ライフサイエンスコーパス: bond

1 e position and stereochemistry of the double bond.

2 eeds via alkene insertion into a Ni(II)-acyl bond.

3 decay is intrinsic to the nature of the Si-O bond.

4 eactions have also evolved to cleave the C-P bond.

5 the two local conformations around a single bond.

6 cleaved rather than the weaker aliphatic O-R bond.

7 or trans-configured Glu(18)-Pro(19) peptide bond.

8 ains of the target protein via an isopeptide bond.

9 nitrogen inversion or rotation about the N-O bond.

10 mplexes have free rotation around the CPh-B1 bond.

11 ndergo rapid internal rotation about the M-O bond.

12 2(H2O)n should be able to form very weak C-H bonds.

13 arization and oriented molecular vibrational bonds.

14 ion and the construction of both C-C and C-N bonds.

15 erparts, disilenes with Si horizontal lineSi bonds.

16 ies (O(MeAN)-LA) able to oxidize C-H and O-H bonds.

17 stead, misfolds, forming incorrect disulfide bonds.

18 chanisms, including force-strengthened catch bonds.

19 R: Cy (1), (i)Pr (2)) with discrete Ge-P exo bonds.

20 ical mechanisms for generating carbon-sulfur bonds.

21 nt cage and then to the symmetry of hydrogen bonds.

22 intramolecular amidation of gamma-C(sp(3))-H bonds.

23 oss nonpolar, polar, ionic, and charge-shift bonds.

24 ar solvent for formation of intramolecular H-bonds.

25 oselective and stereoselective carbon-carbon bonds.

26 n theme related to (changes in) metal-ligand bonding.

27 in-group metal-boron complexes with multiple bonding.

28 ding in all GLUT1 conformations via hydrogen bonding.

29 hin the planes and extremely weak interlayer bonding.

30 en bonds of type YH-X analogous to secondary bonding.

31 ssociated either with the mobilization of pi-bonded 2-pentene or with the equally large activation ba

32 The coparental bond-a relationship of solidarity and commitment between

33 , sulfenic acids), which tend to have high H-bond acidities.

34 ocyclic carbene (NHC) chemistry, a novel C-N bond activation and ring-opening process is described fo

35 ction with fluorobenzene afforded the CAr -H bond activation product [1-F-2-IMe -C6 H4 ](+) I(-) (3).

36 dioxazolone amidating agents via C(sp(3) )-H bond activation to generate the desired amidated product

37 on-carbon, carbon-hydrogen, and carbon-metal bond activation.

38 reactivity of compound I with respect to C-H bond activation.

39 d catalysis proceeds through five steps: C-H bond activation; C-C coupling via a concerted 1,2-aryl t

40 ionally, many transition-metal-catalyzed C-H bond additions to polarized pi bonds occur within cascad

41 DC for 1 min and then bonded with the primer-bonding agent.

42 ed with anthocyanins mainly through hydrogen bonding, although some hydrophobic interaction may also

43 The chemoselectivity for C-H bond amination is greater than 20:1 in all cases.

44 catalyze enantioselective intramolecular C-H bond amination reactions of sulfonyl azides.

45 been engineered to catalyze abiological C-H bond amination reactions, but the yields of these reacti

46 lar attraction and the "windmill" pattern of bonding among the fully halogenated molecules.

47 not have sufficient electrons to give every bond an electron pair.

48 Bonding analyses (NBO and QTAIM) and the isolobal relati

49 omophenyl 4'-nitrobenzoate where the halogen bonding and C-H...O hydrogen bonding are well-matched.

50 s and demonstrate the importance of hydrogen bonding and hydrophobic interactions in the oligomerizat

51 sugar pucker, due to intramolecular hydrogen bonding and hyperconjugation effects.

52 Understanding the nature of chemical bonding and lattice dynamics together with their influen

53 Bonding and stability depend strongly on the trans effec

54 nal change driven by the collective hydrogen bonding and the sequence-mandated topology of the molecu

55 experimental evidence for enhanced hydrogen bonding and/or icebergs in such solutions.

56 al view of the relative orientations between bonds and chemical shielding tensors, respectively, rega

57 the common genetic basis of salutary social bonds and clinically defined psychiatric disorders.

58 charged molecules, held together by hydrogen bonds and Coulomb interactions, have attracted great int

59 approaching the surface, activating the O-H bonds and inducing deprotonation.

