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

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

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

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

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

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

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

11 The electronic absorption and electrochemical properties of

12 Synthesis was monitored by electronic absorption and electron paramagnetic resonanc

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

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

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

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

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

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

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

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

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

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

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

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

25 The transient electronic absorption and fluorescence data evidence tha

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

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

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

29 Electronic absorption and magnetic circular dichroism (M

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

31 Electronic absorption and magnetic circular dichroism sp

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

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

34 Electronic absorption and metal analysis suggest that th

35 In addition, the electronic absorption and reduction stoichiometries with

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

37 Electronic absorption and resonance Raman spectra are pr

38 Electronic absorption and resonance Raman spectra of fer

39 Variable-temperature electronic absorption and resonance Raman spectroscopies

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

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

42 Electronic absorption and resonance Raman spectroscopy r

43 Electronic absorption and resonance Raman spectroscopy w

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

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

46 Electronic absorption and resonance-enhanced Raman spect

47 A combination of femtosecond electronic absorption and stimulated Raman spectroscopie

48 Electronic absorption and stimulated resonance Raman spe

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

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

51 The infrared, electronic absorption, and electron paramagnetic resonan

52 The infrared, electronic absorption, and electron paramagnetic resonan

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

54 Proton NMR, electronic absorption, and fluorescence emission spectro

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

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

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

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

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

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

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

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

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

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

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

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

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

68 Electronic absorption, circular dichroism (CD), magnetic

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

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

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

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

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

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

75 Electronic absorption, electron paramagnetic resonance,

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

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

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

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

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

81 Electronic absorption, EPR, and resonance Raman spectros

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

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

84 2 displayed electronic absorption features (lambdamax =460, 610 nm)

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

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

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

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

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

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

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

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

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

94 The electronic absorption line shape and Stark spectrum of t

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

96 Electronic absorption, magnetic circular dichroism (MCD)

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

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

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

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

101 Electronic absorption, magnetic circular dichroism, and

102 The electronic absorption, magnetic circular dichroism, and

103 Our electronic absorption, magnetic circular dichroism, and

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

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

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

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

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

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

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

111 From electronic absorption measurements binding constants in

112 1:1 complex, which has been characterized by electronic absorption, Mossbauer, and NMR spectroscopies

113 Redox and spectroscopic (electronic absorption, multifrequency electron paramagne

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

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

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

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

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

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

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

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

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

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

124 Electronic absorption, resonance Raman, and ground- and

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

126 The electronic absorption spectra are characterized by low-

127 The electronic absorption spectra are dominated by dithiolen

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

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

130 Electronic absorption spectra of BM3-DDAB films on silic

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

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

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

134 Electronic absorption spectra of the catalytically compe

135 The electronic absorption spectra of the CoII complexes show

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

137 Electronic absorption spectra of thionin-oxidized and CO

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

139 Electronic absorption spectra show significant red-shift

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

141 Correlation of electronic absorption spectra with activity measurements

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

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

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

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

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

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

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

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

150 Electronic absorption spectra, resonance Raman and FTIR

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

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

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

154 so displayed significant variations in their electronic absorption spectra.

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

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

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

158 Electronic absorption spectral titration of a 1 mM sampl

159 Electronic absorption spectral titration of a 1 mM sampl

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

175 Electronic absorption spectroscopy and variable-temperat

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

177 Simultaneous cyclic voltammetry and electronic absorption spectroscopy define reduction pote

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

179 Electronic absorption spectroscopy has been used to stud

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

181 The electronic absorption spectroscopy is an essential tool

182 Additionally, electronic absorption spectroscopy reveals that FeII CBS

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

184 Electronic absorption spectroscopy studies showed that u

185 Analysis by electronic absorption spectroscopy supports the trivalen

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

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

188 Electronic absorption spectroscopy was used to show that

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

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

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

192 1 and 2 were examined by reactivity studies, electronic absorption spectroscopy, and density function

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

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

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

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

197 Using electronic absorption spectroscopy, electrical transport

198 Using electronic absorption spectroscopy, it was observed that

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

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

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

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

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

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

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

206 studied by resonance Raman spectroscopy and electronic absorption spectroscopy.

207 R spectroscopy with assignments confirmed by electronic absorption spectroscopy.

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

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

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

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

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

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

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

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

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

217 The electronic absorption spectrum of 1 exhibits a weak tran

218 The electronic absorption spectrum of 3 features a broad obs

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

220 The electronic absorption spectrum of solubilized beef heart

221 The electronic absorption spectrum of the aqueous electron i

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

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

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

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

226 The electronic absorption spectrum, susceptibility to fluori

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

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

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

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

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

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

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