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New alternatives for estimating the octanol/water partition coefficient and water solubility for volatile organic compounds using GLC data (Kovats retention indices)

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CONTRIBUTORS:
  Author Felicia SPAFIU
  Author Alice MISCHIE
  Author Petre IONITA
  Author Adrian BETERINGHE
  Author Titus CONSTANTINESCU
  Author Alexandru T. BALABAN
JOURNAL:
  ARKIVOC, 2009(X), 174 - 194.
YEAR: 2009
PUB TYPE: Journal Article
SUBJECT(S): chemistry - mathematical
DISCIPLINE: Chemistry
HTTP: http://www.arkat-usa.org/get-file/28920/
LANGUAGE: English
PUB ID: 103-449-961 (Last edited on 2009/06/03 02:17:38 GMT-6)
SPONSOR(S):
 
ABSTRACT:
New possibilities for estimating octanol/water partition coefficients (logP) and the water solubility (Sw) were investigated using Kovāts retention indices (I) obtained from GLC retention data for 132 volatile organic compounds belonging to 7 different chemical classes (hydrocarbons, alcohols, aldehydes, ketones, carboxylic acids, esters and halogen compounds). Application of the multilinear regression method led to six equations, all involving index I, as follows: (i) direct correlation logP vs. I (eq.1); (ii) logP vs. I , molar refractivity, and surface tension (eq. 2); (iii) logP vs. I and structural characteristics (eqs. 3, 4 and 6); (iv) logP vs. the I/Sw ratio (eq. 5). Excepting eq. 1 (which showed relatively weak correlations), eqs. 2 – 6 can provide reliable values for logP and for logSw as proved by the significant statistical parameters. The general models presented through eqs. 2 – 6 may also be applied in estimation of other biological and/or ecological important properties, which are linearly dependent on the logP or log Sw values. By generalization, a new calculation method is suggested (eq. 7), in order to allow the estimation of logP or logSw in terms of the number of bonds and the Kovāts retention index.
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