Fabrication of 3D engineered intestinal tissue producing abundant mucus by air-liquid interface culture using paper-based dual-layer scaffold.

Fabrication of engineered intestinal tissues with the structures and functions as humans is crucial and promising as the tools for developing drugs and functional foods. The aim of this study is to fabricate an engineered intestinal tissue from Caco-2 cells by air-liquid interface culture using a paper-based dual-layer scaffold and analyze its structure and functions. Just by simply placing on a folded paper soaked in the medium, the electrospun gelatin microfiber mesh as the upper cell adhesion layer of the dual-layer scaffold was exposed to the air, while the lower paper layer worked to preserve and supply the cell culture medium to achieve stable culture over several weeks. Unlike the flat tissue produced using the conventional commercial cultureware, Transwell, the engineered intestinal tissue fabricated in this study formed three-dimensional villous architectures. Microvilli and tight junction structures characteristic of epithelial tissue were also formed at the apical side. Furthermore, compared to the tissue prepared by Transwell, mucus production was significantly larger, and the enzymatic activities of drug metabolism and digestion were almost equivalent. In conclusion, the air-liquid interface culture using the paper-based dual-layer scaffold developed in this study was simple but effective in fabricating the engineered intestinal tissue with superior structures and functions.

Photochromism of phenazine-2,3-diol derivatives through excited state intermolecular proton transfer based on keto-enol tautomerization.

Photochromism through excited-state intermolecular proton transfer (ESInterPT) processes based on keto-enol tautomerization was found in phenazine-2,3-diol PD1 and its monoalkoxy derivative PD2 in a glassy matrix at 77 K: the colorless solutions of enol forms PD1-E and PD2-E at 298 K transformed into orange-colored solutions of keto forms PD1-K and PD2-K upon photoirradiation (λ = 385 nm) at 77 K. Furthermore, this report is the first to achieve the single-crystal X-ray structural analyses of phenazine-2,3-diol PD1 and its monoalkoxy derivative PD2, since the report on the synthesis of PD1 70 years ago. Indeed, it was found that PD1 and PD2 molecules exist in the keto form (PD1-K) and the enol form (PD2-E), respectively, in the crystal, and the neighboring PD1-K and PD2-E molecules are linked by one-dimensional intermolecular NH⋯O and OH⋯N hydrogen bonding, respectively. The fact suggests strongly that for PD1 and PD2, the formation of continuous intermolecular hydrogen bonding in aggregates such as in a glassy matrix at 77 K is involved in the keto-enol tautomerization of phenazine-2,3-diol derivatives based on ESInterPT. More interestingly, the color and the photoabsorption spectrum of the solids obtained by sublimation of crystals of PD2-E are similar to those for the crystals of PD1-K, indicating that the PD2 molecule exists in the keto form (PD2-K) in the solid of the sublimate. Therefore, this study provides a valuable insight for a greater understanding of the keto-enol tautomerization of diazaacene-diol derivatives and their photophysical properties in the solution and in the solid state.

Wireless Electrochemical Gel Actuators.

Soft actuators generate motion in response to external stimuli and are indispensable for soft robots, particularly future miniature robots with complex structure and motion. Similarly to conventional hard robots, electricity is suitable for the stimulation. However, previous electrochemical soft actuators require a tethered connection to a power supply, limiting their size, structure, and motion. Here, wireless electrochemical soft actuators composed of hydrogels and driven by bipolar electrochemistry are reported. Viologen, which dimerizes by one-electron reduction and dissociates by one-electron oxidation, is incorporated in the side chains of the gel networks and works as a reversible cross-link. Wireless and reversible electrochemical actuation of the hydrogels, i.e., muscle-like shrinking and swelling, is demonstrated at microscopic and even macroscopic scales.

Thermally Stable Photomechanical Molecular Hinge: Sterically Hindered Stiff-Stilbene Photoswitch Mechanically Isomerizes.

