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以脲基嘧啶酮四重氢键为桥联单元,组装了二茂铁同体二聚体(1·1)。电化学实验显示1·1中两个等同的二茂铁基团的氧化还原电位差值(ΔE)达260 mV,说明1·1中两个二茂铁基团间通过四氢键发生了显著的电子相互作用。在1·1/CHCl3中逐步加入0.5、1和2等摩尔的CF3COOH时,由于脲基嘧啶酮四氢键的逐步解离,二茂铁间的电子相互作用强度逐渐减弱,其ΔE从260 mV逐步减小至150、100和0 mV,此时再加入三乙胺又可以使电子相互作用逐步恢复至初始状态,说明通过加入质子酸、碱可有效调控四氢键体系中发色团间通过氢键的电子相互作用。 相似文献
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主要介绍了利用252Cf标准裂变中子能谱刻度快脉冲LS301型液闪中子探测器的探测效率的实验方法和结果, 简要介绍了实验数据的处理过程, 得到了阈值分别为0.5, 0.7, 1.0和1.6 MeV, 以及中子能量在10 MeV以下的探测器效率, 并对测量结果进行了误差分析。同时为了检验实验结果的准确性, 将实验结果与理论计算结果进行比较, 两者在不确定度范围内符合得很好。Neutron detection efficiency of LS301 fast neutron detector was calibrated by measuring the neutron energy spectrum of 252Cf source, which has a standard fission neutron spectrum. A low mass, fast ionization chamber is used as the fission fragments detector in the time of flight(TOF) spectrometer and afforded the start signal of neutron flight. The stop signal was offered by the anode of LS301. A measured TOF spectrum was turned to the neutron energy spectrum which will be compared with the standard one. Consequently, the fast neutron detection efficiency of LS301 was obtained. Calibration procedures of experimental and data processing was given. Relative detection efficiencies were obtained separately for threshold settings of 0.5, 0.7, 1.0 and 1.6 MeV for neutron energies under 10 MeV. Experimental results accorded with theoretical efficiency curves which were calculated with the Monte Carlo code NEFF50. 相似文献
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建立了基于离子液体的单滴微萃取-毛细管电泳联用测定溴酚类化合物的方法。考察了萃取剂种类与体积、萃取时间、有机溶剂、盐浓度及萃取温度对萃取效率的影响。确定了最佳萃取条件为:以1-丁基-3-甲基咪唑六氟磷酸盐([C4MIM]PF6])离子液体作为萃取剂,萃取时间为8 min,样品溶液中NaCl浓度为10%(质量分数),萃取温度为20 ℃。在最佳条件下,3种溴酚(4-溴酚、2,6-二溴酚和2,4,6-三溴酚)在1~100 mg/L范围内呈良好的线性关系,线性相关系数为0.9939~0.9988;检出限为0.3 mg/L (S/N=3);该方法对3种溴酚的富集倍数分别为115.8、327.0和569.8; 6次平行测定的相对标准偏差为5.21%~6.47%;对本地区自来水、河水和湖水的加标回收率为87.8%~96.7%。结果表明,该方法稳定可靠,适合于水体中溴酚类污染物的测定。 相似文献
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