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活体植物中β-胡萝卜素分子的二级拉曼散射谱
引用本文:赵金涛,张鹏翔,徐存英.活体植物中β-胡萝卜素分子的二级拉曼散射谱[J].光谱学与光谱分析,2002,22(5):790-792.
作者姓名:赵金涛  张鹏翔  徐存英
作者单位:1. 杭州电子工业学院文理分院应用物理系,浙江,杭州,310037
2. 昆明理工大学材料与冶金工程学院,云南,昆明,650051
基金项目:杭州电子学院校内基金资助
摘    要:利用显微拉曼光谱技术对从法国梧桐树新鲜采集得到的树叶做了测试分析,在可见光514.5nm激发下,不对样品做任何提纯,直接得到了树叶中β-胡萝卜素分子的一级和二级拉曼光谱。根据对β-胡萝卜素分子拉曼散射位于2000-3100cm^-1之间和2000cm^-1以下谱线的仔细分析对比,得到了二级拉曼谱和一级谱的倍频、和频关系。实验研究表明,控制样品表面的激光强度和信号积分时间,不破坏活体树叶中的分子结构和构象,这为研究植物在不同的环境生长状况提供一种实时实地测量技术。此外讨论了用共焦显微拉曼研究活体植物的优点及限制。

关 键 词:二级拉曼散射谱  结构  活体植物  光合作用  β-胡萝卜素  功能分子  分析
文章编号:1000-0593(2002)05-0790-03
修稿时间:2001年6月8日

Secondary Raman Spectrum of β-carotene Molecule in Living Leaf of French Phoenix Tree
ZHAO Jin-tao ,ZHANG Peng-xiang ,XU Cun-ying .Dept. of Applied Physics,School of Science and Arts,Hangzhou Institute of Electronic Engineering,Hangzhou ,China .Engineering School of Material and Metallurgy,Kunming University of Scie.Secondary Raman Spectrum of β-carotene Molecule in Living Leaf of French Phoenix Tree[J].Spectroscopy and Spectral Analysis,2002,22(5):790-792.
Authors:ZHAO Jin-tao  ZHANG Peng-xiang  XU Cun-ying Dept of Applied Physics  School of Science and Arts  Hangzhou Institute of Electronic Engineering  Hangzhou  China Engineering School of Material and Metallurgy  Kunming University of Scie
Institution:Dept. of Applied Physics, School of Science and Arts, Hangzhou Institute of Electronic Engineering, Hangzhou 310037, China.
Abstract:Under visible incidence light 514.5 nm, the Raman scattering spectrum from the beta-carotene molecule in the leaf was directly obtained after it was immediately collected from French phoenix tree without any preparing the sample but cleaning. It is very easy to collect the secondary Raman lines addition to the first Raman spectrum in situ by micro Raman. By careful comparing and analyzing the Raman lines between 2,000-3,100 cm-1 and below 2,000 cm-1 regions, we obtained the correlated relation of the first and secondary Raman lines. The study results indicated that there is no damage to the structure and configuration of beta-carotene molecule in the live leaf by controlling laser power on the sample surface and integrating time for Raman signal, but large power laser or long time irradiation on the live sample would cause very strong fluorescence background in Raman spectrum which indicated that there is a photo damage in the center of photo reaction. The Micro Raman would become one of possible in situ methods for investigating live plant molecules growing up in different environment. At last we proposed and discussed the advantages and limits in micro Raman when it is applied to investigating live molecules in botany field.
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