60 r characterising the vibrations of molecular bonds and is therefore ideal for label-free detection of

61 teractions can be dissociated as sacrificial bonds and their facile reformation results in self-recov

62 20 and gp41, an engineered 201-433 disulfide bond, and density corresponding to 22 N-glycans.

63 is acid to polarize the carbon-carbon triple bond, and solid K3PO4 interacts with carbonyl oxygen, pr

64 phobic burial include shorter and stronger H-bonds, and increased entropy in the folded state.

65 ere the halogen bonding and C-H...O hydrogen bonding are well-matched.

66 We find that weak hydrogen bonds are at or near preferred gamma-secretase cleavage

67 Functional groups containing X-X bonds are found in all major classes of natural products

68 reactivity toward tertiary and benzylic C-H bonds are observed.

69 apping is challenged when multiple disulfide bonds are present in complicated patterns.

70 C-H bonds are ubiquitous structural units of organic molecul

71 action employing an internally oxidizing O-N bond as a directing group.

72 e formation of intramolecular phenol-amide H-bonds as a function of solvent composition.

73 y ring-closing, but support instead hydrogen-bond assisted ring-closing to prodrugs.

74 agent, resulting in the formation of two C-C bonds at a single carbon center bearing a C(sp(3)) organ

75 onal methods to investigate small numbers of bonds at the interface between two membranes.

76 umidity), an increase in the amount of ionic bonds at the interface is observed.

77 the synchronized actuation of the mechanical bonds at the molecular level.

78 onsiveness was achieved by using a disulfide bond-based crosslinker.

79 The hydrogen-bond-based resorcinarene capsule represents the first ma

80 se monotonically with force, indicating slip-bond behavior.

81 n surveyed in terms of the nature of the C-H bond being activated (C(sp(2))-H or C(sp(3))-H), the nat

82 an E1 mechanism with the cleavage of Cbeta-H bond being rate determining.

83 antiparallel-beta-sheets (1690cm(-1)) and H-bonded beta-turns (1664cm(-1)).

84 featuring an unsupported, terminal multiple bond between a Ce(IV) ion and a ligand fragment was also

85 in R411A-alpha2 is dynamic, reforming the H-bond between Y731 and Y730 to allow RT to propagate to Y

86 quare-shaped pieces due to the van der Waals bonding between the sulfur atoms of the quintuple layers

87 crystallines, which was believed to form the bonding between these two metals in addition to mechanic

88 hibition relies on the formation of hydrogen bonds between C-terminal residues of lentil peptides and

89 Single bonds between carbon atoms are inherently challenging to

90 terfacial location is stabilized by hydrogen bonds between the 5-HT hydroxyl group and lipid headgrou

91 II active site zinc, as well as two hydrogen bonds between the oxazolidinedione ring oxygen and the C

92 analysis indicated the formation of hydrogen bonds between the polar zone of phospholipid and the OH

93 Their widespread use to forge bonds between two aromatic rings has enabled every branc

94 ized by Arg54 and Glu76, which form hydrogen bonds between two subunits.

95 ated compounds featuring multiply and singly bonded boron spin pairs.

96 elated to illuminate atomic-level details of bond breaking and formation during the hydrolysis of a c

97 tonated phenyl tautomer (2H(+)) prior to C-C bond breaking would produce protonated CO2, an energetic

98 propyl]amine) that featured an elongated O-O bond but did not lead to O-O cleavage or reactivity towa

99 es) and dipole-dipole interactions (hydrogen bonds), but nevertheless represents a distinctive elemen

100 enes preferentially react with the disulfide bond, but not thiol group.

101 gs" arising from strengthened water hydrogen bonding, but there is no experimental evidence for enhan

102 aromatic heterocycles were converted to C-Si bonds by reaction with hydrosilanes under the catalytic

103 tinuous flow protocol has been developed for bond C-H activation which promotes the alpha-cyanation o

104 The directed activation of carbon-hydrogen bonds (C-H) is important in the development of synthetic

105 nhardtii (Cr) ChR2) (i) undergoes a hydrogen bond change in D --> K transition and (ii) deprotonates

106 Bonding characteristics shed light on the reasons for th

107 of hydrogen bond, herein we focus on the Li bond chemistry in Li-S batteries through sophisticated q

108 antly lowers the activation barrier for C-OH bond cleavage from the metallocarboxylic acid intermedia

109 diphenyl sulfide also showed competitive C-S bond cleavage giving phenyl sulfinic acid and ionization

110 ovide a "bottom-up" fundamental insight, C-H bond cleavage in methane over Ni-based catalysts was inv

111 Rate-limiting C-O bond cleavage occurs to generate a three-coordinate prod

112 I2 and TBHP as the green oxidant via the C-H bond cleavage of the benzylic carbon under mild reaction

113 e carotenoids as substrate or perform double-bond cleavage.

