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Catalytic Three-Component Machinery: Control of Catalytic Activity by Machine Speed

机译:催化三组分机械:通过机速控制催化活性

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摘要

Three supramolecular slider-on-deck systems DS1-DS3 were obtained as two-component aggregates from the sliders S1-S3 and deck D with its three zinc porphyrin (ZnPor) binding sites. The binding of the two-footed slider to the deck varies with the donor qualities of and the steric hindrance at the pyridine/pyrimidine (pyr) feet, and was effected by two N(pyr)ZnPor interactions. Accordingly, the sliders move over the three zinc porphyrins in the deck at different speeds, namely with 32.2, 220, and 440kHz at room temperature. The addition of N-methylpyrrolidine as an organocatalyst to DS1-DS3 generates catalytic three-component machineries. By using a conjugate addition as a probe reaction, we observed a correlation between the operating speed of the slider-on-deck systems and the yields of the catalytic reaction. As the thermodynamic binding of the slider decreases, both the frequency of the sliding motion and the yield of the catalytic reaction increase.
机译:获得三个超分子滑块上的甲板系统DS1-DS3作为来自滑块S1-S3和DECK D的双组分聚集体,其三个锌卟啉(Znpor)结合位点。 双脚滑块与甲板的结合随着吡啶/嘧啶(Pyr)脚的施主质量和空间障碍,并通过两种N(Pyr)Znpor相互作用而进行。 因此,滑块以不同的速度在甲板中的三个锌卟啉上移动,即在室温下用32.2,220和440kHz移动。 将N-甲基吡咯烷作为有机催化剂加入DS1-DS3产生催化三组分机械。 通过使用作为探针反应的缀合物添加,我们观察了滑块上甲板系统的操作速度与催化反应的产率之间的相关性。 随着滑块的热力学结合减小,滑动运动的频率和催化反应的产率均增加。

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