ライフサイエンスコーパス: NMR spectra

1 rape varieties and 4 locations based on (1)H NMR spectra.

2 of the amino acids of CaM in (1)H-(15)N HSQC NMR spectra.

3 ransformations could be observed in FTIR and NMR spectra.

4 ssible through the analysis of routine (13)C NMR spectra.

5 up to 100% according to their LC-MS and (1)H NMR spectra.

6 traction in D2O in order to acquire the (1)H NMR spectra.

7 ed by monitoring signal perturbations in the NMR spectra.

8 pid mixtures from 1D (31)P and 2D (1)H-(31)P NMR spectra.

9 btained from high field magic angle spinning NMR spectra.

10 , which do not contribute to the solid state NMR spectra.

11 ilitates visual inspection of the associated NMR spectra.

12 the appearance of a CO2 peak on the FTIR and NMR spectra.

13 rance of two distinct sets of signals in the NMR spectra.

14 C and (13)C-(15)N magic angle spinning (MAS) NMR spectra.

15 the near-silence of the ITC carbon in (13)C NMR spectra.

16 al intensities in magic-angle spinning (MAS) NMR spectra.

17 they greatly simplify the interpretation of NMR spectra.

18 and provides chemical resolution missing in NMR spectra.

19 of one-dimensional (1D) or multidimensional NMR spectra.

20 he corresponding UV/Vis absorption and (13)C NMR spectra.

21 nts from interleaved natural abundance (13)C NMR spectra.

22 n the gel as can be seen from the (29)Si MAS NMR spectra.

23 f the oligomers gave discrete (1)H and (13)C NMR spectra.

24 scape, yet are often "invisible" in standard NMR spectra.

25 d results in large chemical shift changes in NMR spectra.

26 unprecedented shifts up to -24 ppm in (7) Li NMR spectra.

27 f parahydrogen-originating hydrogens in (1)H NMR spectra.

28 ion-based algorithm, to quantify time-series NMR spectra.

29 beling patterns and data from other types of NMR spectra.

30 of cells to the acquisition and analysis of NMR spectra.

31 es of (1)H and (13)C satellite peaks in (1)H NMR spectra.

32 titration curves, but also the lineshapes of NMR spectra.

33 ring experimental and DFT calculated (195)Pt NMR spectra.

34 best or even impossible for some regions in NMR spectra.

35 peaks from individual metabolites in complex NMR spectra.

36 ning process, could be monitored through the NMR spectra.

37 AMEs was achieved based on the recorded (1)H NMR spectra.

38 ving rise to changes in the luminescence and NMR spectra.

39 f time series of nuclear magnetic resonance (NMR) spectra.

40 y (GPC) and (1)H nuclear magnetic resonance (NMR) spectra.

41 (1D) imino (1)H NMR as well as by 2D HyperW NMR spectra acquired upon simultaneous injection of hype

42 efold enhancements were observed in the (1)H NMR spectra after sample transfer to high field (9.4 T).

43 alent-bond 2D (27) Al{(29) Si} J-correlation NMR spectra allow distinct framework Al sites to be iden

44 mensional (1)H-(17)O correlation solid-state NMR spectra allow overlapping oxygen sites to be resolve

45 (15)N NMR spectra allow the extraction of four H37 pKas and sh

46 (17)O NMR spectra allowed identification and distinction of va

47 enhancements observed in the resulting (1)H NMR spectra allowed us to monitor in real time the chang

48 The NMR spectra also show significant peak broadening, indic

49 of the crystal structure of the catalyst and NMR spectra analysis, a bifunctional catalytic model was

50 S models were built on diffusion-edited (1)H NMR spectra and calibrated on HPLC-derived lipoprotein s

51 processing during the interpretation of (1)H NMR spectra and complementary IR spectra.

52 High resolution (1)H NMR spectra and DFT calculations provided evidence for t

53 VT-NMR spectra and DFT calculations were used to determine

54 (31)P NMR spectra and DFT investigation provide indication tha

55 Mytilitol was quantified in the (1)H NMR spectra and its average relative concentration turne

56 range of coalescence temperatures in the VT NMR spectra and occurrence of the isosbestic points in t

57 Solid-state NMR spectra and optimized structures obtained from van d

58 Solid-state (13)C NMR spectra and single-crystal X-ray diffraction structu

59 (31)P NMR spectra and small-angle X-ray scattering (SAXS) data

60 tes were identified by line-fitting of 1D 1H-NMR spectra and the use of statistical total correlation

61 approach that simulates (13) C multiplets in NMR spectra and utilizes mass increments to obtain long-

62 NMR spectra and X-ray structures of hybrid [n]arenes ind

63 pproaches used for acquiring high-resolution NMR spectra, and discuss the information that these spec

64 characterized by infrared, and multinuclear NMR spectra, and elemental analyses.