Molecular photoswitches are extensively used as molecular machines because of the small structures, simple motions, and advantages of light including high spatiotemporal resolution. Applications of photoswitches depend on the mechanical responses, in other words, whether they can generate motions against mechanical forces as actuators or can be activated and controlled by mechanical forces as mechanophores. Sterically hindered stiff stilbene (HSS) is a promising photoswitch offering large hinge-like motions in the E/Z isomerization, high thermal stability of the Z isomer, which is relatively unstable compared to the E isomer, with a half-life of ca. 1000 years at room temperature, and near-quantitative two-way photoisomerization. However, its mechanical response is entirely unexplored. Here, we elucidate the mechanochemical reactivity of HSS by incorporating one Z or E isomer into the center of polymer chains, ultrasonicating the polymer solutions, and stretching the polymer films to apply elongational forces to the embedded HSS. The present study demonstrated that HSS mechanically isomerizes only in the Z to E direction and reversibly isomerizes in combination with UV light, i.e., works as a photomechanical hinge. The photomechanically inducible but thermally irreversible hinge-like motions render HSS unique and promise unconventional applications differently from existing photoswitches, mechanophores, and hinges.

Development of water-soluble phenazine-2,3-diol-based photosensitizers for singlet oxygen generation.

Phenazine-2,3-diol-based dyes, KY-1Na and KY-2Na bearing one and two carboxylic acid sodium salts, respectively, have been newly developed as water-soluble photosensitizers (PSs) possessing the ability to generate singlet oxygen (1O2). In order to evaluate the solubility of KY-1Na and KY-2Na in water, the hydrophobicity/hydrophilicity of the two PSs was investigated by experimental measurement of the logarithms (log Po/w) of the 1-octanol/water partition coefficient (Po/w) for the PS. The log Po/w values of both KY-1Na and KY-2Na were determined to be -0.9, indicating that both the PSs are more hydrophilic than Rose Bengal (-0.6) and have hydrophilicity equivalent to methylene blue (-0.9). Both the PSs in water show a broad photoabsorption band in the range of 500 to 600 nm. Thus, we estimated the 1O2 quantum yields (ΦΔ) of KY-1Na and KY-2Na in water by using 9,10-anthracenediyl-bis(methylene)dimalonic acid (ABDA) as a water-soluble 1O2 scavenger. It was found that in water the ΦΔ value (0.19) of KY-2Na is higher than that of KY-1Na (0.06). Density functional theory (DFT) calculations suggested that the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) distributions for the molecular structure of KY-2Na are adequately separated, leading to a decrease in the energy gap (ΔEST) between the singlet state (S1) and the triplet state (T1) that causes efficient intersystem crossing (ISC), compared to that for the molecular structure of KY-1Na. Indeed, time-dependent DFT (TD-DFT) calculations demonstrated that the ΔEST(S1-T1) value (0.82 eV) of KY-2Na is smaller than that (0.98 eV) of KY-1Na, resulting in a relatively high ΦΔ value of KY-2Na. Consequently, we demonstrate that phenazine-2,3-diol-based PSs bearing carboxylic acid salts possess high solubility and moderate 1O2 generation ability in water.

Thermoelectric Properties of Conductive Freestanding Films Prepared from PEDOT:PSS Aqueous Dispersion and Ionic Liquids.

In this study, freestanding poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) films modified with an ionic liquid (IL) were synthesized assuming modulization. These films were easily peeled off the glass substrate in water, producing hydrophobic and flexible freestanding films that exhibited extremely high mechanical strengths. The thermoelectric properties of the IL-doped PEDOT:PSS films depended on the amount of IL incorporated. To analyze the mechanism of this dependence in detail, the compositions, higher-order structures, and electronic states of the polymer films were studied by X-ray photoelectron spectroscopy, X-ray diffraction analysis, and electronic absorption spectroscopy. In addition, the carrier density in the polymer film was quantified using electrochemical techniques, and its correlation with the thermoelectric conversion properties was analyzed.

Sterically Hindered Stiff-Stilbene Photoswitch Offers Large Motions, 90% Two-Way Photoisomerization, and High Thermal Stability.

