Kinetic and mechanistic studies of polyoxometalate (POM) reaction with lignin and model compounds.

摘要

Polyoxometalates (POMs) are a rapidly growing class of metal-oxygen-cluster anions. The properties of POMs can be modified by altering the POMs chemical composition and structure. Due to low cost, commercial availability, and synthetic tractability POMs have found application in various fields of chemistry and technology. POMs are reusable and thermally stable to oxidative conditions, making them an attractive alternative to chlorine for the delignification of wood pulp.; The research addressed in this dissertation deals with detailed kinetic and mechanistic studies of K5[SiVW11O40]·12H 2O, a POM used in the delignification of wood pulp, oxidation of phenolic lignin model compounds and milled wood lignin (MWL).; Results from lignin model studies suggest an overall second-order reaction rate; first order with respect to both POM and phenolic substrate. It was observed that electron-transfer from neutral phenols was slower than that from the corresponding phenoxide anions. Hammett studies revealed the reaction involved the formation of an electron-deficient radical intermediate where the rate-determining step is electron transfer from a neutral substrate. The structure of the substituted phenol, in terms of its electron donating/withdrawing character, along with the position of the substituent on the aromatic ring heavily influences the reaction rates. Increasing the number of ortho methoxyl groups dramatically increased the reaction rate, e.g. phenol guaiacyl syringyl model structures. The ortho methoxyl group(s) resonance stabilizes and delocalizes the forming phenoxyl radical intermediate. Similarly, the reaction rate of para-substituted guaiacyl and syringyl model compounds showed a dependence on the nature of the para-substituent; inductive or resonance conjugated electron withdrawing effects and inductive donating effects.; The effect of POM oxidation on the chemical structure of a Lodgepole pine MWL is investigated. 13C nuclear magnetic resonance (NMR) spectroscopic data revealed an approximate 28% decrease in beta-O-4 inter-unit linkages after POM treatment, the decrease in beta-O-4 inter-unit linkages being accompanied by an increase in carbonyl content. These results suggest that POM oxidation involves side-chain (such as alpha-OH/beta-O-4) oxidation. 13C NMR spectroscopy along with gel permeation chromatography revealed an increase in the degree of condensation which supports the idea that radical coupling is a major reaction pathway in this process.