ライフサイエンスコーパス: ozonolysis

1 ions of unsaturated hydrocarbons with ozone (ozonolysis).

2 isoprene photo-oxidation and by alpha-pinene ozonolysis.

3 ultilayer model (KM-GAP) simulating triolein ozonolysis.

4 n of secondary organic aerosol formed during ozonolysis.

5 d allylic electrophiles, followed by a rapid ozonolysis.

6 In each case, SOA was produced by a-pinene ozonolysis.

7 ) that would form simultaneously in a-pinene ozonolysis.

8 ns of the Criegee intermediate formed during ozonolysis.

9 edox-catalyzed thiol-ene reaction and alkene ozonolysis.

10 ts in concentrations similar to alpha-pinene ozonolysis.

11 squalene-ozone (SqOz) reaction, or squalene ozonolysis.

12 urce of its production occurs through alkene ozonolysis.

13 organic compounds formed during alpha-pinene ozonolysis.

14 etween hydroxy-carbonyl products of squalene ozonolysis.

15 ethers 12, 15, 28, and 45 include controlled ozonolysis, 1,2-addition of the Normant reagent, and het

16 ne 1 was desymmetrized via a one-pot Criegee ozonolysis/acylation protocol to afford acetal-lactone 2

17 zylidene 2-C-methylerythritol silyl ether by ozonolysis afforded a 1,2,3-triol 3-monobenzoate interme

18 Heck coupling of 17 with styrene followed by ozonolysis afforded the 6-formyl derivative 19.

19 -alkylation followed by a two-step, one-pot, ozonolysis/aldol condensation protocol.

20 An ozonolysis/aldol sequence first produced the trans cyclo

21 To study the nature of multiphase ozonolysis, an unsaturated triglyceride, triolein, of th

22 ular alkylidene C-H insertion to give, after ozonolysis and aldol condensation, (-)-mesembrine 1.

23 Here we report how ozonolysis and copper catalysis under mild reaction cond

24 Ozonolysis and fluoride ion-induced desilylation complet

25 roperties of particulate HOMs generated from ozonolysis and OH oxidation of unsubstituted (C10H16) an

26 d NO3, consistent with previous studies that ozonolysis and oxidation by NO3 are sources of nighttime

27 Oxidative decay via ozonolysis and product formation were monitored by liqui

28 Further elaboration by ozonolysis and reductive amination affords 2b in an over

29 d functional group manipulations followed by ozonolysis and reductive amination.

30 stream oxidative cleavage protocols, such as ozonolysis and the Lemieux-Johnson reaction.

31 SOA yield and composition from alpha-pinene ozonolysis and the photooxidation of toluene and acetyle

32 room-temperature oxidation process that used ozonolysis and ultraviolet irradiation effected both the

33 e ketone, saponification, iodolactonization, ozonolysis, and intramolecular aldol reaction) to a spir

34 ses vinyl triflate formation, site-selective ozonolysis, and reduction.

35 iliary followed by chiral auxiliary removal, ozonolysis, and reductive amination/intramolecular nucle

36 ctional elaboration, by acetal substitution, ozonolysis, and sulfur ylide-mediated epoxidation, provi

37 3 yield is (7.9-0.2+0.4)% from HFO-1234ze(E) ozonolysis, and the PFC-14 yield is (1.04-0.05+0.07)% fr

38 alpha-pinene reacting with secondary OH from ozonolysis are key intermediates in the organic nitrate

39 While the volatile products of squalene ozonolysis are known, the condensed-phase products have

40 Signature products unique to cholesterol ozonolysis are present within atherosclerotic tissue at

41 ecause the reaction products from endocyclic ozonolysis are tethered, this system is ideal for consid

42 Criegee intermediates (CI), formed in alkene ozonolysis, are central for controlling the multiphase c

43 lly deuterated cyclohexene and cis-6-nonenal ozonolysis, as well as the influence of water addition t

