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121.
Theoretical and Experimental Chemistry - The effect of the structure of the catalyst and the type of base on the reaction rate and product yield of the tosylation of dihydroxybenzenes in a...  相似文献   
122.
Optics and Spectroscopy - The population kinetics of a two-level system has been theoretically investigated taking into account the transfer of spontaneous radiation under continuous optical...  相似文献   
123.
Physics of Atomic Nuclei - The article presents the concept of a channel-type reactor with a combined cooled moderator. The moderator consists of ceramic beryllium oxide and a liquid...  相似文献   
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Mixed-graft block copolymers (mGBCPs) consist of two or more types of polymeric side chains grafted on a linear backbone in a random, alternating, or pseudo-alternating sequence. They can phase-separate with the backbone serving as the interface of the blocks, and the side chains dominate their self-assembly behavior. mGBCPs are an accessible polymer architecture for exploring the idea of encoding polymer properties through the macromolecular architecture, as there are two distinct structural components that can be tuned: the backbone and the side chains. In this Concept article, the current literature on the synthesis of mGBCPs is reviewed, and the advantages and disadvantages of each synthetic method are noted. The self-assembly of mGBCPs is also discussed where possible. Finally, directions for future research on mGBCP synthesis and self-assembly are suggested.  相似文献   
126.
Physics of Particles and Nuclei Letters - The Silicon Photomultiplier (SiPM) is a novel semiconducting photodetector which can detect single photons. It consists of many microcells (pixels)...  相似文献   
127.
A simple and efficient nitrile-directed meta-C−H olefination, acetoxylation, and iodination of biaryl compounds is reported. Compared to the previous approach of installing a complex U-shaped template to achieve a molecular U-turn and assemble the large-sized cyclophane transition state for the remote C−H activation, a synthetically useful phenyl nitrile functional group could also direct remote meta-C−H activation. This reaction provides a useful method for the modification of biaryl compounds because the nitrile group can be readily converted to amines, acids, amides, or other heterocycles. Notably, the remote meta-selectivity of biphenylnitriles could not be expected from previous results with a macrocyclophane nitrile template. DFT computational studies show that a ligand-containing Pd–Ag heterodimeric transition state (TS) favors the desired remote meta-selectivity. Control experiments demonstrate the directing effect of the nitrile group and exclude the possibility of non-directed meta-C−H activation. Substituted 2-pyridone ligands were found to be key in assisting the cleavage of the meta-C−H bond in the concerted metalation–deprotonation (CMD) process.  相似文献   
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Physics of Particles and Nuclei Letters - The problem of spontaneous isotopic symmetry breaking in Nambu–Jona-Lasinio quark models is considered. It is shown that, in models with light...  相似文献   
130.
Gurbatov  S. N.  Pelinovsky  E. N. 《Doklady Physics》2020,65(8):269-272
Doklady Physics - In this paper, we study the statistical characteristics of the Riemann wave and the integral of it. Such problems arise in the physics of fronts’ propagation, in particular,...  相似文献   
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