六种蜂花粉的红外光谱三级鉴别研究

采用傅里叶变换红外光谱(FTIR)结合二阶导数谱和热扰动下的二维相关红外光谱技术对6种不同花粉,即杏花花粉、油菜花粉、茶花花粉、西瓜花粉、荷花花粉和虞美人花粉,进行了快速无损的鉴别。结果表明,在一维红外光谱图上,不同花粉的蛋白质、脂肪和糖类物质的特征吸收峰在相对峰强和峰位上均存在一定的差异,在二阶导数谱上差异很明显。而在二维红外谱图上,由于6种花粉的自动峰及相关峰峰簇的位置和数量不同,其差别体现得更为明显和直观。因此,三级红外宏观指纹图谱法是鉴别不同蜂花粉种类的一种有效和快速检测方法。     

基于选择性模型组合的三维荧光光谱水质分析方法

为提高三维荧光光谱水质分析的精度,提出一种选择性模型组合方法,采用相关系数法对三维荧光光谱激发波长进行选择,并将被选中的激发波长下的荧光发射光谱水质分析子模型采用岭回归法进行模型组合,得到对水质指标的组合模型。以一组总有机碳(TOC)范围在3.41～125.35 mg·L-1,化学需氧量(COD)范围在22.80～330.60 mg·L-1的32个地表水和城市生活污水水样做为研究对象,对其三维荧光光谱220～400 nm范围内的10个激发波长采用上述方法进行选择,分别针对TOC和COD指标筛选出260,280,400 nm和220,280,400 nm各3个激发波长。采用部分最小二乘方法建立上述激发波长下荧光发射光谱水质分析子模型,根据岭回归法计算各子模型的组合系数,分别得到对TOC和COD指标的组合模型。实验结果表明：采用该方法得到的组合模型对TOC和COD两种指标的预测误差均方根(RMSEP)相比精度最高的单一荧光发射光谱子模型分别减小了15.4%和17.5%,相比未经模型选择的组合模型分别减小了6.1%和10.9%。     

IR/Raman spectroscopy and DFT calculations of cyclic di‐amino acid peptides. Part III: comparison of solid state and solution structures of cyclo(L‐Ser‐L‐Ser)

B3‐LYP/cc‐pVDZ calculations of the gas‐phase structure and vibrational spectra of the isolated molecule cyclo(L ‐Ser‐L ‐Ser), a cyclic di‐amino acid peptide (CDAP), were carried out by assuming C₂ symmetry. It is predicted that the minimum‐energy structure is a boat conformation for the diketopiperazine (DKP) ring with both L ‐seryl side chains being folded slightly above the ring. An additional structure of higher energy (15.16 kJ mol⁻¹) has been calculated for a DKP ring with a planar geometry, although in this case two fundamental vibrations have been calculated with imaginary wavenumbers. The reported X‐ray crystallographic structure of cyclo(L ‐Ser‐L ‐Ser), shows that the DKP ring displays a near‐planar conformation, with both the two L ‐seryl side chains being folded above the ring. It is hypothesized that the crystal packing forces constrain the DKP ring in a planar conformation and it is probable that the lower energy boat conformation may prevail in the aqueous environment. Raman scattering and Fourier‐transform infrared (FT‐IR) spectra of solid state and aqueous solution samples of cyclo(L ‐Ser‐L ‐Ser) are reported and discussed. Vibrational band assignments have been made on the basis of comparisons with the calculated vibrational spectra and band wavenumber shifts upon deuteration of labile protons. The experimental Raman and IR results for solid‐state samples show characteristic amide I vibrations which are split (Raman: 1661 and 1687 cm⁻¹, IR: 1666 and 1680 cm⁻¹), possibly due to interactions between molecules in a crystallographic unit cell. The cis amide I band is differentiated by its deuterium shift of ∼30 cm⁻¹, which is larger than that previously reported for trans amide I deuterium shifts. A cis amide II mode has been assigned to a Raman band located at 1520 cm⁻¹. The occurrence of this cis amide II mode at a wavenumber above 1500 cm⁻¹ concurs with results of previously examined CDAP molecules with low molecular weight substituents on the C^α atoms, and is also indicative of a relatively unstrained DKP ring. Copyright © 2009 John Wiley & Sons, Ltd.     

结温对高压白光LED光谱特性的影响

高压LED因其自身突出的特点在照明领域有着潜在的应用优势,但作为一种新型功率LED,其光电热特性仍需深入研究。该实验对6和9V GaN基高压LED芯片进行了相同结构和工艺条件的封装,对封装样品进行了10~70℃的变温度光谱测试,并进行了从控温平台温度到器件结温的转换。为保证器件的电流密度相同,6和9V样品光谱测试的工作电流分别设定为150和100mA。结果显示,结温升高会导致蓝光峰值波长红移、波长半高宽增大、光效下降和显色指数上升等现象。在相同平台温度和注入功率下,9V样品的结温低于6V样品;随着温度的升高,9V样品波长半高宽的增加量比6V样品少1.3nm,光效下降量少1.13lm·W~(-1),显色指数上升量少0.28。以上表明,与低压LED相比,高压LED有着更低的工作结温和更小的温度影响。原因在于,相同环境温度下高压LED具有更好的电流扩展性和更少的发热量。此特性在高压LED的研究、发展与应用等方面具有参考价值。此外,峰值波长仍与结温有着较好的线性度,在光谱设备精度较高的情况下可继续作为结温的敏感参数。     

