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- W2803493533 abstract "Meso-tetraarylporphyrins are widely explored due to their facile synthesis, characteristic deep colors, intense fluorescence, and high photochemical stability. Moreover, porphyrinoids have ability to chelate a wide variety of metal ions in their inner core.1 The electronic properties of porphyrins can be easily modulated by appending different substituents at β-and/or meso-positions. The substituents at β-positions of the porphyrins exert much larger steric and electronic effects on the porphyrin π-system than substituents at the meso-aryl positions.2 The optical properties of porphyrin π-system can be tuned by the modification of macrocyclic core through extended π-conjugation3a or by converting into chlorins3b or by tuning the conformation of the macrocycle.3c" @default.
- W2803493533 created "2018-06-01" @default.
- W2803493533 date "2018-01-01" @default.
- W2803493533 modified "2023-10-18" @default.
- W2803493533 title "Synthesis, Structural, Spectral and Intriguing Electrochemical Redox Properties of π-Extended Chlorins and Porphyrins" @default.
- W2803493533 doi "https://doi.org/10.1149/ma2018-01/12/980" @default.
- W2803493533 hasPublicationYear "2018" @default.
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