Molecular photoswitches have been widely used as molecular machines in various fields due to the small structures and simple motions generated in reversible isomerization. However, common photoswitches, as represented by azobenzene (AB), cannot combine both large motions and high thermal stability, which are critically important for some practical applications in addition to high photoisomerization yields. Here, we focus on a promising photoswitch, stiff stilbene (SS), and its derivative, sterically hindered SS (HSS). The detailed investigation of their performance with a comparison to AB demonstrated that HSS is an outstanding photoswitch offering larger motions than AB and SS, ca. 90% photoisomerization in both E-to-Z and Z-to-E directions, and significantly high thermal stability with a half-life of ca. 1000 years at room temperature. The superior performance of HSS promises its use in various applications, even where previous photoswitches have troubles and are unavailable.

Fluorescent polymer films based on photo-induced electron transfer for visualizing water.

As fluorescent materials for visualization, detection, and quantification of a trace amount of water, we have designed and developed a PET (photo-induced electron transfer)-type fluorescent monomer SM-2 composed of methyl methacrylate-substituted anthracene fluorophore-(aminomethyl)-4-cyanophenylboronic acid pinacol ester (AminoMeCNPhenylBPin) and achieved preparation of a copolymer poly(SM-2-co-MMA) composed of SM-2 and methyl methacrylate (MMA). Both SM-2 and poly(SM-2-co-MMA) exhibited enhancement of the fluorescence emission with the increase in water content in various solvents (less polar, polar, protic, and aprotic solvents) due to the formation of the PET inactive (fluorescent) species SM-2a and poly(SM-2-co-MMA)a, respectively, by the interaction with water molecules. The detection limit (DL) of poly(SM-2-co-MMA) for water in the low water content region below 1.0 wt% in acetonitrile was 0.066 wt%, indicating that poly(SM-2-co-MMA) can act as a PET-type fluorescent polymeric sensor for a trace amount of water in solvents, although it was inferior to that (0.009 wt%) of SM-2. It was found that spin-coated poly(SM-2-co-MMA) films as well as 15 wt% SM-2-doped polymethyl methacrylate (PMMA) films produced a satisfactory reversible fluorescence off-on switching between the PET active state under a drying process and the PET inactive state upon exposure to moisture, which is demonstrated by the fact that the both the films are similar in hydrophilicity to each other from the measurement of the water contact angles on the polymer film surface. Herein we propose that PET-type fluorescent polymer films based on a fluorescence enhancement system are one of the most promising and convenient functional dye materials for visualizing moisture and water droplets.

Synthesis, optical and electrochemical properties of (D-π)2-type and (D-π)2Ph-type fluorescent dyes.

The (D-π)2-type fluorescent dye OTT-2 with two (diphenylamino)carbazole-thiophene units as D (electron-donating group)-π (π-conjugated bridge) moiety and the (D-π)2Ph-type fluorescent dye OTK-2 with the two D-π moieties connected through a phenyl ring were derived by oxidative homocoupling of a stannyl D-π unit and Stille coupling of a stannyl D-π unit with 1,3-diiodobenzene, respectively. Their optical and electrochemical properties were investigated by photoabsorption and fluorescence spectroscopy, time-resolved fluorescence spectroscopy, cyclic voltammetry (CV) and molecular orbital (MO) calculations. In toluene the photoabsorption and fluorescence maximum wavelengths (λmax,abs and λmax,fl) of OTT-2 appear in a longer wavelength region than those of OTK-2. The fluorescence quantum yield (Φfl) of OTT-2 is 0.41, which is higher than that (Φfl = 0.36) of OTK-2. In the solid state OTT-2 shows relatively intense fluorescence properties (Φfl-solid = 0.24 nm), compared with OTK-2 (Φfl-solid = 0.15 nm). CV results demonstrated that OTT-2 and OTK-2 exhibit a reversible oxidation wave. Based on photoabsorption, fluorescence spectroscopy and CV for the two dyes, it was found that the lowest unoccupied molecular orbital (LUMO) energy level of OTT-2 is lower than that of OTK-2, but OTT-2 and OTK-2 have comparable highest occupied molecular orbital (HOMO) energy levels. Consequently, this work reveals that compared to the (D-π)2Ph-type structure, the (D-π)2-type structure exhibits not only a bathochromic shift of the photoabsorption band, but also intense fluorescence emission both in solution and the solid state.