基于粪便可见-近红外反射光谱的高山麝慢性肠炎诊断

提出了一种利用粪便可见-近红外反射光谱进行高山麝慢性肠炎诊断的新方法。以FieldSpec？3地物光谱仪采集了125份高山麝粪便（正常粪样70份,慢性肠炎患者粪样55份）的光谱数据,将其随机分成训练集（95份）和检验集（30份）。光谱经S.Golay平滑与一阶导数处理后以主成分分析法（PCA）降维。以前6个主成分（含原始光谱95.16%的特征信息）作为新变量,利用训练集样本,分别以模糊模式识别、BP-神经网络、Fisher线性判别以及Bayes逐步判别四种方法建立高山麝慢性肠炎的诊断模型。对检验集30个未知样的预测表明,Fisher线性判别的准确率为86.7%,模糊模式识别与BP-神经网络模型判别的准确率为90%,Bayes逐步判别的准确率最高,达93.3%。进一步分析发现所有误诊都源于将正常样误判为病样,四种方法对病样的检出率均达100%。说明利用粪便的可见-近红外反射光谱进行高山麝慢性肠炎的快速、非接触性诊断是可行的,且PCA 结合Bayes逐步判别是一种优选方法。     

Two-step laser excitation of the highly excited even-parity states of atomic mercury

We report term energies and quantum defects of highly excited even-parity states of mercury in the 83 876–84 140 cm^-1 energy range, employing a two-step laser excitation scheme via the S₀↦6s6p³P₁ inter-combination transition. Two dye lasers, pumped by a common Nd:YAG laser, were frequency doubled by BBO crystals and used to record the spectra in conjunction with a thermionic diode ion detector. Our new observations include the much extended D₂ (22 ≤n ≤52) series and a few members of the S₁ (24 ≤n ≤30) Rydberg series. Members of the D₂ Rydberg series with such a high n value are reported for the first time. The relative intensities of the D₂ and S₁ transitions (m = 4, 5 and 6) of group II-B elements excited from the P₁ inter-combination states are also discussed.     

Investigation of the local structure and the effects of the orbit reduction factor on the EPR g-factors for octahedral (CrO6) cluster in TiO2:Cr and MgO:Cr systems

A theoretical method for studying the inter-relation between electronic and molecular structure has been proposed based on the complete energy matrices for a d³ configuration ion in a tetragonal ligand-field. By means of this method, the local structure for Cr³⁺ ion doped in oxides TiO₂ (anatase) and MgO has been determined. The calculated results indicate that the local structure of the (CrO₆)⁹⁻ cluster in TiO₂:Cr³⁺ and MgO:Cr³⁺ systems exists as a compressed distortion relative to the regular octahedron. Meanwhile, the dependence of the EPR zero-field splitting parameter D on the local structure parameter ΔR (ΔR=R₁−R₂) has been revealed. In addition, the relation between the EPR g-factors (g,g,Δg) and the orbit reduction factor k has been discussed for the two systems, suggesting that the orbit reduction factor k is very important to understand the EPR g-factors.     

对称陀螺分子NH3的高温谱线强度研究

在直接计算分子配分函数的基础上,将无转动跃迁偶极矩平方近似为一常数,计算了对称陀螺分子NH₃ 0300 a—0000 s跃迁在高温下的线强度.在296K,计算的分子总配分函数与HITRAN数据库的结果符合很好,只有0.19%的百分误差.计算的跃迁线强度在2000 K和3000K的高温与HITRAN数据库的结果也符合相当好,最大百分误差分别为-0.65%和-1.77%.这就表明分子配分函数和线强度的高温计算是可靠的.在此基础上,计算被扩展到更高温度,报道了对称陀螺分子NH_{3< 关键词： 高温光谱 对称陀螺分子 配分函数 氨}     

高压液态重水的拉曼光谱研究

应用金刚石压腔结合拉曼光谱技术研究了重水在291 K,0.1～800 MPa条件下的拉曼谱图。结果表明：压力增大的过程中,重水的拉曼伸缩振动光谱向低频方向移动,并且频移和压力基本呈线性相关。频移没有突变,没有发生相的转变。将重水的拉曼谱峰分解为代表分子内O—D振动的高频峰和代表分子间氢键振动的低频峰。研究这两种不同类型谱峰的性质,发现代表分子间氢键的低频峰峰面积在不同的压力范围内呈现出不同的变化特征,压力对分子间氢键的影响并不是持续不变的。拉曼峰的峰面积反映的是产生这种拉曼峰的振动的数目,峰面积的变化反映了特征振动数目的变化。由于分子间氢键的强相互作用,水分子总是倾向于形成对称的空间五分子四面体结构,因此最大峰面积代表了最稳定的五分子团簇结构。     

Substitution and Solvent Effect of Some Substituted Hydroxy Schiff Bases

Abstract

The uv-vis spectra of eight ortho-hydroxy- andpara-hydroxy schiff bases were recorded in different solvents. Inductive and resonance effect of the substituents affect the electronic spectra of those molecules, while, intra-molecular hydrogen bond formation or breakage have little effect on the uv-visible spectra.