114 erophospholipids (PE, PS, and PC), via ester bond cleavage.

115 ygen but also activates it for efficient O-O bond cleavage.

116 died in view of its ability to form triply H-bonded complexes with a suitably complementary 2,6-diace

117 carbon was present in a non-graphitic sp(2)-bonded configuration.

118 r modeling calculations, rotation around the bond connecting the quinazolin-4(3H)-one nucleus to the

119 rocesses in hand that today achieve the same bond constructions characteristic of traditional organic

120 Spy0125 was in a folded state, its thioester bond could be cleaved with the small-molecule nucleophil

121 bon dioxide (CO2) gave the respective O-[Zr] bonded cyclic boratacarbonate product.

122 in a scaffold organized by multiple hydrogen bonds dictate stereoselectivity.

123 The tetramers consist of hydrogen-bonded dimers that sandwich together through hydrophobic

124 A ladder of H-bond donating residues creates a 'polar track' demarking

125 tic approach through inclusion of a hydrogen bond donor cocatalyst significantly improved enantiosele

126 eorganized and the higher number of hydrogen bond donor sites provides a remarkable enhancement of it

127 p, as it is considered a lipophilic hydrogen bond donor that may act as a bioisostere of hydroxyl, th

128 a new protocol in which an achiral hydrogen bond donor thiourea catalyst was utilized to enhance the

129 form intra- and interprotamine sulfur-sulfur bonds during the final stages of sperm maturation.

130 Chemical bond energies can then be understood in terms of stabili

131 Hypervalent bonding ensues.

132 The mutant R411A(alpha) disrupts the H-bonding environment and conformation of Y731, ostensibly

133 o-oxidation up to O4-5 of mainly high double bond equivalence species (DBE > 9).

134 mass spectrometry (MS) reports on backbone H-bond fluctuations.

135 e microscopic properties of a given hydrogen-bonded fluid.

136 g(110) surfaces leads to the scission of C-I bonds followed by the formation of organometallic zigzag

137 sources: stereoelectronic assistance of C-C bond formation (i.e., "LUMO umpolung") and crossover fro

138 he ER requires core glycosylation, disulfide-bond formation and proline isomerization.

139 em iron enzyme capable of catalysing the C-S bond formation and sulfoxidation, herein, we discovered

140 osulfur ligands, we describe the gold-sulfur bond formation and the nature of the resulting interface

141 weak base, lysine amino groups underwent C-N bond formation at room temperature.

142 synchronous transition state allowing easier bond formation between two sterically hindered carbons.

143 lyst to promote stereocontrolled C-N and C-S bond formation by activation of an achiral sulfenylating

144 vide the first demonstrations of C-N and N-N bond formation from attack of C-based and N-based nucleo

145 Although C-C bond formation has been a staple of organic synthesis, t

146 ir CCA-ends into the PTC thus making peptide bond formation impossible.

147 tes these phosphorylation events and new C-C bond formation in the absence of biotin has remained a m

148 Reversibility in bond formation is essential to generate ordered networks

149 In this process, carbon-nitrogen bond formation proceeds through a key aminium radical ca

150 io calculations suggest that carbon-fluorine bond formation proceeds via a concerted transition state

151 tandem isomerization followed by C-O and C-C bond formation reaction strategy developed by our own gr

152 amic view of corticostriatal activity during bond formation, revealing how social interactions can re

153 ylation; 1,2- 1,3-, or 1,4-addition; and C-O bond formation.

154 is acidic borane with concomitant C-H or C-C bond formation.

155 re energetically accessible pathways for O-O bond formation.

156 hrough inter- and intramolecular C-C and C-N bond formation.

157 developed via C-H functionalization and C-N bond formation.

158 has been accomplished via alkene vicinal C-N bonds formation of 2-bromo-2-alkenones with guanidine av

159 modules in DCM-d2 solution, through halogen bonding, forming oligomeric assemblies.

