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   <subfield code="a">Pyrolysis reactions of various lignin model dimers</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Haruo Kawamoto, Sunao Horigoshi, Shiro Saka]</subfield>
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   <subfield code="a">Primary pyrolysis reactions and relative reactivities for depolymerization and condensation/carbonization were evaluated for various lignin model dimers with α-O-4, β-O-4, β-1, and biphenyl substructures by characterizing the tetrahydrofuran (THF)-soluble and THF-insoluble fractions obtained after pyrolysis at 400°C. Reactivity was quite different depending on the model structure: depolymerization: α-O-4 [phenolic (ph), nonphenolic (nonph)], β-O-4 (ph) &gt; β-O-4 (nonph), β-1 (ph, nonph) &gt; biphenyl (ph, nonph); condensation/carbonization: β-1 (ph) &gt; β-O-4 (ph) &gt; α-O-4 (ph) &gt; β-O-4 (nonph), biphenyl (ph, nonph), α-O-4 (nonph), β-1 (nonph). Major degradation pathways were also identified for β-O-4 and β-1 model dimers: β-O-4 types: Cβ-O cleavage to form cinnamyl alcohols and phenols and Cγ-elimination yielding vinyl ethers; β-1 types: Cα-Cβ cleavage yielding benzaldehydes and styrenes and Cγ-elimination yielding stilbenes. Relative reactivities of these pathways were also quite different between phenolic and nonphenolic forms even in the same types; Cβ-O cleavage (β-O-4) and Cγ-elimination (β-1) were substantially enhanced in phenolic forms.</subfield>
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