Affiliation:
1. Institute of Industrial Science The University of Tokyo 4-6-1, Komaba, Meguro-ku 153-8505 Tokyo Japan
2. Department of Basic Science Graduate School of Arts and Sciences The University of Tokyo 3-8-1, Komaba, Meguro-ku 153-8902 Tokyo Japan
Abstract
AbstractHerein, we propose a novel amphiphilic polythiophene‐based chemosensor functionalized with a Zn(II)‐dipicolylamine side chain (1poly ⋅ Zn) for the pattern recognition of oxyanions. Optical changes in amphiphilic 1poly ⋅ Zn can be induced by the formation of a random coil from a backbone‐planarized structure upon the addition of target oxyanions, which results in blueshifts in the UV‐vis absorption spectra and turn‐on‐type fluorescence responses. Dynamic behavior in a polythiophene wire and/or among wires could be a driving force for obtaining visible color changes, while the molecular wire effect is dominant in obtaining fluorescence sensor responses. Notably, the magnitude of optical changes in 1poly ⋅ Zn has depended on differences in properties of oxyanions, such as their binding affinity, hydrophilicity, and molecular geometry. Thus, various colorimetric and fluorescence response patterns of 1poly ⋅ Zn to oxyanions were obtained, albeit using a single chemosensor. A constructed information‐rich dataset was applied to pattern recognition for the simultaneous group categorization of phosphate and carboxylate groups and the prediction of similar structural oxyanions at a different order of concentrations in their mixture solutions.
Funder
Japan Society for the Promotion of Science
Subject
General Chemistry,Biochemistry,Organic Chemistry
Cited by
3 articles.
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