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Revisiting the mechanism ofβ-O-4 bond cleavage during acidolysis of lignin IV: dependence of acidolysis reaction on the type of acid

✍ Scribed by Takaaki Imai; Tomoya Yokoyama; Yuji Matsumoto


Publisher
Springer
Year
2011
Tongue
English
Weight
138 KB
Volume
57
Category
Article
ISSN
1435-0211

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Influence of C g -OH on pyrolytic cleavage mechanism of b-ether-linkage in lignin dimer was studied in N 2 with C g -deoxy-type dimers, which have various p-substituents (-H, -Cl, -OCH 3 ) at their C b -phenoxy groups. Reactivities at 400 8C and the influence of radical scavenger (tetralin) indicate