期刊文献+
共找到9,965篇文章
< 1 2 250 >
每页显示 20 50 100
Catalytic Effect of Transition Metal Complexes of Triaminoguanidine on the Thermolysis of Energetic NC/DEGDN Composite
1
作者 Mohammed Dourari Ahmed Fouzi Tarchoun +4 位作者 Djalal Trache Amir Abdelaziz Roufaida Tiliouine Tessnim Barkat Weiqiang Pang 《火炸药学报》 EI CAS CSCD 北大核心 2024年第3期209-219,I0003,共12页
The transition metal complexes of triaminoguanidine(TAG-M,where M=Cobalt(Co)or Iron(Fe))have been prepared.The catalytic effect of these complexes on the thermolysis of energetic composite based on nitrocellulose and ... The transition metal complexes of triaminoguanidine(TAG-M,where M=Cobalt(Co)or Iron(Fe))have been prepared.The catalytic effect of these complexes on the thermolysis of energetic composite based on nitrocellulose and diethylene glycol dinitrate,has been investigated.Extensive characterization of the resulting energetic composites was carried out using scanning electron microscopy(SEM),X-ray diffraction(XRD),Fourier transform infrared spectroscopy(FTIR),and differential scanning calorimetry(DSC).Isoconversional kinetic analysis was performed to determine the Arrhenius parameters associated with the thermolysis of the elaborated energetic formulations.It is found that TAG-M complexes have strong catalytic effect on the thermo-kinetic decomposition of NC/DEGDN by decreasing the apparent activation energy and significantly increased the total heat release.The models that govern the decomposition processes are also studied,and it is revealed that different reaction processes are accomplished by introduction metal complexes of triaminoguanidine.Overall,this study serves as a valuable reference for future research focused on the investigation of catalytic combustion features of solid propellants. 展开更多
关键词 triaminoguanidine transition metal complexes NITROCELLULOSE diethylene glycol dinitrate catalytic effect
下载PDF
Subtraction of liposome signals in cryo-EM structural determination of protein-liposome complexes
2
作者 李首卿 李明 +1 位作者 王玉梅 李雪明 《Chinese Physics B》 SCIE EI CAS CSCD 2024年第8期569-577,共9页
Reconstituting membrane proteins in liposomes and determining their structure is a common method for determining membrane protein structures using single-particle cryo-electron microscopy(cryo-EM).However,the strong s... Reconstituting membrane proteins in liposomes and determining their structure is a common method for determining membrane protein structures using single-particle cryo-electron microscopy(cryo-EM).However,the strong signal of liposomes under cryo-EM imaging conditions often interferes with the structural determination of the embedded membrane proteins.Here,we propose a liposome signal subtraction method based on single-particle two-dimensional(2D)classification average images,aimed at enhancing the reconstruction resolution of membrane proteins.We analyzed the signal distribution characteristics of liposomes and proteins within the 2D classification average images of protein–liposome complexes in the frequency domain.Based on this analysis,we designed a method to subtract the liposome signals from the original particle images.After the subtraction,the accuracy of single-particle three-dimensional(3D)alignment was improved,enhancing the resolution of the final 3D reconstruction.We demonstrated this method using a PIEZO1-proteoliposome dataset by improving the resolution of the PIEZO1 protein. 展开更多
关键词 CRYO-EM protein–liposome complexes liposome signal subtraction 2D classification averaging
下载PDF
Synthesis and Physico-Chemical Characterizations of Novel Hydrazone Ligands and Their Metal Complexes against Hormone-Dependent and Independent Cancers
3
作者 Sommai Patitungkho Kingkaew Patitungkho 《Open Journal of Medicinal Chemistry》 2024年第1期1-12,共12页
