ライフサイエンスコーパス: solid-state NMR

1 osquitoes was investigated in vivo using 13C solid-state NMR.

2 re we report high-resolution (17)O (I = 5/2) solid-state NMR spectra of the mixed-conducting solid ox

3 to each site symmetry, render advanced 27Al solid-state NMR a unique spectroscopic tool to fingerpri

4 short-range structure results from 1D and 2D solid-state NMR experiments.

5 1D and 2D solid-state NMR, as well as XRD data on lithiated sample

6 rve resolution approach (MCR), to denoise 2D solid-state NMR spectra, yielding a substantial S/N rati

7 amma-Al(2)O(3) by using two-dimensional (2D) solid-state NMR spectroscopy at high field.

8 Here, we present a proton-detected 4D solid-state NMR assignment procedure that is tailored fo

9 A solid-state NMR temperature series reveals that KirBac1.

10 Additionally, solid-state NMR was used to demonstrate correlation betw

11 Advanced solid-state NMR and quantum-chemical methods allow us to

12 Although highly consistent with all solid-state NMR observables, the ensembles of more than

13 only multidimensional diffusion MR but also solid-state NMR spectroscopy due to the mathematical sim

14 as quantified, using neutron diffraction and solid state NMR.

15 olecular modeling, molecular simulation, and solid state NMR suggests that inversion of the symmetric

16 sed transmission EM, biochemical assays, and solid-state NMR spectroscopy of representative isolates

17 Dye binding and solid-state NMR studies reveal changes in fibril surface

18 g density functional theory calculations and solid-state NMR spectroscopy.

19 ermediates using circular dichroism (CD) and solid-state NMR reveal that the dimer and oligomers have

20 haracterization by X-ray crystallography and solid-state NMR spectroscopy.

21 ouble electron-electron resonance (DEER) and solid-state NMR (ssNMR) spectroscopy to refine the struc

22 branes by combining electrophysiological and solid-state NMR experiments.

23 diffraction, hydrogen-deuterium exchange and solid-state NMR studies map the beta-forming region to a

24 ation lifetime spectroscopy (PALS), FTIR and solid-state NMR spectroscopy) to demonstrate how a hiera

25 Fourier transform infrared and solid-state NMR spectroscopic studies reveal a central b

26 lementary techniques, including infrared and solid-state NMR spectroscopies.

27 According to IR and solid-state NMR, the methyl group remains intact, and do

28 Combining both liquid- and solid-state NMR, we demonstrate that structural rearrang

29 e, fluorescence anisotropy measurements, and solid-state NMR spectroscopy to study the influence of p

30 nformation from cryo-electron microscopy and solid-state NMR spectroscopy is combined in a single str

31 d using transmission electron microscopy and solid-state NMR spectroscopy.

32 idimetry, cryogenic electron microscopy, and solid-state NMR measurements.

33 ssemble into semi-elliptical nanosheets, and solid-state NMR provides insight into the self-assembly

34 ray crystallography, solution-state NMR, and solid-state NMR to follow at the atomic level the assemb

35 ds, ab initio calculated chemical shifts and solid-state NMR experiments are powerful methods for cry

36 all-atom molecular dynamics simulations and solid-state NMR further reveal that the CypA-binding pat

37 nation of molecular dynamics simulations and solid-state NMR shows that a higher propensity for backb

38 all-atom molecular dynamics simulations and solid-state NMR spectroscopy.

39 n of molecular dynamics (MD) simulations and solid-state NMR was used to present an atomistic model o

40 rface has been characterized by solution and solid-state NMR and biochemical techniques but never cry

41 ere determined using a combined solution and solid-state NMR approach.

42 Using a combination of solution and solid-state NMR experiments, cosedimentation assays, dif

43 analyzed with a combination of solution and solid-state NMR techniques, including dynamic nuclear po

44 main of the Het-s protein using solution and solid-state NMR, electron and atomic force microscopies,

45 -validated examples using both solution- and solid-state NMR data.

46 es on the close integration of solution- and solid-state NMR methods and is generally applicable to s

47 that combines the strengths of solution- and solid-state NMR to measure dipolar, chemical shift, and

48 lecular assemblies, using both solution- and solid-state NMR.

49 Fourier transform infrared spectroscopy and solid-state NMR spectroscopy validate the N-H(2) group a

50 Two-dimensional liquid-state and solid-state NMR experiments were used to assign lipid (1

51 A match between the calculated structure and solid-state NMR was found by testing multiple semi-local

52 wder and fiber X-ray diffraction studies and solid-state NMR experiments.

