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1.
The effect of a single water molecule on the OH + HOCl reaction has been investigated. The naked reaction, the reaction without water, has two elementary reaction paths, depending on how the hydroxyl radical approaches the HOCl molecule. In both cases, the reaction begins with the formation of prereactive hydrogen bond complexes before the abstraction of the hydrogen by the hydroxyl radical. When water is added, the products of the reaction do not change, and the reaction becomes quite complex yielding six different reaction paths. Interestingly, a geometrical rearrangement occurs in the prereactive hydrogen bonded region, which prepares the HOCl moiety to react with the hydroxyl radical. The rate constant for the reaction without water is computed to be 2.2 × 10(-13) cm(3) molecule(-1) s(-1) at room temperature, which is in good agreement with experimental values. The reaction between ClOH···H(2)O and OH is estimated to be slower than the naked reaction by 4-5 orders of magnitude. Although, the reaction between ClOH and the H(2)O···HO complex is also predicted to be slower, it is up to 2.2 times faster than the naked reaction at altitudes below 6 km. Another intriguing finding of this work is an interesting three-body interchange reaction that can occur, that is HOCl + HO···H(2)O → HOCl···H(2)O + OH.  相似文献   

2.
在密度泛函理论B3LYP/6-31G*水平上,研究了ClONO2+Cl(2P3/2)Cl2+NO3和ClONO2+Cl(2P3/2)ClO+ClONO(cis)及ClONO2+Cl(2P3/2)ClOCl+NO2的反应机理.计算得到各可能反应途径的过渡态,并经过内禀反应坐标(IRC)分析加以证实.反应ClONO2+Cl(2P3/2)Cl2+NO3反应活化能垒最低,为4.5kJ/mol,是反应主通道.  相似文献   

3.
The reaction of N(4S)+CH3X(X=Cl、Br) was studied by the ab initio method. The geometries of the reactants, transition states and products were optimized at the MP2/6-311+G(d,p) level. The corresponding vibration frequencies were calculated at the same level. The single-point calculations for all the stationary points were carried out at the MP2/6-311++G(3df,2p) and the QCISD(T)/6-311+G(d,p) levels using the MP2/6-311+G(d,p) optimized geometries. The energies of all the stationary points were calculated by the G2MP2 method. The results of this theoretical study indicate that the reaction has three reaction channels: H abstraction reaction channel a, Cl or Br abstraction reaction channel b and substitution reaction channel c. For the N(4S)+CH3Cl reaction, reaction channel a is the main reaction channel. Reaction channels b and c may have a slight contribution in the reaction. For the N(4S)+CH3Br reaction, reaction channel a is the main reaction channel. Reaction channels b and c may have some contribution in the reaction.  相似文献   

4.
A simple and selective voltammetric method based on selenium-gold film modified glassy carbon electrode has been developed for investigating electrochemical reaction mechanism of selenocystine. With N2 saturated, redox reactions between selenocystine (SeC) and selenocysteine (SeCys) were judged to be two simple electron-transfer processes. With air saturated, the reduction reaction was diagnosed to be EC catalytic reaction (the chemical oxidation reaction of the SeCys by O2 (C) following the electron-transfer reaction (E)) and oxidation reaction is a simple electron-transfer process. With pure O2 saturated, only reduction peak was observed and the reaction was judged to be EC catalytic reaction. The electron-transfer numbers of redox reaction were calculated to be 2 by chronocoulometry and rotating disk electrode.  相似文献   

5.
A new polystyrene anchored Pd(II) azo complex has been synthesized and characterized. The present Pd(II) azo complex behaves as a very efficient heterogeneous catalyst in the Suzuki coupling and Sonogashira coupling reaction in water medium. Aryl halides, coupled with phenylboronic acids (Suzuki-Miyaura reaction) or terminal alkyne (Sonogashira reaction), smoothly afford the corresponding cross-coupling products in excellent yields (83-100% yield for Suzuki reaction and 68-96% yield for Sonogashira reaction of aryl halides) under phosphine-free reaction conditions in the presence of polystyrene anchored Pd(II) azo complex catalyst in water medium. Furthermore, the catalyst has shown good thermal stability and recyclability. This polymer-supported Pd(II) catalyst could be easily recovered by simple filtration of the reaction mixture and reused for more than six consecutive trials without a significant loss of its catalytic activity.  相似文献   

