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961.
Hui Zhang Kan Zhan Yulu Chen Guoxia Chen Xiaomei Zhou Junxiu Liu Min Wu Henmei Ni 《Journal of Sol-Gel Science and Technology》2014,71(3):597-605
Three dimensional Liesegang spherical layers of CaHPO4 in gelatin ball were performed by employing CaCl2 and Na2HPO4 as the inner and outer electrolyte, respectively. Effects of concentrations of inner and outer electrolyte as well as pH on the morphologies of Liesegang rings (LRs) were investigated. As a result, it was observed that the time law, spacing law and width law found in 1D/2D gel systems were obeyed in this 3D gelatin system. The interaction of Ca2+ and HPO4 2? with gelatin matrix played a key role to the formation of LRs due to the existence of carboxylic groups on the gelatin chains. Using Ca2+ as the inner electrolyte, LRs were prepared. However, employing HPO4 2? as inner electrolyte, LRs were not obtained. Moreover, pH of gelatin solution greatly impacted on the formation of LRs. The number of LRs increased with the decrease of pH, whereas the width inversely decreased. pH 4.40 was a turn point, from which the spacing coefficient abruptly increased as pH increased. All these results indicated that the network was created by the interaction of Ca2+ and –COO? of gelatin chains, which dominated the formation of CaHPO4 LRs in gelatin. 相似文献
962.
Dunhua Hong Taisong Pan Dayu Feng Zhenlong Huang Feiyi Liao XiaoMei Li Yin Zhang Min Gao 《Journal of Sol-Gel Science and Technology》2014,71(3):464-469
(LaBa)Co2O5+δ (LBCO) thin films were successfully fabricated on Si (001) substrates by polymer-assisted deposition method. Microstructures were examined by X-ray diffraction technique, which confirmed the films were a single phase, pseudo cubic structure. The electrical transport properties of the films were investigated by the temperature dependence of films resistance, which suggested that LBCO films have typical semiconductor properties. After circle tests, the oxygen–hydrogen response rate did not show obvious variation in the specific temperature environment of 580 °C. This demonstrates that the LBCO thin films have a superior stability in both oxygen and hydrogen (6 % H2, 94 % N2) environment. Simultaneously, the drastic changes of films resistance (from ~106 to ~102 Ω) with the switch of redox (O2–H2) environment within such a short time (~2.2 s) indicated that LBCO films have an excellent oxygen sensitive property and extraordinary fast surface exchange rate. 相似文献
963.
利用L-谷氨酸苄酯开环聚合得到聚L-谷氨酸苄酯,对其进行表征,将聚L-谷氨酸苄酯溶于四氢呋喃后涂敷在3-氨丙基三乙氧基硅胶上制得液相色谱固定相,研究了正相色谱条件下聚L-谷氨酸苄酯涂敷型固定相对9种位置异构体及10种手性化合物的拆分能力。以不同比例的正己烷/异丙醇为流动相,有6种位置异构体(o,m,p-氯苯胺、o,m,p-溴苯胺、o,m,p-碘苯胺、o,m,p-硝基苯胺、o,m,p-二硝基苯和o,m,p-苯二胺)和4种手性化合物(1-(对氯苯基)乙醇、5-二硝基-N-(1-苯乙基)苯甲酰胺、华法林和四咪唑)得到不同程度的拆分,表明聚L-谷氨酸苄酯涂敷型固定相对位置异构体具有较好的识别作用,同时也表现出良好的手性拆分能力。 相似文献
964.
高效液相色谱-电喷雾串联质谱法测定畜禽粪便中四环素类抗生素 总被引:1,自引:0,他引:1
建立了高效液相色谱-电喷雾串联质谱法(HPLC-MS/MS)测定畜禽粪便中四环素类抗生素的分析方法。样品经甲醇-乙酸-水(体积比6∶3∶1)溶液提取,OASIS HLB小柱净化后,采用Waters Symmetry C18色谱柱(150×3.9mm,5μm)进行分离,以0.3%甲酸水溶液-0.3%甲酸乙腈溶液梯度洗脱,电喷雾正离子模式多反应监测(MRM)模式定量分析。在优化的色谱条件下,四环素、土霉素和金霉素在0.05~1.0mg/L范围内具有良好的线性,其检出限分别为0.025、0.084、0.098mg/kg;样品回收率为80%~103%。实验结果表明,该方法较液相色谱法具有更高的准确性和灵敏度,可满足畜禽粪便中四环素类抗生素残留的检测要求。 相似文献
965.
Dr. Huizeng Li Wei Fang Zhipeng Zhao An Li Dr. Zheng Li Prof. Mingzhu Li Prof. Qunyang Li Prof. Xiqiao Feng Prof. Yanlin Song 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(26):10622-10626
Precise separation and localization of microdroplets are fundamental for various fields, such as high-throughput screening, combinatorial chemistry, and the recognition of complex analytes. We have developed a droplet self-splitting strategy to divide an impacting droplet into predictable microdroplets and deposit them at preset spots for simultaneous multidetection. No matter exchange was observed between these microdroplets, so they could be manipulated independently. Droplet self-splitting was attributed to anisotropic liquid recoiling on the patterned adhesive surface, as influenced by the droplet Weber number and the width of the low-adhesive stripe. A quantitative criterion was also developed to judge the droplet self-splitting capability. The precise separation and distribution of microdroplets enabled simultaneous arrayed reactions and multiple analyte detection using one droplet of sample. 相似文献
966.