44 ,6-tris(2-chloropropan)-2-yl-1,3,5-trioxane; ozonolysis at -80 degrees C of 2,4,6-tri(propan-2-yliden

45 SOA) can continue mediated by a mechanism of ozonolysis at interfaces, a better understanding about h

46 The products of AH(2) ozonolysis at the relevant air-water interface shift fro

47 d in this synthetic route are regioselective ozonolysis, Au(I)-catalyzed cycloisomerization-induced c

48 the bicyclic myrtenal scaffold prior to the ozonolysis-based ring-opening step that furnishes the ta

49 time scales of SOA formed from alpha-pinene ozonolysis by measuring the dynamic response to a modest

50 ormed from other sources (e.g., alpha-pinene ozonolysis) by affecting gas-phase chemistry and gas-par

51 he primary ozonides initially generated upon ozonolysis can be reduced with Zn/AcOH to afford the car

52 Ozonolysis can be used to determine the db-position and

53 d also study SOA formation from alpha-pinene ozonolysis carried out without an OH scavenger.

54 The steroids produced by cholesterol ozonolysis cause effects that are thought to be critical

55 ionally, we demonstrate that controlling the ozonolysis conditions used for the cleavage enables Clip

56 Accurately characterizing isoprene ozonolysis continues to challenge atmospheric chemists.

57 equently, these synthons were examined in an ozonolysis/cyclization reaction sequence.

58 Several variants of reductive ozonolysis, defined here as the in situ generation of al

59 small diacids or products from alpha-pinene ozonolysis demonstrates that ions are ejected from the s

60 tified in the condensed phase which survived ozonolysis during new particle formation and growth.

61 egradation of unsaturated TGs due to ambient ozonolysis emerged with time and were detectable within

62 Here, the first gas-surface multiphase ozonolysis experiment of BPA thin films, at a constant o

63 an those suggested from many previous alkene ozonolysis experiments and assumed in atmospheric modeli

64 To confirm the hypothesis, ozonolysis experiments as well as direct measurements of

65 nts of peroxy radicals (RO(2)) from flowtube ozonolysis experiments by an iodide-adduct chemical ioni

66 data allowed for the design of a homogeneous ozonolysis flow reactor capable of delivering precise qu

67 We describe a method using ozonolysis for depolymerizing polysaccharides containing

68 idence for mechanisms and products of olefin ozonolysis for reactions of ozone and ethene solely on t

69 e reagents which can mimic the reactivity of ozonolysis for the oxidative conversion of alkenyl bonds

70 ondensed-phase products of squalene particle ozonolysis found that an increase in water vapor concent

71 mine and carboxylate groups of 1 followed by ozonolysis gave methyl ketone 8.

72 acid derived nitroalkenes 9, 10, and 11 and ozonolysis gave the alpha-hydroxy and alpha-amino thiol

73 Alkylation with methallyl halide and ozonolysis gave the ketone 24, which was then converted

74 ger, and the SOA mass yields for unscavenged ozonolysis generally fall within the range of mass yield

75 highly oxygenated products and cis-6-nonenal ozonolysis generated the same monomer product distributi

76 Alkene ozonolysis generates short-lived Criegee intermediates t

77 Ozonolysis has several limitations.

78 suite of oxidation products of alpha-pinene ozonolysis in an aerosol that is assumed to separate int

79 SOA was formed by alpha-pinene ozonolysis in an atmospheric simulation chamber at tempe

80 pact of these emissions on SOA formation via ozonolysis in chamber experiments.

81 Ozonolysis in dried butyl acetate similarly produces mai

82 characterization of Criegee intermediates in ozonolysis in situ were proven difficult in decades of e

83 Aqueous-phase ozonolysis in the atmosphere is an important process dur

84 n to react with ozone are oxidized by direct ozonolysis in the hydrophobic interfacial environment, b

85 olytic production of OH radicals upon alkene ozonolysis in the troposphere.

86 alkenes while mitigating frothing during the ozonolysis in water.