65 ully characterized by infrared, multinuclear NMR spectra, and elemental analysis.

66 uses a combination of conventional 1D and 2D NMR spectra, and residual dipolar couplings (RDCs), is r

67 for rapid and unbiased processing of complex NMR spectra applied for the first time to human faecal m

68 Proton NMR spectra are indispensable for structural characteriz

69 Systematic collections of NMR spectra are often analyzed in terms of the changes i

70 A major problem, however, is that proton NMR spectra are often extensively overlapped, so that in

71 for cryo-EM and in the solution phase where NMR spectra are recorded.

72 However, NMR spectra are sometimes nonconclusive, e.g., if spectr

73 urement of both liquid-state and solid-state NMR spectra as a function of time.

74 shapes and two-dimensional (1)H-(17)O HETCOR NMR spectra as well as accurate internuclear distance me

75 Its simple NMR spectra, as well as HDFT calculations, indicate that

76 The NMR spectra assignment was performed using the novel NOA

77 is not easy to obtain well-resolved in-cell NMR spectra because the detectability and resolution of

78 rred, and these explain the strongly shifted NMR spectra by spin density contributions at the hydroge

79 econvolution and quantification from complex NMR spectra by using the Bayesian automated metabolite a

80 ermediates below the detection limit of (1)H NMR spectra can be applied also to other classes of cata

81 NMR spectra can be fitted or simulated starting with use

82 after dissolving the silica matrix, the (1)H NMR spectra can be resolved for every single component o

83 ty of this para-H2 experiment, the resulting NMR spectra can have hydride signal-to-noise ratios exce

84 nd co-workers describe the use of routine 1D NMR spectra (chemical shifts, chemical shift dispersion,

85 that the detectability and resolution of the NMR spectra clearly depended on the growth phase of the

86 gnals in one-dimensional and two-dimensional NMR spectra, confirming the ligninolytic capabilities of

87 ls in two- and three-dimensional solid-state NMR spectra, conformation-dependent (15)N and (13)C NMR

88 Computational deconvolution of (1)H NMR spectra containing the components for more than one

89 bility and resolution of the E. coli in-cell NMR spectra correlated with the soluble fraction amounts

90 that they possess different melting points, NMR spectra, crystal structures, and stacking patterns i

91 (1)H-NMR spectra datasets of serum, urine, cortex, and stomac

92 yl of W and Ti in (1)H-(1)H multiple-quantum NMR spectra demonstrates that W and Ti species are in cl

93 al heterocovariance analysis (HetCA) of (1)H NMR spectra detecting chemical features that are positiv

94 The NMR spectra display a large (1)H-(19)F J coupling typica

95 H iterative full spin analysis (QM-HiFSA) of NMR spectra distinguished previously unrecognized detail

96 NMR spectra employing a deuterium-labeling approach enab

97 reverse micelles prepared in pentane yields NMR spectra essentially identical to the protein in free

98 Low-temperature (13)C NMR spectra established that (Z)-1 was dissolved as a tr

99 extracted differentially, and the resulting NMR spectra exhibit characteristics favorable for unrave

100 Qualitatively, F508del NMR spectra exhibit significantly more peak broadening t

101 on spectroscopy (STOCY) analysis of the (1)H NMR spectra, followed by a level-1 identification based

102 ence Matching), that uses 2D J-resolved (1)H NMR spectra for enhanced information recovery using the

103 Proton NMR spectra for the dications showed the presence of enh

104 parameters that best reproduce the measured NMR spectra for the selected kinetic model, but to also

105 The proton NMR spectra for these contracted carbaporphyrinoids show

106 (17)O MAS NMR spectra for these systems provide insights into the

107 r polarization (DNP) enable the detection of NMR spectra from low-gamma nuclei with outstanding sensi

108 Previously, it has been shown that (1)H NMR spectra from rat brain extracts can be accurately qu

109 omprehensively evaluated using 617 plasma 1H NMR spectra from the FGENTCARD cohort.

