ライフサイエンスコーパス: electronic absorption

1 modes are detectable as a modulation of the electronic absorption.

2 and unambiguous assignment for the observed electronic absorptions.

3 Raman, resonance Raman, electronic absorption (2-325 K in 2-MeTHF), and emission

4 traviolet/visible/near-infrared (UV/vis/NIR) electronic absorption, (57)Fe Mossbauer, X-band electron

5 based on extensive spectroscopic [UV/vis/NIR electronic absorption, (57)Fe Mossbauer, X-band EPR, res

6 In this study, we have employed electronic absorption (Abs) and magnetic circular dichro

7 vities in biological systems; however, their electronic absorption (Abs) spectra have remained largel

8 Minimal perturbations to the electronic absorption (Abs), circular dichroism (CD), an

9 enzymatic Co-C bond activation, we employed electronic absorption (Abs), magnetic circular dichroism

10 ess as assayed by fluorescence quenching and electronic absorption analyses.

11 been studied at low temperatures, where its electronic absorption and (1)H NMR spectra were recorded

12 tions reproduce the red shifts in the flavin electronic absorption and carbonyl stretch infrared spec

13 chiometry of the holoprotein is supported by electronic absorption and circular dichroism spectra, as

14 Their electronic absorption and electrochemical properties in

15 The electronic absorption and electrochemical properties of

16 Synthesis was monitored by electronic absorption and electron paramagnetic resonanc

17 in peroxidase (LiP) has been investigated by electronic absorption and electron paramagnetic resonanc

18 ents have little influence over the polymers electronic absorption and emission properties in solutio

19 splayed a modest bathochromic shift in their electronic absorption and emission spectra as compared t

20 ffects of small structural variations on the electronic absorption and emission spectra have been exp

21 onding zinc macrocycles and studies of their electronic absorption and emission spectra, electrochemi

22 Variable-temperature (1)H NMR and electronic absorption and emission spectroscopies were u

23 Electronic absorption and emission spectroscopy confirme

24 urfactant suspensions have revealed distinct electronic absorption and emission transitions for more

25 In the present report, electronic absorption and EPR analysis of various substi

26 ms a 1:1 monomeric complex with FeIII, whose electronic absorption and EPR spectra closely resemble t

27 Electronic absorption and EPR spectra of [Co_(DapE)] and

28 The electronic absorption and EPR spectra of [CoCo(AAP)], [C

29 nuclear active site of AAP, we have recorded electronic absorption and EPR spectra of Co(II)Co(II)-,

30 was further supported by the changes in the electronic absorption and EPR spectra when cyanide was a

31 The transient electronic absorption and fluorescence data evidence tha

32 m preparation, and the polarization of their electronic absorption and fluorescence spectra at differ

33 n support of the interaction was obtained by electronic absorption and fluorescence spectroscopy and

34 Ligand-field electronic absorption and magnetic circular dichroism (M

35 verified by high-resolution low-temperature electronic absorption and magnetic circular dichroism (M

36 Electronic absorption and magnetic circular dichroism (M

37 Electronic absorption and magnetic circular dichroism sp

38 ere, we use a combination of low-temperature electronic absorption and magnetic circular dichroism, e

39 Analysis of low-temperature electronic absorption and MCD spectra revealed excitonic

40 Electronic absorption and metal analysis suggest that th

41 ensive single crystal X-ray diffraction, and electronic absorption and Mossbauer spectroscopy.

42 In addition, the electronic absorption and reduction stoichiometries with

43 a(2):eta(2)-O(2)(2-))Cu(II)} complexes (with electronic absorption and resonance Raman (rR) spectrosc

44 ms of sGC activation were investigated using electronic absorption and resonance Raman (RR) spectrosc

45 Electronic absorption and resonance Raman spectra are pr

46 Electronic absorption and resonance Raman spectra of fer

47 The observed trends in electronic absorption and resonance Raman spectral featu

48 Variable-temperature electronic absorption and resonance Raman spectroscopies

49 Characterization of ligand binding by electronic absorption and resonance Raman spectroscopy i

50 tion solely to a low-spin (S = 1/2) species, electronic absorption and resonance Raman spectroscopy p

51 Electronic absorption and resonance Raman spectroscopy r

52 Electronic absorption and resonance Raman spectroscopy w

53 eir structural similarity, as ascertained by electronic absorption and resonance Raman spectroscopy,

54 (57)Fe-Mossbauer spectroscopy as well as by electronic absorption and resonance Raman spectroscopy.

