A QSRR Study on the Relative Retention Time of Halogenated Methyl-phenyl Ethers

Halogenated methyl-phenyl ethers （anisoles） are ubiquitous organic compounds in the environment. In the present study, geometrical optimization and electrostatic potential calculations have been performed for 42 halogenated anisoles at the HF/6-31 G^＊ level. A number of statistically based parameters have been obtained. By multiple regression method, linear relationships between the gas-chromatographic relative retention time （RRT） and structural descriptors have been established for the training set of 32 halogenated anisoles. The result showed that the parameters derived from electrostatic potentials （ESPs） together with the molecular volume （Vmc） could be well used to express the quantitative structure-RRT relationships of halogenated anisoles. The best two-variable regression model gives a correlation coefficient of 0.980 and a standard deviation of 0.07, and the leave-one-out cross-validated correlation coefficient is 0.975. The goodness of the model has been further validated through exploring the predictive power for the testing set of 10 halogenated anisoles.

New monoterpene phenyl ethers from Illicium micranthum

Seven new monoterpene phenyl ethers,namely micranthumnins A-G(1-7),were isolated from the stem bark of Illicium micranthum(Illiciaceae).Their structures were elucidated by comprehensive spectroscopic analyses including MS,IR,1D and 2D NMR.All compounds were evaluated for their anti-AChE activities.

Detection of Claisen Rearrangement Occurring in Allyl Phenyl Ether by in situ GC/MS

We report here a new strategy for revealing the Claisen rearrangement of allyl phenyl ether occurring in the gas phase by in situ GC/MS technique. The Claisen rearrangement has been observed when allyl phenyl ether passed through the capillary column at certain temperatures. The relative proportion of rearrangement products is dependent on the temperature of the capillary column and the substituents on the phenyl ring.

Using multiple site-directed modification of epoxide hydrolase to significantly improve its enantioselectivity in hydrolysis of rac-glycidyl phenyl ether

The epoxide hydrolase gene(SpEH) from Sphingomonas sp. HXN-200 was synthesized and expressed in robust Escherichia coli cells that had a dual protection system. The enantioselectivity(E-value) of the recombinant SpEH was 7.7 and the yield of the remaining(R)-PGE was 24.3% for the hydrolysis of racemic phenyl glycidyl ether(rac-PGE). To improve the catalytic properties of SpEH, the site-directed mutagenesis was carried out based on homology modeling, sequence alignment and molecular docking. Six residues(V195, V196, F218,N226, Q312, and M332) near the active site were mutated to hydrophobic amino acids and the positive mutations were selected for combinatorial mutation. The optimal mutant SpEH^(V196A/N226A/M332A) had an enhanced E-value of 21.2 and a specific activity of 4.57 U·mg^-1-wet cells, which were 2.8-, and 2.3-fold higher than those of wild-type SpEH. The optimal temperature and p H for purified Sp EHV196 A/N226 A/M332 Ato catalyze the hydrolysis of rac-PGE were 25 ℃ and 7.0 with 200 U·mg^-1. The enantioselectivity and yield of the remaining(R)-PGE of E. coliSpEH^(V196A/N226A/M332A)increased from 7.7 to 21.2 and 24.3% to 40.9%, respectively. The molecular docking and kinetic parameter analyses showed that SpEH^(V196A/N226A/M332A) has a greater affinity toward(S)-PGE than(R)-PGE, and that it was more difficult for the O-atom of ASP170 to achieve the nucleophilic attack on the Cα of(R)-PGE, resulting in its improved enantioselectivity.

Insight into the Structural Requirements of Protoporphyrino- gen Oxidase Inhibitors： Molecular Docking and CoMFA of Di- phenyl Ether, Isoxazole Phenyl, and Pyrazole Phenyl Ether

Protoporphyrinogen oxidase （PPO, EC 1.3.3.4） is one of the most significant targets for a large family of in- hibitors that may be used as herbicide, bactericide, fungicide, or photosensitizing activator to treat cancer through photodynamic therapy （PDT）. Molecular docking and CoMFA were combined in a multistep framework with the ultimate goal of identifying important factor contributing to the activity of PPO inhibitors. As a continuation of the previous research work on the development of new PPO inhibitors, the bioassay results indicated that good PPO in- hibitors were discovered in all of the three chemical series with ICs0 values ranging from 0.010 to 0.061 pmol·L ^-1. Using the crystal structure of tobacco mitochondrial PPO （mtPPO） as template, all the compounds were docked into the enzyme active site. The docking pose of each compound was subsequently used in a receptor-based alignment, leading to the development of a significant CoMFA model with r^2 value of 0.98 and q^2 （cross validation r^2） value of 0.63. This novel multistep framework gives insight into the and it can be extended to other classes of PPO inhibitors. In be particularly applicable in virtual screening procedures. structural characteristics for the binding of inhibitors, addition, the simplicity of the proposed approach may

