首页> 外文期刊>Environmental Science & Technology >Thermodynamics of Hg(ll) Bonding to Thiol Groups in Suwannee River Natural Organic Matter Resolved by Competitive Ligand Exchange, Hg L_(III)-Edge EXAFS and ~1H NMR Spectroscopy
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Thermodynamics of Hg(ll) Bonding to Thiol Groups in Suwannee River Natural Organic Matter Resolved by Competitive Ligand Exchange, Hg L_(III)-Edge EXAFS and ~1H NMR Spectroscopy

机译:竞争性配体交换,Hg L_(III)-边缘EXAFS和〜1H NMR光谱解析的Suwannee河天然有机物中Hg(ll)键合至硫醇基团的热力学

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摘要

A molecular level understanding of the thermodynamics and kinetics of the chemical bonding between mercury, Hg(II), and natural organic matter (NOM) associated thiol functional groups (NOM-RSH) is required if bioavailability and transformation processes of Hg in the environment are to be fully understood. This study provides the thermodynamic stability of the Hg(NOM-RS)(2) structure using a robust method in which cysteine (Cys) served as a competing ligand to NOM (Suwannee River 2R101N sample) associated RSH groups. The concentration of the latter was quantified to be 7.5 +/- 0.4 mu mol g(-1) NOM by Hg L-III-edge EXAFS spectroscopy. The Hg(Cys)(2) molecule concentration in chemical equilibrium with the Hg(II)-NOM complexes was directly determined by HPLC-ICPMS and losses of free Cys due to secondary reactions with NOM was accounted for in experiments using H-1 NMR spectroscopy and C-13 isotope labeled Cys. The log K +/- SD for the formation of the Hg(NOM-RS)(2) molecular structure, Hg2+ + 2NOM-RS- = Hg(NOM-RS)(2), and for the Hg(Cys)(NOM-RS) mixed complex, Hg2+ + Cys(-) + NOM-RS- = Hg(Cys)(NOM-RS), were determined to be 40.0 +/- 0.2 and 38.5 +/- 0.2, respectively, at pH 3.0. The magnitude of these constants was further confirmed by H-1 NMR spectroscopy and the Hg(NOM-RS)(2) structure was verified by Hg L-III-edge EXAFS spectroscopy. An important finding is that the thermodynamic stabilities of the complexes Hg(NOM-RS)(2), Hg(Cys)(NOM-RS) and Hg(Cys)(2) are very similar in magnitude at pH values 7, when all thiol groups are protonated. Together with data on 15 low molecular mass (LMM) thiols, as determined by the same method (Liem-Ngyuen et al. Thermodynamic stability of mercury(II) complexes formed with environmentally relevant low-molecular-mass thiols studied by competing ligand exchange and density functional theory. Environ. Chem. 2017, 14, (4), 243-253.), the constants for Hg(NOM-RS)(2) and Hg(Cys)(NOM-RS) represent an internally consistent thermodynamic data set that we recommend is used in studies where the chemical speciation of Hg(II) is determined in the presence of NOM and LMM thiols.
机译:如果需要汞在环境中的生物利用度和转化过程,则需要在分子水平上了解汞,Hg(II)和与天然有机物(NOM)相关的硫醇官能团(NOM-RSH)之间化学键的热力学和动力学。完全理解。这项研究使用一种可靠的方法提供了Hg(NOM-RS)(2)结构的热力学稳定性,其中半胱氨酸(Cys)作为NOM(Suwannee River 2R101N样品)相关RSH基团的竞争配体。后者的浓度通过Hg L-III-edge EXAFS光谱定量为7.5 +/- 0.4μmol g(-1)NOM。通过HPLC-ICPMS直接测定与Hg(II)-NOM配合物化学平衡中的Hg(Cys)(2)分子浓度,并在使用H-1 NMR的实验中解释了由于与NOM的二次反应导致的游离Cys损失光谱学和C-13同位素标记的Cys。 Hg(NOM-RS)(2)分子结构Hg2 + + 2NOM-RS- = Hg(NOM-RS)(2)以及Hg(Cys)(NOM)的log K +/- SD -RS)混合复合物Hg2 + + Cys(-)+ NOM-RS- = Hg(Cys)(NOM-RS)在pH 3.0时分别确定为40.0 +/- 0.2和38.5 +/- 0.2。这些常数的大小通过H-1 NMR光谱进一步证实,并且Hg(NOM-RS)(2)结构通过Hg L-III-edge EXAFS光谱证实。一个重要发现是,复合物Hg(NOM-RS)(2),Hg(Cys)(NOM-RS)和Hg(Cys)(2)在pH值<7时,其热力学稳定性非常相似。所有硫醇基团都质子化。以及通过相同方法测定的15种低分子量(LMM)硫醇的数据(Liem-Ngyuen等人。通过竞争性配体交换和水合物研究,与环境相关的低分子质量硫醇形成的汞(II)配合物的热力学稳定性。密度泛函理论。环境化学.2017,14,(4),243-253。),Hg(NOM-RS)(2)和Hg(Cys)(NOM-RS)的常数表示内部一致的热力学数据我们建议使用的组用于在存在NOM和LMM硫醇的情况下确定Hg(II)的化学形态的研究中。

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  • 来源
    《Environmental Science & Technology》 |2018年第15期|8292-8301|共10页
  • 作者单位

    Swedish Univ Agr Sci, Dept Forest Ecol & Management, SE-90183 Umea, Sweden;

    Swedish Univ Agr Sci, Dept Forest Ecol & Management, SE-90183 Umea, Sweden;

    Swedish Univ Agr Sci, Dept Forest Ecol & Management, SE-90183 Umea, Sweden;

    Umea Univ, Dept Chem, SE-90187 Umea, Sweden;

    Umea Univ, Dept Chem, SE-90187 Umea, Sweden;

    Swedish Univ Agr Sci, Dept Forest Ecol & Management, SE-90183 Umea, Sweden;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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