The Numerical Simulation of the Climatic Change Caused by CO_2 Doubling

The IAP two-level atmospheric general circulation model was coupled to a 60-m-deep mixed layer ocean model and a zero-layer thermodynamic model to simulate the climatic effects induced by a doubling of CO_2 concentration in the atmosphere.The global surface temperature is 1.75℃ when CO_2 is doubled. This value is lower than most of other results in the world, such as those of GFDL, NCAR, UKMO, GISS and OSU models.There are large regional and seasonal differences in the climatic change. Great warming is found in the Northern Hemisphere's high-latitude region anti the Antarctica; and the warming in land areas is greater than in ocean areas, while the precipitation increases in high latitudes and tropical regions but decreases in subtropical regions. In both hemispheres, the warming is greater in winter than in other seasons. As for the changes in China, we find that the precipitation in southwestern and northern China greatly decreases in summer but increases in winter.     

Effects of temperature and sodium carboxylate additives on mineralization of calcium oxalate in silica gel systems

Urolithiasis remains a major medical problem in China, especially in Guangdong Province in the southest of China[1]. A survey in Shenzhen city, the most southern city in China, showed the incidence of renal calculus was 4.87%, being 6.12% in the males and 4.07% in the females[2]. The prevalence of renal calculus has been more as the age advances and in the male population and so was in the less-educated population. The recurrence rate is more than 80%, with a moderate improvement by conventi…     

Simulation of calcium oxalate stone in vitro

Urolithiasis constitutes a serious health problem that affects a significant section of mankind. Between 3% and 14% of the population, depending on the geographical region, suffer from this illness[1]. For example, the incidence of urolithiasis in Florida in the United States of America was 15.7 in 100000 people and increased to 20.8 in 1996. Urolithiasis remains a major medical prob-lem in China, especially in Guangdong Province. A survey in 1997 in Shenzhen City, the most southern city i…     

Preface

Professor Zhou Weishan was born in Shaoxing, Zhejiang Province in 1923. He studied in the Department of Chem-istry, Soochou (Suzhou) University in 1944—1946 and graduated from School of Pharmacy in National Medical College ofShanghai in 1949. Having served as an assistant of organic chemistry under the supervision of Professor Yuen Kechee in thesame place for three years, he moved to the Academy of Military Medical Sciences and served as a research assistant underthe supervision of Professor Huang Minlon in 1952, and then to the Shanghai Institute of Organic Chemistry, Chinese     

Synthesis of 3-hydroxyflavone fluorescent probes and study of their fluorescence properties

<正>Direct measurement of dipole potential in biological membranes has been impossible and 3-hydroxyflavones(3HFs) have allowed detection of changes in dipole potential in biological systems.In the present study,sixteen derivatives of 3HF with aliphatic hydrocarbon chains of different lengths at 4′-position and 6-position were synthesized.The basic fluorescence properties of 3HFs are maintained in all the probes in terms of strong blue shift in maximum fluorescence emission wavelength and100 fold increase in quantum yield in organic solvents and in dioleoylphosphatidylcholine(DOPC) small unilamellar vesicles(SUV) in comparison to in aqueous Hepes buffer(15 mmol/L,pH 7.4).More importantly,the ability of the new compounds to report dipole potential changes in biological systems are also maintained,since all the new probes showed spectrum properties that are similar to yet different from that of F4N1,which potentially may allow more sensitive measurement of the dipole potential change in membranes.     

Kinetic and mechanism of oxidation of thiocarbohydrazide and its metal complex by acid bromate in aqueous and partial aqueous media

The kinetics of oxidation of thiocarbohydrazide in the free and zinc(Ⅱ)-bound states byacid bromate have been studied in aqueous and water-acetic acid(1:1,V/V)media under varyingconditions,both in the absence and presence of added bromide ion.The rates of oxidations show firstorder kinetics in[bromate]in all the cases,but exhibit different kinetic behaviour in[substrate]and[H~+].Oxidation of TCH in aqueous medium shows zero order in[TCH]and nearly second order in[H~+],while oxidation in aqueous acetic acid shows two ranges in[H~+].The rate shows first and fractionalorder kinetics in[TCH]in the first and second acid ranges.Kinetics observed in the presence of Br~-are similar to those observed for oxidation of TCH in second acid range.In addition,the reactionshows fractional order in[Br~-].Oxidation of TCH in Zn(Ⅱ)-bound state exhibits first order kinetics in[substrate]and second order in[H~+].Increase in ionic strength of the medium decreases the rate in allthe cases.Increase in acetic acid composition of the solvent increases the rate.Mechanisms consistentwith the observed results have been considered and the rate laws deduced.The rate limiting steps havebeen identified and the coefficients of these steps have been calculated at different temperatures.Therelated activation parameters have also been computed.The validity of the deduced rate laws has alsobeen tested by recalculating the rate constants from them as[TCH]and[H~+]are varied.     

