ライフサイエンスコーパス: spectroscopy

1 actions via nuclear magnetic resonance (NMR) spectroscopy.

2 lms is investigated by polarization-resolved spectroscopy.

3 metry, deuterium labeling, and UV/Vis action spectroscopy.

4 % efficiency), as evidenced by time-resolved spectroscopy.

5 vements over conventional optoacoustic or IR spectroscopy.

6 s, and compare it with ensemble fluorescence spectroscopy.

7 nt and release profile were studied using UV spectroscopy.

8 phosphine oxide, and in one case by infrared spectroscopy.

9 y peptide-protein interactions by (19) F NMR spectroscopy.

10 th surface-specific sum-frequency generation spectroscopy.

11 stem chemistry from in situ X-ray absorption spectroscopy.

12 tric analysis and nuclear magnetic resonance spectroscopy.

13 te approach for structure calculation by NMR spectroscopy.

14 distribution was quantified ex vivo via EPR spectroscopy.

15 Specific chemical bonds were probed by FTIR spectroscopy.

16 in-coupled hidden Cu(II) was observed by EPR spectroscopy.

17 infrared spectroscopy, and X-ray absorption spectroscopy.

18 ysed by Raman and Fourier-transform infrared spectroscopy.

19 emical transformations by hyperpolarized NMR spectroscopy.

20 ester was confirmed by (1)HNMR, FTIR and UV spectroscopy.

21 lical using nuclear magnetic resonance (NMR) spectroscopy.

22 solids by near and mid-infrared transmission spectroscopy.

23 ved by electron paramagnetic resonance (EPR) spectroscopy.

24 probed via fluorine K-edge X-ray absorption spectroscopy.

25 rtant advances in genetics, cell biology and spectroscopy.

26 using zero-field nuclear magnetic resonance spectroscopy.

27 s characterized by electrochemical impedance spectroscopy.

28 r products, other than ester bonds, with NMR spectroscopy.

29 vibrational signatures from stimulated Raman spectroscopy.

30 on select architectures using in-situ Raman spectroscopy.

31 diffraction, optical and X-ray photoelectron spectroscopy.

32 p towards the untethering of single molecule spectroscopy.

33 4) sites via in-temperature X-ray absorption spectroscopy.

34 can not be readily met by conventional FT-IR spectroscopy.

35 nation factors by nuclear magnetic resonance spectroscopy.

36 uction with K metal and characterized by EPR spectroscopy.

37 by ECD and/or CPL, as well other chiroptical spectroscopies.

38 MR, Raman, and energy-dispersive X-ray (EDX) spectroscopies.

39 ntrations by using proton magnetic resonance spectroscopy ((1)H-MRS) in 28 adults with ASD and 29 age

40 -stressed mice using (1)H-magnetic resonance spectroscopy ((1)H-MRS).

41 soliton microcombs(10) have been applied to spectroscopy(11-13), the search for exoplanets(14,15), o

42 d two-dimensional nuclear magnetic resonance spectroscopy (1D and 2D NMR) and high-resolution tandem

43 , using ultrafast two-dimensional electronic spectroscopy (2DES), we reveal the existence of intermol

44 lusion further supported by X-ray absorption spectroscopy, (57)Fe Mossbauer studies, and DFT calculat

45 sfully detected by electrochemical impedance spectroscopy after electrode functionalization with spec

46 Instruments focusing on near-infrared spectroscopy allow obtaining information about seed and

47 Single-molecule spectroscopy allows us to quantify the effects of crowdi

48 ight scattering (DLS), FESEM, HRTEM, and EDX spectroscopy along with elemental mapping.

49 Combining FTIR and UV-Vis spectroscopy along with molecular dynamics simulations,

50 X-ray absorption spectroscopy analysis discovered that zerovalent Cr(0) c

51 Raman spectroscopy analysis shows a low-intensity or absent D

52 mal denaturation, nuclear magnetic resonance spectroscopy, analytical ultracentrifugation, small-angl

53 using steady-state and transient absorption spectroscopies and quantum chemical calculations.

