| Literature DB >> 32237191 |
Yifan Gu1,2, Jia-Jia Zheng1,3, Ken-Ichi Otake1, Kunihisa Sugimoto1, Nobuhiko Hosono1, Shigeyoshi Sakaki3, Fengting Li2, Susumu Kitagawa1.
Abstract
To achieve unique molecular-recognition patterns, a rational control of the flexibility of porous coordination polymers (PCPs) is highly sought, but it remains elusive. From a thermodynamic perspective, the competitive relationship between the structural deformation energy (Edef ) of soft PCPs and the guest interaction is key for selective a guest-triggered structural-transformation behavior. Therefore, it is vital to investigate and control Edef to regulate this competition for flexibility control. Driven by these theoretical insights, we demonstrate an Edef -modulation strategy via encoding inter-framework hydrogen bonds into a soft PCP with an interpenetrated structure. As a proof of this concept, the enhanced Edef of PCP enables a selective gate-opening behavior toward CHCl3 over CH2 Cl2 by changing the adsorption-energy landscape of the compounds. This study provides a new direction for the design of functional soft porous materials.Entities:
Keywords: energy landscape; flexibility; molecular recognition; porous coordination polymer; structural-deformation energy
Year: 2020 PMID: 32237191 DOI: 10.1002/anie.202003186
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336