Mechanofluorochromism of (D-π-)2A-type azine-based fluorescent dyes.

Bathochromic or hypsochromic shift-type mechanofluorochromism (b-MFC or h-MFC) was found for (D-π-)2A-type azine-based fluorescent dyes OUY-2, OUK-2, and OUJ-2 possessing intramolecular charge-transfer (ICT) characteristics from two (diphenylamino)carbazole-thiophene units as D (electron-donating group)-π (π-conjugated bridge) moieties to a pyridine, pyrazine, or triazine ring as A (electron-withdrawing group): grinding of the recrystallized dyes induced red or blue shifts of the fluorescent colors, that is, bathochromic or hypsochromic shifts of the fluorescence maximum wavelengths (λfl-solid max). The degrees of MFC evaluated by the absolute value of differences (Δλ fl-solid max) in λfl-solid max before and after grinding of the recrystallized dyes increased in the order of OUY-2 (+7 nm) < OUK-2 (-17 nm) < OUJ-2 (+45 nm), so that OUJ-2 exhibits obvious b-MFC, but OUK-2 exhibits h-MFC. X-ray powder diffraction (XRD) and differential scanning calorimetry (DSC) demonstrated that the recrystallized dyes were in the crystalline state but the ground dyes were in the amorphous state. When the ground solids were heated above their crystallization temperatures (T c), the colors and fluorescent colors recovered to the original ones before grinding or converted to other ones, that is, heating the ground solids in the amorphous state induced the recrystallization to recover the original microcrystals or to form other microcrystals due to polymorph transformation. However, (D-π-)2Ph-type fluorescent dye OTK-2 having a phenyl group as a substitute for the azine rings exhibited non-obvious MFC. Molecular orbital (MO) calculations indicated that the values of the dipole moments (µ g) in the ground state were 4.0 debye, 1.4 debye, 3.2 debye, and 2.9 debye for OTK-2, OUY-2, OUK-2, and OUJ-2, respectively. Consequently, on the basis of experimental results and MO calculations, we have demonstrated that the MFC of the (D-π-)2A-type azine-based fluorescent dyes is attributed to reversible switching between the crystalline state of the recrystallized dyes and the amorphous state of the ground dyes with changes in the intermolecular dipole-dipole and π-π interactions before and after grinding. Moreover, this work reveals that (D-π-)2A fluorescent dyes possessing dipole moments of ca. 3 debye as well as moderate or intense ICT characteristics make it possible to activate the MFC.

Synthesis, optical and electrochemical properties of 4,4'-bibenzo[c]thiophene derivatives.