54 Using terahertz (THz) absorption spectroscopy and ab initio molecular dynamics, we have i

55 cture of BTNL2 as determined by solution NMR spectroscopy and also the picosecond-nanosecond timescal

56 In this work, we apply impedance spectroscopy and deep-level transient spectroscopy to ch

57 2)C exchange, coupled with operando infrared spectroscopy and density functional theory (DFT) modelin

58 unction, quantified via fluorescence and NMR spectroscopy and DFT calculations.

59 We measured metabolites by HR-MAS (1)H NMR spectroscopy and DNA cytosine modifications by LC/MS, in

60 MRI techniques including fMRI, MR volumetry, spectroscopy and DTI captured functional, metabolic, and

61 esent study, we employed X-ray photoelectron spectroscopy and Fourier-transform infrared spectroscopy

62 pport the results obtained from fluorescence spectroscopy and give insights into the interactions inv

63 field reflection mode, offering submicron IR spectroscopy and imaging.

64 shed since 2018 which focuses on using Raman spectroscopy and machine learning to address the need fo

65 using (1)H nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry (MS).

66 Nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry of active fractions l

67 and bidimensional Nuclear Magnetic Resonance spectroscopy and mass spectrometry.

68 New approaches in single molecule spectroscopy and microscopy are able to resolve the spat

69 We study these compounds using transient spectroscopy and modelling to unravel the singlet and tr

70 y findings from single-molecule fluorescence spectroscopy and molecular dynamics simulations indicati

71 In situ Raman spectroscopy and molecular dynamics simulations reveal t

72 n this work, we employ single-molecule force spectroscopy and molecular dynamics simulations to disse

73 ing a combination of isotope-edited infrared spectroscopy and molecular dynamics simulations, we char

74 les, as tested in electrochemical absorption spectroscopy and organic electrochemical transistors, an

75 To this end, we coupled Raman spectroscopy and paper spray ionization mass spectrometr

76 ctral coverage; we introduce two-dimensional spectroscopy and present results that demonstrate the ad

77 s of synchrotron-based techniques with Raman spectroscopy and scanning electron microscopy, we invest

78 isotropy is demonstrated via polarized Raman spectroscopy and second-harmonic generation maps of the

79 (Fzd1), using fluorescence cross-correlation spectroscopy and show that the co-receptor, low-density

80 a conformer-specific manner using rotational spectroscopy and theoretical approaches.

81 to underline how the synergy between far-IR spectroscopy and theory can provide an unprecedented pic

82 Fourier-transform infrared spectroscopy and X-ray diffraction observations confirme

83 Complementary experimental (X-ray absorption spectroscopy) and theoretical (Density Functional Theory

84 erent methods are evaluated using PSI, Raman spectroscopy, and AFM.

85 interest to the organic chemistry, molecular spectroscopy, and astrochemistry communities were synthe

86 Using fluorescence microscopy, fluorescence spectroscopy, and cell fractionation experiments, we fou

87 eling studies, variable-temperature (1)H NMR spectroscopy, and density functional theory calculations

88 ass spectrometry, nuclear magnetic resonance spectroscopy, and density functional theory calculations

89 SQUID magnetometry, Mossbauer spectroscopy, and DFT calculations reveal that (P(6)ArC)

90 ring of Pd deposited on Ag using microscopy, spectroscopy, and novel simulation methods.

91 ray scattering/diffraction, X-ray absorption spectroscopy, and Raman techniques, we found that the Cu

92 g recombinant protein expression, absorbance spectroscopy, and tandem mass spectrometry.

93 by X-ray crystallography, electronic and NMR spectroscopy, and theoretical calculations.

94 ission electron microscopy (AC-STEM), UV-vis spectroscopy, and X-ray absorption spectroscopy (XAS).

95 y coupled plasma mass spectrometry, infrared spectroscopy, and X-ray absorption spectroscopy.