53 alculations, diffuse reflectance UV-vis, and solid-state NMR spectroscopies.

54 ted by combining in situ synchrotron XRD and solid-state NMR techniques.

55 Here we report 1.4- and 1.5- angstrom solid-state NMR structures of the transmembrane domain o

56 Here, we describe how one can apply solid-state NMR, ranging from 1D chemical shift assignme

57 Using (11) B solid-state NMR spectroscopy, we show that the majority

58 y improve spectral sensitivity in biological solid-state NMR (ssNMR), thus allowing the study of larg

59 d the edge groups are formed as confirmed by solid state NMR spectroscopy.

60 ure, unobservable by XRD but demonstrated by solid state NMR studies.

61 gh-resolution powder diffraction data and by solid-state NMR spectroscopy.

62 withSiO)Lu[CH(SiMe3)2]2] is characterized by solid-state NMR and EXAFS spectroscopy, which show that

63 cal monomeric composition as demonstrated by solid-state NMR, complemented by spectroscopic, thermal,

64 hNM dynamics was determined by solid-state NMR and revealed that the lamellar gel-to-fl

65 man hormone beta-endorphin was determined by solid-state NMR.

66 recedented two-step process as elucidated by solid-state NMR and molecular dynamics simulation.

67 uid-crystalline lipid bilayer environment by solid-state NMR spectroscopy.

68 in these surface inclusions was examined by solid-state NMR and X-ray powder diffraction.

69 structural analysis of wild-type fibrils by solid-state NMR suggests a molecular repeat unit compris

70 osphate- and carbohydrate-induced fibrils by solid-state NMR.

71 porcine aortic elastin exposed to glucose by solid-state NMR spectroscopic and relaxation methodologi

72 bution of beta-strand segments identified by solid-state NMR, we propose that the DUF583 domain adopt

73 tingly, Q(4) (nAl) Si speciation measured by solid-state NMR can only be modeled with a few combinati

74 e, we show that such data can be obtained by solid-state NMR enhanced by dynamic nuclear polarization

75 zed at the molecular level, in particular by solid-state NMR, and their alkyne metathesis catalytic a

76 These processes are probed by solid-state NMR spectroscopy, including (129) Xe SSNMR.

77 try of membrane-associated HAfp is probed by solid-state NMR.

78 ion-state NMR) and of a membrane protein (by solid-state NMR) were published in 2001 and 2011, respec

79 lycosyl diastereomers to NKA were studied by solid-state NMR (SSNMR), which revealed interactions of

80 Structural and computational studies by solid-state NMR spectroscopy, XAS, and periodic DFT meth

81 intact mosquitoes were monitored using (13)C solid-state NMR and ATR-FTIR.

82 A newly designed 3D (2)H-(13)C-(13)C solid-state NMR magic angle spinning (MAS) experiment is

83 ecular correlation times obtained from (13)C solid-state NMR spectroscopy measurements establish the

84 , and proteins/peptides using advanced (13)C solid-state NMR techniques.

85 The (19)F-(19)F CODEX solid-state NMR experiments performed with ALM in POPC l

86 Here the authors combine solid-state NMR measurements and molecular dynamics simu

87 Here we combine solid-state NMR and structural bioinformatics to determi

88 Here, we combine solid-state NMR spectroscopy, isotherm measurements, and

89 Herein, combined solid-state NMR and synchrotron X-ray powder diffraction

90 structural refinement approach that combines solid-state NMR experiments and molecular simulations to

91 We report nearly complete solid-state NMR (ssNMR) resonance assignments of Rous sa

92 a virus-mimetic lipid membrane and conducted solid-state NMR experiments to probe the membrane-bound

93 rization of materials for which conventional solid-state NMR is impractical due to the lack of sensit

94 Correlated solid-state NMR, X-ray, and electron microscopy analyses

95 osts" and applied 2D (13)C-(13)C correlation solid-state NMR to reveal the carbon-based architecture

96 Two-dimensional (1)H-(17)O correlation solid-state NMR spectra allow overlapping oxygen sites t

97 Surface-selective (133)Cs solid-state NMR spectra show the presence of an addition

98 Here we describe solid state NMR measurements on the dimerization interfa

99 Detailed solid-state NMR analysis of molecular and silica-support

100 ar dynamics simulations, circular dichroism, solid-state NMR and patch clamp to investigate the exten

101 sing variable-temperature X-ray diffraction, solid-state NMR spectroscopy, and periodic DFT calculati

102 Surprisingly, two-dimensional solid state NMR shows that the contact between Phe(19) a

103 nts of signals in two- and three-dimensional solid-state NMR spectra, conformation-dependent (15)N an

104 aracterized by elemental analysis and DRIFT, solid-state NMR, and EXAFS spectroscopy.