This work deals with the synthesis and physicochemical characterizations of a new group of novel retinoidal ligands and their metal complexes. Their in vitro anti-proliferative activities have shown that ligand L1 is ... This work deals with the synthesis and physicochemical characterizations of a new group of novel retinoidal ligands and their metal complexes. Their in vitro anti-proliferative activities have shown that ligand L1 is effective against human breast cancer BT-20 and MCF-7 cell lines. At the same time, compound L2 exerts its effect on human prostate cancer PC-3 and human breast cancer MDA-MB-231 and MCF-7 cell lines respectively. The retinoid ligands exert their pleiotropic action toward retinoic acid receptors (RARs) than their metal complexes but all compounds exhibit concentration-dependent. 展开更多
关键词 Metal complexes CANCERS ANTIOXIDANT Hydrazone Retinoid Receptors
下载PDF
3,6-Bis-β-Dicarbonylsubstituted Carbazoles Bearing N-Spacers and Their Eu(III) Complexes as Immunofluorescent Labelling Agents
4
作者 Dmitry E. Pugachev Georgy V. Zatonsky +2 位作者 Tatyana S. Kostryukova Anna G. Shubina Nikolay V. Vasiliev 《International Journal of Organic Chemistry》 2024年第1期20-31,共12页
New reagents for immunofluorescence analysis of carbazole series containing fluorinated β-dicarbonyl fragments and carboxylic substituent groups separated by spacers of different lengths from the light-gathering carb... New reagents for immunofluorescence analysis of carbazole series containing fluorinated β-dicarbonyl fragments and carboxylic substituent groups separated by spacers of different lengths from the light-gathering carbazole scaffold have been developed. The markers in complex with Eu<sup>3+</sup> ions possess stability in the aqueous phase, intense and prolonged luminescence (τ 550 - 570 μs) with characteristic emission maxima in the region of 615 nm and excitation wavelengths in the region of 380 - 390 nm, which distinguishes them from most of the analogs used. In the study of marker conjugation with streptavidin, a reagent containing 4 - 5 europium labeling complexes based on spacer-containing carbazole tetraketone was obtained. The marker-doped silicate nanoparticles exhibit intense and long-lived luminescence in the characteristic region. 展开更多
关键词 Fluorescence Immunoassay Fluorinated β-Diketones CARBAZOLE Europium complexes STREPTAVIDIN Nanodispersions
下载PDF
Structures and magnetism of dinuclear Co complexes based on imine derivatives
5
作者 SUN Yadan LI Xinfeng +2 位作者 LIU Qiang Hiroki Oshio MENG Yinshan 《无机化学学报》 SCIE CAS CSCD 北大核心 2024年第11期2212-2220,共9页
This study presents the synthesis of three dinuclear cobalt complexes based on three imine derivatives:bis-[4-(2-pyridylmethyleneamino)-phenyl]thioether(L1),bis-[4-(2-pyridylmethyleneamino)-phenyl]ether(L2),and bis-[4... This study presents the synthesis of three dinuclear cobalt complexes based on three imine derivatives:bis-[4-(2-pyridylmethyleneamino)-phenyl]thioether(L1),bis-[4-(2-pyridylmethyleneamino)-phenyl]ether(L2),and bis-[4-(2-pyridylmethyleneamino)-phenyl]methane(L3).Single-crystal X-ray diffraction analysis reveals that the complexes[Co_(2)(L1)3](ClO_(4))4·2CH_(3)CN(1),[Co_(2)(L2)3](ClO_(4))4·2CH_(3)OH(2),and[Co_(2)(L3)3](ClO_(4))4·2CH_(3)OH(3)all exhibit a dinuclear structure.Magnetic test results show that complex 3 exhibited irreversible SCO behavior induced by loss of solvent at 300 K,with the average Co-N bond length increasing from 0.2139(3)to 0.2153(3)nm.Meanwhile,the desolvated complex 3 exhibited paramagnetic behavior similar to that of complexes 1 and 2.Variable-temperature UV-Vis spectroscopic studies also indicate that complex 3 undergoes a solvent-loss-induced spin-state transition.CCDC:2347354,1(120 K);2347355,2(120 K);2347356,3(120 K);2347357,3(400 K). 展开更多
