50 citations as recorded by crossref.

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4. Properties of carbon dioxide absorption and reduction by sodium borohydride under atmospheric pressure Y. Zhao et al. https://doi.org/10.1016/j.fuel.2014.10.070
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6. Measurements of the OH + Octanal and OH, Cl, and Br + Nonanal Reaction Rate Coefficients and the Nonanal Aldehydic Site Branching Ratio M. Spanoudaki et al. https://doi.org/10.1021/acs.jpca.6c01688
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8. Effects of additives on reaction of nucleosides with UV light in presence of uric acid and salicylic acid T. Suzuki & C. Ono https://doi.org/10.3164/jcbn.22-23
9. OH-Initiated Degradation of Unsaturated Esters in the Atmosphere: Kinetics in the Temperature Range of 287−313 K M. Blanco et al. https://doi.org/10.1021/jp901755x
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11. Atmospheric impact of 2-methylpentanal emissions: kinetics, photochemistry, and formation of secondary pollutants M. Asensio et al. https://doi.org/10.5194/acp-23-14115-2023
12. Investigating carbonyl compounds above the Amazon rainforest using a proton-transfer-reaction time-of-flight mass spectrometer (PTR-ToF-MS) with NO+ chemical ionization A. Ringsdorf et al. https://doi.org/10.5194/acp-24-11883-2024
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16. Acyclic halogenated monoterpenes from marine macroalgae: Estimated atmospheric lifetimes, potential degradation products, and their atmospheric impacts M. Khan et al. https://doi.org/10.1080/0035919X.2022.2036264
17. Characterization of Polar Organosulfates in Secondary Organic Aerosol from the Green Leaf Volatile 3-Z-Hexenal M. Shalamzari et al. https://doi.org/10.1021/es503226b
18. Atmospheric Degradation Initiated by OH Radicals of the Potential Foam Expansion Agent, CF3(CF2)2CH═CH2 (HFC-1447fz): Kinetics and Formation of Gaseous Products and Secondary Organic Aerosols E. Jiménez et al. https://doi.org/10.1021/acs.est.5b04379
19. Fluid dynamics modelling of UV reactors in advanced oxidation processes for VOC abatement applications F. Montecchio et al. https://doi.org/10.1016/j.cej.2019.03.094
20. Photochemistry of the sea-surface microlayer (SML) influenced by a phytoplankton bloom: a mesocosm study O. Jibaja Valderrama et al. https://doi.org/10.5194/bg-23-1965-2026
21. UV absorption cross sections between 230 and 350 nm and pressure dependence of the photolysis quantum yield at 308 nm of CF3CH2CHO M. Antiñolo et al. https://doi.org/10.1039/c1cp21368g
22. Terpenoid and carbonyl emissions from Norway spruce in Finland during the growing season H. Hakola et al. https://doi.org/10.5194/acp-17-3357-2017
23. Kinetic Study of the Daytime Atmospheric Fate of (Z)-3-Hexenal J. Xing et al. https://doi.org/10.1021/jp303202h
24. Atmospheric degradation of 2-chloroethyl vinyl ether, allyl ether and allyl ethyl ether: Kinetics with OH radicals and UV photochemistry M. Antiñolo et al. https://doi.org/10.1016/j.chemosphere.2017.04.053
25. Photochemistry of CF3(CH2)2CHO in air: UV absorption cross sections between 230 and 340 nm and photolysis quantum yields at 308 nm M. Antiñolo et al. https://doi.org/10.1016/j.jphotochem.2011.12.023
26. Influence of indoor chemistry on the emission of mVOCs from Aspergillus niger molds C. Kalalian et al. https://doi.org/10.1016/j.scitotenv.2020.140148
27. UV absorption spectra of trans-2-pentenal, trans-2-hexenal and 2-methyl-2-pentenal C. Kalalian et al. https://doi.org/10.1016/j.cplett.2019.01.028
