两个基于2,5-二甲氧基对苯二甲酸和咪唑衍生物的超分子钴配位聚合物的结构及光催化反应

本文以咪唑衍生物为配体,通过水热合成法与钴离子制备出两个配位聚合物:{[Co(DTA)(1,4-DIB)(H₂O)]·H₂O}_n(1)和[Co(DTA)(1,3-BMIB)]_n(2)(1,4-DIB=1,4-二(1H-咪唑-1-基)苯; 1,3-BMIB=1,3-二(4-甲基-1H-咪唑-1-基)苯;H₂DTA=2,5-二甲氧基对苯二甲酸)。利用X射线单晶衍射、粉末衍射、热失重、元素分析、红外光谱以及固体紫外-可见光谱等对两个配合物进行了表征。结构分析证实配合物1和2是通过二维结构堆积成的三维超分子化合物。粉末衍射测试则显示两个配合物在水中有很好的稳定性。固体紫外-可见光谱显示两个配合物属半导体材料,对紫外-可见光有很强的吸收作用。在光催化实验中,配合物1和2可加快亚甲基蓝的降解速度。     

一种新型双吡啶悬臂Mn(Ⅱ)配合物的合成、晶体结构及DNA结合能力研究

通过3,3′-((乙烷-1,2-二基双(2-甲基吡啶杂氮二基)双(亚甲基))双(2-羟基-5-甲基苯甲醛)与2-羟基-1,3-丙二胺的缩合反应得到一种具有双吡啶悬臂的双核锰配合物。通过X射线单晶衍射确定了该配合物结构,结果显示其分子式为[Mn₂(C₃₇H₄₃N₆O₆)]·(ClO₄)₂。该配合物属于单斜晶系,P2₁/c空间群,晶胞参数为:a=1.096 50(19) nm, b=1.419 5(3) nm, c=3.109 4(5) nm, β=108.153(5)°。进一步分析表明两个二价锰离子分别与(N_amine)₂(N_imine)₂O₃和(N_imine)₂O₄体系配位,它们与配位原子形成的几何构型分别是十面体和扭曲的八面体。两个中心锰离子距离为0.331 6 nm,由酚氧原子和醋酸根共同桥联。另外,本文也利用伏安法和黏度法对该配合物与小牛胸腺DNA的结合能力进行研究,实验结果表明它们之间的结合方式为弱的插入作用。     

对氯苯甲酸构筑的铜(Ⅱ)配合物的合成、HSA结合及细胞毒性

本文合成了配合物[Cu(pcba)₂·(phen)(H₂O)] (pcba =对氯苯甲酸,phen = 1,10-邻菲罗啉),该配合物属于三斜晶系,P1空间群,晶胞参数为a=0.790 98(2) nm,b=1.072 40(4) nm,c=1.487 19(6) nm,α=100.613(3)°,β=95.239(3)°,γ=108.334(3)°,Z=2,D_c=1.638 g·cm^-3,F(000)=582,最终结构残差因子R₁=0.035 9,wR₂=0.089 1。采用紫外及荧光研究了配合物和人血清蛋白(HSA)的相互作用方式。结果表明,配合物静态猝灭HSA荧光,可求得配合物与HSA的猝灭常数K_sv=2.35×10⁵ L·mol^-1,猝灭速率常数K_q=2.35×10¹³ L·mol^-1·s^-1,结合常数为K_a=2.14×10¹³ L·mol^-1,结合位点n=2.37。同时,研究了配合物对胃癌细胞A549、宫颈癌细胞Hela和肝癌细胞HepG2的抗增殖能力。     

手性Salen-Ni(Ⅱ)络合物的ECD光谱及其绝对构型关联:可见区第一ECD吸收带的指纹作用

A correlation between the electronic circular dichroism (ECD) spectra and the absolute configurations of a serials' chiral salen-Ni(Ⅱ) complexes was investigated. The solid-state structures, absolute configurations, and preferential conformations in solution of quasi-planar chiral [Ni(salen)] complexes were studied using their crystal structures, solid-state and solution ECD spectra in combination with theoretical ECD calculations. Furthermore, two different nomenclatures for the absolute configurations of square-planar [M(salen)] complexes were inspected carefully, and suggestions for proper use of them are discussed. The calculated ECD spectra of [Ni(sal-R, R-chxn)] [sal-R, R-chxn = (R, R)-1, 2-cyclohexylene bis(salicylicdeneiminate)] in dichloromethane solution revealed that the first ECD band in the visible region was dominated by the ligandto-metal charge transfer transition (LMCT), which was incorrectly assigned to a d-d transition in the literature. When the absolute configuration of [Ni(sal-R, R-chxn)] was Λ, the first ECD absorption band in the visible region was positive. This ECD fingerprint is universally applicable for assigning the absolute configurations of other square-planar chiral [Ni(salen)] and six-coordinate trans-[Co^Ⅲ(salen)L₂] complexes with a "closed-shell" electronic structure. This work provides some insight into the coordination stereochemistry and chiroptical properties of chiral [M(salen)] complexes. Additionally, this work is significant for the understanding of chiral recognition and asymmetric catalytic mechanisms.     