关键词 spin crossover dinuclear cobalt complex imine derivatives
下载PDF
Synergistic Optimization of Buried Interface by Multifunctional Organic-Inorganic Complexes for Highly Efficient Planar Perovskite Solar Cells 被引量:2
6
作者 Heng Liu Zhengyu Lu +7 位作者 Weihai Zhang Hongkang Zhou Yu Xia Yueqing Shi Junwei Wang Rui Chen Haiping Xia Hsing-Lin Wang 《Nano-Micro Letters》 SCIE EI CAS CSCD 2023年第9期505-519,共15页
For the further improvement of the power conversion efficiency(PCE)and stability of perovskite solar cells(PSCs),the buried interface between the perovskite and the electron transport layer is crucial.However,it is ch... For the further improvement of the power conversion efficiency(PCE)and stability of perovskite solar cells(PSCs),the buried interface between the perovskite and the electron transport layer is crucial.However,it is challenging to effectively optimize this interface as it is buried beneath the perovskite film.Herein,we have designed and synthesized a series of multifunctional organic-inorganic(OI)complexes as buried interfacial material to promote electron extraction,as well as the crystal growth of the perovskite.The OI complex with BF4−group not only eliminates oxygen vacancies on the SnO_(2) surface but also balances energy level alignment between SnO_(2) and perovskite,providing a favorable environment for charge carrier extraction.Moreover,OI complex with amine(−NH_(2))functional group can regulate the crystallization of the perovskite film via interaction with PbI2,resulting in highly crystallized perovskite film with large grains and low defect density.Consequently,with rational molecular design,the PSCs with optimal OI complex buried interface layer which contains both BF4−and−NH_(2) functional groups yield a champion device efficiency of 23.69%.More importantly,the resulting unencapsulated device performs excellent ambient stability,maintaining over 90%of its initial efficiency after 2000 h storage,and excellent light stability of 91.5%remaining PCE in the maximum power point tracking measurement(under continuous 100 mW cm−2 light illumination in N2 atmosphere)after 500 h. 展开更多
关键词 Perovskite solar cells Organic Inorganic complexes Multifunctional interfacial material Buried interface layer
下载PDF
DNA-free genome editing in grapevine using CRISPR/Cas9 ribonucleoprotein complexes followed by protoplast regeneration 被引量:1
7
作者 Samaneh Najafi Edoardo Bertini +2 位作者 Erica D’Incà Marianna Fasoli Sara Zenoni 《Horticulture Research》 SCIE CSCD 2023年第1期183-192,共10页
CRISPR/Cas9 genome editing technology can overcome many limitations of traditional breeding,offering enormous potential for crop improvement and food production.Although the direct delivery of Cas9-single guide RNA(sg... CRISPR/Cas9 genome editing technology can overcome many limitations of traditional breeding,offering enormous potential for crop improvement and food production.Although the direct delivery of Cas9-single guide RNA(sgRNA)ribonucleoprotein(RNP)complexes to grapevine(Vitis vinifera)protoplasts has been shown before,the regeneration of edited protoplasts into whole plants has not been reported.Here,we describe an efficient approach to obtain transgene-free edited grapevine plants by the transfection and subsequent regeneration of protoplasts isolated from embryogenic callus.As proof of concept,a single-copy green f luorescent protein reporter gene(GFP)in the grapevine cultivar Thompson Seedless was targeted and knocked out by the direct delivery of RNPs to protoplasts.CRISPR/Cas9 activity,guided by two independent sgRNAs,was confirmed by the loss of GFP f luorescence.The regeneration of GFP−protoplasts into whole plants was monitored throughout development,confirming that the edited grapevine plants were comparable in morphology and growth habit to wild-type controls.We report the first highly efficient protocol for DNA-free genome editing in grapevine by the direct delivery of preassembled Cas9-sgRNA RNP complexes into protoplasts,helping to address the regulatory concerns related to genetically modified plants.This technology could encourage the application of genome editing for the genetic improvement of grapevine and other woody crop plants. 展开更多
