Kinetics of Rapid Covalent Bond Formation of Aniline with Humic Acid: ESR Investigations with Nitroxide Spin Labels
- 作者: Matthies M.1, Glinka K.2, Theiling M.2, Hideg K.3, Steinhoff H.2
-
隶属关系:
- Institute of Environmental Systems Research (USF), University of Osnabrück
- Physics Department, University of Osnabrück
- Department of Organic and Medicinal Chemistry, University of Pécs
- 期: 卷 47, 编号 6 (2016)
- 页面: 627-641
- 栏目: Article
- URL: https://journals.rcsi.science/0937-9347/article/view/247478
- DOI: https://doi.org/10.1007/s00723-016-0782-8
- ID: 247478
如何引用文章
详细
The bioavailability of many soil contaminants depends on their interaction with the soil organic matter. The paper presents a new approach of using stable paramagnetic spin labels for investigating the kinetics of covalent binding of specific xenobiotic functional groups with humic acids, a major organic matter fraction. Leonardite humic acid (LHA) was incubated with the nitroxide spin labels amino-TEMPO (4-amino-2,2,6,6-Tetramethylpiperidin-1-oxyl) and anilino-NO (2,5,5-Trimethyl-2-(3-aminophenyl)pyrrolidin-1-oxyl), respectively, which contain an aliphatic or aromatic functionality susceptible to interaction with LHA. Electron spin resonance spectra of LHA samples without and with the enzyme laccase were recorded at X-band frequency (9.43 GHz) at room temperature and neutral pH. Binding was detected by a pronounced broadening of the spectral lines after incubation of LHA for both spin labels. The development of a broad signal component in the spectrum of anilino-NO indicated the immobilization due to strong binding of the aniline group. The reorientational correlation time of bound anilino-NO is more than two orders of magnitude greater than that of the free label. The ratio of the amount of bound to the unbound species was used to determine the kinetics of the covalent bond formation. Reaction rate constants of 0.16 and 0.01 min−1 were determined corresponding to half-times of 4.3 and 69.3 min, respectively. Treatment of LHA with laccase enhanced the amount of the reacting anilino-NO species by a factor of 7.6, but left the reaction rate unaltered. Oxidative radical coupling was excluded using the spin trap agent n-tert-butyl-alpha-phenylnitrone.
作者简介
Michael Matthies
Institute of Environmental Systems Research (USF), University of Osnabrück
编辑信件的主要联系方式.
Email: matthies@uos.de
德国, Osnabrück, 49069
Kevin Glinka
Physics Department, University of Osnabrück
Email: matthies@uos.de
德国, Osnabrück, 49069
Marius Theiling
Physics Department, University of Osnabrück
Email: matthies@uos.de
德国, Osnabrück, 49069
Kalman Hideg
Department of Organic and Medicinal Chemistry, University of Pécs
Email: matthies@uos.de
匈牙利, Szigeti st. 12, Pécs, 7624
Heinz-Jürgen Steinhoff
Physics Department, University of Osnabrück
Email: matthies@uos.de
德国, Osnabrück, 49069