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Physics of the Solid State - Within the framework of the cluster model using the Mie pair power-law interaction potential with the effective depth of the potential well, whose depth is determined...  相似文献   
164.
An efficient strategy enabling the construction of polysubstituted 1,2-dihydroquinoline derivatives mediated by the commercially available, economical, and environmentally benign iodine (3 mol %) under mild conditions was developed. Various arylamines and α-ketoesters could participate in this cascade reaction, and the desired products were obtained in excellent yields up to 98%.  相似文献   
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Li  Zhisheng  Jiang  Haokai  Cheng  Yanying  Gao  Yunji  Chen  Longfei  Zhang  Yuchun  Li  Tao  Xing  Shaoshuai 《Journal of Thermal Analysis and Calorimetry》2022,147(21):12139-12154
Journal of Thermal Analysis and Calorimetry - Few investigations have focused on the influence of longitudinal fire source location on the temperature profile of smoke induced by fire in a tunnel...  相似文献   
167.
Xu  Rui  Wang  Xin  Zhou  Yuhao 《Nonlinear dynamics》2022,107(3):2345-2362
Nonlinear Dynamics - This paper focuses on the problem of the event-triggered adaptive containment control for a class of nonlinear multiagent systems (MASs) with prescribed performance and...  相似文献   
168.
Chiral Mn Ⅲ (salen) (Jacobsen’s catalyst) was axially immobilized onto a new type of organic polymer-inorganic hybrid materialzirconium poly(styrene-isopropenyl phosphonate)-phosphate(ZPS-IPPA) with different linkage lengths and evaluated as catalysts for the epoxidation of unfunctionalized olefins. The results demonstrated that the prepared catalysts exhibited moderate to good activity and enantioselectivity in the asymmetric epoxidation of unfunctionalized olefins. Furthermore, the immobilized catalysts were relatively stable and could be conveniently separated from the reaction system by simple precipitation in hexane. Moreover, higher enantioselectivity was obtained with catalyst 2c than that of homogeneous counterpart catalyzed even after eight times. The excellent recycling of the catalyst was attributed to its structure feature of ZPS-IPPA which is different from either pure polystyrene or pure zirconium phosphates.  相似文献   
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To elucidate the structure of a compound is a necessary step for its practical applications. To study the structure and properties of metal sulfide fullerene Sc2S@C88 detected by mass spectrometry, 11 194 isomers of C88 and 33 isomers of Sc2S@C88 were systematically examined by density functional theory calculations. The calculations show that the two lowest‐energy isomers are Sc2S@C88:81 738 (IPR‐35) and Sc2S@C88:81 735 (IPR‐32), followed by Sc2S@C88:81 729 (IPR‐26), Sc2S@C88:81 712 (IPR‐9), and Sc2S@C88:81 733 (IPR‐30). Structural analysis shows that the first two energetically favored isomers are bridged by the third and fifth energetically favored isomers, which can transfer into each other via direct Stone–Wales rotation. The calculations of temperature effect show that the first two favored isomers become dominant forms of Sc2S@C88 with decreasing temperature and may coexist in the soot. This structural convertibility among favored isomers of Sc2S@C88 suggest a hidden rule that birds of a feather flock together in metal sulfide fullerenes. This rule may decrease the range of candidate cages for the structural identification of a metal sulfide fullerene. IR spectra are simulated for helping the future experimental identification of Sc2S@C88.  相似文献   
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