AI Article Synopsis

  • An evanescent wave infrared (IR) chemical sensor was created to specifically identify volatile amines that have heterocyclic or phenyl rings.
  • A rhenium-based metallacycle with a "molecular-trap" structure was synthesized to attract these amines through unique interactions, enhancing selectivity.
  • After optimizing the sensor, it demonstrated a quick response and outstanding detection performance for pyridine, with linear detection limits up to 10 mg/L and a sensitivity limit of around 5.7 μg/L, effectively distinguishing it from other volatile organic compounds.

Article Abstract

An evanescent wave infrared chemical sensor was developed to selectively detect volatile amines with heterocyclic or phenyl ring. To achieve this goal, a rhenium-based metallacycle with a "molecular-trap" structure was designed and synthesized as host molecules to selectively trap amines with heterocyclic or phenyl ring through Re-amine and π-π interactions. To explore the trapping properties of the material, a synthesized Re-based molecular trap was treated on an IR sensing element, and wide varieties of volatile organic compounds (VOCs) were examined to establish the selectivity for detection of amines. Based on the observed IR intensities, the Re-based molecular trap favors interaction with amines as evidenced by the variation of absorption bands of the Re molecular trap. With extra π-π interaction force, molecules, such as pyridine and benzylamine, could be detected. After optimization of the parameters for IR sensing, a rapid response in the detection of pyridine was observed, and the linear ranges were generally up to 10 mg/L with a detection limit around 5.7 μg/L. In the presence of other VOCs, the recoveries in detection of pyridine were all close to 100%.

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http://dx.doi.org/10.1021/acsami.6b11767DOI Listing

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