105 elopment of BM2 inhibitors, we have employed solid-state NMR spectroscopy to investigate the conforma

106 dynamic nuclear polarization (DNP)-enhanced solid-state NMR, we were able to analyze the retinal pol

107 They further show that DNP-enhanced solid-state NMR fills the gap for challenging membrane p

108 Conventional and DNP-enhanced solid-state NMR provides a molecular-level understanding

109 ilitated tremendously by use of DNP-enhanced solid-state NMR spectroscopy.

110 pyridine, and (29)Si and (27)Al DNP-enhanced solid-state NMR spectroscopy.

111 also demonstrates the power of DNP-enhanced solid-state NMR to bridge the gap between functional and

112 s was generated and analyzed by DNP-enhanced solid-state NMR.

113 ld and dynamic nuclear polarization-enhanced solid-state NMR utilizing a (13)C-labeled retinal cofact

114 nuclear polarization (DNP) surface-enhanced solid-state NMR techniques.

115 nformer approaches in implicit environments, solid-state NMR restrained ensemble simulations in expli

116 model membrane protein and its experimental solid-state NMR data, we performed restrained ensemble d

117 in explicit membranes that uses experimental solid-state NMR observables to obtain the refined struct

118 art experimental methods including extensive solid-state NMR techniques and HAADF-STEM imaging.

119 the first time, to our knowledge, for (19)F solid-state NMR distance and oligomerization measurement

120 ynthesized and investigated using high-field solid-state NMR spectroscopy, X-ray diffraction, atomic

121 iameter of > ca. 40 nm) can be exploited for solid-state NMR studies on membrane proteins.

122 than the proteoliposomes most often used for solid-state NMR (SSNMR) studies, and differences may aff

123 20/DMD simulation agree well with those from solid state NMR experiments.

124 From solid-state NMR experiments we conclude that the NOE is

125 rrently structural information obtained from solid-state NMR is usually included only after a set of

126 (1)H solid-state NMR allowed the quantification of the hydrog

127 Using spin-lattice relaxation (1)H solid-state NMR at 29.49 and 13.87 MHz in the temperatur

128 n be investigated by applying (17)O and (1)H solid-state NMR spectroscopy and dynamic nuclear polariz

129 idimensional single- and double-quantum (1)H solid-state NMR spectroscopy with density functional the

130 l(-1) These results were confirmed with (2)H solid-state NMR line-shape analysis and spin-lattice rel

131 Furthermore, (31)P and (2)H solid-state NMR spectra show that liquid crystalline 1,2

132 re investigated by variable-temperature (2)H solid-state NMR spectroscopy to reveal the reorientation

133 Variations in solid state NMR signals from certain amino acid side cha

134 ce assignments remains a major bottleneck in solid-state NMR studies of protein structure and dynamic

135 ncy of dynamic nuclear polarization (DNP) in solid-state NMR studies.

136 sed on the analysis of absent cross-peaks in solid-state NMR correlation experiments.

137 which has been used to enhance the signal in solid-state NMR, has also been applied to the study of f

138 ough a multidisciplinary approach, including solid-state NMR (SSNMR) and cryo electron microscopy (cr

139 iew of characterization techniques including solid-state NMR and photothermal induced resonance, and

140 vel using a combination of (31)P and (139)La solid state NMR spectroscopy (SSNMR), extended X-ray abs

141 Li solid-state NMR results show an increase in Li(+) ions (

142 1-42 and 69-77, which are visible in the MAS solid-state NMR spectra, show (13)Calpha chemical shifts

143 Using MAS solid-state NMR, we studied the fibril structure of a re

144 rom phosphorus-31 magic angle spinning (MAS) solid state NMR spectroscopy, bolstering the structural

145 Magic-angle-spinning (MAS) solid-state NMR (ssNMR) spectroscopy allows for the dete

146 olarization (DNP) magic-angle spinning (MAS) solid-state NMR (ssNMR) spectroscopy has the potential t

147 Although magic angle spinning (MAS) solid-state NMR is a powerful technique to obtain atomic

148 Multidimensional magic angle spinning (MAS) solid-state NMR of uniformly (13)C,(15)N-labeled protein

149 beling scheme for magic angle spinning (MAS) solid-state NMR that is based on deuteration in combinat

150 tructure is validated by previously measured solid-state NMR, electron microscopy, and X-ray diffract

151 high-molecular-weight proteins, using modern solid state NMR methods.

