Solvent effects of N,N-dimethylformamide and methanol on mass spectrometry imaging by tapping-mode scanning probe electrospray ionization.

Mass spectrometry imaging (MSI) is an effective technique for visualizing the distribution of lipids in tissues. The direct extraction-ionization methods using minute volumes of solvent for local components have the advantage of rapid measurement without any sample pretreatment. For effective MSI of tissues, it is necessary to understand the effect of solvent physicochemical properties on ion images. In this study, we report solvent effects on the lipid imaging of mouse brain tissue by tapping-mode scanning probe electrospray ionization (t-SPESI) which is capable of extraction-ionization using sub-pL solvents. To precisely measure lipid ions, we developed a measurement system incorporating a quadrupole-time-of-flight mass spectrometer. The differences in signal intensity and spatial resolution of lipid ion images were investigated using N,N-dimethylformamide (non-protic polar solvent), methanol (protic polar solvent) and their mixture. The mixed solvent was suitable for the protonation of lipids, and it provided high spatial resolution MSI. Results indicate that the mixed solvent improves the extractant transfer efficiency and minimizes charged droplets from an electrospray. The solvent selectivity study revealed the importance of solvent selection based on physicochemical properties for the advancement of MSI by t-SPESI.

Multi-energy dissipation mechanisms in supramolecular hydrogels with fast and slow relaxation modes.

Reversible cross-links by non-covalent bonds have been widely used to produce supramolecular hydrogels that are both tough and functional. While various supramolecular hydrogels with several kinds of reversible cross-links have been designed for many years, a universal design that would allow control of mechanical and functional properties remains unavailable. The physical properties of reversible cross-links are usually quantified by thermodynamics, dynamics, and bond energies. Herein, we investigated the relationship between the molecular mobility and mechanical toughness of supramolecular hydrogels consisting of two kinetically distinct reversible cross-links via host-guest interactions. The molecular mobility was quantified as the second-order average relaxation time (〈τ〉w) of the reversible cross-links. We discovered that hydrogels combining fast (〈τ〉w = 1.8 or 18 s) and slowly (〈τ〉w = 6.6 × 103 or 9.5 × 103 s) reversible cross-links showed increased toughness compared to hydrogels with only one type of cross-link because relaxation processes in the former occurred with wide timescales.

Phase equilibrium and dielectric relaxation in mixture of 5CB with dilute dimethyl phthalate: effect of coupling between orientation and composition fluctuations on molecular dynamics in isotropic one-phase state.

Phase equilibrium and dielectric relaxation were examined for mixtures of liquid-crystalline (LC)-forming 4-cyano-4'-pentylbiphenyl (5CB) with dilute dimethyl phthalate (DMP). The mixtures were in an isotropic one-phase state at high temperatures T but were separated into nematic and isotropic phases at low T < TIN (isotropic-to-nematic transition temperature), and the isotropic phase disappeared and a nematic one-phase state was realized on a further decrease of T below another transition temperature . These TIN and data (phase diagram) were described considerably well by a simple model of free energy contributed from a Flory-Huggins type mixing entropy (no enthalpic contribution) and a Landau-de Gennes type nematic interaction. This success of the model, not expected for ordinary (not LC-forming) components exhibiting enthalpically-driven phase separation, suggested that the phase separation in the DMP/5CB mixtures was triggered by the nematic transition of 5CB (possibly governed by the packing entropy) and thus the orientation fluctuation of 5CB molecules was coupled with the composition fluctuation. This coupling was expected to affect the dielectric relaxation detecting the rotational dynamics of 5CB molecules, the major component in the mixtures. This expectation was examined for a representative mixture having the DMP content of wDMP = 3.1 wt% and TIN ≅ 27.0 °C. In a high-T asymptote (T > TIN + 10 °C), the dielectric relaxation of this mixture was close to that of pure 5CB, which suggested no significant effect of the above coupling on 5CB dynamics in the mixture at such high T. Nevertheless, in a significantly wide range of T between TIN and TIN + 10 °C, the dielectric relaxation time τε of the isotropic one-phase mixture increased on cooling much more significantly compared to τε in that high-T asymptote. The kinematic viscosity ν of the mixture exhibited a qualitatively similar increase in the same range of T, but this increase was weaker than that of τε. This difference between the dielectric τε and the rheological ν was attributed to coupling of the orientation and the composition fluctuations mentioned above. Namely, the composition fluctuation enhances the orientation fluctuation in the mixture thereby providing τε (reflecting the orientation fluctuation) with an extra increase. Pure 5CB exhibited similar increases of τε and ν (stronger for the former) but only in a close vicinity of (within 2-3 °C), because the orientation fluctuation in pure 5CB is coupled with the density fluctuation, not with the composition fluctuation being absent in the pure 5CB system. This behavior of pure 5CB in turn suggests an importance of the coupling of orientation and composition fluctuations in the mixture.

