ABSTRACT
A Co(III)-catalyzed vinylene transfer reaction enabled by carboxylic acid is presented. This redox-neutral transformation tolerates various functional groups, including free hydroxyl groups, and features practicality. Five-step routes based on the vinylene transfer reaction and Heck annulation have been devised to the total synthesis of 8-oxodehydrodiscretamine and 2-demethyl-oxypalmatine without the protection of the free hydroxyl functionality.
ABSTRACT
Sulfonic acid-containing bioorganic monomers with wide molecular designability and abundant hydrogen bonding sites hold great potential to design diverse functional biocrystals but have so far not been explored for piezoelectric energy harvesting applications due to the lack of strategies to break the centrosymmetry of their assemblies. Here, a significant molecular packing transformation from centrosymmetric into non-centrosymmetric conformation by the addition of an amide terminus in the sulfonic acid-containing bioorganic molecule is demonstrated, allowing a high electromechanical response. The amide-functionalized molecule self-assembles into a polar supramolecular parallel ß-sheet-like structure with a high longitudinal piezoelectric coefficient d11 = 15.9 pm V-1 that produces the maximal open-circuit voltage of >1 V and the maximal power of 18 nW in nanogenerator devices pioneered. By contrast, molecules containing an amino or a cyclohexyl terminus assemble into highly symmetric 3D hydrogen bonding diamondoid-like networks or 2D double layer structures that show tunable morphologies, thermostability, and mechanical properties but non-piezoelectricity. This work not only presents a facile approach to achieving symmetry transformation of bioorganic assemblies but also demonstrates the terminal group and the property correlation for tailor-made design of high-performance piezoelectric biomaterials.
ABSTRACT
Introduction: Obesity is a growing health problem among young people worldwide and is associated with gut conditions. This study aimed to explore the relationship between obesity, intestinal microbiota, fecal short-chain fatty acids (SCFAs), and lipopolysaccharide (LPS) in young college students. Methods: 16S rRNA gene sequences, SCFA and LPS contents, and obesity status were analyzed in 68 young college students (20-25 years old). Results: There were significant differences in intestinal microbial beta diversity among students with different body mass index (BMI). The abundance and proportion of Firmicutes and Bacteroides had no significant correlation with BMI. The contents of butyric acid and valeric acid in the feces of obese students were low, and the content of SCFAs had no significant correlation with BMI and LPS. The content of LPS in the feces of obese people was significantly higher than that in healthy people, and there was a significant positive correlation between LPS content and BMI. Conclusion: In general, there was a correlation between intestinal microbiota, SCFA, LPS, and BMI in young college students. Our results may enrich the understanding of the relationship between intestinal conditions and obesity and contribute to the study of obesity in young college students.
ABSTRACT
Methane is not only the main cause of coal mine accidents but also a contributor to global warming, meanwhile, it is clean energy. It is necessary to find an advanced material which can capture methane efficiently for its utilization. In this paper, the adsorption of CH4 gas molecules on Nb2CTx(T = O, F, Cl, OH) is studied by first-principles calculation. The results indicate that the adsorption of CH4 on Nb2CTx(T = O, F, Cl, OH) is weak, and the adsorption of CH4 on Nb2C(OH)2 is the best. The calculation results of binding energy and cohesive energy show that Nb2CO2 has the best stability. The adsorption behavior of CH4 on Nb2CO2 under charge control is further studied. With the increase of negative charge state in the system, the adsorption of CH4 on Nb2CO2 is significantly enhanced, from physical adsorption to chemical adsorption; when the charge state of the system is greater than or equal to -2, Nb2CO2 can capture CH4 effectively, and the charges transferred from Nb2CO2 to CH4 mainly come from Nb atom. After the removal of the extra charge, the adsorption of CH4 on Nb2CO2 becomes weak and returns to physical adsorption state; CH4 gas molecules are easy to desorb. Therefore, Nb2CO2 can capture and release CH4 molecules by regulating the charge state of Nb2CO2, and Nb2CO2 is expected to become an excellent candidate material for CH4 capture/release.
Subject(s)
Methane , Niobium , Adsorption , Tomography, X-Ray ComputedABSTRACT
The relationship between moisture transportation and efflorescence in sodium hydroxide- or sodium silicate-activated fly ash/slag geopolymers was investigated. The results show that the efflorescence products are sodium carbonate hydrates, mainly composed of natron, heptahydrate, trona and sodium carbonate. The efflorescence induces compressive strength loss, water absorption increases and pore structure degradation in the geopolymer. When the curved surface of a geopolymer cylinder is covered with plastic film, the moisture transportation drives the free alkalis to the top surface to initiate efflorescence. In comparison, the efflorescence occurring on the curved surface of an uncovered geopolymer cylinder results in a more intensive alkalinity loss. For the uncovered geopolymers prepared with sodium hydroxide activator, efflorescence deposits are formed on the lower half of cylinder. A low capillary absorption capacity developed in the pore structure can only drive the moisture to the middle of cylinder, which is confronted with the drying front. More efflorescence products are formed on the upper half of the uncovered geopolymer cylinder prepared with sodium silicate activator. A relatively higher capillary absorption capacity, developed in the more compact pore structure, transports the moisture from the bottom to the top of cylinder, so no drying line is observed in the cylinder.
