Comparison between Abel test stability and thermal decomposition behavior of nitrocellulose

Journal of Thermal Analysis and Calorimetry - Nitrocellulose (NC) is prone to spontaneous decomposition with exothermic heat release and thus is generally evaluated for stability during the storage...     

Unitary representations of the quantum group SU q (1,1): Structure of the dual space ofU q (sl(2))

Real forms of the quantum universal enveloping algebraU _q (sl(2)) and a topological quantum group associated with this algebra are discussed.     

CpRuIIPF6/quinaldic acid-catalyzed chemoselective allyl ether cleavage. A simple and practical method for hydroxyl deprotection

A cationic CpRu(II) complex in combination with quinaldic acid shows high reactivity and chemoselectivity for the catalytic deprotection of hydroxyl groups protected as allyl ethers. The catalyst operates in alcoholic solvents without the need for any additional nucleophiles, satisfying the practical requirements of operational simplicity, safety, and environmental friendliness. The wide applicability of this deprotection strategy to a variety of multifunctional molecules, including peptides and nucleosides, may provide new opportunities in protective group chemistry. [structure: see text]     

Synthesis and structure of 1-zirconacyclopent-3-yne complexes without substituents adjacent to the triple bond

Five-membered metallacyclic alkynes that have no substituents adjacent to the triple bond have been synthesized, isolated, and structurally characterized. Zirconocene dichlorides, Cp'2ZrCl2 (Cp' = C5H5, C5H4-t-Bu), reacted with 1,4-dichlorobut-2-yne in the presence of magnesium to give 1-zirconacyclopent-3-yne compounds (5 (a) Cp' = C5H5, (b) Cp' = C5H4-t-Bu) that have a -CH2CCCH2- moiety in good yields. They are stable enough to be isolated in a pure form, despite the absence of substituents. 5a reacted with an equimolar amount of Cp2Zr(but-1-ene)(PMe3) to produce a bimetallic complex in which the zirconacyclopentyne coordinates to the other zirconocene moiety as an alkyne.     

Martensitic transformations in some ferrous and non-ferrous alloys under magnetic field and hydrostatic pressure

Martensitic transformations are extensively influenced by external fields, such as temperature and uniaxial stress, in transformation temperatures, crystallography and amount and morphology of the product martensites. Therefore, to clarify the effect of external fields on martensitic transformations it is very important to understand the essential problems of the transformation, such as thermodynamics, kinetics and the origin of the transformation, whose information is naturally useful in technological applications using the transformation. Magnetic field and hydrostatic pressure are important in such external fields because there exist some significant differences in magnetic moment and atomic volume between the parent and martensitic states. In the present paper, therefore, we summarizz the effects of magnetic field and hydrostatic pressure on martensitic transfonnations in some ferrous and non-ferrous alloys by referring to past and recent works made by our group and many other researchers. The transformation start temperatures of all the ferrous alloys examined increase with increasing magnetic field, but those of non-ferrous alloys, such as Ti-Ni and Cu-Al-Ni shape memory alloys, are not affected. On the other hand, the transformation start temperature decreases with increasing hydrostatic pressure in some ferrous alloys, but increases in Cu-Al-Ni alloys. The magnetic field and hydrostatic pressure dependencies of the martensitic start temperature are in good agreement with those calculated by our proposed equations.

During investigations of ferrous Fe-Ni-Co-Ti shape memory alloy, we found that a magnetoelastic martensitic transformation appears and, in addition, several martensite plates grow nearly parallel to the direction of the applied magnetic field in a specimen of Fe-Ni alloy single crystal.

We further found that the isothermal process in Fe-Ni-Mn alloy changes to athermal under a magnetic field and the athermal process changes to isothermal under hydrostatic pressure. Based on these facts, a phenomenological theory has been constructed, which unifies the two transformation processes.     

MicroRNA‐2861 and nanofibrous scaffold synergistically promote human induced pluripotent stem cells osteogenic differentiation

Tissue engineering using new strategies has become a growing and promising method for treating large tissue lesions in the body. On the other hand, microRNAs (miRNAs), which are small non‐coding regulatory RNAs, are a new class of genetic materials that can have effective pharmacological roles. The combination of these two themes has created promising prospects for the treatment of diseases. Herein, human induced pluripotent stem cells (iPSCs) were transduced with miRNA‐2861 and then the osteogenic differentiation potential of transduced iPSCs and non‐transduced iPSCs was investigated while cultured on the electrospun poly lactic‐co‐glycolic acid (PLGA) nanofibrous scaffold and culture plate. MiR‐2861‐transduced iPSCs showed a significantly higher viability, mineralization, alkaline phosphatase (ALP) activity, calcium content, and bone‐related gene expression in comparison with those iPSCs that non‐transduced. The results also indicated that this increase is improved when miR‐2861 transduced iPSCs are cultured on the PLGA nanofibrous scaffold synergistically. This synergy was also confirmed by the results obtained from of Western blot analysis. It can be concluded that, miR‐2861, by negative regulation of those proteins that decrease/inhibit osteogenic differentiation and PLGA nanofibrous scaffold by preparation of a suitable artificial extracellular matrix, have a great positive impact in improving iPSCs osteogenic differentiation potential and this blend can be proposed to use in bone tissue engineering application.     

Catalytic asymmetric hydrogenation of cyclic anhydrides using ruthenium (II) chiral phosphine complex

Optically active γ- and δ-lactones are obtained by the hydrogenation of five- and six-membered cyclic anhydrides using a Ru(II) complex with chiral phosphine ligand, DIOP, as a catalyst.     

Protein adsorption and wetting of the protein adsorbed surfaces studied by a new type of laser reflectometer

We have devised a new type of laser reflectometer that can measure adsorption behavior of (bio)-polymers, such as proteins, on the substrate surface and also the wetting for the surface of adsorbed layer of such (bio)-polymers. The adsorption and the wetting experiments can be conducted in a sequential manner using the same sample by this apparatus. So, the wetting of the surface of protein-adsorbed layer can be measured in virtually intact state. The reflectometry is based on the traditional optical polarimetry and the wetting measurement is due to the dropping time method (DTM) that has been reported before by the authors. The two methods are combined in an apparatus and hence we can correlate the wetting of protein layer adsorbed on the substrate surfaces with the amounts of protein molecules on the surface. As a model case we demonstrate the adsorption of several typical water soluble globular proteins on stainless steel surfaces. For this combination of the adsorbent with adsorbates, it is found that the water wetting of the protein adsorbed surface is closely related with the adsorbed amounts of proteins not depending on species.     

Asymmetric hydrogenation of methyl 3,5-dioxohexanoate catalyzed by ru-binap complex: a short step asymmetric synthesis of dihydro-60methyl-2-H-pyran-2-one

Hydrogenation of methyl 3,5-dioxohexanoate 3 using Ru₂Cl₄((R) or (S)-binap)₂(NEt₃) as the catalyst gave dominantly anti 3,5-dihydroxyester 9, which was then converted into unsaturated lactone 4. The pathway of the hydrogenation reaction was also investigated.