152 We find that multidimensional solid state NMR spectra of (15)N,(13)C-labeled CA assemb

153 Multidimensional solid-state NMR (SSNMR) spectroscopy experiments reveal

154 Here, we use (13)C multidimensional solid-state NMR to analyse the polymer interactions in n

155 Oriented (15)N solid-state NMR indicates that in membranes composed of

156 ate to AuNPs is obtained by (13)C and (23)Na solid-state NMR in combination with computational modell

157 e of spectroscopic methods, including (23)Na solid-state NMR, Mossbauer, and X-ray photoelectron spec

158 (93)Nb solid-state NMR spectra of 1a-3a and (31)P solid-state N

159 Here we report new solid-state NMR constraints that indicate antiparallel i

160 Presented here is a new solid-state-NMR-based quantification method for componen

161 ometry (ESI-TOF and LC-MS), as well as (17)O solid state NMR (for the (17)O labeled species).

162 new DNP-based measurements that extend (17)O solid-state NMR beyond its current capabilities.

163 Labeling studies and (17)O solid-state NMR data confirm that two-thirds of the oxyg

164 Unfortunately, (17)O solid-state NMR experiments are often hindered by a comb

165 ance the sensitivity and resolution of (17)O solid-state NMR experiments.

166 ted the application and development of (17)O solid-state NMR spectroscopy as a probe of molecular str

167 Here, the authors use (17)O solid-state NMR spectroscopy to discriminate between oxy

168 We used (17)O solid-state NMR spectroscopy to follow this process and

169 al model for proteins with recently obtained solid-state NMR spectroscopy data and amino acid contact

170 er to molecular level by the combined use of solid state NMR and X-ray scattering.

171 Herein, we demonstrate the application of solid-state NMR spectroscopy on native, heterogeneous th

172 onstrates the principles and applications of solid-state NMR by unifying dipolar and quadrupolar inte

173 ure was established through a combination of solid-state NMR (SSNMR) experiments, including J-resolve

174 A combination of solid-state NMR and circular dichroism experiments found

175 e studied in detail through a combination of solid-state NMR experiments, using labeled ethylene, and

176 Here we use a combination of solid-state NMR spectroscopy and potential energy landsc

177 The results show that the combination of solid-state NMR, XRD, and DFT can improve structure refi

178 Concepts of solid-state NMR spectroscopy and applications to fluid m

179 cording, in a matter of minutes to hours, of solid-state NMR spectra suitable for quantitative analys

180 s, as they are under the strong influence of solid-state NMR restraints.

181 By means of solid-state NMR, we confirm this prediction, demonstrati

182 1alpha phases and showcases the potential of solid-state NMR to detect an elusive biophysical regime

183 ransporter protein and presents the power of solid-state NMR in this growing field.

184 ique to improve the signal to noise ratio of solid-state NMR experiments.

185 ent approach for boosting the sensitivity of solid-state NMR (ssNMR) spectroscopy, thereby enabling t

186 rged as a tool to enhance the sensitivity of solid-state NMR experiments.

187 s elucidated through the combined studies of solid-state NMR and X-ray absorption near-edge structure

188 Most structure calculations based on solid-state NMR observables are performed using simulate

189 In oriented-sample (OS) solid-state NMR of membrane proteins, the angular-depend

190 Our solid-state NMR data showed that these fibrils consist o

191 Previously, our solid-state NMR studies of isolated melanized cell walls

192 b solid-state NMR spectra of 1a-3a and (31)P solid-state NMR on their PMe3 derivatives 1b-3b led to t

193 Here, we employ nondestructive (31)P solid-state NMR spectroscopy to investigate the chemical

194 a strategy that combines sparse paramagnetic solid-state NMR restraints with physics-based atomistic

