半拓扑系统

本文旨在建立Ｓ系统理论，它具有相当的广泛性，以及应用背景性，同时又以拓扑空间、模糊拓扑空间、拓扑分子格以及拓扑系统为特例．     

超声雾化进样微波诱导等离子体原子发射光谱法测定痕量磷的研究

本文提出了一种测定水溶液样品中痕量磷的微波诱导等离子体原子发射光谱法(MIPAES)。样品经超声雾化并去溶后引入等离子体。考查了Ar和He MIP中磷的发射光谱特性和一些实验参数对磷发射强度的影响。用Ar和He作工作气体时,检出限分别为0.03和0.0045μg/ml,方法的相对标准偏差小于5％。     

The ultraviolet radiation environment of high southern latitudes: springtime behavior over a decadal timescale

Four spectroradiometers located at latitudes from 55 degrees to 90 degrees S conducted near-continuous measurements of ground-level solar ultraviolet irradiance from 1990 through 2001. The behavior during months from October through December is of special interest because this period includes the springtime loss in column ozone and the naturally large irradiances of early summer. Monthly integrated irradiances using biological weightings for erythema and damage to DNA show a distortion of the normal annual cycle in irradiance, with enhanced values occurring in October and November. In some cases, these irradiances exceed those near summer solstice in December. Changes in local cloudiness and column ozone both contribute significantly to interannual variability in erythemal irradiance. This is particularly the case at Palmer Station, near 65 degrees S, where the monthly integrated erythemal irradiance in November 1997 was more than double that observed 5 years earlier. In general, at sites on the Antarctic continent, interannual variability in monthly integrated erythemal irradiance is greatest in November, when the observation for any given year can fall 40% above or below the multiyear mean. Near the tip of South America, interannual variability is approximately half that seen in Antarctica.     

含多个(R)-1,1′-联萘手性高分子合成与结构表征

单体(R)-3,3′-二碘-2,2′-二正丁氧基-1,1′-联萘((R)-M-1),(R)-6,6′-二溴-2,2′-二正丁氧基-1,1′-联萘((R)-M-2)分别与1,4-二乙烯基-2,3-二丁氧基萘(M-3),在钯催化下,通过Heck交叉耦合反应合成手性高分子P-1与P-2.单体和高分子进行了1H-NMR1、3C-NMR、FT-IR、旋光度、GPC、UV、热分析、荧光光谱和CD等测试分析.高分子侧链上引入丁氧基后使得手性高分子溶解性增强并具有良好的成膜性,手性高分子P-1和P-2都能发射较强的蓝绿色荧光,荧光量子效率分别为0.42和0.48.     

微波等离子体增强辉光放电光源激发温度的研究

研究了一种改进型的微波等离子体增强辉光放电光源在光谱分析中的应用，对其重要的参数指标－激发温度进行了较为较细的考察。结果表明引入微波等离子体后辉光放电的激发温度明显高于单纯辉光放电时的激发温度。     

Distinguishing Sulfotyrosine Containing Peptides from their Phosphotyrosine Counterparts Using Mass Spectrometry

Sulfotyrosine and phosphotyrosine are two post-translational modifications present in higher eukaryotes. A simple and direct mass spectrometry method to distinguish between these modifications is crucial to advance our understanding of the sulfoproteome. While sulfation and phosphorylation are nominally isobaric, the accurate mass of the sulfuryl moiety is 9.6 mDa less than the phosphoryl moiety. Based on this difference, we have used an Orbitrap Fusion Lumos mass spectrometer to characterize, resolve, and distinguish between sulfotyrosine and phosphotyrosine modifications using a set of model peptides. Multiple fragmentation techniques, namely HCD, CID, ETD, ETciD, and EThcD, have been used to compare the different fragmentation behaviors between peptides modified with these species. Sulfotyrosine undergoes neutral loss using HCD and CID, but the sulfuryl moiety is largely stable under ETD. In contrast, phosphotyrosine is stable during fragmentation using all these methods. This differential stability provides a mechanism to distinguish sulfopeptides from phosphopeptides. Based on the rigorous characterization presented herein, this work serves as a model for accurate identification of phosphotyrosine and, more challenging, sulfotyrosine, in complex proteomic samples.

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Reversibly switching the conformation of short peptide through in-tether chiral sulfonium auxiliary

A novel approach for reversibly switching the conformation of short constraint λ-helical peptides through chemselective alkylation of the in-tether thioether and dealkylation of the chiral sulfonium was developed and it provides a valuable modifiable site to functionalize the peptides.     

Rapid dissolution of spruce cellulose in H<Subscript>2</Subscript>SO<Subscript>4</Subscript> aqueous solution at low temperature

Dissolution of cellulose is the key challenge in its applications. It has been discovered that spruce cellulose with high molecular weight (4.10 × 10⁵ g mol^?1) can be dissolved in 64 wt% H₂SO₄ aqueous solution at low temperature within 2 min, and the cellulose concentration in solution can reach as high as 5 % (w/v). FT-IR spectra and XRD spectra proved that it is a direct solvent for cellulose rather than a derivative aqueous solution system. The cold H₂SO₄ aqueous solution broke the hydrogen bonds among cellulose molecules and the low temperature dramatically slowed down the hydrolysis, which led to the dissolution of cellulose. The resultant cellulose solution was relatively stable, and the molecular weight of cellulose only slightly decreased after storage at ?20 °C for 1 h. Due to the high molecular weight of cellulose, cellulose solution could form regenerated films with good mechanical properties and transparency at low concentration (2 % w/v). This work has not only provided the new evidence of cellulose dissolution which facilitated the development of cellulose solvent, but also suggested a convenient way to directly transfer cellulose with high molecular weight into materials without structure modifications.     

邻羟基苯基(乙炔基)次膦酸酯的合成方法

邻羟基(乙炔基)次膦酸酯是一个多官能团的有用中间体，本文提出了此化合物的有效而切实可行的合成方法     

Trace Ir(III) complex enhanced electrochemiluminescence of AIE-active Pdots in aqueous media

Science China Chemistry - Trace Ir(III) complex enhanced aggregation-induced electrochemiluminescence (AIECL) of poly-tetraphenylethene (pTPE) in aqueous media was investigated for the first time....