96 y diffraction; UV/vis, MCD, IR, EPR, and NMR spectroscopy; and quantum chemistry.

97 xt] measured by angle-resolved photoemission spectroscopy (ARPES).

98 function assessed by electron spin resonance spectroscopy as well as conventional and 2-dimensional s

99 econd Fe K(alpha) and K(beta) X-ray emission spectroscopy at an X-ray free-electron laser (FEL).

100 total reflectance Fourier-transform infrared spectroscopy (ATR-FTIR) combined with chemometric method

101 Optical spectroscopy-based online monitoring offers a powerful a

102 By photoemission spectroscopy below the Curie temperature, we observe top

103 h in a wide range of applications, including spectroscopy, bio-medical sensing, astronomical and spac

104 combination of vibrational and photoemission spectroscopies, bonding of the two peptides to TiO(2) su

105 hGrx1, Atox1 and WLN5-6 were detected by NMR spectroscopy both in the presence and absence of Cu at a

106 provide a proof-of-concept to show how Raman spectroscopy can be used to identify the types of tissue

107 ow that visible and near infra-red (Vis/NIR) spectroscopy can classify rice according to sub-populati

108 Here, through extraction, derivatization, spectroscopy, chromatography, and mass spectrometry, we

109 as steady-state & time-resolved fluorescence spectroscopy, Circular Dichroism (CD) and Fluorescence C

110 d Total Reflectance - Mid-Infrared (ATR-MIR) spectroscopy combined with Partial Least Squares Discrim

111 tigated by scanning tunneling microscopy and spectroscopy, complemented by theoretical calculations.

112 the convergence of biochemistry, structure, spectroscopy, computation, and model chemistry.

113 ve (EW) with high-sensitive cavity ring-down spectroscopy (CRDS) technique using a diode laser at 644

114 copy (SEIRAS), in situ soft X-ray absorption spectroscopy (Cu L-edge), and online gas chromatography

115 riate classification analysis of vibrational spectroscopy data (FTIR, Raman and near-IR) highlighting

116 ons using a unit cell approach reproduce the spectroscopy data and explain how periodic microstructur

117 Electrochemical impedance spectroscopy data generated under illuminated, catalytic

118 yses of the one and two-dimensional infrared spectroscopy data show that the intermediates are more f

119 EPR spectroscopy data suggests particles cleared more slowly

120 dissolution begins and electrical impedance spectroscopy demonstrated that diffusive transport accel

121 asurements such as electrochemical impedance spectroscopy (EIS) (which measure the movement of only t

122 ents were based on Electrochemical Impedance Spectroscopy (EIS) and Differential Pulse Voltammetry (D

123 ical processes and electrochemical impedance spectroscopy (EIS) in the characterization of different

124 rs and, using ultrafast transient absorption spectroscopy, elucidate the critical role of electron tr

125 Therefore, Raman spectroscopy enables reliable neutrophil phenotyping and

126 s is evidenced by nuclear magnetic resonance spectroscopy, end group analysis, and chain extension ex

127 and YchJ, also copurified with iron, and NMR spectroscopy experiments indicated that YecA binds iron

128 ge, electron paramagnetic resonance, and NMR spectroscopy experiments reveal that a disorder-to-order

129 is proposed to refer to the class of all NMR spectroscopy experiments that rely on viscous solvents f

130 nomenon was observed during in situ infrared spectroscopy experiments.

131 nt for comparison with high-resolution force spectroscopy experiments.

132 uch as colorimetric, flame atomic absorption spectroscopy (FAAS), and inductively coupled plasma opti

133 techniques such as fluorescence correlation spectroscopy (FCS) and spectral imaging.

134 el electrophoresis, fluorescence correlation spectroscopy (FCS), and microfluidic experiments.

135 Dichroism (CD) and Fluorescence Correlation Spectroscopy (FCS).

136 Here, we present fiber-enhanced Raman spectroscopy (FERS) of headspace gases as an alternate t

137 cal chemistry analysis, 1D (1)H NMR and mass spectroscopy (FIA-MS/MS and LC-MS/MS) techniques.

