Autoxidation Reaction Research Articles

Multi-scheme chemical ionization inlet (MION) for fast switching of reagent ion chemistry in atmospheric pressure chemical ionization mass spectrometry (CIMS) applications

Abstract. A novel chemical ionization inlet named the Multi-scheme chemical IONization inlet (MION), Karsa Ltd., Helsinki, Finland) capable of fast switching between multiple reagent ion schemes is presented, and its performance is demonstrated by measuring several known oxidation products from much-studied cyclohexene and α-pinene ozonolysis systems by applying consecutive bromide (Br−) and nitrate (NO3-) chemical ionization. Experiments were performed in flow tube reactors under atmospheric pressure and room temperature (22 ∘C) utilizing an atmospheric pressure interface time-of-flight mass spectrometer (APi-ToF-MS, Tofwerk Ltd., Thun, Switzerland) as the detector. The application of complementary ion modes in probing the same steady-state reaction mixture enabled a far more complete picture of the detailed autoxidation process; the HO2 radical and the least-oxidized reaction products were retrieved with Br− ionization, whereas the highest-oxidized reaction products were detected in the NO3- mode, directly providing information on the first steps and on the ultimate endpoint of oxidation, respectively. While chemical ionization inlets with multiple reagent ion capabilities have been reported previously, an application in which the charging of the sample occurs at atmospheric pressure with practically no sample pretreatment, and with the potential to switch the reagent ion scheme within a second timescale, has not been introduced previously. Also, the ability of bromide ionization to detect highly oxygenated organic molecules (HOM) from atmospheric autoxidation reactions has not been demonstrated prior to this investigation.

Thin epoxy layers on native aluminium oxide: Specific ageing processes in mild conditions

Post-cured epoxy layers (EP, approx. 100 nm and 1 µm) of three amine hydrogen – oxirane ratios are prepared in dried air on natively oxidised aluminium substrate. A less crosslinked interphase forms as the consequence of adhesive interactions. Even though the layers exhibit very good durability in moist-warm air for up to 100 d, two stages of chemical ageing are revealed. During a short initial stage, some water absorbs firmly in the EP networks. Residual oxirane rings and secondary amine groups are shown to hydrolyse, while network chains remain intact. Marking the 2nd stage, dedicated autoxidation reactions are proven to simultaneously attack tertiary amine crosslinks and α-CH2 groups at phenylene ether units. These reactions destroy network chains, and the release of network fragments was established. Moreover, network destruction proceeds more effectively in 100 nm layers as the surface erodes slightly, even under the given environmentally mild conditions. That observation proves a specifically reduced durability for the interphase at the contact with native aluminium oxide.

Quality characteristics of fried fish crackers packaged in gelatin bags: Effect of squalene and storage time

The influence of bags from fish skin gelatin (GEL) film prepared by substituting glycerol (GLY) with squalene (SQ) at 50% was evaluated on the quality characteristics of fried fish crackers (FFCs) stored for 30 days at 28.0 ± 0.5 °C and 70 ± 5% RH, in comparison with control bags from glycerol plasticized gelatin films (GEL/GLY) and commercial nylon/linear low-density polyethylene (LLDPE) films. The prepared GEL/GLY/SQ films had improved water vapor and oxygen barrier properties. FFCs stored in GEL/GLY/SQ bags had lower moisture content and water activity, compared to those stored in GEL/GLY bags and without packaging (p < 0.05). After 30 days, FFCs stored in GEL/GLY/SQ and nylon/LLDPE bags had lower concentration of hydroperoxides and secondary lipid oxidation products than others. In addition, FFCs stored in GEL/GLY/SQ and nylon/LLDPE bags had less volatile compounds, especially those formed from autoxidation and non-enzymatic browning reaction. Therefore, GEL/GLY/SQ bags lowered the oxidation and loss of polyunsaturated fatty acids, mainly n-3 and n-6 when compared to other bags. Moreover, FFCs stored in GEL/GLY/SQ bags exhibited negligible changes in color and texture. Therefore, the prepared GEL/GLY/SQ bags improved oxidative stability of FFCs.