160 eversible under conventional low temperature bond-forming conditions have been underexplored.

161 ons, but difficult to access with modern C-C bond-forming reactions.

162 Inspired by the hydrogen-bonded G-quadruplexes found frequently in guanine-rich D

163 Detailed information on the hydrogen bond geometry upon hydrogen-to-deuterium isotope exchang

164 rect nucleophilic substitution of aryl C-OMe bond has been described.

165 asses of enantioselective silylations of C-H bonds have been reported recently, but little mechanisti

166 n, the mixture of 2-5 and 3-5 phosphodiester bonds have emerged as a plausible structural element in

167 ng controversy on the nature of the hydrogen bond (HB) can be settled by looking at the effect of a v

168 Inspired by the concept of hydrogen bond, herein we focus on the Li bond chemistry in Li-S b

169 table and biologically active as a disulfide-bonded heterodimer, whereas it forms inactive disulfide-

170 yridinyl)isophthalamide-barbiturate hydrogen-bonding host-guest complexes are separately incorporated

171 iction endonucleases catalyze phosphodiester bond hydrolysis within or close to their DNA target site

172 te scission of the B horizontal lineB double bond in 6 was achieved by the treatment with an isonitri

173 t cleave the proline-phenylalanine dipeptide bond in Ang II.

174 see text] bond in dizincocene, and the Mn-Mn bond in dimanganese decacarbonyl.

175 the [Formula: see text]-[Formula: see text] bond in dizincocene, and the Mn-Mn bond in dimanganese d

176 effects are illustrated by comparing the C-C bond in ethane against that in bis(diamantane), and disp

177 The bonding in 25 and the mechanism and thermodynamics of th

178 Significantly, the weakened N-H bonds in ((iPr)PDI)Mo(NH3)2(eta(2)-C2H4) enabled hydroge

179 Recently, it was reported that C-H bonds in aromatic heterocycles were converted to C-Si bo

180 curately determining intermolecular hydrogen bonds in carbohydrate-protein complexes.

181 that NAC was efficient in reducing disulfide bonds in circulating VWF multimers.

182 Finally, three metal-metal bonds in experimentally characterized compounds are exam

183 nd the important roles of CF2-H...O hydrogen bonds in influencing intermolecular interactions and con

184 of detecting specific organic and inorganic bonds in metal complexes and minerals and therefore, has

185 atom abstraction from the nitrogen-hydrogen bonds in purine nucleosides produces reactive intermedia

186 he GGA yields expanded lattices and softened bonds in relation to the LDA, but the SCAN meta-GGA syst

187 This species reacts with weak O-H bonds in TEMPO-H and 4-dimethylaminophenol ((NMe2)PhOH),

188 The electrophilic activation of double bonds in the bicyclic products with m-CPBA is an efficie

189 diboranes featuring two-center-two-electron bonds in the context of related compounds featuring mult

190 olecule on top by strengthening the hydrogen bonds in the layer that it contacts.

191 the overall formation of one C-C and two C-N bonds, in moderate to excellent yields.

192 ion-pair formation, and we obtain NBO-based bonding indices to characterize other electronic, struct

193 le the benzonitrile group accepts a hydrogen-bonding interaction from the side chain residue of Asn31

194 nce combined with a weak allosteric hydrogen-bonding interaction that significantly lowers the activa

195 An interesting substrate-solvent hydrogen-bonding interaction was observed.

196 O6 coordination, and 3) binding via hydrogen-bonding interaction with the first-shell water molecules

197 ound aminoacyl-tRNA is initiated by hydrogen bond interactions between the first two nucleotides of t

198 he crystal structure shows that the hydrogen bonding interactions between pairs of 3 result in the fo

199 the prevalence and applications of chalcogen-bonding interactions continues to develop, debate still

200 c structure and orbitals responsible for the bonding interactions in the Sc-OCPPCO-Sc skeleton but al

201 Furthermore, G40 can also establish hydrogen bonding interactions with the nonbridging oxygen of the

202 HF moiety of GRL-09510 forms strong hydrogen-bond-interactions with HIV-1 protease (PR) active-site a

203 tigated the microstructure and phases at the bonding interface of ultrasonically welded aluminum to c

204 ctrochemical conversion of the dative Au<--N bond into a new type of Au-N contact.

205 re of the reaction is that the stronger Ph-O bond is cleaved rather than the weaker aliphatic O-R bon

206 Upon blue light activation, a covalent bond is formed between VVD residue Cys108 and its cofact

207 he relative contribution of the trans double-bond isomer in the mixed samples.