87 erically relevant AAHPs through liquid-phase ozonolysis, in which two types of monoterpene-derived SC

88 re significantly higher than SOA yields from ozonolysis including an OH scavenger, and the SOA mass y

89 then converted by hydrogenation and a second ozonolysis into the keto aldehyde 26.

90 ated ketone; (b) a domino sequence involving ozonolysis, intramolecular aldol reaction, and acetaliza

91 Ozonolysis is a major tropospheric removal mechanism for

92 Ozonolysis is a widely used and practical synthetic tech

93 In an office setting, ozonolysis is also the dominant degradation pathway for

94 A) with organolithium reagents and reductive ozonolysis is presented.

95 le component of SOM produced by alpha-pinene ozonolysis is quantified for 20- to 50-mum particles at

96 the importance of product quantification and ozonolysis kinetics in determining the overall environme

97 This study employs ozonolysis kinetics to distinguish these isomers based o

98 ocessing of alkenes, including isoprene, via ozonolysis leads to the formation of zwitterionic reacti

99 liquid chromatography is coupled to in-line ozonolysis/mass spectrometry (Ag(+)-LC/O3-MS).

100 These highly oxidized products of squalene ozonolysis may accumulate on indoor dust and surfaces an

101 Such a mechanism, reminiscent of ozonolysis, may prevail in most permanganate oxidations.

102 ainly secondary CI, in contrast to gas-phase ozonolysis mechanisms.

103 Here, we introduce a new ozonolysis method inside the matrix-assisted laser desor

104 The simulations reveal that ozonolysis occurs near the surface and is O3-transport l

105 Ozonolysis of (S)-18 afforded a stable diketo ester (R)-

106 Ozonolysis of 1 selectively removed pdac ligands to gene

107 radical was produced in the dark through the ozonolysis of 2,3-dimethyl-2-butene (DMB).

108 Controlled ozonolysis of 2b-NBu4 followed by 1H and 15N NMR spectro

109 hydroxy-i-steroid 11 as a byproduct from the ozonolysis of 9 and an attempt to effect conversion of s

110 The kinetics and products of ozonolysis of a series of model compounds with different

111 Criegee intermediates, derived from ozonolysis of alkenes and recognized as key species in t

112 The ozonolysis of alkenes contributes substantially to the f

113 In the indoor air, the ozonolysis of alkenes has been suggested as an alternati

114 Conversely, the ozonolysis of alkenes has been suggested as the main pat

115 tion rate accelerations between 15-fold (for ozonolysis of alkenes in ionised lipids) and 90-fold (fo

116 carbonyl oxides that play critical roles in ozonolysis of alkenes in the atmosphere.

117 Ozonolysis of alkenes in the presence of solubilized wat

118 Ozonolysis of alkenes in the troposphere produces Criege

119 ueous-phase ozonolysis, we herein report the ozonolysis of alkenes in water assisted by surfactants.

120 Coolade-assisted ozonolysis of alkenes in water provided the desired carb

121 Ozonolysis of alkenes is known to produce reactive inter

122 Ozonolysis of alkenes, an important nonphotolytic source

123 Ozonolysis of alkenes, an important nonphotolytic source

124 These oxidative reactions, together with the ozonolysis of alkenes, are also responsible for the nigh

125 mediates (CIs), mainly formed from gas-phase ozonolysis of alkenes, are considered as atmospheric oxi

126 now often called "Criegee intermediates," in ozonolysis of alkenes.

127 lsilylperoxyketals and -acetals derived from ozonolysis of alkenes.

128 sis of ozone and nitrous acid (HONO) and the ozonolysis of alkenes.

129 HOM formation from ozonolysis of alpha-cedrene was explained by an autoxida

130 nd radical concentrations, estimated for the ozonolysis of alpha-pinene (0.020 +/- 0.0050 nmol/mug),

131 18.9 +/- 3.2% of the mass of SOA formed from ozonolysis of alpha-pinene and beta-pinene, respectively

132 es of several major dimer esters in SOA from ozonolysis of alpha-pinene and beta-pinene-substantial g

133 poration kinetics of SOA particles formed by ozonolysis of alpha-pinene and limonene.

