ライフサイエンスコーパス: spectroscopy

1 , electron microscopy, Raman, and UV-visible spectroscopies).

2 e high-valent state may be probed by in situ spectroscopy.

3 exclusion chromatography and Solid-state NMR spectroscopy.

4 lysis and Fourier transform infra-red (FTIR) spectroscopy.

5 as proved by elemental analysis, IR, and NMR spectroscopy.

6 s, trace element analysis, and time-resolved spectroscopy.

7 cs of active and inactive TNFalpha using NMR spectroscopy.

8 Raman and wavelength/energy dispersive X-ray spectroscopy.

9 copy in the UV and IR regions, and microwave spectroscopy.

10 ymers, as detected by solid-state (13) C NMR spectroscopy.

11 n frequency metrology, precision clocks, and spectroscopy.

12 zed and characterized structurally using NMR spectroscopy.

13 ytical Ultracentrifugation (AUC), and UV/Vis spectroscopy.

14 gical developments of 2D vibrational surface spectroscopy.

15 their polymer composition using micro-Raman spectroscopy.

16 ne nanoparticles and studied by solution NMR spectroscopy.

17 vivo (1)H-[(13)C]-nuclear magnetic resonance spectroscopy.

18 rostructure studied using XPS and UV-Vis-NIR spectroscopy.

19 for prokaryotic production to be used in NMR spectroscopy.

20 with (7) Li nuclear magnetic resonance (NMR) spectroscopy.

21 analyzed by excitation-emission fluorescence spectroscopy.

22 e been injvestigated by deep level transient spectroscopy.

23 henols has been investigated using (19)F NMR spectroscopy.

24 d glutamine) levels using magnetic resonance spectroscopy.

25 was carried out, using UV-visible absorption spectroscopy.

26 (7)Li solid-state nuclear magnetic resonance spectroscopy.

27 etry (hydrophilic fraction) and fluorescence spectroscopy.

28 n counting studies, and transient absorption spectroscopy.

29 ammetry, and electron paramagnetic resonance spectroscopy.

30 the resulting solids using (57)Fe Mossbauer spectroscopy.

31 nterrogated with Raman and photoluminescence spectroscopy.

32 especially for devices exploiting evanescent spectroscopy.

33 l phase, which was identified using infrared spectroscopy.

34 oscopy and spatio-temporal image correlation spectroscopy.

35 (31)P solid-state nuclear magnetic resonance spectroscopy.

36 ned by electron paramagnetic resonance (EPR) spectroscopy.

37 modes as also evidenced from THz time domain spectroscopy.

38 and diffusion using fluorescence correlation spectroscopy.

39 chlorophylls complexes was confirmed by FTIR spectroscopy.

40 e, UV-vis-NIR, and ultraviolet photoelectron spectroscopy.

41 ns including sugars were evaluated using NMR spectroscopy.

42 -MS/MS) and nuclear magnetic resonance (NMR) spectroscopy.

43 an be monitored in real time by fluorescence spectroscopy.

44 chrotron Radiation Circular Dichroism (SRCD) spectroscopy.

45 etric conformers can be distinguished by NMR spectroscopy.

46 inductively coupled plasma-optical emission spectroscopy.

47 constant of 9 M(-1) s(-1) as measured by NMR spectroscopy.

48 by dynamic light scattering (DLS) and UV/Vis spectroscopy.

49 nd time-resolved absorption and fluorescence spectroscopy.

50 acterized as intrinsically disordered by NMR spectroscopy.

51 evidenced by electron paramagnetic resonance spectroscopy.

52 nd humidity, using electrochemical impedance spectroscopy.

53 sured by fluorescence and circular dichroism spectroscopy.

54 imultaneously by FT-IR and 2D IR correlation spectroscopies.

55 posed procedure with laser-induced breakdown spectroscopy allowed the precise copper determination (c

56 ligands and verified using small angle x-ray spectroscopy, allows us to calculate the heat released i

57 Counterintuitively, we found that spectroscopy alone does not provide sufficient informati

58 etal ions was investigated with fluorescence spectroscopy, amongst them Fe(3+) ions showed quenching

59 e crystal was obtained by Andreev reflection spectroscopy analysis.

60 and further confirmed by X-ray photoelectron spectroscopy analysis.

61 effect is further supported by IR-MS action spectroscopy and ab initio calculations.

62 Bi target and characterized by photoelectron spectroscopy and ab initio calculations.

63 regions, as confirmed by X-ray photoelectron spectroscopy and atomic force microscopy experiments.