55 Electronic absorption and resonance-enhanced Raman spect

56 A combination of femtosecond electronic absorption and stimulated Raman spectroscopie

57 Electronic absorption and stimulated resonance Raman spe

58 Here we employ a combination of electronic absorption and variable-temperature magnetic

59 ination of in situ powder X-ray diffraction, electronic absorption and vibrational spectroscopy, dc r

60 The infrared, electronic absorption, and electron paramagnetic resonan

61 The infrared, electronic absorption, and electron paramagnetic resonan

62 have been studied by (1)H NMR, 2D ROESY NMR, electronic absorption, and emission spectroscopies.

63 Proton NMR, electronic absorption, and fluorescence emission spectro

64 On the basis of circular dichroism (CD), electronic absorption, and fluorescence spectra, the sec

65 ed by electron paramagnetic resonance (EPR), electronic absorption, and magnetic circular dichroism (

66 Electronic paramagnetic resonance (EPR), electronic absorption, and magnetic circular dichroism s

67 copic techniques, including resonance Raman, electronic absorption, and variable temperature/variable

68 lkoxide cluster was established by infrared, electronic absorption, and X-ray photoelectron spectrosc

69 ical methods, including (1)H NMR, UV/vis/NIR electronic absorption, as well as EPR spectroscopy and S

70 sitions arising from this species yielded an electronic absorption band at 324 nm with a shoulder at

71 apidly inactivates the enzyme and shifts the electronic absorption band from 420 to 325 nm.

72 nce compounds, including a unique low-energy electronic absorption band, attributed to an IVCT-type t

73 ular hypsochromic shift of its lowest energy electronic absorption band.

74 onfirm that at least one of the lower-energy electronic absorption bands (E(max) approximately 16300

75 in a full assignment of the observed MCD and electronic absorption bands, a detailed understanding of

76 tuted extended pentafulvenes feature intense electronic absorption bands, extending over the entire v

77 Through the use of electronic absorption, circular dichroism (CD), and magn

78 properties of this highly reactive species, electronic absorption, circular dichroism (CD), magnetic

79 Electronic absorption, circular dichroism (CD), magnetic

80 Using redox potentiometry, electronic absorption, circular dichroism (CD), magnetic

81 The electronic absorption data also indicated that both Co(I

82 On the basis of EPR and electronic absorption data for Co(II)-substituted AAP, n

83 The electronic absorption data imply that the type 1 site in

84 The compounds show intense electronic absorptions due to metal-to-bridge charge tra

85 Electronic absorption, electron paramagnetic resonance,

86 heme sites of SoxAX have been analyzed using electronic absorption, electron paramagnetic resonance,

87 d field of the Mn(IV) center, as assessed by electronic absorption, electron paramagnetic resonance,

88 An array of spectroscopic characterizations (electronic absorption, electron paramagnetic resonance,

89 iffraction and opto-electronic properties by electronic absorption/emission spectra and electrochemic

90 work focuses on theoretical understanding of electronic absorption energies of N,N-dimethylaniline wi

91 urally probe the metal binding site in VanX, electronic absorption, EPR, and extended x-ray absorptio

92 Electronic absorption, EPR, and resonance Raman spectros

93 te inhibitor is observed to be protonated in electronic absorption experiments.

94 Electronic absorption, Fe K-edge X-ray absorption, reson

95 2 displayed electronic absorption features (lambdamax =460, 610 nm)

96 is cross-links that give rise to distinctive electronic absorption features between 300-400 nm.

