The separation and synthesis of lipidic 1,2- and 1,3-diols from natural phenolic lipids for the complexation and recovery of boron |
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Authors: | Tyman John H P Mehet Satinderjit K |
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Affiliation: | Department of Chemistry, Brunel University, Uxbridge, Middlesex UB8 3PH, UK. jhptyman@hotmail.com |
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Abstract: | A study has been made of the semi-synthesis of 1,3-diols (anacardic alcohols) from natural phenolic lipid resources from Anacardium occidentale and Anacardium giganteum which have given C15 and C11 derivatives, respectively. An isomeric 1,3-diol (isoanacardic alcohol) has been obtained from cardanol separated from technical cashew nut-shell liquid. Homologous 1,3-diols have been synthesised from a range of synthetic 2-alkyl-, 3-alkyl- and 4-alkylphenols and from 6-alkylsalicylic acids. The natural 1,2-diol, urushiol, from Rhus vernicifera has been purified. All these lipidic compounds have been studied for their complexation and the potential recovery of boron as boric acid. |
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Keywords: | Alkyl- and arylalkyl-1,3-diols Alkylsalicyl alcohols Saligenins Aryl-1,2-diols Boric acid complexation Solvent extraction of boron compounds |
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