64 ry degradation was monitored using impedance spectroscopy and capacity tests; the results show that t

65 combinations was investigated by using FTIR spectroscopy and compared with the change in enzyme acti

66 We have used fluorescence correlation spectroscopy and cross-correlation spectroscopy to quant

67 re we show, using nuclear magnetic resonance spectroscopy and density functional theory, that a six-p

68 Circular dichroism spectroscopy and dynamic light scattering experiments ve

69 ter photobleaching, fluorescence correlation spectroscopy and electron microscopy in live cells, we s

70 Perry and colleagues now combine NMR spectroscopy and electrophysiological experiments to exp

71 n anti-inflammatory drug Piroxicam using THz spectroscopy and employed Principal Component Analysis t

72 the acid-induced unfolding of HdeA using NMR spectroscopy and fluorescence measurements, and obtained

73 X-ray absorption spectroscopy and high-energy X-ray scattering demonstrat

74 re characterized in the solid state by Raman spectroscopy and low-temperature single-crystal X-ray di

75 ucidated by Nuclear Magnetic Resonance (NMR) spectroscopy and mass spectrometry (MS).

76 total reflection Fourier-transform infrared spectroscopy and measuring the zeta potential.

77 Here, we combine advanced spectroscopy and microscopy on model Pd/C samples to dec

78 Here we utilize in situ spectroscopy and microscopy to identify and characterize

79 d a combination of relaxation dispersion NMR spectroscopy and molecular dynamics simulations to deter

80 ombine ultrafast two-dimensional vibrational spectroscopy and molecular dynamics simulations to study

81 native state as probed by heteronuclear NMR spectroscopy and multiple conformer simulations of cryst

82 Using raster image correlation spectroscopy and number and brightness analysis combined

83 easing concentrations quantifiable by UV-vis spectroscopy and obvious to the naked eye.

84 systems is crucial for achieving fidelity in spectroscopy and quantum computing, but inherent nonline

85 c system combines chemical handling, in-line spectroscopy and real-time feedback and analysis with an

86 electronic states, as observed from optical spectroscopy and resonant inelastic X-ray scattering.

87 threitol is measured using both fluorescence spectroscopy and single droplet paper spray mass spectro

88 a nanostructures, using widely available NMR spectroscopy and small amounts of sample.

89 This complex was fully characterized by NMR spectroscopy and X-ray crystallography.

90 , as previously proposed on the basis of NMR spectroscopy and X-ray crystallography.

91 X-ray absorption spectroscopy and X-ray photoelectron spectroscopy studie

92 exclusion chromatography, circular dichroism spectroscopy, and electron microscopy; compared the prop

93 ident X-ray diffraction, X-ray photoelectron spectroscopy, and Fourier transform infrared spectroscop

94 -angle x-ray scattering, high-resolution NMR spectroscopy, and limited proteolysis coupled with mass

95 th SEM, XRD, TEM, SAED, EDX, XPS, UV-visible spectroscopy, and open-circuit potential versus time exp

96 e were identified by Front-Face fluorescence spectroscopy, and the emission intensity trend was inves

97 tructure, which can be useful in sensing and spectroscopy applications.

98 EPR spectroscopy applying stable hydrophilic and hydrophobic

99 ic nuclear polarization surface enhanced NMR spectroscopy approach that induces a 200-fold increase i

100 It might also be beneficial for other spectroscopy approaches which require harmonic analysis

101 Most phonon spectroscopies are selectively sensitive to either surfa

102 erg theory, and angle-resolved photoemission spectroscopy (ARPES), we show that surface states in few

103 to conventional angle-resolved photoemission spectroscopy (ARPES).

104 Here, such optimization using ultrafast spectroscopy as a tool to optimize the material bandgap

105 )P magnetization transfer magnetic resonance spectroscopy as described previously.

106 n X-ray Kbeta emission and K-edge absorption spectroscopy as well as quantum chemistry to determine m

107 Proton magnetic resonance spectroscopy at 7T was performed in 21 patients with chr

108 chizophrenia using proton magnetic resonance spectroscopy at 7T, which allows separation of metabolit

109 X-ray absorption near-edge structure (XANES) spectroscopy at the carbon K-edge (280-350 eV) is a very

110 ), as evidenced by operando X-ray absorption spectroscopy at the Co K-edge.

111 total reflection Fourier transform infrared spectroscopy (ATR-FTIR) nicely agreed with interaction e

112 ttenuated total reflection Fourier transform spectroscopy (ATR-FTIR) without the need for collimated

113 ctrometry (ICP-MS), amino acid analysis, and spectroscopy (ATR-IR, Raman).

