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211.
Hollow multishelled structure(HoMS)is one of the most promising multifunctional structures.The high complexity of its structure makes the general and controllable synthesis of HoMS rather challenging.By integration of multidisciplinary knowledge,a great achievement in HoMSs has been obtained in the past decade.Especially,the developed sequential templating approach has significantly boomed the progress of HoMS in composition and structure diversity and application area.The implementation of the temporal-spatial ordering in HoMS makes it indispensable in solving the key scientific problems in energy conversion,catalysis and drug delivery areas.Further development in HoMSs with novel intricate structures will bring new understandings.In this review,we systematically introduce the development history of HoMSs,summarize the inspiration inherited from the previous research on hollow structures,and discuss the milestones in the development of HoMSs,with a focus on the sequential templating approach for HoMS fabrication,attractive temporal-spatial ordering property and dynamic smart behavior for advanced applications.We hope to reveal the inherent relationship between the precise synthesis of HoMS and its highly tunable compositional and structural characteristics,and point out its future direction to boost HoMS area further. 相似文献
212.
Electropolymerization is one of the most important methodologies to synthesize and develop conducting polymers. The complexity of the polymerization mechanism, ion doping processes and structural defects are considered to be symbiotic and unavoidable, making the stagnant state and huge band gap with advanced interdisciplinary research fields and important applications in the last three decades. Herein, we provide a point of view into controlled electropolymerization by regioselective activation reactions of monomers, where self-dimerizations instead of self-electropolymerizations were utilized. The resulting dimers play a role in the connections between functional building blocks to form functional polymers on demand. This account highlights the typical findings in controlled electropolymerizations as a forum for discussing new opportunities in exploiting novel designs and applications. 相似文献
213.
Mn4+-activated double perovskite phosphors with composition diversity have presented excellent luminescent performances. However, the charge imbalance between Mn4+ and matrix cations would increase non-radiative recombination and reduce the structural stability. Here, novel high-efficiency stable Li+/Mn4+ co-incorporated Sr2YSbO6 red phosphors are successfully synthesized via a solid-state reaction method for warm w-LEDs, where the Li+ ions have the effect of charge balance for Sr2YSbO6:Mn4+ and reduce the non-radiative energy transfer among Mn4+ ions. It is demonstrated that the substitution of Li+–Mn4+ pairs for Sb5+ can enhance the bonding with low-shifted diffraction peaks and high emission intensity, and prolong the decay lifetime, compared with those of Mn4+ single-doped ones. Impressively, the thermal stability is enhanced to 89.72% from 84.61% at the original value of 303 K. Finally, a w-LED device based on the optimal phosphor Sr2YSbO6:0.01Mn4+/0.01Li+ red component exhibits a correlated color temperature of 4487 K and color rendering index of 80.2. Therefore, the incorporated Li+ ions serve as both charge compensator and co-activator in Mn4+-activated double perovskite phosphors with the aim of high luminescent performance and thermal stability. 相似文献
214.
Chiral 2-oxazolines are valuable building blocks and famous ligands for asymmetric catalysis. The most common synthesis involves the reaction of an amino alcohol with a carboxylic acid. In this paper, an efficient synthesis of 2-oxazolines has been achieved via the stereospecific isomerization of 3-amido-2-phenyl azetidines. The reactions were studied in the presence of both Brønsted and Lewis acids, and Cu(OTf)2 was found to be the most effective. 相似文献
215.
San-E Zhu Jian-Hui Zhang Yu Gong Li-Feng Dou Li-Hua Mao Hong-Dian Lu Chun-Xiang Wei Hong Chen Xue-Fei Wang Wei Yang 《Molecules (Basel, Switzerland)》2021,26(5)
A broadband visible light-absorbing [70]fullerene-BODIPY-triphenylamine triad (C70-B-T) has been synthesized and applied as a heavy atom-free organic triplet photosensitizer for photooxidation. By attaching two triphenylmethyl amine units (TPAs) to the π-core of BODIPY via ethynyl linkers, the absorption range of the antenna is extended to 700 nm with a peak at 600 nm. Thus, the absorption spectrum of C70-B-T almost covers the entire UV–visible region (270–700 nm). The photophysical processes are investigated by means of steady-state and transient spectroscopies. Upon photoexcitation at 339 nm, an efficient energy transfer (ET) from TPA to BODIPY occurs both in C70-B-T and B-T, resulting in the appearance of the BODIPY emission at 664 nm. Direct or indirect (via ET) excitation of the BODIPY-part of C70-B-T is followed by photoinduced ET from the antenna to C70, thus the singlet excited state of C70 (1C70*) is populated. Subsequently, the triplet excited state of C70 (3C70*) is produced via the intrinsic intersystem crossing of C70. The photooxidation ability of C70-B-T was studied using 1,5-dihydroxy naphthalene (DHN) as a chemical sensor. The photooxidation efficiency of C70-B-T is higher than that of the individual components of C70-1 and B-T, and even higher than that of methylene blue (MB). The photooxidation rate constant of C70-B-T is 1.47 and 1.51 times as that of C70-1 and MB, respectively. The results indicate that the C70-antenna systems can be used as another structure motif for a heavy atom-free organic triplet photosensitizer. 相似文献
216.
Transformation thermodynamics as a major extension of transformation optics has recently received considerable attention. In this paper, we present two-dimensional (2D) and three-dimensional (3D) diamond-shaped transient thermal cloaks with non-singular homogeneous material parameters. The absence of singularity in the parameters results from the fact that the linear coordinate transformation is performed by expanding a line segment rather than a point into a region, while the mechanism behind the homogeneity is the homogeneous stretching and compression along orthogonal directions during the transformation. Although the derived parameters remain anisotropic, we further show that this can be circumvented by considering a layered structure composed of only four types of isotropic materials based on the effective medium theory. Numerical simulation results confirm the good performance of the proposed cloaks. 相似文献
217.
A phase transition was observed at 63-69 GPa and room temperature in vanadium with synchrotron x-ray diffraction. The transition is characterized as a rhombohedral lattice distortion of the body-centered-cubic vanadium without a discontinuity in the pressure-volume data, thus representing a novel type of transition that has never been observed in elements. Instead of driven by the conventional s-d electronic transition mechanism, the phase transition could be associated with the softening of C44 trigonal elasticity tensor that originates from the combination of Fermi surface nesting, band Jahn-Teller distortion, and electronic topological transition. 相似文献
218.
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220.
Beryllium fluorides are widely used in protein phosphorylation studies to get stable transition state analogs or near attack conformers, which has attracted much attention. BeF3? is one of the optimal phosphoryl (PO3?) analogs for its identical geometry and charge, and Mg2+ naturally participates in the phosphoryl binding in biological systems. In solutions, BeF3? coexists with other beryllium fluorides (BeF42?, BeF2 and BeF+) and magnesium fluorides, and there are equilibriums between these species. In this article, 19F NMR spectroscopy was applied to the investigation of the impact of magnesium(II) on beryllium fluorides. It has been found that when Mg2+ was introduced into the solutions, the chemical shifts, the intensities and the line widths of 19F signals of various beryllium fluoride complexes were changed. After ionic strength correction, these effects were remarkable only for BeF42? and BeF3?, especially BeF42?, when the concentration of the fluoride ion is relatively low. Mechanism of the effects is proposed which involves ion pair formation between Mg2+ and beryllium fluorides. 相似文献