110 nowledge, this is the first time that MS and NMR spectra have been combined to determine the PDI of c

111 Various algorithms comparing 2D NMR spectra have been explored for their ability to dere

112 CONCISE and PCA of NMR spectra have discovered novel states of a well-studi

113 he in-line flow cell gives excellent quality NMR spectra having little impact on peak shape.

114 l (1)H and (13)C nuclear magnetic resonance (NMR) spectra, high-resolution mass spectrometry, and cal

115 Their similar NMR spectra in chloroform clearly suggest the same 1,3-a

116 predicted and compared with the experimental NMR spectra in order to identify the molecular structure

117 formational signatures observed in simple 1D NMR spectra in the optimization of compounds for medicin

118 The variable-temperature (7) Li NMR spectra in THF confirm the presence of three types o

119 onfigurational ensemble in the simulation of NMR spectra, in combination with solid-state NMR experim

120 A detailed analysis of the NMR spectra (including 2D experiments) revealed previous

121 Deuterium NMR spectra indicate that bound cholesterol is approxima

122 (15)N NMR spectra indicate that removal of the second histidin

123 erature (1)H, (15)N, and 2-D (1)H-(1)H ROESY NMR spectra indicated rapid exchange of the proton and h

124 (1)H nuclear magnetic resonance ((1)H NMR) spectra indicated that the oxidation of fluorescing

125 Both mimics fold cooperatively and exhibit NMR spectra indicative of a closely packed conformation,

126 Data processing for 1D NMR spectra is a key bottleneck for metabolomic and othe

127 The use of 1D and 2D NMR spectra is indeed very helpful to investigate the co

128 ation content of nuclear magnetic resonance (NMR) spectra is routinely used to identify and character

129 nsing behavior of L was corroborated by (1)H NMR spectra, mass spectrometry, and theoretical calculat

130 tionship between multiplets typical for (1)H NMR spectra must be abandoned.

131 analysis of up to three two-dimensional (2D) NMR spectra, namely, (13)C-(1)H HSQC (heteronuclear sing

132 separation by mathematically dissecting the NMR spectra obtained from chromatographic fractions.

133 han 60 metabolites have been assigned in the NMR spectra obtained from the fresh fecal buffer extract

134 r of a few minutes and the simplicity of the NMR spectra obtained make this approach well-suited to t

135 emonstrate the utility of high-quality (13)C NMR spectra obtained using a custom (13)C-optimized prob

136 pressure NMR probe was used to collect (13)C NMR spectra of (13)C-labeled CO2 reactions with NaOH sol

137 We observed ligand-specific changes in the NMR spectra of (13)CH(3)-epsilon-methionine probes in th

138 We find that multidimensional solid state NMR spectra of (15)N,(13)C-labeled CA assemblies are rem

139 NMR spectra of (S)-alanine and (S)-proline derived compo

140 Here we show that the (19)F NMR spectra of 1 (~1:1 diastereomer mixture prepared by

141 (93)Nb solid-state NMR spectra of 1a-3a and (31)P solid-state NMR on their

142 and their splitting patterns in multinuclear NMR spectra of 2H indicate that the chiral Cu20H11 core

143 The (31)P NMR spectra of 3% CLWMS at pH 12 showed decreased cyclic

144 Laser-enhanced 2D NMR spectra of 5 muM proteins at 600 MHz display 30-fold

145 Line shape analysis of solid state (2)H NMR spectra of a phenylene-d4 isotopologue, obtained as

146 DNP-SENS), to obtain the (195)Pt solid-state NMR spectra of a prototypical example of highly disperse

147 ing NOE-derived distance restraints, and the NMR spectra of a series of designed eta-helices were alt

148 Detailed NMR spectra of all complexes as well as IR and single cr

149 he work has implications for the analysis of NMR spectra of all materials with anisotropic magnetic s

150 (1)H and (13)C NMR spectra of allyl isothiocyanate (AITC) were measured

151 However, (31)P MAS NMR spectra of analyzed series display a higher number o

152 Here, we use multidimensional NMR spectra of animal and in vitro model tissues as fing

153 l protocol for acquiring high-quality HR-MAS NMR spectra of biological tissues at low spinning rates

154 Using NMR spectra of blood samples, taken at different time po

155 The simulated and experimental NMR spectra of caffeoylquinic acids are in excellent agr

156 -(1)H heteronuclear single-quantum coherence NMR spectra of CcdB at pH 4 and 7 suggests that the pH 4

