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Preparation of Highly Porous Coordination Polymer Coatings on Macroporous Polymer Monoliths for Enhanced Enrichment of Phosphopeptides
Published on: July 14, 2015
Coordination polymers based on aluminum(III) porphyrins
Gregory J E Davidson1, Laura A Lane, Paul R Raithby
1Department of Chemistry and Biochemistry, University of Windsor, Windsor, Ontario N9B 3P4, Canada. gjed2@uwindsor.ca
Aluminum(III) porphyrin carboxylate complexes bind to nitrogenous ligands. This study formed one-dimensional coordination polymers using isonicotinic or nicotinic acid, confirmed by spectroscopy and X-ray analysis.
Area of Science:
- Coordination Chemistry
- Materials Science
- Supramolecular Chemistry
Background:
- Aluminum(III) porphyrin carboxylate complexes exhibit a known affinity for coordinating with nitrogenous ligands.
- The design of ligands offering multiple donor sites is crucial for constructing complex supramolecular architectures.
Purpose of the Study:
- To investigate the formation of coordination polymers using aluminum(III) porphyrin carboxylates and bifunctional ligands.
- To explore the structural characteristics of the resulting one-dimensional (1-D) coordination polymers.
Main Methods:
- Synthesis of aluminum(III) porphyrin carboxylate complexes.
- Utilized isonicotinic acid and nicotinic acid as bifunctional ligands (carboxylate and nitrogen donors).
- Characterization techniques included proton nuclear magnetic resonance ((1)H NMR) spectroscopy, nanoelectrospray ionization spectrometry, and X-ray diffraction analysis.
Main Results:
- The reaction successfully yielded one-dimensional (1-D) coordination polymers.
- Complexes and their linear oligomers were spectroscopically identified.
- Solid-state X-ray diffraction confirmed the polymeric, one-dimensional structure.
Conclusions:
- Bifunctional ligands like isonicotinic and nicotinic acid are effective in directing the self-assembly of aluminum(III) porphyrin carboxylates into 1-D coordination polymers.
- The study demonstrates a viable synthetic route for creating novel coordination polymer architectures with potential applications in materials science.
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