Efficient Identification for Alcohol Homologues and Hyperthermy Based on Coordination Polymer Multiple Structural Transformations.

Recently, coordination polymer materials are of high interest due to the potential applications for chemical sensing and luminescent materials. In this work, we designed a photofluorescence coordination polymer material based on a donor-metal-acceptor structure. The donor-metal-acceptor architecture showed unusual multiple environmental responsiveness accompanied by a great change of fluorescence behaviors. Generally, organic homologue molecules are not easily distinguished by coordination polymer sensors because they have similar molecular structures and interaction sites. However, using the feature of multiple structural transformations, the accurate identification for organic homologue molecules can be realized, especially in a short time to quickly identify MeOH in other alcohol homologues (even in mixed atmospheres with only 10% MeOH). The visualization transformation of fluorescence can also be realized by single crystal to single crystal thermal-induced coordination bond ON/OFF behavior. The reversible structure conversion strategy provides new ideas for the accurate identification of organic homolog molecules or external environmental stimuli.