首页 | 本学科首页   官方微博 | 高级检索  
     检索      


Photodiscoloration of western hemlock (Tsuga heterophylla) sapwood III Early stage of photodiscoloration reaction with lignans
Authors:Fumio Kawamura  Megumi Miyachi  Shingo Kawai  Hideo Ohashi
Institution:(1) Present address: Institute of Wood Technology, Akita Prefectural College of Agriculture, 016 Noshiro, Japan;(2) The united Graduate School of Agricultural Science, Gifu University, Yanagido, Gifu 501-11, Japan;(3) Faculty of Agriculture, Gifu University, Yanagido, Gifu 501-11, Japan
Abstract:The reaction during the early stage of photodiscoloration of constituents in western hemlock Tsuga heterophylla (Raf. Sarg., Pinaceae] sapwood was investigated with chemical methods. The main photodiscoloring constituents, hydroxymatairesinol, allohydroxymatairesinol, agr-conidendrin, and oxomatairesinol, were used as substrates for light-irradiation experiments in vitro. The structures of photodiscoloration reaction products were elucidated by isolation and instrumental analyses and/or co-high-performance liquid chromatography analyses with authentic specimens. The experiment was undertaken to distinguish each series of liquid phases using chloroform, water (both including a trace of methanol), and methanol, and the solid phase. The reaction products allohydroxymatairesi (2), oxomatairesinol (3), agr-conidendrin (4), allo-7prime-methoxymatairesinol (5), 7prime-methoxymatairesinol (6), and vanillin (7) were isolated or detected in the reaction mixture of a hydroxymatairesinol system. The reaction products hydroxymatairesinol (1), 3, 4, 5, 6, and 7 were confirmed in the reaction system of allohydroxymatairesinol, which was an epimer of hydroxymatairesinol. Product 3 was confirmed from the agr-conidendrin system, and reaction product 7 was confirmed from oxomatairesinol. The photodiscoloration reaction of western hemlock sapwood could be initiated by the formation of phenoxy radicals from the respective constituents. The reaction was then presumed to progress via formation of a quinonemethide intermediate in many of them. It was suggested that the reactive species, such as phenoxy radical or quinonemethide intermediate, formed by lightirradiation might be converted to quinone derivatives and colored oligomers. Products 1, 2, 3, 4, and 7, formed from substrates such as hydroxymatairesinol, allohydroxymatairesinol, agr-conidendrin, and oxomatairesinol, were the same as the original metabolic constituents of western hemlock. Therefore it was concluded that the photodiscoloration of western hemlock depends not on the quantitative level of a few respective metabolites but, rather, on the coexistence of many metabolites.Part of this paper was presented at the 46th Annual Meeting of Japan Wood Research Society at Kumamoto, April 1996
Keywords:Tsuga heterophylla sapwood  Photodiscoloration  Phenoxy radical  Quinonemethide intermediate  Lignan
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号