关键词 complexes FIR EDITING
下载PDF
Encapsulation of Ru(II) Polypyridine Complexes for Tumor-Targeted Anticancer Therapy
8
作者 Johannes Karges 《Biomedical Engineering Frontiers》 CAS 2023年第1期52-65,共14页
Ru(II)polypyridine complexes have attracted much attention as anticancer agents because of their unique photophysical,photochemical,and biological properties.Despite their promising therapeutic profile,the vast majori... Ru(II)polypyridine complexes have attracted much attention as anticancer agents because of their unique photophysical,photochemical,and biological properties.Despite their promising therapeutic profile,the vast majority of compounds are associated with poor water solubility and poor cancer selectivity.Among the different strategies employed to overcome these pharmacological limitations,many research efforts have been devoted to the physical or covalent encapsulation of the Ru(II)polypyridine complexes into nanoparticles.This article highlights recent developments in the design,preparation,and physicochemical properties of Ru(II)polypyridine complex-loaded nanoparticles for their potential application in anticancer therapy. 展开更多
关键词 properties. PYRIDINE complexes
下载PDF
Study on the Reaction Behavior of Some Trinuclear Complexes of Transition Metals: [Fe_2M(μ_3-O) (μ-O_2CCH_3)_6(H_2O)_3]·xH_2O by the Method of Probe Reaction of Acetic Acid
9
作者 HE Ling-Jie CHEN Bo +5 位作者 CAI Su-Hua WANG Yan-Ming ZHOU Wen-Bo ZHANG Lin-Na (Fujnin Institute of Research on the Structure of Matter,the Chinese Academy of Sciences, Fuzhou, Fujian 350002, China)XIE Qing-Shan (Present address:Shishi Organizing Committee ,Sh 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 1998年第5期365-371,共7页
The reaction behaviors of the title complexes have been studied in thesystem of dinitrogen gas by means of in situ IR. It has been found that some activefragments created at some stage of the thermal decomposition pro... The reaction behaviors of the title complexes have been studied in thesystem of dinitrogen gas by means of in situ IR. It has been found that some activefragments created at some stage of the thermal decomposition process of the complexes.enable.the acetic acid both obtained from the ligand of the complexes and introducedfrom outside to convert to acetone by decarboxylation. Their optimum reaction temperatures are of 240~270℃ for [Fe2MnO(O2CCH3),(H2O)3], 290~320 C for [Fe3Q(O2CCH3)6(H2O)3], 300~330℃ for [Fe2CoO(O2CCH3),(H2O)3] and 320~ 350℃for [Fe2NiO(O2CCH3)6(H2O)3], indicating the lowering sequence of the activity of active species. At the same time it has been shown that this activity may come from thejoined contributions of both the coordinating capability of the hetero-metals in the complexes and their structural factors. On the basis of the TGA, DTA and EI-MS data,the composition of the active fragments has been tentatively inferred as [Fe2MnO(O2CCH3)3-2]. 展开更多
关键词 in situ IR carboxylato complexes iron complexes manganese complexes cobalt complexes nickel complexes
全文增补中
Probing electronic structures of transition metal complexes using electron paramagnetic resonance spectroscopy
10
作者 Shengfa Ye 《Magnetic Resonance Letters》 2023年第1期43-60,I0003,共19页