157 NMR spectra of deuterated glycine-2-(13)C revealed inter

158 es of photocatalytic reactions and to obtain NMR spectra of dilute solutions with a single pulse of a

159 P addition (5 mM) had no impact on the (31)P NMR spectra of DP-MPC; addition of 5 mM SHMP to control

160 Next, NMR spectra of each member of the structural manifold ar

161 When species contain sparse fluorine atoms, NMR spectra of fluorine-containing spin systems can be e

162 efficient protocol for the rapid analysis of NMR spectra of green and roasted coffee extracts, enabli

163 Here we show that solution NMR spectra of H-RasGTPgammaS mixed with a functional fr

164 g a few identified for the first time in the NMR spectra of human serum.

165 NMR spectra of isolated MOS indicated minimal amounts of

166 me in order to give access to the individual NMR spectra of mixture components.

167 The (1)H, (2)H and (13)C NMR spectra of mixtures of racemic mono- and prochiral b

168 The NMR spectra of multiple time points were formulated as a

169 NMR spectra of NBD1 lacking the N-terminal tail, NBD1-De

170 Solid-state NMR spectra of new P-Se heterocycles based on peri-subst

171 veloped for the simulation of (13)C and (1)H NMR spectra of oligo- and polysaccharides and their deri

172 the near-silence of the ITC carbon in (13)C NMR spectra of organic isothiocyanates.

173 High resolution (13)C NMR spectra of plasma triacylglycerols and glucose provi

174 The imino NMR spectra of pre-let-7 loops and LREs contain resonanc

175 Further, we show that 2D (13)C NMR spectra of protease-cleaved Fc and Fab fragments can

176 Analysis of (113)Cd NMR spectra of PrP(C), along with relevant control prote

177 It was possible to extract NMR spectra of pure N-glycans that were heavily overlapp

178 NMR spectra of quadrupolar nuclei (I > (1)/2) are often

179 exciting and challenging new applications of NMR spectra of quadrupolar nuclei in the fields of energ

180 OGe)4 environments are expected in (31)P MAS NMR spectra of R3c NASICON samples.

181 observed from chemical shift changes in the NMR spectra of residues in the helices and on the surfac

182 carbon signatures are observed in the (13)C NMR spectra of samples and are determined to vary in int

183 High-resolution (195)Pt NMR spectra of select regions of the broad (195)Pt powde

184 we analyzed previously acquired (1)H HR-MAS NMR spectra of separated cortex and medulla samples usin

185 NMR spectra of several small molecules as well as a prot

186 The NMR spectra of simple binary complexes of the TAZ1 and T

187 The approach is tested on the (7)Li NMR spectra of single crystals and powders of LiFePO(4).

188 agic angle spinning (MAS) [(13)C,(13)C]-DARR NMR spectra of single- and multi-span membrane proteins

189 n also facilitated the interpretation of the NMR spectra of small molecule models of phenanthriplatin

190 spin parameters against experimental 1D-(1)H NMR spectra of small molecules.

191 (23)Na MAS NMR spectra of sodium-oxygen (Na-O2) cathodes reveals a

192 We enhance the (7)Li, (1)H and (19)F NMR spectra of solid-electrolyte interphase species sele

193 help in the interpretation and assignment of NMR spectra of solids, but the statistical representatio

194 ilicic acid (Q(1)) can be observed in (29)Si NMR spectra of solutions containing PEG 10000 with inten

195 been suggested to bind to the SRA1 RNA, but NMR spectra of SRA1p in the presence of its 80-nt RNA ta

196 We were able to produce high-quality NMR spectra of substrate bound to microcrystalline LeuT

197 The 1H NMR spectra of synthetic 26 in deuterated chloroform and

198 The (1)H NMR spectra of the CO and deoxy forms of these mutants i

199 al spin systems are extracted from 2D and 3D NMR spectra of the complex mixture.

200 esent in a measurable quantity in the (23)Na NMR spectra of the cycled electrodes.

