scholarly journals Unexpected polymerization mechanism of dilignol in the lignin growing

2019 ◽  
Vol 6 (7) ◽  
pp. 190445 ◽  
Author(s):  
Yasuyuki Matsushita ◽  
Yuto Oyabu ◽  
Dan Aoki ◽  
Kazuhiko Fukushima

Lignin is an essential component of higher plants, which is built by the enzymatic dehydrogenative polymerization of monolignols. First, monolignol is enzymatically oxidized to produce the phenoxy radical, which can form resonance hybrids. Two radical resonant hybrids are coupled with each other to yield dilignol with various linkage types, of which the main structures are β- O -4′ ( I ), β-5′ ( II ) and β-β′ ( III ). However, the reaction mechanism behind the addition lignol radicals to dilignol is not yet fully understood. Here, we show an unexpected reaction with structure II during enzymatic dehydrogenative polymerization, which involves cleavage of a covalent linkage and creation of a new radical coupling site. This implied that the β-5 dilignol diversifies the growing pattern of lignin. This discovery elucidates a novel mechanism in lignin polymerization.

2014 ◽  
Vol 47 (22) ◽  
pp. 7812-7822 ◽  
Author(s):  
Xuepu Wang ◽  
Jian Huang ◽  
Lingdi Chen ◽  
Yujie Liu ◽  
Guowei Wang

2015 ◽  
Vol 12 (4) ◽  
pp. 753-760
Author(s):  
Baghdad Science Journal

An attempt to synthesize the benzoimidazol derivatives from the reaction of o-phenylenediamine and benzoic acid derivatives in the presence of ethanol and various ketones under microwave irradiation, 1 , 5 - benzodiazepinum salt derivatives were obtained instead of them. Unexpected reaction was happened for synthesis a new series of benzodiazepinium salt derivatives in a selective yield . The reaction mechanism was also discussed. The new compounds were purified and identified their structures were elucidated using various physical techniques like; FT- IR spectra, micro elemental analysis (C.H.N) and 1H NMR spectra.


2005 ◽  
Vol 16 (4) ◽  
pp. 398-406 ◽  
Author(s):  
Laurence B Davin ◽  
Norman G Lewis

Science ◽  
1997 ◽  
Vol 275 (5298) ◽  
pp. 362-367 ◽  
Author(s):  
L. B. Davin ◽  
H.-B. Wang ◽  
A. L. Crowell ◽  
D. L. Bedgar ◽  
D. M. Martin ◽  
...  

2019 ◽  
Vol 6 (11) ◽  
pp. 1863-1867 ◽  
Author(s):  
Xinxing Gong ◽  
Xiaofang Li ◽  
Wenlin Xie ◽  
Jie Wu ◽  
Shengqing Ye

A photoinduced synthesis of S-aryl thiosulfonates through a three-component reaction of aryldiazonium tetrafluoroborates, sodium metabisulfite, and thiourea is achieved. In this transformation, a radical coupling pathway is proposed.


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