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941.
Bernice H. L. Oh Alexander Bismarck Mary B. Chan‐Park 《Macromolecular rapid communications》2015,36(4):364-372
High‐porosity interconnected, thermoresponsive macroporous hydrogels are prepared from oil‐in‐water high internal phase emulsions (HIPEs) stabilized by gelatin‐graft‐poly(N‐isopropylacrylamide). PolyHIPEs are obtained by gelling HIPEs utilizing the thermoresponsiveness of the copolymer components. PolyHIPEs properties can be controlled by varying the aqueous phase composition, internal phase volume ratio, and gelation temperature. PolyHIPEs respond to temperature changes experienced during cell seeding, allowing fibroblasts to spread, proliferate, and penetrate into the scaffold. Encapsulated cells survive ejection of cell‐laden hydrogels through a hypodermic needle. This system provides a new strategy for the fabrication of safe injectable biocompatible tissue engineering scaffolds.
942.
So Young An Seung Man Noh Joon Hyun Nam Jung Kwon Oh 《Macromolecular rapid communications》2015,36(13):1255-1260
Polymer‐based crosslinked networks with intrinsic self‐repairing ability have emerged due to their built‐in ability to repair physical damages. Here, novel dual sulfide–disulfide crosslinked networks (s‐ssPxNs) are reported exhibiting rapid and room temperature self‐healability within seconds to minutes, with no extra healing agents and no change under any environmental conditions. The method to synthesize these self‐healable networks utilizes a combination of well‐known crosslinking chemistry: photoinduced thiol‐ene click‐type radical addition, generating lightly sulfide‐crosslinked polysulfide‐based networks with excess thiols, and their oxidation, creating dynamic disulfide crosslinkages to yield the dual s‐ssPxNs. The resulting s‐ssPxN networks show rapid self‐healing within 30 s to 30 min at room temperature, as well as self‐healing elasticity with reversible viscoelastic properties. These results, combined with tunable self‐healing kinetics, demonstrate the versatility of the method as a new means to synthesize smart multifunctional polymeric materials.
943.
Yidong Zhang Zhenwei Dong Lei Zhao Huijuan Guan 《Surface and interface analysis : SIA》2022,54(6):600-606
ZnO film-based ultraviolet (UV) detector was fabricated by photoassisted peak force tunnel atomic force (PFTUNA) on fluorine tin oxide (FTO) substrate. The PFTUNA current in dark and in UV light was ~0.1 and 2.0 nA, respectively. The UV sensitivity (photocurrent/dark current) is more than 20. The response time and the recovery time are ~0.12 and 0.32 s, respectively. The UV sensing mechanism is that the holes will transport to the ZnO surface to capture the adsorbed oxygen ions to weaken the depletion layer under UV illumination. The PFTUNA current between the tip and the ZnO film is consistent with the Richardson–Schottky (RS) thermionic emission model. 相似文献
944.
Wang Hua-Shun Zhang Ling-Fang Liu Ming-Xin Gu Xue-jiao Li Man-fei Zheng Chao-Pei Wang Kai Xiao Dong Zhou Min Li Xue-Mei Hu Qiu-Fen Li Yin-Ke 《Chemistry of Natural Compounds》2022,58(5):888-891
Chemistry of Natural Compounds - Two new CPA-type indole alkaloids (1 and 2) were isolated from the fungus Aspergillus versicolor. Their structures were determined by means of HR-ESI-MS and... 相似文献
945.
Journal of Structural Chemistry - A new bis(salamo)-type ligand has been designed and synthesized, and its hetero-trinuclear [Cu(II)2Ca(II)] complex has been successfully prepared. It is... 相似文献
946.