201 The (31)P NMR spectra of the degraded olive oils, which contain OH

202 two-dimensional (13)C and (15)N solid-state NMR spectra of the formulations while preserving the mic

203 nal packing is also consistent with (1)H-MAS NMR spectra of the L(o) phase, NMR diffusion experiments

204 high-resolution (17)O (I = 5/2) solid-state NMR spectra of the mixed-conducting solid oxide fuel cel

205 Comparison of NMR spectra of the nonselective NaK and potassium-select

206 In contrast, the NMR spectra of the peptides labeled with (13)C at the sa

207 re, the high resolution afforded by the (1)H NMR spectra of the permethylated switchgrass and poplar

208 Re-examination of NMR spectra of the previously reported d-allo-ShK protei

209 (1) H NMR spectra of the protonolysis product of 2 synthesized

210 mical shift differences observed in the (1)H NMR spectra of the racemic and the enantio-enriched comp

211 to remarkably clean homo- and heteronuclear NMR spectra of the serum metabolome that compare favorab

212 The NMR spectra of the three trisaccharides were fully assig

213 es of binding to two sites directly from the NMR spectra of the titrations.

214 matic process is introduced to compare (13)C NMR spectra of two (or more) candidate samples of known

215 a of urine of subjects with T2DM and 62 (1)H NMR spectra of urine of control subjects.

216 mixture; (ii) metabolites present in 62 (1)H NMR spectra of urine of subjects with T2DM and 62 (1)H N

217 previously published crystal structures and NMR spectra of various NBD1 mutants, we propose that del

218 lar tensors and peak intensities from 3D MAS NMR spectra of wild-type and the A92E and G94D CypA esca

219 NMR spectra of WT NBD1 reveal significant concentration-

220 e spinning (MAS) nuclear magnetic resonance (NMR) spectra of 5-30 kDa proteins.

221 tionally, we have included predicted MS- and NMR-spectra of thousands of compounds for assignment of

222 restraints from four-dimensional solid-state NMR spectra on extensively deuterated and (1)H back-exch

223 Fidelity of reconstruction of series of NMR spectra or images requires more PCs than needed to p

224 The splitting of signals in the NMR spectra originating from enantiotopic sites in proch

225 ity of a database containing many comparable NMR spectra produced by different spectrometers is cruci

226 The operando NMR spectra provide molecularly specific, time-resolved

227 c-angle-spinning nuclear magnetic resonance (NMR) spectra provide atomic level information for each a

228 , 7616 - 7623 ] and exploits the simplified NMR spectra provided by the extraction of metabolites un

229 The ability to both simulate and fit NMR spectra provides the user the opportunity to not onl

230 g (NUS) data acquisition and high-resolution NMR spectra reconstruction.

231 Variable-temperature (17)O NMR spectra recorded from 22 to 214 degrees C were inter

232 e that a profiling strategy based on fast 2D NMR spectra recorded in 2.4min is more efficient than th

233 The (1)H NMR spectra recorded in deuterated dichloromethane indic

234 uple this application of PCA to an automated NMR spectra recording and processing protocol and obtain

235 (RED)-STORM to identify other signals in the NMR spectra relating to the same molecule.

236 Solid-state (2)H NMR spectra report the folding and orientation of the co

237 The resonance for Met-187 in our NMR spectra reported on the ability of the enzyme to che

238 in-house library of 210 pure component (1)H NMR spectra represented the design matrix in the related

239 features observed in both (27)Al and (71)Ga NMR spectra result from both the deviations in the polyh

240 However, NMR spectra reveal sharp resonances with chemical shifts

241 NMR spectra reveal that EmrE can simultaneously bind and

242 Moreover, NMR spectra revealed that the CaM-F142L-CaMBD interactio

243 The (1)H NMR spectra revealed that the halides formed tight ion-p

244 2D (19)F NMR spectra show correlation peaks between MPER residues

245 In each case, low-temperature (6)Li NMR spectra show stereoisomerically pure homoaggregates

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

247 (13)C CP/MAS NMR spectra show that the Fe(CO)3 moiety in polycrystall

248 embranes mimicking the virus envelope, (15)N NMR spectra show that the His-27 tetrad protonates with

249 (31)P NMR spectra show that the peptide retains the lamellar s

250 NMR spectra show that the structural heterogeneity is su

251 se relaxation-optimized spectroscopy (TROSY) NMR spectra show the N-terminal and C-terminal catalytic

252 Surface-selective (133)Cs solid-state NMR spectra show the presence of an additional (133)Cs N

253 77, which are visible in the MAS solid-state NMR spectra, show (13)Calpha chemical shifts that are hi

254 The (13)C NMR spectra showed further evidence of the formation of

255 (1)H NMR spectra showed large upfield shifts of the protons i

256 ross-polarization magic angle spinning (13)C NMR spectra showed that CO2 binds chemically to IRMOF-74

257 strongly aromatic properties, and the proton NMR spectra showed the N-methyl resonances near -3 ppm.