Assessment of the autoxidation mechanism of p-toluenediamine by air and hydrogen peroxide and determination of mutagenic environmental contaminant in beauty salon effluent

The present work investigated the autoxidation reaction of p-toluenediamine (PTD) - a precursor - widely used in permanent hair dyeing formulation, under experimental conditions close to the hair dyeing process (oxygen and/or peroxide in ammoniacal medium), by chromatographic and spectroscopic techniques. In additional, evaluated the mutagenicity of the PTD oxidation products and the presence of PTD and this products in wastewater from beauty salon, as well as in surface water and drinking water using HPLC coupled to a diode array detector and linear scan voltammetry. Through this study, it was possible the identification of semi-quinonediimine, quinonediimine, dimers (derived from toluenediamine), and trimer radical identified as Bandrowski's Base derivative (BBD) formed during autoxidation of PTD. Salmonella Typhimurium YG1041 assay with and without metabolic activation induced rat-liver (S9) indicated mutagenic activity for BBD. Levels of PTD were determined by the standard addition method in samples collected from the wastewater of a beauty salon, as well as from the water before and after treatment in a drinking water treatment plant (DWTP) reached concentrations of 2.08 ± 0.21, 2.36 ± 0.10 × 10−3, and 1.77 ± 0.13 × 10−3 mg L−1, respectively. In addition, linear sweep voltammetry was used to monitor the BBD found at the concentration of 1.59 ± 0.35 mg L−1 in wastewater collected from the beauty salon.

Revising the structure of a new eicosanoid from human platelets to 8,9–11,12-diepoxy-13-hydroxyeicosadienoic acid

Eicosanoids are critical mediators of fever, pain, and inflammation generated by immune and tissue cells. We recently described a new bioactive eicosanoid generated by cyclooxygenase-1 (COX-1) turnover during platelet activation that can stimulate human neutrophil integrin expression. On the basis of mass spectrometry (MS/MS and MS3), stable isotope labeling, and GC-MS analysis, we previously proposed a structure of 8-hydroxy-9,11-dioxolane eicosatetraenoic acid (DXA3). Here, we achieved enzymatic synthesis and 1H NMR characterization of this compound with results in conflict with the previously proposed structural assignment. Accordingly, by using LC-MS, we screened autoxidation reactions of 11-hydroperoxy-eicosatetraenoic acid (11-HpETE) and thereby identified a candidate sharing the precise reverse-phase chromatographic and MS characteristics of the platelet product. We optimized these methods to increase yield, allowing full structural analysis by 1H NMR. The revised assignment is presented here as 8,9–11,12-diepoxy-13-hydroxyeicosadienoic acid, abbreviated to 8,9–11,12-DiEp-13-HEDE or DiEpHEDE, substituted for the previous name DXA3. We found that in platelets, the lipid likely forms via dioxolane ring opening with rearrangement to the diepoxy moieties followed by oxygen insertion at C13. We present its enzymatic biosynthetic pathway and MS/MS fragmentation pattern and, using the synthetic compound, demonstrate that it has bioactivity. For the platelet lipid, we estimate 16 isomers based on our current knowledge (and four isomers for the synthetic lipid). Determining the exact isomeric structure of the platelet lipid remains to be undertaken.