114 this study, nuclear magnetic resonance (NMR) spectroscopy-based metabolomic analysis was used to iden

115 n vitro alphaB- and gammaD-crystallin, 2D IR spectroscopy can identify the highly ordered beta-sheets

116 e process monitoring with a focus on optical spectroscopy can provide a fast, nondestructive method f

117 Here, we show that solid-state (17) O NMR spectroscopy can provide unique information about the en

118 13 ((13)C)-pyruvate magnetic resonance (MR) spectroscopy, can serve as indicators of response in ova

119 -SIMS imaging and coherent anti-Stokes Raman spectroscopy (CARS) microspectroscopy allowed us to loca

120 PPP-NN were investigated by EPR and optical spectroscopy combined with DFT calculations.

121 ble lasers have far-reaching applications in spectroscopy, communication, metrology and basic science

122 A combination of spectroscopy, computational modeling, and crystallograph

123 l classification of saffron using UV-visible spectroscopy, conventionally adopted for quality grading

124 To address this problem, we use SPR spectroscopy correlated with surface enhanced Raman scat

125 These findings suggest that fluorescence spectroscopy could offer a rapid and high-throughput scr

126 The unprecedented resolution of cold-ion spectroscopy coupled with tandem MS may render this the

127 e were studied by steady-state and transient spectroscopies, cyclic voltammetry, and electron paramag

128 Nuclear magnetic resonance spectroscopy demonstrated that the N-terminal inhibitory

129 (82.8%), loading capacity (35.38%) and FT-IR spectroscopy demonstrated the interaction between oil an

130 Compounds 1-3 were analyzed by EPR and NMR spectroscopy, DFT calculations, and X-ray crystallograph

131 e reflectance mid-infrared Fourier-transform spectroscopy (DRIFTS) is capable of detecting specific o

132 The diffuse reflectance infra-red spectroscopy (DRIFTS) results show the absence of nitrat

133 ffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS).

134 characterized via, UV-Vis spectroscopy, FTIR spectroscopy, dynamic light scattering and scanning elec

135 emically analysed by energy dispersive X-ray spectroscopy (EDX), inductively coupled plasma mass spec

136 emical techniques; electrochemical impedance spectroscopy (EIS) and Mott-Schottky analysis on the sam

137 were monitored by electrochemical impedance spectroscopy (EIS).

138 Using electronic absorption spectroscopy, electrical transport measurements and elec

139 Molecular dispersion spectroscopy encompasses a group of spectroscopic techni

140 H NMR, EPR, and X-ray absorption (near-edge) spectroscopy, ESI mass spectrometry, and DFT methods.

141 and two-dimensional (COSY, NOESY, DOSY) NMR spectroscopy, ESI-MS, ion-mobility mass spectrometry (IM

142 ciferase, by combining single-molecule force-spectroscopy experiments and coarse-grained simulation.

143 ble-temperature (VT) NMR and exchange (EXSY) spectroscopy experiments.

144 tion results to iron K-edge X-ray absorption spectroscopy fitting results allowed to quantify the rel

145 Functional near infrared spectroscopy (fNIRS) is a field-deployable optical brain

146 Using functional near-infrared spectroscopy (fNIRS), we examined hemodynamic responses

147 present study reveal the potential of Raman spectroscopy for rapid determination (45s) of erucic aci

148 Femtosecond stimulated Raman spectroscopy (FSRS) is a vibrational spectroscopy techni

149 ay-tomography and Fourier-Transform Infrared spectroscopy (FTIR); releases were quantified by Inducti

150 solution was then characterized via, UV-Vis spectroscopy, FTIR spectroscopy, dynamic light scatterin

151 NMR spectroscopy further demonstrated that DREB2A underwent

152 -femtosecond extreme UV transient absorption spectroscopy (FXTAS) at the vanadium M2,3 edge is used t

153 ence and grazing emission X-ray fluorescence spectroscopy (GI/GE-XRF) are techniques that enable nond

154 Raman spectroscopy has been growing as a fast tool to food ana

155 Fluorescence correlation spectroscopy has been previously used to investigate pep

156 Infrared spectroscopy has been used in the past to probe the dyna

157 Surface-enhanced Raman scattering (SERS) spectroscopy has evolved into a cross-disciplinary analy

158 Spatially resolved electron energy loss spectroscopy has previously been used to image plasmonic

159 The nanoprobe based NMR spectroscopy has the potential to enable rapid screening

160 Until recently, NMR spectroscopy has yielded structures of small or medium-s

161 -ray based techniques combined with mu-Raman spectroscopy have been applied to demonstrate that the o

162 ystallography and nuclear magnetic resonance spectroscopy have revealed the structures of nearly all

163 Combining UV-visible spectroscopy, heme quantification, and site-directed mut

164 inductively coupled plasma optical emission spectroscopy (ICP-OES).