6.
Lü Ling-Ling 《结构化学》2008,27(9):1039-1044
The insertion reaction mechanism of CF2 with CH2O was investigated at the B3LYP/6-311G(d)//MP2/6-311G(d) level. The geometric conformations at each stationary point in reaction potential surface were fully optimized and the transition states were verified by intrinsic reaction coordinate (IRC) and frequency analysis. The energies of all reactants were calculated with CCSD(T)/6-311G(d)//G2MP2 methods. Results indicated that the P1 reaction route with difuoroaldehyde as product is the dominant reaction pathway, which exhibits nucleophilic character. According to NBO analysis, the starting point of insertion reaction is the interaction between carbene LP(C3) and formaldehyde π(Cl-O2). Besides, the thermodynamic and dynamic properties of dominated reaction (1) at different temperature were studied with statistic thermodynamic method and Eyring transition state theory adjusted by Wigner means, from which the proper temperature (500- 1200 K) of reaction (1) could be estimated. Finally, the thermo- dynamic and dynamic properties of insertion reaction mechanisms (CF2, CX2 (X = Cl, Br) with CH2O) were compared and discussed.  相似文献   

7.
A kinetic study of the hexacyanoferrate(III)-cyanide redox reaction has been made in connection with development of a new catalytic method for copper. The reaction kinetics change with time from first- to second-order dependence with respect to hexacyanoferrate(III). The reaction is nearly inverse first-order with respect to hexacyanoferrate(II) and first-order with respect to cyanide. The reaction shows a strong positive primary salt effect, but a very small increase in the reaction rate with temperature is found. A parallel reaction proceeds with a first-order dependence with respect to hydroxide. A tentative mechanism is proposed for the first reaction, involving the formation of cyanogen radicals. The second reaction corresponds to the well-known decomposition of hexacyanoferrate(III) in alkaline medium. The catalysed reaction exhibits similar kinetics with respect to hexacyanoferrate(II) and (III) but is zero-order with respect to cyanide and hydroxide and first-order with respect to catalyst. The proposed mechanism involves two consecutive interactions of the hexacyanoferrate(III) with copper(I) and with copper(II) cyanide complexes respectively, followed by a 2-electron oxidation of a co-ordinatively bridging cyanide group.  相似文献   

8.
The catalytic water formation reaction on Pt(111) was investigated by kinetic Monte Carlo simulations, where the interaction energy between reaction species and the high mobility of H(2)O molecule was considered. Results obtained clearly reproduce the scanning tunneling microscopy images which show that the reaction proceeds via traveling the reaction fronts on the O-covered Pt(111) surface by creating H(2)O islands backwards. The reaction front is a mixed layer of OH and H(2)O with a (square root 3 x square root 3)R30(o) structure. Coverage change during the reaction is also reproduced in which the reaction consists of three characteristic processes, as observed by the previous experiments. The simulation also revealed that the proton transfer from H(2)O to OH plays an important role to propagate the water formation.  相似文献   

9.
实验发现偏二甲肼(UDMH)在溴酸钾-鲁米诺化学发光反应体系中的后化学发光反应.在对这一后化学发光反应的动力学性质、发光条件,包括溴酸钾浓度、鲁米诺浓度、管长、流速和酸碱度条件等研究的基础上,建立了后化学发光反应法测定偏二甲肼的新方法,并讨论了其可能的反应机理.该方法的线性范围为1.0×10-7~1.0×10-5g/L...  相似文献   

10.
In contrast to the reaction of benzoquinones with β-enaminoesters providing indoles (Nenitzescu reaction), the tandem one-pot reaction of the Blaise reaction intermediate, zinc bromide complex of β-enaminoesters, with benzoquinone affords 5-hydroxy-α-(aminomethylene)benzofuran-2(3H)-ones in good to excellent yields (tandem Blaise-Nenitzescu reaction).  相似文献   