138 demonstrated using functional near-infrared spectroscopy (fNIRS).

139 ication of FRET and fluorescence correlation spectroscopy for the analysis of oligomerization of tran

140 ese results underline the suitability of NMR spectroscopy for the identification and quantification o

141 ospectroscopic technique, for example, Raman spectroscopy, for assessing endoscopic disease severity

142 techniques, such as fiber optic reflectance spectroscopy (FORS), Raman spectroscopy, multispectral i

143 were investigated using X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, X

144 of hot intracluster gas, while deep imaging spectroscopy from the European Space Agency's X-ray Mult

145 application of femtosecond stimulated Raman spectroscopy (FSRS) to a multichromophoric biological co

146 Fourier transform infrared spectroscopy (FTIR) imaging with automated data analysis

147 nation of grazing incidence X-ray absorption spectroscopy (GIXAS) and X-ray diffraction (GIXRD).

148 state magnetic studies, and (57)Fe Mossbauer spectroscopy has been applied to characterize complexes

149 genic single-particle photoluminescence (PL) spectroscopy has been used with great success to directl

150 Solution-state NMR spectroscopy has emerged as a leading structural techniq

151 terization and quantification by (29) Si NMR spectroscopy has received significant attention, it is a

152 igh-resolution magic-angle-spinning (1)H NMR spectroscopy (HR-MAS NMR) is a well-established techniqu

153 High-resolution ultrasonic spectroscopy (HR-US) was applied for real-time monitorin

154 y X-ray crystallography, X-ray photoelectron spectroscopy, hydrogen evolution experiments, electrospr

155 X-ray spectroscopy (i.e., XAS and EDX) and diffraction indicat

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

157 aracterized by Raman and X-ray photoelectron spectroscopies in addition to microscopies.

158 -fiber reflectance/single-fiber fluorescence spectroscopy in 15 patients with a dysplastic colorectal

159 y means of Fourier Transform Infrared (FTIR) spectroscopy in a very broad range (from near- via mid-

160 ection Fourier-transform infrared (ATR-FTIR) spectroscopy in conjunction with chemometric techniques,

161 highlight the importance of single-particle spectroscopy in revealing the diverse optical properties

162 he use of microfluidic single-cell impedance spectroscopy in the field of calcifying algae.

163 dues) when examined by single molecule force spectroscopy in vitro displays the properties of a rando

164 munoprecipitation of FGFR1 coupled with mass spectroscopy indicated that FGFR1 forms a physical compl

165 We conclude that ICIRD spectroscopy is a noninvasive, label-free approach for a

166 Auger electron spectroscopy is applied to demonstrate a postdeposition

167 An introduction to the field of far-IR spectroscopy is given, thereby highlighting the opportun

168 In this work, ultrafast spectroscopy is used to explore the nature of the carrie

169 ndomized lesions was 41.6%; by near-infrared spectroscopy-IVUS, the median plaque burden was 73.7%, t

170 tes the potential of laser-induced breakdown spectroscopy (LIBS) for the direct analysis of liquid fo

171 BCAAs were quantified via NMR spectroscopy, log-transformed, and standardized.

172 n the van der Pauw geometry, THz time-domain spectroscopy mapping and calibrated Kelvin probe force m

173 based method of 2D ultraviolet fragmentation spectroscopy-mass spectrometry (2D UV-MS) of cold ions.

174 Our angle-resolved photoemission spectroscopy measurements and first-principles calculati

175 dge X-ray absorption fine structure (NEXAFS) spectroscopy measurements at the carbon K edge on thin m

176 on times obtained from (13)C solid-state NMR spectroscopy measurements establish the occurrence of mo

177 n demonstrated, both by transient absorption spectroscopy measurements on the femto, pico-, nano-, an

178 cale and have the potential to revolutionize spectroscopy, metrology and timing.

