-light and even near-infrared regions.

63 Visible-light and infrared-light persistent phosphors ar

64 the manganese-calcium cluster are tracked by visible-light and X-ray spectroscopy.

65 oped using the organic photocatalyst 4CzIPN, visible light, and N-(acyloxy)phthalimides as radical pr

66 O emission can be shifted into the green for visible light applications through the introduction of d

67 sed for fabricating optical metasurfaces for visible light applications.

68 ors based on oxindole which can be driven by visible light are presented.

69 t temporal and spatial resolution using only visible light as stimulus.

70 ilized on the combined photobioanode for the visible light assisted glucose oxidation (GCE|MWCNT|g-C(

71 toelectrochemical biofuel cell (PBFC) with a visible light assisted photobioanode.

72 Substitution of UV irradiation with visible light benefits bioimaging, while the spectral be

73 imultaneous monitoring of RAS signaling with visible-light biosensors, enabling all-optical approach.

74 gy to transcend the energetic limitations of visible light by electrochemically priming a photocataly

75 ess organic carbon and was more sensitive to visible light by exhibiting greater changes.

76 The NIR light is thus upconverted into visible light by T1 and excited PS.

77 otocol involves the successful harvesting of visible light by TETPY assemblies to catalyze the coupli

78 However, due to the attenuation of visible light by tissue, and the limited set of near-inf

79 s were synchronized with a second high-speed visible light camera and two thermocouples to provide in

80 ) photoredox catalyst, upon irradiation with visible light, can be either reduced or oxidized by the

81 Visible light catalysis allows the regioselective synthe

82 we show that colloidal quantum dots serve as visible-light chromophores, photocatalysts and reusable

83 n illustration of this, we have demonstrated visible light communication using OLEDs with data rates

84 Visible Light Communications (VLC) can provide both illu

85 rsible photoswitching, and multiplexing with visible-light-controllable optogenetic tools.

86 n the development of a new system to achieve visible-light-controlled metathesis by merging olefin me

87 (3) photocatalysts possess great promise for visible light driven photodegradation of AO dye.

88 nfrared Raman spectroscopy revealed that the visible light-driven rotation of the molecular motor pro

89 ted high turnover frequency of 29.5 h(-1) in visible-light-driven acceptorless dehydrogenation of tet

90 irectly reducing O(2) to produce H(2) O(2) , visible-light-driven AQ reduction occurs in the DSPEC an

91 le of a chiral molecular switch in which the visible-light-driven azobenzene motif is directly linked

92 xample of a 1,2-dithienyldicyanoethene-based visible-light-driven chiral fluorescent molecular switch

93 i.e., nematic liquid crystals, enabled by a visible-light-driven chiral molecular switch.

94 n of FDH on dye-sensitized TiO(2) allows for visible-light-driven CO(2) reduction to formate in the a

95 iding a practical and efficient strategy for visible-light-driven H(2) O(2) production.

96 th high sensitivity and selectivity based on visible-light-driven heterojunction and biopolymer-enhan

97 Here we describe the visible-light-driven installation of side chains at dehy

98 A visible-light-driven molecular imprinting film was prepa

99 Visible-light-driven molecular switches endowing reversi

100 hich subsequently works as an efficient wide-visible-light-driven photocatalyst for converting CO(2)

101 rful strategy for expanding the potential of visible-light-driven radical synthetic chemistry.

102 hly investigated for CO2 electrochemical and visible-light-driven reduction.

103 lar switch with terminal iodo atoms exhibits visible-light-driven reversible unwinding, that is, a ch

104 The visible-light-driven rotation of an overcrowded alkene-b

105 Finally, the visible-light-driven water oxidation activity of type 1

106 The reaction, which is enabled by visible-light-driven, acridine-catalyzed decarboxylation

107 This visible-light-driven, reversible handedness inversion, e

108 which has good catalytic activity to absorb visible light due to the localized surface plasmon reson

109 re presented, suggesting the occurrence of a visible-light EDA complex which generates the aryl radic

110 We herein report the development of a visible light-enabled aza Paterno-Buchi reaction that su

111 totoxicity, minimal spectral cross talk with visible light excitable optogenetic tools and fluorescen

112 mains the significant hydrophobicity of most visible-light excitable photocaging groups.

