Boston ivy has received much attention from researchers owing to its exceptional climbing abilities. However, many aspects of their adhesion behavior remain unresolved. Our research has discovered a phenomenon of oxidation and discoloration in Boston ivy pads, which leads to a significant decrease in adhesion force. In this study, we conducted a comprehensive investigation into the oxidation discoloration phenomenon. Through XPS analysis, we confirmed that the transition from Fe2+ to Fe3+ in the pad is the primary cause of the oxidation discoloration reaction. Furthermore, by conducting in situ adhesion testing using AFM, we observed a decrease in adhesion during the oxidation of iron ions. The magnitude of adhesion is closely related to the amount of pyrocatechol. Following the oxidation reaction, iron ions chelate with more pyrocatechol, resulting in a decrease in the available pyrocatechol content for adhesion. To validate this mechanism, we designed and prepared a biomimetic composite adhesion surface of a PDMS hydrogel. This composite surface improved oxidation resistance through the hydrogel, demonstrating improved adhesion performance. These findings offer promising prospects for the application of bionic materials in various fields.
Fluorescence recognition for the antimalarial cinchonidine could be achieved efficiently and rapidly through bamboo-like carbon nanotubes based on chiral conjugated H8BINOL derivatives. Herein, it was proved that the chiral fluorescence probe H8BINOL exhibited excellent fluorescence identification ability for cinchonidine. The structure and size of the S-1 (S-(3,3′-phenyl)-5,5′6,6′,7′,8,8′-octahydro-[1,1′-dinaphthalene]-2,2′-diol) and R-1 (R-(3,3′-phenyl)-5,5′6,6′,7′,8,8′-octahydro-[1,1′-dinaphthalene]-2,2′-diol) were studied by using the DLS, TEM, and SEM spectra, which exhibited a self-assembled bamboo-like carbon nanotube structure. In the CD (circular dichroism) test, cinchonidine was added to a pair of enantiomers of H8BINOL derivatives. The different configurations of H8BINOL derivatives showed significantly different Cotton effects for cinchonidine, indicating that cinchonidine formed diastereoisomer π–π complexes with different configurations of H8BINOL derivatives. From the AFM tests, it was revealed that cinchonidine could effectively quench the fluorescent spot of the probes quickly. The fluorescence titration tests demonstrated that 6.4 × 10−7 mol of cinchonidine could completely quench the fluorescence sensor of S-1 (2 × 10−5 M, 2 mL) through the formation of a 1 : 1 complex. The limit of detection (LOD) of S-1 was calculated to be 6.08 × 10−10, which indicates that S-1 has a high sensitivity and can be applied effectively to the practice of identifying cinchonidine. Meanwhile, the fluorescence sensor R-1 also exhibited the same sensibility with a low limit of detection (7.60 × 10−10).
危险品化学品经营许可证（带存储）