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Study on Hyperspectral Estimation Model of Chlorophyll Content in Grape Leaves 被引量:1
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作者 Luyan NIU chunyan gao +3 位作者 Jiabo SUN Yanzhong LIU Xiaoyan ZHANG Fengyun WANG 《Agricultural Biotechnology》 CAS 2018年第4期55-58,61,共5页
In view of the shortage of using traditional methods to monitor chlorophyll content, hyperspectral technology was used to estimate the chlorophyll content of grape leaves rapidly, accurately and non-destructively. Bas... In view of the shortage of using traditional methods to monitor chlorophyll content, hyperspectral technology was used to estimate the chlorophyll content of grape leaves rapidly, accurately and non-destructively. Based on the data of hyperspectral reflectivity and SPAD value of grape leaves collected from Wanjishan grape planting base in Tai an, the correlations of SPAD value with the original spectral reflectivity of grape leaves and its first derivative were analyzed to select sensitive bands, and an estimation model of chlorophyll content in grape leaves based on hyperspectral reflectivity was established. The best model was SPAD = 59.352+ 44 836.313 R 601 . 展开更多
关键词 GRAPE CHLOROPHYLL Hyperspectral reflectivity Spectral features
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基于共轭驱动的Cu(Ⅱ)氧化仲胺合成氯桥联双核Cu(Ⅰ)配合物
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作者 张永坡 李鑫峰 +4 位作者 宋亚菲 孙萌瑶 殷丛丛 高春艳 赵晋忠 《大学化学》 CAS 2024年第5期44-51,共8页
现行的实验教材中缺乏双核桥联配合物合成的实验,关于仲胺合成和Cu(Ⅱ)氧化性的知识也较少。本实验从有机化学理论知识中的基本反应出发,设计了两条路线合成目标仲胺配体,即基于亲核取代反应的路线一和亲核加成缩合-还原的路线二。运用... 现行的实验教材中缺乏双核桥联配合物合成的实验,关于仲胺合成和Cu(Ⅱ)氧化性的知识也较少。本实验从有机化学理论知识中的基本反应出发,设计了两条路线合成目标仲胺配体,即基于亲核取代反应的路线一和亲核加成缩合-还原的路线二。运用配位化学原理及有机化学中的共轭驱动效应,使弱氧化性的Cu(Ⅱ)将仲胺氧化成共轭的芳香亚胺(希夫碱)结构,同时利用希夫碱的配位作用和氯离子的桥联配位作用形成稳定的氯桥联双核Cu(Ⅰ)配合物。为适应普通高校的实验教学条件,本实验还设计了一套操作简单、现象直观的Cu(Ⅰ)配合物中铜离子价态的鉴定实验。本实验所涉实验原理既包含基础化学反应知识,又体现最新的科学研究成果,反应条件温和、实验现象直观、重现性好、收率高,能有效提高学生的综合实验操作技能,锻炼学生的有机合成、配位合成能力。 展开更多
关键词 双核配合物 桥联 仲胺 氧化还原反应 亚铜
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分子器件中的光致异构效应
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作者 高春燕 程丽 +1 位作者 贾传成 郭雪峰 《中国科学:化学》 CAS CSCD 北大核心 2022年第2期294-308,共15页
基于光致异构分子构筑单分子光电子器件或分子膜器件,探究器件中分子在光诱导下构型的变化规律,并在单分子水平上探索其异构效应对电荷传输、器件光电性能的影响,对推动有关分子器件的基础应用研究至关重要.本文系统阐述近些年关于光致... 基于光致异构分子构筑单分子光电子器件或分子膜器件,探究器件中分子在光诱导下构型的变化规律,并在单分子水平上探索其异构效应对电荷传输、器件光电性能的影响,对推动有关分子器件的基础应用研究至关重要.本文系统阐述近些年关于光致异构分子器件的研究成果,着重梳理了关于分子器件的制备、电荷传输机理、器件性能调控以及应用等方面的代表性进展,为未来开发功能性分子器件以及实现复杂集成电路或计算系统应用提供一定的思路. 展开更多
关键词 单分子器件 光致异构 电荷传输
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Phosphorus-doped Fe_(7)S_(8)@C nanowires for efficient electrochemical hydrogen and oxygen evolutions:Controlled synthesis and electronic modulation on active sites
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作者 Thanh-Tung Le Xiao Liu +7 位作者 Peijun Xin Qing Wang chunyan gao Ye Wu Yongjiang Zhangjun Hu Shoushuang Huang Zhiwen Chen 《Journal of Materials Science & Technology》 SCIE EI CAS CSCD 2021年第15期168-175,共8页
Developing low-cost,efficient,and stable non-precious-metal electrocatalysts with controlled crystal structure,morphology and compositions are highly desirable for hydrogen and oxygen evolution reactions.Herein,a seri... Developing low-cost,efficient,and stable non-precious-metal electrocatalysts with controlled crystal structure,morphology and compositions are highly desirable for hydrogen and oxygen evolution reactions.Herein,a series of phosphorus-doped Fe_(7)S_(8)nanowires integrated within carbon(P-Fe_(7)S_(8)@C)are rationally synthesized via a one-step phosphorization of one-dimensional(1D)Fe-based organicinorganic nanowires.The as-obtained P-Fe_(7)S_(8)@C catalysts with modified electronic configurations present typical porous structure,providing plentiful active sites for rapid reaction kinetics.Density functional calculations demonstrate that the doping Fe_(7)S_(8)with P can effectively enhance the electron density of Fe_(7)S_(8)around the Fermi level and weaken the Fe-H bonding,leading to the decrease of adsorption free energy barrier on active sites.As a result,the optimal catalyst of P-Fe_(7)S_(8)-600@C exhibits a relatively low overpotential of 136 mV for hydrogen evolution reaction(HER)to reach the current density of 10 mA/cm^(2),and a significantly low overpotential of 210 mV for oxygen evolution reaction(OER)at 20 mA/cm^(2)in alkaline media.The work presented here may pave the way to design and synthesis of other prominent Fe-based catalysts for water splitting via electronic regulation. 展开更多
关键词 Ron sulfide P-DOPING Hydrogen and oxygen evolution reaction ELECTROCATALYSIS
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Oscillatory behavior of p53-Mdm2 system driven by transcriptional and translational time delays
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作者 chunyan gao Haihong Liu +2 位作者 Zengrong Liu Yuan Zhang Fang Yan 《International Journal of Biomathematics》 SCIE 2020年第5期63-95,共33页
Biological experiments clarify that p53-Mdm2 module is the core of tumor network and p53 oscillation plays an important role in determining the tumor cell fate.In this paper,we investigate the effect of time delay on ... Biological experiments clarify that p53-Mdm2 module is the core of tumor network and p53 oscillation plays an important role in determining the tumor cell fate.In this paper,we investigate the effect of time delay on the oscillatory behavior induced by Hopf bifurcation in p53-Mdm2 system.First,the stability of the unique positive equilibriurm point and the existence of Hopf bifurcation are investigated by using the time delay as the bifurcation parameter and by applying the bifurcation theory.Second,the explicit criteria determining the direction of Hopf bifurcation and the stability of bifurcating periodic solutions are developed based on the normal form theory and the center manifold theorem.In addition,the combination of numerical simulation results and theoretical calculation results indicates that time delays in p53-Mdm2 system are critical for p53 oscillations.The results may help us to better understand the biological functions of p53 pathway and provide clues for treatment of cancer. 展开更多
关键词 Time delays stability Hopf bifurcation p53-Mdm2 pathway
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