113 The recent emergence of visible-light excitable photoprotecting groups has the p

114 ly generates increased amounts of H(2) under visible light exposure with the highest H(2) generation

115 3.3 and 44.2 muM in the dark, whereas, after visible light exposure, the photosensitizers exhibited I

116 es in an external electric field with simple visible-light exposure.

117 hes were illuminated with linearly polarised visible light for 5, 15, 25 and 50 h.

118 netics is an optical technique that exploits visible light for selective neuromodulation with spatio-

119 enerating enhanced anodic photocurrent under visible light for signaling.

120 ein, we report a novel transition-metal- and visible-light-free room-temperature radical approach for

121 rformed at ambient temperature and driven by visible light from commercially available LEDs.

122 vert to spiropyran moieties upon exposure to visible light have been extensively studied as they can

123 abilized alkyl radicals when irradiated with visible light; however, they are not known to form unsta

124 ntum yield of 50+/-4 % (lambda=400 nm) under visible light illumination (AM 1.5G, 100 mW cm(-2) , lam

125 Under visible light illumination, the onset potential for CO(2

126 ligand capped CsPbBr(3) perovskite QDs under visible light illumination.

127 a turnover number (TON) of over 52,000 under visible light illumination.

128 Acridine orange dye (AO) was evaluated over visible light illumination.

129 a large open-circuit voltage of 0.61 V under visible light illumination.

130 alization of DNA is presented, notably using visible light in combination with NADH, the ubiquitous r

131 reduce vinyl pyridines when irradiated with visible light in the presence of a photoredox catalyst.

132 ntaneous optical enrichment upon exposure to visible light in the presence of three distinct molecula

133 Illumination with linearly polarised visible light indicated changes in the crystalline struc

134 ded with the compound, millisecond pulses of visible light induce a transient hyperpolarization follo

135 ble efficient sequential reactions involving visible light-induced aerobic hydroxylation of 4-nitroph

136 Development of a visible light-induced and singlet oxygen-mediated green

137 Visible light-induced borylation may provide access to s

138 Herein, we report a general, metal-free visible light-induced photocatalytic borylation platform

139 A new visible light-induced photocatalytic protocol enabling t

140 involving an imine condensation followed by visible light-induced photocyclization.

141 00 that mediates the previously unachievable visible light-induced single electron reduction of pheno

142 In addition, use of visible light-induced XPS for chemically resolved electr

143 Herein, we report visible-light-induced B-H insertions of HBpin with acyls

144 ydroperoxidation has been realized through a visible-light-induced Csp(3)-H activation.

145 Here visible-light-induced formation of a helical superstruct

146 Here we report a visible-light-induced intermolecular radical hydroalkyla

147 Visible-light-induced metal-free trifluoromethylation of

148 A mild visible-light-induced Pd-catalyzed intramolecular C-H ar

149 d transition-metal (TM)-catalyzed systems or visible-light-induced photocatalytic systems that would

150 Very recently, transition-metal-free visible-light-induced radical approaches have emerged as

151 with alpha-halo carbonyl compounds through a visible-light-induced radical hydroalkylation, which cou

152 stic studies support that this unprecedented visible-light-induced reactivity is enabled by the abili

153 owever, due to limited tissue penetration of visible light, invasive craniotomy and intracranial impl

154 yst retains 60 % CO evolution activity under visible light irradiation (lambda>400 nm) and displays m

155 ion of the ethylenic junctions is induced by visible light irradiation (with a thermal back conversio

156 nt radicals derived from alkyl iodides under visible light irradiation add to the central strained bo

157 se reactions occur at room temperature under visible light irradiation and are catalyzed by the combi

158 However, photosubstitution by visible light irradiation in acetonitrile was possible f

159 mediates and occur at room temperature under visible light irradiation in the presence of an iridium

160 Visible light irradiation induced the selective crystall

161 rogen peroxide oxidation with broad spectrum visible light irradiation of the entire specimen.

