Triptycene‐based organic molecules of intrinsic microporosity (OMIMs) with extended functionalized π‐surfaces are excellent materials for gas sorption and separation. In this study, the affinities of triptycene‐based OMIM affinity materials on 195 MHz high‐fundamental‐frequency quartz crystal microbalances (HFF‐QCMs) for hazardous and illicit compounds such as piperonal and (–)‐norephedrine were determined. Both new and existing porous triptycene‐based affinity materials were investigated, resulting in very high sensitivities and selectivities that could be applied for sensing purposes. Remarkable results were found for safrole – a starting material for illicit compounds such as ecstasy. A systematic approach highlights the effects of different size of π‐surfaces of these affinity materials, allowing a classification of the properties that might be optimal for the design of future OMIM‐based affinity materials.
The combination of an (−)‐isosteviol‐derived building block and 9,9’‐spirobifluorene or tetraphenylmethane generated highly potent new affinity materials for the detection of volatile organic compounds (VOCs). Comparison of their affinity behaviour with different core structures showed remarkable influence on selectivity and sensitivity due to structural rigidity and their pre‐organization. Their unique supramolecular properties were investigated in an affinity assay using high fundamental frequency quartz crystal microbalances.
Resorcin[4]arene cavitands are well‐known supramolecular hosts, and their outstanding guest‐binding abilities in solution have been studied in detail in recent decades. In a systematic approach, different resorcin[4]arene cavitands and container molecules are characterized as affinity materials for gravimetric sensing using high‐fundamental‐frequency quartz crystal microbalances. Analysis of their affinity toward a series of various analytes reveals a remarkable dependence of both selectivity and sensitivity on the shape, accessibility, and size of the cavity, along with their supramolecular interactions with the host molecules.
The severely ozone‐depleting trichlorofluoromethane is still appearing in several recycling processes or industrial applications. A simple and selective supramolecular complex formation of
per
‐methylated α‐cyclodextrin (
1
) with the highly volatile trichlorofluoromethane (
2
) is reported. This interaction moreover leads to thermally stable crystals.
Per
‐methylated α‐cyclodextrin is successfully exploited as a reversible and selective adsorption material for liquid and airborne trichlorofluoromethane as well as an affinity material for the chemical sensing and detection of this particular volatile organic component.
Trichlorofluoromethane was once a promising and versatile applicable chlorofluorocarbon. Unaware of its ozone-depleting character, for a long time it was globally applied as propellant and refrigerant and thus led to significant thinning of the ozone layer and contributed to the formation of the so-called ozone hole. Although production and application of this substance were gradually reduced at an early stage, we still face the consequences of its former careless use. Today, trichlorofluoromethane is released during recycling processes of waste cooling devices, traded on the black market, and according to recent findings still illegally manufactured. Here, we present an optical sensor device for real-time in-situ detection and measurement of this environmentally harmful chlorofluorocarbon. The described sensor is based on a planar Bragg grating that is functionalized with cyclodextrin derivatives and operates on the principle of a chemical sensor. In our study, the sensor is sensitized using per-methyl-, per-ethyl-, and per-allyl-substituted α -, β -, and γ -cyclodextrins as affinity materials for airborne trichlorofluoromethane. These functional coatings have been proven to be highly efficient, as an up to 400-times stronger signal deflection could be achieved compared to an identical but uncoated sensor. The presented sensor device shows instantaneous response to trichlorofluoromethane exposure, and features a limit-of-detection of less than 25 ppm, depending on the applied affinity material.
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