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111.
Hairan Zhang Qiuyue Zhang Ling Zhang Tingting Pei Erni Li Huiting Wang Prof. Qian Zhang Prof. Lixin Xia 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(6):1535-1542
Poly(N-isopropylacrylamide)-modified graphene oxide (PNIPAm-GO), which is a type of thermally responsive GO, was designed and synthesized through a covalent “grafting-from” strategy. The as-prepared modified nanosheets integrated the individual advantages of two components, such as the thermal sensitivity of the PNIPAm terminal as well as the conductivity and the open 2D structure of the GO substrate. PNIPAm-GO was able to perform the reversible regulation of hydrophilicity/hydrophobicity in aqueous solution upon variations in the temperature. Such a unique property might also lead to the utilization of PNIPAm-GO as an intelligent electrode material to achieve a switchable electrochemical response toward a [Fe(CN)6]3−/4− probe. The PNIPAm-GO modified glassy carbon electrode (PNIPAm-GO/GC electrode) was able to exhibit better electrochemical performance in an ON/OFF switching effect than the PNIPAm-modified glassy carbon electrode (PNIPAm/GC electrode) without GO owing to the intrinsic properties and large surface area of the introduced GO. Moreover, it was found that the PNIPAm-GO/GC electrode also displayed excellent thermally responsive electrocatalysis toward the detection of 1,4-dihydro-β-nicotinamide adenine dinucleotide (NADH) and dopamine (DA), which resulted in two different catalytic statuses on the same electrode. This kind of switchable catalytic performance of the PNIPAm-GO/GC electrode might greatly enhance the flexibility of its application, and thus it is expected to have wide potential for applications in the fields of biosensors and biocatalysis. 相似文献
112.
Xingguang Li Xu Ma Zhixun Wang Pei‐Nian Liu Liming Zhang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(48):17340-17344
By using biphenyl‐2‐ylphosphines functionalized with a remote tertiary amino group as a ligand, readily available acetylenic amides are directly converted into 2‐aminofurans devoid of any electron‐withdrawing and hence deactivating/stabilizing substituents. These highly electron‐rich furans have rarely been prepared, let alone applied in synthesis, because of their high reactivities and low stabilities associated with the electron‐rich nature of the furan ring. In this work, these reactive furans smoothly undergo either in situ intermolecular Diels–Alder reactions to deliver highly functionalized/substituted aniline products or intramolecular ones to furnish carbazole‐4‐carboxylates in mostly good to excellent yields. This work offers general and expedient access to this class of little studies electron‐rich furans and should lead to exciting opportunities for their applications. 相似文献
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The steam-assistant heteroatoms of sulfur and phosphorus dual-doped graphene film fabricated via an ice-template and thermal-activation approach demonstrates an excellent pseudocapacitive behavior in flexible electrochemical capacitors. 相似文献
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We propose a new general type of splitting methods for accretive operators in Banach spaces. We then give the sufficient conditions to guarantee the strong convergence. In the last section, we apply our results to the minimization optimization problem and the linear inverse problem including the numerical examples. 相似文献
118.
Size controlled synthesis of ornithine‐based polypeptides by ring‐opening polymerization of α‐(amino acid)‐N‐carboxyanhydrides 下载免费PDF全文
119.
Synthesis of multi‐functionalized carbonyl compounds by palladium–catalysed γ‐substitution of MBH adducts with activated amides 下载免费PDF全文
Gao Pei‐Sen Zhang Jin‐Lei Li Ning Zheng Zhan Jiang Yuan Yang Gao Zi‐Wei Zhang Weiqiang Xu Li‐Wen 《应用有机金属化学》2018,32(3)
Catalytic allylic γ‐substitution with Morita‐Baylis‐Hillman (MBH) adducts for creating a new family of unsymmetrical dicarbonyl compounds was presented in this work, in which a variety of allylated amide products were achieved in good yields and high regioselectivity with excellent linear‐to‐branched ratios. Especially, it was found that the Pd/HZNU‐Phos complex exhibited remarkably high activity (with a TON up to 16800) in this transformation between dicarbonyl amides and MBH adducts. In addition, the possibly multisite interaction between multifunctional Pd/HZNU‐Phos catalyst system and substrates might responsible for its exceptionally high efficiency in this reaction. 相似文献
120.
Physical gelation and macromolecular mobility of sustainable polylactide during isothermal crystallization 下载免费PDF全文
Huagao Fang Qizheng Xie Haibing Wei Pei Xu Yunsheng Ding 《Journal of Polymer Science.Polymer Physics》2017,55(16):1235-1244
The mobility of free macromolecular chains is of importance to the growth of crystallites in a crystallizing sustainable polylactide (PLA), which was scarcely explored by rheology. In this study, the time‐resolved rheological properties for PLA during isothermal crystallization were investigated first, showing that the storage and loss modulus experience 2–3 decades of increase. The Avrami analysis reveals that the crystallization kinetics in rheological measurement protocol follows the homogeneous nucleation and three‐dimensional growth mechanism. The linear viscoelastic properties in the vicinity of physical gelation point were then studied at the inverse quenching temperature of 165 °C. The results show that physical gelation occurs when the critical absolute crystallinity reaches 13% as determined by the rheological method. Relaxation time spectra reveal that the interfacial relaxation is greatly retarded but the presence of growing spherulites possesses little constraint on the mobility of free chains in matrix especially before physical gelation point. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2017 , 55, 1235–1244 相似文献