134 ry organic aerosols (SOA) resulting from the ozonolysis of alpha-pinene and photooxidation of toluene

135 paction surface to study SOA formed from the ozonolysis of alpha-pinene at relative humidities (RHs)

136 In addition, ozonolysis of alpha-pinene contributes substantially to

137 ntration and particle mass concentration for ozonolysis of alpha-pinene exceed those from ozonolysis

138 Ozonolysis of alpha-pinene has been chosen as a proof-of

139 inland) suggesting that DMA might affect the ozonolysis of alpha-pinene in ambient conditions.

140 Ozonolysis of alpha-pinene in the presence of candle gas

141 In the present study, ozonolysis of alpha-pinene in the presence of dimethylam

142 morphologies of SOA particles formed during ozonolysis of alpha-pinene in the presence of dioctyl ph

143 nd incorporated into SOA particles formed by ozonolysis of alpha-pinene in the presence of PAH vapor.

144 Ozonolysis of alpha-pinene, Delta(3)-carene, and a 1:1 m

145 The SOA was generated by the dark ozonolysis of alpha-pinene, extracted into the water, an

146 aerosol (SOA) mixtures produced through the ozonolysis of alpha-pinene, limonene, and ocimene.

147 secondary organic aerosol (SOA) produced by ozonolysis of alpha-pinene.

148 ondary organic aerosol (SOA) formed from the ozonolysis of alpha-pinene.

149 d from the photo-oxidation of mesitylene and ozonolysis of alpha-pinene.

150 oxygenated molecules (HOMs) are produced by ozonolysis of alpha-pinene.

151 ndary organic aerosol (SOA) arising from the ozonolysis of alpha-pinene.

152 secondary organic material (SOM) produced by ozonolysis of alpha-pinene.

153 easured product yields for the heterogeneous ozonolysis of alpha-terpineol adsorbed on glass, NaCl, a

154 We investigated the multiphase ozonolysis of alpha-terpineol, an oxygenated derivative

155 ducts and kinetics differ from the gas-phase ozonolysis of alpha-terpineol.

156 This transformation proceeds by Criegee ozonolysis of an alkene, reductive cleavage of the resul

157 Multiphase ozonolysis of aqueous organics presents a potential path

158 )H(9)CHOO, and C(5)H(11)CHOO), produced from ozonolysis of asymmetrical 1-alkenes (1-butene, 1-penten

159 ctrometry (DART-MS), kinetics studies of the ozonolysis of BaP in thin films exhibited fast initial l

160 Ozonolysis of beta-caryophyllonic (BCA) and limononic (L

161 The ozonolysis of bicyclic 1,2-dioxines was investigated usi

162 formed in a variety of systems, ranging from ozonolysis of biogenic volatile organic compounds to aro

163 de of four pericyclic reactions initiated by ozonolysis of C=N bonds.

164 The ozonolysis of CH(3)SeCH(3) proceeded with a rate constan

165 sterol, which is only a minor product during ozonolysis of cholesterol in solution.

166 of highly oxidized organic compounds in the ozonolysis of cyclohexene (C6H10) was investigated by me

167 the double bond similar to that found in the ozonolysis of cyclohexene and limonene.

168 CIs from the ozonolysis of cyclohexene, acting as surrogate for cycli

169 ozonolysis of alpha-pinene exceed those from ozonolysis of Delta(3)-carene alone, while their mixture

170 ary organic aerosol (SOA) formation from the ozonolysis of dominant GLVs, their mixtures and grass cl

171 pressure becomes important in the gas-phase ozonolysis of endocyclic alkenes for a carbon number bet

172 simplest Criegee intermediate, CH(2)OO, from ozonolysis of ethene by cavity ring-down spectroscopy in

173 Ozonolysis of fragrance additives served as a secondary

174 hase oxidation by hydroxyl radicals (OH) and ozonolysis of gaseous alpha-terpineol.

