Electrochemical production of hydrogen from water requires the development ofelectrocatalysts that are active,stable,and low-cost for water splitting.To address these challenges,researchers are increasingly exploring ...Electrochemical production of hydrogen from water requires the development ofelectrocatalysts that are active,stable,and low-cost for water splitting.To address these challenges,researchers are increasingly exploring binder-free electrocatalytic integratedelectrodes (IEs) as an alternative to conventional powder-based electrode preparation methods,for the former is highly desirable to improve the catalytic activity and long-term stability for large-scale applications of electrocatalysts.Herein,we demonstrate a laser-inducedhydrothermal reaction (LIHR) technique to grow NiMoO4nanosheets on nickel foam,which is then calcined under H2/Ar mixed gases to prepare the IE IE-NiMo-LR.This electrode exhibits superior hydrogen evolution reaction performance,requiring overpotentials of 59,116 and143 mV to achieve current densities of 100,500 and 1000 mA·cm-2.During the 350 h chronopotentiometry test at current densities of 100 and 500 m A·cm-2,the overpotentialremains essentially unchanged.In addition,NiFe-layered double hydroxide grown on Ni foam is also fabricated with the same LIHR method and coupled with IE-NiMo-IR to achieve water splitting.This combination exhibits excellent durability under industrial current density.The energy consumption and production efficiency of the LIHR method are systematicallycompared with the conventional hydrothermal method.The LIHR method significantly improves the production rate by over 19 times,while consuming only 27.78%of the total energy required by conventional hydrothermal methods to achieve the same production.展开更多
A series of experiments were conducted in a self-made smog chamber at （300 ＋ 1） K and 1.01 × 10^5 Pa to simulate the photochemical reaction of ethyl methyl sulfide （EMS） and NOx. The results showed that the ...A series of experiments were conducted in a self-made smog chamber at （300 ＋ 1） K and 1.01 × 10^5 Pa to simulate the photochemical reaction of ethyl methyl sulfide （EMS） and NOx. The results showed that the higher the initial concentration of EMS, the more ozone was generated in the simulative reactions. It was found that the light intensity plays a very important role in the evaluation of ozone formation potential for EMS. The parameters of d（Oa-NO） and IR （incremental reactivity） were used to quantify the potential of EMS on ozone formation. The obtained maximum IR values in this article for the five simulative reactions were 1.55 × 10^-2, 0.99 × 10^-2, 1.36 × 10^-2, 2.47 × 10^-2, and 1.65 × 10^-2, respectively. A comparison between the results we obtained here and the results we obtained previously for di-tert-butyl peroxide and acetylene showed that the potential reactivity of EMS on ozone formation was at a relatively low level.展开更多
The photochemical reaction of magnesium tetraphenyl porphyrin （MgTPP） with O2 was studied in CH2Cl2 by steady-state fluorescence, UV-vis absorption, FTIR and MALDI-TOF MS measurements. These spectra indicate that O2...The photochemical reaction of magnesium tetraphenyl porphyrin （MgTPP） with O2 was studied in CH2Cl2 by steady-state fluorescence, UV-vis absorption, FTIR and MALDI-TOF MS measurements. These spectra indicate that O2 can react with MgTPP excited by irradiation, forming the stable 1：1 coordinated adduct of MgTPP-O2. In the adduct, the oxygen atoms of O2 may insert in the Mg-N bonds in MgTPP and bind with the nitrogen atoms of MgTPP to form N-O-Mg bonds.展开更多
The photochemical reaction of magnesium tetraphenyl porphyrin（MgTPP） with sulfur dioxide（SO_2） was investigated in dichloromethane（CH_2Cl_2） by steady-state fluorescence,UV-vis absorption,MS,and XRD spectroscopi...The photochemical reaction of magnesium tetraphenyl porphyrin（MgTPP） with sulfur dioxide（SO_2） was investigated in dichloromethane（CH_2Cl_2） by steady-state fluorescence,UV-vis absorption,MS,and XRD spectroscopic techniques.These spectra showed that under irradiation MgTPP reacted with SO_2 to form 1：1 molecular adduct at first step.During the process of keeping irradiation and maintaining the flow of SO_2,SO_2 was reduced into S^（2-） by MgTPP and the results were detected using MS and XRD techniques.Understanding the photochemical reaction of MgTPP with SO_2 is of key interest in elucidating fundamental photochemical reaction mechanisms associated with this class of chlorophyll in the presence of SO_2.展开更多
