ライフサイエンスコーパス: dipolar

1 In dipolar(6,8), quadrupolar(8-12) and hexadecapolar(13) ne

2 Dipolar absorption of x-rays is thus diminished, which m

3 Second, we have introduced a supplemental dipolar AC waveform to the quadrupole mass filter of a c

4 the noncovalent synthesis approach based on dipolar aggregation is suitable for the design of well-d

5 s both inward and outward transport of small dipolar amino acids (serine, proline, cysteine, alanine,

6 ead to excitation of significantly different dipolar and charge transfer plasmon (CTP) resonances, re

7 nst experimental spectra, error analysis and dipolar and chemical shift wave plotting.

8 Here, we demonstrate the excitation of dipolar and CTP resonant modes in metallic nanodimers br

9 an analytical expression accounting for both dipolar and exchange coupling to simulate the time trace

10 n the triangular lattice with an intertwined dipolar and ferro-multipolar order.

11 of plasmon-emitter interactions ranging from dipolar and multipolar spontaneous emission enhancement,

12 g very small inhomogeneous broadening due to dipolar and nuclear fields.

13 While this structure hosts both dipolar and quadrupolar electric and magnetic delocalize

14 applications of solid-state NMR by unifying dipolar and quadrupolar interactions and highlights the

15 of Huygens dipoles excited in an individual dipolar antenna.

16 free-space wavelength, thus invalidating the dipolar approximation for meta-atoms.

17 micyanine dyes bearing Btz (1) or Ind (2) in dipolar aprotic solvent-water mixtures.

18 erostructured tetrapod that is capable of 1D dipolar assembly into colloidal polymers that carry tetr

19 The thermal (3 + 2) dipolar azide-alkyne cycloaddition, proceeding without c

20 eads to GQD-Fe-GQD units with D(2) symmetry, dipolar bonding potential, and linear assemblies.

21 of solution- and solid-state NMR to measure dipolar, chemical shift, and quadrupolar tensors in aque

22 an electron donor-acceptor (D-A) substituted dipolar chromophore (BTPA-TCNE) is developed to serve as

23 ul design of the spacer moieties linking the dipolar chromophores within the bis(merocyanine) dyes al

24 ained in high yields in copper-catalyzed 1,3-dipolar "click" cycloaddition using bis(TMS)butadiyne an

25 identical chemical shift but that is not in dipolar contact with (15)N.

26 ation of DNP-enhanced (13) C spins in direct dipolar contact with electron spins, thereby leading to

27 loit the presence of sizable quadrupolar and dipolar contributions in the uranium L3-edge X-ray absor

28 These new arene-annulated dipolar coumarins display interesting absorption and flu

29 on CEACAM1-IgV dimerization and use residual dipolar coupling (RDC) measurements to characterize the

30 ow the plasticity in the model-free residual dipolar coupling (RDC) order parameters and in an ensemb

31 ngle, small-angle X-ray scattering, residual dipolar coupling and inter-domain NOE nuclear Overhauser

32 inction spectra of coupled resonators is the dipolar coupling band.

33 ally, measurements of the distance-dependent dipolar coupling between the two spins are used to obtai

34 one-shot determination of accurate residual dipolar coupling constants from a single NMR spectrum.

35 NMR chemical shifts and residual dipolar coupling data reveal Ca(2+)-dependent difference

36 The collection of residual dipolar coupling data, amide protection factors, and par

37 present NMR resonance assignments, residual dipolar coupling data, functional analysis, and a struct

38 analysis and by application of the residual dipolar coupling method, the rearrangement occurs withou

39 Heteronuclear dipolar coupling modulation schemes allowed to character

40 teraction strength, we elucidate the role of dipolar coupling of molecular monolayers to their enviro

41 Hamiltonian for the hydride electron-nuclear dipolar coupling to its "anchoring" Fe ions, an approach

42 alone, but the addition of NMR RDC (residual dipolar coupling) restraints improves the structure mode

43 ombination of DNA hybridization and particle dipolar coupling, a property dependent on particle compo

44 s transitions between qubit states, a strong dipolar coupling, and leading-order protection from elec

45 at approximately 165 ppm and lacks (15)N for dipolar coupling.

