ABSTRACT
Bulk molybdenum disulfide (MoS2 ) itself is virtually insoluble in common organic solvents because of the tight stacks of multiple MoS2 nanosheets. Here we report that V-shaped polyaromatic compounds with non-ionic side chains can efficiently exfoliate and disperse the inorganic nanosheets. Simple grinding and sonication (less than total 1â h) of MoS2 powder with the V-shaped compounds gave rise to large MoS2 nanosheets highly dispersed in NMP through efficient host-guest S-π interactions. DLS and AFM analyses revealed that the lateral sizes (ca.â 150-270â nm) and thicknesses (ca.â 2-8â nm) of the products depend on the identity of the non-ionic side chains on the V-shaped dispersant.
ABSTRACT
By the covalent linkage of two bent bisanthracene amphiphiles with a biphenyl spacer bearing hydrophilic pendants, we synthesized a new molecular clip with a C-shaped conformation. The molecular clip provides an acyclic, open cavity surrounded by four anthracene panels in water. In contrast to previous clip- and tweezers-like compounds as well as cage-shaped compounds, the C-shaped polyaromatic cavity displays unusual wide-ranging capturing abilities toward not only planar perylene-based pigments and cylindrical single-walled carbon nanotubes but also highly branched macromolecules (carbazole dendrimers).
ABSTRACT
Complexation of novel multiply N-confused expanded calix[n]phyrins with boron difluoride afforded a new class of cyclic BODIPY (boron-dipyrromethene) arrays. The structures of circularly arranged BODIPY subunits linked in an N-confused fashion give rise to such photophysical properties unique to the macrocycles as redshifted emission wavelengths along with apparent large Stokes shifts, long emission lifetimes, and solid-state lasing. The DFT calculations support the size-dependent excited-state dynamics of the macrocycles.
