Geometric and Electronic Behavior of C60 on PTCDA Hydrogen Bonded Network

Self-assembled supramolecular networks are promising spacer layer for electronic decoupling from the metal substrate.However,the mechanism behind of how the intrinsic electronic structure of spacer layers affects the adsorbate is still unclear.Here a hydrogen bonded network composed of n-type semiconducting molecules 3,4,9,10-perylene-tetracarboxylic-dianhydride(PTCDA)is prepared under ultra-high vacuum to serve as a spacer layer for functional organics C60 on Au(111).The geometric and electronic information of C60 was investigated by scanning tunneling microscopy and scanning tunneling spectroscopy(STM/STS)at 5 K.Effective decoupling from the metal surface yields an energy gap of 3.67 eV for C602nd,merely considering the HOMO-LUMO peak separation.The broadening of resonance peaks in STS measurements however indicates unneglected interlayer interactions in this hetero-organic system.Moreover,we scrutinize the nucleation sites of C60 on PTCDA layer and attribute this to the decreased diffusion capability on a less dense molecular arrangement possessing inhomogeneous spatial distribution of unoccupied molecular orbitals.     

湖泊沉积物中镉的测定及环境意义研究

建立了氢化物发生-原子荧光光谱法测定湖泊沉积物中镉的分析方法.优化了沉积物中镉的提取条件和测定条件,研究了Cu元素对测定镉的干扰及消除方法.以武汉市涨渡湖为例,通过对总镉和有效态镉的测定揭示了涨渡湖近百年来镉的各形态垂直分布特征.结果表明:自上世纪50年代以来,涨渡湖沉积物中的总镉由深层到表层呈上升趋势,有效态镉变化不大但其含量维持在较高水平.镉的潜在风险性较大.     

高温液体实时分子光谱测量装置

主要报导自行与制作的高温实时分子光谱测量装置。它主要在红外光谱仪和激光拉曼光谱仪的基础上加设了一套实时高温红外光学泵浦采集系统和样品高温加热炉。该装置可用于研究高温晶体生长过程中母液相的结构以及固 -液相转变过程中结构的变化。     

Synthesis,Crystal Structure and Luminescent Property of Cadmium Complex Based on 2-（2-（1Hbenzo[d]imidazol-2-yl）benzyl）-1H-benzo[d]-imidazole

The complex [Cd(bbb)Cl2]·DMF·H2O, where bbb is 2-(2-(1H-benzo[d]imidazol-2-yl)benzyl)-1H-benzo[d]imidazole, was synthesized and characterized by X-ray single-crystal structure analyses. For the complex: C24H25Cl2CdN5O2, Mr = 598.77, crystal system, triclinic, space group P1, a = 9.9878(12), b = 10.0008(12), c = 13.2217(15) , α = 80.674(2), β = 72.158(2), γ = 86.776(2)°, V = 1240.5(3) 3, Z = 2, Dc = 1.598 g/cm3, λ = 0.71073, μ(MoKα) = 1.127 mm–1, F(000) = 600, S = 1.04, R = 0.0905 and wR = 0.3088 for 4805 observed reflections with I 2σ(I). It is a neutral complex. The distorted tetrahedral geometry of cadmium ion is coordinated by two nitrogen atoms of ligand and two chloride ions. The complex emits blue green luminescence with emission peaks at 480 nm in DMF solution.     

应用于局域表面等离激元共振扫描显微探针的球形Au@Ag纳米粒子的合成及介电敏感性检测

局域表面等离激元共振(LSPR)显微探针的检测灵敏性主要取决于针尖上修饰的纳米粒子的LSPR性质.本文采用阴离子辅助法,在水溶液中通过调节Au核与Ag⁺的物质的量之比,实现Au核上不同厚度的Ag壳层包覆,可控地一步合成均一性好、银壳层较厚(≥10 nm)的核壳比不同的球形Au@Ag纳米粒子.通过扫描电镜(SEM)、透射电镜(TEM)及扫描透射电子显微镜X射线能谱(STM-EDS)线扫描分析对不同核壳比的Au@Ag纳米粒子进行形貌组成表征,证实了所合成核壳结构的可控性.将不同核壳比的Au@Ag纳米粒子置于不同折射率溶液中进行纳米粒子介电敏感性的研究,表明7.5 nm Au@28 nm Ag的纳米结构具有最高的品质因子.同时将不同核壳比的Au@Ag纳米粒子置于不同折射率的非导电性基底上进行单颗纳米粒子散射性质的研究,结果表明7.5 nm Au@28 nm Ag纳米粒子适合作为LSPR显微探针的高检测灵敏性纳米结构之一.     