We designed and synthesized unsubstituted 4,4'-bibenzo[c]thiophene 4,4'-BBT and its silyl-substituted derivatives 1,1'-Si-4,4'-BBT and 1,1',3,3'-Si-4,4'-BBT with one or two tert-butyldimethylsilyl groups on each thiophene ring, as new π-building blocks in emitters, photosensitizers and semiconductors for organic optoelectronic devices. The characterization of 4,4'-BBT, 1,1'-Si-4,4'-BBT and 1,1',3,3'-Si-4,4'-BBT was successfully determined by FTIR, 1H and 13C NMR measurements, high-resolution mass spectrometry (HRMS) analysis, photoabsorption and fluorescence spectroscopy, cyclic voltammetry (CV) and density functional theory (DFT) calculations. Moreover, a single-crystal X-ray structural analysis was successfully made for 1,1'-Si-4,4'-BBT and 1,1',3,3'-Si-4,4'-BBT. The photoabsorption and fluorescence maxima (λ abs max and λ fl max) of the three 4,4'-bibenzo[c]thiophene derivatives in toluene exhibit bathochromic shifts in the order of 4,4'-BBT (359 nm and 410 nm) < 1,1'-Si-4,4'-BBT (366 nm and 420 nm) < 1,1',3,3'-Si-4,4'-BBT (371 nm and 451 nm). The HOMO and LUMO energy levels rise in the order of 4,4'-BBT (-5.55 eV and -2.39 eV) < 1,1'-Si-4,4'-BBT (-5.45 eV and -2.34 eV) < 1,1',3,3'-Si-4,4'-BBT (-5.34 eV and -2.30 eV), but the rise of the HOMO energy level is larger than that of the LUMO energy level, resulting in the bathochromic shift of the photoabsorption band from 4,4'-BBT to 1,1',3,3'-Si-4,4'-BBT. The fluorescence quantum yields (Φ fl) of 4,4'-BBT, 1,1'-Si-4,4'-BBT and 1,1',3,3'-Si-4,4'-BBT in toluene are 0.41, 0.41 and 0.36, respectively. It is worth mentioning that in the solid state 1,1'-Si-4,4'-BBT and 1,1',3,3'-Si-4,4'-BBT show relatively high Φ fl-solid values of 0.22 and 0.25, respectively, whereas 4,4'-BBT exhibits poor solid-state fluorescence properties (Φ fl-solid < 0.02). This work provides an efficient synthetic method for the 4,4'-bibenzo[c]thiophene derivatives and their photophysical properties in the solution and solid state, electrochemical properties and X-ray crystal structures.

Polymer films doped with fluorescent sensor for moisture and water droplet based on photo-induced electron transfer.

Anthracene-(aminomethyl)phenylboronic acid pinacol ester (AminoMePhenylBPin) OF-2 acts as a PET (photo-induced electron transfer)-type fluorescent sensor for determination of a trace amount of water: the addition of water to organic solvents containing OF-2 causes a drastic and linear enhancement of fluorescence emission as a function of water content, which is attributed to the suppression of PET. Indeed, detection limits (DLs) for OF-2 were as low as 0.01-0.008 wt% of water in solvents, that is, the PET method makes it possible to visualize, detect, and determine a trace amount of water. Thus, in this work, in order to develop fluorescent polymeric materials for visualization and detection of water, we have achieved the preparation of various types of polymer films (polystyrene (PS), poly(4-vinylphenol) (PVP), polyvinyl alcohol (PVA), and polyethylene glycol (PEG)) which were doped with OF-2, and investigated the optical sensing properties of the OF-2-doped polymer films for water. As-prepared OF-2-doped polymer films initially exhibited green excimer emission in the PET active state, but blue monomer emission in the PET inactive state upon exposure to moisture or by water droplet. Moreover, it was found that the OF-2-doped polymer films show the reversible fluorescence properties in the dry-wet process. Herein we propose that polymer films doped with PET-type fluorescent sensors for water based on a fluorescence enhancement (turn-on) system are one of the most promising and convenient functional materials for visualizing moisture and water droplets.

Fluorescent supramolecular mechanophores based on charge-transfer interactions.

Supramolecular mechanofluorophores based on charge-transfer (CT) interactions between fluorescent pyrene and naphthalene diimide(s) with a tandem structure are newly developed and incorporated into the mid-chain of poly(ε-caprolactone)s. The fluorescence (FL) is quenched by the intramolecular CT interactions even at low concentrations both in solution and in the polymer matrix, and turn-on FL is induced upon application of mechanical forces.

Cell adhesion control by photoinduced LCST shift of PNIPAAm-based brush scaffolds.

Poly(N-isopropylacrylamide) (PNIPAAm)-brush substrates are one of the most successful dynamic scaffolds for thermally controlling cell adhesion. Endowing substrates with photocontrollability promises further development and applications in the biomedical and bioengineering fields. In this study, we developed photoresponsive PNIPAAm copolymers by incorporation of spiropyran into the polymer chain, enabling the photoinduced shift of the lower critical solution temperatures. Their brush substrates were fabricated in a simple, facile grafting-to manner. Co-grafting with non-cell-adhesive poly(ethylene glycol) enhanced the modulation of surface chemical properties upon photostimulation; it enabled significant photocontrol of cell adhesion of several types with keeping culture temperature constant.

