原子配分参数、配分连接性指数及其应用

结构决定性质，性质反映结构，这是化学、生物学等学科的一条基本规律。因此，分子的微观结构与性质之间存在着密切关系。物质的理化性质、生物活性等数据的获取，迄今主要来自于实验。如能建立结构与性能之间的数量关系用以估算与预测分子的性质，这无疑是一项十分有意义的工作。拓扑指数法以其计算简单、准确性高、应用范围广而在上述领域中发挥重要作用犤１～４犦。拓扑指数是对分子结构进行的定量描述，使分子之间的结构差异定量化。自Wiener提出第一个拓扑指数（W）犤５犦以来，迄今已有２００余种拓扑指数问世。其中一部分能够有效地…     

Liquid chromatographic study of two methoxypsoralen isomers with β-cyclodextrin

Abstract

The inclusion into β-cyclodextrin (β-Cyd) by the two methoxypsoralen isomers (5-methoxypsoralen (5-MOP) and 8-methoxypsoralen (8-MOP)) has been extensively studied by reverse phase liquid chromatography (RP-HPLC). Some important quantitative data concerning the complexation in a dynamic flow system have been drawn. The stoichiometry of the complex formation (1:1 in all instances), and the affinity constants with the β-Cyd cavity (K_f) of the two guest compounds, have been established. By taking into account the competitive effect of the organic modifier of the eluent (methanol), the K_fs of both compounds have been extrapolated to pure water (233 M^?1 and 106 M^?1 for 5-MOP and 8-MOP, respectively). On the other hand, the established stoichiometry and affinity constants have been interpreted in terms of enthalpy and entropy changes. Finally, the importance of the position of the methoxy substituent has been underlined and seems to rule the quality of the fit of each isomer within the inner cavity of β-cyclodextrin.     

An Aqueous Thermodynamic Model for the Solubility of Potassium Ferrate in Alkaline Solutions to High Ionic Strengths from 283.15 to 333.15 K

Potassium ferrate, K₂FeO₄(cr), has numerous promising environmental applications. An aqueous thermodynamic model applicable to high ionic strengths is essential for guiding its applications. In this study, a thermodynamic model is developed for the solubility of K₂FeO₄(cr) in aqueous alkali metal hydroxide solutions, from 283.15 to 333.15 K to high ionic strengths, up to saturation of KOH and NaOH, based on the Pitzer activity coefficient model for aqueous species. The solubility products for K₂FeO₄(cr) at infinite dilution in the temperature range from 283.15 to 333.15 K were obtained. Based on the thermodynamic solubility product of K₂FeO₄(cr) at 298.15 and its temperature dependence, in combination with thermodynamic properties for $ {\text{FeO}}_{4}^{2 - } $ FeO 4 2 ? and K⁺ from the literature, standard thermodynamic properties of K₂FeO₄(cr) at 298.15 K and 0.1 MPa (1 bar) are derived for the first time as follows: Δ_f G ⁰ = ?(896 ± 8) kJ·mol^?1, Δ_f H ⁰ = ?(1026 ± 4) kJ·mol^?1, and S ⁰ = (130 ± 17) J·mol^?1·K^?1. Using the above thermodynamic properties for K₂FeO₄(cr), the potential presence or preservation of K₂FeO₄(cr) in the Martian soils under the conditions relevant to Mars were quantitatively evaluated. Thermodynamic calculations pertaining to the Martian conditions indicate that the presence or preservation of K₂FeO₄(cr) as a strong oxidant in the Martian soils can be supported.     