Relationship between global and segmental dynamics of poly(butylene oxide) studied by broadband dielectric spectroscopy.

Relationship between segmental relaxation and normal-mode relaxation has been studied for molten poly(butylene oxide)s having various molecular weights by broadband dielectric spectroscopy over a wide temperature (T) range. We found that T dependence of the segmental relaxation time, τs, was weaker than the normal mode time, τn, at high T(>250 K ∼ Tg + 50 K), and the τn/τs ratio systematically decreased with increasing temperature. This high temperature complexity, whose mechanism has not been discussed in detail so far, was quantitatively explained by assuming the two step processes: local conformation change of polymers (elementary process) occurs first, and then the motion of a segment unit (second process) occurs. It was also found that the elementary process was strongly correlated with the experimentally observed ß-relaxation.

Viscoelastic Relaxation of Polymerized Ionic Liquid and Lithium Salt Mixtures: Effect of Salt Concentration.

Polymerized ionic liquids (PILs) doped with lithium salts have recently attracted research interests as the polymer component in lithium-ion batteries because of their high ionic mobilities and lithium-ion transference numbers. To date, although the ion transport mechanism in lithium-doped PILs has been considerably studied, the role of lithium salts on the dynamics of PIL chains remains poorly understood. Herein, we examine the thermal and rheological behaviors of the mixture of poly(1-butyl-3-vinylimidazolium bis(trifluoromethanesulfonyl)imide (PC4-TFSI)/lithium TFSI (LiTFSI) in order to clarify the effect of the addition of LiTFSI. We show that the glass transition temperature Tg and the entanglement density decrease with the increase in LiTFSI concentration wLiTFSI. These results indicate that LiTFSI acts as a plasticizer for PC4-TFSI. Comparison of the frequency dependence of the complex modulus under the iso-frictional condition reveals that the addition of LiTFSI does not modify the stress relaxation mechanism of PC4-TFSI, including its characteristic time scale. This suggests that the doped LiTFSI, component that can be carrier ions, is not so firmly bound to the polymer chain as it modifies the chain dynamics. In addition, a broadening of the loss modulus spectrum in the glass region occurs at high wLiTFSI. This change in the spectrum can be caused by the responses of free TFSI and/or coordination complexes of Li and TFSI. Our detailed rheological analysis can extract the information of the dynamical features for PIL/salt mixtures and may provide helpful knowledge for the control of mechanical properties and ion mobilities in PILs.

Synthesis of dibenz[b,f]oxepins via manganese(III)-based oxidative 1,2-radical rearrangement.

The oxidation of monoalkyl 2-(9H-xanthenyl)malonates 1 with Mn(OAc)(3) gave the 9- or 10-dibenz[b,f]oxepincarboxylates 2 in good yields. The reaction proceeds with high regioselectivity except for the case of (1-methoxyxanthenyl)malonate 1 (R(1) = Me, R(2) = 1-MeO), which gave two regioisomers. It was proposed that the process for the formation of 2 must include the 1,2-aryl radical rearrangement followed by oxidative decarboxylation.

Glass Transition Behaviors of Poly (Vinyl Pyridine)/Poly (Vinyl Phenol) Revisited.

We examined the composition and molecular weight dependence of the glass transition temperature in detail for two types of hydrogen bonding miscible blends: poly (2-vinyl pyridine)/poly (vinyl phenol) (2VPy/VPh) and poly (4-vinyl pyridine)/poly (vinyl phenol) (4VPy/VPh). Regarding the functional form of the glass transition temperature, Tg, as a function of the weight fraction, we found a weak deviation from the Kwei equation for 2VPy/VPh blends. In contrast, such a deviation was not observed for the 4VPy/VPh blend. By relating the difference in the functional forms of Tg between the two blend systems to the difference in hydrogen bonding ability, we proposed a modified version of the Kwei equation. As for the interaction parameter, q in the Kwei equation, clear molecular weight dependence was observed for 2VPy/VPh blends: the lower the VPh molecular weight in the oligomer level, the higher the q values, suggesting the higher hydrogen bonding formability near the polymer chain ends than the middle part of a polymer chain.

Polymerized Ionic Liquids: Correlation of Ionic Conductivity with Nanoscale Morphology and Counterion Volume.