ALLELIC FREQUENCIES OF PLASMA ALPHA-1-ANTITRYPSIN IN CHINESE

Alpha-1-antitrypsin (Pi) types and subtypes in a Chinese population of 1049 unrelatedindividuals in Beijing were determined by separator isoelectric focusing. The low activityPi variant S and the deficient Pi variant Z, common in most Caucasian populations, are ab-sent in the Chinese population. The frequent Pi variant found in the Chinese population isa neutral mutant, Etokyo, which was only found in Japanese before. Thus, it is concludedthat, as a predisposition of obstructive or some other lung diseases and liver diseases, thegenetic determined deficiency of alpha-1-antitrypsin in Chinese is not so important as in mostCaucasian populations.     

Could gingko foliage serve as a bio-monitor for organochlorine pesticides in air?

The feasibility of gingko (Gingo Biloba) foliage as a passive bio-monitor for organochlorine pesticides in air was explored. The accumulation patterns of hexachlorocyclohexanes (HCHs), dichlorodiphenyl- trichloroethanes (DDTs) and hexachlorobenzene (HCB) in gingko foliage were similar; the amounts of HCHs, DDTs and HCB increased with foliage growth in spring and decreased thereafter. This accumu-lation pattern is likely related to the growing process of the gingko foliage, which was observed for the first time in our work, giving a piece of evidence for the "bud burst effect" in plants. Compared with those in pine needles in 1980's, the residual levels of HCHs and DDTs have declined obviously in Bei-jing, indicating that the ban on the production and use of organochlorine pesticides (OCPs) in our country is effective; however, the amount of HCB has increased, indicating great progress of chemical industry in Beijing. The analysis for the source of OCPs in the gingko foliage showed that the technical HCHs and DDTs were used largely in history, but were not used in recent years. A little lidane has been used and there was a new input of o,p′-DDT in recent years; dicofol usage may be the main source of o,p′-DDT. Concentrations of HCHs, DDTs and HCB in gingko foliages were similar to those in pine nee-dles in the corresponding period and there is a strong positive correlation between the OCPs concen-tration data obtained from these two kinds of trees. It presents no difference in the accumulation style between these two kinds of trees. The level of OCPs in the gingko foliage reflects the pollution status of OCP in air. The result of this work shows that the gingko foliage can be used as a bio-monitor of OCPs in air.     

N pollution sources and denitrification in waterbodies in Taihu Lake region

Herein presented are the researches of the past few years related to characteristics of N pollution of waterbodies and N transport from croplands to the waterbodies in Suzhou and Wuxi regions, the center of the Taihu Lake valley. Based on the types of waterbodies, concentrations of inorganic N of different forms, concentrations of PO_4~(3-), δ15NH4 values in river and lake waterbodies, the pollution sources of N in the river, lake and well waters are distinguished, and comparisons are made of trend of variation and amplitude of concentration between years, seasons and N pollutants in waterbodies. The increase in N2O concentration in different waterbodies and high δ15NO_3~(-) value in different waterbodies are deemed as an evidence of the existence of denitrification in the river, lake and well waters. Moreover, the role of denitrification in the waterbodies plays in stabilizing chronically concentration of N as pollutant in the waterbodies and mitigating N load in the waterbodies.     

Electrochemical behaviors of novel electroactive Au nanoparticles protected by self-assembled monolayers

There has been substantial recent interest in studying monolayer-protected gold clusters (MPCs) owing to their diverse applications. The present work is an electrochemical study of novel gold nanoparticles covered with a monolayer of mercapto-dodecanol ended chloro-dicyano-quinone (HS-C12O-CDQ), which was adsorbed on the electrode (CDQ-MPCs film). Our findings reveal a redox behavior for CDQ-MPCs film similar to the solution electrochemistry of dichloro-dicyano-quinone. Furthermore, a diffusion-like mechanism was found for electron transfer, which may have occurred due to proton diffusion towards or outwards the electrode through the film casted. Chronoamperometry confirmed diffusion behavior of the ET process. Finally, EIS was used to find the rate constant of ET process for the redox reaction that occurred and the contribution of MPCs in total interfacial capacitance.     