Larval Tenebrio molitor (Coleoptera: Tenebrionidae) Fat Body Extracts Catalyze Firefly D-Luciferin- and ATP-Dependent Chemiluminescence: A Luciferase-like Enzyme*

Ultraweak light emission was detected upon injection of firefly luciferin into live Tenebrio larvae. A chemilumi-nescent enzymatic activity dependent on molecular oxygen, D-luciferin and MgATP was then isolated from larval fat body extracts by precipitation with 70% ammonium sulfate. D-Luciferin and ATP can be replaced by luciferyl-adenylate. Pyrophosphate is a main product from the chemiluminescent reaction. The in vitro chemiluminescence intensity was not affected by peroxidase inhibitors such as N₃^?_- (0.5 mM) and CN^? (1 mM), attesting to its nonperoxidatic nature but was strongly inhibited by AMP (1 mM), luciferin 6′-ethyl ether (1 mM) and sodium pyrophosphate (2 mM), well-known firefly lucifer-ase inhibitors. Some physical-chemical properties of this enzymatic activity were similar to those of firefly lucif-erase (K_MATP = 195 μM; K_0.5 luciferin - 0.8 mM; optimum pH 8.5; δ_max= 610 nm at pH 8.5; firefly lucifer-ase: δ_max= 565 nm at pH 8.0 and 619 mm at pH 6.0), but the chemiluminescence was not affected by addition of polyclonal antibodies raised against Photinus pyralis luciferase. These data suggest that this chemiluminescence results from a ligase with luciferase activity.     

Nucleophilic displacement in polyhalogenoaromatic compounds. Part 12.[1] Additivity of fluorine substituent effects in methoxydefluorination

The rates of methoxydefluorination of all twelve polyfluorobenzenes in dimethyl sulphoxide-methanol mixtures (DMSO-MeOH; 9:1, v/v; 298.2 K) have been measured. Three substituent rate factors (f_o, 60; f_m, 180; f_p, 0.75) are sufficient to reproduce the effect of the fluorine substituent in this reaction upon each member of the series. The solvent effect, comparing these results with an earlier and more limited study in methanol is predominantly a simple acceleration. The effects of substituents upon the rate of methoxydefluorination of fluorobenzene itself are slightly greater (?^?, 6.9) than in the corresponding reaction of pentafluorobenzene derivatives (?^?, 5.8), but the change in sensitivity is much less than that found with nitrobenzene derivatives.     

MZn2HPO4PO4 (M=Na+, K+)的合成、表征和标准摩尔生成焓

采用低温固相法和水热法制备MZn2HPO4PO4 (M=Na+, K+) 并用XRD, FT-IR, TG and SEM对其进行表征,用等温量热计测定热化学性质。按照Hess’s定律,设计一新的热化学循环。结果表明,所合成的物质是等结构三斜晶系的目标产物,具有片层结构,分解温度分别为： 415 ℃和430 ℃。从测定的溶解焓和其他的标准热化学数据,计算出MZn2HPO4PO4 (M=Na+, K+) 的标准摩尔生成焓分别为：ΔfHm [NaZn2HPO4PO4, s]=-3042.38±0.31 kJ·mol-1; ΔfHm [KZn2HPO4PO4,s]=-3093.46 ±0.27 kJ·mol-1。     

多溴代二苯胺热力学性质的密度泛函理论研究

在B3LYP/6-31G*水平上对209个多溴代二苯胺(PBDPA)系列化合物进行了全优化和振动分析计算, 得到各分子在298.15 K, 101.3 kPa标准状态下的热力学参数. 设计等键反应, 计算了PBDPA系列化合物的标准生成热(ΔfHÖ)和标准生成自由能(ΔfGÖ). 研究了热力学参数SÖ与溴原子的取代位置及取代数目(NPBS)之间的关系, 结果表明: PBDPA系列化合物的SÖ, ΔfHÖ和ΔfGÖ与NPBS之间有很强的相关性(R2≥0.984). 根据异构体标准生成自由能的相对大小, 从理论上求得异构体的相对稳定性. 以Gaussian 03程序的输出文件为基础, 采用统计热力学程序计算了PBDPA化合物在200 K至1000 K的摩尔恒压热容(Cp,m), 并用最小二乘法求得Cp,m与温度之间的相关方程, 发现Cp,m与T, T－1和T－2之间有着很好的相关性(R2＝1.000).     

