Organic Chemistry I, Chemistry Faculty, Bielefeld University, Universitätsstrasse 25, 33615 Bielefeld, Germany.
Phys Chem Chem Phys. 2010 Sep 28;12(36):10981-7. doi: 10.1039/c0cp00227e. Epub 2010 Jul 27.
The specific interaction of a supramolecular binding motif was quantitatively evaluated by dynamic single-molecule force spectroscopy (SMFS) using an atomic force microscope (AFM). The supramolecular capsule forms by two different cavitands stitched together by four hydrogen bonds between carboxylic acid and pyridyl groups. The tetra(carboxyl)cavitand is monofunctionalized at the lower rim with a flexible poly(ethylene glycol) linker and attached to the AFM sensor tip. Single-molecule association experiments are accomplished using a diluted self-assembled monolayer (SAM) of the tetra(pyridyl)cavitand on a gold substrate. The measured single-molecule dissociation forces of the heterodimeric capsule represent the mechanical stability of the supramolecular system and allow a quantitative evaluation of the interaction according to the Bell-Evans model yielding dissociation rate constant k(off) = (0.14 +/- 0.14) s(-1), reaction length x(beta) = (0.56 +/- 0.076) nm and an estimated value of DeltaG(0) = -27 kJ mol(-1).
通过原子力显微镜(AFM)的动态单分子力谱(SMFS),定量评估了超分子结合基序的特定相互作用。超分子胶囊由两个不同的穴醚通过羧酸和吡啶基团之间的四个氢键缝合而成。四(羧酸)穴醚在较低的边缘上被单官能化,具有柔性的聚(乙二醇)接头,并连接到 AFM 传感器尖端。使用金基底上的四(吡啶)穴醚的稀释自组装单层(SAM)进行单分子缔合实验。异二聚体胶囊的测量单分子解离力代表了超分子体系的机械稳定性,并根据贝尔-埃文斯模型进行定量评估,得到解离速率常数 k(off) = (0.14 +/- 0.14) s(-1)、反应长度 x(beta) = (0.56 +/- 0.076) nm 和估计的DeltaG(0) 值为 -27 kJ mol(-1)。