Autoxidation of the sea ice biomarker proxy IPSO25 in the near-surface oxic layers of Arctic and Antarctic sediments

Over the last decade or so, the mono- and di-unsaturated highly branched isoprenoid (HBI) lipids IP25 (Ice Proxy with 25 carbon atoms) and IPSO25 (Ice Proxy for the Southern Ocean with 25 carbon atoms) have emerged as useful proxies for sea ice in the Arctic and Antarctic, respectively. A more complete understanding of their respective proxy signatures, however, requires more detailed knowledge of their stability in the water column and in sediments. In the current study, we focused on the autoxidation of IPSO25, first by performing laboratory-based oxidation reactions on a purified sample and characterizing products based on detailed mass spectral analysis. We then analysed for the same oxidation products in near-surface sediments retrieved from the Arctic and the Antarctic, and some suspended organic matter from the Antarctic. Our data show that IPSO25 is susceptible to partial autoxidation within the oxic layers of Arctic and Antarctic sediments, while the same processes appear not to be so important in the water column. Although the number of primary autoxidation reactions identified in sediments was not as large as in laboratory experiments, there was evidence for their subsequent modification by biotic degradation. Quantifying the extent of degradation of IPSO25 and IP25 in sediments, and thus the impact of such process on the use of these biomarkers as paleo sea ice proxies, remains challenging at this stage, since most of the primary oxidation products do not accumulate, likely due to secondary biodegradation reactions. Some interesting differences in reactivity were also observed between IPSO25 and IP25 present in the same Arctic sediments. This suggests that factors other than environmental control may influence the IPSO25/IP25 ratio (i.e. DIP25) in Arctic sediments.

Dopamine Autoxidation Is Controlled by Acidic pH.

We studied the reaction mechanism of dopamine autoxidation using quantum chemical methods. Unlike other biogenic amines important in the central nervous system, dopamine and noradrenaline are capable of undergoing a non-enzymatic autoxidative reaction giving rise to a superoxide anion that further decomposes to reactive oxygen species. The reaction in question, which takes place in an aqueous solution, is as such not limited to the mitochondrial membrane where scavenging enzymes such as catalase and superoxide dismutase are located. With the experimental rate constant of 0.147 s−1, the dopamine autoxidation reaction is comparably as fast as the monoamine oxidase B catalyzed dopamine decomposition with a rate constant of 1 s−1. By using quantum chemical calculations, we demonstrated that the rate-limiting step is the formation of a hydroxide ion from a water molecule, which attacks the amino group that enters intramolecular Michael addition, giving rise to a pharmacologically inert aminochrome. We have shown that for dopamine stability on a time scale of days, it is essential that the pH value of the synaptic vesicle interior is acidic. The pathophysiologic correlates of the results are discussed in the context of Parkinson's disease as well as the pathology caused by long-term amphetamine and cocaine administration.

A Curcumin Degradation Product, 7-Norcyclopentadione, Formed by Aryl Migration and Loss of a Carbon from the Heptadienedione Chain.

Evidence that anti-inflammatory and other biological effects of curcumin may at least in part be mediated by its metabolites underscores the importance of identifying novel transformation products. Spontaneous degradation of curcumin in buffer pH 7.5 results mainly in dioxygenated products with a characteristic cyclopentadione ring composed of carbons 2 through 6 of the former heptadienedione chain. When analyzing degradation reactions of 4'- O-methylcurcumin, a product was identified missing one of the terminal carbons of the heptadienedione moiety while containing a cyclopentadione ring and adjacent hydroxy group typical of curcumin degradation products. Analysis of curcumin autoxidation reactions showed formation of an analogous compound, 7-norcyclopentadione, a degradation product exhibiting net loss of a carbon and gain of an oxygen atom. Removal of the carbon is proposed to occur via a peroxide-linked curcumin dimer in conjunction with radical-mediated 1,2-aryl migration of a guaiacol moiety. Oxidation reactions of demethoxycurcumin gave demethoxy-7-norcyclopentadione, whereas an analogous product was not observed from bis-demethoxycurcumin. Incubation of RAW264.7 macrophage-like cells with curcumin showed the presence of 7-norcyclopentadione, the formation of which was not increased upon activation of the cells with 12- O-tetradecanoylphorbol-13-acetate . 7-Norcyclopentadione is a novel type of degradation product that is most likely formed via autoxidative processes when cells are incubated with curcumin.