Geranyl phenyl ethers from Illicium micranthum and their anti-HBV activity

Fourteen new geranyl phenyl ethers(1–14)along with three known compounds(15–17)were isolated from Illicium micranthum,and their structures were elucidated by comprehensive spectroscopic methods.Illimicranins A–H(1–8)were characterized as geranyl vanillin ethers,while 9 and 10 were dimethyl acetal derivatives.Illimicranins I and J(11 and 12)were rare geranyl isoeugenol ethers.Illimicranins K and L(13 and 14)represented the first example of geranyl guaiacylacetone ether and geranyl zingerone ether,respectively.Compounds 1,2 and 15 exhibited anti-HBV(hepatitis B virus)activity against HBsAg(hepatitis B surface antigen)and HBeAg(hepatitis B e antigen)secretion,and HBV DNA replication.

Hydrolysis kinetics of benzyl phenyl ether in high temperature liquid water

The application of high temperature liquid water（HTLW） to decomposition of lignin as efficient and green solution for phenolic compounds recovery was studied.Benzyl phenyl ether（BPE）,the lignin model compound,was treated at temperatures ranging from 220 to 250℃.BPE undergo hydrolysis in HTLW,and main products were phenol and benzyl alcohol with the minimum selectivities of 75.7%and 82.8%,respectively.Lower temperature led to higher selectivity in 220-250℃temperature range.The kinetics on BPE hydrolysis was studied and the activation energy was determined as 150.3±12.5 kJ/mol with the first-order kinetic equations.Based on products distribution,the reaction mechanism for decomposition of benzyl phenyl ether was proposed.The investigated process provides insights into the design of a commercial method for utilization of lignin.

Theoretical Analysis of Mass Transfer with Chemical Reaction Using Absorption of Carbon Dioxide into Phenyl Glycidyl Ether Solution

Theoretical analysis corresponding to the diffusion and reaction kinetics in a chemical reaction between carbon dioxide and phenyl glycidyl ether solution is presented. Analytical expressions pertaining to the concentration of carbon dioxide (CO2), phenyl glycidyl ether solution (PGE) and flux are obtained in terms of reaction rate constants. In this paper, a powerful analytical method, called the Adomian decomposition method (ADM) is used to obtain approximate analytical solutions for nonlinear differential equations. Furthermore, in this work the numerical simulation of the problem is also reported using Scilab/Matlab program. An agreement between analytical and numerical results is noted.

A Facile One-pot Method for the Synthesis of Vinyl Ethers from 2-Hydroxyalkyl Phenyl Selenides

A mild, one-pot procedure for the synthesis of vinyl ethers in good yields from 2-hydroxyalkyl phenyl selenides with primary or secondary organic halides has been developed.

Formation of Hybrid Ring Structure of Cyanurate/Isocyanurate in the Reaction be-tween 2,4,6-Tris(4-Phenyl-Phenoxy)-1, 3,5-Triazine and Phenyl Glycidyl Ether

Reaction products of 2,4,6-tris(4-phenyl-phenoxy)-1,3,5-triazine derived from 4-phenylphenol cyanate ester and phenyl glycidyl ether were analyzed. In addition to an isocyanurate compound and an oxazolidone compound which were well known as reaction products of cyanate esters and epoxy resins, compounds with hybrid ring structure of cyanurate/isocyanurate were determined. Gibbs free energies of the compound having hybrid ring structure of cyanurate/isocyanurate with two isocyanurate moiety were found to be lower than that of the compound with cyanurate ring structure through calculations. Calculation data supported the existence of hybrid ring structure of cy-anurate/isocyanurate. It was revealed that isomerization from cyanurate to isocyanurate occurs via hybrid ring structure of cyanurate/isocyanurate in the reaction of aryl cyanurate and epoxy.

Synthesis and Adsorption Property of Two Polymeric Adsorbents with Pendent Ether Bonds

Two polymeric adsorbents, poly(methyl p-vinylbenzyl ether) and poly(phenyl p-vinylbenzyl ether), were synthesized from chloromethylated polystyrene. Their adsorption property for phenol in hexane solution was investigated. The results showed that the two adsorbents adsorb phenol from hexane solution through hydrogen-bonding and π-π stacking interaction.

