2019
DOI: 10.1142/s1088424619501451
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Synthesis, characterization and modeling of self-assembled porphyrin nanorods

Abstract: Porphyrin nanorods were prepared by ion-association between free-base meso 5,10,15,20-tetrakis-(4-[Formula: see text]-methylpyridinium)porphyrin cations and tetraphenylborate anions. The nanorods have variable lengths (up to a few micrometers long) and diameters ([Formula: see text]50–500 nm). Their structure at the molecular level was elucidated by combining multinuclear solid state NMR spectroscopy, synchrotron X-ray powder diffraction and DFT calculations.

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Cited by 2 publications
(3 citation statements)
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“…The origin of this spectral evolution may be attributed either to the formation of porphyrin J-aggregates in the nanostructures or to the flattening of the porphyrin within the nanostructures inducing a larger π conjugation between the macrocycle and meso aryl groups. 38 Fluorescence spectra of the precursor 2 and nanoparticles are displayed in Figure 3d (λ exc = 430 nm). The two emission bands of porphyrins within nanoparticles at 664 and 732 nm are slightly red-shifted compared to those of the corresponding silylated porphyrin precursor (659 and 725 nm).…”
Section: ■ Results and Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…The origin of this spectral evolution may be attributed either to the formation of porphyrin J-aggregates in the nanostructures or to the flattening of the porphyrin within the nanostructures inducing a larger π conjugation between the macrocycle and meso aryl groups. 38 Fluorescence spectra of the precursor 2 and nanoparticles are displayed in Figure 3d (λ exc = 430 nm). The two emission bands of porphyrins within nanoparticles at 664 and 732 nm are slightly red-shifted compared to those of the corresponding silylated porphyrin precursor (659 and 725 nm).…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…Compared with the porphyrin precursor, absorption bands of the porphyrins within nanoparticles are red-shifted. The origin of this spectral evolution may be attributed either to the formation of porphyrin J-aggregates in the nanostructures or to the flattening of the porphyrin within the nanostructures inducing a larger π conjugation between the macrocycle and meso aryl groups . Fluorescence spectra of the precursor 2 and nanoparticles are displayed in Figure d (λ exc = 430 nm).…”
Section: Resultsmentioning
confidence: 99%
“…Porphyrins have significant applications in the electrochemical industry. Porphyrin derivatives, solid as well as liquid, have been used in fuel cells and solar cells and as catalysts in batteries for high-performance devices for the past few years. Interestingly, porphyrins aggregate forming complex structures such as nanorods, nanotubes, nanorings, and so forth by stacking and other self-assembly methods. , Porphyrins are covalently bonded to each other forming a complex arrangement of covalent organic frameworks (COFs). The periodic boundary of each porphyrin is bonded to another by strong covalent bonds forming a new phase of advanced materials.…”
Section: Introductionmentioning
confidence: 99%