RESUMEN
A pyrrolodithiin-derived box-like cyclophane (ProBox), featuring an adaptive geometry with stimuli-responsiveness, was designed and successfully constructed. The dynamic and foldable dithiin subunit endowed the cyclophane with a compressible cavity which can transform from a hex-nut geometry to a nearly rectangular box upon complexing guests with various sizes and shapes. The resulting pseudorotaxane complexes could be dethreaded via electrochemical oxidation. Such an adaptive cavity along with redox-switchable host-guest binding of ProBox could enable further applications in complex molecular switches and machines.
RESUMEN
A series of novel hinge-like molecules, namely dipyrrolo-1,4-dithiins (PDs), were prepared and fully characterized by NMR, UV/vis, cyclic voltammogram, ESR, and single crystal X-ray diffraction (SCXRD) analysis. The lateral fusion of pyrroles with 1,4-dithiins has led to not only retained key features of a dithiin, but also enhanced redox-activity with increased susceptibility to radical cations via redox or chemical oxidation. Stabilization of their radicals are observed for the N,N-tert-butyl or N,N-triphenylmethyl PD as evidenced by ESR measurements. DFT calculations and SCXRD analysis revealed PDs are extremely flexible with adaptive molecular geometries that can be mechanically regulated via crystal packing or host-guest complexation. The excellent donor nature of PDs renders inclusion complexes with the cyclophane bluebox (cyclobis(paraquat-p-phenylene)), featuring association constants up to 104 â M-1 . Additionally, a planarized transition intermediate associated with inversion dynamics of a PD has been preserved in the pseudorotaxane structure with assistances of πâ â â π and Sâ â â π interactions. The hinged structure, excellent redox-activity, and adaptive nature of PDs could further enable accesses to exotic redox switchable host-guest chemistry and functional materials.
RESUMEN
An unprecedented bisthianthrene dipyridyl ligand was designed and synthesized for coordination driven self-assembly. The combination of this conformationally dynamic linker with a 90° convergent metal corner exclusively afforded a novel M2L2 truncated square-like metallamacrocycle. The single crystal X-ray structure reveals a belt-shaped geometry with a cavity diameter of ca. 13.7 Å. The breathable cavity and electron-rich thianthreno panels enable the highly efficient binding of the fullerenes C60 (Ka = 5.1 × 106 M-1) and C70 (Ka = 3.7 × 106 M-1). The encapsulation of C60 is fully confirmed by NMR, mass spectroscopy and single crystal X-ray diffraction analyses. The cyclic voltammograms further reveal that the truncated square is redox active. The strong binding affinity, adaptive complexation, and redox activity of the thianthrene-incorporated metallamacrocycle provide new insights into the design of supramolecular hosts.
RESUMEN
Leucine aminopeptidase (LAP), one of the important cancer-related biomarkers, is significantly over-expressed in many malignant tumor cells. Developing an effective fluorescent probe for high-specificity and in situ trapping of endogenous LAP in living samples is still challenging. In this project, we report a water-soluble near-infrared (NIR) fluorescent probe (CHMC-M-Leu) for specific monitoring of LAP in vitro and in vivo. The novel fluorescent probe (CHMC-M-Leu) contains a NIR-emitting fluorophore (CHMC-M) as the reporter and l-leucine as the enzyme-active trigger moiety which are linked together by a p-aminobenzyl alcohol (PABA) section. Upon exposure to LAP, the fluorescence at 625 nm gets impressively enhanced, which belongs to the near-infrared region and is beneficial for imaging in vivo. Furthermore, the novel fluorescent probe exhibits fast response and highly chemoselective detection of LAP in various bio-related species. In addition, CHMC-M-Leu shows favourable cellular uptake and was successfully used to monitor endogenous LAP in living cells.