Position-specific isotope effects during alkaline hydrolysis of 2,4-dinitroanisole resolved by compound-specific isotope analysis, 13C NMR, and density-functional theory

Author:

Wang ChunleiORCID,Heraty Linnea J.ORCID,Wallace Adam F.,Liu Changjie,Li Xiaoqiang,McGovern Gregory P.,Horita Juske,Fuller Mark E.,Hatzinger Paul B.,Sturchio Neil C.ORCID

Funder

US Department of Energy Basic Energy Sciences

Strategic Environmental Research and Development Program

National Science Foundation

Publisher

Elsevier BV

Subject

General Medicine,General Chemistry,Environmental Chemistry,Environmental Engineering,Pollution,Health, Toxicology and Mutagenesis,Public Health, Environmental and Occupational Health

Reference46 articles.

1. NMR-based isotopic and isotopomic analysis;Akoka;Prog. Nucl. Magn. Reson. Spectrosc.,2020

2. C-N bond forming cross-coupling reactions: an overview;Bariwal;Chem. Soc. Rev.,2013

3. Internal referencing for 13C position-specific isotope analysis measured by NMR spectrometry;Bayle;Anal. Chem.,2015

4. Mineral identity, natural organic matter, and repeated contaminant exposures do not affect the carbon and nitrogen isotope fractionation of 2,4-dinitroanisole during abiotic reduction;Berens;Environ. Sci.: Proces. Impact.,2019

5. Assessment of 2,4-dinitroanisole transformation using compound-specific isotope analysis after in situ chemical reduction of iron oxides;Berens;Environ. Sci. Technol.,2020

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