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Assessment of 2,4-dinitroanisole transformation using compound-specific isotope analysis after <em>in situ</em> chemical reduction of iron oxides
Berens, M. J., Hofstetter, T. B., Bolotin, J., & Arnold, W. A. (2020). Assessment of 2,4-dinitroanisole transformation using compound-specific isotope analysis after in situ chemical reduction of iron oxides. Environmental Science and Technology, 54(9), 5520-5531. https://doi.org/10.1021/acs.est.9b07616
Dual-element isotope analysis of desphenylchloridazon to investigate its environmental fate in a systematic field study: a long-term lysimeter experiment
Melsbach, A., Torrentó, C., Ponsin, V., Bolotin, J., Lachat, L., Prasuhn, V., … Elsner, M. (2020). Dual-element isotope analysis of desphenylchloridazon to investigate its environmental fate in a systematic field study: a long-term lysimeter experiment. Environmental Science and Technology, 54(7), 3929-3939. https://doi.org/10.1021/acs.est.9b04606
Kinetic isotope effects of the enzymatic transformation of <i>γ</i>-hexachlorocyclohexane by the lindane dehydrochlorinase variants LinA1 and LinA2
Schilling, I. E., Hess, R., Bolotin, J., Lal, R., Hofstetter, T. B., & Kohler, H. P. E. (2019). Kinetic isotope effects of the enzymatic transformation of γ-hexachlorocyclohexane by the lindane dehydrochlorinase variants LinA1 and LinA2. Environmental Science and Technology, 53(5), 2353-2363. https://doi.org/10.1021/acs.est.8b04234
Molecularly imprinted polymers for compound-specific isotope analysis of polar organic micropollutants in aquatic environments
Bakkour, R., Bolotin, J., Sellergren, B., & Hofstetter, T. B. (2018). Molecularly imprinted polymers for compound-specific isotope analysis of polar organic micropollutants in aquatic environments. Analytical Chemistry, 90(12), 7292-7301. https://doi.org/10.1021/acs.analchem.8b00493
Formation of brominated trihalomethanes during chlorination or ozonation of natural organic matter extracts and model compounds in saline water
Liu, Z. Q., Shah, A. D., Salhi, E., Bolotin, J., & von Gunten, U. (2018). Formation of brominated trihalomethanes during chlorination or ozonation of natural organic matter extracts and model compounds in saline water. Water Research, 143, 492-502. https://doi.org/10.1016/j.watres.2018.06.042
Different mechanisms of alkaline and enzymatic hydrolysis of the insensitive munition component 2,4-dinitroanisole lead to identical products
Ulrich, B. A., Palatucci, M., Bolotin, J., Spain, J. C., & Hofstetter, T. B. (2018). Different mechanisms of alkaline and enzymatic hydrolysis of the insensitive munition component 2,4-dinitroanisole lead to identical products. Environmental Science and Technology Letters, 5(7), 456-461. https://doi.org/10.1021/acs.estlett.8b00258
Measurement of oxygen isotope ratios (<SUP>18</SUP>O/<SUP>16</SUP>O) of aqueous O<SUB>2</SUB> in small samples by gas chromatography/isotope ratio mass spectrometry
Pati, S. G., Bolotin, J., Brennwald, M. S., Kohler, H. P. E., Werner, R. A., & Hofstetter, T. B. (2016). Measurement of oxygen isotope ratios (18O/16O) of aqueous O2 in small samples by gas chromatography/isotope ratio mass spectrometry. Rapid Communications in Mass Spectrometry, 30(6), 684-690. https://doi.org/10.1002/rcm.7481
Isotope fractionation associated with the direct photolysis of 4-chloroaniline
Ratti, M., Canonica, S., McNeill, K., Erickson, P. R., Bolotin, J., & Hofstetter, T. B. (2015). Isotope fractionation associated with the direct photolysis of 4-chloroaniline. Environmental Science and Technology, 49(7), 4263-4273. https://doi.org/10.1021/es505784a
Isotope fractionation associated with the indirect photolysis of substituted anilines in aqueous solution
Ratti, M., Canonica, S., McNeill, K., Bolotin, J., & Hofstetter, T. B. (2015). Isotope fractionation associated with the indirect photolysis of substituted anilines in aqueous solution. Environmental Science and Technology, 49(21), 12766-12773. https://doi.org/10.1021/acs.est.5b03119
Isotope fractionation associated with the photochemical dechlorination of chloroanilines