175 Ozonolysis of HXL results in formation of low volatility

176 the novel LC-OzID-IMS-MS configuration where ozonolysis of ionized lipids occurred rapidly (10 ms) wi

177 Here, the photooxidation and ozonolysis of isoprene were examined under a range of co

178 Ozonolysis of isoprene, one of the most abundant volatil

179 onomeric malonic anhydrides were prepared by ozonolysis of ketene dimers, a procedure validated by mo

180 xamine chemical aging of SOA produced by the ozonolysis of limonene (LSOA) in the presence of gaseous

181 f secondary organic aerosol produced through ozonolysis of limonene (LSOA).

182 condary organic aerosol (SOA) formation from ozonolysis of limonene at total aerosol mass loadings ra

183 Thus ozonolysis of octyl cyclobutene-1-carboxylate followed b

184 that SOZs and other oxygenates will form via ozonolysis of oily indoor surfaces and skin oil.

185 Proof-of-principle measurements of the ozonolysis of oleic acid aerosol (20 mug/m(3)) revealed

186 Negative ion spectra from the ozonolysis of oleic acid show azelaic acid and 9-oxonona

187 phthalene into a water-methanol droplet, the ozonolysis of oleic acid, and localization of the carbon

188 To examine the ozonolysis of organic molecules, gas-phase ozone generat

189 Herein, we quantify "transient AMFs" from ozonolysis of pulse-emitted limonene in a ventilated cha

190 Previous studies have focused on surface ozonolysis of pure unsaturated compounds on impermeable

191 are robust reagents capable of withstanding ozonolysis of remote alkenes, thus providing a new route

192 The ozonolysis of sesquiterpenes resulted in molar HOM yield

193 wipe samples and known gaseous products from ozonolysis of skin lipids.

194 dicals (OH) in the presence of ozone via the ozonolysis of skin-emitted alkenes.

195 For example, ozonolysis of spirodienone 12c in CH2Cl2 and reductive w

196 Here, we examine the heterogeneous ozonolysis of squalene, a key species in indoor air chem

197 ents produces organic hydroperoxides via the ozonolysis of terpene flavoring chemicals.

198 The ozonolysis of tetramethylethylene (TME) in solution to h

199 Ozonolysis of the 2,6-divinyl derivative of a naphthalen

200 The beta-elimination step after the ozonolysis of the chemodosimeter was too slow to be prac

201 anone derivatives in H(2)SO(4)/CH(3)CN or by ozonolysis of the corresponding cyclohexanone methyl oxi

202 lves alkylation of 1 with an allylic halide, ozonolysis of the double bond, and catalytic hydrogenati

203 highly substituted form and in high yield by ozonolysis of the enamine bond of 1,2,3,4-tetrahydro-9H-

204 Ozonolysis of the gas phase photochemical products in th

205 Direct ozonolysis of the ketones followed by in situ acidificat

206 Furthermore, ozonolysis of the latter products led to polycarbonyl co

207 Ozonolysis of the mechanochemical products further shows

208 ence of VOC-cross-product dimers in SOA from ozonolysis of the monoterpene mixture: a VOC-cross-produ

209 its hydroxyl function followed by reductive ozonolysis of the olefin and a subsequent one-pot three-

210 Ozonolysis of the olefin followed by brief treatment wit

211 Ozonolysis of the pyrazole moiety affords pharmaceutical

212 hydrides by methyl (S)-prolinate followed by ozonolysis of the resulting carboxylic acids is used to

213 entatively identified as products of aqueous ozonolysis of the two unsaturated terpenoic acids invest

214 Ozonolysis of these vinyl sulfones and vinyl phosphonate

215 Here, the gas-surface ozonolysis of three oleic acid-based compounds was studi

216 functional organic compounds (HOMs) from the ozonolysis of three sesquiterpenes, alpha-cedrene, beta-

