Bartelmann Thomas, Gnannt Frederik, Zitzmann Max, Mayer Peter, Dube Henry
Ludwig-Maximilians-Universität München, Department of Chemistry, Center for Integrated Protein Science CIPSM Butenandtstr. 5-13 81377 München Germany
Friedrich-Alexander-Universität Erlangen-Nürnberg, Department of Chemistry and Pharmacy Nikolaus-Fiebiger-Str. 10 91058 Erlangen Germany.
Chem Sci. 2021 Jan 14;12(10):3651-3659. doi: 10.1039/d0sc04981f.
Introducing responsive elements into supramolecular recognition systems offers great advantages for the control of intermolecular interactions and represents an important stepping stone towards multi-purpose and reprogrammable synthetic systems. Of particular interest is implementation of light-responsiveness because of the unique ease and precision of this signal. Here we present visible light responsive hemithioindigo-based molecular tweezers that bear a highly polar sulfoxide function as an additional recognition unit inside their binding site. Sulfur oxidation allows to simultaneously enhance all crucial properties of this receptor type photoswitching capability, thermal stability of individual switching states, binding affinity, and binding modulation upon switching. With a novel titration method the thermodynamic binding parameters were determined using reduced sample amounts. Employing these strongly enhanced molecular tweezers allowed to demonstrate photocontrol of intermolecular charge transfer in a reversible manner.
将响应性元件引入超分子识别系统,对于控制分子间相互作用具有极大优势,并且是迈向多功能和可重新编程合成系统的重要一步。由于光信号具有独特的简便性和精确性,光响应性的实现尤其令人关注。在此,我们展示了基于半硫代靛蓝的可见光响应分子镊子,其在结合位点内具有高度极性的亚砜官能团作为额外的识别单元。硫氧化能够同时增强这类受体的所有关键特性——光开关能力、各个开关状态的热稳定性、结合亲和力以及开关时的结合调节。通过一种新颖的滴定方法,使用减少的样品量确定了热力学结合参数。利用这些增强效果显著的分子镊子,得以可逆地展示分子间电荷转移的光控作用。