Photochemical reactions of poly(3-butoxythiophene-2,5-diyl) with chloroform under irradiation with light were studied. The reactions were separately carried out under air, oxygen, and nitrogen. The obtained results sh...Photochemical reactions of poly(3-butoxythiophene-2,5-diyl) with chloroform under irradiation with light were studied. The reactions were separately carried out under air, oxygen, and nitrogen. The obtained results showed that this reaction belongs to the pseudo-first-order reaction with a rate constant kobs of 1.4×10?5 s?1 at room temperature. The presence or absence of air, oxygen, and nitrogen did not have obvious effects on the reaction rate under irradiation with light.展开更多
Biobased aromatic-aliphatic polyols were previously synthesized from a thermal thiol-ene reaction of propoxylated cardanol with 2-mercaptoethanol(ME)in the presence of azobisisobutyronitrile(AIBN)as a radical initiato...Biobased aromatic-aliphatic polyols were previously synthesized from a thermal thiol-ene reaction of propoxylated cardanol with 2-mercaptoethanol(ME)in the presence of azobisisobutyronitrile(AIBN)as a radical initiator.Cardanol used for this purpose was obtained as a dark-brown liquid(Gardner Color Reference^18).The photochemical thiol-ene reaction can also be used to prepare aromatic-aliphatic polyols by employing cardanol.Via the photochemical thiol-ene reaction,2-mercaptoethanol was added successfully to C=C double bond of cardanol,suggesting that phenolic group may not play an inhibitory role in the radical thiol-ene reaction.However,we preferred to alkoxylate the phenolic hydroxyl group of cardanol,which is much more reactive with isocyanates than phenolic hydroxyls,to generate a new aliphatic hydroxyl group.Furthermore,the functionality of polyols was also improved by two methods:1)using 1-thio-glycerol instead of 2-mercaptoethanol and 2)using alkoxylated cardanol with glycidol(Cardanol-GLY)instead of propoxylated cardanol(Cardanol-PO).These polyols were then used in preparation of rigid polyurethane foams that can be useful in various applications such as insulation of freezers,pipes and storage tanks in food and chemical industries.展开更多
The photochemical reaction of bicyclo[4.1.0]heptane was studied at the complete active space SCF（CASSCF） level with a 6-31G^＊ basis set. A muhireference MP2 algorithm that has been implemented in the Gaussian progr...The photochemical reaction of bicyclo[4.1.0]heptane was studied at the complete active space SCF（CASSCF） level with a 6-31G^＊ basis set. A muhireference MP2 algorithm that has been implemented in the Gaussian program was used to correct the energetics for the dynamic correlation. Starting from the Franck-Condon excitation of bicyclo [ 4.1.0 ] heptane, the reaction is via two bonds＇ breakage to give rise to 1,6-heptdiene. One internal conversion （IC） and two intersystem crossing points（ISC） were located and are discussed separately. The reaction proceeds to its own characteristic product on the ground state.展开更多
Photoreaction of particle-bound 1-nitropyrehe (1-NP) under simulated atmospheric condition has been studied. When 1-NP coated on the surface of silica gel was suspended in a stream of nitrogen, oxygen or air, respecti...Photoreaction of particle-bound 1-nitropyrehe (1-NP) under simulated atmospheric condition has been studied. When 1-NP coated on the surface of silica gel was suspended in a stream of nitrogen, oxygen or air, respectively, and exposed to intensive light of xenon lamp, photochemical reaction took place. The result of kinetic study showed it to be of the second order. The photoreaction products were identified by off-line HPLC/MS as 1,6-pyrenequinone, 1,8-pyrenequinone, trinitro-hydroxypyrene, dinitrohydroxypyrene, 6,6'- dipyrenenone, etc. The mutagenicity of photochemical reaction products is higher in oxygen and air, and lower in nitrogen than that of the precursor 1-NP, as detected by the Ames Bioassay.展开更多
A new rhodium(Ⅱ)porphyrin complex was isolated by chromatography from the photochemical reac- tion of(μ—tetraphenylporphyrinato)bis[dicarbonylrhodium(Ⅰ)]with pyridine in benzene and has been charac- terized.From t...A new rhodium(Ⅱ)porphyrin complex was isolated by chromatography from the photochemical reac- tion of(μ—tetraphenylporphyrinato)bis[dicarbonylrhodium(Ⅰ)]with pyridine in benzene and has been charac- terized.From the results,the reaction mechanism is proposed.展开更多
The solid state photochemical reaction of nitrobenzaldehyde with indole was investigated. Seven hey products were identified by IR, MS,^(1)H HMR and elemental analysis.