Electron paramagnetic resonance(EPR)or electron spin resonance(ESR)has been widely employed to characterize transition metal complexes.However,because of the high degree of complexity of transition metal EPR spectra,h... Electron paramagnetic resonance(EPR)or electron spin resonance(ESR)has been widely employed to characterize transition metal complexes.However,because of the high degree of complexity of transition metal EPR spectra,how to extract the underlying electronicstructure information inevitably poses a major challenge to beginners,in particular for systems with S>1/2.In fact,the physical principles of transition metal EPR have long been well-established and since 1970s a series of dedicated voluminous monographs have been published already.Not surprisingly,they are not appropriate stating points for novices to grasp a panorama of the profound theory prior to scrutinizing in-depth references.The present review aims to fill this gap to provide a perspective of transition metal EPR and unveil some peculiar subtleties thereof on the basis of our recent work. 展开更多
关键词 EPR Electronic structures Transition metal complexes Spin Hamiltonian
下载PDF
A Theoretical Study of Tris-(o-benzoquinonediimine)-First-Row Divalent Transition Metal Complexes
11
作者 Mohammad Abdul Matin Samiran Bhattacharjee Anwar Hossain 《Advances in Chemical Engineering and Science》 CAS 2023年第2期172-188,共17页
The ligand o-phenylenediamine (opda) and its oxidized form, o-benzoquinonediimine (bqdi), act as a fascinating candidate coordinating toward transition metal ions leading to the photochemical hydrogen production in ab... The ligand o-phenylenediamine (opda) and its oxidized form, o-benzoquinonediimine (bqdi), act as a fascinating candidate coordinating toward transition metal ions leading to the photochemical hydrogen production in absence of photosensitizers. Herein, we report the systematic study of the interaction between the oxidized form bqdi ligand, tris-(o-benzoquinonediimine) with divalent first-row transition metal series using DFT calculations. The lowest energy structures, bond length, binding energies, frontier molecular orbital analysis, natural bond orbitals, and global reactivity descriptor were calculated using B3LYP/6-311G(d,P) level of theory. The time dependent-DFT at the CAM-B3LYP/6-311+G(d,p) level of theory was applied to determine the electronic structures and the optical spectra. The theoretical binding trend of the divalent first-row transition metal series is decreasing as follows: Cu >Ti > V > Co > Ni > Fe > Cr > Zn >Mn. Among them, the binding potency of iron (II) by the bqdi ligand was not predominantly sturdy as compared to other first-row divalent transition metal ions. The origin of strong coordination with Fe(II) is attributed to its extra capability to induce covalent coordination of bqdi ligands. The complex exhibited two strong peaks at 370 nm and 452 nm, due to the HOMO-3 to LUMO+1 and HOMO-1 to LUMO transitions, respectively. Natural bond orbital analysis showed that the major interaction happens between the N lone pair electrons of the ligand with an anti-bonding orbital of metal ions, in which Ti showed the highest interaction energy than other metal ions. The present systemic DFT study of bqdi ligands with the first-row transition metals strongly encourages the future establishment of photochemical hydrogen production in absence of photosensitizers. 展开更多
关键词 DFT O-PHENYLENEDIAMINE o-benzoquinodiimine First-Row Divalent Transition Metals Time Dependent–DFT Coordination complexes
下载PDF
Synthesis and Characterisation of Cr(III) and Co(II) Schiff Base Complexes
12
作者 Fatin M. Elmagbari Ahmed N. Hammouda +2 位作者 Hamdi A. M. Bennour Rashd M. EL-Ferjani Younis O. Ben Amer 《Materials Sciences and Applications》 CAS 2023年第2期53-62,共10页