A Novel Micro—hole Electrode Used to Investigate Electron Transfer Reactions at ITIES

A novel micro-hole electrode was fabricated to investigate the electron transfer reaction at the interface between two immiscible electrolyte solutions (ITIES). The electron transfer reaction between feero/ferricyanide in aqueous phase(W) and ferrocene in 1,2-dichloroethane (O) phase was studied as a test experiment. The results showed that the diffusion coefficient obtained from the micro-hole electrode was consistent with that obtained at macro-interface. Due to its simplicity and the very small IR drop it will be a useful tool for the study of ITIES systems.     

Scanning electrochemical microscopy determination of organic soluble MPC electron-transfer rates

In this paper, we describe a novel method for measuring the forward heterogeneous electron-transfer rate constant (kf) through the thiol monolayer of gold monolayer protected clusters (MPCs) in solution using scanning electrochemical microscopy (SECM). Applying the equations for mixed mass-transfer and electron-transfer processes, we develop a new formula using only the diffusion coefficient and the tip radius and use it as part of a new method for evaluating SECM approach curves. This method is applied to determine the electron-transfer rates from a series of SECM approach curves for monodisperse hexanethiol MPCs and for polydisperse hexanethiol, octanethiol, decanethiol, dodecanethiol, and 2-phenyethylthiol gold MPCs. Our results show that as the alkanethiol length increases the rate of electron transfer decreases in a manner consistent with the previously proposed tunneling mechanism for the electron transfer in MPCs. However, the effective tunneling coefficient, Beta, is found to be only 0.41 A-1 for alkanethiol passivated MPCs compared to typical values of 1.1 A-1 for alkanethiols as self-assembled monolayers on two-dimensional gold substrates. Similar SECM approach curve results for Pt and Au MPCs indicate that the electron-transfer rate is dependent mostly on the composition of the thiol layer and not on differences in the core metal.     

Achieving Direct Electrical Connection to Glucose Oxidase Using Aligned Single Walled Carbon Nanotube Arrays

Direct electron transfer between an electrode and the redox active centre of glucose oxidase, flavin adenine dinucleotide (FAD), is probed using carbon nanotube modified gold electrodes. Gold electrodes are first modified with a self‐assembled monolayer of cysteamine and then shortened single walled carbon nanotubes (SWNT) are aligned normal to the electrode surface by self‐assembly. The electrochemistry of these aligned nanotube electrode arrays is initially investigated using potassium ferricyanide which showed SWNT act as nanoelectrodes with the ends of the tubes more electrochemically active than the walls. Subsequently the nanotubes are plugged into the enzymes in one of two ways. In the first method, native glucose oxidase is covalently attached to the ends of the aligned tubes which allowed close approach to FAD and direct electron transfer to be observed with a rate constant of 0.3 s^?1. In the second strategy, FAD was attached to the ends of the tubes and the enzyme reconstituted around the surface immobilized FAD. This latter approach allowed more efficient electron transfer to the FAD with a rate constant of 9 s^?1.     

金电极上L-半胱氨酸短链分子自组装单层的电化学性能和拉曼光谱研究

用循环伏安法分别测定了金电极表面L-半胱氨酸(L-Cys)和十二硫醇自组装单分子层的电化学行为, 实验发现虽然单层结构排列致密, 但并不能有效地阻碍铁氰化钾与电极间异相电子转移过程, 同时观察到十二烷基硫醇自组装层能较好地阻碍电子转移作用. 运用表面增强拉曼散射光谱技术, 以十二烷基硫醇作为缺陷探针, 从分子水平上证实了L-半胱氨酸自组装单层的稳定性和致密性.     

