Conversion of Lignin Models by Photoredox Catalysis
One prominent goal of 21st century research is to develop a sustainable carbon‐neutral biorefinery. Lignin is an important component of lignocellulosic biomass; however, it is currently underutilized owing to its highly cross‐linked, complex, and randomly polymerized composition, which poses a signi...
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Published in | ChemSusChem Vol. 11; no. 18; pp. 3071 - 3080 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
Germany
Wiley Subscription Services, Inc
21.09.2018
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Subjects | |
Online Access | Get full text |
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Summary: | One prominent goal of 21st century research is to develop a sustainable carbon‐neutral biorefinery. Lignin is an important component of lignocellulosic biomass; however, it is currently underutilized owing to its highly cross‐linked, complex, and randomly polymerized composition, which poses a significant challenge to its depolymerization and valorization. Chemical catalytic approaches based on transition metals represent the primary research area to drive degradation reactions. Recently, alternative photocatalytic strategies that employ sustainable solar energy to initiate the transformation of lignin have started to emerge. This Concept article examines new developments of photocatalyzed reactions and provides insight into C−O and C−C bond‐cleavage reactions of lignin models in both homogeneous and heterogeneous systems.
Bring to light: Lignin is an important component of lignocellulosic biomass but is underutilized. This article examines the development of photocatalyzed reactions and provides insight into C−O and C−C bond‐cleavage reactions of lignin models in both homogeneous and heterogeneous systems. The opportunities and challenges of the ultimate photoredox catalytic conversion of lignin into value‐added commodity and fine chemicals are outlined. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1864-5631 1864-564X 1864-564X |
DOI: | 10.1002/cssc.201801370 |