Some reactions of 2-(4-substitutedphenyl)-2-(N-methyl-N-4-substitutedbenzamido) acetic acids

In situ generated 2,4-diaryl substituted münchnones from 2-(4-substitutedphenyl)-2-(N-methyl-N-4-substitutedbenzamido)acetic acids react with acetic anhydride in the presence of 2-nitromethylene thiazolidine, which is most likely acting as a base, and unexpectedly undergo a Dakin–West type reaction and a concurrent autoxidation reaction leading to the formation of (E)-1-(N,4-dimethylbenzamido)-1-(4-fluorophenyl)prop-1-en-2-yl acetate, 4-substitutedphenyl-N-methyl-N-(4-substitutedbenzoyl) benzamides and p-substituted benzoic acids. In addition, a novel and efficient access to N-acyl urea derivatives is described by the reaction between 2-(4-substitutedphenyl)-2-(N-methyl-N-4-substitutedbenzamido)acetic acids and cyclohexyl, isopropyl carbodiimides in the presence of a base. The structures of all new products were identified on the basis of NMR and IR spectra, along with X-ray diffraction data and HRMS measurements.

Kinetics and Degradation Mechanism of Adrenaline Derivative CpQ in Diluted Aqueous Solutions

The degradation kinetics of an adrenaline (epinephrine) derivative, CpQ, was studied in solution in the pH range of 1-12 at 40-80 °C by high-performance liquid chromatography and ultraviolet-visible spectroscopy. The pH-rate profile exhibits a bell-shaped curve with two sigmoidal regions in the specific acid-catalyzed and specific base-catalyzed regions. The pH range of maximum stability was 2.5-4.5 with the main degradation pathway being the oxidative N-dealkylation of the aliphatic amino moiety followed by fast interconversion of the resulting fragments to stable degradation products. The autoxidation reaction was slower than the reaction of the oxygen reactive species. The chiral center underwent R to S racemization by a polar reaction mechanism under acidic conditions with a rate minimum at pH 4. The rates of degradation of the R and S enantiomers were similar across all pHs. CpQ degradation in the presence of hydrogen peroxide at 40 °C was significantly faster, and the extent of increases with pH. Metal ions bind to CpQ and catalyze its hydrolysis in the order Fe3+ > Fe2+ > Mg2+ > Mn2+ > Ti3+ > Sr2+ > Zn2+, with a rate enhancement of ≤1 order of magnitude at the studied pH values of 1 and 5. There was no buffer catalysis observed in the hydrolysis of the studied compound for maleate and phosphate but significant buffer catalysis in the case of citrate and malate.

Experimental and Numerical Study on Oxidation Deposition Properties of Aviation Kerosene

In the fuel cooling system of an engine, the heating of aviation kerosene causes it to exhibit complicated, unsteady physicochemical processes and forms undesirable coke deposition. To understand these processes better, we investigated the coupling relationship between turbulent flow, heat transfer, autoxidation, and deposition reactions of fuel in a cooling heat exchanger. The experiments were performed to investigate the whole process within 105 min, separated into five continuous phases of 20, 40, 60, 80, and 105 min, with a heat flux of 38.6 kW/m2. On the basis of the experimental results, we established a three-dimensional model to study the influence of kerosene’s heat-transfer process on oxidation deposition in a long, straight, horizontal pipe under supercritical pressure condition. A modified six-step, pseudo-detailed chemical kinetic and global deposition mechanism has been incorporated into the numerical model with particular attention to temperature variation. The model was validated based on ...

Protection of dopamine towards autoxidation reaction by encapsulation into non-coated- or chitosan- or thiolated chitosan-coated-liposomes.