基于噪声误差模型的不规则区域室内定位和锚点分布优化

结合实际工业背景,研究了一类在不规则区域且误差不服从高斯分布的室内无线定位问题.给出了噪声误差模型,在对多个传统定位算法进行性能分析的基础上,研究了待定位区域内锚点阵列的分布,改进了多锚点阵列下的定位方法,并提出基于Delaunay三角剖分锚点分布优化模型和求解方法.     

Functional sample path properties of subsequence's C-R increments for a Wiener process in Hlder norm

In this paper, with the aid of large deviation formulas established in strong topology of functional space generated by H¨older norm, we discuss the functional sample path properties of subsequence's C-R increments for a Wiener process in H¨older normThe obtained results,generalize the corresponding results of Chen and the classic Strassen's law of iterated logarithm for a Wiener process.     

Conformational Changes and Redox Properties of Bimetallic Single Helicates of Hexapyrrole-α,ω-dicarbaldehydes

The hexapyrrole-α,ω-dicarbaldehydes 1 a and 1 b were metallated with Cu^II, Ni^II, and Pd^II to give bimetallic complexes where a pair of 3 N+O four-coordinate metal planes are helically distorted and the central 2,2′-bipyrrole subunit adopts a cis or trans conformation. X-ray crystallographic analysis of the bisCu complex revealed a closed form with a cis-2,2′-bipyrrole subunit and an open form with a trans-2,2′-bipyrrole subunit. The bisPd complexes took a closed form both in the solid state and in solution. They are regarded as single helicates of two turns and the energy barrier for the interchange between an M helix and a P helix was remarkably influenced by the bulky 3,3′-substituent of the central 2,2′-bipyrrole subunit. Although the bisNi complexes adopt a closed form in the solid state, they exist as a homohelical open C₂-symmetric form or a heterohelical open C_i-symmetric form in solution. A theoretical study suggested that the closed form of 1 a Pd was stabilized by the Pd–Pd interaction. Compound 1 a Pd was reversibly oxidized by one electron at 0.14 V versus ferrocene/ferrocenium (Fc/Fc⁺) and this oxidized species showed Vis/NIR absorption bands at λ=767 and 1408 nm.     

可见/近红外光谱图像在作物病害检测中的应用

农作物病害严重影响了我国正常的农业生产，现代农业迫切需要快速、准确、高效的作物病害诊断方法。首先简单介绍了常用病害检测技术，如：聚合酶链式反应技术、人工感官判定技术、统计学方法等，这些方法或是比较费时、或是只能用于产生明显病斑后的病害诊断，而光谱技术在植物病害的快速检测方面有一定的潜力，目前已有大量的研究成果。主要围绕可见/近红外光谱图像在病害检测的应用展开分析和讨论，讨论了该技术所涉及的仪器，并从细胞、植物组织、冠层及更大尺度层面分析了该技术在病害检测中的现况。目前大部分与植物病害有关的可见/近红外光谱研究都以植物叶片为对象，而在更小尺度（细胞至显微尺度）和更大尺度（冠层至航空/航天遥感方面）上的研究较少，特别是单细胞级别的病害研究，只在动物细胞领域展开，而且以荧光、拉曼、红外光谱为主。可见/近红外在以植物叶片为主要研究对象的器官尺度上有大量的成功应用，目前的研究已涉及了大部分的常见作物及其主要病害，包括真菌性、细菌性等各种病原引起的病害的检测。植物叶片尺度的研究主要从以下三个方面展开：(1）基于计算机图像处理和模式识别的病害信息自动快速判断；(2）基于化学计量学方法的高光谱或高光谱图像病害程度模型；(3）建立与作物病害有关的叶片某些理化参数的光谱模型，从而量化病害的程度。在植物叶片这一尺度相关研究的主要问题是：研究过于碎片化，往往只研究了某一种或少数几种病害，所建的模型只能用于特定实验条件，无法直接自动判断任意田间样本的染病种类与程度。在近地冠层尺度，植株的三维形态对光谱模型有较大的干扰，有文献表明以植株近地冠层2D图像作为病害检测数据，偏差较大，所建模型不稳定，基于卫星影像的病害模型较少。还讨论了常用光谱及光谱图像建模与分类方法。目前可见/近红外光谱在农作物病害方面有一定的应用潜力，但存在研究内容的不平衡、研究系统性不够、各学科合作研究不够深入等几大问题。最后提出可见/近红外光谱在病害检测领域中应更注重多学科的深入合作，并急需相关的仪器设备、方法模型方面的突破。