| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10225162 | Dyes and Pigments | 2019 | 48 Pages |
Abstract
A series of β-functionalized D-A porphyrins have been synthesized via Suzuki coupling reaction. Synthesized free base porphyrins exhibited very high protonation constants (logβ2â¯=â¯9.59-10.45). An efficient Förster resonance through bond energy transfer (78-88%) from β-substituents to macrocyclic core was supported by steady state and time resolved fluorescence measurements. Free base β-trisubstituted porphyrins exhibited highest protonation constants so far known in the literature.329
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Physical Sciences and Engineering
Chemical Engineering
Chemical Engineering (General)
Authors
Nitika Grover, Nivedita Chaudhri, Muniappan Sankar,