46 By measuring (1)H-(15)N dipolar-coupling as well as (15)N R1 and R1rho relaxatio

47 coupling constants ((1) J(OH)) or (1)H-(17)O dipolar couplings ( D(OH)), respectively, the latter of

48 NMR dipolar couplings (DCs) depend intrinsically on both mol

49 e difference between two successive residual dipolar couplings (DeltaRDCs) involving C6/8-H6/8, C3'-H

50 spectroscopy (NOESY) spectroscopy, residual dipolar couplings (RDCs) and paramagnetic relaxation enh

51 se of anisotropic NMR data, such as residual dipolar couplings (RDCs) and residual chemical shift ani

52 Experimentally measured residual dipolar couplings (RDCs) are highly valuable for atomic-

53 Residual dipolar couplings (RDCs) can provide a means of assignin

54 Alternatively, one can measure residual dipolar couplings (RDCs) for natural abundance lipid sam

55 Residual Dipolar Couplings (RDCs) have become an alternate approa

56 rotein that NMR and, in particular, residual dipolar couplings (RDCs) measured for the folded portion

57 However, NMR residual dipolar couplings (RDCs) measured under three different

58 tes between dipolar interactions to residual dipolar couplings (RDCs) of individual consecutive H(N)-

59 pproach based on the measurement of residual dipolar couplings (RDCs) to probe the structural and mot

60 ramagnetic relaxation enhancements, residual dipolar couplings (RDCs), chemical shifts, and small-ang

61 entional 1D and 2D NMR spectra, and residual dipolar couplings (RDCs), is reported.

62 an ideal model alpha-helix for its residual dipolar couplings (RDCs), measured in a filamentous phag

63 e experimental data afforded by NMR residual dipolar couplings (which yield both orientational and sh

64 However, so far only (1) H-(15) N dipolar couplings and (15) N chemical shifts have been r

65 of membrane proteins, the angular-dependent dipolar couplings and chemical shifts provide a direct i

66 troscopy, including measurements of residual dipolar couplings and molecular dynamics simulations, to

67 Residual dipolar couplings and residual chemical shift anisotropy

68 Here we use NMR chemical shifts and residual dipolar couplings as structural restraints in replica-av

69 Further, NMR residual dipolar couplings collected under three anisotropic cond

70 sly inaccessible (1) H(alpha) -(13) C(alpha) dipolar couplings have been measured, which make it poss

71 cular alignment model that predicts residual dipolar couplings of small molecules aligned by poly(gam

72 Refinement of this library with NMR residual dipolar couplings provided an atomistic ensemble model f

73 )N relaxation rates, and (1)H-(15)N residual dipolar couplings suggest structural changes and rapid m

74 ng chemical shift perturbations and residual dipolar couplings was employed to obtain a structural mo

75 shifts, nuclear Overhauser effects, residual dipolar couplings) to predictions from molecular dynamic

76 rrelation experiments, (1)H-(17)O scalar and dipolar couplings, and plane-wave DFT calculations provi

77 d peptide would be evident in local residual dipolar couplings, and possibly differences in homonucle

78 ution NMR methodology that combines residual dipolar couplings, J-couplings, and intramolecular hydro

79 f the proteins and chemical shifts, residual dipolar couplings, paramagnetic relaxation enhancement,

80 ion of holo-ACPP to ACPS by fitting residual dipolar couplings.

81 strongly favoring magnetization transfer by dipolar cross-relaxation.

82 ive pentacyclic intermediate formed by a 1,3 dipolar cyclo-addition of prFMN with the alpha-beta doub

83 that prFMN can function as a dipole in a 1,3 dipolar cyclo-addition reaction as the initial step in a

84 However, enzyme-catalyzed 1,3 dipolar cyclo-additions are unprecedented and other mech

85 nes by using copper(I)-catalyzed Huisgen 1,3-dipolar cycloaddition ("click chemistry").

