Halogen- and hydrogen-bonding triazole-functionalised porphyrin-based receptors for anion recognitionElectronic supplementary information (ESI) available: 1H and 13C NMR spectra and ESI mass spectra or porphyrins 5 and 6; titration protocols and UV/visible titration curves. CCDC 953393. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c3dt52093e
Iodotriazole and triazole anion recognition groups have been integrated into a picket-fence zinc( ii )-metalloporphyrin scaffold to produce receptors for anion recognition and sensing applications. 1 H NMR and UV/visible spectroscopic investigations reveal both host systems exhibit strong anion bind...
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creator | Gilday, Lydia C White, Nicholas G Beer, Paul D |
description | Iodotriazole and triazole anion recognition groups have been integrated into a picket-fence zinc(
ii
)-metalloporphyrin scaffold to produce receptors for anion recognition and sensing applications.
1
H NMR and UV/visible spectroscopic investigations reveal both host systems exhibit strong anion binding affinities in a range of solvent media. Importantly, the halogen-bonding iodotriazole-containing porphyrin-based host displays halide binding affinities substantially larger than the protic-functionalised analogue concomitant with a reduced strength of oxoanion complexation.
Halogen-bonding iodotriazole anion recognition groups have been integrated into a picket-fence zinc(
ii
)-metalloporphyrin scaffold to produce a receptor with enhanced halide anion recognition and sensing applications. |
doi_str_mv | 10.1039/c3dt52093e |
format | Article |
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ii
)-metalloporphyrin scaffold to produce receptors for anion recognition and sensing applications.
1
H NMR and UV/visible spectroscopic investigations reveal both host systems exhibit strong anion binding affinities in a range of solvent media. Importantly, the halogen-bonding iodotriazole-containing porphyrin-based host displays halide binding affinities substantially larger than the protic-functionalised analogue concomitant with a reduced strength of oxoanion complexation.
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ii
)-metalloporphyrin scaffold to produce receptors for anion recognition and sensing applications.
1
H NMR and UV/visible spectroscopic investigations reveal both host systems exhibit strong anion binding affinities in a range of solvent media. Importantly, the halogen-bonding iodotriazole-containing porphyrin-based host displays halide binding affinities substantially larger than the protic-functionalised analogue concomitant with a reduced strength of oxoanion complexation.
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ii
)-metalloporphyrin scaffold to produce receptors for anion recognition and sensing applications.
1
H NMR and UV/visible spectroscopic investigations reveal both host systems exhibit strong anion binding affinities in a range of solvent media. Importantly, the halogen-bonding iodotriazole-containing porphyrin-based host displays halide binding affinities substantially larger than the protic-functionalised analogue concomitant with a reduced strength of oxoanion complexation.
Halogen-bonding iodotriazole anion recognition groups have been integrated into a picket-fence zinc(
ii
)-metalloporphyrin scaffold to produce a receptor with enhanced halide anion recognition and sensing applications.</abstract><doi>10.1039/c3dt52093e</doi><tpages>8</tpages></addata></record> |
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title | Halogen- and hydrogen-bonding triazole-functionalised porphyrin-based receptors for anion recognitionElectronic supplementary information (ESI) available: 1H and 13C NMR spectra and ESI mass spectra or porphyrins 5 and 6; titration protocols and UV/visible titration curves. CCDC 953393. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c3dt52093e |
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