High quality ultrafine Si powders have been synthesized from SiH4 by laser induced gas phase reaction. The powders prduced under different synthesis conditions have mean particle size of 10-120nm in diam. with narrow ...High quality ultrafine Si powders have been synthesized from SiH4 by laser induced gas phase reaction. The powders prduced under different synthesis conditions have mean particle size of 10-120nm in diam. with narrow particle size distribution, and free of hard agglomerates.The powders are polycrystalline with the ratio of mean grain to particle diameter being between 0.3-0.7. The size of the powder increases with increasing laser power and reaction pressure,but decreases with increasing silane gas flow rate and the addition of Ar diluent. Grain sizes drop distinctly with the rise of the addition of Ar gas and laser power, but change little with the gas flow rate and reaction temperature. The formation of Si particles under different synthesis conditions is discussed展开更多
Bovine serum albumin (BSA) was labeled with 9,10-anthraquinone and the photochemical fluorimetric reactivity of the covalently conjugated 9,10-anthraquinone was remarkably improved. The mechanism for the enhancement i...Bovine serum albumin (BSA) was labeled with 9,10-anthraquinone and the photochemical fluorimetric reactivity of the covalently conjugated 9,10-anthraquinone was remarkably improved. The mechanism for the enhancement in the photochemical reactivity of conjugated 9,10-anthraquinone with BSA was discussed.展开更多
Photochemical reactions of microcystin-LR, a toxic compound produced by some blue green algae, were investigated. Ultraviolet absorption of microcystin-LR was assessed. Time-dependent density functional theory (TDDFT)...Photochemical reactions of microcystin-LR, a toxic compound produced by some blue green algae, were investigated. Ultraviolet absorption of microcystin-LR was assessed. Time-dependent density functional theory (TDDFT) calculations indicated that absorption peak at 238 nm was mainly due to excitation of electrons from the linear chain structure Adda of microcystin-LR. Irradiation of microcystin-LR with UV light resulted in the reduction of the 238 nm absorption peak and the appearance of a new peak at 300 nm. Density functional theory (DFT) and TDDFT calculations with a model molecule suggested that this 300 nm peak was due to tricyclo-Adda microcystin-LR, an intermediate in photochemical reactions of microcystin-LR. Analysis of the rate of this photochemical reaction showed that it was a first order reaction.展开更多
We report on the successful fabrication of highly branched Cu S nanocrystals by laser-induced photochemical reaction.Surprisingly, the single-crystalline nature with preferential alignment of the（107） orientation ca...We report on the successful fabrication of highly branched Cu S nanocrystals by laser-induced photochemical reaction.Surprisingly, the single-crystalline nature with preferential alignment of the（107） orientation can be well improved during the moderate growth process. The branch length drastically increases from about 5 nm to 6 μm with an increase of photochemical reaction time（0-40 min）. The absorption spectra of as-prepared Cu S nanodendrites show that localized surface plasmon resonance（LSPR） peaks can be modulated from about 1037 nm to 1700 nm with an increase of branch length. Our results have a promising potential for photodynamic therapy and biological imaging application.展开更多
In the quest for new agrochemicals and pharmaceuticals,chemists seek access to reliable and mild synthetic techniques to allow for the systematic modification of chemical structures,exploration of unexplored chemical ...In the quest for new agrochemicals and pharmaceuticals,chemists seek access to reliable and mild synthetic techniques to allow for the systematic modification of chemical structures,exploration of unexplored chemical space,and facilitation of practical synthesis in their search for novel agrochemicals and pharmaceuticals.In this regard,photocatalytic reactions enabled the synthesis of intricate and more functionalized compounds.This review overviews the developed synthetic methodologies and their utility in the chemical synthesis of pharmaceuticals.This review also offers in-depth insights into contemporary photoredox reactions such as allylic additions,cyclization,reductive cross-coupling,C–H activation,ring opening,oxidative cross-coupling,dehydrogenation,desulphonation,and decarboxylation.It provides a positive outlook for the promising future of this field.展开更多