86 prolinates, obtained by enantiocatalyzed 1,3-dipolar cycloaddition (1,3-DC) of imino esters and nitro

87 Optimization of the 1,3-dipolar cycloaddition (1,3-DC), original methods includi

88 ation, dehydrogenative coupling, Huisgen 1,3-dipolar cycloaddition (click reaction), hydroheteroaryla

89 Cu(I)-catalyzed azide-alkyne 1,3-dipolar cycloaddition (CuAAC), popularly known as the "c

90 The 1,3-dipolar cycloaddition (Prato reaction) of Y(3)N@I(h)-C(8

91 uent contributes to stereoselectivity of 1,3-dipolar cycloaddition and structural features of beta-pr

92 formation and subsequent stereoselective 1,3-dipolar cycloaddition as key steps.

93 utyl)dipyrrin) facilitate intramolecular 1,3-dipolar cycloaddition as well as C-H amination to furnis

94 Catalytic enantioselective 1,3-dipolar cycloaddition between imino esters and electroph

95 hereby combining the key features of the 1,3-dipolar cycloaddition chemistry of azides and cyclopropa

96 y a nonpeptidic coupling method based on 1,3-dipolar cycloaddition chemistry of azomethine ylides.

97 omoting the noncopper catalyzed azide-alkyne dipolar cycloaddition click reaction between either a li

98 a catalytic asymmetric azomethine ylide 1,3-dipolar cycloaddition followed by an intramolecular Au(I

99 the reaction can be considered a normal 1,3-dipolar cycloaddition involving M horizontal lineC bonds

100 Finally, we showed that Cu-catalyzed 1,3-dipolar cycloaddition is also chemically compatible with

101 ones, and azepino-pyrrolizinones via [3 + 2]-dipolar cycloaddition is described.

102 The oxidized prFMN supports a 1,3-dipolar cycloaddition mechanism that underpins reversibl

103 A regio- and diastereoselective 1,3-dipolar cycloaddition of 2 H-azirines with azomethine yl

104 The first 1,3-dipolar cycloaddition of 2H-azirines with nitrones, a st

105 hexadienones has been developed by using the dipolar cycloaddition of an N-alkenylnitrone and an aryn

106 with the virtues of the Cu(i)-catalyzed-1,3-dipolar cycloaddition of azides and alkynes (the CuAAC o

107 This reaction proceeds as a sequence of 1,3-dipolar cycloaddition of azomethine ylide generated in s

108 Cu-catalyzed 1,3-dipolar cycloaddition of iododiacetylenes with organic a

109 An efficient catalytic asymmetric 1,3-dipolar cycloaddition of N-benzylidineiminoglycinate-der

110 oits a known bioorthogonal reaction, the 1,3-dipolar cycloaddition of nitrileimines and electron-poor

111 A green and efficient 1,3-dipolar cycloaddition of nitrones with different styrene

112 The intramolecular 1,3-dipolar cycloaddition of ortho-substituted 1,1,1-trifluo

113 A stereo- and regioselective 1,3-dipolar cycloaddition of the stable ninhydrin-derived az

114 The process involves 1,3-dipolar cycloaddition of unsymmetrical azomethine ylide

115 synthesis involved (i) the azide-alkyne 1,3-dipolar cycloaddition or (ii) the formation of the ester

116 t (de)carboxylation through a reversible 1,3-dipolar cycloaddition process.

117 lly active synthetic steroid, by using a 1,3-dipolar cycloaddition reaction (Prato's protocol) result

118 or templates its own synthesis through a 1,3-dipolar cycloaddition reaction between a nitrone compone

119 gment, using the Cu(I)-catalyzed Huisgen 1,3-dipolar cycloaddition reaction of azides and alkynes.

120 omologation, transphosphorylation, and a 1,3-dipolar cycloaddition reaction of diazoalkylphosphonates

121 A 1,3-dipolar cycloaddition reaction of nonstabilized azomethi

122 harides can be visualized "on chip" by a 1,3-dipolar cycloaddition reaction with an alkynyl-modified

123 dation that were subsequently subjected to a dipolar cycloaddition reaction with trimethylsilyl amino

124 )Cu]-ADIBO-NOTA) via copper-free Huisgen-1,3-dipolar cycloaddition reaction.