162 ivity with almost 100 % yield achieved under visible light irradiation using [Ru(bpy)(3) ](2+) as the

163 the rate of Congo red dye degradation under visible light irradiation, and the decomposition efficie

164 m pure water under simulated solar light and visible light irradiation, respectively.

165 s metal-metal to ligand charge transfer upon visible light irradiation, which is responsible for cata

166 ) ion at mild electrochemical potential with visible light irradiation.

167 imide esters using an Ir photocatalyst under visible light irradiation.

168 base, and proceeds at room temperature under visible light irradiation.

169 ion, triggered by alternating between UV and visible light irradiation.

170 ehalogenation reaction of aryl halides under visible light irradiation.

171 r carbon dioxide conversion to formate under visible light irradiation.

172 ocages allow the release of substrates using visible light irradiation.

173 s with conversion efficiency above 99% under visible light irradiation.

174 xy-dimethyl aniline was modulated in situ by visible light irradiation.

175 and oxidative potential (OP) of soot due to visible-light irradiation and its underlying mechanisms

176 t Grignard monomers readily polymerize under visible-light irradiation at room temperature in the abs

177 Finally, we have found that visible-light irradiation has a positive impact under el

178 r visible-light stimuli; however, the use of visible-light irradiation has intrinsic challenges.

179 their corresponding aldehydes/ketones under visible-light irradiation in air at room temperature, wh

180 These reactions occur under visible-light irradiation in the presence of an Ir(III)

181 proposed that elemental carbon in soot under visible-light irradiation initiated an inside-to-outside

182 perature and under metal-free conditions and visible-light irradiation using pyrylium salt as a photo

183 proceed in 1,2-dichloroethane solvent under visible-light irradiation, and the active catalyst is ge

184 y, enabled by metal catalysts, additives, or visible-light irradiation, can be applied in transannula

185 l diazonium salts and pyridine allows, under visible-light irradiation, the synthesis of biaryls in m

186 time, and extremely large on/off ratio upon visible-light irradiation.

187 s well as high-rate production of H(2) under visible-light irradiation.

188 cross-links remain stabilized for as long as visible light is present, thereby retaining the material

189 amides from alcohols and amines mediated by visible light is presented.

190 rescence switches, particularly triggered by visible light, is of increasing interest for the potenti

191 the catalyst shows significant absorption of visible light, it has been applied for the photocatalyti

192 hotoscission upon exposure to cytocompatible visible light (lambda ~ 400 nm) in a dose-dependent mann

193 Conventional silicon solar panels block visible light making them unfeasible to cover all the su

194 es is usually below the diffraction limit of visible light, making it impossible to resolve their val

195 Regardless of the presence of O(3), visible light markedly promoted oxidation of soot, which

196 rein, we use these probes to demonstrate the visible light mediated bidirectional control over the ac

197 Visible-light mediated aerobic dehydrogenation of N-hete

198 A general platform for visible-light mediated intermolecular [2 + 2] cycloaddit

199 as well as electron transfer pathways in the visible light-mediated C-N bond formation.