Ratti, M., Canonica, S., McNeill, K., Bolotin, J., & Hofstetter, T. B. (2015). Isotope fractionation associated with the photochemical dechlorination of chloroanilines. Environmental Science and Technology, 49(16), 9797-9806. https://doi.org/10.1021/acs.est.5b02602
Compound-specific carbon, nitrogen, and hydrogen isotope analysis of <I>N</I>-nitrosodimethylamine in aqueous solutions
Spahr, S., Bolotin, J., Schleucher, J., Ehlers, I., von Gunten, U., & Hofstetter, T. B. (2015). Compound-specific carbon, nitrogen, and hydrogen isotope analysis of N-nitrosodimethylamine in aqueous solutions. Analytical Chemistry, 87(5), 2916-2924. https://doi.org/10.1021/ac5044169
Isotope effects as new proxies for organic pollutant transformation
Hofstetter, T. B., Bolotin, J., Pati, S. G., Skarpeli-Liati, M., Spahr, S., & Wijker, R. S. (2014). Isotope effects as new proxies for organic pollutant transformation. Chimia, 68(11), 788-792. https://doi.org/10.2533/chimia.2014.788
Isotope effects of enzymatic dioxygenation of nitrobenzene and 2-nitrotoluene by nitrobenzene dioxygenase
Pati, S. G., Kohler, H. P. E., Bolotin, J., Parales, R. E., & Hofstetter, T. B. (2014). Isotope effects of enzymatic dioxygenation of nitrobenzene and 2-nitrotoluene by nitrobenzene dioxygenase. Environmental Science and Technology, 48(18), 10750-10759. https://doi.org/10.1021/es5028844
Compound-specific isotope analysis of benzotriazole and its derivatives
Spahr, S., Huntscha, S., Bolotin, J., Maier, M. P., Elsner, M., Hollender, J., & Hofstetter, T. B. (2013). Compound-specific isotope analysis of benzotriazole and its derivatives. Analytical and Bioanalytical Chemistry, 405(9), 2843-2856. https://doi.org/10.1007/s00216-012-6526-1
Isotope fractionation associated with the biodegradation of 2- and 4-nitrophenols via monooxygenation pathways
Wijker, R. S., Kurt, Z., Spain, J. C., Bolotin, J., Zeyer, J., & Hofstetter, T. B. (2013). Isotope fractionation associated with the biodegradation of 2- and 4-nitrophenols via monooxygenation pathways. Environmental Science and Technology, 47(24), 14185-14193. https://doi.org/10.1021/es403876u
Isotopic analysis of oxidative pollutant degradation pathways exhibiting large H isotope fractionation
Wijker, R. S., Adamczyk, P., Bolotin, J., Paneth, P., & Hofstetter, T. B. (2013). Isotopic analysis of oxidative pollutant degradation pathways exhibiting large H isotope fractionation. Environmental Science and Technology, 47(23), 13459-13468. https://doi.org/10.1021/es403597v
Using compound-specific isotope analysis to assess biodegradation of nitroaromatic explosives in the subsurface
Wijker, R. S., Bolotin, J., Nishino, S. F., Spain, J. C., & Hofstetter, T. B. (2013). Using compound-specific isotope analysis to assess biodegradation of nitroaromatic explosives in the subsurface. Environmental Science and Technology, 47(13), 6872-6883. https://doi.org/10.1021/es3051845
δ<SUP>15</SUP>N enrichment suggests possible source for halogenated 1′-methyl-1,2′-bipyrroles (MBPs)
Pangallo, K. C., Reddy, C. M., Poyton, M., Bolotin, J., & Hofstetter, T. B. (2012). δ15N enrichment suggests possible source for halogenated 1′-methyl-1,2′-bipyrroles (MBPs). Environmental Science and Technology, 46(4), 2064-2070. https://doi.org/10.1021/es203143c
Carbon and nitrogen isotope effects associated with the dioxygenation of aniline and diphenylamine
Pati, S. G., Shin, K., Skarpeli-Liati, M., Bolotin, J., Eustis, S. N., Spain, J. C., & Hofstetter, T. B. (2012). Carbon and nitrogen isotope effects associated with the dioxygenation of aniline and diphenylamine. Environmental Science and Technology, 46(21), 11844-11853. https://doi.org/10.1021/es303043t
Carbon, hydrogen, and nitrogen isotope fractionation associated with oxidative transformation of substituted aromatic <I>N</I>-alkyl amines
Skarpeli-Liati, M., Pati, S. G., Bolotin, J., Eustis, S. N., & Hofstetter, T. B. (2012). Carbon, hydrogen, and nitrogen isotope fractionation associated with oxidative transformation of substituted aromatic N-alkyl amines. Environmental Science and Technology, 46(13), 7189-7198. https://doi.org/10.1021/es300819v