125 a novel enantioselective triple cascade 1,3-dipolar cycloaddition reaction.

126 A single pot dipolar cycloaddition reaction/Cope elimination sequence

127 azoles to form nitrile imines primed for 1,3-dipolar cycloaddition reactions is of widespread utility

128 arylacridines has been developed via the 1,3-dipolar cycloaddition reactions of arynes with N-oxides.

129 nition sites-that react pairwise through 1,3-dipolar cycloaddition reactions to create a network of f

130 hich are prepared in situ, is exemplified by dipolar cycloaddition reactions with nitrones to give hi

131 series of products through irreversible 1,3-dipolar cycloaddition reactions with the four nitrones p

132 dine recognition site can participate in 1,3-dipolar cycloaddition reactions with two maleimides that

133 le imines are important intermediates in 1,3-dipolar cycloaddition reactions, and they are also known

134 The geometries, stabilities, and 1,3-dipolar cycloaddition reactivities of 24 mesoionic azome

135 Nitrile oxide 1,3-dipolar cycloaddition to arylsulfonyl- and dialkylaminoa

136 thine ylides via the domino Mannich reaction-dipolar cycloaddition to form 3,3-disubstituted pyrrolid

137 alkyl enol ethers undergo intramolecular 1,3-dipolar cycloaddition to generate stable triazolines; in

138 to oximes, cyclization to nitrones, and 1,3-dipolar cycloaddition to tricyclic isoxazolidines as sin

139 A Cu(II) -catalyzed asymmetric 1,3-dipolar cycloaddition using beta-fluoroalkyl alkenyl ary

140 a/azanorbornadienes as dipolarophiles in 1,3-dipolar cycloaddition with benzyl azide.

141 ed even a difluorinated cyclooctyne in a 1,3-dipolar cycloaddition with benzylazide.

142 s confirmed by spectroscopic methods and 1,3-dipolar cycloaddition with methyl acrylate.

143 2-Diazomethylpyridine 1D undergoes 1,3-dipolar cycloaddition with tetracyanoethylene (TCNE) at

144 -intramolecular proton transfer, Huisgen 1,3-dipolar cycloaddition, and dehydrogenative aromatization

145 of this work contributes to the study of 1,3-dipolar cycloaddition, as well as enriches chemistry of

146 This greener approach involves 1,3-dipolar cycloaddition, regioselective ring expansion, fo

147 nnamic acid-type compounds to reversible 1,3-dipolar cycloaddition, while the formation of dead-end p

148 /isoxazoline hybrids were synthesized by 1,3-dipolar cycloaddition.

149 ia an improved protocol for Cu-catalyzed 1,3-dipolar cycloaddition.

150 mplex as a catalyst following a two-step 1,3-dipolar cycloaddition/intramolecular alkylation sequence

151 The scope of this tandem 1,3-dipolar cycloaddition/rDA reaction was studied with thir

152 include [2 + 2] cycloadditions, [3 + 2] 1,3-dipolar cycloadditions (with azides, nitrones, azomethin

153 developed, especially those based on the 1,3-dipolar cycloadditions and Diels-Alder reactions owing t

154 lidene carbene mediated Li-N insertions, and dipolar cycloadditions by controlling the reaction param

155 y cycloaddition reactions in general and 1,3-dipolar cycloadditions in particular.

156 t from the mechanism of prFMN-associated 1,3-dipolar cycloadditions in related enzymes.

157 We report the first 1,3-dipolar cycloadditions of 1,2-cyclohexadiene, a rarely e

158 ives, which are not accessible by direct 1,3-dipolar cycloadditions of azomethine ylide with frequent

159 lic pyrrolines that are inaccessible through dipolar cycloadditions of exocyclic cyclohexenones and p

160 razolo[1,5-a]pyridin-2(1H)-ones, whereas 1,3-dipolar cycloadditions of these dipoles to typical acety

161 en's 1960 announcement of the concept of 1,3-dipolar cycloadditions was published the year before Ald

162 to give tetrahydroindolizines (stepwise 1,3-dipolar cycloadditions with 3) and cyclopropanes (with 4

163 4pi components (covering Diels-Alder and 1,3-dipolar cycloadditions).

