排序方式: 共有37条查询结果,搜索用时 15 毫秒
1.
Guan X Lin X Kwok WM Du Y Li YL Zhao C Wang D Phillips DL 《The journal of physical chemistry. A》2005,109(6):1247-1256
Ultraviolet photolysis of low concentrations of CH2I2 in methanol solution found that CH2I2 is converted into dimethoxymethane and some H+ and I- products. Picosecond time-resolved resonance Raman (ps-TR3) experiments observed that the isodiiodomethane (CH2I-I) photoproduct decayed faster as the concentration of methanol increases, suggesting that isodiiodomethane is reacting with methanol. Ab initio calculations indicate isodiiodomethane is able to react with methanol via an O-H insertion/HI elimination to form an iodoether (ICH2-O-CH3) and HI products. The iodoether can then further react via another O-H insertion/HI elimination reaction to form the dimethoxymethane (CH3-O-CH2-O-CH3) observed in the photochemistry experiments. A reaction mechanism consistent with these experimental and theoretical observations is proposed. 相似文献
2.
Kwok WM Zhao C Guan X Li YL Du Y Phillips DL 《The Journal of chemical physics》2004,120(19):9017-9032
A combined experimental and theoretical study of the ultraviolet photolysis of CH2I2 in water is reported. Ultraviolet photolysis of low concentrations of CH2I2 in water was experimentally observed to lead to almost complete conversion into CH2(OH)2 and 2HI products. Picosecond time-resolved resonance Raman spectroscopy experiments in mixed water/acetonitrile solvents (25%-75% water) showed that appreciable amounts of isodiiodomethane (CH2I-I) were formed within several picoseconds and the decay of the CH2I-I species became substantially shorter with increasing water concentration, suggesting that CH2I-I may be reacting with water. Ab initio calculations demonstrate the CH2I-I species is able to react readily with water via a water-catalyzed O--H-insertion and HI-elimination reaction followed by its CH2I(OH) product undergoing a further water-catalyzed HI-elimination reaction to make a H2C=O product. These HI-elimination reactions produce the two HI leaving groups observed experimentally and the H2C=O product further reacts with water to produce the other final CH2(OH)2 product observed in the photochemistry experiments. These results suggest that CH2I-I is the species that reacts with water to produce the CH2(OH)2 and 2HI products seen in the photochemistry experiments. The present study demonstrates that ultraviolet photolysis of CH2I2 at low concentration leads to efficient dehalogenation and release of multiple strong acid (HI) leaving groups. Some possible ramifications for the decomposition of polyhalomethanes and halomethanols in aqueous environments as well as the photochemistry of polyhalomethanes in the natural environment are briefly discussed. 相似文献
3.
Yinwu Li Jiahao Liu Dr. Xiao Huang Prof. Dr. Ling-Bo Qu Prof. Dr. Cunyuan Zhao Prof. Dr. Robert Langer Prof. Dr. Zhuofeng Ke 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(60):13785-13798
As a new type of bifunctional catalyst, the Lewis acid transition-metal (LA-TM) catalysts have been widely applied for hydrogen activation. This study presents a mechanistic framework to understand the LA-TM-catalyzed H2 activation through DFT studies. The mer(trans)-homolytic cleavage, the fac(cis)-homolytic cleavage, the synergetic heterolytic cleavage, and the dissociative heterolytic cleavage should be taken as general mechanisms for the field of LA-TM catalysis. Four typical LA-TM catalysts, the Z-type κ4-L3B-Rh complex tri(azaindolyl)borane-Rh, the X-type κ3-L2B-Co complex bis-phosphino-boryl (PBP)-Co, the η2-BC-type κ3-L2B-Pd complex diphosphine-borane (DPB)-Pd, and the Z-type κ2-LB-Pt complex (boryl)iminomethane (BIM)-Pt are selected as representative models to systematically illustrate their mechanistic features and explore the influencing factors on mechanistic variations. Our results indicate that the tri(azaindolyl)borane-Rh catalyst favors the synergetic heterolytic mechanism; the PBP-Co catalyst prefers the mer(trans)-homolytic mechanism; the DPB-Pd catalyst operates through the fac(cis)-homolytic mechanism, whereas the BIM-Pt catalyst tends to undergo the dissociative heterolytic mechanism. The mechanistic variations are determined by the coordination geometry, the LA-TM bonding nature, the electronic structure of the TM center, and the flexibility or steric effect of the LA ligands. The presented mechanistic framework should provide helpful guidelines for LA-TM catalyst design and reaction developments. 相似文献
4.
Wanxia Huang Chaogang Li Maosheng Wang Yong Zhou Cunyuan Zhu Kuanguo Li Xinyan Yang Fabao Zhang 《Physics letters. A》2019,383(13):1520-1525
We investigate simulated and theoretically the optical properties of the metamaterial, composed of two bigger split ring resonators and one smaller split ring resonator in unit cell. We observe the magic phenomena that one mode B is inhibited from strong to weak then disappears while another mode A appears and becomes stronger and stronger as asymmetric degree increases. The results show the mode A originates from the destructive interference between the dipole mode and the quadrapole mode, and its strength is proportional to the cross coupling coefficient of near-field. The disappearance of the mode B is due to the competition between the mode B and the mode A, and the variation of strength is proportional to the frequency shift of the dark mode. That is, with asymmetric degree increasing, the mode B converts into the mode A. These phenomena are explained very well by the temporal coupled-mode theory. Our metamaterial provides a kind of new design for understanding the interaction between light and matter. 相似文献
5.
