RESUMEN
We describe the preparation of oil-in-water (o/w) colloidal particles with a polypyrrole (pPy) shell in which cyclodextrin has been incorporated at the oil-water interface via either physical adsorption or reaction with the pPy shell. The utility of these particles was assessed by the extraction of organic dyes from water. In all cases, we found that cyclodextrin incorporation significantly improved dye uptake, giving up to 78 ± 11% dye extraction in the case of a 100 ppm solution of 4-nitroaniline with a covalently incorporated cyclodextrin. We demonstrated the ability of our colloidal particles to extract nicotine-derived nitrosamine ketone (NNK), a potent carcinogen, from aqueous solution. By treating the solution containing 100 ppm NNK with our particles over 24 and 48 h, we found that NNK removal reached 65 ± 2 and 83 ± 1%, respectively. The uptake could be improved by re-treating a solution with additional freshly prepared particles, to achieve 95 ± 1% NNK extraction with a covalently incorporated cyclodextrin.
RESUMEN
We designed porous polymers with a tungsten-calix[4]arene imido complex as the nitrosamine receptor for the efficient extraction of tobacco-specific nitrosamines (TSNAs) from water. The interaction between the metallocalix[4]arene and the TSNA, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (nicotine-derived nitrosamine ketone, NNK) was investigated. We found that the incorporation of the nitrosamine receptor into porous polymers increased their selectivity toward NNK over nicotine. The polymer with an optimal ratio of calixarene-containing and porosity-inducing building blocks showed a high maximum adsorption capacity of up to 203 mg/g toward NNK under sonication, which was among the highest values reported. The adsorbed NNK could be removed from the polymer by soaking it in acetonitrile, enabling the adsorbent to be reused. A similar extraction efficiency to that under sonication could be achieved using the polymer-coated magnetic particles under stirring. We also proved that the material could efficiently extract TSNAs from real tobacco extract. This work not only provides an efficient material for the extraction of TSNAs but also offers a design strategy for efficient adsorbents.
RESUMEN
Herein, we present the synthesis and characterization of a macrocyclic polyamide cage that incorporates redox-active 1,4-dithiin units. UV/vis titration experiments with eight anions in acetonitrile revealed high affinity for H2AsO4- (logâ¯ß2 = 10.4-0.4+0.4) and HCO3- (logâ¯ß2 = 8.3-0.4+0.3) over other common anionic guests, such as Cl- (logâ¯K1:1 = 3.20-0.02+0.03), HSO4- (logâ¯K1:1 = 3.57-0.03+0.02), and H2PO4- (logâ¯K1:1 = 4.24-0.04+0.05), by the selective formation of HG2 complexes. The recognition of arsenate over phosphate is rare among both proteins and synthetic receptors, and though the origin of selectivity is not known, exploiting the difference in the binding stoichiometry represents an underexplored avenue toward developing receptors that can differentiate between the two anions. Additional analysis by 1H NMR in 1:3 CD2Cl2/MeCN-d3 found a strong dependence of anion binding stoichiometry with the solvent employed. Finally, titration experiments with cyclic voltammetry provided varying and complex responses for each anion tested, though reaction between the anion and receptors was observed in most cases. These results implicate 1,4-dithiins as interesting recognition moieties in the construction of supramolecular receptors.
RESUMEN
We demonstrate the broad applicability of the annulation protocol combining, in one pot, a direct arylation and cross aldol condensation for the straightforward synthesis at gram-scale of π-extended thiophene-based scaffolds. The regiospecific direct arylation drives the subsequent cross-aldol condensation proceed under the same basic conditions, and the overall protocol has broad applicability in the synthesis of extended aromatics wherein the thiophene ring is annulated with furans, pyridines, indoles, benzothiophenes, and benzofurans. These scaffolds can be further elaborated into π-extended, highly fluorescent oligomers with a central deficient benzothiadiazole unit with up to nine aromatic rings through coupling reactions.
RESUMEN
The synthesis and characterization of four novel donor-acceptor-donor π-extended oligomers, incorporating naphtha(1-b)thiophene-4-carboxylate or benzo(b)thieno(3,2-g) benzothiophene-4-carboxylate 2-octyldodecyl esters as end-capping moieties, and two different conjugated core fragments, is reported. The end-capping moieties are obtained via a cascade sequence of sustainable organic reactions, and then coupled to benzo(c)(1,2,5)thiadiazole and its difluoro derivative as the electron-poor π-conjugated cores. The optoelectronic properties of the oligomers are reported. The novel compounds revealed good film forming properties, and when tested in bulk-heterojunction organic photovoltaic cell devices in combination with PC61BM, revealed good fill factors, but low efficiencies, due to their poor absorption profiles.