200 We report a visible light-mediated flow process for C-N cross-coupli

201 The method combines a visible light-mediated Ni/Ir-photoredox dual catalytic N

202 Visible light-mediated photocatalytic organic transforma

203 ss to the key tetrahydropyran core through a visible light-mediated photoredox reaction from an allyl

204 This one-pot method features a visible-light-mediated [4+2] cycloaddition between an ar

205 ene-arenophile para-cycloadducts, formed via visible-light-mediated [4+2]-photocycloaddition that und

206 The development of visible-light-mediated allylation of unactivated sp(3) C

207 We report a visible-light-mediated benzylic C-H oxygenation reaction

208 Herein, we report a visible-light-mediated carboxylation of benzylic C-H bon

209 y, the reaction proceeds smoothly under mild visible-light-mediated conditions at room temperature, p

210 Here we report a visible-light-mediated intermolecular aza Paterno-Buchi

211 A visible-light-mediated late-stage aminocarbonylation of

212 lization, and (c) transition-metal catalyzed visible-light-mediated light photoredox catalysis.

213 We report a general visible-light-mediated strategy that enables the constru

214 An efficient protocol for visible-light-mediated synthesis of a specific class of

215 e investigation was made of a unique kind of visible light metamaterial absorber comprising elliptica

216 Alternately, a visible light method has been used for deprotection of N

217 ever, the limited deep-tissue penetration of visible light needed for QD activation, and concern over

218 reversible photoisomerization in response to visible light of different wavelengths due to the band s

219 be photoisomerized in both directions using visible light of different wavelengths, a promising attr

220 versible photoisomerization upon exposure to visible light of different wavelengths.

221 helical superstructure upon irradiation with visible light of different wavelengths.

222 esteric phases can be reversibly tuned using visible light of two different wavelengths.

223 urpose, here we report on MChD detected with visible light on a chiral magnetic helix formulated as [

224 de with a digital micromirror device shining visible light onto silicon acts as the spatial THz modul

225 retinal oxygen metabolic rate in rats using visible-light optical coherence tomography.

226 t fulfills multiple functions by 1) enabling visible-light pai->pai* excitation of the catalyst-bound

227 A colloidal system for visible-light photo-H(2) generation is made by building

228 sitization of mammalian cells and neurons by visible-light photoactivation of signaling molecules.

229 Visible-light photocatalysis and electrocatalysis are tw

230 s similar to those recently discovered using visible-light photocatalysis but without the use of an e

231 al phosphoric acid based organocatalysis and visible-light photocatalysis have both emerged as promis

232 We describe the synthesis through visible-light photocatalysis of novel functionalized tet

233 To this end, visible-light photocatalysis offers unique opportunities

234 nsequently, the catalyst exhibits a superior visible-light photocatalytic hydrogen production rate (~

235 Along with paragraphs discussing the visible-light photocatalytic synthetic protocols so far

236 ng low-cost plasmonic material for prompting visible-light photochemical reactions.

237 A transition metal- and oxidant-free visible light-photoinduced protocol for direct functiona

238 In this report, we describe the visible light photolysis of aryl diazoacetates in the pr

239 ed by triplet photosensitizers, which absorb visible-light photons and transfer the energy to the sub

240 edox catalyst to harness the energy from two visible-light photons to affect a single, high-energy ch

241 We report the use of a rhodium(II) dimer in visible light photoredox catalysis for the aerobic oxida

242 bered alpha-3 degrees primary amines through visible light photoredox catalysis.

243 we disclose the use of polysulfide anions as visible light photoredox catalysts for aryl cross-coupli

244 The discovery of this visible light photoredox reaction was enabled through th

245 The focus of this Minireview is the use of visible-light photoredox catalysis in the synthesis of t

246 Employing visible-light photoredox catalysis, primary sulfonamides

247 and chromone-3-carboxylic acids by means of visible-light photoredox catalysis.

248 Visible-light photoredox chlorosulfonation of alkenes an

249 In particular, with the Ru-dye as visible light photosensitizer, hierarchical Ni(OH)(2) na

250 A substantial photoconductance and visible-light photovoltaic effect are found in radical h

251 he methanol oxidation reaction (MOR) and the visible-light plasmonic response of Ag.

