High-Field Electron Paramagnetic Resonance and Density Functional Theory Study of Stable Organic Radicals in Lignin: Influence of the Extraction Process, Botanical Origin, and Protonation Reactions on the Radical g Tensor

被引:68
作者
Baehrle, Christian [1 ]
Nick, Thomas U. [2 ]
Bennati, Marina [2 ]
Jeschke, Gunnar [3 ]
Vogel, Frederic [1 ]
机构
[1] Paul Scherrer Inst, Res Dept Gen Energy, CH-5232 Villigen, Switzerland
[2] Max Planck Inst Biophys Chem, D-37077 Gottingen, Germany
[3] Swiss Fed Inst Technol, EPR Res Grp, CH-8093 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
PARRINELLO MOLECULAR-DYNAMICS; HUMIC ACIDS; BASIS-SETS; INDIGENOUS RADICALS; SCAVENGING ACTIVITY; CORRELATION-ENERGY; REACTION CENTERS; HARTREE-FOCK; EPR; ENDOR;
D O I
10.1021/acs.jpca.5b02200
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The radical concentrations and g factors of stable organic radicals in different lignin preparations were determined by X-band EPR at 9 GHz. We observed that the g factors of these radicals are largely determined by the extraction process and not by the botanical origin of the lignin. The parameter mostly influencing the g factor is the pH value during lignin extraction. This effect was studied in depth using high-field EPR spectroscopy at 263 GHz. We were able to determine the g(xx), g(yy), and g(zz) components of the g tensor of the stable organic radicals in lignin. With the enhanced resolution of high-field EPR, distinct radical species could be found in this complex polymer. The radical species are assigned to substituted o-semiquinone radicals and can exist in different protonation states SH3+, SH2, SH1-, and S2-. The proposed model structures are supported by DFT calculations. The g principal values of the proposed structure were all in reasonable agreement with the experiments.
引用
收藏
页码:6475 / 6482
页数:8
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