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Article << Previous     |     Next >>   Contents Vol 58(12)

Quaternary Ammonium Arylspiroborate Esters as Organo-Soluble, Environmentally Benign Wood Protectants

Jenny M. Carr A, Peter J. Duggan B C H, David G. Humphrey A F H, James A. Platts D, Edward M. Tyndall E G

A ENSIS—Wood Processing and Products, CSIRO, Clayton South VIC 3169, Australia.
B School of Chemistry, Monash University, Melbourne VIC 3800, Australia.
C CSIRO Molecular and Health Technologies, Clayton South VIC 3169, Australia.
D School of Chemistry, Cardiff University, Cardiff CF10 3AT, UK.
E Centre for Green Chemistry, Monash University, Melbourne VIC 3800, Australia.
F Present address: Koppers Arch Wood Protection, Tullamarine VIC 3043, Australia.
G Present address: Biota Holdings Ltd, Notting Hill VIC 3168, Australia.
H Corresponding authors. Email: peter.duggan@csiro.au; david_humphrey@koppersarch.com.au
 
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Abstract

As part of a larger project aimed at the development of leach resistant boron-based wood preservatives, the anti-fungal and termiticidal activities, and the resistance to leaching from timber, of three related tetra-n-butylammonium spiroborates, tetra-n-butylammonium bis(ortho-hydroxymethylphenolato)borate 2, tetra-n-butylammonium bis[catecholato(2–)-O,O′]borate 3, and tetra-n-butylammonium bis[salicylato(2-)-O,O']borate 4, have been examined. All three borates are found to be active against test organisms, with the following orders of activity being observed: 2 > 3 > 4 > boric acid against wood decay fungi, and 2 > 34 > boric acid against termites. The most active compound in both assays 2 also has the highest calculated lipophilicity. In a test for permanence in wood, the following order of leach resistance is observed: 4 >> 32 > boric acid. This order appears to correlate more closely with the stability constants of the borate esters, as determined using 11B NMR spectroscopy, rather than calculated lipophilicities.

   
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