Coordination-driven assembly of a 3d-4f heterometallic organic framework with 1D Cu4I4 and Eu-based chains: syntheses, structures and various properties
DALTON TRANSACTIONS
Authors: Guo, Feng; Su, Changhua; Fan, Yuhang; Shi, Wenbing; Zhang, Xiuling; Xu, Jiakun
Abstract
A three-dimensional porous 3d-4f heterometallic organic framework, namely, {[Eu-3(Cu4I4)(3)(INA)(9)(DMF)(4)]center dot 3DMF}(n)(YNU-2), was successfully prepared under solvothermal conditions. There are two different one-dimensional metal chains in the structure, namely, Cu4I4 and Eu-III-based chains, resulting in an excellent stability of the prepared sample. A N-2 sorption isotherm at 77 K revealed that the activated sample exhibits a Brunauer-Emmett-Teller surface area of 371 m(2) g(-1), while, YNU-2 can adsorb obviously higher CO2 amounts than CH4 at 273 K and 298 K under 1 atm because of the stronger interaction force between CO2 and the porous skeleton. Furthermore, YNU-2 is highly efficient heterogeneous catalyst for chemical fixation of the CO2 and epoxides into cyclic carbonates with a preferable recyclability. Taking into account its excellent stability, the prepared sample can be used to construct an electrochemical adapter sensor for detecting cocaine with a detection limit of 0.27 pg mL(-1) in the wide range of 0.001-0.5 ng mL(-1).
Analysis of the role played by ligand-induced folding of the cocaine-binding aptamer in the photochrome aptamer switch assay
TALANTA
Authors: Shoara, Aron A.; Churcher, Zachary R.; Steele, Terry W. J.; Johnson, Philip E.
Abstract
The Photochrome Aptamer Switch Assay (PHASA) relies on ligand binding by an aptamer to alter the local environment of a stilbene compound covalently attached to the 5' end of the aptamer. We used the PHASA with both structure switching and non-structure switching versions of the cocaine-binding aptamer. We show that the largest change in fluorescence intensity and the lowest concentration limit of detection (C(Lo)o(D)) is obtained using the structure-switching cocaine-binding aptamer. Fluorescence anisotropy measurements were used to quantify the affinity of the conjugated aptamer to cocaine. We also used thermal melt analysis and Nuclear Magnetic Resonance (NMR) spectroscopy to show that the addition of the stilbene to the aptamer increases the melt temperature of the cocaine-bound structure-switching aptamer by (6.4 +/- 0.3) degrees C compared to the unconjugated aptamer while the free form of the structure-switching aptamer-stilbene conjugate remains unfolded.