Literature DB >> 20162309

Theoretical calculation of partition coefficients of dimethoxypyrimidinylsalicylic acids.

Eduardo J Delgado1.   

Abstract

Despite their importance as herbicides, dimethoxypyrimidinylsalicylic acids has been poorly characterized from a physical-chemical point of view. This lack of information has prevented the assessment of their impact in the environment once they are released. In this study, environmentally important properties (free energy of solvation, Henry's law constant, octanol/air, and octanol/water partition coefficients) of 39 dimethoxypyrimidinylsalicylic derived compounds are calculated by density functional theory (DFT) methods at B3LYP/6-31G(d,p) level of theory using the Poisson-Boltzmann solvation model. These properties have not been reported previously for this family of compounds, neither experimentally or theoretically.

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Year:  2010        PMID: 20162309     DOI: 10.1007/s00894-010-0668-x

Source DB:  PubMed          Journal:  J Mol Model        ISSN: 0948-5023            Impact factor:   1.810


  3 in total

1.  On the calculation of Henry's law constants of chlorinated benzenes in water from semiempirical quantum chemical methods.

Authors:  Eduardo J Delgado; Joel Alderete
Journal:  J Chem Inf Comput Sci       Date:  2002 May-Jun

2.  Prediction of Henry's law constants of triazine derived herbicides from quantum chemical continuum solvation models.

Authors:  Eduardo J Delgado; Joel B Alderete
Journal:  J Chem Inf Comput Sci       Date:  2003 Jul-Aug

3.  Estimating octanol-air partition coefficients with octanol-water partition coefficients and Henry's law constants.

Authors:  William M Meylan; Philip H Howard
Journal:  Chemosphere       Date:  2005-11       Impact factor: 7.086

  3 in total

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