Light Down-Converter Based on Luminescent Nanofibers from the Blending of Conjugated Rod-Coil Block Copolymers and Perovskite through Electrospinning.

We demonstrated a novel strategy for the preparation of light down-converter by combining rod-coil block copolymers with perovskite quantum dots (QDs) through electrospinning. Reports have shown that polymer deformability can be enhanced by incorporating a soft segment and controlled by varying the rod/coil ratio. Therefore, we first synthesized the rod-coil block copolymer through the click reaction of polyfluorene (PF) and poly(n-butyl acrylate) (PBA). Next, the CsPbBr3@PF8k-b-PBA12k composite fibers were fabricated by blending perovskite through electrospinning. Optical spectral evidence demonstrated the success of the strategy, as light down-converters were prepared through the controlled variance of QD/polymer ratios to achieve tunable color and stretchability. This result reveals the potential of using rod-coil block copolymers to fabricate color-tunable perovskite light down-converters.

Programmed folding into spiro-multicyclic polymer topologies from linear and star-shaped chains.

The development of precise folding techniques for synthetic polymer chains that replicate the unique structures and functions of biopolymers has long been a key challenge. In particular, spiro-type (i.e., 8-, trefoil-, and quatrefoil-shaped) polymer topologies remain challenging due to their inherent structural complexity. Herein, we establish a folding strategy to produce spiro-type multicyclic polymers via intramolecular ring-opening metathesis oligomerization of the norbornenyl groups attached at predetermined positions along a synthetic polymer precursor. This strategy provides easy access to the desired spiro-type topological polymers with a controllable number of ring units and molecular weight while retaining narrow dispersity (Ɖ < 1.1). This effective strategy marks an advancement in the development of functionalized materials composed of specific three-dimensional nanostructures.

A versatile synthetic strategy for macromolecular cages: intramolecular consecutive cyclization of star-shaped polymers.

Cage-shaped polymers, or "macromolecular cages", are of great interest as the macromolecular analogues of molecular cages because of their various potential applications in supramolecular chemistry and materials science. However, the systematic synthesis of macromolecular cages remains a great challenge. Herein, we describe a robust and versatile synthetic strategy for macromolecular cages with defined arm numbers and sizes based on the intramolecular consecutive cyclization of highly reactive norbornene groups attached to each end of the arms of a star-shaped polymer precursor. The cyclizations of three-, four-, six-, and eight-armed star-shaped poly(ε-caprolactone)s (PCLs) bearing a norbornenyl group at each arm terminus were effected with Grubbs' third generation catalyst at high dilution. 1H NMR, SEC, and MALDI-TOF MS analyses revealed that the reaction proceeded to produce the desired macromolecular cages with sufficient purity. The molecular sizes of the macromolecular cages were controlled by simply changing the molecular weight of the star-shaped polymer precursors. Systematic investigation of the structure-property relationships confirmed that the macromolecular cages adopt a much more compact conformation, in both the solution and bulk states, as compared to their linear and star-shaped counterparts. This synthetic approach marks a significant advance in the synthesis of complex macromolecular architectures and provides a platform for novel applications using cage-shaped molecules with polymer frameworks.