165 In operando X-ray absorption spectroscopy identified reduced Pt covered with an amorp

166 otron small-angle X-ray scattering and Raman spectroscopy in a controlled gas-phase environment.

167 ultanate of Oman and were measured using NIR spectroscopy in absorption mode in the wavelength range

168 icroscopy (STEM) and energy dispersive X-ray spectroscopy in STEM (EDX-STEM).

169 ate the direct applicability of infrared ion spectroscopy in the field of drug metabolism and, more g

170 total reflectance Fourier transform infrared spectroscopy in the Kretschmann geometry (ATR-FTIR Krets

171 ion mass spectrometry, absorption and action spectroscopy in the UV and IR regions, and microwave spe

172 id from various structural elements, and NMR spectroscopy indicated complete de-esterification of ara

173 entrations of Fe(2+), while Sb L1-edge XANES spectroscopy indicated no reduction of Sb(V).

174 2008-2016) in infrared reflection absorption spectroscopy (IRRAS) studies on oxide powders achieved b

175 ning calorimetry and (1)H NMR and UV-vis-NIR spectroscopies is presented, demonstrating this DHAP pro

176 Mid-infrared (MIR) spectroscopy is a powerful tool for characterising the v

177 Studying PTMs by NMR spectroscopy is a promising method to analyze proteins a

178 Saturation transfer difference (STD) NMR spectroscopy is extensively used to obtain epitope maps

179 Deep UV resonance Raman spectroscopy is introduced as an analytical tool for ult

180 Using NMR spectroscopy, isothermal titration calorimetry and molec

181 Here, using CD spectroscopy, isothermal titration calorimetry, and smal

182 steady-state fluorescence polarization (FP) spectroscopy, kinetically resolves the dissociation of d

183 ared and studied by variable temperature NMR spectroscopy leading to the conclusion that the rate-det

184 est the potential of laser-induced breakdown spectroscopy (LIBS) analysis combined with chemometrics

185 tive method based on Laser Induced Breakdown Spectroscopy (LIBS) to the quality control, traceability

186 Laser-induced breakdown spectroscopy (LIBS) was investigated to estimate the via

187 In ZrSiS, angle-resolved photoemission spectroscopy measurements have shown an unusually robust

188 nts of electron paramagnetic resonance (EPR) spectroscopy measurements of various food products.

189 liquid chromatography-mass spectrometry/mass spectroscopy method quantifying circulating and equilibr

190 ystem, a prerequisite for all kinds of force spectroscopy methods, to obtain reliable values independ

191 identify unambiguously using linear optical spectroscopy methods.

192 timised to enable simultaneous in-situ Raman spectroscopy monitoring of 2D dispersed flakes during th

193 erebral metabolism, (13)C magnetic resonance spectroscopy (MRS) allows following the fate of (13)C-en

194 ng near-ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) we show that a time scale of hour

195 cs of a model OMP (tOmpA) using fluorescence spectroscopy, native mass spectrometry, and molecular dy

196 While near-infrared spectroscopy (NIRS) haemodynamic measures have proven to

197 We exploited a Near-Infrared Spectroscopy (NIRS) method to monitor the onset of fat p

198 Using (1)H Nuclear Magnetic Resonance spectroscopy (NMR) and Gas Chromatography - Mass Spectro

199 e-dimension (31)P nuclear magnetic resonance spectroscopy (NMR) has greatly advanced our understandin

200 trate that quantum interpolation can achieve spectroscopy of classical magnetic fields and individual

201 in bilayer graphene (BLG) using photocurrent spectroscopy of high-quality BLG encapsulated in hexagon

202 carried out metabolomic analysis by (1)H NMR spectroscopy of media from astrocyte-spinal neuron co-cu

203 We report a measurement by neutron spin echo spectroscopy of the diffusion of hemoglobin in solutions

204 specificity by high-resolution photoelectron spectroscopy of the vinylidene anions H2CC- and D2CC- an

205 r-infrared and ultrafast optical Kerr effect spectroscopies on carefully selected ions with a greater

206 Their applications include spectroscopy, optical tomography, wavefront sensing, and

207 Using force spectroscopy optimized for 1-microsecond resolution, we

208 is commonly measured using indirect tracer, spectroscopy, or electrical methods, no direct observati

209 ith extreme ultraviolet transient absorption spectroscopy paves the way for investigating few- to sub

210 X-ray absorption spectroscopy provides firm evidence for the presence of

211 s measurement using time-resolved absorption spectroscopy provides information on temporal dynamics o

212 alytical method using surface-enhanced Raman spectroscopy reduces sample preparation and analysis tim

213 e detected by magnetic resonance imaging and spectroscopy, respectively.