164 N@I(h)-C(80), obtained by regioselective 1,3-dipolar cycloadditions, were elucidated by single crysta

165 ipally described the state of the art of 1,3-dipolar cycloadditions-his golden offspring.

166 he electronic and structural features of 1,3-dipolar cycloadditions.

167 e chemoselectivity of the diazo group in 1,3-dipolar cycloadditions.

168 This was the result of his research into 1,3-dipolar cycloadditions.

169 , which can be captured as corresponding 1,3-dipolar cycloadducts in the presence of DHPO.

170 antum spin dynamics become protected against dipolar decoherence.

171 ies from delocalized/multipolar to localized/dipolar depending on the environment.

172 nza A full length M2 protein, the buildup of dipolar-dephased (15)N signals from the tetrad of His37

173 CsPbBr(3) crystal structure, and theoretical dipolar dephasing curves considering all possible (1)H-(

174 Dipolar dephasing curves that report on the distance bet

175 Intramolecular (13)C-(15)N dipolar dephasing is consistent with close (<5 A) contac

176 -dimensional artificial spin ice system, the dipolar dice lattice.

177 The evolution from exchange to dipolar-dominated interactions is experimentally capture

178 ved only when using donor-acceptor-acceptor' dipolar donors in the photoactive heterojunctions.

179 e of the covalent bond to form a fluorescent dipolar dye.

180 igitated centrosymmetric organization of the dipolar dyes and concomitant annihilation of the ground

181 ontext of molecular engineering of push-pull dipolar dyes, we introduce a structural modification of

182 ral phase transitions, structural phases and dipolar dynamics in the mixed methylammonium/dimethylamm

183 We demonstrate that dipolar effects lead to significantly faster loss for an

184 lectric and magnetic delocalized modes, only dipolar electric and quadrupolar magnetic modes remain a

185 Pulse-dipolar electron spin resonance spectroscopy and site-sp

186 Pulse-dipolar electron spin resonance spectroscopy was also us

187 ed by site-directed spin-labeling with pulse-dipolar electron-spin resonance spectroscopy (PDS), smal

188 Dipolar EPR spectroscopy has proven to be a valuable too

189 the molecules in the trap leads to efficient dipolar evaporative cooling, yielding a rapid increase i

190 show how DEER experiments can be extended to dipolar evolution times of ca. 80 mus, permitting distan

191 We have investigated numerically toroidal dipolar excitation at optical frequency in metamaterials

192 tic dipolar resonances leads to the toroidal dipolar excitation, when space-inversion symmetry is bro

193 etry-broken states could thus be produced by dipolar excitations.

194 ults will facilitate further developments of dipolar exciton-polariton gases and condensates in hybri

195 ensate in a long-lived dark spin state of 2D dipolar excitons.

196 Our models predicted a dipolar far field and a polarity reversal at the center

197 er moments turn in-plane and act to yoke the dipolar fields from the adjacent hard layer perpendicula

198 SrTiO(3)) is a quantum paraelectric in which dipolar fluctuations grow upon cooling, although a long-

199 g access to new electron-acceptor groups and dipolar fluorophores displaying near-infrared emission i

200 h that the inclusions cannot achieve ordered dipolar ground states.

201 Synthetic accessibility to this dipolar heterostructured tetrapod enabled the use of the

202 Fast MAS (1)H{(195)Pt} dipolar-HMQC and S-REDOR experiments were implemented on

203 00-nanosecond gate time that uses the strong dipolar interaction between trapped Rydberg ions, which

204 es as Smax V cr(-0.37), which tallies with a dipolar interaction exponent of 2/3 in EC materials and

205 They emerge as a result of dipolar-interaction-induced transfer of angular momentum

206 ooperative atomic displacements aligned from dipolar interactions as in insulating phases.