195 By performing solid-state NMR measurements at very fast (100 kHz) magi

196 We present solid-state NMR measurements of beta-strand secondary st

197 We present solid-state NMR measurements of this open mutant at neut

198 imulations accurately predicted our previous solid-state NMR data and newly acquired electron paramag

199 ectroscopy (DNP-SENS), to obtain the (195)Pt solid-state NMR spectra of a prototypical example of hig

200 s experimentally studied by (2)H and (195)Pt solid-state NMR spectroscopy (powder pattern changes wit

201 PGLa are in excellent agreement with recent solid state NMR experiments.

202 its relation to the fibril core, we recorded solid-state NMR and EPR data on fibrils formed by the fi

203 However, (13)C-(13)C dipolar recoupling solid-state NMR measurements also identify nonnegligible

204 We report solid-state NMR (ssNMR) measurements on spherical virus-

205 r and outer membranes, yield high-resolution solid-state NMR spectra that reflect the structure of Ai

206 lts highlight the utility of high-resolution solid-state NMR spectroscopy for studying ligand binding

207 High-resolution solid-state NMR spectroscopy shows water interacting wit

208 om Caulobacter crescentus by high-resolution solid-state NMR spectroscopy.

209 enhance the sensitivity of surface-selective solid-state NMR experiments by 1-2 orders of magnitude.

210 lear polarization enhanced (27)Al and (29)Si solid-state NMR experiments.

211 DOR process through a combination of in situ solid-state NMR spectroscopy and powder X-ray diffractio

212 The use of in situ solid-state NMR to probe the transition from intracrysta

213 a combination of reactivity studies, in situ solid-state NMR, and an extensive series of DFT calculat

214 identify the challenges and devise a (119)Sn solid-state NMR protocol for the determination of the lo

215 out by X-ray diffraction, mass spectrometry, solid-state NMR, and diffuse reflectance UV-vis (DR UV-v

216 amined by DFT calculations, IR spectroscopy, solid-state NMR spectroscopy, and analysis of the Cambri

217 measurement, photoluminescence spectroscopy, solid-state NMR, and X-ray absorption spectroscopy, etc.

218 and neutron diffraction, Raman spectroscopy, solid-state NMR, transmission electron microscopy and fi

219 estraints obtained from magic-angle spinning solid-state NMR experimental data.

220 eparin analogue enabled magic-angle spinning solid-state NMR of the GAG bound to 3Q fibrils, and meas

221 infrared spectroscopy, magic angle spinning solid-state NMR spectroscopy, and van der Waals-correcte

222 describe (1)H-detected magic angle spinning solid-state NMR studies of monomeric IL-8 (1-66) bound t

223 Here we present a magic angle spinning solid-state NMR study demonstrating that the NSAID sulin

224 e use multi-dimensional magic angle spinning solid-state NMR to characterize the sorghum secondary ce

225 r polarization enhanced magic angle spinning solid-state NMR to study this challenging membrane prote

226 Using advanced magic angle spinning solid-state NMR, we directly probe the structure of the

227 Using magic-angle-spinning solid-state NMR spectroscopy, we show that the TMD of th

228 Using (2)H static solid-state NMR approaches, we compare the dynamics in t

229 Here, we used (2)H static solid-state NMR methods to probe the dynamics of selecte

230 The (105)Pd static solid-state NMR illustrates how different types (and lev

231 agic-angle-spinning (MAS) and (105)Pd static solid-state NMR nuclear magnetic resonance (NMR), synchr

232 ayers and its membrane topology using static solid-state NMR spectroscopy.

233 Surprisingly, solid-state NMR reveals that these amorphous deposits ha

234 ting a multitude of experimental techniques (solid-state NMR, AFM, SLS, DLS, FT-IR, CD) with large- a

235 stances using dipolar recoupling techniques, solid state NMR chemical shifts, and long-range side cha

236 mixing, freeze-trapping, and low-temperature solid-state NMR (ssNMR) with signal enhancements from dy

237 X-ray diffraction, and variable-temperature solid-state NMR by (13)C cross-polarization magic angle

238 Herein, we demonstrate that solid-state NMR spectroscopy allows the unambiguous assi

239 membrane protein green proteorhodopsin that solid-state NMR could identify specific interactions at

240 helix 9 segments from the cryoEM study, the solid state NMR data lead to a unique high-resolution st

241 red segments, which do not contribute to the solid state NMR spectra.