Development of optical sensor for water in acetonitrile based on propeller-structured BODIPY-type pyridine-boron trifluoride complex.

A propeller-structured 3,5,8-trithienyl-BODIPY-type pyridine-boron trifluoride complex, ST-3-BF3, which has three units of 2-(pyridin-4-yl)-3-(thiophen-2-yl)acrylonitrile at the 3-, 5-, and 8-positions on the BODIPY skeleton, was designed and developed as an intramolecular charge transfer (ICT)-type optical sensor for the detection of a trace amount of water in acetonitrile. The characterization of ST-3-BF3 was successfully determined by FTIR, 1H and 11B NMR measurements, high-resolution mass spectrometry (HRMS) analysis, thermogravimetry-differential thermal analysis (TG-DTA), photoabsorption and fluorescence spectral measurements, and density functional theory (DFT) calculations. ST-3-BF3 showed a broad photoabsorption band in the range of 600 to 800 nm, which is assigned to the S0 → S1 transition of the BODIPY skeleton with the expanded π-conjugated system over the 2-(pyridin-4-yl)-3-(thiophen-2-yl)acrylonitrile units at the 3-, 5-, and 8-positions onto the BODIPY core. In addition, a photoabsorption band was also observed in the range of 300 to 550 nm, which can be assigned to the ICT band between the 2-(pyridin-4-yl)-3-(thiophen-2-yl)acrylonitrile units at 3-, 5-, and 8-positions and the BODIPY core. ST-3-BF3 exhibited a characteristic fluorescence band originating from the BODIPY skeleton at around 730 nm. It was found that by addition of a trace amount of water to the acetonitrile solution of ST-3-BF3, the photoabsorption band at around 415 nm and the fluorescence band at around 730 nm increased linearly as a function of the water content below only 0.2 wt%, which could be ascribed to the change in the ICT characteristics due to the dissociation of ST-3-BF3 into ST-3 by water molecules. Thus, this work demonstrated that the 3,5,8-trithienyl-BODIPY-type pyridine-boron trifluoride complex can act as a highly-sensitive optical sensor for the detection of a trace amount of water in acetonitrile.

Synthesis, photophysical and electrochemical properties of pyridine, pyrazine and triazine-based (D-π-)2A fluorescent dyes.

The donor-acceptor-π-conjugated (D-π-)2A fluorescent dyes OUY-2, OUK-2 and OUJ-2 with two (diphenylamino)carbazole thiophene units as D (electron-donating group)-π (π-conjugated bridge) moiety and a pyridine, pyrazine or triazine ring as electron-withdrawing group (electron-accepting group, A) have been designed and synthesized. The photophysical and electrochemical properties of the three dyes were investigated by photoabsorption and fluorescence spectroscopy, Lippert-Mataga plots, cyclic voltammetry and density functional theory calculations. The photoabsorption maximum (λmax,abs) and the fluorescence maximum (λmax,fl) for the intramolecular charge-transfer characteristic band of the (D-π-)2A fluorescent dyes show bathochromic shifts in the order of OUY-2 < OUK-2 < OUJ-2. Moreover, the photoabsorption bands of the (D-π-)2A fluorescent dyes are nearly independent of solvent polarity, while the fluorescence bands showed bathochromic shifts with increasing solvent polarity (i.e., positive fluorescence solvatochromism). The Lippert-Mataga plots for OUY-2, OUK-2 and OUJ-2 indicate that the Δµ (= µe - µg) value, which is the difference in the dipole moment of the dye between the excited (µe) and the ground (µg) states, increases in the order of OUY-2 < OUK-2 < OUJ-2. Therefore, the fact explains our findings that OUJ-2 shows large bathochromic shifts of the fluorescence maxima in polar solvents, as well as the Stokes shift values of OUJ-2 in polar solvents are much larger than those in nonpolar solvents. The cyclic voltammetry of OUY-2, OUK-2 and OUJ-2 demonstrated that there is little difference in the HOMO energy level among the three dyes, but the LUMO energy levels decrease in the order of OUY-2 > OUK-2 > OUJ-2. Consequently, this work reveals that for the (D-π-)2A fluorescent dyes OUY-2, OUK-2 and OUJ-2 the bathochromic shifts of λmax,abs and λmax,fl and the lowering of the LUMO energy level are dependent on the electron-withdrawing ability of the azine ring, which increases in the order of OUY-2 < OUK-2 < OUJ-2.