HFBAPP/6FDA/BPADA含氟苯醚型聚酰亚胺薄膜的制备与性能研究

以2,2-双[4-(4-氨基苯氧基)苯基]六氟丙烷(HFBAPP)为二胺单体,2,2′-双(3,4-二羧酸)六氟丙烷二酐(6FDA)和双酚A型二醚二酐(BPADA)为二酐单体制备了一系列HFBAPP/6FDA/BPADA含氟苯醚型PI薄膜。通过改变二酐单体比例,分析比较醚键与三氟甲基对PI薄膜综合性能的影响。结果表明:随着三氟甲基含量的升高和醚键含量的降低,HFBAPP/6FDA/BPADA含氟苯醚型PI薄膜的光学性能和热学性能提高,而力学性能下降,玻璃化转变温度最高可达247.3℃,800℃时的残炭率最高可达56.3%,可见光范围内的透光率最高可达88.2%,拉伸强度最高可达84.7 MPa。

STRUCTURE AND PROPERTIES OF PHOSPHROUS-CONTAINING POLY(ARYLETHER KETONE)WITH BISPHENOL-A MOIETY

A phosphrous-containing poly（aryl ether ketone） was synthesized derived from bisphenol-A and bis[4-（4- fluorobenzoyl）phenyl] phenyl phosphine oxide （FPPPO） by nucleophilic substitution reaction. The structure of the polymer was characterized by FT-IR, ^1H-NMR and ^31p-NMR. The thermal property of the PAEK was measured by DSC and TGA. The glass transition temperature （Tg） of the polymer was 205℃, and the 5% weight loss temperature under nitrogen was 475℃. Good solubility of the polymer in organic solvents, such as N-methylpyrrolidone, dimethylformamide, dimethylacetamide, dimethylsulfoxide and chloroalkanes was observed, flexible film was obtained from the polymer＇s CH2Cl2 solution. The limiting oxygen index （LOI） of the PAEK was 40, which indicated that organic phosphorus moiety can offer good flame retardant property to the polymer.

烯丙基苯基醚Claisen重排反应的量化计算研究——介绍一个计算化学实验

烯基烯丙基醚或芳基烯丙基醚受热发生[3,3]-σ重排,生成γ,δ-不饱和醛酮或邻对位烯丙基酚,即为Claisen重排反应。本研究利用Gaussian 16程序的DFT方法对烯丙基苯基醚在加热条件的Claisen重排反应进行了量化计算研究。通过本实验的练习,我们旨在加深学生对Claisen重排反应过渡态结构的认识,促进学生应用计算化学工具解决化学问题,提升学生在学习、科研中的实践与创新能力。

用三角相图法研究药用微乳的形成条件

目的 用建立的改良三角相图法制备低毒药用微乳。方法 选磷脂和聚氧乙烯辛基苯基醚 (OP)为乳化剂 ,乙醇和正辛醇为助乳化剂 ,油酸乙酯和橄榄油为油相 ,以改良三角相图法即固定水相和助乳化剂的比值 (W /A)或油相和助乳化剂的比值 (O/A) ,对比经典三角相图法即固定乳化剂和助乳化剂的比值 (Km)制备的微乳所需乳化剂和助乳化剂的量及相体积比的大小。结果 对磷脂为乳化剂形成的微乳系统 ,改良三角相图法所需乳化剂的量为 6 % - 2 8% ,而经典三角相图法所需乳化剂的量为 2 8% - 2 9 6 %。对OP为乳化剂形成的微乳系统 ,改良三角相图法所需乳化剂为 2 3 % - 40 % ;而经典三角相图法所需乳化剂为 2 7 6 % - 49 8% ,以上两种系统 ,前者均较后者用量小。结论 用改良三角相图代替经典三角相图研究形成药用微乳的理论 ,对寻找低毒性的微乳有积极的指导意义。

改性聚苯醚(MPPO)工程塑料国内外发展现状

综述了聚苯醚、共混改性聚苯醚、相容剂改性聚苯醚、热固性聚苯醚和阻燃聚苯醚工程塑料的国内外进展。介绍了其在工程塑料领域的消费量和消费分布以及在覆铜板中的应用。

Ni基催化剂上木质素模型化合物苯基苯乙醚C–O键的加氢裂解

研究了Ni基催化剂上木质素模型化合物苯基苯乙醚中C–O–C键加氢裂解性能.结果表明,Ni/C催化剂显示出优异的加氢裂解能力,苯基苯乙醚的转化率达到99%以上.Ni/C催化剂的还原方法对裂解选择性有重要影响;氢气还原制备的Ni/C-H催化剂上,C–O–C键裂解选择性为85%.Ru/C和Pd/C催化剂上裂解选择性分别为40%和69%.采用碳热还原方法制备的Ni/C-C催化剂,可以实现高选择性加氢和裂解,C–O–C键裂解选择性达到99%以上,其中芳烃化合物收率为44%.这可能与镍组分和载体碳之间的相互作用有关.

ZnMgAl复合氧化物催化合成丙二醇苯醚

以不同类水滑石化合物为前驱体制得的复合氧化物作为合成丙二醇苯醚反应的固体碱催化剂,考察了催化剂组成、结构及反应条件对催化合成丙二醇苯醚反应的影响。结果发现,在所制备的固体碱催化剂中ZnMgAl复合氧化物显示出高效的催化活性和选择性,在催化剂用量为1.1%,C6H5OH/PO摩尔比为1∶1,反应温度为413K和反应时间为5h的条件下,环氧丙烷的转化率达到97.2%,丙二醇苯醚的选择性达93.4%。