二阶导数光谱-峰面积积分法同时测定芦荟中痕量铁(Ⅱ)和钴(Ⅱ)

在 1,10 -邻菲罗啉显色体系中 ,引入二阶导数光谱 -峰面积积分技术 ,建立了同时测定痕量铁 ( )和钴 ( )的新方法。该法可有效消除共存离子的干扰 ,提高了准确度和灵敏度。对铁和钴的表观摩尔吸光系数分别为 εFe5 .4 5× 10 6 L·mol-1·cm-1,εCo 1.1× 10 4 L· mol-1· cm-1;铁含量在 0 .0— 8.5 μg·m L-1,钴含量在 0 .0— 7.3μg· m L-1范围内遵守比耳定律。可用于芦荟中铁和钴的同时测定 ,结果令人满意     

聚苯乙烯负载的β-溴乙烯基硒化合物的合成及其在固相合成多取代烯烃中的应用

多取代烯烃的合成一直是有机合成的重要内容之一,在维生素、前列腺素和昆虫信息素等天然产物中都含有（Z）-或（E）-构型的多取代烯基结构单元,元素及金属有机化合物组成的1,2-双官能团化合物在立体选择性地合成多取代烯烃方面的应用研究一直是有机合成的热点。     

Characterization of the Nanoscale Microstructure of an Immersion Silver on Sputtered Copper

1 INTRODUCTION Silver and its compounds have received much attention due to their current and potential applica- tions in many areas[1, 2]. As a metal with the highest electrical and thermal conductivities, silver was one of the most important noble metals used in electrical industries in the last century. Several decades ago, however, the development of silver application in electronic area seemed not so quick. The fear for some undesirable phenomena involving silver, like “electrochemi…     

THE FORMATION AND CRYSTAL STRUCTURE OF DIHYDRONITIDINE AND DISCUSSION OF ANTICANCER MECHANISM OF NITIDINE CATION

The paper reports the formation and crystal structure of dihydronitidine, expounds thereasons and conditions of easily formed oxynitidine, and discusses anticancer mechanism ofnitidine (cation). The crystallographic parameters of dihydronitidine are: space group P2_(1/n),a= 12.54(1), b = 9. 148(5), c = 14.748(8)A, β= 92. 12(6)°,Z =4. 4108 independent reflec-tions were collected within the range of 3°≤2θ≤54°, of which 2137 intensity data with I≥3σ(I) were used in the structural determination. The crystal structure has been refined byfull matrix least-square method to a final R of 0.050.     

A Novel Fluorescent Probe for ATP Detection Based on Synergetic Effect of Aggregation-induced Emission and Counterion Displacement

In this work,a fluorescent probe(TPEBe-I)was developed for adenosine triphosphate(ATP)detection based on the synergetic effect of aggregation-induced emission and counterion displacement.TPEBe-I gave weak emission in aqueous solution due to the heavy-atom effect of counter iodide ion.However,upon the addition of ATP,the new aggregate complex(TPEBe-ATP)was formed between the cationic unit of TPEBe-I and ATP through electrostatic interactions,which not only restricted the intramolecular motion of luminogen but also eliminated the quenching effect of iodide ion.As a result,the fluorescent light-up detection for ATP was successfully achieved.Moreover,TPEBe-I exhibited high selectivity towards ATP and showed a wide linear detection region towards the logarithm of ATP concentration(5—600μmol/L)with a detection limit of 1.0μmol/L,enabling TPEBe-I as a promising probe for ATP quantitative analysis.