The aim of this work is to evaluate the potential of non-coated-, chitosan-(CS)- or chitosan-glutathione conjugate- (CS-GSH)-coated liposomes to protect the neurotransmitter Dopamine (DA) from the autoxidation reaction in neutral/alkaline conditions. This may be of interest in the development of nanotechnology-based approaches to improve Parkinson's disease treatment because decreased ROS production and reduced DA associated neurotoxicity are expected. For the mentioned purposes, DA-loaded vesicles were prepared by the Dried Reconstituted Vesicles (DRV) method, and were subsequently coated using solutions of polycations. As for the mean diameters of liposomes so prepared, the CS-GSH coated liposomes showed a significant decrease in size compared to the corresponding non-coated and CS-coated vesicles. The surface charge of DA-loaded non-coated liposomes was -10.8 mV, whereas the CS or CS-GSH coated vesicles showed a slightly positive ζ-potential. The capability of the herein studied vesicles to prevent DA autoxidation was evaluated by visual inspection, monitoring DA/lipid ratio as such and under stressed conditions. The results suggest that liposome formulations partially protect the neurotransmitter from the autoxidation reaction. In particular, the CS-GSH coated liposomes were more stable than the corresponding CS-coated and non-coated ones against the oxidative damage and were found to deliver the neurotransmitter in a sustained manner. Probably, this is due to the localization of the neurotransmitter in the core of the vesicles as indicated by XPS which confirmed the absence of the neurotransmitter on the surface of these vesicles.

Iodometric Determination of Hydroperoxides in Hydrocarbon Autoxidation Reactions Using Triphenylphosphine Solution as a Titrant: A New Protocol

Hydroperoxides are important oxidants in epoxidation processes and play a central role in the industrial hydrocarbon autoxidation. This paper presents a new and water-free/low-water iodometric titration technique that can be utilized to quantify organic hydroperoxides. In this protocol, the aqueous thiosulfate titrant used in the conventional iodometric titration method was replaced with a new titrant (triphenylphosphine solution) in order to prevent the need for aqueous solutions. In addition, a comparison of two methods showed that titration time in this new method is shorter than that of thiosulfate titrant based one. It is predicted that a colorless charge-transfer complex is formed from interaction between triphenylphosphine and iodine. The proposed protocol can be utilized in the industrial processes that go through hydroperoxide intermediates.

Photoxidation of Benzyl Alcohol with Heterogeneous Photocatalysts in the UV Range: The Complex Interplay with the Autoxidative Reaction

AbstractIn conventional studies of heterogeneous photocatalytic oxidation, it is crucial to evaluate by means of control experiments the relevance of the “non‐catalyzed” autoxidation reaction under irradiation. If the autoxidation is found to be negligible, it is usually considered that it can be safely disregarded. However, in the case of aromatic aldehydes’ synthesis such as benzaldehyde, irradiating with UV light may lead to a more complex mechanism than previously thought. Herein, we prove that neglecting the autoxidative reaction can lead to a misinterpretation of the mechanism as well as an overestimation of the catalyst's efficiency, even if the control experiment exhibits zero yield. As an example, we studied the synthesis of benzaldehyde from benzyl alcohol by UV‐A irradiation with and without TiO2 and CdS nanoparticles; without catalyst, after a long induction time, the aldehyde enhances its own production through an autocatalytic reaction activated by the same light wavelengths utilized for the nanocatalysts. The long induction time leads to considering the autocatalysis to be deceptively negligible. However, the nanoparticles act as a fast initiator of the benzaldehyde autocatalysis, in such a way that the oxidation rate reached a similar performance with nanoparticles and after removing them. This suggests that the commonly ignored autocatalysis of benzaldehyde indeed is a relevant parallel pathway to the heterogeneous catalysis mechanism.