97 eport and demonstrate the importance of weak electronic absorption features, normally ignored or not

98 acterized by a range of techniques including electronic absorption, fluorescence emission, NMR and ti

99 th (1)H, (11)B, (13)C, (15)N, and (19)F NMR, electronic absorption, fluorescence spectroscopies, and

100 Cyclic voltammetric studies, as well as NMR, electronic absorption, fluorescence, and femtosecond pum

101 Calculated electronic absorptions for the protonated (356 nm) and n

102 effect of octyl substituents on the onset of electronic absorption in annelated beta-trithiophenes is

103 d component in that it promotes lower energy electronic absorption in its metal complexes and also pr

104 The electronic absorption in the UV and visible region (UV-v

105 The carbene exhibits a weak electronic absorption in the visible spectrum (lambda(ma

106 ally locked pi system and shows very intense electronic absorptions in the Q range of the electronic

107 e transient broadening and spectral shift of electronic absorption is induced by a picosecond THz fie

108 Upon irradiation into the near-UV electronic absorption (lambdamax 350 nm), MeC3Me ((3)3)

109 The electronic absorption line shape and Stark spectrum of t

110 y(2)(Me))](+), were examined in detail using electronic absorption, low-temperature magnetic circular

111 Electronic absorption, magnetic circular dichroism (MCD)

112 n addition to EPR spectroscopy, we have used electronic absorption, magnetic circular dichroism (MCD)

113 es of Co (2+)Cbl and Co (2+)Cbi (+) by using electronic absorption, magnetic circular dichroism, and

114 ay overcome this challenge, we have employed electronic absorption, magnetic circular dichroism, and

115 peroxidase (C420) have been characterized by electronic absorption, magnetic circular dichroism, and

116 aracterized several enzyme variants by using electronic absorption, magnetic circular dichroism, and

117 Electronic absorption, magnetic circular dichroism, and

118 The electronic absorption, magnetic circular dichroism, and

119 Our electronic absorption, magnetic circular dichroism, and

120 nanocrystals were synthesized and studied by electronic absorption, magnetic circular dichroism, tran

121 ) nanocrystals and their characterization by electronic absorption, magnetic circular dichroism, X-ra

122 reported in cupredoxins before, with intense electronic absorption maxima at ~410 and 760 nm.

123 The value of the electronic absorption maximum for the HAV 3C (C24S) acyl

124 ns of E75 and Rev-erbbeta were studied using electronic absorption, MCD, resonance Raman, and EPR spe

125 BxRcoM-2 was studied using electronic absorption, MCD, resonance Raman, and EPR spe

126 From electronic absorption measurements binding constants in

127 Ultrafast time-resolved electronic absorption measurements revealed lifetimes fo

128 1:1 complex, which has been characterized by electronic absorption, Mossbauer, and NMR spectroscopies

129 Redox and spectroscopic (electronic absorption, multifrequency electron paramagne

130 R) vibrational, ultraviolet/visible (UV/vis) electronic absorption, multinuclear NMR, X-band electron

131 as (57)Fe Mossbauer, IR vibrational, UV/vis electronic absorption, multinuclear NMR, X-band EPR, and

132 or variants with axial ligand substitutions, electronic absorption, near-UV circular dichroism, and e

133 tuted ImiS was prepared and characterized by electronic absorption, NMR, and EPR spectroscopies.

134 lationships that lead to near-infrared (NIR) electronic absorption of chromophores are described.

135 rgon laser was used to resonantly excite the electronic absorption of the carotenoid pigments, and sc

136 hing of the laser excitation source with the electronic absorption of the target molecule.

137 dge potentials of ZnO was investigated using electronic absorption, photoluminescence, and magnetic c

138 to separate the vibrational signal from the (electronic) absorption processes.

139 of the FAD, although considerable changes in electronic absorption properties are observed in oxidize

140 The electronic absorption properties of the Co(2+) ion were

141 ted backbone of the bipyridine moiety on the electronic absorption properties of the title chromophor

142 roscopic characterization of heme binding by electronic absorption, resonance Raman, and EPR has show

143 Electronic absorption, resonance Raman, and ground- and

144 ployed a multidimensional approach involving electronic absorption, S and Cu K-edge XAS, EPR, and res

145 ues including nuclear magnetic resonance and electronic absorption specrtoscopies.