207 th of the external field strength versus the dipolar interactions between the rotors, different colle

208 chemical reaction rates by inducing resonant dipolar interactions by means of an external electric fi

209 mental effects of inter-radical exchange and dipolar interactions can be minimised by placing the rad

210 in which strong, long-range and anisotropic dipolar interactions can drive the emergence of exotic m

211 ) polar molecules, in which elastic, tunable dipolar interactions dominate over all inelastic process

212 tial TiO2 coating, during which the magnetic dipolar interactions induced the anisotropic self-assemb

213 effect of the interplay of spatial order and dipolar interactions on the collective properties of the

214 Our studies reveal the effects of the dipolar interactions on the structure and the osmotic pr

215 We introduce a lattice model based on dipolar interactions plus a competing, frustrating term

216 f electrostatic ion-solvent correlations and dipolar interactions that act at separations well beyond

217 ss-correlated relaxation (CCR) rates between dipolar interactions to residual dipolar couplings (RDCs

218 , when the external field dominates over the dipolar interactions, the rotors undergo full rotations,

219 oton interaction strengths(5) and long-range dipolar interactions, these interlayer excitons are prom

220 ficient identification of numerous (1)H-(1)H dipolar interactions, which provide distance constraints

221 materials can significantly reduce magnetic dipolar interactions, which tend to favor large skyrmion

222 stigations identified dominant electrostatic dipolar interactions, while others implicated lone pair

223 olariton gases and condensates with inherent dipolar interactions.

224 fluorine as acceptor, and different types of dipolar interactions.

225 om the non-interacting case, indicating weak dipolar interactions.

226 is complicated by the long-ranged nature of dipolar interactions.

227 l moment, solely arising from intramolecular dipolar interactions.

228 inductive polarisation augment electrostatic dipolar interactions.

229 ing with the arylboronic acid; the resulting dipolar intermediate evolves by antiperiplanar 1,2-migra

230 motion is generated through a combination of dipolar interparticle gradient forces, time-dependent to

231 or the first time as dipolarophiles in a 1,3-dipolar intramolecular cycloaddition reaction, leading t

232 r anatomy and measures timing and density of dipolar, ionic activation (ie, charge density) across th

233 shown to occur experimentally in spin ice, a dipolar lattice system.

234 e of their surface chemistry, in particular, dipolar ligands and exciton-delocalizing ligands, on the

235 is suggested to be relevant to more general dipolar liquids.

236 aritons - coupled excitations of photons and dipolar matter excitations - can propagate along anisotr

237 lectrics, modulated polar phases such as the dipolar maze and the nano-bubble state have been apprais

238 ed by the longitudinal optical phonon in the dipolar medium and the exciton.

239 ency and the excitation strength of toroidal dipolar mode are studied in detail.

240 ction we adjusted the extinction peak of the dipolar mode at the telecommunication band (lambda 1.55

241 the modulation depths of relaxation-induced dipolar modulation enhancement (RIDME) EPR experiments.

242 mperature dependence of reorientation of the dipolar molecular cations systematically described here

243 strategy for achieving quantum degeneracy in dipolar molecular gases in which strong, long-range and

244 ere, we show that a two-dimensional array of dipolar molecular rotors can undergo simultaneous rotati

245 d to behave as an acceptor and thus generate dipolar molecule with mu above 5 D, whereas in 2b and 2d

246 le the creation of deeply quantum degenerate dipolar molecules and raises the possibility of using st

247 For ultracold dipolar molecules at sub-microkelvin temperatures, inter

248 Here, we report how single dipolar molecules can be oriented with maximum precision

249 designed for two-photon absorption behave as dipolar molecules in the S1 electronic excited state.

250 ta value due to significant variation of the dipolar moment (mu) value.

251 tetrapod from CdSe@CdS that carries a single dipolar nanoparticle tip from a core-shell colloid of Au

252 halide perovskites can be attributed to the dipolar nature and the dynamic behavior of these cations

253 ic interaction, changing it to predominantly dipolar or even to exponential one at lateral distances

254 of particle-particle spacing enabled either dipolar or quadrupolar lattice modes to be selectively a

255 diffraction mode relative to single-particle dipolar or quadrupolar resonances.

