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201.
Inside Cover: An Extra‐Large‐Pore Zeolite with 24×8×8‐Ring Channels Using a Structure‐Directing Agent Derived from Traditional Chinese Medicine (Angew. Chem. Int. Ed. 22/2018)
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Jiahui Liu Guangming Wang Xuepu Wang Yan Sun Bei Zhou Yunlong Zou Prof. Dr. Biaobing Wang Prof. Dr. Kaka Zhang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(67):16735-16743
The fabrication of room-temperature organic phosphorescence and afterglow materials, as well as the transformation of their photophysical properties, has emerged as an important topic in the research field of luminescent materials. Here, we report the establishment of energy landscapes in dopant-matrix organic afterglow systems where the aggregation states of luminescent dopants can be controlled by doping concentrations in the matrices and the methods of preparing the materials. Through manipulation by thermodynamic and kinetic control, dopant-matrix afterglow materials with different aggregation states and diverse afterglow properties can be obtained. The conversion from metastable aggregation state to thermodynamic stable aggregation state of the dopant-matrix afterglow materials to leads to the emergence of intriguing afterglow transformation behavior triggered by thermal and solvent annealing. The thermodynamically unfavorable reversible afterglow transformation process can also be achieved by coupling the dopant-matrix afterglow system to mechanical forces. 相似文献
203.
正The Chang'E-3(CE-3)mission began with a smooth countdown and flawless launch on the Long March 3B rocket from the Xichang satellite launch center at 01:30 CST on December 2,2013.It landed on the northeastern Imbrium basin(340.49°E,44.12°N)at 21:11 CST on December 14,2013,and the Yutu rover was deployed from the lander the next morning at 04:35.The lander was equipped with a number of remote-sensing 相似文献
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A “Mitsubishi emblem” tetrauclear aluminum complex containing two unsymmetric N2O2‐ligands and a symmetric NO3‐ligand as initiator for polymerization of rac‐lactide
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Minggang Hu Fugui Wang Fuzhong Han Qigang Deng Wenhui Ma Hailong Yan Guohua Dong Weiming Song 《Journal of polymer science. Part A, Polymer chemistry》2017,55(12):2084-2091
A novel hydroxy‐, methoxy‐, and phenoxy‐bridge “Mitsubishi emblem” tetranuclear aluminum complex ( 1 ) is synthesized from an unsymmetric amine‐pyridine‐bis(phenol) N2O2‐ligand (H2L1) and a symmetric amine‐tris(phenol) NO3‐ligand (H2L2). Two same configuration chiral nitrogen atoms are formed in the tetranuclear Al complex upon coordination of the unsymmetric tertiary amine ligand to central Al. Complex 1 initiates controlled ring‐opening polymerization (ROP) of rac‐lactide and afford polylactide (PLA) with narrow molecular weight distributions (Mw/Mn = 1.05–1.19). The analysis of 1H NMR spectra of the oligomer indicates that the methoxy group is the initiating group and the ring‐opening polymerization of lactide follows a coordination‐insertion mechanism. The Homonuclear decoupled 1H NMR spectroscopy suggests the isotactic‐rich chains is preferentially formed in PLA. The study on kinetics of the ROP of lactide reveals the homopropagation rate is higher than the cross‐propagation rate, which is in agreement with the observed isotactic selectivity in the ROP of rac‐lactide. The stereochemistry of the polymerization was also supported by activation parameters. The introduction of unsymmetric ligand H2L1 has an effect on stereoslectivity of polymerization. This result may be of interest for the design of multinuclear metal complex catalysts containing functionalized ligands. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 2084–2091 相似文献
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X. Yang R.-Y. Zou R. Li J.-L. Yang Y. Ye Y.-F. Zhao 《Phosphorus, sulfur, and silicon and the related elements》2013,188(6):722-727
Abstract A series of novel side group-modified cyclotriphosphazene derivatives were synthesized by the reaction of hexachlorocyclotriphosphazene [N3P3Cl6] with 2,2′-diphenol and the potassium salt of 4-hydroxybenzaldehyde, and subsequent reduction of aldehyde groups to alcohol groups by the use of sodium borohydride. The bromination reaction was carried out with PBr3 to give N3P3(O2C12H8) (p-BrCH2-C6H4-O-)4. This compound was employed in reactions with macrocyclic polyamides, imidazole, or morpholine to produce title compounds. The target compounds were characterized by 1H NMR, 31P NMR, 13C NMR, and electrospray ionization mass spectrometry. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file. 相似文献
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A methodology for improving antistatic property of polyetherimide (PEI) composite using polyaniline (PANI) grafted multi‐walled carbon nanotubes (MWNTs) as conductive medium was proposed. First, the MWNTs grafted with PANI (PANI‐g‐MWNTs) were prepared by in‐situ polymerization in an emulsion system. Subsequently, PANI‐g‐MWNTs were blended with PEI using N‐methyl‐2‐pyrrolidone as solvent. After removing the solvent, the PEI/PANI‐g‐MWNT composite was prepared. As assisted conductive medium, the grafted PANI molecular chains on MWNT surface were dispersed in the PEI matrix to decrease the percolation value of the antistatic composites. The structure and morphology of PANI‐g‐MWNTs were characterized by Fourier transform infrared spectroscopy, transmission electron microscope, thermogravimetric analysis, and X‐ray powder diffraction, respectively. The dispersion of PANI‐g‐MWNTs in PEI matrix was studied by scanning electron microscope. The electrical performance was characterized by highly resistant meter. The volume resistivity of the conductivity percolation threshold was 1.781 × 10?8 S/cm when the loading of PANI‐g‐MWNTs was 1.0 wt%. The conductivity of PANI‐g‐MWNTs/PEI composites was found to be higher than that of pristine MWNTs/PEI composite. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献