[1] TIMELL T E. Recent progress in the chemistry of wood hemicelluloses[J]. Wood Science and Technology,1967,1(1):45-70. [2] 王治民,杨晓慧,周永红. 木质素基聚氨酯薄膜的研究进展[J]. 化工新型材料,2013,41(7):13-15. WANG Z M,YANG X H,ZHOU Y H. The preparation of lignin polyurethane films and its modification research[J]. New Chemical Materials,2013,41(7):13-15. [3] HERNES P J,BENNER R. Photochemical and microbial degradation of dissolved lignin phenols:Implications for the fate of terrigenous dissolved organic matter in marine environments[J]. Journal of Geophysical Research Oceans,2003,108(C9):351-378. [4] 杨淑蕙. 植物纤维化学[M]. 3版. 北京:中国轻工业出版社,2001:69. YANG S H. Lignocellulosic Chemistry[M]. 3rd ed. Beijing:China Light Industry Press,2001:69. [5] YANG H P,YAN R,CHEN H P,et al. Characteristics of hemicellulose,cellulose and lignin pyrolysis[J]. Fuel,2007,86(12/13):1781-1788. [6] BOERJAN W,RALPH J,BAUCHER M. Lignin biosynthesis[J]. Annual Review of Plant Biology,2003,54:519-546. [7] BRUNOW G,LUNDQUIST K,CARLSTRÖM K,et al. A new synthesis of model compounds for the beta-5 structural unit in lignins[J]. Acta Chemica Scandinavica,1984,B38(4):335-336. [8] FAUSTINO H,GIL N,BAPTISTA C,et al. Antioxidant activity of lignin phenolic compounds extracted from Kraft and sulphite black liquors[J]. Molecules,2010,15:9308-9322. [9] 张莹,雷中方. 造纸黑液提取木质素的抗氧化性研究[J]. 复旦学报:自然科学版,2010,49(1):60-64. ZHANG Y,LEI Z F. Study on antioxidant activity of lignin from pulping black liquor[J]. Fudan University Journal:Natural Science,2010,49(1):60-64. [10] VINARDELL M P,UGARTONDO V,MITJANS M. Potential applications of antioxidant lignins from different sources[J]. Industrial Crops & Products,2008,27(2):220-223. [11] 聂明才,霍淑平,孔振武. 木质素模型化合物的研究进展[J]. 林产化学与工业,2010,30(5):115-121. NIE M C,HUO S P,KONG Z W. Research progress of lignin model compounds[J]. Chemistry and Industry of Forest Products,2010,30(5):115-121. [12] CATHALA B,AGUIÉ-BÉGHIN V,DOUILLARD R,et al. Properties of model compounds of lignin (dehydrogenation polymers=DHPs) at the air/water interface[J]. Polymer Degradation &Stability,1998,59(1):77-80. [13] 叶哲孜,谢益民,吴晨曦,等. 多糖存在下异丁香酚的脱氢聚合及LCC的形成[J]. 林产化学与工业,2016,36(2):45-50. YE Z Z,XIE Y M,WU C X,et al. Dehydrogenation polymerization of isoeugenol and formation of lignin-carbohydrate complexes with presence of polysaccharide[J]. Chemistry and Industry of Forest Products,2016,36(2):45-50. [14] CATHALA B,SAAKE B,FAIX O,et al. Evaluation of the reproducibility of the synthesis of dehydrogenation polymer models of lignin[J]. Polymer Degradation & Stability,1998,59(1):65-69. [15] HOBALLAH M E,STUURMAN J,TURLINGS T C J,et al. The composition and timing of flower odour emission by wild Petunia axillaris coincide with the antennal perception and nocturnal activity of the pollinator Manduca sexta[J]. Planta,2005,222(1):141-150. [16] KOEDUKA T,FRIDMAN E,GANG D R,et al. Eugenol and isoeugenol,characteristic aromatic