Hydrogen‐transfer polymerization of vinyl monomers derived from 4‐methylbenzoyl isocyanate and acrylamide derivatives

The anionic polymerization of N‐acryloyl‐N′‐(4‐methylbenzoyl)urea (1) was carried out at 80°C for 24 h in DMF, DMSO, acetonitrile, or toluene by t‐BuOK or DBU (3 mol %) as an initiator to obtain polymer 3 in a good yield. The structure of 3 was dependent upon the initiator used, in which t‐BuOK selectively conducted the hydrogen‐transfer polymerization, while DBU partially induced the vinyl polymerization (16–20%). Likewise, N‐acryloyl‐N‐methyl‐N′‐(4‐methylbenzoyl)urea (2, i.e., an N‐methylated derivative of 1) was subjected to the hydrogen‐transfer polymerization. Although the yield of the polymer was lower in comparison with 1, the structure of the obtained polymer 4 was similarly governed by the initiator. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 465–472, 1999     

Topological Hall effect in pyrochlore lattice with varying density of spin chirality

The three-site spin correlation, S(i)·(S(j)×S(k)) on the neighboring triangular sites i, j and k, termed scalar spin chirality, can endow the conduction electron with a quantum Berry phase and resultant transverse (Hall) transport. The paramagnetic barely metallic state was prepared in hole-doped Y2Mo2O7 with pyrochlore lattice using a high-pressure synthesis method, which is further endowed with the spin chirality by partially replacing Y site with Tb (content x). The local spin chirality formed by the adjacent three Tb Ising moments on the pyrochlore lattice can couple to the conduction electrons to give rise to the topological Hall effect whose magnitude increases in proportion to x3 or the density of the Tb-moment triangular clusters.     

Electronic Structures and Magnetic Properties of Transition Metal Doped CsPbI3 Perovskite Compounds by First-Principles Calculation

Physics of the Solid State - Transition metal doped cesium lead halide (CsPbI3) perovskite compounds were studied for application in photovoltaic solar cells. Electronic structures, chemical shifts...