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AbstractCovalent Organic Frameworks (COFs), an emerging class of crystalline porous materials, are a new type of support for grafting lanthanide ions (Ln3+), which can be employed as ratiometric luminescent thermometers. In this work we have shown that COFs co‐grafted with lanthanide ions (Eu3+, Tb3+) and Cu2+ (or potentially other d‐metals) can synchronously be employed both as a nanothermometer and catalyst during a chemical reaction. The performance of the thermometer could be tuned by changing the grafted d‐metal and solvent environment. As a proof of principle, the Glaser coupling reaction was investigated. We show that temperature can be precisely measured during the course of the catalytic reaction using luminescence thermometry. This concept could be potentially easily extended to other catalytic reactions by grafting other d‐metal ions on the Ln@COF platform.
catalysis, thermometry, FACILE SYNTHESIS, NANOSHEETS, ULTRAFINE, Chemistry, in-situ thermometry, COF, Taverne, luminescence, NANOPARTICLES, SENSORS, lanthanides, ratiometric thermometers, covalent organic frameworks, Glaser coupling reaction
catalysis, thermometry, FACILE SYNTHESIS, NANOSHEETS, ULTRAFINE, Chemistry, in-situ thermometry, COF, Taverne, luminescence, NANOPARTICLES, SENSORS, lanthanides, ratiometric thermometers, covalent organic frameworks, Glaser coupling reaction
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 65 | |
popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 1% | |
influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 1% |