Nano-Structural Investigation on Cellulose Highly Dissolved in Ionic Liquid: A Small Angle X-ray Scattering Study.

We investigated nano-structural changes of cellulose dissolved in 1-ethyl-3-methylimidazolium acetate-an ionic liquid (IL)-using a small angle X-ray scattering (SAXS) technique over the entire concentration range (0-100 mol %). Fibril structures of cellulose disappeared at 40 mol % of cellulose, which is a significantly higher concentration than the maximum concentration of dissolution (24-28 mol %) previously determined in this IL. This behavior is explained by the presence of the anion bridging, whereby an anion prefers to interact with multiple OH groups of different cellulose molecules at high concentrations, discovered in our recent work. Furthermore, we observed the emergence of two aggregated nano-structures in the concentration range of 30-80 mol %. The diameter of one structure was 12-20 nm, dependent on concentration, which is ascribed to cellulose chain entanglement. In contrast, the other with 4.1 nm diameter exhibited concentration independence and is reminiscent of a cellulose microfibril, reflecting the occurrence of nanofibrillation. These results contribute to an understanding of the dissolution mechanism of cellulose in ILs. Finally, we unexpectedly proposed a novel cellulose/IL composite: the cellulose/IL mixtures of 30-50 mol % that possess liquid crystallinity are sufficiently hard to be moldable.

Structural Analysis of Crystalline R(+)-α-Lipoic Acid-α-cyclodextrin Complex Based on Microscopic and Spectroscopic Studies.

R(+)-α-lipoic acid (RALA) is a naturally-occurring substance, and its protein-bound form plays significant role in the energy metabolism in the mitochondria. RALA is vulnerable to a variety of physical stimuli, including heat and UV light, which prompted us to study the stability of its complexes with cyclodextrins (CDs). In this study, we have prepared and purified a crystalline RALA-αCD complex and evaluated its properties in the solid state. The results of ¹H NMR and PXRD analyses indicated that the crystalline RALA-αCD complex is a channel type complex with a molar ratio of 2:3 (RALA:α-CD). Attenuated total reflection/Fourier transform infrared analysis of the complex showed the shift of the C=O stretching vibration of RALA due to the formation of the RALA-αCD complex. Raman spectroscopic analysis revealed the significant weakness of the S-S and C-S stretching vibrations of RALA in the RALA-αCD complex implying that the dithiolane ring of RALA is almost enclosed in glucose ring of α-CD. Extent of this effect was dependent on the direction of the excitation laser to the hexagonal morphology of the crystal. Solid-state NMR analysis allowed for the chemical shift of the C=O peak to be precisely determined. These results suggested that RALA was positioned in the α-CD cavity with its 1,2-dithiolane ring orientated perpendicular to the plane of the α-CD ring.

Investigation of accessibility and reactivity of cellulose pretreated by ionic liquid at high loading.

High loading of cellulose in ionic liquid (IL) pretreatment is potentially a key technique for cellulose conversion to glucose in biorefining. In this work, to expand the potential use of this high loading technique, the accessibility of microcrystalline cellulose pretreated with an IL across a wide cellulose loading range (5-50mol%) and its relationship with the hydrolytic reactivity were comprehensively investigated. The results show that the estimated cellulose accessibility based on the crystallinity and specific surface area was notably higher in 25mol% loading than that for a conventional loading of 5mol%. Consistently, acid-catalyzed glucose conversion was faster at this high loading, showing that a higher cellulose loading improves the pretreatment efficiency. In contrast, enzymatic hydrolysis was not enhanced by a high cellulose loading. A key difference between the activities in these two hydrolytic reactions is the catalyst size.

Anion Bridging-Induced Structural Transformation of Cellulose Dissolved in Ionic Liquid.

We performed structural investigations of cellulose mixed with 1-ethyl-3-methylimidazolium acetate ([Emim][OAc]) in the entire concentration range (0-100 mol %) by wide-angle X-ray scattering with the aid of quantum chemical calculations and 13C solid-state NMR spectroscopy. We particularly focused on a highly concentrated region (≥30 mol %), which has previously been overlooked. At concentrations of 15-30 mol %, a periodic peak corresponding to cellulose chain alignment emerged; this is associated with a lyotropic cholesteric liquid-crystalline phase. At concentrations of ≥30 mol %, the structure is transformed into ordered layers where OAc anions and Emim cations intercalate. This transformation is found to be driven by a change in the interaction between the IL anions and the OH groups of cellulose. At low concentrations, the anion mainly interacts with the OH group of cellulose in a 1:1 ratio, as previously reported; at high concentrations, the anions bridge the OH groups of two cellulose chains.