Measurement and ANN prediction of pH-dependent solubility of nitrogen-heterocyclic compounds. (September 2015)

• Record Type: Journal Article
• Authors: Sun, Feifei; Yu, Qingni; Zhu, Jingke; Lei, Lecheng; Li, Zhongjian; Zhang, Xingwang
• Is Part Of: Chemosphere. Volume 134(2015)
• Page Start: 402
• Page End: 407
• Publication Date: 2015-09
• Subjects: Nitrogen-heterocyclic compounds -- pH-dependent solubility -- QSPR -- ANN; Pollution -- Periodicals; Pollution -- Physiological effect -- Periodicals; Environmental sciences -- Periodicals; Atmospheric chemistry -- Periodicals; 551.511
• DOI: 10.1016/j.chemosphere.2015.04.092
• Languages: English
• ISSNs: 0045-6535

Abstract

Highlights: An ANN model for the prediction of pH-dependent solubility of NHCs was built. The charge on the nitrogen atom of NHCs ( Q N ) was proposed as an input of the model. The accuracy of the model was improved compared with the model based on HH equation. The solubilities of 25 NHCs were determined in buffer solutions of different pH. Abstract: Based on the solubility of 25 nitrogen-heterocyclic compounds (NHCs) measured by saturation shake-flask method, artificial neural network (ANN) was employed to the study of the quantitative relationship between the structure and pH-dependent solubility of NHCs. With genetic algorithm-multivariate linear regression (GA-MLR) approach, five out of the 1497 molecular descriptors computed by Dragon software were selected to describe the molecular structures of NHCs. Using the five selected molecular descriptors as well as pH and the partial charge on the nitrogen atom of NHCs ( Q N ) as inputs of ANN, a quantitative structure–property relationship (QSPR) model without using Henderson–Hasselbalch (HH) equation was successfully developed to predict the aqueous solubility of NHCs in different pH water solutions. The prediction model performed well on the 25 model NHCs with an absolute average relative deviation (AARD) of 5.9%, while HH approach gave an AARD of 36.9% for the same model NHCs. It was found that Q N played a very important role in the description of NHCs and, with Q N, ANN became a potential tool for the prediction of pH-dependent solubility of NHCs.