Co(II) and Cr(III) metal complexes of Schiff bases were synthesized from the condensation reaction between 4-(dimethylamino)benzaldehyde and 4-amino-3-hydroxy-naphthalene-1-sulfonic acid. Their structures were investi... Co(II) and Cr(III) metal complexes of Schiff bases were synthesized from the condensation reaction between 4-(dimethylamino)benzaldehyde and 4-amino-3-hydroxy-naphthalene-1-sulfonic acid. Their structures were investigated by elemental analysis, molar conductance measurements, infrared spectroscopy, electronic spectroscopy, and 1HNMR spectroscopy. The elemental analysis data suggested a 1:1 [M:L] ratio for the complexes. The molar conductance measurements of the complexes indicate their electrolytic nature in DMSO as a solvent. The absorption bands in the electronic spectra verified an octahedral environment around the metal ions in the complexes. 展开更多
关键词 Schiff Base Ligand complexes 1HNMR Spectra
下载PDF
Syntheses and Crystal Structures of Di-, Tri- and Tetra-nuclear Cobalt(II)-Lanthanide(III) Carboxylate Complexes
13
作者 崔勇 郑发鲲 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2001年第2期112-119,共8页
关键词 lanthanide complexes cobalt complexes carboxylate complexes SYNTHESES crystal structures
下载PDF
Physicochemical and Analytical Studies of Some Monomer and Polymer Complexes Derived from Selected Aroyl Hydrazone
14
作者 Aymen Hussien Ahmed Mohsen Mahmoud Mostafa 《Open Journal of Inorganic Chemistry》 CAS 2022年第1期1-17,共17页
New solid complexes derived from the reaction of aroyl hydrazones, 2-hydroxy-1-naphthaldehyde benzene sulphonyl hydrazone (HNB), and 2-hydroxy-1-naphthaldehyde p-toluene sulphonyl hydrazone (HNT), with Co<sup>2+... New solid complexes derived from the reaction of aroyl hydrazones, 2-hydroxy-1-naphthaldehyde benzene sulphonyl hydrazone (HNB), and 2-hydroxy-1-naphthaldehyde p-toluene sulphonyl hydrazone (HNT), with Co<sup>2+</sup>, Ni<sup>2+</sup>, and Cu<sup>2+</sup> salts have been isolated and characterized using elemental analyses, spectral (UV-vis., IR), molar conductivity and magnetic measurements. The modes of bonding as well as the stereochemistry of the isolated solid complexes were discussed. The results suggested that both HNB and HNT coordinated with the metal ions in a bidentate manner forming a polymeric chain in the case of HNB while monocular complexes were formed in the case of HNT. The amounts of solvent in the solid complexes were determined by TGA measurements. Also, spectral studies of HNT with Co<sup>2+</sup> and Fe<sup>3+</sup> ions in solution were carried and the ratio of complexes was determined by continuous variation, molar ratio, and slope ratio methods. Moreover, the results suggest the formation of 1:1 (M:L) for Co<sup>2+</sup> ions while three species with ratios of 1:1, 1:2, and 2:1 (M:L) have been observed in the case of Ni<sup>2+</sup> and Cu<sup>2+</sup>. Finally, conductance titration of HNB and HNT with Co<sup>2+</sup> ion elucidates the formation of two species with ratios 1:1 and 1:2 (M:L) in the case of the Co<sup>2+</sup>-HNB while 1:1 (M:L) belongs to the Co<sup>2+</sup>-HNT system. 展开更多
关键词 Aroyl Hydrazones complexes Polymer and Monomer complexes FTIR Synthesis Stoichiometry of complexes
下载PDF
Pathfinder-Based Simulation and Optimization of Evacuation of Large Commercial Complexes
15
作者 Jiuju Liu Shuhan Li 《Journal of Building Construction and Planning Research》 2023年第2期27-35,共9页