179 Using NMR spectroscopy, molecular dynamics simulations, and isothe

180 Hyperpolarized (13)C magnetic resonance spectroscopy (MRS) is a developing imaging technique tha

181 maging techniques such as magnetic resonance spectroscopy (MRS) may cover anatomically and functional

182 ified using micro-Fourier-transform infrared spectroscopy (muFTIR).

183 optic reflectance spectroscopy (FORS), Raman spectroscopy, multispectral imaging (MSI), and macro X-r

184 ica coffee blends by combining near infrared spectroscopy (NIRS) and total reflection X-ray fluoresce

185 A portable near infrared spectroscopy (NIRS) instrument was evaluated for the dis

186 her a wavelet method that uses near-infrared spectroscopy (NIRS) or intracranial pressure (ICP) decre

187 etic resonance imaging (f-MRI) near-infrared spectroscopy (NIRS), and positron-emission tomography (P

188 re analysed using nuclear magnetic resonance spectroscopy (NMR) with the aim of building and evaluati

189 determined using nuclear magnetic resonance spectroscopy (NMR).

190 chrotron-based nuclear resonance vibrational spectroscopy (NRVS) using the Mossbauer isotope (161) Dy

191 d using various techniques, such as infrared spectroscopy, nuclear magnetic resonance spectroscopy, u

192 aser-based off-axis integrated cavity output spectroscopy (OA-ICOS) technique.

193 acquired near-whole-brain magnetic resonance spectroscopy of N-acetyl compounds, glutamate+glutamine,

194 w that electron paramagnetic resonance (EPR) spectroscopy of oligonucleotides spin-labelled with tria

195 developed technique of laser-photodetachment spectroscopy of radioisotopes opens the path for future

196 ICIRD spectroscopy on the light, oxygen, or voltage (LOV) doma

197 ticles with search terms (magnetic resonance spectroscopy OR MRS) AND (glutamate OR glut* OR GLX) AND

198 gether with micro-Fourier transform infrared spectroscopy, Pb is shown to be associated with fatty ac

199 se field gradient nuclear magnetic resonance spectroscopy (PFG-NMR, which gives movement of all of th

200 Longitudinal acoustic mode Raman spectroscopy provides a complementary measurement of the

201 on was followed by electrochemical impedance spectroscopy, proving that the new system can be applied

202 ection Fourier transform infrared (ATR-FTIR) spectroscopy ready for use in commercial FTIR spectromet

203 diabatic Molecular Dynamics, and Theoretical Spectroscopy represent the three pillars of the virtual

204 sis method to correlate characteristic Raman spectroscopy response of MoSe(2) at ca. 242 cm(-1) (A(1g

205 Furthermore, Raman spectroscopy results revealed that the 9th-week GBs has

206 ctance Fourier transform infrared (ATR-FTIR) spectroscopy revealed a presence of oxygen-containing fu

207 Further FT-IR spectroscopy revealed the presence of a W=O moiety arisi

208 Circular dichroism spectroscopy revealed the presence of largely disordered

209 Solid-state UV-vis spectroscopy reveals that azobenzene molecules undergo r

210 UV/vis and fluorescence spectroscopy reveals that the anthracene-substituted der

211 Holding m = 1, spectroscopy reveals that the n = 1 superlattice contain

212 y, we investigate the potential use of Raman spectroscopy (RS) as a label-free, non-invasive and non-

213 olor fluorescence lifetime cross-correlation spectroscopy (sc-FLCCS).

214 crystals is confirmed by low-frequency Raman spectroscopy, scanning transmission electron microscopy,

215 in situ surface-enhanced infrared absorption spectroscopy (SEIRAS), in situ soft X-ray absorption spe

216 near-field emission, is widely being used in spectroscopy, sensing, and microscopy.

217 A rapid Surface Enhanced Raman Spectroscopy (SERS) method to detect SO(2) in wine is pr

218 rochemically assisted surface-enhanced Raman spectroscopy (SERS) platform with the capability to reve

219 The use of surface-enhanced Raman spectroscopy (SERS) to determine spectral markers for th

220 th minimally invasive surface-enhanced Raman spectroscopy (SERS).