146 e S(Cys)-Cu charge transfer (CT) band in the electronic absorption spectra and < 8 gauss changes in t

147 rmational preferences are identified through electronic absorption spectra and associated computation

148 Cryogenic UV/Vis electronic absorption spectra and vibrational Raman spec

149 The electronic absorption spectra are characterized by low-

150 The electronic absorption spectra are dominated by dithiolen

151 differences in the experimental NMR data and electronic absorption spectra for pKSI and tKSI, two hom

152 Electronic absorption spectra of 2, 3, and 4 reveal a ch

153 Both the calculated and experimental electronic absorption spectra of 4 are comparable to tho

154 Electronic absorption spectra of BM3-DDAB films on silic

155 Electronic absorption spectra of Co(II)-loaded H178A EcM

156 Furthermore, the electronic absorption spectra of Co(II)-loaded MetAP ind

157 We track the evolution of highly-resolved electronic absorption spectra of gold nanoclusters with

158 Examination of the electronic absorption spectra of the bridging ligands sh

159 Electronic absorption spectra of the catalytically compe

160 The electronic absorption spectra of the CoII complexes show

161 The electronic absorption spectra of the phenothiazine deriv

162 In contrast to the EPR spectra, the electronic absorption spectra of the rotamers of triplet

163 The electronic absorption spectra of the tropone-fused porph

164 Electronic absorption spectra of thionin-oxidized and CO

165 Electronic absorption spectra of water cluster anions (H

166 R spectrum and the temperature dependence of electronic absorption spectra revealed that the heme iro

167 Electronic absorption spectra show significant red-shift

168 layered structure, electronic structure, and electronic absorption spectra were determined.

169 Correlation of electronic absorption spectra with activity measurements

170 racterized by comparison of its (1)H NMR and electronic absorption spectra with calculated spectra.

171 His79Ala apoenzyme and the comparison of its electronic absorption spectra with other variants sugges

172 dged annulene structures have porphyrin-like electronic absorption spectra with strong Soret bands ne

173 ic structure, spin and charge distributions, electronic absorption spectra, and electron affinity and

174 y, electronic and thermodynamic stabilities, electronic absorption spectra, and electron detachment e

175 ochromic shift ( approximately 10 nm) in the electronic absorption spectra, and the long wavelength a

176 iable-temperature (1)H NMR/ESR measurements, electronic absorption spectra, and theoretical calculati

177 s documented by signature changes in NMR and electronic absorption spectra, as well as by cyclic volt

178 W51H/H52W), and CcP(W51H/H52L), have altered electronic absorption spectra, indicating that the heme

179 Electronic absorption spectra, recorded at pH 7.5 of [Co

180 Electronic absorption spectra, resonance Raman and FTIR

181 ce of a shoulder feature on the blue edge of electronic absorption spectra, which many have attribute

182 bathochromic shift of their Q bands in their electronic absorption spectra.

183 complexes showed a remarkable shift in their electronic absorption spectra.

184 so displayed significant variations in their electronic absorption spectra.

185 ors) and amiodarone (AM) was performed using electronic absorption spectra.

186 )H, (13)C, and (15)N NMR chemical shifts and electronic absorption spectra.

187 e conformation via striking variation in its electronic absorption spectra.

188 nding network on the NMR chemical shifts and electronic absorption spectra.

