Thermoresponsive Property of Poly(,-bis(2-methoxyethyl)acrylamide) and Its Copolymers with Water-Soluble Poly(,-disubstituted acrylamide) Prepared Using Hydrosilylation-Promoted Group Transfer Polymerization.

The group-transfer polymerization (GTP) of ,-bis(2-methoxyethyl)acrylamide (MOEAm) initiated by MeEtSiH in the hydrosilylation-promoted method and by silylketene acetal (SKA) in the conventional method proceeded in a controlled/living manner to provide poly(,-bis(2-methoxyethyl)acrylamide) (PMOEAm) and PMOEAm with the SKA residue at the α-chain end (MCIP-PMOEAm), respectively. PMOEAm--poly(dimethylacrylamide) (PDMAm) and PMOEAm--PDMAm and PMOEAm--poly(-bis(2-ethoxyethyl)acrylamide) (PEOEAm) and PMOEAm--PEOEAm were synthesized by the block and random group-transfer copolymerization of MOEAm and dimethylacrylamide or -bis(2-ethoxyethyl)acrylamide. The homo- and copolymer structures affected the thermoresponsive properties; the cloud point temperature () increasing by decreasing the degree of polymerization (x).

Maltotriose-Chlorin e6 Conjugate Linked Tetraethyleneglycol as an Advanced Photosensitizer for Photodynamic Therapy. Synthesis and Antitumor Activities against Canine and Mouse Mammary Carcinoma Cells.

Glycoconjugated chlorins represent a promising class of compounds that meet the requirements for the third-generation photosensitizer (PS) for photodynamic therapy (PDT). We have focused on the use of glucose (Glc) to improve the performance of the PS based on the Warburg effect-a phenomenon where tumors consume higher Glc levels than normal cells. However, as a matter of fact, Glc-conjugation has a poor efficacy in hydrophilic modification; thus, the resultant PS is not suitable for intravenous injection.

Planar tetracoordinate carbon species CLi3E with 12-valence-electrons.

We exhibit theoretically a series of 12-valence-electron pentaatomic species CLi3E (E = N, P, As, Sb, Bi) and CLi3E(+) (E = O, S, Se, Te, Po). The analyses of potential energy surfaces indicate that the C2v structures with a planar tetracoordinate carbon are the global minimum in these species except for E = N, P. A localized C[double bond, length as m-dash]E double bond is found in the planar tetracoordinate carbon species.

Correction: Efficient singlet oxygen generation from sugar pendant C60 derivatives for photodynamic therapy.

Correction for 'Efficient singlet oxygen generation from sugar pendant C60 derivatives for photodynamic therapy' by Shigenobu Yano et al., Chem. Commun.

Efficient singlet oxygen generation from sugar pendant C60 derivatives for photodynamic therapy.

The amidation reaction between C60 with an activated ester group (1) and acetylated Glc (AcGlc) with an amino group (2) was performed to yield the target AcGlc-pendant C60 compound (3). The water soluble deacetylated compound, Glc-pendant C60 compound (4), exhibited high photocytotoxicity against HeLa cells due to the more efficient singlet oxygen generation as compared with that of Glc-pendant azafulleroids.

Unconventional charge distribution in the planar wheel-type M©B6H6(-/0/+) (M = Mn, Fe and Co): central M with negative charges and peripheral boron ring with positive charges.

Planar wheel-type D6h M©B6H6(-/0/+) (M = Mn, Fe and Co for anion, neutral and cation, respectively.) clusters with a planar hexacoordinate transition-metal at the center of the boron ring were designed and investigated by density functional theory. These planar clusters are chemically stable as a result of their large binding energy, vertical ionization potential, and vertical electron affinity.

Mechanical ball-milling preparation of fullerene/cobalt core/shell nanocomposites with high electrochemical hydrogen storage ability.

The design and synthesis of new hydrogen storage nanomaterials with high capacity at low cost is extremely desirable but remains challenging for today's development of hydrogen economy. Because of the special honeycomb structures and excellent physical and chemical characters, fullerenes have been extensively considered as ideal materials for hydrogen storage materials. To take the most advantage of its distinctive symmetrical carbon cage structure, we have uniformly coated C60's surface with metal cobalt in nanoscale to form a core/shell structure through a simple ball-milling process in this work.

Controlled synthesis and chiral recognition of immobilized cellulose and amylose tris(cyclohexylcarbamate)s/3-(triethoxysilyl)propylcarbamates as chiral packing materials for high-performance liquid chromatography.

The cyclohexylcarbamates of cellulose and amylose bearing a controlled amount of 3-(triethoxysilyl)propyl residue were synthesized by a one-pot process and efficiently immobilized onto silica gel through the intermolecular polycondensation of triethoxysilyl group. Their chiral recognition abilities were evaluated as chiral packing materials (CPMs) for high-performance liquid chromatography (HPLC). The immobilized CPMs exhibited comparable or higher recognition abilities than the conventional coated-type CPMs.

Immobilization and chromatographic evaluation of novel regioselectively substituted amylose-based chiral packing materials for HPLC.

The regioselectively substituted amylose derivatives bearing a 4-tert-butylbenzoate or 4-chlorobenzoate group at 2-position, and 3,5-dichlorophenylcarbamate and a small amount of 3-(triethoxysilyl)propylcarbamate groups at 3- and 6-positions were synthesized by a two-step process based on the esterification of 2-position of a glucose unit. The obtained derivatives were effectively immobilized onto macroporous silica gel by intermolecular polycondensation of triethoxysilyl groups. Their chiral recognition abilities were evaluated as chiral packing materials (CPMs) for high-performance liquid chromatography.

Preparation and chiral recognition in HPLC of cellulose 3,5-dichlorophenylcarbamates immobilized onto silica gel.

The 3,5-dichlorophenylcarbamates (2) of cellulose bearing a small amount of 3-(triethoxysilyl)propyl residues were synthesized by a one-pot process and immobilized onto a silica gel through intermolecular polycondensation of the triethoxysilyl groups. The obtained cellulose derivatives were characterized by (1) H NMR and elemental analysis (EA), and their recognition abilities were evaluated by high-performance liquid chromatography (HPLC). The cellulose derivatives containing about 1-5% of the 3-(triethoxysilyl)propyl residue were efficiently immobilized with a high chiral recognition ability.

Determination of nitrobenzene in water and ice samples collected from the Songhua River after an explosion of a petrochemical plant and investigation on enclosing behavior of nitrobenzene into ice.

In this study, nitrobenzene in water and ice samples collected from the Songhua River after the explosion of a petrochemical plant was determined by GC/MS. The results showed that nitrobenzene was detected in most of the water and ice samples taken from the Songhua River. However, the concentration of nitrobenzene in all water and ice samples was from 0 to 0.