在盘状液晶分子外围柔性链中引入功能不同的基团, 是设计和合成具有良好液晶性能化合物的常用策略. 本工作从苯并菲2,3-二甲酸和酸酐出发, 通过亲核取代和点击反应, 分别合成了两类三唑环修饰的苯并菲二羧酸酯和苯并菲酰亚胺化合物. 热重分析仪(TGA)测试表明, 新制备的主要中间产物与目标化合物失重为5%时的温度在274~389 ℃之间, 均表现出良好的热稳定性. 我们通过差示扫描量热法(DSC)、偏光显微镜(POM)和变温X射线衍射(XRD)实验对这些化合物的热力学行为和介晶性进行了研究. 除三唑环修饰的酯3a和3b无液晶性外, 主要中间产物(2和5)与三唑环修饰的酰亚胺产物(6a和6b)均有一个六方柱状液晶相. 此外, 制备的以三唑为桥联基团的酰亚胺二聚体10为室温液晶, 具有173 ℃的液晶范围. XRD证实了该二聚体中存在有序度不同的两种柱状液晶相(Colh1和Colh2). 另外, 由于三唑环的引入, 三唑环修饰的酯类和酰亚胺两类化合物在某些有机溶剂中都能形成有机凝胶. 其中, 二聚体10在1,2-二氯乙烷和1,4-二氧六环中表现出优异的凝胶能力, 其临界凝胶浓度(CGC)可低至1 mg/mL. 相比之下, 不含三唑环的中间产物2和5则不能形成凝胶, 表明三唑环之间的偶极-偶极作用和液晶刚性核π-π堆积的协同作用对于超分子凝胶的形成起着重要的作用. 因此, 同时表现出液晶和凝胶性质的三唑环修饰的苯并菲2,3-二酰亚胺分子具有成为一种多功能材料的潜在应用价值. 相似文献
947.
Dong Yunzhao Li Tingcheng You Xiangqian You Qingliang Sun Lang Xie Guangyong 《Research on Chemical Intermediates》2022,48(3):1151-1158
Research on Chemical Intermediates - Dichlorobenzonitriles are important organic intermediates for the production of many fine chemicals and are produced most economically and environment-friendly... 相似文献
948.
Huang Qiying Xue Hanjing Dong Ruitao Xue Yun Zhou Xiaodong Li Zichao Li Qun 《Cellulose (London, England)》2022,29(3):1759-1774
Cellulose - Aiming to improve the thermal stability and flame retardant properties of calcium alginate, calcium alginate (CaAlg)/hydroxyapatite (HAP) hybrid material was synthesized in situ by the... 相似文献
949.
Dr. Zhaowen Dong Dr. Andrzej Sienkiewicz Dr. Abdusalom A. Suleymanov Cesare Berton Dr. Farzaneh Fadaei-Tirani Dr. Rosario Scopelliti Prof. Kay Severin 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(32):e202200893
Dichalcogenolenes are archetypal redox non-innocent ligands with numerous applications. Herein, a diselenolene ligand with fundamentally different electronic properties is described. A mesoionic diselenolene was prepared by selenation of a C2-protected imidazolium salt. This ligand is diamagnetic, which is in contrast to the paramagnetic nature of standard dichalcogenolene monoanions. The new ligand is also redox-active, as demonstrated by isolation of a stable diselenolene radical dianion. The unique electronic properties of the new ligand give rise to unusual coordination chemistry. Thus, preparation of a hexacoordinate aluminum tris(diselenolene) complex and a Lewis acidic aluminate complex with two ligand-centered unpaired electrons was achieved. 相似文献
950.
Some short peptides can spontaneously self-assemble into various nanostructures via the synergistic driving forces of non-covalent interactions. These non-covalent interactions,including electrostatic interaction,hydrogen bonding,aromatic interactions and other non-covalent interactions,are usually highly coupled together. Through rational sequence design and proper modification of short peptide molecules,the driving forces could be regulated purposively,and the nanostructures and morphologies of the self-assemblies could be controlled accordingly,and thus so as to achieve the fabrication of peptide-based supramolecular biomaterials and develop their functions. In this paper,the effects of hydrogen bonding,π-π stacking, electrostatic interaction,hydrophobic interaction,metal ion coordination and chiral center on the self-assembly behavior of peptide self-assembly have been reviewed. The driving force regulation strategies, including sequence design,pH and concentration adjustment and metal ion coordination,and the resulted nanostructures have also been discussed. We also make the outlooks on the development of peptide-based supramolecular biomaterials with specific functions in biomedicines and biocatalysis. © 2022, Science Press (China). All rights reserved. 相似文献