Poole Colin F
Department of Chemistry, Wayne State University, Detroit, MI 48202, USA.
J Chromatogr A. 2024 Apr 26;1721:464850. doi: 10.1016/j.chroma.2024.464850. Epub 2024 Mar 27.
The solvation parameter model uses five system independent descriptors to characterize compound properties defined as excess molar refraction, E, dipolarity/polarizability, S, hydrogen-bond acidity, A, hydrogen-bond basicity, B, and McGowan's characteristic volume, V, to model transfer properties between condensed phases. The V descriptor is assigned from structure. For compounds liquid at 20 °C the E descriptor can be assigned from the characteristic volume and its refractive index. The E descriptor for compounds solid at 20 °C and the S, A, and B descriptors are experimental properties traditionally assigned from chromatographic, liquid-liquid partition, and solubility measurements. In this report liquid-liquid partition constants in totally organic and aqueous biphasic systems are evaluated as a standalone technique for descriptor assignments. Using six totally organic biphasic systems the S, A, and B descriptors were assigned with an average absolute deviation (AAD) of about 0.04, 0.03, and 0.04, respectively, compared with the best estimate of the true descriptor values for 65 compounds. The E descriptor for compounds solid at 20 °C can only be estimated with an AAD of approximately 0.1. For six aqueous biphasic systems the B descriptor is assigned with a lower AAD of 0.028 and higher AAD of 0.08 and 0.05 for the S and A descriptors, respectively, than for the totally organic biphasic systems for compounds with a reliable value for the E descriptor. The preferred system for descriptor assignments utilizes both totally organic biphasic systems (heptane-1,1,1-trifluoroethanol, isopentyl ether-propylene carbonate, isopentyl ether-ethanolamine, heptane-ethylene glycol, heptane-formamide, and 1,2-dichloroethane-ethylene glycol) and aqueous biphasic systems (octanol-water, cyclohexane-water) with the possible substitution of some systems with alternative systems of similar selectivity. For 55 varied compounds this combination of eight organic and aqueous biphasic systems resulted in an AAD of approximately 0.03, 0.02, and 0.02 for the S, A, and B descriptors compared to the best estimate of the true descriptor value. For 30 compounds solid at 20 °C the AAD for the E descriptor of 0.11 is poorly assigned. The relative average absolute deviation in percent (RAAD) corresponds to 9.7 %, 3.1 %. 4.0 % and 8.3 % for E, S, A, and B, respectively, for the eight biphasic systems. Liquid-liquid partition is compared to reversed-phase liquid and gas chromatography as a standalone technique for descriptor assignments.
溶剂化参数模型使用五个与体系无关的描述符来表征化合物的性质,这些性质被定义为过量摩尔折射度(E)、偶极矩/极化率(S)、氢键酸度(A)、氢键碱度(B)和麦高恩特征体积(V),以模拟凝聚相之间的转移性质。V描述符是根据结构指定的。对于在20°C时为液体的化合物,E描述符可以根据特征体积及其折射率来指定。对于在20°C时为固体的化合物,E描述符以及S、A和B描述符是传统上通过色谱、液-液分配和溶解度测量得到的实验性质。在本报告中,全有机和水相双相体系中的液-液分配常数被评估为一种用于描述符赋值的独立技术。使用六个全有机双相体系,与65种化合物的真实描述符值的最佳估计值相比,S、A和B描述符的平均绝对偏差(AAD)分别约为0.04、0.03和0.04。对于在20°C时为固体的化合物,E描述符只能以约0.1的AAD进行估计。对于六个水相双相体系,对于具有可靠E描述符值的化合物,B描述符的AAD为0.028,S和A描述符的AAD分别为0.08和0.05,比全有机双相体系的AAD更低。用于描述符赋值的首选体系同时使用全有机双相体系(庚烷-1,1,1-三氟乙醇、异戊基醚-碳酸丙烯酯、异戊基醚-乙醇胺、庚烷-乙二醇、庚烷-甲酰胺和1,2-二氯乙烷-乙二醇)和水相双相体系(辛醇-水、环己烷-水),并可能用一些具有相似选择性的替代体系替换某些体系。对于55种不同的化合物,这八个有机和水相双相体系的组合,与真实描述符值的最佳估计值相比,S、A和B描述符的AAD分别约为0.03、0.02和0.02。对于30种在20°C时为固体的化合物,E描述符的AAD为0.11,赋值效果较差。八个双相体系中,E、S、A和B的相对平均绝对偏差百分比(RAAD)分别为9.7%、3.1%、4.0%和8.3%。作为一种用于描述符赋值的独立技术,将液-液分配与反相液相色谱和气相色谱进行了比较。