The reaction of triethylamine with bromine. An evaluation of the formation constant of the transient 1:1 complex and a study of its conversion into products.

Triethylamine and bromine in 1,2-dichloroethane give a non isolable 1:1 charge transfer complex with K_f>10⁷ M^?1, which undergoes a fast intramolecular oxidation to N,N-diethylethyldeneiminium bromide and hydrogen bromide.     

Lithium tetrahydridoaluminate LiAlH4 and hexahydridoaluminate Li3AlH6: molar heat capacity and thermodynamic properties from 10 to 300 K

The heat capacity of lithium tetra- and hexa-hydridoaluminate have been determined by adiabatic calorimetry over the range 10 to 300 K and associated thermodynamic functions have been computed. At 298.15 K the heat capacities C_p and entropies S^o are respectively 83.19 J K^?1 mol^?1 and 78.8 J K^?1 mol^?1 for LiAlH₄ and 127.75 J K^?1 mol^?1 and 102.6 J K^?1 mol^?1 for Li₃AlH₆.     

THE pKa OF DIPROTONATED SEMIMETHYLENE BLUE, IN 5% ETHANOL AND 50% ACETONITRILE AQUEOUS SOLUTIONS

Abstract— Semimethylene blue was generated by reductive quenching of triplet methylene blue, ³MBH²⁺, with diphenylamine at pH 0.62–3.4. A Q-switched ruby laser flash-photolysis-kinetic spectro-photometric apparatus was used to characterize the absorption spectrum of semimethylene blue from 350 to 900 nm and a number of physical constants at 25°C with μ= 0.4 M and Cl^? as the anion. The specific rate of quenching of ³MBH²⁺ by DPA is 2.8 × 10⁹M^?1 s^?1 in 5% EtOH-95% water and 1.2×10⁹M^?1 s^?1 in 50 v/v% aq. CH₃CN. Corresponding efficiencies of net electron transfer are, respectively, 0.15 and 0.62. Spectral characteristics in 5% EtOH are, for MBH²₂±, λ_max= 375 nm, ε₃₇₅= 9000 M^?1 cm^?1; λ_max= 880 nm, ε₈₈₀= 12700 M^?1 cm^?1; for MBH±, λ_max= 410 nm, ε₄₁₀= 9800 M^?1 cm^?1, λ_max= 880 nm, ε₈₈₀= 33000 M^?1 cm^?1; for MBH± in 50 v/v% AN, λ_max= 400 nm, ε₄₀₀= 11000 M^?1 cm^?1 and λ_max= 880 nm,ε₈₈₀= 39000 M^?1 cm^?1. The pK_a of MBH²₂ε calculated from the pH dependence of the absorption spectrum is 1.86 × 0.04 in 5% EtOH and 1.15 in 50 v/v% AN. Rate constants, k_decay, for reaction DPAH±⁺ with MBH²₂ε and MBH± in 5% EtOH are, respectively, 3.9 × 10⁹ and 9.5 × 10⁹M^?1 s^?1. The value of pK_a of MBH²₂ε calculated from the dependence of k_decay on pH is 1.75 in 5% EtOH.     

4-硝基苯甲醇的低温热容和标准摩尔生成焓

用精密自动绝热量热计测定了4-硝基苯甲醇（4-NBA）在78 ~ 396 K温区的摩尔热容。其熔化温度、摩尔熔化焓及摩尔熔化熵分别为:(336.426 ± 0.088) K, (20.97 ± 0.13) kJ×mol-1 和 (57.24 ± 0.36) J×K-1×mol-1.根据热力学函数关系式,从热容值计算出了该物质在80 ~ 400 K温区的热力学函数值 [HT - H298.15 K] 和[ST - S298.15 K]. 用精密氧弹燃烧量热计测定了该物质在T＝298.15 K的恒容燃烧能和标准摩尔燃烧焓分别为 (C7H7NO3, s)＝- ( 3549.11 ± 1.47 ) kJ×mol-1 和 (C7H7NO3, s)＝- ( 3548.49 ± 1.47 ) kJ×mol-1. 利用标准摩尔燃烧焓和其他辅助热力学数据通过盖斯热化学循环, 计算出了该物质标准摩尔生成焓 (C7H7NO3, s)＝- (206.49 ± 2.52) kJ×mol-1 .     

