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Evidence for π-πElectron Donor-Acceptor Interactions between π-Donor Aromatic Compounds and π-Acceptor Sites in Soil Organic Matter through pH Effects on Sorption

机译:pH吸附对土壤有机质中π供体芳香族化合物与π受体位点之间ππ电子供体-受体相互作用的证据

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Elucidation of molecular-level interactions controlling the sorption of organic compounds in soils is of major theoretical and practical interest. Sorption ofπ-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, π-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-π-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'-tetrachlorobi-phenyl, and 3,3',4,4'-tetrachlorobiphenyl. The opposite pH effect was observed for 2-nonanol and 2-nonanone, which are non-π-donors, but capable of H-bonding. Also, no pH-dependent sorption was observed between theπ-donor PHEN and alumina, a model inorganic surface. We propose that theπ-donor solutes interact withπ-acceptor sites in soil organic matter (SOM), including aromatic rings with multiple carboxyl groups, aromatic amines, or heteroaromatic amines. The π-acceptor ability of such aromatic moieties would increase with protonation. π-πInteractions between PMB, NAPH, and PHEN, and model SOM acceptors, 1,3,5-benzenetricarboxylic acid (BTA), 1,4,5,8-naphthalenetet-racarboxylic acid (NTA), and pyridine (PY) in methanol and methanol-water, were verified by the appearance of pH-dependent upfield 1{sup left}H 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.
机译:阐明控制土壤中有机化合物吸附的分子级相互作用具有重要的理论和实践意义。发现在许多土壤中,π电子给体化合物,五甲基苯(PMB),萘(NAPH)和菲(PHEN)的吸附随着pH的降低而增加,pH值约为2.5-7。这种行为不能归因于腐殖质疏水特性的pH依赖性变化,π-H键,与矿物表面的相互作用,与黑碳的相互作用,溶质共面性或pH对溶质活性系数的影响。对于非π-给体疏水性化合物,无论是否为平面,均未观察到pH的显着影响:反式1,2-二氯环己烷(DCCH),六氯-1,3-丁二烯(HCBD),1,2,4-三氯苯(TCB),2,2',5,5'-四氯联苯和3,3',4,4'-四氯联苯。对于2-壬醇和2-壬酮,它们是非π-供体,但能够进行H键键合,观察到相反的pH效应。另外,在π供体PHEN与模型无机表面氧化铝之间未观察到pH依赖性吸附。我们提出,π-供体溶质与土壤有机质(SOM)中的π-受体位点相互作用,包括具有多个羧基的芳环,芳族胺或杂芳族胺。此类芳族部分的π-受体能力将随着质子化而增加。 PMB,NAPH和PHEN与模型SOM受体,1,3,5-苯三甲酸(BTA),1,4,5,8-萘基-萘甲酸(NTA)和吡啶(PY)之间的π-π相互作用甲醇和甲醇-水通过环电流效应引起的pH依赖性高场1 {H} NMR化学位移的出现进行了验证。 UV / vis光谱显示了各种NTA供体的pH依赖性电荷转移带。对于与模型受体配对的非供体化合物,未发现NMR位移或电荷转移带。

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