Ordered Transfer from 3D‐oriented MOF Superstructures to Polymeric Films: Microfabrication, Enhanced Chemical Stability, and Anisotropic Fluorescent Patterns

Abstract Films and patterns of 3D‐oriented metal‐organic frameworks (MOFs) afford well‐ordered pore structures extending across centimeter‐scale areas. These macroscopic domains of aligned pores are pivotal to enhance diffusion along specific pathways and orient functional guests. The anisotropic properties emerging from this alignment are beneficial for applications in ion conductivity and photonics. However, the structure of 3D‐oriented MOF films and patterns can rapidly degrade under humid and acidic conditions. Thus, more durable 3D‐ordered porous systems are desired for practical applications. Here, oriented porous polymer films and patterns are prepared by using heteroepitaxially oriented N 3 ‐functionalized MOF films as precursor materials. The film fabrication protocol utilizes an azide–alkyne cycloaddition on the Cu 2 (AzBPDC) 2 DABCO MOF. The micropatterning protocol exploits the X‐ray sensitivity of azide groups in Cu 2 (AzBPDC) 2 DABCO, enabling selective degradation in the irradiated areas. The masked regions of the MOF film retain their N 3 ‐functionality, allowing for subsequent cross‐linking through azide‐alkyne coupling. Subsequent acidic treatment removes the Cu ions from the MOF, yielding porous polymer micro‐patterns. The polymer has high chemical stability and shows an anisotropic fluorescent response. The use of 3D‐oriented MOF systems as precursors for the fabrication of oriented porous polymers will facilitate the progress of optical components for photonic applications. This article is protected by copyright. All rights reserved