岷江上游汶川县耕地景观变化及空间驱动力

基于遥感影像和地理信息系统技术,应用景观指数和Kappa指数系列方法对岷江上游耕地景观变化进行研究,并引入二项Logistic逐步回归模型,选择海拔、坡度、坡向、到道路、河流和居民点距离为驱动因子对汶川县耕地景观变化的空间驱动力进行分析.结果表明:研究期间耕地景观面积一直处于增长趋势,1974—1986年间耕地景观面积增幅最大.1986—2000年间耕地面积增加不明显,但是耕地景观与其它景观类型相互转换频繁,空间位置变化剧烈,特别是1994—2000年期间.耕地景观面积变化的驱动力主要为政策变化.耕地景观变化的空间驱动力在不同时间段内存在较大差异.

北京地区气候变化和植被的关系:基于遥感数据和物候资料的分析

气候变化对陆地生态系统的影响及其反馈是全球变化研究的焦点之一。本文利用1951～2000年的气温、降水等气候资料、1982～2000年的NOAA/AVHRR遥感数据和1951～2000年北京春季物候的代表性指标———山桃(Prunusdavidiana)始花的物候数据,分析了在年际和年内时间尺度上北京地区各气候参量与植被变化之间的关系。结果显示:植物生长与温度之间的关系远比其与降水之间的关系密切;各气候参量和植被生长状况之间的关系因时间尺度而不同。1)月际水平上,具有显著生态学意义的气候指标对植被生长状况

饮用水消毒副产物暴露评价研究进展

介绍了饮用水消毒副产物暴露评价的基本定义,对饮用水暴露评价的主要消毒副产物进行了归纳总结,综述了现阶段饮用水消毒副产物暴露评价方法的进展及不足,并结合具体案例对饮用水消毒副产物暴露评价的具体步骤进行较为详细阐述,并对饮用水消毒副产物暴露评价研究的发展趋势及将来研究的重点进行了展望。

Manipulating charge-transfer character with electron-withdrawing main-group moieties for the color tuning of iridium electrophosphors

A new and synthetically versatile strategy has been developed for the phosphorescence color tuning of cyclometalated iridium phosphors by simple tailoring of the phenyl ring of ppy (Hppy=2-phenylpyridine) with various main-group moieties in [Ir(ppy-X)(2)(acac)] (X=B(Mes)(2), SiPh3, GePh3, NPh2, POPh2, OPh, SPh, SO2Ph). This can be achieved by shifting the charge-transfer character from the pyridyl groups in some traditional iridium ppy-type complexes to the electron-withdrawing main-group moieties and these assignments were supported by theoretical calculations.

交联型聚乙烯亚胺智能基因载体的制备及PEG化影响

使用胱胺双丙烯酰胺(CBA)对低分子量聚乙烯亚胺(PEI)进行交联反应制备智能降解型聚阳离子基因载体.通过与聚乙二醇(PEG)反应得到不同程度PEG化的聚阳离子载体.利用核磁、黏度测试、粒度仪、zeta电位仪和凝胶电泳对聚阳离子载体及其与DNA的复合物进行了表征.研究表明随着PEG含量的增加,聚阳离子载体/DNA复合物颗粒粒径变小、表面正电荷降低,PEG具有明显的屏蔽作用,但过多的PEG也使载体与DNA复合能力下降.通过MTT细胞毒性测试和荧光素酶质粒转染实验得出,含二硫键的交联型阳离子聚合物在测试范围内显示了非常低的细胞毒性,最佳转染效率是PEI25k的4倍,PEG化后其细胞毒性得到进一步改善,转染效率却明显降低.

SYNTHESIS AND CHARACTERIZATION OF A CROSSLINKING POLYETHYLENIMINE AS SMART GENE CARRIER AND EFFECTS OF PEGYLATION DEGREE

A smart biodegradable cationic polymer (CBA-PEI) based on the disulfide bond-containing cross-linker cystamine bisacrylamide (CBA) and low molecular weight branched polyethylenimine (1800-Da, PEI1800) was successfully synthesized by Michael addition reaction in our recent study. Furthermore, a series of copolymers (CBA-PEI-PEG) with different PEGylation degree were obtained by the mPEG-SPA (5000-Da) reacting with CBA-PEI at various weight ratios directly. The molecular structures of the resulting polymers CBA-PEI and CBA-PEI-PEG were evaluated by nuclear magnetic resonance spectroscopy (H-1-NMR) and capillary viscosity measurements, all of which had successfully verified formation of the copolymers. The polymer/DNA complexes based on CBA-PEI and CBA-PEI-PEG were measured by dynamic light scattering and gel retardation assay. The results showed that the particle size and zeta potential of complexes were reduced with increasing amount of PEG grafting, even no particle formation. The particle size of CBA-PEI/DNA complexes was in range of 103.1 to 129.1 nm, and the zeta potential was in range of 14.2 to 24.3 mV above the 2:1 weight ratio. In the same measure condition, the particle size of CBA-PEI-PEG complexes was reduced to a range of 32.2 to 55 nm, and the zeta potential was in range of 9.3 to 13.8 mV at the 2:1 weight ratio.

Electrochemistry of hydroquinone derivatives at metal and iodine-modified metal electrodes

The difference in the electrochemical behavior of hydroquinone and pyrocatechol. at platinum and gold surfaces was analyzed using voltammetry and attenuated total reflection Fourier transform infrared spectroscopy. The results show that the hydroquinone derivatives are adsorbed on a gold surface with vertical orientation, which makes the electron transfer between the bulk species and the electrode surface easier than that in the case of flat adsorption of hydroquinone derivatives that occurs at a platinum electrode. The formation of the vertical conformation and the rapid process of electron transfer were also confirmed by quantum chemistry calculations. In addition, the pre-adsorbed iodine on the electrodes played a key role on the adsorbed configuration and. electron transfer of redox species.