11.
研究在高氯酸银作用下,三苯基环戊二烯扩环氧化生成三苯基取代吡喃盐的反应,并初步探讨了反应机理  相似文献   

12.
2-苯基吲哚 (1a) 在甲醇中的染料敏化光氧化反应给出2-苯基-2-(2'-苯基-3'-吲哚基)二氢吲哚-3-酮 (2a) 和2-甲氧基-2-苯基二氢吲哚-3-酮 (4a), 相应N-甲基取代产物由1-甲基-2-苯基吲哚 (1b) 的类似反应获得。发现反应产物分布随吲哚 (1) 的浓度和介质酸度的变化而变化。对反应机理进行了推测, 其中当1a的反应在乙腈中进行时, 分离到了相应的反应中间体: 2-苯基-3H-吲哚-3-酮 (3a)。  相似文献   

13.
A sodium chloride (NaCl) catalyst (0.1 w/w %) lowers the oxidation temperature of graphitized multiwalled carbon nanotubes: MWCNT-20 (diameter: 20-70 nm) and MWCNT-80 (diameter: 80-150 nm). The analysis of the reaction kinetics indicates that the oxidation of MWCNT-20 and MWCNT-80 mixed with no NaCl exhibits single reaction processes with activation energies of E(a) = 159 and 152 kJ mol(-1), respectively. The oxidation reaction in the presence of NaCl is shown to consist of two different reaction processes, that is, a first reaction and a second reaction process. The first reaction process is dominant at a low temperature of around 600 degrees C, while the second reaction process becomes more dominant than the first one in a higher temperature region. The activation energies of the first reaction processes (MWCNT-20: E(a1) = 35.7 kJ mol(-1); MWCNT-80: E(a1) = 43.5 kJ mol(-1)) are much smaller than those of the second reaction processes (MWCNT-20: E(a2) = 170 kJ mol(-1); MWCNT-80: E(a2) = 171 kJ mol(-1)). The comparison of the kinetic parameters and the results of the spectroscopic and microscopic analyses imply that the lowering of the oxidation temperature in the presence of NaCl results from the introduction of disorder into the graphitized MWCNTs (during the first reaction process), thus increasing the facility of the oxidation reaction of the disorder-induced nanotubes (in the second reaction process). It is found that the larger nanopits and cracks on the outer graphitic layers are caused by the catalytic effect of NaCl. Therefore, the NaCl-mixed samples showed more rapid and stronger oxidation compared with that of the nonmixed samples at the same residual quantity.  相似文献   

14.
双噁唑啉手性配体已广泛用于不对称Henry反应、环丙烷化反应、Aldol反应、烷基化反应、环加成反应中,并表现出很高的对映选择性和催化活性,成为最有用的手性配体之一。文章综述了近10年来双噁唑啉手性配体及高分子受载手性双噁唑啉在不对称合成中的研究进展。  相似文献   

15.
In this article, a simple method for the synthesis of bis(di(indolyl)aryl)methanes is described. The iodine‐catalyzed (5 mol %) reaction of indoles with various bis(salicylaldehyde) derivatives affords the bis(di(indolyl)aryl)methanes in excellent yields. The reaction works well under mild reaction condition with shorter reaction time.  相似文献   

16.
Metathesis (exchange) reactions offer the possibility of controlling temperature through a judicious choice of precursors. Here, a reaction between AlCl(3) and Ca(3)N(2) is found to produce phase-pure aluminum nitride (AlN) in seconds. The CaCl(2) byproduct salt, whose formation drives this highly exothermic reaction, is simply washed away after reaction completion. SEM images demonstrate that the AlN product is a micron-sized powder, while TEM shows well-formed crystallites. Thermodynamic calculations indicate that a reaction temperature of 2208 K could be reached under adiabatic conditions. Using an in situ thermocouple and a stainless steel reactor vessel to hold the precursors, a reaction temperature of 1673 K is measured 0.8 s after initiation. Switching to a thermally insulating ceramic vessel produces a maximum reaction temperature of 2010 K because of the more nearly adiabatic conditions. The high reaction temperature appears to be critical to forming phase-pure AlN. Experiments with Li(3)N, instead of Ca(3)N(2), produce lower temperatures (1513 K), resulting in both Al and Al(2)O(3) impurities.  相似文献   