189 Electronic absorption spectral titration of a 1 mM sampl

190 Electronic absorption spectral titration of a 1 mM sampl

191 ite with N2S2-donor ligands, consistent with electronic absorption spectroscopic results indicating t

192 Spectroscopic analysis using infrared and electronic absorption spectroscopies affords resolution

193 ng various techniques including (1)H NMR and electronic absorption spectroscopies and cyclic voltamme

194 rized via multinuclear NMR, vibrational, and electronic absorption spectroscopies and, in some cases,

195 characterized using (1)H NMR, infrared, and electronic absorption spectroscopies as well as X-ray cr

196 Electron paramagnetic resonance and electronic absorption spectroscopies, combined with addi

197 biophysical approach involving Mossbauer and electronic absorption spectroscopies, electron paramagne

198 GH2 (2+) ) was investigated by (1) H NMR and electronic absorption spectroscopies, electrospray mass

199 ures elucidated using multinuclear NMR, EPR, electronic absorption spectroscopies, SQUID magnetometry

200 y single-crystal X-ray diffraction, NMR, and electronic absorption spectroscopies.

201 n has involved various techniques, including electronic absorption spectroscopy and cyclic voltammetr

202 salts by using various techniques including electronic absorption spectroscopy and cyclic voltammetr

203 erized by using various techniques including electronic absorption spectroscopy and cyclic voltammetr

204 erized by using various techniques including electronic absorption spectroscopy and cyclic voltammetr

205 rized by using various techniques, including electronic absorption spectroscopy and cyclic voltammetr

206 salts by using various techniques including electronic absorption spectroscopy and cyclic voltammetr

207 cucurbit[6]uril (CB6), were investigated by electronic absorption spectroscopy and DFT computational

208 in dichloromethane using ultrafast transient electronic absorption spectroscopy and quantum chemical

209 Electronic absorption spectroscopy and variable-temperat

210 d the structure of this protein (SbHbN) with electronic absorption spectroscopy and X-ray crystallogr

211 tal-to-ligand stoichiometry as determined by electronic absorption spectroscopy and X-ray diffraction

212 e basis of (57)Fe Mossbauer, EPR, and UV/vis electronic absorption spectroscopy as well as quantum ch

213 X-ray crystallography, EPR spectroscopy, and electronic absorption spectroscopy as well as SQUID magn

214 Simultaneous cyclic voltammetry and electronic absorption spectroscopy define reduction pote

215 Near-IR electronic absorption spectroscopy for 1 and 2 reveals a

216 Electronic absorption spectroscopy has been used to stud

217 NCO(-), N(3)(-)), has been characterized by electronic absorption spectroscopy in the visible and ne

218 The electronic absorption spectroscopy is an essential tool

219 Additionally, electronic absorption spectroscopy reveals that FeII CBS

220 Stopped-flow electronic absorption spectroscopy reveals the rapid for

221 mperature, and temperature-dependent NMR and electronic absorption spectroscopy studies show the ener

222 Electronic absorption spectroscopy studies showed that u

223 Analysis by electronic absorption spectroscopy supports the trivalen

224 aper reports the application of ligand-field electronic absorption spectroscopy to probe Co(2+) dopan

225 We used fluorescence and electronic absorption spectroscopy to study the molecula

226 at exploit variable-temperature ground-state electronic absorption spectroscopy unambiguously demonst

227 Electronic absorption spectroscopy was used to show that

228 ctrometry, N-terminal sequence analysis, and electronic absorption spectroscopy we show that fumagill

229 pic (S K-edge X-ray absorption spectroscopy, electronic absorption spectroscopy, and circular dichroi

230 f X-ray crystallography, Raman spectroscopy, electronic absorption spectroscopy, and density function

231 1 and 2 were examined by reactivity studies, electronic absorption spectroscopy, and density function

232 on of variable-temperature EPR spectroscopy, electronic absorption spectroscopy, and magnetic suscept

233 dazyl radicals were characterized by EPR and electronic absorption spectroscopy, and results were ana

234 zinyl radicals were characterized by EPR and electronic absorption spectroscopy, and the results were

235 Resonance Raman spectroscopy, electronic absorption spectroscopy, and the time-depende

236 1)P nuclear magnetic resonance spectroscopy, electronic absorption spectroscopy, cyclic voltammetry,

237 Using electronic absorption spectroscopy, electrical transport

238 Using electronic absorption spectroscopy, it was observed that

239 zed and studied by X-ray powder diffraction, electronic absorption spectroscopy, magnetic circular di