221 ing pH nanoprobes and surface-enhanced Raman spectroscopy (SERS).

222 and surface enhanced spatially offset Raman spectroscopy (SESORS), and reviews the progress made in

223 s same H(2)O coverage, transmission infrared spectroscopy showed that forsterite dissolution begins a

224 rformed by proton-nuclear magnetic resonance spectroscopy showed that the particulate organic carbon

225 Ambient-pressure x-ray photoelectron spectroscopy showed that water added to methane and oxyg

226 Spectroscopy shows that, in contrast to other alphaKG-de

227 In this work, (71) Ga NMR spectroscopy shows the presence of [Ga(arene)(n) ](+) sa

228 Single molecule force spectroscopy (SMFS) reveals that the force necessary to

229 ganic substrates using single-molecule force spectroscopy (SMFS).

230 As a new type of imaging spectroscopy, SMOLM exposes the organizational and funct

231 duced micro- and submicro-X-ray fluorescence spectroscopy (SR-XRF), gadolinium was detected in human

232 Recent advanced EPR and Mn K-edge X-ray spectroscopy studies converge upon the HO model.

233 However, most prior magnetic resonance spectroscopy studies had small samples (all <60, most <2

234 In addition, the electrochemical impedance spectroscopy studies observed that L-MT sample performed

235 ectance-surface-enhanced infrared absorption spectroscopy) study of a sputtered thin film Ag cathode

236 sses SORS and related variants of deep Raman spectroscopy such as transmission Raman spectroscopy (TR

237 tron vacuum ultraviolet photoionization mass spectroscopy (SVUV-PIMS), which uncovers the existence o

238 antitative Nuclear Magnetic Resonance (qNMR) spectroscopy technique has certain advantages such as lo

239 re and dynamics via imaging or combined with spectroscopy techniques such as fluorescence correlation

240 roscopy coupled with energy dispersive X-ray spectroscopy (TEM-EDX) is a powerful tool for determinin

241 tion, and vibrational, electronic, and X-ray spectroscopies that exist, along with the results of the

242 t enhanced sequences, and magnetic resonance spectroscopy that may provide insight into the biologica

243 chroism and nuclear magnetic resonance (NMR) spectroscopy that Spp2 is intrinsically disordered in so

244 Using solid-state (15)N NMR spectroscopy, the cis/trans isomerization in a two-dimen

245 ctron microscopy, Fourier-transform infrared spectroscopy, thermogravimetric analysis and X-ray diffr

246 resonance spectroscopy, ultraviolet-visible spectroscopy, thermogravimetric analysis, scanning elect

247 With the aid of positron annihilation spectroscopy, this study, for the first time, demonstrat

248 erefore demonstrate the capability for Raman spectroscopy to be used as an analytical tool to measure

249 edance spectroscopy and deep-level transient spectroscopy to characterize the ionic defect landscape

250 n (XRD) and nuclear magnetic resonance (NMR) spectroscopy to demonstrate that the apparent first-cycl

251 d employing nuclear magnetic resonance (NMR) spectroscopy to determine the reaction kinetic profile.

252 nking and immunoprecipitation (CLIP) and NMR spectroscopy to identify and characterise physiological

253 Here we used NMR and optical spectroscopy to identify conditions that enable the capt

254 This work uses nuclear magnetic resonance spectroscopy to investigate metabolic differences betwee

255 spectroscopy and Fourier-transform infrared spectroscopy to investigate the conversion pathway of Cr

256 We use magnetic tweezers force spectroscopy to measure changes in extension and mechani

257 ontrol subjects underwent magnetic resonance spectroscopy to measure glutamate, glutamate+glutamine (

258 luorescence microscopy and image correlation spectroscopy to monitor and map diffusion of fluorescent

259 lly demonstrate the capability of deep Raman spectroscopy to noninvasively monitor changes in the wat