17.
The dynamic cure kinetics of thermosetting acetylene-terminated sulfone (ATS) and two blends prepared by the ATS and thermoplastic bisphenol A polysulfone (PSF), polyary-lethersulfone with cardo group (PES-C) were determinated by differential scanning calori-metry (DSC). The addition of polysulfone's resin increases the temperature of initial reaction and decreases the activation energy of cure reaction(E), pre-exponnential factor (LnA), and heat of cure reaction (AH). The temperature of reaction peak and final reaction and the reaction order(n) have been no effect.  相似文献   

18.
近年来,半互穿聚合物网络(SIPN)概念被用来研制能结合热塑性聚合物的加工性和热固性聚合物的高温性能的大分子体系,用于复合材料耐高温树脂基体。例如:乙炔端基酰亚胺低聚物与热塑性聚酰亚胺基SIPN,线性聚酰亚胺与热固性双马来酰亚胺基SIPN以及热塑性树脂与双腈基SIPN已有报道。研究结果表明共混物起到协同作用,易于加工并具有优异的性能。乙炔端基砜(ATS)树脂具有与聚砜树脂相类似的结构,被认为在将来代替环氧用于高性能粘合剂和复合材料树脂基体的候选者之一。其另  相似文献   

19.
朱益忠  张喜全  刘飞  顾红梅 《应用化学》2015,32(11):1240-1245
以(5R)-3-(4-溴-3-氟苯基)-5-羟甲基噁唑烷-2-酮为起始原料,在[PdCl2(dppf)]·CH2Cl2催化下与联硼酸频那醇酯反应得到硼化物,继而与5-溴-2-(2-甲基-2H-四唑-5-基)吡啶进行Suzuki反应得到特地唑胺,收率82.9%。 分别考察了催化体系对硼化反应和Suzuki反应的影响,确定了较佳的反应条件。 特地唑胺与二苄基N,N-二异丙基亚磷酰胺反应得到二苄基保护的磷酸特地唑胺,随后经Pd/C脱苄得到磷酸特地唑胺,总收率66.2%。  相似文献   

20.
Nanosecond time-resolved resonance Raman (ns-TR(3)) spectroscopy was employed to investigate the photoinduced reactions of 3-(hydroxymethyl)benzophenone (1) in acetonitrile, 2-propanol, and neutral and acidic aqueous solutions. Density functional theory calculations were utilized to help the interpretation of the experimental spectra. In acetonitrile, the neutral triplet state 1 [denoted here as (m-BPOH)(3)] was observed on the nanosecond to microsecond time scale. In 2-propanol this triplet state appeared to abstract a hydrogen atom from the solvent molecules to produce the aryphenyl ketyl radical of 1 (denoted here as ArPK of 1), and then this species underwent a cross-coupling reaction with the dimethylketyl radical (also formed from the hydrogen abstraction reaction) to form a long-lived light absorbing transient species that was tentatively identified to be mainly 2-(4-(hydroxy(3-(hydroxymethyl)phenyl)methylene)cyclohexa-2,5-dienyl)propan-2-ol. In 1:1 H(2)O:CH(3)CN aqueous solution at neutral pH, (m-BPOH)(3) reacted with water to produce the ArPK of 1 and then underwent further reaction to produce a long-lived light absorbing transient species. Three photochemical reactions appeared to take place after 266 nm photolysis of 1 in acidic aqueous solutions, a photoreduction reaction, an overall photohydration reaction, and a novel photoredox reaction. TR(3) experiments in 1:1 H(2)O:CH(3)CN aqueous solution at pH 2 detected a new triplet biradical species, which is associated with an unusual photoredox reaction. This reaction is observed to be the predominant reaction at pH 2 and seems to face competition from the overall photohydration reaction at pH 0.  相似文献   

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