RESUMO
Carbon nanothreads are one-dimensional materials obtained by controlled compression of aromatic molecules. Benzene and other six-membered ring molecules are normally used as precursors, but recent experiments have shown that carbon nanothreads can also be synthesized from five-membered ring heterocyclic compounds such as thiophene and furan, with an improved control of the structure of the final material and potentially easier scalability. In this work we use Density Functional Theory calculations to unveil the structural, electronic and mechanical properties of carbon nanothreads derived not only from thiophene and furan, but also from pyrrole, aiming to encourage experimental efforts towards the synthesis of equivalent 1D materials. Our results show that these new structures are remarkably stable when compared to similar nanothreads derived from benzene and pyridine. The presence of heteroatoms may lead to significant variations on the electronic band gap of these materials compared to conventional nanothreads, without compromising their mechanical properties. These findings suggest that nanothreads derived from five-membered rings are suitable for the same applications proposed for conventional NTs and potential candidates for new ones.
RESUMO
Nimodipine (NIM) is a calcium channel-blocking agent, which in the solid state exhibits two crystalline modifications, Mode I and Mode II. The first one is a racemic mixture, while the second is a conglomerate. Because the drug has poor aqueous solubility and Mode I is twice as soluble as Mode II, the former is widely preferred for the development of pharmaceutical forms. In order to study the effect of thermal stimuli on the behavior of NIM, an analytical method was developed coupling ATR-FTIR spectroscopy to Multivariate Curve Resolution with Alternating Least Squares (MCR-ALS). The method allowed to monitor the transformations of each polymorph, their respective mixtures and commercial samples, during the thermal treatment. It was observed that Mode II experienced changes during the experiments and the chemometric technique provided the abundance profile and the pure spectra of the different species involved. In this way, it was established that Mode II has two transitions, at 116.8⯰C and 131.9⯰C, which reflect that Mode II is first transformed into Mode I, which then melts. The liquid phase solidifies to give an amorphous (AM) vitreous solid, which does not revert to the crystalline state. The analysis of a commercial sample of NIM exhibited the similar transformations than Mode II; however, a pronounced decrease was noted in the first transition temperature (95⯰C), whereas the second remained essentially unchanged (131.6⯰C). This could be a result of the presence of mixtures of Mode I and Mode II (0.32:0.68) in the bulk solid, as confirmed by the analysis of a physical mixture of crystals of Modes I and II. Therefore, it was concluded that the developed ATR-FTIR/MCR-ALS method is suitable for the detailed analysis of the crystalline forms of NIM in bulk drug and enables de study of their possible thermally promoted interconversions.
Assuntos
Bloqueadores dos Canais de Cálcio/química , Composição de Medicamentos/normas , Nimodipina/química , Química Farmacêutica , Cristalização , Armazenamento de Medicamentos , Análise dos Mínimos Quadrados , Controle de Qualidade , Solubilidade , Espectroscopia de Infravermelho com Transformada de Fourier/instrumentação , Espectroscopia de Infravermelho com Transformada de Fourier/métodos , Temperatura de Transição , ÁguaRESUMO
The successful incorporation of functionalized single-walled carbon nanotubes (f-SWCNTs) into a silica matrix prepared by the sol-gel method is reported herein. SWCNTs produced through catalytic chemical-vapor deposition (CCVD) have been purified and functionalized with sulfuric, nitric and hydrochloric acids to ensure a good dispersion in an aqueous solution. The nanotube composites are prepared using three concentrations of f-SWCNTs (0.025, 0.050 and 0.075 wt%.) in a silica matrix, resulting in translucent monoliths after gelation. Dense, crack-free and hard compacts are obtained by high-pressure processing at 7.7 GPa and room temperature. Compared to the pure silica compact, compacts containing 0.025 and 0.050 wt% f-SWCNTs show an increased toughness of about 54% and 69%, respectively. The influence of f-SWCNTs on some microstructural aspects of the silica matrix has been studied using nitrogen adsorption/desorption isotherms. Raman spectroscopy has been applied to analyze the effect of the silica matrix and high-pressure compaction on the f-SWCNTs incorporated into the silica matrix. These measurements showed that f-SWCNTs remained in the silica matrix under pressure, suggesting an important interaction with the matrix.