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991.
Shen X Boswell CA Wong EH Weisman GR Anderson CJ Tomellini SA 《Biomedical chromatography : BMC》2006,20(1):37-47
The use of copper radioisotopes in imaging and therapy has prompted an increased interest in chelators which form stable copper complexes, such as Cu(II)-azamacrocyclic complexes. The effects of charge, stability and the size of the macrocyclic backbone of the Cu(II)-azamacrocyclic complexes on biological behavior have been evaluated. Here we report a reversed-phase high-performance liquid chromatography (HPLC) method to separate several Cu(II)-azamacrocyclic complexes, including Cu(II) complexes of 1,4,8,11-tetraazacyclotetradecane-1,4,8,11-tetraacetic acid (TETA), 4,11-bis(carboxymethyl)-1,4,8,11-tetraazabicyclo[6.6.2]hexadecane (CB-TE2A) and 4,10-bis(carboxymethyl)-1,4,7,10-tetraazabicyclo[5.5.2]tetradecane (CB-DO2A). Absorbance at 280 nm was used to monitor the complexes as they eluted from the reversed-phase column. The effects of the concentration of the buffer, the pH of the buffered mobile phase and the concentration of the organic modifier, methanol, on the separation were investigated. Separation of these copper complexes by ion-pair HPLC with the use of a mass spectrometry-compatible ion-pair reagent, triethylammonium acetate, in the mobile phase at pH 6.3 is also presented. The reversed-phase chromatographic conditions utilized also allow the pK(a)s of Cu-TETA and the log(k'w) values of Cu-CB-TE2A, Cu-TETA and Cu-CB-DO2A to be estimated. 相似文献
992.
Highly sensitive sensor for detection of NADH based on catalytic growth of Au nanoparticles on glassy carbon electrode 总被引:1,自引:0,他引:1
Lin Tang Guangming Zeng Guoli Shen Yi Zhang Yuanping Li Changzheng Fan Can Liu Chenggang Niu 《Analytical and bioanalytical chemistry》2009,393(6-7):1677-1684
In this work, an electrochemical dihydronicotinamide adenine dinucleotide (NADH) sensor based on the catalytic growth of Au nanoparticles (Au NPs) on glassy carbon electrode was developed. Catalyzed by Au NPs immobilized on pretreated glassy carbon electrode, the reduction of AuCl4 ? in the presence of hydroquinone and cetyltrimethyl ammonium chloride led to the formation of enlarged Au NPs on the electrode surface. Spectrophotometry and high-resolution scanning electronic microscope (SEM) analysis of the sensor morphologies before and after biocatalytic reaction revealed a diameter growth of the nanoparticles. The catalytic growth of Au NPs on electrode surface remarkably facilitated the electron transfer and improved the performance of the sensor. Under optimal conditions, NADH could be detected in the range from 1.25?×?10?6 to 3.08?×?10?4 M, and the detection limit was 2.5?×?10?7 M. The advantages of the proposed sensor, such as high precision and sensitivity, fast response, low cost, and good storage stability, made it suitable for on-line detection of NADH in complex biological systems and contaminant degradation processes. Figure
Schematic presentation of the bioelectrocatalytic sensing of NADH 相似文献
993.
Honglan Cai Chang Yi Xueqin An Weiguo Shen 《The Journal of chemical thermodynamics》2009,41(5):639-644
To examine the critical behavior of the microemulsion, we have determined the coexistence curves for two ternary microemulsion systems of {water + sodium di(2-ethylhexyl) sulfosuccinate (AOT) + n-decane} with the molar ratios ω = (45.2 and 50.0) of water to AOT, respectively, by measuring refractive index at a constant pressure in the critical region. The critical exponent β and the critical amplitude B have been deduced from the coexistence curves. It was found that the values of β for both systems were consistent with the 3D-Ising exponent in a critical region. By increasing ω, i.e. the droplet size, the critical temperature and, to a lesser extent, the critical concentration decrease. The region of coexisting two phases was drastically reduced by an increase in the droplet size. 相似文献
994.