constituents of spices,are biosynthesized via reduction of a coniferyl alcohol ester[J]. Proceedings of the National Academy of Sciences,2006,103(26):10128-10133. [17] MUHLEMANN J K,WOODWORTH B D,MORGAN J A,et al. The monolignol pathway contributes to the biosynthesis of volatile phenylpropenes in flowers[J]. The New phytologist,2014,204(3):661-670. [18] FREUDENBERG K,JONES K,RENNER H. Radioaktive isotope und lignin. IX:Künstliches lignin ausmarkiertem coniferylalkohol[J]. Berichte Der Deutschen Chemischen Gesellschaft,1963,96(7):1844-1849. [19] TERASHIMA N,ATALLAL R H,RALPH S A,et al. New preparations of lignin polymer models under conditions that approximate cell wall lignification. Ⅱ:Structural characterization of the models by thioacidolysis[J]. Holzforschung,1995,50(1):9-14. [20] 中野准三,高洁. 木质素的化学:基础与应用[M]. 北京:轻工业出版社,1988:545. NAKANO J,GAO J. Chemistry of Lignin Basic and Application[M]. Beijing:Light Industry Press,1988:545. [21] 吴保国,赵菊兰. 差示紫外光谱法测定木素酚羟基含量[J]. 东北林业大学学报,1993,21(2):56-65. WU B G,ZHAO J L. Determination of phenolic hydroxyl groups by differential UV spectrophotometry[J]. Journal of Northeast Forestry University,1993,21(2):56-65. [22] SHARMA O P,BHAT T K. DPPH antioxidant assay revisited[J]. Food Chemistry,2009,113(4):1202-1205. [23] 韦献雅,殷丽琴,钟成,等. DPPH法评价抗氧化活性研究进展[J]. 食品科学,2014,35(9):317-322. WEI X Y,YIN L Q,ZHONG C,et al. Advances in the DPPH radical scavenging assay for antioxidant activity evalua[J]. Food Science,2014,35(9):317-322. [24] 高云涛,魏薇,叶丽清,等. DPPH自由基清除活性的光度微量滴定模型及应用[J]. 光谱学与光谱分析,2015,35(2):492-496. GAO Y T,WEI W,YE L Q,et al. Photometric micro-titration model of DPPH radicals scavenging activity and its application[J]. Spectroscopy and Spectral Analysis,2015,35(2):492-496. [25] NIHORIMBERE V,钱和,汪何雅,等. DPPH自由基比色法测定番石榴叶提取物抗氧化活性的研究[J]. 食品科学,2004,25(7):36-42. NIHORIMBERE V,QIAN H,WANG H Y,et al. Evaluation of antioxidant activity of Psidium guajava Linn (Guava) leaf extracts by means of DPPH free radical[J]. Food Science,2004,25(7):36-42. [26] 莫文杰,余丽璇,周明松,等. 酚羟基对木质素磺酸钠染料分散剂性能的影响[J]. 高校化学工程学报,2016,30(2):423-430. MO W J,YU L X,ZHOU M S,et al. Influence of phenolic hydroxyl groups on the performance of lignosulfonate as a dye dispersant[J]. Journal of Chemical Engineering of Chinese Universities,2016,30(2):423-430. [27] LIN S Y,DENCE C W. Methods in Lignin Chemistry[M]. Heidelberg:Springe,1992:429. [28] EVLIYA H,OLCAY A. Oxidative polymerisation of isoeugenol and mild oxidation of synthetic polymers with alkaline cupric hydroxide[J]. Holzforschung,1974,28(4):130-135. [29] 顾瑞军. 木素和木素-碳水化合物复合体的化学结构及形成机理[D]. 广州:华南理工大学硕士学位论文,2002. GU R J. Study on lignin and lignin-carbohydrate complexes from monolignol[D]. Guangzhou:Mastre Degree Thesis of South China University of Technology,2002. [30] HUNNAY E. 13C NMR Studies of a dehydropolymer (DHP) from isoeugenol; comparison with spruce lignin[J]. Holzforschung,1989,43(1):61-64. |