Biotic and abiotic degradation of the sea ice diatom biomarker IP25 and selected algal sterols in near-surface Arctic sediments

The organic geochemical IP25 (Ice Proxy with 25 carbon atoms) has been used as a proxy for Arctic sea ice in recent years. To date, however, the role of degradation of IP25 in Arctic marine sediments and the impact that this may have on palaeo sea ice reconstruction based on this biomarker have not been investigated in any detail. Here, we show that IP25 may be susceptible to autoxidation in near-surface oxic sediments. To arrive at these conclusions, we first subjected a purified sample of IP25 to autoxidation in the laboratory and characterised the oxidation products using high resolution gas chromatography–mass spectrometric methods. Most of these IP25 oxidation products were also detected in near-surface sediments collected from Barrow Strait in the Canadian Arctic, although their proposed secondary oxidation and the relatively lower abundances of IP25 in other sediments probably explain why we were not able to detect them in material from other parts of the region. A rapid decrease in IP25 concentration in some near-surface Arctic marine sediments, including examples presented here, may potentially be attributed to at least partial degradation, especially for sediment cores containing relatively thick oxic layers representing decades or centuries of deposition. An increase in the ratio of two common phytoplanktonic sterols – epi-brassicasterol and 24-methylenecholesterol – provides further evidence for such autoxidation reactions given the known enhanced reactivity of the latter to such processes reported previously. In addition, we provide some evidence that biodegradation processes also act on IP25 in Arctic sediments. The oxidation products identified in the present study will need to be quantified more precisely in downcore records in the future before the effects of degradation processes on IP25-based palaeo sea ice reconstruction can be fully understood. In the meantime, a brief overview of some previous investigations of IP25 in relatively shallow Arctic marine sediments suggests that overlying climate conditions were likely dominant over degradation processes, as evidenced from often increasing IP25 concentration downcore, together with positive relationships to known sea ice conditions.

A DFT investigation of the blue bottle experiment: E∘half-cell analysis of autoxidation catalysed by redox indicators.

The blue bottle experiment is a collective term for autoxidation reactions catalysed by redox indicators. The reactions are characterized by their repeatable cycle of colour changes when shaken/left to stand and intricate chemical pattern formation. The blue bottle experiment is studied based on calculated solution-phase half-cell reduction potential of related reactions. Our investigation confirms that the reaction in various versions of the blue bottle experiment published to date is mainly the oxidation of an acyloin to a 1,2-dicarbonyl structure. In the light of the calculations, we also propose new non-acyloin reducing agents for the experiment. These results can help guide future experimental studies on the blue bottle experiment.

Highly Oxygenated Molecules from Atmospheric Autoxidation of Hydrocarbons: A Prominent Challenge for Chemical Kinetics Studies

Recent advances in chemical ionization mass spectrometry have allowed the detection of a new group of compounds termed highly oxygenated molecules (HOM). These are atmospheric oxidation products of volatile organic compounds (VOC) retaining most of their carbon backbone, and with O/C ratios around unity. Owing to their surprisingly high yields and low vapor pressures, the importance of HOM for aerosol formation has been easy to verify. However, the opposite can be said concerning the exact formation pathways of HOM from major aerosol precursor VOC. While the role of peroxy radical autoxidation, i.e., consecutive intramolecular H-shifts followed by O2 addition, has been recognized, the detailed formation mechanisms remain highly uncertain. A primary reason is that the autoxidation process occurs on sub-second timescales and is extremely sensitive to environmental conditions like gas composition, temperature, and pressure. This, in turn, poses a great challenge for chemical kinetics studies to be able to mimic the relevant atmospheric reaction pathways, while simultaneously using conditions suitable for studying the short-lived radical intermediates. In this perspective, we define six specific challenges for this community to directly observe the initial steps of atmospherically relevant autoxidation reactions and thereby facilitate vital improvements in the understanding of VOC degradation and organic aerosol formation.