The resonance light-scattering (RLS) of human serum albumin (HSA) and bovine serum albumin (BSA) is reported for the first time, and applied to study photochemical reaction of HSA and BSA. The fact of photocrosslinkin...The resonance light-scattering (RLS) of human serum albumin (HSA) and bovine serum albumin (BSA) is reported for the first time, and applied to study photochemical reaction of HSA and BSA. The fact of photocrosslinking self-association effect in HSA and BSA solutions is identified by the enhancement of RLS. The fluorescence quenching at about 350 nm and 700 nm proves that tryptophan (Trp) residues are one of the photochemical activity sites in HSA and BSA molecules. The Rayleigh scattering (RS) spectra of HSA and BSA that were neglected in fluorescence spectra before are found at about 296 nm, 592 nm and 888 nm for the first time, and are of adventageous to studying the aggregation of HSA or BSA. The possible photochemical reaction mechanism is also proposed.展开更多
The photochemical kinetics of phenanthrenequinone （PQ） doped poly （methyl methacrylate） photopolymer in holographic recording was studied theoretically and experimentally. The diffusion of PQ molecules during holo...The photochemical kinetics of phenanthrenequinone （PQ） doped poly （methyl methacrylate） photopolymer in holographic recording was studied theoretically and experimentally. The diffusion of PQ molecules during holographic recording was negligible because of its small diffusion coefficient at room temperature. A photochemical reaction kinetics model of PQ/PMMA was established. The analytical expressions for the temporal variations of transmittance and diffraction efficiency were derived. By fitting the experimental curves, some parameters related with the polymer components were obtained by the proposed model, which can be used to analyze the photochemical process and will be helpful to the optimization of material preparation.展开更多
基金financial support from The University of Manchester to cover his PhD tuition fees for him to carry out this workChina National High-end Foreign Experts Recruitment Plan Project (G2023018001L) for partially supporting the work。
文摘Electrochemical production of hydrogen from water requires the development ofelectrocatalysts that are active,stable,and low-cost for water splitting.To address these challenges,researchers are increasingly exploring binder-free electrocatalytic integratedelectrodes (IEs) as an alternative to conventional powder-based electrode preparation methods,for the former is highly desirable to improve the catalytic activity and long-term stability for large-scale applications of electrocatalysts.Herein,we demonstrate a laser-inducedhydrothermal reaction (LIHR) technique to grow NiMoO4nanosheets on nickel foam,which is then calcined under H2/Ar mixed gases to prepare the IE IE-NiMo-LR.This electrode exhibits superior hydrogen evolution reaction performance,requiring overpotentials of 59,116 and143 mV to achieve current densities of 100,500 and 1000 mA·cm-2.During the 350 h chronopotentiometry test at current densities of 100 and 500 m A·cm-2,the overpotentialremains essentially unchanged.In addition,NiFe-layered double hydroxide grown on Ni foam is also fabricated with the same LIHR method and coupled with IE-NiMo-IR to achieve water splitting.This combination exhibits excellent durability under industrial current density.The energy consumption and production efficiency of the LIHR method are systematicallycompared with the conventional hydrothermal method.The LIHR method significantly improves the production rate by over 19 times,while consuming only 27.78%of the total energy required by conventional hydrothermal methods to achieve the same production.
