Partition of Poly(Oxyethylene)s with 5-Chloro-8-Quinolinoxyl End-Groups between 1-Octanol and Water
Author:
Affiliation:
1. Institute of Polymers, Bulgarian Academy of Sciences, Sofia 1113, Bulgaria
2. Medical Academy, Clinical Hospital Lozenets, Sofia 1407, Bulgaria
Abstract
Publisher
SAGE Publications
Subject
Materials Chemistry,Polymers and Plastics,Biomaterials,Bioengineering
Link
http://journals.sagepub.com/doi/pdf/10.1177/088391159601100103
Reference20 articles.
1. Preparation and properties of poly(oxyethylene)s with 5-chloro-8-quinolinoxyl end-groups
2. Metal ion complex formation of poly(oxyethylene) with 5-chloro-8-quinolinoxyl end-groups
3. The Use of Substituent Constants and Regression Analysis in the Study of Enzymatic Reaction Mechanisms
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1. Linear Solvation Energy Relationship (LSER) Analysis of Liquid–Liquid Distribution Constants of 8-Hydroxyquinoline and Its Derivatives;Journal of Chemical & Engineering Data;2011-10-17
2. Novel Materials and Systems Based on Synthetic and Natural Polymers Targeted for Use in the Biomedical Field;Advanced Biomaterials for Medical Applications;2004
3. Preparation, characterization and biological activity of Schiff base compounds derived from 8-hydroxyquinoline-2-carboxaldehyde and Jeffamines ED®;European Polymer Journal;2002-05
4. Preparation, Characterization, and Biological Activity of Amides and Esters from 8-Hydroxyquinoline-2-Carboxylic Acid and Jeffamines ED® Or Poly(Ethylene Glycol)S;Journal of Bioactive and Compatible Polymers;2001-07
5. Synthesis and fluorescent applications of novel fluoroalkylated end-capped oligomers containing 5-chloro-8-quinolyl segments;Journal of Fluorine Chemistry;2000-04
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