Enzymatic and free radical formation of cis- and trans- epoxyeicosatrienoic acids in vitro and in vivo

Epoxyeicosatrienoic acids (EETs) are metabolites of arachidonic acid (AA) oxidation that have important cardioprotective and signaling properties. AA is an ω-6 polyunsaturated fatty acid (PUFA) that is prone to autoxidation. Although hydroperoxides and isoprostanes are major autoxidation products of AA, EETs are also formed from the largely overlooked peroxyl radical addition mechanism. While autoxidation yields both cis- and trans-EETs, cytochrome P450 (CYP) epoxygenases have been shown to exclusively catalyze the formation of all regioisomer cis-EETs, on each of the double bonds. In plasma and red blood cell (RBC) membranes, cis- and trans-EETs have been observed, and both have multiple physiological functions. We developed a sensitive ultra-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) assay that separates cis- and trans- isomers of EETs and applied it to determine the relative distribution of cis- vs. trans-EETs in reaction mixtures of AA subjected to free radical oxidation in benzene and liposomes in vitro. We also determined the in vivo distribution of EETs in several tissues, including human and mouse heart, and RBC membranes. We then measured EET levels in heart and RBC of young mice compared to old. Formation of EETs in free radical reactions of AA in benzene and in liposomes exhibited time- and AA concentration-dependent increase and trans-EET levels were higher than cis-EETs under both conditions. In contrast, cis-EET levels were overall higher in biological samples. In general, trans-EETs increased with mouse age more than cis-EETs. We propose a mechanism for the non-enzymatic formation of cis- and trans-EETs involving addition of the peroxyl radical to one of AA's double bonds followed by bond rotation and intramolecular homolytic substitution (SHi). Enzymatic formation of cis-EETs by cytochrome P450 most likely occurs via a one-step concerted mechanism that does not allow bond rotation. The ability to accurately measure circulating EETs resulting from autoxidation or enzymatic reactions in plasma and RBC membranes will allow for future studies investigating how these important signaling lipids correlate with heart disease outcomes.

Autoxidation of Heterocyclic Aminals.

The autoxidation reactions of 2-acyl-2,3-dihydroquinazolin-4(1H)-ones 4a and 5a and 2,2′-bis(dihydroquinazolinone) 6a are described. These reactions generate aminyl radicals that undergo β-C–C cleavage, and subsequent reactions of the resulting C-based radicals with O2 lead to diverse products with good selectivity, depending on the structure of the substrate. Oxidation of 4a, in which the 2-acyl group is part of a cyclic acenaphthenone unit, yields a heterocyclic C-hydroperoxylaminal via 1,2-acyl migration. Oxidation of 5a, which contains a 2-acetyl group, yields peracetic acid and a quinazolinone product. Oxidation of 6a forms a bis(quinazolinone) by net dehydrogenation.

Highly Oxygenated Multifunctional Compounds in α-Pinene Secondary Organic Aerosol

Highly oxygenated multifunctional organic compounds (HOMs) originating from biogenic emissions constitute a widespread source of organic aerosols in the pristine atmosphere. However, the molecular forms in which HOMs are present in the condensed phase upon gas-particle partitioning remain unclear. In this study, we show that highly oxygenated molecules that contain multiple peroxide functionalities are readily cationized by the attachment of Na+ during electrospray ionization operated in the positive ion mode. With this method, we present the first identification of HOMs characterized as C8-10H12-18O4-9 monomers and C16-20H24-36O8-14 dimers in α-pinene derived secondary organic aerosol (SOA). Simultaneous detection of these molecules in the gas phase provides direct evidence for their gas-to-particle conversion. Molecular properties of particulate HOMs generated from ozonolysis and OH oxidation of unsubstituted (C10H16) and deuterated (C10H13D3) α-pinene are investigated using coupled ion mobility spectrometry with mass spectrometry. The systematic shift in the mass of monomers in the deuterated system is consistent with the decomposition of isomeric vinylhydroperoxides to release vinoxy radical isotopologues, the precursors to a sequence of autoxidation reactions that ultimately yield HOMs in the gas phase. The remarkable difference observed in the dimer abundance under O3- versus OH-dominant environments underlines the competition between intramolecular hydrogen migration of peroxy radicals and their bimolecular termination reactions. Our results provide new and direct molecular-level information for a key component needed for achieving carbon mass closure of α-pinene SOA.