217 The ozonolysis of TME in the participating solvent, methanol

218 cept, we characterized HOM formed during the ozonolysis of two biogenic compounds (alpha-pinene and l

219 lar-level composition of SOA formed from the ozonolysis of two GLVs: cis-3-hexenol (HXL) and cis-3-he

220 condary organic aerosol (SOA) generated from ozonolysis of two structural monoterpene isomers: D-limo

221 In this work, we examine the ozonolysis of two synthesized unsaturated carbonyl isome

222 hemical kinetics associated with the ambient ozonolysis of unsaturated triacylglycerols (TGs), a majo

223 ultaneously quantifies CIs produced from the ozonolysis of volatile organic compounds in the gas and

224 cles were produced in a flow tube reactor by ozonolysis of volatile organic compounds, including the

225 to the synthesis of 2 was a first-generation ozonolysis/olefination/aldol strategy to convert a [2.2.

226 position of SOA formed via dark alpha-pinene ozonolysis on either (NH(4))(2)SO(4) or Fe-containing (N

227 The stepwise nature of isoprene ozonolysis on the aqueous surface is more consistent wit

228 Ozonolysis or oxidative cleavage of peracetylated allyl

229 ns (NOx photo-oxidation, photolysis of H2O2, ozonolysis, or thermal decomposition of N2O5).

230 ne intermediate; (iii) development of a safe ozonolysis process conducted in an aqueous solvent mixtu

231 01+0.04)% from HFO-1234yf, while HCFO-1233xf ozonolysis produces CFC-13 in (0.034-0.006+0.009)% yield

232 exocyclic or the compound itself is acyclic, ozonolysis produces less ELVOC and the role of the OH ra

233 cts with the conjugated double bonds forming ozonolysis product aldehydes.

234 human occupancy on the dynamics of skin oil ozonolysis products (SOOPs) in an office in a LEED-certi

235 accurate mass and arrival time extraction of ozonolysis products facilitated correlation of precursor

236 Ozonolysis products from LPA (18:1) unambiguously demons

237 Here we report detection of cholesterol ozonolysis products in human brains.

238 n CSE-119 cells was strongly affected by the ozonolysis products of 6PPD but not by those of the othe

239 OCs were measured, including common skin oil ozonolysis products such as acetone, 6-MHO, and 4-OPA; h

240 locks with formulas corresponding to primary ozonolysis products such as pinic and pinonic acids, whe

241 challenges owing to the explosive nature of ozonolysis products(8,9).

242 SOA is primarily formed from low-volatility ozonolysis products, with a small contribution from high

243 ake coefficient that is 1.6% of that for the ozonolysis products.

244 involves the cleavage of olefinic groups via ozonolysis, providing the resulting two-merged net MOFs

245 The BTx ozonolysis rate constant measured by ELISA was 5.74 +/-

246 s toward the gas phase exhibit heterogeneous ozonolysis rate constants that are 2 times faster than d

247 strating the rapid nature of this multiphase ozonolysis reaction at atmospherically relevant ozone le

248 rofiles benchmark the modeling of the ethene ozonolysis reaction network and mechanism, allowing for

249 pies along with GC-MS identified the aqueous ozonolysis reaction products as trans- and cis-lactols [

250 Reactions between ozonolysis reaction products of alpha-pinene, such as pi

251 in the aerosol cycle and in the atmospheric ozonolysis reaction sequence.

252 ted in the gas phase of a beta-caryophyllene ozonolysis reaction system.

253 During the ozonolysis reaction, water molecules trapped within the

254 We found that CIs from ozonolysis reactions can be directly probed by means of

255 Results are presented for ozonolysis reactions of four biogenic monoterpenes (alph

256 solvents on ozone solubility and the rate of ozonolysis reactions using rapid injection NMR spectrosc

257 tion of several early intermediates in these ozonolysis reactions.

258 nge of different CIs formed from atmospheric ozonolysis reactions.