二元无机物标准熵 So298的拓扑研究

为了预测二元无机物的标准熵,基于分子图的连接矩阵和离子参数gi、qi,提出了一种新的连接性指数mQ, mG及其逆指数mQ’, mG’。 qi、gi定义为：qi=(1.1+Zi1.1) /(1.7+ni), gi=(1.4+Zi) /(0.9+ri+ri-1),其中Zi 、ni和 ri分别代表离子i的电荷数、最外层主量子数和半径。从0Q, 0Q’, 1G,和1G’,利用多元线性回归分析方法和人工神经网络方法,可以构建优良的QSPR模型。对371个二元无机物,其多元线性模型及神经网络模型的相关系数、标准偏差和平均绝对偏差分别是：0.9905, 8.29 J.K-1.mol-1, 6.48 J. K-1.mol-1, 0.9960, 5.37 J.K-1.mol-1 和 3.90 J.K-1.mol-1。留一法交叉验证表明,其多元线性模型具有良好的稳定性。两个模型对187个未进入模型的二元无机物的标准熵的预测值和实验值之间的相关系数、标准偏差和平均绝对偏差分别是：0.9897, 8.64 J. K-1.mol-1, 6.84 J. K-1.mol-1, 0.9957, 5.63 J.K-1.mol-1, 和 4.18 J.K-1.mol-1。研究表明,本文方法在预测二元无机物标准熵时比文献方法更有效,两种模型均能较精确的预测二元无机物的标准熵,且神经网络模型的预测结果更精确。     

Electrochemical properties of the AlBr3/MBr/ArH solvent system and polarography of metal ions in it

Physical and electrochemical properties of the AlBr₃/MBr/ArH system with different metal ions added were studied. Nernst plots for the Hg/Hg²⁺ and Zn/Zn²⁺ couples were measured and the formal potentials were found to be 0.65–0.68 V (RAIE) for the former and 0.08 V (RAIE) for the latter. The slopes of the Nernst plots were 29±1 mV as expected. The exchange current density for deposition and dissolution of mercury was found to be 18.5 μA cm^?2 and 73 μA cm^?2 in 0.1 mM and 1.0 mM solutions of HgBr₂, respectively,The density of the solution was found to increase linearly with increasing concentration of AlBr₃, and its values in toluence and mesitylene were practically identical. The viscosity increased rapidly from a value of ca. 0.5–0.6 cP for the pure solvents to 1.9 cP and 4.0 cP for 2.3 M AlBr₃, 0.76 M KBr in toluence and mesitylene, respectively. The measured diffusion coefficients of Hg²⁺ were in the range of (0.8–2.0)×10^?6 cm²s^?1 in mesitylene (depending on the concentration of AlBr₃ and KBr) and 4.0×10^?6 cm²s^? in toluene. The calculated ionic radius was 6.3±1 Å in mesitylene and 2.3±0.5 Å in toluene. The diffusion coefficient for Ag⁺, ions was found to have similar values.The specific conductivity was found to increase with concentration of (KAl₂Br₇). The molar conductivity also increases with increasing concentration. When corrected for the change of viscosity, the normalized molar conductivity increases linearly with the square of the concentration of (KAl₂Br₇).A detailed survey of existing literature data for this and similar systems is presented.     