214 AFM force-spectroscopy results showed that the adhesion of C. albi

215 Importantly, Raman spectroscopy revealed molecular-level perturbations of f

216 As K-edge XANES spectroscopy revealed some reduction of As(V) to As(III)

217 spectroscopy, and Fourier transform infrared spectroscopy, revealing that the enhanced sensing perfor

218 X-ray photoelectron spectroscopy reveals that, at pH </= 3.5, a significant

219 use of low-temperature, rapid injection NMR spectroscopy (RI-NMR), kinetic studies, and computationa

220 Here, a combined reflectometric interference spectroscopy (RIfS) and QCM is developed to simultaneous

221 t back to undergo outcome magnetic resonance spectroscopy scans, which were identical to the scans co

222 opsis thaliana, using surface-enhanced Raman spectroscopy (SERS) and gold nanoprobes at single-cell r

223 h Raman, a label-free surface-enhanced Raman spectroscopy (SERS) approach can be implemented to detec

224 Developing surface-enhanced Raman spectroscopy (SERS) based biosensors requires not only s

225 The application of surface-enhanced Raman spectroscopy (SERS) in biological and biomedical detecti

226 mple preparation with surface-enhanced Raman spectroscopy (SERS)-based detection for quantitative ana

227 coupled to a high-stability cavity-ring-down-spectroscopy setup.

228 osphate, 25 degrees C) monitored by (1)H NMR spectroscopy show benign acetic acid as the only signifi

229 Extended X-ray absorption fine-structure spectroscopy showed red amorphous Se(0) with a first she

230 croscopy (TEM) and operando X-ray absorption spectroscopy showed that oxygen species can survive in t

231 reaction, quasi in situ X-ray photoelectron spectroscopy showed that the surface is metallic under r

232 Single molecule spectroscopy (SMS) has matured to a point where it can b

233 ve developed handheld spatially offset Raman spectroscopy (SORS) for the first time in a food or beve

234 EPR spectroscopy, SQUID magnetometry, and DFT calculations t

235 Offline microscopy and spectroscopy studies have shown that dry supermicron SSA

236 rable to or greater than previous vigabatrin spectroscopy studies in healthy epilepsy-naive subjects.

237 We also report CD and UV-Vis spectroscopy studies of adducted human Hb that revealed

238 orption spectroscopy and X-ray photoelectron spectroscopy studies of SNNO/LSMO heterostructures revea

239 ic voltammetry and electrochemical impedance spectroscopy studies showed that the fabricated aptasens

240 Experimental spectroscopy studies with purified proteins validate our

241 s confirmed using X-ray absorption near edge spectroscopy, suggesting substitution on both Ca and Zr

242 Based on the THz time-domain spectroscopy system, THz nano-metamaterial sensing chips

243 d Raman spectroscopy (FSRS) is a vibrational spectroscopy technique that has been used in a wide vari

244 DOSY is an NMR spectroscopy technique that resolves resonances accordin

245 re we show, using Fourier transform infrared spectroscopy, that COR15A starts to fold into alpha-heli

246 gh X-ray diffraction and X-ray photoelectron spectroscopy, the as-grown tungsten(VI) sub-oxide was id

247 selectively detected CN(-) under the UV-vis spectroscopy through the rapid appearance of deep pink c

248 ctance Fourier transform infrared (ATR-FTIR) spectroscopy to analyze urine samples collected from rod

249 We used X-ray absorption spectroscopy to characterize the structural order of mer

250 Our results demonstrate the power of Raman spectroscopy to detect apparition of skin toxicity in pa

251 pulsed electron paramagnetic resonance (EPR) spectroscopy to determine their coherence times.

