330 resultados para 7 (2 hydroxyethyl)guanine


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研究了两种新型芴类衍生物9,9-二(2-乙基已基)-2,7-二咔唑-9H-芴(简记为DCZF)和9,9-二(2-乙基已基)-2,7-二(2-(4-甲氧基)苯-2,1-乙烯基)芴(简记为BMOSF)在N,N-二甲基甲酰胺(DMF)中的线性吸收和单光子荧光行为,并用脉冲宽度为38ps,重复频率为10Hz的1064 nm Nd:YAG脉冲激光研究了两种化合物的三光子吸收性质.结果表明:两种新材料的最大线性吸收峰分别位于330和380nm,吸收区域覆盖了270-420nm波段.两种化合物的荧光带位于蓝-紫区,中心

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合成了具有大π共轭性的对称型芴类衍生物9,9-二(2-乙基已基)-2,7-(2-(4-甲氧基)苯-2,1-乙烯基)芴(简写为MO-F1u—MO)。通过元素分析、质谱、紫外-可见光谱和红外光谱对其进行了表征。测试了该染料在乙腈、二氯甲烷、四氢呋喃和正己烷4种不同极性溶剂中的线性吸收光谱和单光子荧光谱。结果发现溶剂效应对吸收光谱和荧光光谱表现出不同程度的影响,对产生这些光谱行为的主要原因进行了讨论。

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研究了摩尔组分为70TeO2-(20-x)ZnO-xPbO-5La2O3-2.5K2O-2.5Na2O(x=0,5,10,15,20)的新型多元铅锌镧碲酸盐激光玻璃,外掺Yb2O3为玻璃摩尔组分的1%,测试了试样的物理性质及吸收光谱、荧光光谱和荧光寿命,计算了Yb^3+的吸收截面、受激发射截面、荧光有效线宽等光谱参数,结果表明:该系列玻璃都具有良好的热学稳定性((Tx-Tg)>195℃,高于TZN玻璃(118℃));当X=15时,样品具有较好的光谱性质:高的受激发射截面(1.25pm^2)、长的荧光寿命(

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Ce3+ ions were introduced into the Er3+/Yb3+ -codoped TeO2-WO3-ZnO glasses, and the effect of Ce3+ on the emission properties at 1.5 mu m band and the upconversion luminescence of Er3+ in the glasses was investigated. With the increasing of Ce3+ concentration, the emission intensity of Er3+ at 1.5 mu m band increases firstly, and then decreases. The optimal doping concentration of Ce3+ is about 2.07 x 10(20)/cm(3). As for the Er3+ emission at 1.5-mu m band, the fluorescence lifetime decreases a little from 3.4ms to 3.0ms, while the full width at half maximum (FWHM) hardly changes with the increase of Cc 3+ concentration. Due to the effective cross relaxation between Ce3+ and Er3+ : Er3+ (I-4(11/2)) + Ce3+ (F-2(5/2)) -> Er3+ (I-4(13/2)) + Ce3+ (F-2(7/2)), the upconversion emission intensity of Er3+ is reduced greatly. But when Ce3+ -doping concentration is too high, the other cross relaxation between Ce3+ and Er3+ : Er3+ (4I(13/2)) + Ce3+ (F-2(5/2)) -> Er3+ (I-4(15/2)) + Ce3+ (F-2(7/2)) happens, which depopulates the I-4(13/2) level of Er3+ and results in the decrease of the emission intensity and fluorescence lifetime of Er3+ at 1.5 mu m band.

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An interesting fluorescence intensity reverse photonic phenomenon between red and green fluorescence is investigated. The dynamic range. of intensity reverse between red and green fluorescence of Er( 0.5) Yb( 3): FOV oxyfluoride nanophase vitroceramics, when excited by 378.5nm and 522.5nm light respectively, is about 4.32 x 10(2). It is calculated that the phonon- assistant energy transfer rate of the electric multi- dipole interaction of {(4)G(11/2)( Er3+) -> F-4(9/2)( Er3+), F-2(7/2)( Yb3+). F-2(5/2)( Yb3+)} energy transfer of Er( 0.5) Yb( 3): FOV is around 1.380 x 10(8) s(-1), which is much larger than the relative multiphonon nonradiative relaxation rates 3.20 x 10(5) s(-1). That energy transfer rate for general material with same rare earth ion's concentration is about 1.194 x 10(5) s(-1). These are the reason to emerge the unusual intensity reverse phenomenon in Er( 0.5) Yb( 3): FOV. (C) 2007 Optical Society of America.

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The spectroscopic and fluorescent decay behaviors of Yb3+-doped SiO2-PbO-Na2O-K2O glass is reported in this work. Yb2O3 contents of 1, 1.5 and 2mol% are added into the glass. Through the measurement of absorption and fluorescence spectra, and fluorescent decay rate at room temperature and at low temperature (18 K), it is found that the nonradiative decay rate of Yb3+ ions is mainly determined by the interaction between residual hydroxyl groups and Yb3+ ions. Concentration quenching effect can be omitted in this glass up to the Yb3+ ion concentration of 8.98 x 10(20)/cm(3). Multiphonon decay rate is also very small because of the large energy gap between F-2(5/2) and F-2(7/2) levels of Yb3+ ions. (c) 2004 Elsevier B.V. All rights reserved.

