Hypsochromically‐shifted Emission of Metal‐organic Frameworks Generated through Post‐synthetic Ligand Reduction

Author:

Smith Kyle T.12,Hunter Kye2,Chiu Nan‐Chieh12,Zhuang Hao3,Jumrusprasert Peemapat14,Stickle William F.5,Reimer Jeffrey A.3,Zuehlsdorff Tim J.2,Stylianou Kyriakos C.12ORCID

Affiliation:

1. Materials Discovery Laboratory (MaD Lab) Oregon State University Corvallis OR 97331 USA

2. Department of Chemistry Oregon State University Corvallis OR97331 USA

3. Department of Chemical and Biomolecular Engineering University of California Berkeley CA 94720 USA

4. Chulalongkorn University Bangkok 10330 Thailand

5. Hewlett-Packard Co. 1000 NE Circle Blvd. Corvallis OR 97330 USA

Abstract

AbstractLuminescent materials with tunable emission are becoming increasingly desirable as we move towards needing efficient Light Emitting Diodes (LEDs) for displays. Key to developing better displays is the advancement of strategies for rationally designing emissive materials that are tunable and efficient. We report a series of emissive metal‐organic frameworks (MOFs) generated using BUT‐10 (BUT: Beijing University of Technology) that emits green light with λmax at 525 nm. Post‐synthetic reduction of the ketone on the fluorenone ligand in BUT‐10 generates new materials, BUT‐10‐M and BUT‐10‐R. The emission for BUT‐10‐R is hypsochromically‐shifted by 113 nm. Multivariate BUT‐10‐M structures demonstrate emission with two maxima corresponding to the emission of both fluorenol and fluorenone moieties present in their structures. Our study represents a novel post‐synthetic ligand reduction strategy for producing emissive MOFs with tunable emission ranging from green, white‐blue to deep blue.

Funder

Oregon State University

Publisher

Wiley

Subject

General Medicine

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