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101.
Xiaopin Duan Christina Chan Wenbin Lin 《Angewandte Chemie (International ed. in English)》2019,58(3):670-680
Cancer immunotherapies that train or stimulate the inherent immunological systems to recognize, attack, and eradicate tumor cells with minimal damage to healthy cells have demonstrated promising clinical responses in recent years. However, most of these immunotherapeutic strategies only benefit a small subset of patients and cause systemic autoimmune side effects in some patients. Immunogenic cell death (ICD)‐inducing modalities not only directly kill cancer cells but also induce antitumor immune responses against a broad spectrum of solid tumors. Such strategies for generating vaccine‐like functions could be used to stimulate a “cold” tumor microenvironment to become an immunogenic, “hot” tumor microenvironment, working in synergy with immunotherapies to increase patient response rates and lead to successful treatment outcomes. This Minireview will focus on nanoparticle‐based treatment modalities that can induce and enhance ICD to potentiate cancer immunotherapy. 相似文献
102.
Weichao Xue Wenbin Mao Liangliang Zhang Martin Oestreich 《Angewandte Chemie (International ed. in English)》2019,58(19):6440-6443
Robust procedures for two mechanistically distinct C(sp3)?Ge bond formations from alkyl electrophiles and germanium nucleophiles are reported. The germanium reagents were made available as bench‐stable solutions by lithium‐to‐magnesium and lithium‐to‐zinc transmetalation, respectively. The germanium Grignard reagent reacts with various primary and secondary alkyl electrophiles by an ionic nucleophilic displacement. Conversely, the coupling of the corresponding zinc reagent requires a nickel catalyst, which then engages in radical bond formations with primary, secondary, and even tertiary alkyl bromides. Both methods avoid the regioselectivity issue of alkene hydrogermylation and enable the synthesis of a wide range of functionalized alkyl‐substituted germanes. 相似文献
103.
Xiaojuan Deng Wenbin Li Guosheng Ding Tao Xue Xiaoping Chen 《Separation & Purification Reviews》2019,48(1):14-29
Efficient enantioselective separation is a challenging task due to the identical physical and chemical properties of enantiomers. Functionalized magnetic nanomaterials modified with chiral ligands on their surface possess both magnetic property and chiral recognition ability, and have demonstrated great potential in chiral discrimination. This review summarizes the applications of magnetic nanomaterials modified with various chiral selectors (e.g., β-cyclodextrins, polymers, proteins, amino acids and cellulose) in enantioselective separation. After proper preparation and modification, these functionalized magnetic nanomaterials are effective for enantioseparation. Therefore, enantioseparations based on functionalized magnetic nanomaterials are convenient, economical and effective. 相似文献
104.
The photoluminescence of porous silicon with and without carbon deposition fabricated by plasma-enhanced chemical vapor deposition technique has been investigated. After the deposition, the rapid thermal processes in the temperature ranging from 500 to 1100 °C have been carried out. It was found that after the carbon deposition a new intense blue emission appeared. The rapid thermal processes at 800and 900 °C could enhance the blue emission, while the other rapid thermal processes quenched it. Finally, the mechanism for the effect of carbon deposition and rapid thermal processes on photoluminescence properties of porous silicon was discussed. 相似文献
105.
Youji Li Mingyuan Ma Shuguo Sun Wenbin Yan Yuzhu Ouyang 《Applied Surface Science》2008,254(13):4154-4158
TiO2-carbon surface (TCS) composites were prepared by pretreatment of a sealing substrate in supercritical carbon dioxide using paraffin as a plugging agent, and sol-gel processing using tetrabutyl orthotitanate as a precursor. The samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectrum (XPS), optical absorption spectroscopy and nitrogen absorption. The photoactivity of TCS was checked by monitoring the decomposition of methylene blue (MB) in aqueous solution under UV irradiation. The results indicated that compared with TC prepared only by the sol-gel method, the small nanosize TiO2 particles are well dispersed on carbon surface with large amount of micropores and high Eg values, meanwhile TCS have high Ti3+ concentration due to supercritical pretreatment providing a amount of carbon on the composite surface with interfacial energy effects, which controls the growth of TiO2 nanoparticles, baffles the agglomeration of TiO2 nanoparticles and easily produces Ti3+ ions. These are reasons why TCS has a higher efficiency of decomposing MB than TiO2-carbon (TC) composites and pure TiO2. Additional, it is also attributed to the fact that TCS produce a high concentration of organic compounds near TiO2 in comparison with TC and pure TiO2, because their surface area are greater than that of TC and pure TiO2. 相似文献
106.
