激光诱导Ni等离子体发射光谱的空间演化特性研究

在350- 600nm 波长范围内测定了激光烧蚀Ni等离子体中Ni原子的空间分辨发射光谱.测定了385.83 nm发射光谱线的相对强度和STARK展宽及其随径向的变化特性。结果表明, 在沿激光束方向上, 当距离靶表面0-2.5mm范围内变化时,谱线的STARK展宽和谱线的强度都随距靶面距离的增大先增大,但增大到最大值后随距离的进一步增大而减小。谱线强度和STARK加宽的最大值都出现在离靶面约1.5mm处。     

强碱胁迫枯草芽孢杆菌芽孢致死的拉曼光谱研究

应用单细胞拉曼分析技术结合PCA方法,以枯草芽孢杆菌芽孢为对象,以强碱为诱导剂实时记录芽孢生理变化过程,探究芽孢在强碱胁迫下的致死机制。实验表明,枯草芽孢杆菌芽孢和其萌发后芽孢在一定范围均有一定的耐受强碱能力,但萌发后芽孢的耐受力明显下降,主要原因是释放了维持其抗性及稳定性的特有Ca2+-DPA的保护;芽胞受强碱胁迫也会有少量Ca2+-DPA释放过程的行为特征,但通过分析所记录的光谱数据结果表明,其释放行为不同于由L-丙氨酸引起的芽孢的正常Ca2+-DPA释放过程。通过PCA比较分析强碱胁迫芽孢和萌发后芽孢Ca2+-DPA释放过程,主要是强碱破坏芽孢膜结构,膜损伤后强碱比较容易进到芽孢内部从而破坏蛋白质的主链结构链及核酸;芽孢膜通道也可能受到强碱的伤害,造成微量Ca2+-DPA的释放。     

基于高/多光谱图像空天一体融合仿真方法

提出了一种基于高/多光谱图像的空天一体融合仿真方法. 以航空高光谱数据为基础, 根据航天多光谱遥感相关参数, 通过空天一体光谱维变换、尺度空间变换、辐射强度变换、混合像素变换和噪声变换将 航空高光谱图像中的地物目标进行空天一体映射到航天多光谱图像中, 得到特定地物目标的航天多光谱融合模拟仿真图像. 仿真实验表明该方法简便易行, 有效地减少了地物目标的三维建模和探测器响应建模的巨大工作量, 较好地实现了对特定地物目标航天多光谱图像的模拟, 开拓了遥感图像仿真模拟方法的新领域, 具有重要的研究和应用价值. 关键词： 遥感图像 空天一体 融合仿真 光谱维变换     

结直肠癌细胞株及细胞核的傅里叶变换红外光谱研究

运用傅里叶变换红外光谱技术研究了正常组织(30例)和细胞株(SW 620),正常细胞核和癌变细胞核的红外光谱特征,为红外光谱诊断结直肠癌奠定了细胞及亚细胞水平的实验基础。将所得光谱图的峰位及峰强比进行统计分析发现:细胞株(SW 620)和癌变细胞核中谱带(2 925,1 240和1 085cm-1)的峰位均向高波数移动(p<0.05),而谱带1 400cm-1的峰位均向低波数移动(p<0.05);细胞株(SW 620)中峰强比(I1 650/I1 460,I1 400/I1 460,I1 240/I1 460,)较正常组织升高(p<0.05),而I1 740/I1 460则降低(p<0.01)。癌变细胞核中(I1 650/I1 460,I1 400/I1 460,I1 240/I1 460)较正常细胞核亦升高(p<0.05).这些差异可作为区别组织良恶性的指标。     

大气压冷等离子体射流灭活子宫颈癌Hela细胞

研究了大气压冷等离子体射流对子宫颈癌Hela细胞的灭活机制. 在倒置显微镜下观察不同等离子体处理条件下的细胞形态, 并通过中性红吸收测试定量测定各个条件下的细胞存活率. 将功率维持在18 W, 在900 mL/min 氩等离子体中添入氧气的百分含量分别为1%, 2%, 4% 和8%的条件下处理Hela细胞, 探讨活性气体氧气在惰性气体氩气中的百分含量对Hela癌细胞灭活效率的影响, 发现添加2%氧气时, 氩/氧等离子体灭活效果最佳, 处理180 s后细胞存活率可降至7%. 当继续添加氧超过2%时, 灭活效果逐渐减弱, 直至8%时, 其效果反而不如单纯氩等离子体. 通过测量等离子体发射光谱, 结果表明活性氧自由基在癌细胞灭活过程中可能起关键作用. 关键词： 大气压冷等离子体射流 Hela癌细胞 存活率 发射光谱     