240 pported by means of (15)N-isotopic labeling, electronic absorption spectroscopy, magnetometry, electr

241 re studied by cyclic voltammetry, UV-vis-NIR electronic absorption spectroscopy, NMR, X-ray crystallo

242 A combination of X-ray crystallography, electronic absorption spectroscopy, resonance Raman spec

243 ned for reactivity, by using low-temperature electronic absorption spectroscopy, toward a number of b

244 e have investigated the enzyme mechanism via electronic absorption spectroscopy, using chemometric an

245 examined using Mossbauer spectroscopy, EPR, electronic absorption spectroscopy, X-ray absorption spe

246 mx1), and human cytochrome P450 CYP3A4 using electronic absorption spectroscopy.

247 y characterized by X-ray crystallography and electronic absorption spectroscopy.

248 studied by resonance Raman spectroscopy and electronic absorption spectroscopy.

249 and elemental analysis, and by infrared and electronic absorption spectroscopy.

250 )N(3)(Et,Pr))](+) using variable-temperature electronic absorption spectroscopy.

251 circular dichroism, circular dichroism, and electronic absorption spectroscopy.

252 R spectroscopy with assignments confirmed by electronic absorption spectroscopy.

253 terized by single-crystal and solution-state electronic absorption spectroscopy.

254 me a, b, and c centers were quantified using electronic absorption spectroscopy.

255 Moreover, we study the electronic absorption spectrum and calculate the rate co

256 Moreover, we study the electronic absorption spectrum and calculate the rate co

257 at even if reported anisotropy values in the electronic absorption spectrum are low, the dissociation

258 panying rather small changes in the observed electronic absorption spectrum are suggestive of a modif

259 The electronic absorption spectrum of (k33)(2)PD(+) is calcu

260 itals, a splitting that is manifested in the electronic absorption spectrum of 1 (lambda = 610 nm, ep

261 The electronic absorption spectrum of 1 exhibits a weak tran

262 The electronic absorption spectrum of 2 displayed features (

263 The electronic absorption spectrum of 3 features a broad obs

264 greater than the anisotropy reported in the electronic absorption spectrum of gas-phase leucine ense

265 EPR spectrum of I(+)PF(6) in 2-MeTHF and the electronic absorption spectrum of I(+)PF(6)(-) in THF ar

266 py, which simultaneously probes the size and electronic absorption spectrum of molecules and particle

267 The electronic absorption spectrum of solubilized beef heart

268 The electronic absorption spectrum of the aqueous electron i

269 The electronic absorption spectrum of the Co(II)-substituted

270 In addition, the temperature-dependent electronic absorption spectrum of the Ni(II) complex, Tp

271 We also show that the electronic absorption spectrum of the triple pancake bon

272 intermediate with a hypsochromically shifted electronic absorption spectrum relative to the starting

273 opper, the protein is active and displays an electronic absorption spectrum with lambda(max) at 504 n

274 The electronic absorption spectrum, susceptibility to fluori

275 rmational change evidenced by changes in the electronic absorption spectrum.

276 phyrin that exhibited a strongly red-shifted electronic absorption spectrum.

277 Electronic absorption studies of Co(II)(1)-ImiS revealed

278 ture of these dimers in solution is unknown, electronic absorption studies suggest that they have [TT

279 ghlights how photochemistry in the neglected electronic absorption tail makes an important addition t

280 X-ray absorption spectroscopy (XAS) is an electronic absorption technique for which the initial st

281 supported by both the cyclic voltammetry and electronic absorption titrations.

282 erred site of reduction, while time-resolved electronic absorption (TrA) spectroscopy highlights the

283 antum mechanical (QM) treatment to calculate electronic absorption (UV-vis) and circular dichroism (C

284 R, (57)Fe Mossbauer spectroscopy, UV-visible electronic absorption, variable-temperature X-ray diffra

285 ratures, has been monitored by CD as well by electronic absorption (with the oxidized protein) and by