Living Anionic Addition Reaction of 1,1-Diphenylethylene Derivatives: One-Pot Synthesis of ABC-type Chain-End Sequence-Controlled Polymers.

In this study, a 1:1 addition reaction using 1,1-diphenylethylene (DPE) derivatives, referred to as the "living anionic addition reaction", was established to regulate the sequence of vinyl compounds having negligible homopolymerizability. The stoichiometric and successive addition reaction between a DPE anion and more reactive DPE derivatives proceeded quantitatively when the electrophilicity of the DPE derivatives was sufficiently enhanced by electron-withdrawing groups such as (trimethylsilyl)ethynyl and acyl groups. The relative electrophilicity of the DPE derivatives was predicted by Hammett's law and the ß-carbon chemical shifts of the carbon-carbon double bonds. AB- and ABC-type chain-end sequence-controlled polystyrenes with well-defined structures were synthesized by reacting two or three DPE derivatives with difunctional anionic living polystyrene in increasing order of their electrophilicity in a one-pot reaction.

Bioinspired structural transition of synthetic polymers through biomolecular ligand binding.

Inspired by ligand binding-triggered structural transition of biopolymers in living systems, we demonstrated the structural transition of thermoresponsive poly(N-isopropylacrylamide) through specific ligand binding of artificially evolved peptides to the polymer.

A thermoresponsive dynamic polymer brush fabricated by the segregation of amphiphilic diblock copolymers.

A highly dense polymer brush was previously fabricated by the spontaneous segregation of amphiphilic diblock copolymers in an elastomer matrix into water and a hydrophobic polymer interface and named a 'dynamic polymer brush'. We fabricated a lower critical solution temperature (LCST)-type thermoresponsive dynamic polymer brush by mixing polyisoprene-b-poly[tri(ethylene glycol)methyl ether methacrylate] (PI-b-PME3MA) into a polystyrene-b-polyisoprene-b-polystyrene (SIS) elastomer. The LCST of PME3MA in water is 52 °C. The structure of the polymer brush was determined at several different temperatures using neutron reflectivity. With increasing temperature, the brush thickness of the LCST-type thermoresponsive dynamic polymer brush decreases, similar to the conventional fixed brush with the LCST-type thermoresponse. However, the graft density of the dynamic polymer brush surprisingly increases with increasing temperature. The change of the brush density of the conventional fixed polymer brush is not allowed. However, we observed for the first time that dynamic polymer brushes uniquely respond to increasing temperature with increasing brush densities.

Biomimetic Synthesis of Antireflective Silica/Polymer Composite Coatings Comprising Vesicular Nanostructures.

Antireflective (AR) silica/polymer composite coatings on glass and poly(methyl methacrylate) (PMMA) substrates were prepared by silica mineralization of layer-by-layer (LbL) assembled films composed of polystyrene-block-poly(l-lysine)/poly(l-glutamic acid) (PS-b-PLL/PGA) complex vesicles without any post-treatments. PS-b-PLL AB and A2B block copolymers with appropriate block ratio can self-assemble to form vesicles, which can be deposited onto substrates without dissociation. Silica deposition specifically onto the complex vesicles in the multilayer films through amine-catalyzed polycondensation results in the continuous, intact composite coatings comprising vesicular nanostructures, which provided an additional parameter for tuning their optical properties. The film thickness and porosity are mainly dictated by the bilayer number and the degree of deformation/fission of vesicles upon complexation and mineralization, depending on polymer composition. The coated PMMA substrate with maximum transmission over 98% can be achieved at the optimized wavelength region. The AR composite films were mechanically stable to withstand both the wipe and adhesion tests due to the preparation of continuous, intact films. This study demonstrated that the concept of preparing composite films comprising vesicular nanostructures through the combination of LbL assembly and biomineralization is feasible.

Affinity-based thermoresponsive precipitation of proteins modified with polymer-binding peptides.

A 12-mer peptide with an affinity for the meso diad sequence of poly(N-isopropylacrylamide) (PNIPAM) was identified through affinity-based peptide screening. A model protein (i.e., human serum albumin (HSA)) chemically modified with the peptide was successfully precipitated with PNIPAM above the lower critical solution temperature (LCST) of PNIPAM.

Synthesis and Characterization of Multicomponent ABC- and ABCD-Type Miktoarm Star-Branched Polymers Containing a Poly(3-hexylthiophene) Segment.