Large commercial complexes are large in scale, complex in function, and located in densely populated areas that are prone to casualties due to unfavorable evacuation. To comprehend the safety evacuation of large comme... Large commercial complexes are large in scale, complex in function, and located in densely populated areas that are prone to casualties due to unfavorable evacuation. To comprehend the safety evacuation of large commercial complex buildings in China, investigate the safety evacuation problems encountered during the evacuation process and the evacuation optimization design strategy, the paper uses Pathfinder to build a simulation model based on literature research and study to simulate the evacuation of personnel in a large commercial complex in Dalian and explore its problems during the evacuation process. The results show that the type of personnel has an effect on the large commercial complex’s evacuation simulation results;the total number of evacuees is non-linearly correlated with the time change curve;some staircases take a long time to evacuate and have a low utilization rate. To improve evacuation efficiency, optimization suggestions for safety exits, evacuation stairs, and evacuation channels are made based on the results. 展开更多
关键词 Commercial Complex Safe Evacuation SIMULATION PATHFINDER
下载PDF
2,4-Dinitrophenyl Ether of Polyvinyl Alcohol and Polymer Bound Anionic SIGMA Complexes
16
作者 John C. Phelan Michael J. Strauss 《International Journal of Organic Chemistry》 2023年第3期87-95,共9页
A new electrophilic polymer, 2,4-dinitrophenyl ether of polyvinyl alcohol (PVA-DNP), having a degree of substitution of 0.5 was prepared from polyvinyl alcohol (PVA) and 1-fluro-2,4-dinitrobenzene (DNFB). The PVA-DNP ... A new electrophilic polymer, 2,4-dinitrophenyl ether of polyvinyl alcohol (PVA-DNP), having a degree of substitution of 0.5 was prepared from polyvinyl alcohol (PVA) and 1-fluro-2,4-dinitrobenzene (DNFB). The PVA-DNP polymer was characterized by NMR, IR, and UV-visible spectroscopy. The reaction of PVA-DNP with sodium methoxide was followed by NMR and UV-visible spectroscopy. Evidence of polymer bound spirocyclic SIGMA complex, C-1 and C-3 polymer bound DNP-methoxy SIGMA complexes and the formation and C-1 methoxy complex of 2,4-dinitroanisole was observed. 展开更多
关键词 2 4-Dinitrophenyl Ether Polyvinyl Alcohol Anionic SIGMA Complex Thermal Stability Nucleophilic Aromatic Substitution
下载PDF
Resonance Raman Spectra of Purified PS Ⅱ Core Antenna Complexes CP43 and CP47 被引量:2
17
作者 单际修 杨昆云 +7 位作者 冯丽洁 李良璧 匡廷云 王居硕 赵南明 刘玉龙 朱恪 杨国桢 《Acta Botanica Sinica》 CSCD 1999年第3期280-284,共5页
PSⅡ core antenna complexes, CP43 and CP47, were purified from spinach (Spinacia oleracea L.) by DEAE Fractogel TSK 650S anion exchange chromatography. Their normal temperature (298 K) resonance Raman spectra were... PSⅡ core antenna complexes, CP43 and CP47, were purified from spinach (Spinacia oleracea L.) by DEAE Fractogel TSK 650S anion exchange chromatography. Their normal temperature (298 K) resonance Raman spectra were measured. The results suggest that all β carotenoids bound to CP43 and CP47 are in all trans configuration and likely in twisted conformations. 展开更多
关键词 PSⅡ Core antenna complexes CP43 CP47 Resonance Raman spectrum β carotene
下载PDF
STUDY ON THE ANTI-TUMOR EFFICACY INDUCED BY HEAT SHOCK PROTEIN 70-PEPTIDE COMPLEXES DERIVED FROM TUMOR CELLS 被引量:6
18
作者 傅庆国 张玮 +2 位作者 孟凡东 郭仁宣 姚振宇 《Chinese Medical Sciences Journal》 CAS CSCD 2002年第3期153-156,共4页
OBJECTIVE: To study the efficacy and explore the mechanism of the anti-tumor immunity elicited by heat shock protein 70-peptide complexes (HSP70-PC) derived from tumor cells. METHODS: Cells culture, flow cytometric an... OBJECTIVE: To study the efficacy and explore the mechanism of the anti-tumor immunity elicited by heat shock protein 70-peptide complexes (HSP70-PC) derived from tumor cells. METHODS: Cells culture, flow cytometric analysis, affinity chromatography for protein purification, SDS-PAGE, Western-blotting and animal experiment were used. RESULTS: HSP70-PC immunization rendered protective effect to both naive tumorl-bearing mice. All of the naive mice obtained complete resistance to Hcaf cell attack; 40% of the tumor-bearing mice survived for over 90 days, whereas the mice of control group died within 2 weeks (P 展开更多