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30. OH radical and Cl atom initiated Reactions of Methyl n-propyl ether: Kinetics and Atmospheric Implications B. Kar & B. Rajakumar https://doi.org/10.1016/j.atmosenv.2024.120717
31. Structure–Activity Relationships for 1,3-Dipolar Cycloaddition Reactions of Criegee Intermediates with Carbonyls Z. Cornwell et al. https://doi.org/10.1021/acsearthspacechem.5c00398
32. Laboratory Studies of CHF2CF2CH2OH and CF3CF2CH2OH: UV and IR Absorption Cross Sections and OH Rate Coefficients between 263 and 358 K M. Antiñolo et al. https://doi.org/10.1021/jp2111633
33. Atmospheric fate of hydrofluoroolefins, CxF2x+1CH CH2 (x = 1,2,3,4 and 6): Kinetics with Cl atoms and products B. Ballesteros et al. https://doi.org/10.1016/j.chemosphere.2016.09.156
34. Temperature Effects on the Removal of Potential HFC Replacements, CF3CH2CH2OH and CF3(CH2)2CH2OH, Initiated by OH Radicals M. Antiñolo et al. https://doi.org/10.1021/es103931s
35. Kinetic and Products Study of the Atmospheric Degradation of trans-2-Hexenal with Cl Atoms A. Grira et al. https://doi.org/10.1021/acs.jpca.2c05060
36. Studies in search of selective detection of isomeric biogenic hexen‐1‐ols and hexanal by flowing afterglow tandem mass spectrometry using [H3O]+ and [NO]+ reagent ions F. Dhooghe et al. https://doi.org/10.1002/rcm.6294
37. Green Leaf Volatiles in the Atmosphere—Properties, Transformation, and Significance K. Sarang et al. https://doi.org/10.3390/atmos12121655
38. Production of oxygenated volatile organic compounds from the ozonolysis of coastal seawater D. Kilgour et al. https://doi.org/10.5194/acp-24-3729-2024
39. Development of an irradiation and kinetic model for UV processes in volatile organic compounds abatement applications F. Montecchio et al. https://doi.org/10.1016/j.cej.2018.05.009
40. Photolysis, OH reactivity and ozone reactivity of a proxy for isoprene-derived hydroperoxyenals (HPALDs) G. Wolfe et al. https://doi.org/10.1039/c2cp40388a
41. Rate constants of the gas‐phase reactions of OH radicals with trans‐2‐hexenal, trans‐2‐octenal, and trans‐2‐nonenal T. Gao et al. https://doi.org/10.1002/kin.20424
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43. Hydroxyl radical reaction rate coefficients as a function of temperature and IR absorption cross sections for CF3CH=CH2 (HFO-1243zf), potential replacement of CF3CH2F (HFC-134a) S. González et al. https://doi.org/10.1007/s11356-014-3426-2
44. Reactions of carbonyl oxide with aldehydes: accurate electronic structure methods, kinetic insights, and atmospheric implications C. Xie & B. Long https://doi.org/10.5194/acp-26-6973-2026
45. Photooxidation of Leaf-Wound Oxygenated Compounds, 1-Penten-3-ol, (Z)-3-Hexen-1-ol, and 1-Penten-3-one, Initiated by OH Radicals and Sunlight E. Jiménez et al. https://doi.org/10.1021/es8027814
46. Influence of temperature on the chemical removal of 3-methylbutanal, trans-2-methyl-2-butenal, and 3-methyl-2-butenal by OH radicals in the troposphere E. Jiménez et al. https://doi.org/10.1016/j.atmosenv.2009.05.005
47. Mechanism and Product Distribution of the O3-Initiated Degradation of (E)-2-Heptenal, (E)-2-Octenal, and (E)-2-Nonenal E. Gaona Colmán et al. https://doi.org/10.1021/acs.jpca.7b01857
48. Quantitative kinetics reveal that reactions of HO2 are a significant sink for aldehydes in the atmosphere and may initiate the formation of highly oxygenated molecules via autoxidation Q. Gao et al. https://doi.org/10.1039/D4CP00693C
49. Quantifying the reactive uptake of OH by organic aerosols in a continuous flow stirred tank reactor D. Che et al. https://doi.org/10.1039/b904418c
50. Evaluation of the daytime tropospheric loss of 2-methylbutanal M. Asensio et al. https://doi.org/10.5194/acp-22-2689-2022