Qingqing Shao Shujiang Tu Chunmei Li Longji Cao Dianxiang Zhou Bo Jiang Yan Zhang Wenjuan Hao Qian Wang 《Journal of heterocyclic chemistry》2008,45(2):411-416
Triaza‐benzo[b]fluoren‐6‐one derivatives were synthesized via the three‐component reaction of aldehyde, cyclohexane‐1,3‐dione compound and 2‐aminobenzimidazole in water under microwave irradiation. The new protocol has the advantages of excellent yield, low cost, reduced environment impact, wide scope and convenient procedure. 相似文献
995.
Guan SH Xia JM Lu ZQ Chen GT Jiang BH Liu X Guo DA 《Magnetic resonance in chemistry : MRC》2008,46(2):186-190
Three new lignan glycosides (1-3) were isolated from the stems of Akebia trifoliata. Their structures were elucidated as (7R,8R,7'R,8'R)3,3',5,5'tetramethoxy-4,4'dihydroxy-7,9':7',9-diepoxylignan-4-O-beta-D-glucopyranoside (1), (7S,8S,8'R)-4,4',9-trihydroxy-3,3',5,5'-tetramethoxy-7,9'-epoxylignan-7'-one 9-O-beta-D-glucopyranoside (2), (7R,8R,8'S)-4,4',9-trihydroxy3,3',5,5'-tetramethoxy-7,9'-epoxylignan-7'-one 9-O-beta-D-glucopyranoside (3) by spectral analyses, primarily NMR, MS and CD. The NMR assignments for the compounds were carried out using 1H, 13C, DEPT, COSY, HSQC, HMBC and ROESY NMR experiments. 相似文献
996.
Dr. Zhen-Zhen Shen Dr. Shuang-Yan Lang Rui-Zhi Liu Dr. Chi Zhou Yao-Zu Zhang Prof. Dr. Bing Liu Prof. Dr. Rui Wen 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2024,136(1):e202316781
Lithium–carbon dioxide (Li–CO2) battery technology presents a promising opportunity for carbon capture and energy storage. Despite tremendous efforts in Li–CO2 batteries, the complex electrode/electrolyte/CO2 triple-phase interfacial processes remain poorly understood, in particular at the nanoscale. Here, using in situ atomic force microscopy and laser confocal microscopy-differential interference contrast microscopy, we directly observed the CO2 conversion processes in Li–CO2 batteries at the nanoscale, and further revealed a laser-tuned reaction pathway based on the real-time observations. During discharge, a bi-component composite, Li2CO3/C, deposits as micron-sized clusters through a 3D progressive growth model, followed by a 3D decomposition pathway during the subsequent recharge. When the cell operates under laser (λ=405 nm) irradiation, densely packed Li2CO3/C flakes deposit rapidly during discharge. Upon the recharge, they predominantly decompose at the interfaces of the flake and electrode, detaching themselves from the electrode and causing irreversible capacity degradation. In situ Raman shows that the laser promotes the formation of poorly soluble intermediates, Li2C2O4, which in turn affects growth/decomposition pathways of Li2CO3/C and the cell performance. Our findings provide mechanistic insights into interfacial evolution in Li–CO2 batteries and the laser-tuned CO2 conversion reactions, which can inspire strategies of monitoring and controlling the multistep and multiphase interfacial reactions in advanced electrochemical devices. 相似文献
997.
Dr. Yutao Sang Dr. Qirong Zhu Dr. Xiaoqin Zhou Dr. Yuqian Jiang Prof. Li Zhang Prof. Minghua Liu 《Angewandte Chemie (International ed. in English)》2023,62(8):e202215867
Herein we describe the self-assembly of an achiral molecule into macroscopic helicity as well as the emergent chiral-selective spin-filtering effect. It was found that a benzene-1,3,5-tricarboxamide (BTA) motif with an aminopyridine group in each arm could coordinate with AgI and self-assemble into nanospheres. Upon sonication, symmetry breaking occurred and the nanospheres transferred into helical nanofibers with strong CD signals. Although the sign of the CD signals appeared randomly, it could be controlled by using the as-made chiral assemblies as a seed. Furthermore, it was found that the charge transport of the helical nanofibers was highly selective with a spin-polarization transport of up to 45 %, although the chiral nanofibers are composed exclusively from achiral building blocks. This work demonstrates symmetry breaking under sonication and the chiral-selective spin-filtering effect. 相似文献
998.