Min Wang Jia-Qi Wang Cong Xi Chuan-Qi Cheng Cheng-Qin Zou Rui Zhang Ya-Meng Xie Zhong-Lu Guo Prof. Cheng-Chun Tang Dr. Cun-Ku Dong Prof. Yong-Jun Chen Prof. Xi-Wen Du 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(28):11607-11612
Developing highly efficient and low-cost photocatalysts for overall water splitting has long been a pursuit for converting solar power into clean hydrogen energy. Herein, we demonstrate that a nonstoichiometric nickel–cobalt double hydroxide can achieve overall water splitting by itself upon solar light irradiation, avoiding the consumption of noble-metal co-catalysts. We employed an intensive laser to ablate a NiCo alloy target immersed in alkaline solution, and produced so-called L-NiCo nanosheets with a nonstoichiometric composition and O2−/Co3+ ions exposed on the surface. The nonstoichiometric composition broadens the band gap, while O2− and Co3+ ions boost hydrogen and oxygen evolution, respectively. As such, the photocatalyst achieves a H2 evolution rate of 1.7 μmol h−1 under AM 1.5G sunlight irradiation and an apparent quantum yield (AQE) of 1.38 % at 380 nm. 相似文献
967.
Dr. Chao Wang Min Hu Dr. Yueying Chu Xue Zhou Dr. Qiang Wang Dr. Guodong Qi Dr. Shenhui Li Prof. Dr. Jun Xu Prof. Dr. Feng Deng 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(18):7265-7269
The understanding of catalyst deactivation represents one of the major challenges for the methanol-to-hydrocarbon (MTH) reaction over acidic zeolites. Here we report the critical role of intermolecular π-interactions in catalyst deactivation in the MTH reaction on zeolites H-SSZ-13 and H-ZSM-5. π-interaction-induced spatial proximities between cyclopentenyl cations and aromatics in the confined channels and/or cages of zeolites are revealed by two-dimensional solid-state NMR spectroscopy. The formation of naphtalene as a precursor to coke species is favored due to the reaction of aromatics with the nearby cyclopentenyl cations and correlates with both acid density and zeolite topology. 相似文献
968.
Min Zhou Ximian Xiao Zihao Cong Yueming Wu Wenjing Zhang Pengcheng Ma Sheng Chen Haodong Zhang Danfeng Zhang Donghui Zhang Xiangfeng Luan Prof. Yiyong Mai Prof. Runhui Liu 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(18):7307-7311
Biocompatible and proteolysis-resistant poly-β-peptides have broad applications and are dominantly synthesized via the harsh and water-sensitive ring-opening polymerization of β-lactams in a glovebox or using a Schlenk line, catalyzed by the strong base LiN(SiMe3)2. We have developed a controllable and water-insensitive ring-opening polymerization of β-amino acid N-thiocarboxyanhydrides (β-NTAs) that can be operated in open vessels to prepare poly-β-peptides in high yields, with diverse functional groups, variable chain length, narrow dispersity and defined architecture. These merits imply wide applications of β-NTA polymerization and resulting poly-β-peptides, which is validated by the finding of a HDP-mimicking poly-β-peptide with potent antimicrobial activities. The living β-NTA polymerization enables the controllable synthesis of random, block copolymers and easy tuning of both terminal groups of polypeptides, which facilitated the unravelling of the antibacterial mechanism using the fluorophore-labelled poly-β-peptide. 相似文献
969.
Dr. Min Luo Dr. Chensheng Lin Donghong Lin Prof. Ning Ye 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(37):16112-16115
The first fluorosulfonic ultraviolet (UV) nonlinear optical (NLO) material, C(NH2)3SO3F, is rationally designed by taking KBe2BO3F2 (KBBF) as the parent compound. C(NH2)3SO3F features similar topological layers as KBBF by replacing inorganic (BO3)3− with organic C(NH2)3+ trigonal units and BeO3F with SO3F− tetrahedra. Therefore, C(NH2)3SO3F is a metal-free UV NLO crystal. Benefiting from the coplanar configuration of the C(NH2)3+ cationic groups, it possesses a large SHG response of 5×KDP and moderate birefringence of 0.133@1064 nm. Besides, it has a short UV cutoff edge of 200 nm. The calculated results reveal the shortest SHG phase-matching wavelengths can reach 200 nm. These findings highlight the exploration of metal-free compounds as nontoxic and low-cost UV NLO materials as a new research area. 相似文献
970.
Ruibing An Xiaoyang Cheng Shixuan Wei Yuxuan Hu Yidan Sun Zheng Huang Prof. Hong-Yuan Chen Prof. Deju Ye 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(46):20817-20825
Stimuli-responsive smart photosensitizer (PS) nanoassemblies that allow enhanced delivery and controlled release of PSs are promising for imaging-guided photodynamic therapy (PDT) of tumors. However, the lack of high-sensitivity and spatial-resolution signals and fast washout of released PSs from tumor tissues have impeded PDT efficacy in vivo. Herein, we report tumor targeting, redox-responsive magnetic and fluorogenic PS nanoassemblies ( NP-RGD ) synthesized via self-assembly of a cRGD- and disulfide-containing fluorogenic and paramagnetic small molecule ( 1-RGD ) for fluorescence/magnetic resonance bimodal imaging-guided tumor PDT. NP-RGD show high r1 relaxivity but quenched fluorescence and PDT activity; disulfide reduction by glutathione (GSH) promotes efficient disassembly into a small-molecule probe ( 2-RGD ) and an organic PS (PPa-SH), which could further bind with intracellular albumin, allowing prolonged retention and cascade activation of fluorescence and PDT to ablate tumors. 相似文献