Ascherl Laura, Evans Emrys W, Gorman Jeffrey, Orsborne Sarah, Bessinger Derya, Bein Thomas, Friend Richard H, Auras Florian
Department of Chemistry and Center for NanoScience (CeNS) , University of Munich (LMU) , Butenandtstraße 5-13 , 81377 Munich , Germany.
Cavendish Laboratory , University of Cambridge , Cambridge CB3 0HE , United Kingdom.
J Am Chem Soc. 2019 Oct 2;141(39):15693-15699. doi: 10.1021/jacs.9b08079. Epub 2019 Sep 24.
Traditionally, the properties and functions of covalent organic frameworks (COFs) are defined by their constituting building blocks, while the chemical bonds that connect the individual subunits have not attracted much attention as functional components of the final material. We have developed a new series of dual-pore perylene-based COFs and demonstrated that their imine bonds can be protonated reversibly, causing significant protonation-induced color shifts toward the near-infrared, while the structure and crystallinity of the frameworks are fully retained. Thin films of these COFs are highly sensitive colorimetric acid vapor sensors with a detection limit as low as 35 μg L and a response range of at least 4 orders of magnitude. Since the acidochromism in our COFs is a cooperative phenomenon based on electronically coupled imines, the COFs can be used to determine simultaneously the concentration and protonation strength of nonaqueous acid solutions, in which pH electrodes are not applicable, and to distinguish between different acids. Including the imine bonds as function-determining constituents of the framework provides an additional handle for constructing multifunctional COFs and extending the range of their possible applications.
传统上,共价有机框架(COF)的性质和功能由其构成的结构单元决定,而连接各个亚基的化学键作为最终材料的功能组分并未受到太多关注。我们开发了一系列新型的基于苝的双孔COF,并证明其亚胺键可发生可逆质子化,导致显著的质子化诱导颜色向近红外方向转变,同时框架的结构和结晶度得以完全保留。这些COF薄膜是高灵敏度的比色酸蒸气传感器,检测限低至35 μg L,响应范围至少为4个数量级。由于我们的COF中的酸致变色是基于电子耦合亚胺的协同现象,因此这些COF可用于同时测定非水酸性溶液的浓度和质子化强度(pH电极在此不适用),并区分不同的酸。将亚胺键作为框架的功能决定成分,为构建多功能COF和扩展其可能的应用范围提供了额外的手段。