Fluorescent sensor for water based on photo-induced electron transfer and Förster resonance energy transfer: anthracene-(aminomethyl)phenylboronic acid ester-BODIPY structure.

An anthracene-(aminomethyl)phenylboronic acid ester-BODIPY (DJ-1) was designed and developed as a fluorescent sensor based on photo-induced electron transfer (PET) and Förster resonance energy transfer (FRET) for the detection of a trace amount of water in solvents, where the anthracene skeleton and BODIPY skeleton are the donor fluorophore and the acceptor fluorophore in the FRET process, respectively. It was found that the addition of water to organic solvents containing DJ-1 causes both the suppression of PET in the anthracene-(aminomethyl)phenylboronic acid ester as the PET-type fluorescent sensor skeleton and the energy transfer from the anthracene skeleton to the BODIPY skeleton through a FRET process, thus resulting in the enhancement of the fluorescence band originating from the BODIPY skeleton. This work demonstrates that the PET/FRET-based fluorescent dye composed of the donor fluorophore possessing PET characteristics and the acceptor fluorophore in the FRET process can act as a fluorescent sensor with a large SS for the detection of a trace amount of water in solvents.

Development of an intramolecular charge transfer-type colorimetric and fluorescence sensor for water by fusion with a juloidine structure and complexation with boron trifluoride.

An optical sensor with the ability to detect and determine water over a wide concentration range is highly desirable in the laboratory and industry. Here the sensitivity and spectral responses of an intramolecular charge transfer-type colorimetric and fluorescence sensor with ß-carboline structure are tuned and improved significantly over various water contents in the organic solvent by fusion with an electron-donating juloidine structure and complexation with boron trifluoride (BF3). The sensors, ET-1 and ET-1-BF3, developed in this study can respond differently depending on water content. ET-1-BF3 releases BF3 to generate ET-1 by addition of a trace amount of water, and ET-1 forms hydrogen bonds with one water molecule in low water contents and a hydrogen-bonded proton transfer complex with several water molecules in high water contents, accompanying gradual color and fluorescence changes. This work shows a promising approach to the sensitive detection and precise determination of water over the whole concentration range using a simple and practical method with optical sensors.

The photoregulation of a mechanochemical polymer scission.

Control over mechanochemical polymer scission by another external stimulus may offer an avenue to further advance the fields of polymer chemistry, mechanochemistry, and materials science. Herein, we demonstrate that light can regulate the mechanochemical behavior of a diarylethene-conjugated Diels-Alder adduct (DAE/DA) that reversibly isomerizes from a weaker open form to a stronger closed form under photoirradiation. Pulsed ultrasonication experiments, spectroscopic analyses, and density functional theory calculations support the successful photoregulation of the reactivity of this DAE/DA mechanophore, which is incorporated at the mid-chain of a polymer, and indicate that higher force and energy are required to cleave the closed form of the DAE/DA mechanophore relative to the open form. The present photoregulation concept provides an attractive approach toward the generation of new mechanofunctional polymers.

Photoresponsive fiber scaffolds with a core-sheath nanostructure for regulating cell behaviors.

Herein, we report the fabrication of photoresponsive three-dimensional (3D) fiber scaffolds for the first time, where photoresponsive polymers are localized on their fiber surfaces of nano thickness, using a simple and practical co-axial (core-sheath) electrospinning technique. Cell adhesion to the 3D scaffolds was regulated by photostimulation.