This article reports on a novel type of microspheres (∼720 nm in diameter) prepared via precipitation polymerization and constructed by optically active helical substituted polyacetylene (PSA). The microspheres were obtained in high yield (>80%), with regular morphology and narrow size distribution. PSA forming the microspheres was found to adopt helices with predominant one-handed screw sense, according to circular dichroism and UV−vis absorption spectroscopies and specific optical rotation measurements. The helical conformations of PSA endowed the microspheres thereof with considerable optical activity. The chiral microspheres feature in combining in one entity the advantages of both chiral polymers and the micrometer-sized particles in scale and spherical morphology and thus are expected to find some significant applications. This is well exemplified by successful induction of enantioselective crystallization with the chiral microspheres. Such chiral microspheres efficiently induced enantioselective crystallization of alanine enantiomers: (S)-PSA preferably induced L-alanine to form octahedral crystals while (R)-PSA toward D-alanine forming needle-like crystals, with a remarkably high ee (85%). This is the first precipitation polymerization of substituted acetylenes for preparing chiral polymeric microspheres. The present chiral microspheres represent a new type of advanced functional chiral materials.

This article presents two novel artificial helical polymers, substituted polyacetylenes with urea groups in side chains. Poly(4) and poly(5) can be obtained in high yields (≥97%) and with moderate molecular weights (11,000–14,000). Poly(4) contains chiral centers in side chains, and poly(5) is an achiral polymer. Both of the two polymers adopted helical structures under certain conditions. More interestingly, poly(4) exhibited large specific optical rotations, resulting from the predominant one‐handed screw sense. The helical conformation in poly(5) was stable against heat, while poly(4) underwent conformational transition from helix to random coil upon increasing temperature from 0 to 55 °C. Solvents had considerable influence on the stability of the helical conformation in poly(4). The screw sense adopted by the helices was also largely affected by the nature of the solvent. Poly(4‐co‐5)s formed helical conformation and showed large optical rotations, following the Sergeants and Soldiers rule. By comparing the present two polymers (with one NH groups) with the three polymers previously reported (with two NH groups in side chains), the nature of the hydrogen bonds formed between the neighboring urea groups played big roles in the formation of stable helical conformation. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 4112–4121, 2008

A novel and general strategy for the synthesis of carbon-encapsulated metal oxide hollow nanoparticles (HNPs) and pure metal oxide HNPs was developed from carbon-encapsulated metal nanoparticles by controlled oxidation in the air. The materials were characterized by transmission electron microscopy, scanning electron microscopy, and X-ray diffraction measurements. It was found that the morphologies and compositions of HNPs were easily tailored through adjustment of the oxidation conditions. When used as the anode materials for lithium-ion batteries, carbon-encapsulated α-Fe2O3 HNPs exhibit excellent cycling performance and a higher reversible capacity of about 700 mA h g−1 after the 60th cycle and possess great potential application in lithium-ion batteries.

A novel chiral N‐propargylsulfamide monomer (1a) and its enantiomer (1b) were synthesized and polymerized with (nbd)Rh+B−(C6H5)4 as a catalyst providing poly(1) (poly(1a) and poly(1b)) in high yields (≥99%). Poly(1) could take stable helices in less polar solvents (chloroform and THF), demonstrated by strong circular dichroism signals and UV–vis absorption peaks at about 415 nm and the large specific rotations; but in more polar solvents including DMF and DMSO, poly(1) failed to form helix. Quantitative evaluation with anisotropy factor showed that the helical screw sense had a relatively high thermal stability. These results together with the IR spectra measured in solvents showed that hydrogen bonding between the neighboring sulfamide groups is one of the main driving forces for poly(1) to adopt stable helices. In addition, copolymerization of monomer 1a and monomer 2 was conducted, the solubility of poly(1) was improved drastically. However, the copolymerization had adverse effects on the formation of stable helices in the copolymers. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 500–508, 2007

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