The impact of the chemical structure on ion transport, nanoscale morphology, and dynamics in polymerized imidazolium-based ionic liquids is investigated by broadband dielectric spectroscopy and X-ray scattering, complemented with atomistic molecular dynamics simulations. Anion volume is found to correlate strongly with Tg-independent ionic conductivities spanning more than 3 orders of magnitude. In addition, a systematic increase in alkyl side chain length results in about one decade decrease in Tg-independent ionic conductivity correlating with an increase in the characteristic backbone-to-backbone distances found from scattering and simulations. The quantitative comparison between ion sizes, morphology, and ionic conductivity underscores the need for polymerized ionic liquids with small counterions and short alkyl side chain length in order to obtain polymer electrolytes with higher ionic conductivity.

Rapid Stretching Vibration at the Polymer Chain End.

Stretching vibrations of aliphatic C-D bonds at the chain end and midchain site of partially deuterated polystyrene (PS) were determined by Fourier transform infrared (FT-IR) spectroscopy. It was first found that the stretching vibration at the chain end is more rapid compared to that at the midchain site in the glassy bulk state. The difference in the frequencies of the stretching vibrations at the chain end and midchain site changed little even when the PS was dissolved in toluene. Moreover, the DFT vibrational frequency calculations showed that the C-D bonds at the end site intrinsically have higher vibrational frequency because of lower intramolecular interactions at the chain end. From these results, it was concluded that the main origin for the local rapid stretching vibration at the chain end is not intermolecular effects but reduced intramolecular interactions induced by the discontinuity of the repeating unit at the chain end.

Dielectric relaxation of guest molecules in a clathrate structure of syndiotactic polystyrene.

Structure and dynamics of semicrystalline polymer films composed of syndiotactic polystyrene (sPS) and 2-butanone were examined through X-ray diffraction, polarized FTIR, and dielectric relaxation measurements. The X-ray and FTIR measurements revealed its crystal structure to be δ-clathrate containing 2-butanone molecules inside. The carbonyl group of 2-butanone in the crystal was found to orient preferentially parallel to the ac plane of the crystal through the polarized ATR FTIR measurements. Dielectric measurements were also conducted on these film samples to see only the relaxation dynamics of 2-butanone thanks to the high dielectric intensity of 2-butanone compared to sPS. Two relaxation modes denoted by slow and fast modes appeared. The former was assigned to the motion of 2-butanone molecules entrapped in the cavities of the crystalline (δ-form) and the latter to those in the amorphous region. We focused on the slow mode in order to elucidate the specific dynamics of the guest molecule confined in the crystalline region. The relaxation time of the slow mode was about 4 orders of magnitude longer than that of liquid 2-butanone. This suggests that the dynamics of guest molecules is highly restricted due to the high barrier to conformational and/or orientational change of the guest molecule in the cavity of δ-crystal. Furthermore, the dielectric intensity Δε of the slow mode was much smaller than the one calculated from that of bulk liquid 2-butanone and the guest concentration in the crystalline region (the intensity was only 10% of the estimated value from the bulk liquid data). This result also indicates that the free rotational motion of 2-butanone molecules is restricted inside the crystal. This will be consistently related to the weak uniplanar orientation of the carbonyl group of 2-butanone parallel to the ac plane revealed by the X-ray and polarized ATR FTIR measurements.

Glass transition temperature and ß relaxation temperature around chain end of polystyrene determined by site specific spin labeling.

A glass transition temperature, T(g), and a ß relaxation temperature, T(ß), of spin-labeled polystyrene (PS) having a number average molecular weight (M(n)) of ca. 25 kDa were determined by the microwave power saturation (MPS) method of electron spin resonance (ESR). Spin labeling was selectively carried out at chain ends or midchain segments. This method allowed us to determine the local T(g) and the local T(ß) around the spin-labeled sites, selectively. The T(g) determined by the ESR, T(g,ESR), was in good agreement with that determined by differential scanning calorimetry, T(g,DSC); the T(g,ESR) decreased with decreasing M(n) with blending oligomers as well as the T(g,DSC). The T(g,ESR) for the end-labeled PS (PS-E) was equal to that for the midchain-labeled PS (PS-M) irrespective of the M(n). However, we previously reported that the PS-E showed distinctly higher segmental mobility than the PS-M in the temperature range 423-463 K (above T(g)). Therefore, we conclude that the chain ends intrinsically have higher segmental mobility than midchain segments due to the discontinuity of repeat units; however, the mobilities of chain ends and midchain segments are averaged out in the vicinity of T(g) due to the cooperativities with neighboring numerous chain segments. Concerning the ß relaxation, the T(ß) determined by the MPS was in good agreement with those determined by dielectric and dynamic mechanical spectroscopies and dilatometry. The T(ß) of the PS-E was the same with that of the PS-M within experimental uncertainties; the T(ß) was insensitive to the M(n) in contrast to the T(g). Therefore, we conclude that the effect of chain end is little on the ß relaxation of PS due to its local character. In addition, the effect of annealing at 353 K was found to be the same for the T(ß)s of the PS-E and PS-M.