RESUMO
A series of novel titanium complexes (2a-2e) bearing [N, P] aniline-chlorodiphenylphosphine ligands (1a-1e) featuring CH3 and F substituents have been synthesized and characterized. Surprisingly, in the presence of polar additive, the complexes (2a-2e) all displayed high catalytic activities (up to 1.04 × 106 gPolymer (mol·Ti)-1·h-1 and produced copolymer with the ultrahigh molecular weight up to 1.37 × 106 g/mol. The catalytic activities are significantly enhanced by introducing electron-withdrawing group (F) into the aniline aromatic ring. Especially, the increase in activity based on different complexes followed the order of 2e > 2d > 2c > 2b > 2a. Simultaneously, density functional theory (DFT) calculations have been performed to probe the polymerization mechanism as well as the electronic and steric effects of various substituents on the catalyst backbone. DFT computation revealed that the polymerization behaviors could be adjusted by the electronic effect of ligand substituents; however, it has little to do with the steric hindrance of the substituents. Furthermore, theoretical calculation results keep well in accordance with experimental measurement results. The article provided an appealing design method that the employment of fluorine atom as electron-withdrawing to be studied is the promotive effect of transition-metal coordination polymerization.
RESUMO
We experimentally demonstrate self-accelerating Bessel-like optical beams propagating along arbitrary trajectories in free space. With computer-generated holography, such beams are designed to follow different controllable trajectories while their main lobe transverse profiles remain nearly invariant and symmetric. Examples include parabolic, snake-like, hyperbolic, hyperbolic secant, and even three-dimensional spiraling trajectories. The self-healing property of such beams is also demonstrated. This new class of optical beams can be considered as a hybrid between accelerating and nonaccelerating nondiffracting beams that may find a variety of applications.