关键词 NEOPLASM heat shock protein 70 peptide complexes tumor vaccineObjective. To study the efficacy and explore the mechanism of the anti tumor immunity elicited by heat shock protein 70 peptide complexes (HSP70 PC) derived from tumor cells. M
下载PDF
Synthesis and Photophysical Properties of Dy^(3+) and Gd^(3+) Polymeric Complexes with Functionalized Polybenzimidazole Containing β-Diketone Side Group 被引量:1
19
作者 吴骞 钟超凡 +2 位作者 郭荣芳 何爱红 黄华良 《Journal of Rare Earths》 SCIE EI CAS CSCD 2007年第5期562-567,共6页
The polymeric ligand PBIa (functionalized polybenzimidazole containing β-diketone side group) was successfully synthesized via the reaction of polybenzimidazole (PBI) with 3-Br-acetylacetone in DM SO solvent usin... The polymeric ligand PBIa (functionalized polybenzimidazole containing β-diketone side group) was successfully synthesized via the reaction of polybenzimidazole (PBI) with 3-Br-acetylacetone in DM SO solvent using Nail as the deprotonation reagent. Its corresponding polymeric complexes of Dy^3+ and Gd^3+ were prepared and characterized by FT-IR, ^1H NMR, molar conductance measurements, and thermal analysis. The photoluminescence properties and the probable mechanism of the Dy and Gd complexes were studied. The measurement and analysis of the thermal properties showed that these were thermal stable. 展开更多
关键词 lanthanide complexes POLYBENZIMIDAZOLE polymeric complexes photophysical properties rare earths
下载PDF
Theoretical Studies on Structures and Spectroscopic Properties of Highly Efficient Phosphorescent [Ru(terpy)(phen)X]+ Complexes
20
作者 金丽 张建坡 +1 位作者 张红星 白福全 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2011年第4期391-398,I0003,共9页
The ground and the lowest-lying triplet excited state geometries, electronic structures, and spectroscopic properties of three mixed-ligand Ru(II) complexes [Ru(terpy)(phen)X]+ (terpy=2,2',6',2″-terpyridine... The ground and the lowest-lying triplet excited state geometries, electronic structures, and spectroscopic properties of three mixed-ligand Ru(II) complexes [Ru(terpy)(phen)X]+ (terpy=2,2',6',2″-terpyridine, phen=l,10-phenanthroline, and X=-C-=CH (1), X=Cl (2), X-CN (3)) were investigated theoretically using the density functional theory method. The ground and excited state geometries have been fully optimized at the B3LYP/LanL2DZ and UB3LYP/LanL2DZ levels, respectively. The absorption and emission spectra of the com- plexes in CHaCN solutions were calculated by time-dependent density functional theory with the PCM solvent model. The calculated bond lengths of Ru-C, Ru-N, and Ru-Cl in the ground state agree well with the corresponding experimental results. The highest occupied molecular orbital were dominantly localized on the Ru atom and monodentate X ligand for 1 and 2, Ru atom and terpy ligand for a, while the lowest unoccupied molecular orbital were π*(terpy) type orbital. Therefore, the lowest-energy absorptions of 1 and 2 at 688 and 631 nln are attributed to a dyz (Ru)+Tr/p(X)--π* (terpy) transition with MLCT/XLCT (metal-to-ligand charge transfer/X ligand to terpy ligand charge transfer) character, whereas that of 3 at 529 nm is related to a dyz (Ru)+π(terpy)-π* (terpy) transition with MLCT and ILCT transition character. The calculated phosphorescence of three complexes at 1011 nm (1), 913 nm (2), and 838 nm (3) have similar transition properties to that of the lowest-lying absorption. It is shown that the lowest lying absorptions and emissions transition character of these Ru(II) complexes can be tuned by changing the electron-withdrawing ability of the monodentate ligand. 展开更多
关键词 Mixed-ligand Ru(II) complexes Electronic structure Spectroscopic property DFT calculation UB3LYP method
下载PDF
上一页 1 2 250 下一页 到第
使用帮助 返回顶部