新法制备铁氰化钴修饰玻碳电极及多巴胺的电催化氧化

过渡金属铁氰化物由于可用于电催化、离子选择性电极以及固态电池和电致变色装置的材料等而受到关注[1 ] 。铁氰化钴 (CoHCF)由于性能优越 ,常被作为模型化合物加以研究[2 ] ,如Kulesza等[3] 利用电化学石英晶体微天平和X光吸收光谱技术研究了它的结构 ,Sato等[4] 对其表现出的磁性进行了研究 ,我们曾报道过CoHCF修饰电极催化NADH和抗坏血酸的氧化[5,6] 等。用电化学制备CoHCF修饰电极的方法可分为 2种 ,一种是电化学共沉积法 ,另一种是所谓的“新生金属法”。电化学共沉积法是将电极放在含有Co2 +盐和K3Fe(CN) 6的溶液中于一定电位范围内循环扫描。由于Co2 +盐和K3Fe(CN) 6存在同一溶液中 ,所以它们的浓度不宜太高 ,一般控制在 0 5～ 1 0mmol/L范围内。若浓度太高 ,就会在溶液中发生化学沉积使溶液变浑浊。如浓度较低 ,要得到较厚的CoHCF膜 ,循环次数必须很多 ,耗时较长。“新生金属法”是先在Co2 +盐溶液中 ,控制电极电位使Co2 +被还原成Co沉积在电极表面 ,然后将电极转入K3Fe(CN) 6溶液中进行电位扫描 ,从而在电极表面沉积C...

Synthesis of phenyl/amino-capped tetraaniline by chemical and electrochemical methods

Phenyl/amino-capped tetraaniline was prepared by chemical oxidation coupling and electrochemical cyclic voltammetry methods. The MacDiarmid's method of oxidation coupling was improved. The aqueous HCl was replaced with a mixture solution of HCl and acetone and (NH4)(2)S(2)O(0)8 was used as oxidant instead of FeCl3. The reaction displays a higher yield and the product tetraaniline has a higher purity owing to the improvement. In the mixture solution system, tetraaniline can be synthesized by electrochemical cyclic voltammetry method. The mechanism by which tetraaniline was prepared from p-amino diphenylamine was proposed. The product was characterized by MALDI-TOF MS and FTIR.

化学和电化学方法合成苯/胺封端苯胺四聚体

利用改进了的 Mac Diarmid氧化偶联方法合成了苯 /胺封端的苯胺四聚体 .通过对循环伏安曲线的分析 ,给出二聚体经由电化学氧化 -化学偶联成为四聚体的机理 .利用基质辅助激光解吸质谱和红外光谱对产物进行了表征

Synthesis and crystallization of a novel poly(ether ketone ether ketone ketone) containing meta-phenylene linkage: PEKEKK(T/I)

Poly(ether ketone ether ketone ketone) containing meta-phenylene linkage (PEKEKK(T/I)) was synthesized by electrophilic Friedel-Crafts acylation condensation of 1, 4-diphenoxybenzophenone with terephthaloyl chloride (T) and isophthaloyl chloride (I) with a T/I ratio of 1 and characterized by LR,DSC,TGA and WAXD. PEKEKK(T/I) has two different crystal structures: a conventional Farm I structure, the same as that observed in PEEK and PEK, wich is usually developed from melt crystallization, and a new Form II structure which can be developed from cold crystallization or solvent induced crystallization (by exposing the glassy sample to methylene chloride).

Half-sandwich metal diselenolate complexes Cp#M(NO)(SePh)(2) (M = Mo or W; Cp# = Cp or MeCp) as ligands. Synthesis of selenolate-bridged heterobimetallic compounds

The reactions of half-sandwich diselenolate Mo and W complexes (CpM)-M-#(NO)(SePh)(2) (M = Mo; Cp-# = Cp' (1a), MeCp (1b); M = W; Cp-# = Cp' (1c)) with (Norb)Mo(CO)(4), Ni(COD)(2) and Fe(CO)(5) have been investigated. Treatment of (1a), (1b) and (1c) with (Norb)Mo(CO)(4) in PhMe gave the bimetallic complexes: Cp'Mo(NO)(mu -SePh)(2)Mo(CO)(4) (2a), MeCpMo(NO)(mu -SePh)(2)Mo(CO)(4) (2b) and Cp'W(NO)(mu -SePh)(2)Mo(CO)(4) (2c) in moderate yields. Irradiation of (1a) and (1c) in the presence of Fe(CO)(5) gave heterobimetallic complexes Cp'Mo(CO)(mu -SePh)(2)Fe(CO)(3) (3a) and Cp'W(NO)(mu -SePh)(2)Fe(CO)(3) (3c). Ni(COD)(2) reacts with two equivalents of (1a), (1b) and (1c) to give [Cp'Mo(NO)(mu -SePh)(2)](2)Ni (4a), [MeCpMo(NO)(mu -SePh)(2)](2)Ni (4b) and [Cp'W(NO)(mu -SePh)(2)](2)Ni (4c) in good yields. The new heterobimetallic complexes were characterized by i.r., H-1-n.m.r., C-13-n.m.r. and EI-MS spectroscopy.