252 The UV and visible light portions of the solar light spectrum are e

253 Only recently, visible light-promoted carbene transfer reactions of dia

254 This review summarises the impact of visible light-promoted chemistry on the functionalizatio

255 An organic dye-catalyzed visible light-promoted ketocarbonylation protocol of vin

256 Biaryls were synthesized via a novel visible-light-promoted Gomberg-Bachmann reaction that do

257 A continuous-flow, visible-light-promoted method has been developed to over

258 The protocol involves the visible-light-promoted oxidative amidation of amines wit

259 A visible-light-promoted regioselective C(sp(2))-H/C(sp(3)

260 In this sequence, we have developed a visible-light-promoted regioselective C3-H trifluorometh

261 A visible-light-promoted regioselective coupling of C(sp(3

262 A visible-light-promoted three-component isocyanide-based

263 o dyes (Acid Blue-113, AB-113) (~ 99%) under visible light radiation.

264 To address the limitation of visible light readouts-namely high background-IRDye 800C

265 imultaneous, yet independent, exploration of visible-light reflection alongside audible sound-wave ge

266 hobic film showed transparency of 90% in the visible light region with a static water contact angle o

267 s of the human visual system even beyond the visible light region.

268 d gap of TC-GQD nanocomposite was shifted to visible lights relative to its components (1.3 eV), and

269 deeper structures of the nervous system, by visible light, remains a technical challenge.

270 Significantly, upon exposure to air and visible light residing in their absorption regime (365-6

271 benzene is well compatible for the design of visible-light-responsive systems, providing stable and b

272 ch are responsible for sensitivity to UV and visible light), retinal photoreceptors, and ocular lense

273 sphoric acid backbones presenting one or two visible-light-sensitive thioxanthone moieties have been

274 C(3)N(5) was also shown to be an effective visible light sensitizer for TiO(2) photoanodes in photo

275 perovskite solar cells under gamma-rays and visible light simultaneously is reported.

276 liquid polymer formulation by switching one visible light source on-and-off without the need for any

277 d FAF simultaneously with a single broadband visible light source.

278 ion, settling/centrifugation, pipetting, and visible-light spectroscopy, we developed a novel techniq

279 These HDP materials emit over the entire visible light spectrum, centered at 600 +/- 30 nm with f

280 absorption band in the yellow region of the visible light spectrum, no adequate explanation of the m

281 Within the visible light spectrum, red light induces stomatal openi

282 chemistry, and describe the use of localised visible light stimuli on photoconductor/liquid and semic

283 l of these reactions require ultraviolet- or visible-light stimuli; however, the use of visible-light

284 Under the visible light, the photobioanode shows an anodic photocu

285 Even when the two precursors do not absorb visible light, the resulting EDA complex often does.

286 Upon visible-light, the substrates interacted with the vitami

287 For example, the penetration of visible light through most reaction media is very low, l

288 Optogenetics, which uses visible light to control the cells genetically modified

289 ical dication undergoes photoexcitation with visible light to produce an excited-state species with o

290 OPT uses visible light to visualize the 3D morphology of large tr

291 An ultrasensitive Visible light-triggered photoelectrochemical (PEC) senso

292 its open, merocyanine form, and exposure to visible light triggers dissociation of polymer cross-lin

293 of mammalian origin by use of photoswitches, visible light (typically), and genetic modification.

294 Polymerizations are performed under visible light using an oxygen tolerant porphyrin-catalyz

295 ived phenyliodonium ylide in the presence of visible light using experiment and theory.

296 photocatalytic degradation of rhodamine B by visible light using two different structurally well-defi

297 The effect of the infrared (IR) and visible light (Vis) components of solar radiation on ski

298 erstanding of thiol-ene curing kinetics with visible light, we varied the printing parameters (e.g.,

299 onal device onto a window glass transmitting visible light while simultaneously guiding near infrared

300 ferent air/fuel ratios (A/F) were aged under visible light with or without ozone (O(3)) at an atmosph