Cunyuan Pei Yameng Yin Xiaobin Liao Fangyu Xiong Qinyou An Mengda Jin Yan Zhao Liqiang Mai 《Journal of Energy Chemistry》2021,(7):586-592
The selection of the most suitable crystal structure for ions storage and the investigation of the corresponding reaction mechanism is still an ongoing challeng... 相似文献
6.
Li ZF Fan Y DeYonker NJ Zhang X Su CY Xu H Xu X Zhao C 《The Journal of organic chemistry》2012,77(14):6076-6086
The mechanism and intermediates of hydroalkylation of aryl alkynes via C(sp(3))-H activation through a platinum(II)-centered catalyst are investigated with density functional theory at the B3LYP/[6-31G(d) for H, O, C; 6-31+G(d,p) for F, Cl; SDD for Pt] level of theory. Solvent effects on reactions were explored using calculations that included a polarizable continuum model for the solvent (THF). Free energy diagrams for three suggested mechanisms were computed: (a) one that leads to formation of a Pt(II) vinyl carbenoid (Mechanism A), (b) another where the transition state implies a directed 1,4-hydrogen shift (Mechanism B), and (c) one with a Pt-aided 1,4-hydrogen migration (Mechanism C). Results suggest that the insertion reaction pathway of Mechanism A is reasonable. Through 4,5-hydrogen transfer, the Pt(II) vinyl carbenoid is formed. Thus, the stepwise insertion mechanism is favored while the electrocyclization mechanism is implausible. Electron-withdrawing/electron-donating groups substituted at the phenyl and benzyl sp(3) C atoms slightly change the thermodynamic properties of the first half of Mechanism A, but electronic effects cause a substantial shift in relative energies for the second half of Mechanism A. The rate-limiting step can be varied between the 4,5-hydrogen shift process and the 1,5-hydrogen shift step by altering electron-withdrawing/electron-donating groups on the benzyl C atom. Additionally, NBO and AIM analyses are applied to further investigate electronic structure changes during the mechanism. 相似文献
7.
Zhao C Lin X Kwok WM Guan X Du Y Wang D Hung KF Phillips DL 《Chemistry (Weinheim an der Bergstrasse, Germany)》2005,11(4):1093-1108
A combined experimental and theoretical study of the UV photolysis of a typical tetrahalomethane, CBr4, in water and acetonitrile/water was performed. Ultraviolet photolysis of low concentrations of CBr4 in water mostly leads to the production of four HBr leaving groups and CO2. Picosecond time-resolved resonance Raman (Ps-TR3) experiments and ab initio calculations indicate that water-catalyzed O-H insertion/HBr elimination of the isomer of CBr4 and subsequent reactions of its products lead to the formation of these products. The UV photolyses of di-, tri-, and tetrahalomethanes at low concentrations in water-solvated environments are compared to one another. This comparison enables a general reaction scheme to be deduced that can account for the different products produced by UV photolysis of low concentrations of di-, tri-, and tetrahalomethanes in water. The fate of the (halo)formaldehyde intermediate in the chemical reaction mechanism is the key to determining how many strong acid leaving groups are produced and which carbon atom final product is likely formed by UV photolysis of a polyhalomethane at low concentrations in a water-solvated environment. 相似文献
8.
A systematic ab initio investigation of the water-assisted decomposition of chloromethanol, dichloromethanol, and formyl chloride as a function of the number of water molecules (up to six) building up the solvation shell is presented. The decomposition reactions of the chlorinated methanols and formyl chloride are accelerated substantially as the reaction system involves additional explicit coordination of water molecules. Rate constants for the decomposition of chlorinated methanols and formyl chloride were found to be in reasonable agreement with previous experimental observations of aqueous phase decomposition reactions of dichloromethanol [CHCl(2)(OH)] and formyl chloride. For example, using the calculated activation free energies in conjunction with the stabilization free energies from the ab initio calculations, the rate constant was predicted to be 1.2-1.5 x 10(4) s(-1) for the decomposition of formyl chloride in aqueous solution. This is in good agreement with the experimental rate constant of about 10(4) s(-1) reported in the literature. The mechanism for the water catalysis of the decomposition reactions as well as probable implications for the decomposition of these chlorinated methanol compounds and formaldehydes in the natural environment and as intermediates in advanced oxidation processes are briefly discussed. 相似文献
9.
The trivalent samarium carbenoid I2SmCH2I-promoted cyclopropanation reactions with ethylene have been investigated and are predicted to be highly reactive, similarly to the divalent samarium carbenoid ISmCH2I. The methylene transfer and carbometalation pathways were explored and compared with and without coordination of THF solvent molecules to the carbenoid. The methylene transfer was found to be favored, with the barrier to reaction going from 12.9 to 9.2 kcal/mol compared to barriers of 15.4-17.5 kcal/mol for the carbometalation pathway upon the addition of one THF molecule. 相似文献
10.