基金supported by the Knowledge Innovation Program of the Chinese Academy of Sciences(No. KZCX2-YW-205)the National Natural Sci-ence Foundation of China (No. 20577052, 20673123,20503035).
文摘A series of experiments were conducted in a self-made smog chamber at （300 ＋ 1） K and 1.01 × 10^5 Pa to simulate the photochemical reaction of ethyl methyl sulfide （EMS） and NOx. The results showed that the higher the initial concentration of EMS, the more ozone was generated in the simulative reactions. It was found that the light intensity plays a very important role in the evaluation of ozone formation potential for EMS. The parameters of d（Oa-NO） and IR （incremental reactivity） were used to quantify the potential of EMS on ozone formation. The obtained maximum IR values in this article for the five simulative reactions were 1.55 × 10^-2, 0.99 × 10^-2, 1.36 × 10^-2, 2.47 × 10^-2, and 1.65 × 10^-2, respectively. A comparison between the results we obtained here and the results we obtained previously for di-tert-butyl peroxide and acetylene showed that the potential reactivity of EMS on ozone formation was at a relatively low level.
基金Jiangxi Boyuan Industry Co.Ltd.(Jiangxi Province,China).
文摘The photochemical reaction of magnesium tetraphenyl porphyrin （MgTPP） with O2 was studied in CH2Cl2 by steady-state fluorescence, UV-vis absorption, FTIR and MALDI-TOF MS measurements. These spectra indicate that O2 can react with MgTPP excited by irradiation, forming the stable 1：1 coordinated adduct of MgTPP-O2. In the adduct, the oxygen atoms of O2 may insert in the Mg-N bonds in MgTPP and bind with the nitrogen atoms of MgTPP to form N-O-Mg bonds.
基金financed by Yongfeng Boyuan Industry Co.,Ltd.,(Jiangxi province,China).Thanks to Professor Wenting Hua and Professor Hongcheng Gao(Peking University,China) for their suggestions on the photochemical interaction mechanism of MgTPP with SO_2.
文摘The photochemical reaction of magnesium tetraphenyl porphyrin（MgTPP） with sulfur dioxide（SO_2） was investigated in dichloromethane（CH_2Cl_2） by steady-state fluorescence,UV-vis absorption,MS,and XRD spectroscopic techniques.These spectra showed that under irradiation MgTPP reacted with SO_2 to form 1：1 molecular adduct at first step.During the process of keeping irradiation and maintaining the flow of SO_2,SO_2 was reduced into S^（2-） by MgTPP and the results were detected using MS and XRD techniques.Understanding the photochemical reaction of MgTPP with SO_2 is of key interest in elucidating fundamental photochemical reaction mechanisms associated with this class of chlorophyll in the presence of SO_2.
文摘Photochemical reactions of poly(3-butoxythiophene-2,5-diyl) with chloroform under irradiation with light were studied. The reactions were separately carried out under air, oxygen, and nitrogen. The obtained results showed that this reaction belongs to the pseudo-first-order reaction with a rate constant kobs of 1.4×10?5 s?1 at room temperature. The presence or absence of air, oxygen, and nitrogen did not have obvious effects on the reaction rate under irradiation with light.