Zejing Xing Xiaodan Gou Prof. Dr. Li-Ping Jiang Prof. Dr. Jun-Jie Zhu Dr. Cheng Ma 《Angewandte Chemie (International ed. in English)》2023,62(39):e202308950
Protein coronas are present extensively at the bio-nano interface due to the natural adsorption of proteins onto nanomaterials in biological fluids. Aside from the robust property of nanoparticles, the dynamics of the protein corona shell largely define their chemical identity by altering interface properties. However, the soft coronas are normally complex and rapidly changing. To real-time monitor the entire formation, we report here a self-regulated electrochemiluminescence (ECL) microscopy based on the interaction of the Ru(bpy)33+ with the nanoparticle surface. Thus, the heterogeneity of the protein corona is in situ observed in single nanoparticle “cores” before and after loading drugs in nanomedicine carriers. The label-free, optical stable and dynamic ECL microscopy minimize misinterpretations caused by the variation of nanoparticle size and polydispersity. Accordingly, the synergetic actions of proteins and nanoparticles properties are uncovered by chemically engineered protein corona. After comparing the protein corona formation kinetics in different complex systems and different nanomedicine carriers, the universality and accuracy of this technique were well demonstrated via the protein corona formation kinetics curves regulated by competitive adsorption of Ru(bpy)33+ and multiple proteins on surface of various carriers. The work is of great significance for studying bio-nano interface in drug delivery and targeted cancer treatment. 相似文献
999.
Yunpeng Zhong Xuesong Xie Prof. Zhiyuan Zeng Prof. Bingan Lu Prof. Gen Chen Prof. Jiang Zhou 《Angewandte Chemie (International ed. in English)》2023,62(40):e202310577
Aqueous rechargeable zinc-ion batteries (ARZBs) are impeded by the mutual problems of unstable cathode, electrolyte parasitic reactions, and dendritic growth of zinc (Zn) anode. Herein, a triple-functional strategy by introducing the tetramethylene sulfone (TMS) to form a hydrated eutectic electrolyte is reported to ameliorate these issues. The activity of H2O is inhibited by reconstructing hydrogen bonds due to the strong interaction between TMS and H2O. Meanwhile, the preferentially adsorbed TMS on the Zn surface increases the thickness of double electric layer (EDL) structure, which provides a shielding buffer layer to suppress dendrite growth. Interestingly, TMS modulates the primary solvation shell of Zn2+ ultimately to achieve a novel solvent co-intercalation ((Zn-TMS)2+) mechanism, and the intercalated TMS works as a “pillar” that provides more zincophilic sites and stabilizes the structure of cathode (NH4V4O10, (NVO)). Consequently, the Zn||NVO battery exhibits a remarkably high specific capacity of 515.6 mAh g−1 at a low current density of 0.2 A g−1 for over 40 days. This multi-functional electrolytes and solvent co-intercalation mechanism will significantly propel the practical development of aqueous batteries. 相似文献
1000.
Dongdong Li Prof. Dr. Chaoren Shen Zhiyao Si Prof. Dr. Lu Liu 《Angewandte Chemie (International ed. in English)》2023,62(42):e202310283
An unprecedented Pd-catalyzed fluorinative bifunctionalization of aziridines and azetidines was successfully developed via regioselective C−C and C−F bond cleavage of gem-difluorocyclopropanes, leading to various β,β′-bisfluorinated amines and β,γ-bisfluorinated amines. This reaction was achieved by incorporating a 2-fluorinated allyl group and a fluorine atom scissored from gem-difluorocyclopropane in 100 % atom economy for the first time. The mechanistic investigations indicated that the reaction underwent amine attacking 2-fluorinated allyl palladium complex to generate η2-coordinated N-allyl aziridine followed by fluoride ligand transfer affording the final β- and γ-fluorinated amines. 相似文献