飞秒激光低压N2等离子体特性的实验研究

在低于一个标准大气压的条件下对飞秒激光产生的N₂等离子体光谱进行了实验研究.结果表明, 各种样品气压下的激光N₂等离子体光谱均表现为连续谱和线状谱的叠加.随着样品气压的降低, 连续谱和原子谱线的强度经历了由缓慢增强发展为缓慢降低再到迅速降低的过程, 而正一价离子谱线强度呈现逐步增强的特征.在气压低于0.3 atm (1 atm=101325 Pa)时, 出现了正二价态的离子谱线. 给出了低压N₂等离子体对于飞秒激光传输和能量吸收的物理特性, 并初步讨论了低压等离子体通道特性.这些结果有助于加深了解飞秒激光等离子体的特性和机理, 特别是给出了在实验上测量不同价态离子光谱的条件, 为今后的研究提供了有益的实验依据. 关键词： 飞秒激光 气压 等离子体光谱 激光传输     

Preparation of trimethyl-2-hydroxyethylarsonium (arsenocholine) compounds

Trimethyl-2-X-ethylarsonium salts (X=OH, Cl, Br, CH₃COO; anion=Br) and trimethyl-2-diethoxyethylarsonium bromide were prepared from trimethylarsine and the appropriate organic bromides in sealed tubes at elevated temperatures or by refluxing the neat reagents. The yields ranged from 33 to 85%. Anion exchange reactions produced the arsonium iodides, nitrates, acetates, tosylates, tetraphenylborates, picrates, hydroxides, and carbonates. Arsenocholine bromide (X=OH) was phosphorylated with concentrated phosphoric acid. The product was isolated as the barium salt. Treatment of the barium salt with sulfuric acid yielded trimethyl-2-(dihydrogen phosphato)ethylarsonium bromide. These substances were synthesized to serve as precursors for arsenic- containing phospholipids and as standards for the chromatographic identification of arsenocholines. The synthesized compounds were characterized by elemental analyses and ¹H and ¹³C NMR spectroscopy. The shifts of the arsenic compounds were compared with those of the corresponding nitrogen compounds and found to be sufficiently different to be used for the identification of these compounds in their mixtures.     

Radiative frequency shift without ultraviolet divergency in a two-level hydrogenic atom

Summary By taking into account the retardation effects a finite result for the frequency shift of the Lyman α-radiation from a two-level hydrogenic atom is obtained. This result shows a nonnegligible correction as compared to previous results obtained in the dipole approximation with a cut-off frequency.     

Formation of an Unusual Guaiane Ketopentaenolide from Dehydroisoleucomisin by the Action of Anhydrous DMF and HCl

Dehydroisoleucomisin (anhydroaustricin) was converted in good yield to guai-1(10),3,5,7(11), 8-pentaen-2-on-12,8-olide by the action of anhydrous HCl in dry DMF. The chemical structure of the product was established using spectral data. The probable formation scheme of this lactone was proposed to include a series of prototopic transformations and ionic dehydrogenation of intermediates. __________ Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 339–340, July–August, 2005.     

Synthesis of a calix[4]crown modified with germanium‐containing side chains

A germacalix‐crown, 25,27‐bis[1‐(3‐trimethylgermylpropyl)oxy]calix[4]arene‐crown‐6, 1,3‐alternate ( 1a ), and its carbon analog, 25,27‐bis‐[1‐(4,4‐dimethylpentyl)oxy]calix[4]arene‐crown‐6, 1,3‐alternate ( 1b ), were prepared and their structures were confirmed by elemental analysis and ¹H and ¹³C NMR spectroscopy. A cation transport test indicated that both compounds exhibited much the same cation transport ability, so that the role of the germanium moiety in capturing and transporting counteranions is not yet clear. Copyright © 2005 John Wiley & Sons, Ltd.