文摘Biobased aromatic-aliphatic polyols were previously synthesized from a thermal thiol-ene reaction of propoxylated cardanol with 2-mercaptoethanol(ME)in the presence of azobisisobutyronitrile(AIBN)as a radical initiator.Cardanol used for this purpose was obtained as a dark-brown liquid(Gardner Color Reference^18).The photochemical thiol-ene reaction can also be used to prepare aromatic-aliphatic polyols by employing cardanol.Via the photochemical thiol-ene reaction,2-mercaptoethanol was added successfully to C=C double bond of cardanol,suggesting that phenolic group may not play an inhibitory role in the radical thiol-ene reaction.However,we preferred to alkoxylate the phenolic hydroxyl group of cardanol,which is much more reactive with isocyanates than phenolic hydroxyls,to generate a new aliphatic hydroxyl group.Furthermore,the functionality of polyols was also improved by two methods:1)using 1-thio-glycerol instead of 2-mercaptoethanol and 2)using alkoxylated cardanol with glycidol(Cardanol-GLY)instead of propoxylated cardanol(Cardanol-PO).These polyols were then used in preparation of rigid polyurethane foams that can be useful in various applications such as insulation of freezers,pipes and storage tanks in food and chemical industries.
基金Supported by the Yunnan Provincial Science and Technology Department(No. 2003A0003M)
文摘The photochemical reaction of bicyclo[4.1.0]heptane was studied at the complete active space SCF（CASSCF） level with a 6-31G^＊ basis set. A muhireference MP2 algorithm that has been implemented in the Gaussian program was used to correct the energetics for the dynamic correlation. Starting from the Franck-Condon excitation of bicyclo [ 4.1.0 ] heptane, the reaction is via two bonds＇ breakage to give rise to 1,6-heptdiene. One internal conversion （IC） and two intersystem crossing points（ISC） were located and are discussed separately. The reaction proceeds to its own characteristic product on the ground state.
文摘Photoreaction of particle-bound 1-nitropyrehe (1-NP) under simulated atmospheric condition has been studied. When 1-NP coated on the surface of silica gel was suspended in a stream of nitrogen, oxygen or air, respectively, and exposed to intensive light of xenon lamp, photochemical reaction took place. The result of kinetic study showed it to be of the second order. The photoreaction products were identified by off-line HPLC/MS as 1,6-pyrenequinone, 1,8-pyrenequinone, trinitro-hydroxypyrene, dinitrohydroxypyrene, 6,6'- dipyrenenone, etc. The mutagenicity of photochemical reaction products is higher in oxygen and air, and lower in nitrogen than that of the precursor 1-NP, as detected by the Ames Bioassay.
基金Project Supported by Science Research Foundation of Zhongshan University,National Natural Science Foundation of P.R.China and Resarch Fund of Royal Society of Chemistry
文摘A new rhodium(Ⅱ)porphyrin complex was isolated by chromatography from the photochemical reac- tion of(μ—tetraphenylporphyrinato)bis[dicarbonylrhodium(Ⅰ)]with pyridine in benzene and has been charac- terized.From the results,the reaction mechanism is proposed.
文摘The solid state photochemical reaction of nitrobenzaldehyde with indole was investigated. Seven hey products were identified by IR, MS,^(1)H HMR and elemental analysis.
文摘High quality ultrafine Si powders have been synthesized from SiH4 by laser induced gas phase reaction. The powders prduced under different synthesis conditions have mean particle size of 10-120nm in diam. with narrow particle size distribution, and free of hard agglomerates.The powders are polycrystalline with the ratio of mean grain to particle diameter being between 0.3-0.7. The size of the powder increases with increasing laser power and reaction pressure,but decreases with increasing silane gas flow rate and the addition of Ar diluent. Grain sizes drop distinctly with the rise of the addition of Ar gas and laser power, but change little with the gas flow rate and reaction temperature. The formation of Si particles under different synthesis conditions is discussed
文摘Bovine serum albumin (BSA) was labeled with 9,10-anthraquinone and the photochemical fluorimetric reactivity of the covalently conjugated 9,10-anthraquinone was remarkably improved. The mechanism for the enhancement in the photochemical reactivity of conjugated 9,10-anthraquinone with BSA was discussed.