The new series of ABC-type miktoarm star polymer (ABC star, A = polyisoprene (PI), B = polystyrene (PS), and C = poly(3-hexylthiophene) (P3HT)) and ABCD-type miktoarm star polymer (ABCD star, A = PI, B = PS, C = poly(α-methylstyrene) (PαMS), and D = P3HT) could be synthesized by the combination of the controlled KCTP, anionic linking reaction, and Click chemistry. By the copper(I)-catalyzed Huisgen 1,3-dipolar cycloaddition click reaction of the azido-chain-end-functional P3HT (P3HT-N3) with the alkyne-in-chain-functional AB diblock copolymer (A = PI and B = PS) (AB-alkyne) or alkyne-core-functional ABC miktoarm star polymer (A = PI, B = PS, and C = PαMS) (ABC-alkyne), the target ABC star and ABCD star, respectively, were obtained, as confirmed by size exclusion chromatography (SEC) and proton nuclear magnetic resonance (1H NMR). The thermal and optical properties of these star polymers were examined by thermal gravimetric analysis (TGA) and UV-vis spectroscopy. The dynamic scattering calorimetry (DSC), atomic force micrograph (AFM) image, and grazing incidence small-angle X-ray scattering (GISAXS) results showed that the periodic P3HT fibril nanostructures rather than microphase separation occurred in the ABCD star film. In addition, it was found that highly crystalline P3HT domains aligned in the "edge-on" orientation, as supported by grazing incidence wide-angle X-ray scattering (GIWAXS).

Living Anionic Polymerization of Benzofulvene: Highly Reactive Fixed Transoid 1,3-Diene.

Anionic polymerization of benzofulvene (BF, α-methyleneindene), an exomethylene monomer having a fixed transoid 1,3-diene moiety, quantitatively proceeded with sec-BuLi or diphenylmethylpotassium in THF at -78 °C for 1 h. The resulting poly(BF)s possessed the predicted molecular weights based on the molar ratios between monomer and initiators and narrow molecular weight distributions (Mw/Mn = 1.1). High anionic polymerizability of BF was realized by the fact that a well-defined diblock copolymer, poly(methyl methacrylate)-block-poly(BF), was obtained by the sequential copolymerization of BF with a low nucleophilic enolate anion of living poly(methyl methacrylate) in quantitative efficiency. NMR analyses indicated that the repeating units of poly(BF) consisted of a 1,2-addition unit (41%) and a 1,4-addition unit (59%) without a 3,4-addition unit, suggesting that the exomethylene group of BF always participated in the polymerization. Thus, BF acted as a novel polymerizable transoid 1,3-diene in the anionic polymerization.

Reduced hydrophobic interaction of polystyrene surfaces by spontaneous segregation of block copolymers with oligo (ethylene glycol) methyl ether methacrylate blocks: force measurements in water using atomic force microscope with hydrophobic probes.

Reduction of hydrophobic interaction in water is important in biological interfaces. In our previous work, we have found that poly(styrene- b-triethylene glycol methyl ether methacrylate) (PS-PME3MA) segregates the PME3MA block to the surface in hydrophobic environment, such as in air or in a vacuum, and shows remarkable resistance against adsorption or adhesion of proteins, platelets, and cells in water. In this paper, we report that atomic force microscopy (AFM) with hydrophobic probes can directly monitor the reduced hydrophobic interaction of the PS surfaces modified by poly(styrene- b-origoethylene glycol methyl ether methacrylate) (PS-PME NMA), where N is the number of ethylene glycol units. The pull-off forces between the hydrophobic probes that are coated with octyltrichlorosilane (OLTS) and the PS-PME NMA modified polystyrene (PS) surfaces in water were measured. The absolute spring constants and tip-curvatures of the AFM cantilevers were measured to compute the work of adhesion by the Johnson, Kendall, and Roberts (JKR) theory, which relates the pull-off force at which the separation occurs between a hemisphere and a plane to the work of adhesion. The hydrophobic interactions between the hydrophobic tip and polymer surfaces in water were greatly reduced with the segregated PME NMA blocks. The hydrophobic interactions decrease with increasing N of the series of PS-PME NMA and show a correlation with the amount of protein adsorbed.

Formation of alternating copolymers via spontaneous copolymerization of 1,3-dehydroadamantane with electron-deficient vinyl monomers.

Copolymerizations of 1,3-dehydroadamantane, 1, and various vinyl monomers were carried out in THF at room temperature. On mixing 1 with electron-deficient vinyl monomers, such as acrylonitrile and methyl acrylate, in the absence of any initiator, the copolymerization spontaneously proceeded to give alternating copolymers in 28-88% yield. By contrast, no reaction of 1 occurred at all when isobutyl vinyl ether or styrene was mixed under similar conditions. These contrastive results indicate the high electron density of a central sigma-bond in a strained [3.3.1]propellane derivative, 1. Alternating sequences of the resulting copolymers were characterized by NMR and MALDI-TOF-MS measurements. DSC and TGA measurements revealed the high thermal stability of the alternating copolymers containing bulky, stiff, and strain-free adamantane skeletons.