259 an anionic oxy-Cope rearrangement, a one-pot ozonolysis-reductive amination, and a Lewis acid promote

260 dary organic aerosols (SOA) from monoterpene ozonolysis represent another type.

261 Deuterated cyclohexene ozonolysis resulted in a less oxidized product distribut

262 nsaturated TGs were found to undergo ambient ozonolysis resulting in a decrease over time.

263 - 2](+) product ions was probed by gas-phase ozonolysis revealing the presence of two new carbon-carb

264 s, which are highly abundant in alpha-pinene ozonolysis SOA (22 +/- 5% by weight), have an atmospheri

265 demonstrated by application to alpha-pinene ozonolysis SOA for which increased filter aerosol mass l

266 cular formulas matching those of monoterpene ozonolysis SOA were observed; they include organonitrate

267 latile compounds and ozone from alpha-pinene ozonolysis SOA with three 1-m-long denuders, and exposin

268 ol particles of adipic acid and alpha-pinene ozonolysis SOM.

269 Ozonolysis successfully depolymerized PS A into structur

270 Specifically, in the a-pinene ozonolysis system, the extents of ion signal reduction i

271 in terpenes capable of generating OH through ozonolysis, the much larger amount of ethanol solvent ac

272 h our previous studies on ethene and propene ozonolysis, the nascent sCI yields demonstrated an intri

273 however, are still limited, as they rely on ozonolysis to generate the key peroxide intermediates fr

274 oquinoline with formaldehyde produced in the ozonolysis to give a methyl (+/-)-1-methyl-2-alkyl-1,2,3

275 d the microwave characterization of isoprene ozonolysis to prereactive complexes.

276 idation (IMP), we address the limitations of ozonolysis to rescue previously inaccessible alkene subs

277 s, as well as the first reported use of "dry ozonolysis" to reveal a masked carboxylic acid in the to

278 a presynthesized microporous UiO-type MOF to ozonolysis, to confer it with mesopores sufficiently lar

279 ctionalized ozonides by a wide range of post-ozonolysis transformations.

280 orders of magnitude, increasing the rate of ozonolysis under low (<10 ppb) ozone levels.

281 all the organic linkers (in this study, via ozonolysis under reductive conditions) liberates the SBU

282 in the range of mass yields for alpha-pinene ozonolysis under various conditions.

283 be the partitioning of SOA from alpha-pinene ozonolysis using measurements from a dual-thermodenuder

284 tant typically required for the conventional ozonolysis using organic solvents.

285 A mild, organometallic alternative to ozonolysis utilizing oxone and OsO(4) is presented.

286 s and O/C > 0.55 in dimers) from cyclohexene ozonolysis was determined as (4.5 +/- 3.8)%.

287 The rate of squalene loss due to ozonolysis was lower than its replenishment on the skin

288 ormed in a flow tube reactor by alpha-pinene ozonolysis, was studied by passing the fresh SOA into a

289 Inspired by the atmospheric aqueous-phase ozonolysis, we herein report the ozonolysis of alkenes i

290 ve organic species generated by alpha-pinene ozonolysis, we show that combining diethylammonium and n

291 rosol chamber investigations of alpha-pinene ozonolysis were conducted under near environmental precu

292 and LA that were produced following aqueous ozonolysis were identified as keto-BCA and keto-LA, resp

293 SOA yields from alpha-pinene ozonolysis were measured in the presence of a variety of

294 Products of BCA and LA ozonolysis were quantified with LC-MS as well as with th

295 c double bond efficiently produce ELVOC from ozonolysis, whereas the yields from OH radical-initiated

296 micity is exhibited in the initial stages of ozonolysis, which has a powerful influence on the CHF(3)

297 tal piece of molecular insight into isoprene ozonolysis, which has broad tropospheric implications du

298 Multiphase ozonolysis will therefore be competitive with multiphase

299 reaction rates for sCIs formed from isoprene ozonolysis with SO2 along with systematic discrepancies

300 produced with 21 to 23% yield from isoprene ozonolysis, yet its reactivity has not been directly stu