Evidence for π-π electron donor-acceptor interactions between π-donor aromatic compounds and π-acceptor sites in soil organic matter through pH effects on sorption

被引:247
作者
Zhu, DQ
Hyun, SH
Pignatello, JJ
Lee, LS
机构
[1] Connecticut Agr Expt Stn, Dept Soil & Water, New Haven, CT 06504 USA
[2] Purdue Univ, Dept Agron, W Lafayette, IN 47907 USA
关键词
D O I
10.1021/es035379e
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Elucidation of molecular-level interactions controlling the sorption of organic compounds in soils is of major theoretical and practical interest. Sorption of T-electron donor compounds, pentamethylbenzene (PMB), naphthalene (NAPH), and phenanthrene (PHEN), in a number of soils was found to increase with decreasing pH in the range of approximately pH 2.5-7. This behavior could not be attributed to pH-dependent alteration of the hydrophobic character of humic substances, pi-H-bonding, interaction with mineral surfaces, interaction with black carbons, solute coplanarity, or pH effects on solute activity coefficient. No significant effect of pH was observed for non-pi-donor hydrophobic compounds, whether planar or not: trans-1,2-dichlorocyclohexane (DCCH), hexachloro-1,3-butadiene (HCBD), 1,2,4-trichlorobenzene (TCB), 2,2',5,5'-tetrachlorobiphenyl, and 3,3',4,4'-tetrachlorobiphenyl. The opposite pH effect was observed for 2-nonanol and 2-nonanone, which are non-pi-donors, but capable of H-bonding. Also, no pH-dependent sorption was observed between the pi-donor PHEN and alumina, a model inorganic surface. We propose that the pi-donor solutes interact with pi-acceptor sites in soil organic matter (SOM), including aromatic rings with multiple carboxyl groups, aromatic amines, or heteroaromatic amines. The pi-acceptor ability of such aromatic moieties would increase with protonation. pi-pi Interactions between PMB, NAPH, and PHEN, and model SOM acceptors, 1,3,5-benzenetricarboxylic acid (NTA), 1,4,5,8-naphthalenetetracarboxylic acid (NTA), and pyridine (PY) in methanol and methanol-water, were verified by the appearance of pH-dependent upfield H-1 NMR chemical shifts induced by ring current effects. UV/vis spectra showed pH-dependent charge-transfer bands for various donors with NTA. No NMR shifts or charge-transfer bands were found for nondonor compounds paired with the model acceptors.
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页码:4361 / 4368
页数:8
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