Low-temperature thermodynamic properties of L- and DL-valines

Heat capacities C _p(T) of L-valine and DL-valine were measured in the temperature range 6–300 K with an adiabatic calorimeter; thermodynamic functions were calculated based on these measurements. At 298.15 K, the values of heat capacity, C _p; entropy, S _m ⁰ (T) ? S _m ⁰ (0); enthalpy, H _m ⁰ (T) ? H _m ⁰ (0) of L-valine are equal, respectively, to 167.9 ± 0.3 J K^?1 mol^?1; 178.5 ± 0.4 J K^?1 mol^?1; and 27510 ± 60 J mol^?1. For DL-valine, these values are equal, respectively, to 167.3 ± 0.3 J K^?1 mol^?1, 174.4 ± 0.3 J K^?1 mol^?1, and 27000 ± 50 J mol^?1. The difference between the heat capacities of enantiomer and racemate has been calculated and compared with the similar data for serines, cysteines, and phenylglycines.     

Hydroxo and Chloro Complexes/Ion Interactions of Hf4+ and the Solubility Product of HfO2(am)

The solubility of HfO₂(am) was determined at different equilibration periods from the over- and undersaturation directions, in very acidic to basic solutions (0.1 m HCl to 3.2 m NaOH), and in NaCl solutions ranging in concentrations from very dilute to as high as 5.59 m and in a ${\text{p}}C_{{\text{H}} + }$ range from 1 to 4 to obtain reliable thermodynamic data for the Hf⁴⁺–Cl^?–Na⁺–H⁺–OH^?–H₂O system. The studies indicate that equilibrium is reached rapidly (<5 days) and that HfO₂(am) solubility shows amphoteric behavior. The solubility data obtained in this study, along with the data reported in the literature, at NaOH molalities as high as 21.7 m were interpreted using the ion-interaction model of Pitzer. The log K ⁰ for the solubility of HfO₂(am) [HfO₂(am) + 2H₂O ? Hf⁴⁺ + 4OH^?] was determined to be ?55.1 ± 0.7. The log K ⁰ values for the formation of HfOH³⁺, Hf(OH)⁰ ₄, Hf(OH)₅ ^?, and Hf(OH)₆ ^2? according to the reaction (Hf⁴⁺ + xOH^? ? Hf(OH)^4?x _x) were determined to be 13.8, <44.8, 49.7 ± 0.2, and 51.2 ± 0.2, respectively. The thermodynamic model developed in this study is valid for a wide range of conditions (as high as 0.1 m HCl, 21.7 m NaOH, and 5.59 m NaCl). The binary ion-interaction parameters for Hf⁴⁺–Cl^?, HfOH³⁺–Cl^?, and Hf(OH)^2? ₆–Na⁺ were determined in this study to accurately define the observed solubility behavior of hafnium in various systems.     

A thermodynamic study of α-, β-, and γ-cyclodextrin-complexed m-methyl red in alkaline solutions

The UV/Visible spectra of m-methyl red (m-MR) ({3-[4-(dimethyl-amino) phenylazo] benzoic acid}) were examined in basic, acidic and strongly acidic aqueous solutions. The observed spectra of m-MR were analyzed and compared with the tautomeric and resonance structures that suggested theoretically. Three isosbestic points in the spectra were observed around 508, 464 and 443 nm representing three different equilibriums between four different species of m-MR. The inclusion constant (K_f) for the inclusion of basic form of m-MR with alpha-, Beta-, and gamma-Cyclodextrin (α-, β- and γ-CD) was evaluated at different temperatures using Benesi-Hildebrand method. The values of K_f at 25 °C were found to be 8.70 × 10³, 4.93 × 10³ mol^?1 dm³ and 2.95 × 10⁷ mol^?2 dm⁶ basis on the inclusion complex ratios (m-MR:CD) of 1:1, 1:1, and 2:1 respectively. The values of the thermodynamic quantities ΔH°, ΔS°, ΔG° for the different inclusion processes were calculated by using Van’t Hoff plot. For all cases of the studied inclusion processes, these inclusions were favored through entropy and enthalpy changes.