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kinds of Yb3+- and Na+-codoped CaF2 laser crystal with different Na:Yb ratios of 0, 1.5, and 10 are grown by the temperature gradient technique. Room-temperature absorption, photoluminescence spectra, and fluorescence lifetimes belonging to the transitions between ground state F-2(7/2) and excited state F-2(5/2) of Yb3+ ions in the three crystals are measured to study the effect of Na+. Experimental results show that codoping Na+ ions in different Na:Yb ratios can modulate the spectroscopy and photoluminescence properties of Yb3+ ions in a CaF2 lattice in a large scope. (c) 2005 Optical Society of America

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Y3Al5O12:Eu nanophosphors were synthesized by a gel combustion method. The structure of phosphors was characterized by XRD and FTIR. YAG phase came to occur when YAG:Eu precursors were sintered at 800 ℃, although the phase was mainly amorphous. The organ

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For the first time, a high optical quality Yb3+-doped lutetium pyrosilicate laser crystal Lu2Si2O7 (LPS) was grown by the Czochralski (Cz) method. The segregation coefficient of ytterbium ion in Yb:LPS crystal detected by the inductively coupled plasma atomic emission spectrometer (TCP-AES) method is equal to 0.847. X-ray powder diffraction result confirms the C2/m phase monoclinic space group of the grown crystal and the peaks corresponding to different phases were indexed. The absorption and fluorescence spectra, as well as fluorescence decay lifetime of Yb3+ ion in LPS have been investigated. The absorption and fluorescence cross-sections of the transitions F-2(7/2) <-> F-2(5/2) of Yb3+ ion in LPS crystal have been determined. The advantages of the Yb:LPS crystal including high crystal quality, quasi-four-level laser operating scheme, high absorption cross-sections (1.33 x 10(-2) cm(2)) and particularly broad emission bandwidth (similar to 62 nm) indicated that the Yb:LPS crystal seemed to be a promising candidate used as compact, efficient thin chip lasers when LD is pumped at 940 and 980 nm due to its low-symmetry monoclinic structure and single crystallographic site. (c) 2007 Elsevier B.V. All rights reserved.

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通过助熔剂固相反应法制备了5%Yb掺杂的硫氧化钇(Y2O2S)粉体。通过对其漫反射光谱和荧光光谱的测量,估算得Yb3+离子在Y2O2S晶格中的晶场分裂。由光谱数据计算得Yb3+离子的2F7/2能级在Y2O2S中的分裂值为709cm-1,适合于Yb3+离子的准三能级的激光运转。由5%Yb:Y2O2S的发射光谱拟合得出其峰位,峰高及峰宽。为了比较,相关的5%Yb:YAG的数据也被给出。

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该成果收集了近10年来我们对光合作用与环境方面研究的主要文章共57篇,概括为6个方面的内容,其中原始论文52篇,技术方法5篇。主要的新进展与特色为:a)阐 明CAM植物代谢与PEPCK的调节特殊性。鉴别菠萝和芦荟为CAM-PEPCK亚型,PEPCK是其光下C4酸的脱羧酶。首次证明PEPCK受底物和碳代谢中间产物的调控,纯化酶的负效应剂G6P、FBP、PEP及正效应剂Mn2+的作用在于改变酶蛋白的构象。b)首先指出PEPC也是活性氧攻击的靶蛋白,其失活原因在于酶蛋白氧化降解和构象改变。不同光合途径植物对光氧化的敏感性有别。光氧化条件下C3与C4植物产生.O2- 速率、耗散激发能和PSII稳定性有一定差异。脂氧合酶(LOX)抑制光合电子传递的位点在PSII氧化侧和Q和PQ上。c)指出较强的抗氧化能力(清除自由基能力)、抗UV-B能力(积累较多的UV-B吸收物质),提高叶片吸收的光能中非光化学耗散的比例,增高光合电子流向光呼吸、O2和NO2-光还原等电子传递支路的传递速率和比例是森林植物适应于自然光环境的强光的重要保护策略。d)从马尾松年轮的δ13C分析追踪了前80年来亚热带自然林区CO2浓度的上升速率(0.7~2.3μl/L/年)。对森林中不同人类活动干扰地点大气CO2、NOX和SO2浓度的现场检测和主要树种的生理、生化变化研究,证明其与人类干扰活动的形式和强度有关,为全球变化及其后效应提供了有力的证据。通过电脑调控水稻生长大棚的CO2浓度发现不同品种间对高CO2浓度适应性的显著差别,明确了适应性较强的4个品种,并从多种指标证明高CO2浓度对水稻的光氧化损伤具有缓解或防护效应。e)盐藻细胞中甘油和蛋白质受介质盐浓度调控,固定化培养提高甘油分泌量。改进和发展了利用对有机自由基DPPH. 的清除比例与数量来评价植物抗氧化性的简易可行的分光光度法。

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