260 Here we apply NMR spectroscopy to patient-derived samples of alpha(1)-anti

261 We also used transient absorption spectroscopy to study the best performing system and we

262 ndent two-dimensional electronic-vibrational spectroscopy to study the origin and dynamics of the mix

263 nd showed the feasibility of MRI and (1)H MR spectroscopy to track disease progression over a wide ra

264 e have utilized label-free spontaneous Raman spectroscopy to understand the structural differences in

265 icularly operando X-ray absorption and Raman spectroscopy, to study the mechanism of OER on cobalt ox

266 ing electron microscopy, X-ray photoelectron spectroscopy, transmission electron microscopy and energ

267 cated in its center using transmission Raman spectroscopy (TRS) by monitoring the change of the OH (~

268 aman spectroscopy such as transmission Raman spectroscopy (TRS), micro-SORS and surface enhanced spat

269 red spectroscopy, nuclear magnetic resonance spectroscopy, ultraviolet-visible spectroscopy, thermogr

270 We performed Raman spectroscopy under pressure on this porous composite to

271 ay absorption near edge structure (HR-XANES) spectroscopy, under conditions of high MeHg production (

272 th conventional and two-dimensional infrared spectroscopy, vibrational circular dichroism, and optica

273 Fourier-transform infrared (FTIR) spectroscopy was applied to predict the degree of hydrol

274 cing and fecal/urinary metabolites by 1H-NMR spectroscopy was complemented with targeted quantificati

275 ts of quartz in amorphous silica gels by NMR spectroscopy was developed and tested on commercially av

276 metry (UHPLC-HRMS) supported by 1 and 2D NMR spectroscopy was used for unambiguous metabolic profilin

277 Using single-molecule force spectroscopy, we also define the response of the protein

278 heoretical computation and time-resolved EPR spectroscopy, we confirmed that the ISC of the bodipy re

279 l characterization of the knot region by NMR spectroscopy, we identify the SAM-binding region and obs

280 sing FRET and fluorescence cross-correlation spectroscopy, we introduce a method to measure surface p

281 Using radiofrequency spectroscopy, we probed the energy, spectral width, and

282 To demonstrate computational spectroscopy, we provide our algorithm with the measured

283 igration using operando electron energy-loss spectroscopy, we reveal that facile transport in Li(4+)

284 electron microscopy and electron energy-loss spectroscopy, we show that beryllium oxide crystallizes

285 ), and electron paramagnetic resonance (EPR) spectroscopy were used to estimate structural characteri

286 ful approach is angle-resolved photoelectron spectroscopy, whereby the kinetic energy and angle of ph

287 published fluorescence lifetime correlation spectroscopy which relies on lifetime differences as a m

288 s performed via TEM and electron energy loss spectroscopy, which indicated a high level of sp(2) bond

289 sentative areas of the filter by micro-Raman spectroscopy will allow proper quantification of micropl

290 brational sum frequency generation (TR-vSFG) spectroscopy with ab initio DFT-based molecular dynamics

291 By combining Raman spectroscopy with two-dimensional (2D) perturbation corr

292 salts are characterized by multinuclear NMR spectroscopy, X-ray analysis, as well as their calculate

293 ron spectroscopy, Fourier transform infrared spectroscopy, X-ray diffraction, and electron microscopy

294 Fourier transform infrared spectroscopy, X-ray diffraction, and gelatinization assa

295 During the last decades, X-ray absorption spectroscopy (XAS) has become an indispensable method fo

296 ), UV-vis spectroscopy, and X-ray absorption spectroscopy (XAS).

297 econd Fe K(alpha) and K(beta) X-ray emission spectroscopy (XES) with Fe K-edge X-ray absorption near-

298 upation is determined through X-ray emission spectroscopy (XES).

299 X-ray photoelectron spectroscopy (XPS) and attenuated total reflectance Four

300 Raman and X-Ray photoelectron spectroscopy (XPS) revealed that the synthesized few-lay