252 g that included optimized magnetic resonance spectroscopy to measure anterior cingulate (AC) glutamat

253 Here we demonstrate use of pulsed EPR spectroscopy to measure the interaction between two ineq

254 We use clock spectroscopy to prepare lattice band populations, intern

255 s m-C8H8 in gas phase; we used photoelectron spectroscopy to probe the first two electronic states of

256 plied handedness-resolved optical reflection spectroscopy to probe the inter-LL transitions at indivi

257 range, 50-79 years) using magnetic resonance spectroscopy to quantify GABA levels as well as resting-

258 rrelation spectroscopy and cross-correlation spectroscopy to quantify the diffusion, photobleaching,

259 Here we use charge modulation spectroscopy to reveal a bipolaron sheet density >10(10)

260 by variable-temperature (2)H solid-state NMR spectroscopy to reveal the reorientation mechanisms with

261 chelman et al. applied single-molecule force spectroscopy to show that an adhesin protein can regener

262 pectroscopy with polarization-resolved Raman spectroscopy to show that the induced monoclinic phase p

263 sotope labeling and two-dimensional infrared spectroscopy to spectrally resolve an oligomeric interme

264 y-mass spectrometry coupled to infrared (IR) spectroscopy to study the amyloid formation mechanism an

265 relaxation enhancement (PRE) measured by NMR spectroscopy to study the transient intermolecular inter

266 Here, we utilize EPR spectroscopy to target the conformational changes that t

267 s question, we used functional near-infrared spectroscopy to test 40 healthy newborns on their abilit

268 the use of magnetic circular dichroism (MCD) spectroscopy to validate the results of TD-DFT calculati

269 femtosecond XANES, combined with UV-visible spectroscopy, to reveal sequential structural evolution

270 2D total correlation spectroscopy (TOCSY) provides unique spin connectivity i

271 me-resolved and angle-resolved photoemission spectroscopy (TRARPES) study of WSe2, a layered semicond

272 ion, Raman spectroscopy, X-ray photoelectron spectroscopy, UV-vis absorption spectra, and photolumine

273 n the active alpha2:beta2 complex by HYSCORE spectroscopy validate that the perturbed conformation of

274 in lymphocytes by nuclear magnetic resonance spectroscopy was altered in septic patients.

275 In this study, label-free fluorescence spectroscopy was used for the first time to determine sp

276 Far-UV circular dichroism spectroscopy was used to confirm the secondary structure

277 (1)H HR-MAS NMR spectroscopy was used to track the metabolic changes thr

278 ional analysis by both wavelength dispersive spectroscopy (WDS) and Rutherford backscattering spectro

279 Using UV-vis spectroscopy, we could measure the amount of Fe(3+) in t

280 g methyl transverse relaxation-optimized NMR spectroscopy, we demonstrate that only three of the six

281 live-cell superresolution cross-correlation spectroscopy, we demonstrate that the two flows are corr

282 Using 2D NMR spectroscopy, we established for the first time that MK-

283 Using force spectroscopy, we have measured here the forces that ense

284 By solid-state (13)C NMR spectroscopy, we observed that about one-third of hemice

285 solid-state nuclear magnetic resonance (NMR) spectroscopy, we show that mineral deposition is biologi

286 nsient absorption and time-resolved infrared spectroscopies were used to characterize the identity an

287 IR polarization selective pump-probe (PSPP) spectroscopies were used to investigate CO2 reorientatio

288 High-field and low-field proton NMR spectroscopy were used to analyse lipophilic extracts fr

289 own to be suitable for photon counting X-ray spectroscopy when coupled to a low-noise charge-sensitiv

290 Using time-resolved spectroscopy with broadband capability, we clearly demon

291 gle- and double-quantum (1)H solid-state NMR spectroscopy with density functional theory calculations

292 We also combine second-harmonic generation spectroscopy with polarization-resolved Raman spectrosco

293 , scanning electron microscopy (SEM), UV-Vis spectroscopy, X-ray diffraction (XRD) analysis and Fouri

294 lectron microscopy, X-ray diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy, UV-vis a

295 Here, X-ray absorption spectroscopy (XAS) and rR studies have been used to esta

296 e pathway, we have employed X-ray absorption spectroscopy (XAS) to investigate the relationship betwe

297 UID, UV-vis absorption, and X-ray absorption spectroscopy (XAS)) coupled with advanced theoretical ca

298 ttering (WAXS) with X-ray photon-correlation spectroscopy (XPCS) in the small-angle X-ray scattering

299 trode (GCE), as shown by X-ray photoelectron spectroscopy (XPS) measurements.

300 ular dichroism (CD), and X-ray photoelectron spectroscopy (XPS).