ABSTRACT
Higher-ordered architectures self-assembly of nanomaterials have recently attracted increasing attention. In this work, we report a spontaneous and efficient route to simultaneous synthesis and self-assembly of 3D layered beta-FeOOH nanorods depending on a pH-induced strategy, in which the continuous change of pH is achieved by hydrolysis of FeCl(3).6H(2)O in the presence of urea under hydrothermal conditions. The electron microscopy observations reveal that the square-prismic beta-FeOOH nanorods are self-assembled in a side-by-side fashion to form highly oriented 2D nanorod arrays, and the 2D nanorod arrays are further stacked in a face-to-face fashion to form the final 3D layered architectures. On the basis of time-dependent experiments, a multistage reaction mechanism for the formation of the 3D layered beta-FeOOH nanorods architecture is presented, involving the fast growth and synchronous self-assembly of the nanorods toward 1D, 2D, and 3D spontaneously. The experimental evidence further demonstrates that the urea-decomposition-dependent pH continuously changing in the solution, spontaneously altering the driving force competition between the electrostatic repulsive force and the attractive van der Waals force among the nanorods building blocks, is the essential factor to influence the self-assembly of the beta-FeOOH nanorods from 1D to 3D.
ABSTRACT
The title compound, C(13)H(9)BrO, has been synthesized by the intra-molecular Friedel-Crafts reaction of 1-(1-bromo-4-naphth-yl)-3-chloro-propan-1-one. There are two approximately planar [maximum deviations of 0.8â (2) and 0.4â (2)â Å in the two mol-ecules] molecules in the asymmetric unit. The dihedral angle between their mean planes is 19.72â (8)°. Weak inter-molecular C-Hâ¯O hydrogen bonding is present in the crystal structure.