256 In contrast, dipolar order in dielectric crystals is typically limite

257 (13)C-(1)H dipolar order parameters, (1)H rotating-frame spin-latti

258 tions that cannot be explained by a magnetic dipolar order, but instead is the direct consequence of

259 gigahertz (GHz) regime, where the effect of dipolar oscillation is important.

260 Here we report the strength of dipolar oscillation modes for a sample of 3,600 red gian

261 The pronounced dipolar oscillations observed for most of the double spi

262 The dipolar oxathiazyne-like sulfinylnitrene RS(O)N, a highl

263 ically exist in three-dimensional systems of dipolar particles with weakly broken time-reversal symme

264 heastern Arctic Ocean with a dominant Arctic dipolar pattern, may be a recurrent feature under "warm

265 lasmon peak of Au nanoparticles and in-plane dipolar peak of Ag@Au NPLs relies on the intensity and d

266 esonance (LSPR) intensity change of in-plane dipolar peak.

267 hase transitions and indications of a glassy dipolar phase.

268 Couplings between protons, whether scalar or dipolar, provide a wealth of structural information.

269 r response of a meta-atom, resulting in e.g. dipolar, quadrupolar, or multipolar emission on demand.

270 tum memory and for precision measurements on dipolar quantum matter.

271 Designed repeat proteins catalyze the 1,3-dipolar reaction between an imine and a pai-deficient di

272 multiple two-dimensional NMR and (13)C-(13)C dipolar recoupling experiments.

273 gic-angle spinning (MAS) in combination with dipolar recoupling methods.

274 However, (13)C-(13)C dipolar recoupling solid-state NMR measurements also ide

275 (13)C{(14)N} dipolar-recoupling NMR showed that the formation of carb

276 um is sensitive to the lipid composition and dipolar relaxation arising from water penetration, but d

277 ve-absorbing mechanism reveal a unique Debye dipolar relaxation with an Eddy current effect in the ab

278 o determine the contribution of polarity and dipolar relaxations of LAURDAN in each pixel of an image

279 hting the increasing dominance of E(+) -C(-) dipolar resonance form (sp(3) -C) over the E=C ene pai-b

280 The strong coupling among three magnetic dipolar resonances leads to the toroidal dipolar excitat

281 nanodisks and substrate forms three magnetic dipolar resonances, at normal incidence of plane electro

282 he excited state evolves further to a purely dipolar S1 state with the excitation localized entirely

283 tching in organic molecules and violation of dipolar selection rules in atoms.

284 This dipolar sensor can determine the magnetic moments of ind

285 he creation of new states of matter (such as dipolar skyrmions, hedgehog states) and associated pheno

286 pping separation using mixed aqueous-aprotic dipolar solvent (N,N-dimethylacetamide (DMA) and N,N-dim

287 in-crystal ground state of artificial kagome dipolar spin ices and high-energy, low-entropy 'monopole

288 en, disordered ensemble of about one million dipolar spin impurities in diamond at room temperature.

289 ion pairing indeed stabilizes an asymmetric dipolar structure in the electronic ground state.

290 pon NaBH(4) reduction leading to a resonance dipolar structure of the [18]pai-conjugated system as th

291 pair association, stabilizing an asymmetric dipolar structure, similar to the situation in the cryst

292 tics from a spin-1 quadrupolar to a spin-1/2 dipolar system, evidencing the loss of spin isomer disti

293 high precision the (1)H(alpha)-(13)C(alpha) dipolar tensor and carboxylate chemical shift anisotropy

294 tural degrees of freedom beyond the familiar dipolar terms responsible for (anti)ferroelectric order.

295 Instead, dipolar torque activity may either tighten or unwind the

296 and experimental observation of the inverse dipolar transition in BiFeO(3) suggest the universality

297 tudies on the low-temperature physics of the dipolar trident lattice, but also demonstrate how this f

298 ok into an artificial frustrated system, the dipolar trident lattice, where the balance of competing

299 r to AQP channels, that encapsulate oriented dipolar water-wires in a confined chiral conduit.

300 n powder samples by mixing with the strongly dipolar zwitterionic p-benzoquinonemonoimine C6 H2 (-cdo