242 The solid-state NMR approach developed here is generally app

243 The solid-state NMR chemical shifts of the PLP pyridine ring

244 ion of Bronsted acid sites: By enhancing the solid-state NMR signals of (17) O at natural abundance w

245 tions and the concentrated conditions of the solid-state NMR samples, we found substantial amounts of

246 lyses, are shown to be inconsistent with the solid-state NMR results.

247 Though solid-state NMR spectroscopy has the potential to reveal

248 e homogeneous fibril population according to solid-state NMR analysis.

249 We apply our approach to solid-state NMR data for the model protein GB1 labeled w

250 um corneum (SC), using polarization transfer solid-state NMR on natural abundance (13)C in intact SC.

251 MAX1 fibril network is kinetically trapped, solid-state NMR data show that fibrils within this netwo

252 Here the authors use solid-state NMR to study prion protein (PrP) amyloids fr

253 To address this question, we use solid-state NMR and FTIR spectroscopy to define the orie

254 Here we use solid-state NMR relaxation dispersion measurements with

255 Here we use solid-state NMR spectroscopy to derive for the first tim

256 Here we use solid-state NMR spectroscopy to investigate the conforma

257 Here we use solid-state NMR spectroscopy to investigate the global f

258 Here, we use solid-state NMR spectroscopy to investigate the structur

259 Here we use solid-state NMR spectroscopy to investigate the water in

260 Here we use solid-state NMR spectroscopy to track the conformational

261 Here, we use solid-state NMR to determine the 3D structure of the amy

262 Here we use solid-state NMR to determine the atomic-resolution struc

263 We use solid-state NMR to determine the molecular and supramole

264 Here we use solid-state NMR, X-ray diffraction methods and mus-long

265 Here we used solid state NMR to specifically characterize the bound l

266 In the present study we have used solid-state NMR and restrained MD simulations to refine

267 ton conduction property of BM2, we have used solid-state NMR to characterize the pH-dependent structu

268 To tackle this question, we used solid-state NMR strategies providing assignments of non-

269 ily as ammonium carbamates, we observe using solid state NMR that the major chemisorption product for

270 Using solid-state NMR and deprotonation energy calculations, t

271 Using solid-state NMR and molecular dynamics simulations in a

272 Using solid-state NMR, we found that the overall structure of

273 Using solid-state NMR, we solved the structure of P1 bound to

274 ntacts in virus-mimetic lipid bilayers using solid-state NMR spectroscopy, and augmented these experi

275 he M2 protein in phospholipid bilayers using solid-state NMR spectroscopy.

276 now investigated a H27A mutant of BM2 using solid-state NMR.

277 By using solid-state NMR with fast magic-angle spinning (MAS) at

278 an and wall teichoic acid compositions using solid-state NMR.

279 transmembrane domain (ETM), determined using solid-state NMR spectroscopy.

280 f the Rh...H-C motif can be determined using solid-state NMR spectroscopy.

281 l packing alters microsecond dynamics, using solid-state NMR measurements and multi-microsecond MD si

282 function study on the SMR protein EmrE using solid-state NMR spectroscopy in lipid bilayers and resis

283 Here, using solid-state NMR spectroscopy in combination with coarse-

284 n of their protein-ligand interactions using solid-state NMR.

285 of teixobactins in cellular membranes using solid-state NMR, microscopy, and affinity assays.

286 rst study on membrane-associated pHLIP using solid-state NMR spectroscopy.

287 electronic and mechanical properties, using solid-state NMR spectroscopy to examine a variety of nuc

288 S), bound to mesoporous silica (SBA15) using solid-state NMR and FTIR spectroscopy.

289 complex on an amorphous silica surface using solid-state NMR measurements, enabled through a dynamic

290 membrane proteins in lipid environments via solid-state NMR.

291 ic studies of the membrane-bound protein via solid-state NMR and optical spectroscopy.

292 Whereas solid-state NMR (SSNMR) spectroscopy has recently been u

293 While solid-state NMR spectroscopic techniques have helped cla

294 mulation of NMR spectra, in combination with solid-state NMR experiments.

295 scale force measurements in combination with solid-state NMR spectroscopy to show that the cohesive p

296 prerequisite for distance measurements with solid-state NMR.

297 e devices have been extensively studied with solid-state NMR spectroscopy.

298 In this work, solid-state NMR spectroscopy is used to address these ce

299 The combined XAS, solid state NMR, and DFT data argue that the bulky catal

300 In the last few years, solid-state NMR spectroscopy enabled the determination o