Investigation of interparticle interactions of larger (4.63 nm) monolayer protected gold clusters during quantized double layer charging

In this article, the effect of interparticle interactions of 4.63 nm sized monolayer protected gold clusters (Au MPCs) during quantized double layer (QDL) charging has been investigated using electrochemical techniques. Voltammetry and scanning tunneling microscopy have been used to compare their electron transfer behavior. Furthermore, since the QDL process is diffusion controlled, the diffusion coefficient values have been estimated at various charge steps using two independent electroanalytical techniques, viz. chronoamperometry and impedance. These results show that higher core charge facilitates higher diffusion coefficient values, and indicate that repulsive interactions dominate for charged MPCs compared to those of its neutral analogue, which are mainly attractive in nature. Additionally, the electron transfer rate constants at various charge steps have been estimated from the impedance results, showing comparatively faster electron transfer rate at higher charge states.     

Effect of SDBS on interfacial electron transfer at the liquid/liquid interface by thin layer method

The effect of an adsorbed anionic surfactant sodium dodecyl benzene sulfonate(SDBS) on electron transfer(ET) reaction between ferricyanide aqueous solution and decamethylferrocene(DMFc) located on the adjacent organic phase was investigated for the first time by thin layer method.The adsorption of SDBS at the interface resulted in a decay in the cathodic plateau current of bimolecular reaction with increasing concentrations of SDBS in aqueous phase.However,the rate constant of electron transfer(k_(et)) i...     

On the Role of Pre‐ and Post‐Electron‐Transfer Steps in the SmI2/Amine/H2O‐Mediated Reduction of Esters: New Mechanistic Insights and Kinetic Studies

The mechanism of the SmI₂‐mediated reduction of unactivated esters has been studied using a combination of kinetic, radical clocks and reactivity experiments. The kinetic data indicate that all reaction components (SmI₂, amine, H₂O) are involved in the rate equation and that electron transfer is facilitated by Brønsted base assisted deprotonation of water in the transition state. The use of validated cyclopropyl‐containing radical clocks demonstrates that the reaction occurs via fast, reversible first electron transfer, and that the electron transfer from simple Sm(II) complexes to aliphatic esters is rapid. Notably, the mechanistic details presented herein indicate that complexation between SmI₂, H₂O and amines affords a new class of structurally diverse, thermodynamically powerful reductants for efficient electron transfer to carboxylic acid derivatives as an attractive alternative to the classical hydride‐mediated reductions and as a source of acyl‐radical equivalents for C?C bond forming processes.     

Structure and photophysical properties of porphyrin-modified metal nanoclusters with different chain lengths

Three-dimensional porphyrin-monolayer-protected gold clusters with different chain lengths (MPCs) have been prepared to examine the structure and photophysical properties, in comparison with self-assembled monolayers (SAMs) of the porphyrins on a flat gold surface. The three-dimensional porphyrin MPCs exhibit electrochemical and photophysical properties that are much closer to those of a porphyrin reference compound in solution than those of two-dimensional porphyrin SAMs on the flat gold surface. The three-dimensional architectures of porphyrin MPCs with large surface area have improved the light-harvesting efficiency relative to the corresponding porphyrin SAM on the two-dimensional flat gold surface. Time-resolved single photon counting fluorescence and transient absorption spectroscopic studies have demonstrated that undesirable quenching of the porphyrin excited singlet state via energy transfer to the gold surface of the three-dimensional MPCs is much suppressed, as compared to the quenching of the porphyrin SAMs on the two-dimensional flat gold surface. Both the quenching rate constants of the porphyrin excited singlet state by the surfaces of bulk gold and gold nanoclusters reveal weak chain length dependence of the energy transfer quenching.     

Heterophase ligand exchange and metal transfer between monolayer protected clusters

This paper describes reactions in which ligands are exchanged and metals are transferred between monolayer-protected metal clusters (MPCs) that are in different phases (heterophase exchange) or are in the same phase. For example, contact of toluene solutions of alkanethiolate-coated gold MPCs with aqueous solutions of tiopronin-coated gold MPCs yields toluene-phase MPCs that have some tiopronin ligands and aqueous-phase MPCs that have some alkanethiolate ligands. In a second example, heterophase transfer reactions occur between toluene solutions of alkanethiolate-coated gold MPCs and aqueous solutions of tiopronin-coated silver MPCs, in which tiopronin ligands are transferred to the former and gold metal to the latter phase. These ligand and metal exchange reactions are inhibited when conducted under N(2). The results implicate participation of an oxidized form of Au (such as a Au(I) thiolate, Au(I)-SR) as both a ligand and metal carrier in the exchange reactions. Au(I)-SR is demonstrated to be an exchange catalyst.