107.
Wenbin Guo Dr. Nathalie Daro Dr. Sébastien Pillet Dr. Mathieu Marchivie Dr. El-Eulmi Bendeif Dr. Elodie Tailleur Dr. Kittipong Chainok Dominique Denux Dr. Guillaume Chastanet Prof. Philippe Guionneau 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(57):12927-12930
The current craze for research around the spin crossover phenomenon can be justified to some extent by the mechanical properties due to the decrease of volume associated with the transition of the metal ion from the HS state to the LS state. As demonstrated here, the molecular complex [Fe(PM-pBrA)2(NCS)2] exhibits, on the contrary, an increase of the unit-cell volume from HS to LS. This counter-intuitive and unprecedented behavior that concerns both the thermal and the photoexcited spin conversions is revealed by a combination of single-crystal and powder X-ray diffraction complemented by magnetic measurements. Interestingly, this abnormal volume change appears concomitant with the wide rotation of a phenyl ring which induces a drastic modification, though reversible, of the structural packing within the crystal. In addition, the light-induced HS state obtained through the Light-Induced Excited Spin-State Trapping shows a remarkably high relaxation temperature, namely T(LIESST), of 109 K, one of the highest so far reported. The above set of quite unusual characteristics opens up new fields of possibilities within the development of spin crossover materials. 相似文献
108.
109.
Mengmeng Zhang Dr. Jiajun Wang Hui Xue Dr. Jinfeng Zhang Prof. Dr. Shengjie Peng Dr. Xiaopeng Han Prof. Dr. Yida Deng Prof. Dr. Wenbin Hu 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(42):18621-18625
Cu2O is a typical photoelectrocatalyst for sustainable hydrogen production, while the fast charge recombination hinders its further development. Herein, Ni2+ cations have been doped into a Cu2O lattice (named as Ni-Cu2O) by a simple hydrothermal method and act as electron traps. Theoretical results predict that the Ni dopants produce an acceptor impurity level and lower the energy barrier of hydrogen evolution. Photoelectrochemical (PEC) measurements demonstrate that Ni-Cu2O exhibits a photocurrent density of 0.83 mA cm−2, which is 1.34 times higher than that of Cu2O. And the photostability has been enhanced by 7.81 times. Moreover, characterizations confirm the enhanced light-harvesting, facilitated charge separation and transfer, prolonged charge lifetime, and increased carrier concentration of Ni-Cu2O. This work provides deep insight into how acceptor-doping modifies the electronic structure and optimizes the PEC process. 相似文献
110.
Wenbin Wang Yutang Wang Ruoou Yang Qunlei Wen Youwen Liu Zheng Jiang Huiqiao Li Tianyou Zhai 《Angewandte Chemie (International ed. in English)》2020,59(39):16974-16981
Electrochemical synthesis based on electrons as reagents provides a broad prospect for commodity chemical manufacturing. A direct one‐step route for the electrooxidation of amino C?N bonds to nitrile C≡N bonds offers an alternative pathway for nitrile production. However, this route has not been fully explored with respect to either the chemical bond reforming process or the performance optimization. Proposed here is a model of vacancy‐rich Ni(OH)2 atomic layers for studying the performance relationship with respect to structure. Theoretical calculations show the vacancy‐induced local electropositive sites chemisorb the N atom with a lone pair of electrons and then attack the corresponding N(sp3)?H, thus accelerating amino C?N bond activation for dehydrogenation directly into the C≡N bond. Vacancy‐rich nanosheets exhibit up to 96.5 % propionitrile selectivity at a moderate potential of 1.38 V. These findings can lead to a new pathway for facilitating catalytic reactions in the chemicals industry. 相似文献