208 M back to D involves only one C13=C14 double-bond isomerization.

209 The role of hydrogen bonding led us to the rotation of NH4(+) within its solv

210 Trends in crystallographic bond lengths and angles shed light on the structural cha

211 Bk(III)-O and Bk(IV)-O bond lengths are shorter than anticipated and provide fu

212 Experimentally measured bond lifetimes (1/koff) and dissociation constants (Kd =

213 n N-terminal catalytic domain (LC) disulfide bond linked to a C-terminal heavy chain (HC) which inclu

214 is triggered by the formation of a disulfide bond linking two tailpieces.

215 l chromophore featuring a C(11)=C(12) double bond locked in its cis conformation (Rh6mr), employs an

216 shown that on the Au(111) surface this sigma-bond metathesis can be combined with Glaser coupling to

217 We propose a sigma-bond metathesis mechanism in which an Fe-H intermediate

218 n transfer, halogen atom transfer, and sigma-bond methatesis.

219 ctivity Value (OAV) and the number of double bonds mostly contributed to the modulation of habituatio

220 4 maintains solvent exclusion and the core H-bond network in the active site by relocating to replace

221 A complex hydrogen bond network of four active site residues, which was ins

222 sitions, or communication along the hydrogen-bonded network depends on the protonation state of the K

223 d fucosylation mechanism facilitated by an H-bonded network, which is corroborated by mutagenesis exp

224 nds crystallize to form robust open hydrogen-bonded networks with parallel indenofluorenyl cores, sig

225 We next addressed one-bond NMR coupling constants in ethers and the reverse an

226 g the number of internal and external double bonds, number of methyl- and ethyl- functional groups, m

227 catalyzed C-H bond additions to polarized pi bonds occur within cascade reaction sequences to provide

228 eactions involving cleavage of the C(acyl)-O bond of aryl esters that proceed under mild conditions a

229 p*RhCl to accelerate the cleavage of the C-H bond of N-pentafluorophenylbenzamides, providing a new s

230 al via the homolytic cleavage of the S-C(5') bond of SAM.

231 Furthermore, the structure and bonding of compound 1 has been investigated by theoretic

232 s (G4), which are stabilized by the hydrogen bonding of guanine residues.

233 nships between the functional groups and C-H bonds of a substrate has been exploited to achieve meta-

234 Here we show that iron forms chemical bonds of similar strengths in basaltic glasses and iron-

235 e of interaction, leading to normal hydrogen bonds of type YH-X analogous to secondary bonding.

236 rodimer, whereas it forms inactive disulfide-bonded oligomers at neutral pH that are caused by activa

237 ALP, but CES-catalyzed cleavage of the ester bond on the molecules results in disassembly of the nano

238 mental observation of Bi-B double and triple bonds, opening the door to design main-group metal-boron

239 Three further VP24 mutations change hydrogen bonding or cause conformational changes.

240 tum theory of atoms in molecules and natural bond orbital analysis.

241 ized-covalent Zr=P double bond, with a Mayer bond order of 1.48, and together with IR spectroscopic d

242 pecies whenever the benefits of building new bonds outweigh the costs.

243 ow chemoselectivity for the amination of C-H bonds over competing reduction of the azide substrate to

244 for insertion of the nitrene units into C-H bonds over reduction of the azides to the sulfonamides t

245 ning formation of aggregates (1604cm(-1)), H-bonded parallel- and antiparallel-beta-sheets (1690cm(-1

246 Formal removal of two bonding partners from boranes, BR3, yields borylenes, RB

247 the Trpin/Metout conformation, the hydrogen-bonding pattern conducive to the proton relay is not the

248 d did not occur with a linear (non-disulfide-bonded) peptide, or when the double disulfide-bonded Wnt

249 pentene in ZSM-5 and the localized hydrogen-bonded pi-complex at Bronsted acid sites, -36 kJ/mol.

250 ed endosomal escape in living cells.Hydrogen bonding plays a major role in determining the tridimensi

251 ) AChRs respond strongly to ACh because an H-bond positions the QA to interact optimally with the rin

252 d accurate determination of experimental one-bond proton-carbon coupling constants ((1)JCH) in small

253 reveals distinguishing features of chemical bonds ranging across nonpolar, polar, ionic, and charge-

254 y oxidase enzymes, includes the critical O-O bond reductive cleavage step.

