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http://hdl.handle.net/1942/26749
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DC Field | Value | Language |
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dc.contributor.author | Kruk, M.M. | - |
dc.contributor.author | Vershilovskaya, I.V. | - |
dc.contributor.author | Ngo, T. | - |
dc.contributor.author | Scheblykin, I.G. | - |
dc.contributor.author | Dehaen, W. | - |
dc.contributor.author | MAES, Wouter | - |
dc.date.accessioned | 2018-09-26T08:09:18Z | - |
dc.date.available | 2018-09-26T08:09:18Z | - |
dc.date.issued | 2016 | - |
dc.identifier.citation | Proceedings of BSTU, 4, p. 12-15 | - |
dc.identifier.issn | 1683-0377 | - |
dc.identifier.uri | http://hdl.handle.net/1942/26749 | - |
dc.description.abstract | Fluorescence spectra for a series of mixed phenyl-mesityl 5,10,15,20-tetraarylporphyrins – with Mes4, Mes3Ph, Mes2Ph2-trans, Mes2Ph2-cis, MesPh3 and Ph4 type architecture (Mes – mesityl, Ph – phenyl) – in their free base, mono- and diprotonated form are reported. Substitution of a single mesophenyl group with a sterically more demanding mesityl group is found to be sufficient to provide stabilization of the monoprotonated porphyrin species. A decrease in the number of mesityl substituents in the macrocycle leads to a decrease in the fluorescence quantum yield for protonated forms. The progressive replacement of ortho,ortho’-substituted mesityl groups with unhindered phenyls results in the additive pattern of spectral changes for the free base porphyrins, whereas for both protonated species a specific jump at the trans to cis transition is observed, along with a gradual additive pattern before and afterwards. This feature is interpreted as a signature of the transition between the hindered-like and unhindered-like conformations of the tetrapyrrolic macrocycles in the protonated forms. These two molecular conformations provide a different interaction of the two one-electron (a1u,eg) and (a2u,eg) configurations, which leads to changes of their contributions into electronic transitions. | - |
dc.language.iso | en | - |
dc.subject.other | porphyrins; free bases; protonated forms; molecular conformation; fluorescence | - |
dc.title | Free base and protonated form fluorescence of the mixed 5,10,15,20-arylporphyrins | - |
dc.type | Journal Contribution | - |
dc.identifier.epage | 15 | - |
dc.identifier.spage | 12 | - |
dc.identifier.volume | 4 | - |
local.bibliographicCitation.jcat | A2 | - |
local.type.refereed | Refereed | - |
local.type.specified | Article | - |
item.accessRights | Open Access | - |
item.contributor | Kruk, M.M. | - |
item.contributor | Vershilovskaya, I.V. | - |
item.contributor | Ngo, T. | - |
item.contributor | Scheblykin, I.G. | - |
item.contributor | Dehaen, W. | - |
item.contributor | MAES, Wouter | - |
item.fulltext | With Fulltext | - |
item.fullcitation | Kruk, M.M.; Vershilovskaya, I.V.; Ngo, T.; Scheblykin, I.G.; Dehaen, W. & MAES, Wouter (2016) Free base and protonated form fluorescence of the mixed 5,10,15,20-arylporphyrins. In: Proceedings of BSTU, 4, p. 12-15. | - |
crisitem.journal.issn | 1683-0377 | - |
Appears in Collections: | Research publications |
Files in This Item:
File | Description | Size | Format | |
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Kruk.Free base (1).pdf | Published version | 650.5 kB | Adobe PDF | View/Open |
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