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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Simultaneous determination of the lipophilicity and dissociation constants of dialkyl phosphinic acids by negligible depletion hollow fiber membrane-protected liquid-phase microextraction
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Simultaneous determination of the lipophilicity and dissociation constants of dialkyl phosphinic acids by negligible depletion hollow fiber membrane-protected liquid-phase microextraction

机译:通过可忽略的耗尽中空纤维膜保护液相微萃取同时测定二烷基膦酸的亲脂素和解离常数

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Determination of the physicochemical properties, especially the lipophilicity (expressed as the logarithm of distribution coefficient, log D) and dissociation constant (pK(a)), is of great importance in the early stage of environmental risk assessment for an ionizable compound without these data. Currently, the log D and pk(a) values of dialkyl phosphinic acids (DPAs), the environmental hydrolysates of aluminum dialkyl phosphinates (ADPs) that is one class of emerging phosphorus-containing flame retardants, are not available. In this study, the log D and pK(a) values of three DPAs including methylethylphosphinic acid (MEPA), diethylphosphinic acid (DEPA) and methylcyclohexyl phosphinic acid (MHPA), were simultaneously determined by negligible depletion hollow fiber supported liquid phase microextraction (nd-HF-LPME) followed by ultra-performance liquid chromatography coupled with tandem mass spectrometry (UPLC-MS/MS). The pK(a) and log D of DPAs were determined by curve-fitting the experimental data with equations derived on the basis of the Henderson-Hasselbalch equation and compared with model calculated data. For MEPA, DEPA and MHPA, the pK(a) values were close and around 3, but the log Ds were strongly pH-dependent with values from -5.01 to 1.01. The log K-ow of the neutral form (()LogK(ow),(HA)) and ionic form (logK(ow,A)) were in the range of -0.67-1.02 and -3.86-1.33, respectively. The experimentally determined pK(a) values were highly in good agreement with ACD/pK(a) predicted values and the measured log K-OW,K-HA values were closely related to KOWWIN calculated ones, suggesting ACD/pK(a), and KOWWIN are good alternative methods to estimate pKa and log ICow of DPAs, respectively. As far as we know, this is the first report on the pL(a) and log D data for DPAs, which are fundamental for the product design and evaluating the environmental behavior and effects of DPAs and ADPs. (C) 2017 Elsevier B.V. All rights reserved.
机译:测定物理化学性质,尤其是亲脂性(表达为分布系数,log d)和解离常数(PK(a)),在没有这些数据的可电离化合物的环境风险评估的早期阶段具有重要意义。目前,对二烷基膦酸(DPA)的Log D和PK(A)值,铝二烷基磷酸二烷基膦酸盐(ADP)的环境水解产物,即一类新出现的含磷阻燃剂,不可用。在该研究中,通过可忽略的耗尽中空纤维负载的液相微萃取(ND -HF-LPME)随后是超高效液相色谱,耦合,串联质谱(UPLC-MS / MS)。 DPA的PK(A)和Log D通过曲线拟合具有基于Henderson-Hasselbalch方程的等式的实验数据来确定,并与模型计算数据进行比较。对于MEPA,DEPA和MHPA,PK(A)值近距离且3左右,但LOG DS强烈地依赖于-5.01至1.01的值。中性形式(()逻辑(OW),(HA))和离子形式(逻辑(OW,A))的LOG K-OR分别为-0.67-1.02和-3.86-1.33。通过实验确定的PK(A)值与ACD / PK(A)预测值良好的协议非常吻合,并且测量的日志k-ow,K-HA值与Kowwin计算的值密切相关,暗示ACD / PK(A), Kowwin是估计PKA和DPA的MODOM的良好替代方法。据我们所知,这是DPA的PL(a)和Log d数据的第一个报告,这对于产品设计和评估DPA和ADP的环境行为和影响是基础的。 (c)2017年Elsevier B.V.保留所有权利。

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