Adhering hydrogel systems are important particularly in the medical field because they can be used as adhesives cross-linking between living tissues. In this research, hydrogels including cationic substituents prepared via free-radical polymerization were brought into contact after applying an aqueous dispersion of the layered inorganic compound Micromica to their surfaces. As a result, the hydrogels adhered to each other due to the intercalation of cationic substituents included in the gel networks into the interlayers of Micromica. As the water content ratio of hydrogels decreased, the adhesive strength came to be higher, and finally the adhesively bonded joint supported a tensile load of 10 kg. Moreover, it was confirmed that the adhered hydrogels have high tolerance toward various environments, such as high or low temperatures and solvents.
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http://dx.doi.org/10.1021/acsmacrolett.6b00337 | DOI Listing |
ChemSusChem
December 2024
Tokyo Institute of Technology, Department of Chemical Science and Engineering, 4259 G1-9, Nagatsuta, Midori-ku,, 226-8501, Yokohama, JAPAN.
To realize the robust anion exchange membrane (AEM)-based water splitting modules and fuel cells, the design and synthesis of tetraarylphosphonium (TAP) cations are described as a new class of cationic building blocks that exhibit remarkable alkaline stability under harsh conditions. TAP cations with highly sterically demanding aromatic substituents were efficiently synthesized from triarylphosphine derivatives and highly reactive arynes, whose alkaline degradation proved to be suppressed dramatically by the sterically demanding substituents. In the case of bis(2,5-dimethylphenyl)bis(2,4,6-trimethylphenyl)phosphonium, for example, approximately 60% of the cation survived for 27 d under the forced conditions (i.
View Article and Find Full Text PDFJ Chromatogr A
January 2025
Restek Corporation, 110 Benner Circle, Bellefonte, PA, 16823, USA. Electronic address:
The chemical structure of nine imidazolium sulfonate and triflimide zwitterionic liquids (ZILs) were systematically tuned to increase their thermal stability for gas chromatography (GC) separations. Substituents for imidazolium and 2-phenylimidazolium cation systems, comprised of alkyl, benzyl, and oligoether groups of varying chain lengths, were studied as stationary phases in GC. Propanesulfonate, ethanesulfonate, and propanetriflimide anions were examined to understand the effect of linker length and nucleophilicity on ZIL thermal stability.
View Article and Find Full Text PDFJ Phys Chem Lett
December 2024
Solid State and Structural Chemistry Unit, Indian Institute of Science, Bengaluru 560012, India.
The synthesis of organic radicals continues to garner significant interest due to their fascinating optical, electronic, and magnetic properties. Moreover, the growing demand for chemically stable organic radicals is driven by the rapid expansion of the market for electronic devices utilizing organic semiconductors. In this context, the development of multifaceted approaches for the design of stable organic radicals is of great importance.
View Article and Find Full Text PDFJ Org Chem
December 2024
Department of Organic Chemistry and Biochemistry, Rud̵er Bošković Institute, Bijenička Cesta 54, Zagreb 10 000, Croatia.
BODIPY photocages (photocleavable protective groups) have stirred interest because they can release biologically active cargo upon visible light excitation. We conducted combined theoretical and experimental investigations on selected BODIPY photocages to elucidate the mechanism of the competing photocleavage at the boron and -position. Based on the computations, the former reaction involves elongation of the B-C bond, yielding a tight borenium cation and methyl anion.
View Article and Find Full Text PDFJ Med Chem
December 2024
Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences, Leninsky pr., 31, Building 4, Moscow 119071, Russia.
To investigate the influence of phthalocyanine aggregation on their photodynamic activity, a series of six cationic water-soluble zinc(II) phthalocyanines bearing from four to sixteen 4-((diethylmethylammonium)methyl)phenoxy substituents was synthesized. Depending on their structure, the phthalocyanines have different aggregation behaviors in phosphate buffer solutions ranging from fully assembled to monomeric states. Remarkably, independent of aggregation in buffer, very high photodynamic efficiencies against the tumor cell lines MCF-7 and MDA-MB-231 in the nanomolar range were found for all investigated phthalocyanine, and the IC(light) varied from 27 to 358 nM (3.
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