255 From a molecular orbital perspective, the bonding scheme is reminiscent of XeO4 : an octet of elec

256 zation via stereoelectronically assisted C-C bond scission.

257 ding nonpolar, aromatic, polar, and hydrogen bonding solvents.

258 bone's carbonyl and amide groups in hydrogen-bond stabilization of helical structures is a major fact

259 n approach of local, randomized tailoring of bond stiffness via microalloying enhances creep performa

260 pecifically in response to sexual and couple-bonding stimuli.

261 Here, we use genetic tethering and disulfide bonding strategies to construct HslU pseudohexamers cont

262 Fn-binding repeat-9 can significantly affect bond strength and influence the conformation of Fn upon

263 group is found to stabilize the metal-arene bond strength in 5 by roughly 3 kcal/mol compared to tha

264 The Bi-B double and triple bond strengths are calculated to be 3.21 and 4.70 eV, re

265 ased intensity of the cardiolipin cis-double-bond stretching modes.

266 ated by its crystalline, fully tetrahedrally bonded structure.

267 tronger quantum couplings between covalently bonded subsystems.

268 is able to abstract H-atoms from weaker X-H bonds such as TEMPO-H to re-form 2.

269 Proper pretreatment of the bonding surfaces and application of primers or composite

270 ngs, and weakly to Cho because a different H-bond tethers the ligand to misalign the QA and form weak

271 t SdrC is engaged in low-affinity homophilic bonds that promote cell-cell adhesion.

272 The identification of essential disulfide bonds that underlie this process lays the basis for a si

273 oxidative addition of an activated amide C-N bond to a Ni(0) catalyst and proceeds via alkene inserti

274 lium groups that act together to CH-hydrogen-bond to halide anions when the macrocycle is located on

275 process only occurred when a nitro group is bonded to the 4-position of the initial enantiomerically

276 B hemispheres, geometrically rigidified by H-bonding to eight MeOH molecules and encapsulation of two

277 being coupled with assistance from hydrogen-bonding to the ammonium moiety.

278 es O-O homolysis, where the phenol remains H-bonding to the peroxo OCu in the transition state (TS) a

279 rincipal amine compounds imposed by hydrogen bonding to water, where a pH-dependent excitation energy

280 sting of molecules connected by coordination bonds to Ag adatoms.

281 e concept of forcing covalent and reversible bonds to mix at molecular scale to create a homogenous n

282 a non-metal-catalyzed hydrosilylation of P-P bonds to produce silylphosphines (R(1)R(2)P-SiR(3)R(4)R(

283 ho-specific nitration of aromatic C(sp(2))-H bonds using chelation-assisted removable vicinal diamine

284 lecular cross-coupling of C(sp(2))-H and N-H bonds using N-iodosuccinimide (NIS) has been demonstrate

285 from Gram-negative bacteria and a disulfide-bonded variant of the I91 human cardiac titin polyprotei

286 quent dissociation of the electron-rich HO-H bond via H transfer to N on the nickel surface, benefici

287 d hydrocarbons and unactivated aliphatic C-H bonds via a metal-hydride pathway.

288 r reaction with halides in solution, halogen bonding was detected only in cases where brominated and

289 the biomimetic and organometallic Fe-C sigma bond, which enables bidirectional activity reminiscent o

290 ed to the population of the Fe(3+) -O-Co(3+) bonds, while the suppressed ferroelectric polarization i

291 d its inhibitory efficacy through a covalent bond with BTK Cys481.

292 X, which formed a metastable mixed disulfide bond with TG2, we demonstrated that these proteins speci

293 nd treated with 0.3 M EDC for 1 min and then bonded with the primer-bonding agent.

294 NESs also participate in main chain hydrogen bonding with human CRM1 Lys568 side chain, which acts as

295 drophilic exfoliated flakes and subsequently bonding with water, not possible in Nafion composites ba

296 ions reveal a polarized-covalent Zr=P double bond, with a Mayer bond order of 1.48, and together with

297 n process that generates two C-C and two C-N bonds, with water as the only side product.

298 ted by the disruption of conserved disulfide bonds within the substrate.

299 onded) peptide, or when the double disulfide-bonded Wnt peptide contained Ala substituted for the Ser

300 tively cleaves the nicotinamide's glycosidic bond yielding (tz)ADP-ribose.