258 Their (1)H NMR spectra showed the typical pattern of four atropisom

259 Nuclear magnetic resonance (NMR) spectra showed that dephosphorylation depleted the

260 inite-pulse radiofrequency-driven recoupling NMR spectra, spatial proximities between I32 and V40 as

261 The NMR spectra suggest that the carbohydrate links to hydro

262 a matter of minutes to hours, of solid-state NMR spectra suitable for quantitative analysis of protei

263 In addition, the two lines in the (14)N NMR spectra superposed into one line near T(C), indicati

264 NMR spectra support this model and raise the possibility

265 hieves higher resolution and sensitivity for NMR spectra than classical covariance NMR reducing offse

266 was confirmed by X-ray crystallography, has NMR spectra that are very similar, but not identical, to

267 acceptability range are qualified to produce NMR spectra that can be considered statistically equival

268 ses by selecting subsets of homogeneous (1)H NMR spectra that contain specific spectroscopic metaboli

269 pulses, very high-resolution proton-based 3D NMR spectra that correlate single-quantum (SQ), DQ and S

270 membranes, yield high-resolution solid-state NMR spectra that reflect the structure of Ail and reveal

271 We present 1H-NMR spectra that reveal (NEt4)[MoO(S2)2picolinate] (Mo-p

272 in two-dimensional and three-dimensional MAS NMR spectra the CL-bound cyt-c displays a spectral resol

273 , complex refractive indices, (1)H and (13)C NMR spectra, thermograms, aerosol and electrospray ioniz

274 y depend upon chemists' ability to interpret NMR spectra, though research demonstrates that cultivati

275 resolution 1D (1)H-CPMG and diffusion edited NMR spectra to identify the potential molecular biomarke

276 l-line-shape (CTLS) approach applied to (1)H NMR spectra to quantify metabolites present in onion spe

277 covered that one-dimensional (13)C and (15)N NMR spectra, together with spectroscopic selections base

278 2D NMR spectra, total correlated spectroscopy and nuclear O

279 ative-like circular dichroism spectra and 1D-NMR spectra typical of folded structures.

280 ted directly from noninterpreted, complex 2D NMR spectra using principal component analysis (PCA) to

281 ized [1-(13)C]pyruvate during acquisition of NMR spectra using selective excitation to maximize detec

282 Chemometric analysis of the NMR spectra, utilizing both (1)H and (1)H-(13)C HSQC NMR

283 + dipyrromethanedicarbinol routes, and their NMR spectra, UV-vis spectra, X-ray crystal structures, a

284 (13)C NMR spectra were acquired using a z-stored spin-echo seq

285 ities of coenzymes and antioxidants in blood NMR spectra were established combining 1D/2D NMR techniq

286 and signal-to-noise ratio (SNR) of the (1)H NMR spectra were evaluated.

287 roduct characterization in terms of matching NMR spectra were experienced; our studies reveal that th

288 (+)-1 a-1 b-for those instances in which the NMR spectra were obtained in CD3OD-to their correspondin

289 mplete 2D (17)O -> (1)H D-RINEPT correlation NMR spectra were typically obtained in less than 10 h fr

290 Hyperpolarized (13)C NMR spectra were used to characterize product tacticity

291 Nuclear magnetic resonance (NMR) spectra were obtained for five cations, and the che

292 l of 36 NMR data sets (corresponding to 1260 NMR spectra) were produced by 30 participants using 34 N

293 address decoupling artifacts in (13)C{(1)H} NMR spectra which contain a strong (13)C signal with a h

294 ion is constructed from variable-temperature NMR spectra with (13) C-labeled agostic complexes.

295 rmation, allowing then to record single-spin NMR spectra with 13 Hz resolution at room temperature.

296 l NV-based sensor device records single-spin NMR spectra with 13 Hz resolution at room temperature.Di

297 (19)F-T2 NMR spectra with different relaxation delays were record

298 simplify and resolve complex, congested (1)H NMR spectra with many overlapping spin multiplets, while

299 readily be observed in one-dimensional (1)H NMR spectra without any isotope labeling.

300 on approach (MCR), to denoise 2D solid-state NMR spectra, yielding a substantial S/N ratio increase w