文摘Photochemical reactions of microcystin-LR, a toxic compound produced by some blue green algae, were investigated. Ultraviolet absorption of microcystin-LR was assessed. Time-dependent density functional theory (TDDFT) calculations indicated that absorption peak at 238 nm was mainly due to excitation of electrons from the linear chain structure Adda of microcystin-LR. Irradiation of microcystin-LR with UV light resulted in the reduction of the 238 nm absorption peak and the appearance of a new peak at 300 nm. Density functional theory (DFT) and TDDFT calculations with a model molecule suggested that this 300 nm peak was due to tricyclo-Adda microcystin-LR, an intermediate in photochemical reactions of microcystin-LR. Analysis of the rate of this photochemical reaction showed that it was a first order reaction.
基金Project supported by National Natural Science Foundation of China(Grant Nos.11575102,11105085,11405098,and 11375108)the Fundamental Research Funds of Shandong University,China(Grant No.2015JC007)
文摘We report on the successful fabrication of highly branched Cu S nanocrystals by laser-induced photochemical reaction.Surprisingly, the single-crystalline nature with preferential alignment of the（107） orientation can be well improved during the moderate growth process. The branch length drastically increases from about 5 nm to 6 μm with an increase of photochemical reaction time（0-40 min）. The absorption spectra of as-prepared Cu S nanodendrites show that localized surface plasmon resonance（LSPR） peaks can be modulated from about 1037 nm to 1700 nm with an increase of branch length. Our results have a promising potential for photodynamic therapy and biological imaging application.
文摘In the quest for new agrochemicals and pharmaceuticals,chemists seek access to reliable and mild synthetic techniques to allow for the systematic modification of chemical structures,exploration of unexplored chemical space,and facilitation of practical synthesis in their search for novel agrochemicals and pharmaceuticals.In this regard,photocatalytic reactions enabled the synthesis of intricate and more functionalized compounds.This review overviews the developed synthetic methodologies and their utility in the chemical synthesis of pharmaceuticals.This review also offers in-depth insights into contemporary photoredox reactions such as allylic additions,cyclization,reductive cross-coupling,C–H activation,ring opening,oxidative cross-coupling,dehydrogenation,desulphonation,and decarboxylation.It provides a positive outlook for the promising future of this field.
基金the National Natural Science Foundation of China ! 29961001the Foundation for Talents Striding across the Century of Guangxi
文摘The resonance light-scattering (RLS) of human serum albumin (HSA) and bovine serum albumin (BSA) is reported for the first time, and applied to study photochemical reaction of HSA and BSA. The fact of photocrosslinking self-association effect in HSA and BSA solutions is identified by the enhancement of RLS. The fluorescence quenching at about 350 nm and 700 nm proves that tryptophan (Trp) residues are one of the photochemical activity sites in HSA and BSA molecules. The Rayleigh scattering (RS) spectra of HSA and BSA that were neglected in fluorescence spectra before are found at about 296 nm, 592 nm and 888 nm for the first time, and are of adventageous to studying the aggregation of HSA or BSA. The possible photochemical reaction mechanism is also proposed.
基金Project supported by the Fundamental Research Foundation of COSTIND (Grant No 2320060089)the MOST of China (973 Project Grant No 2007CB307001)Program of Excellent Team in Harbin Institute of Technology
文摘The photochemical kinetics of phenanthrenequinone （PQ） doped poly （methyl methacrylate） photopolymer in holographic recording was studied theoretically and experimentally. The diffusion of PQ molecules during holographic recording was negligible because of its small diffusion coefficient at room temperature. A photochemical reaction kinetics model of PQ/PMMA was established. The analytical expressions for the temporal variations of transmittance and diffraction efficiency were derived. By fitting the experimental curves, some parameters related with the polymer components were obtained by the proposed model, which can be used to analyze the photochemical process and will be helpful to the optimization of material preparation.
