Push–pull quinoidal porphyrins
A family of push–pull quinoidal porphyrin monomers has been prepared from a meso-formyl porphyrin by bromination, thioacetal formation, palladium-catalyzed coupling with malononitrile and oxidation with DDQ. Attempts at extending this synthesis to a push–pull quinoidal/cumulenic porphyrin dimer were...
| Main Authors: | , , , |
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| Format: | Journal article |
| Language: | English |
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Royal Society of Chemistry
2018
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| _version_ | 1826281510395707392 |
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| author | Smith, M Blake, I Clegg, W Anderson, H |
| author_facet | Smith, M Blake, I Clegg, W Anderson, H |
| author_sort | Smith, M |
| collection | OXFORD |
| description | A family of push–pull quinoidal porphyrin monomers has been prepared from a meso-formyl porphyrin by bromination, thioacetal formation, palladium-catalyzed coupling with malononitrile and oxidation with DDQ. Attempts at extending this synthesis to a push–pull quinoidal/cumulenic porphyrin dimer were not successful. The crystal structures of the quinoidal porphyrins indicate that there is no significant contribution from singlet biradical or zwitterionic resonance forms. The crystal structure of an ethyne-linked porphyrin dimer shows that the torsion angle between the porphyrin units is only about 3°, in keeping with crystallographic results on related compounds, but contrasting with the torsion angle of about 35° predicted by computational studies. The free-base quinoidal porphyrin monomers form tightly π-stacked layer structures, despite their curved geometries and bulky aryl substituents. |
| first_indexed | 2024-03-07T00:29:53Z |
| format | Journal article |
| id | oxford-uuid:7f686b5d-22f5-42ac-b025-ecee92634d2f |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T00:29:53Z |
| publishDate | 2018 |
| publisher | Royal Society of Chemistry |
| record_format | dspace |
| spelling | oxford-uuid:7f686b5d-22f5-42ac-b025-ecee92634d2f2022-03-26T21:16:44ZPush–pull quinoidal porphyrinsJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:7f686b5d-22f5-42ac-b025-ecee92634d2fEnglishSymplectic Elements at OxfordRoyal Society of Chemistry2018Smith, MBlake, IClegg, WAnderson, HA family of push–pull quinoidal porphyrin monomers has been prepared from a meso-formyl porphyrin by bromination, thioacetal formation, palladium-catalyzed coupling with malononitrile and oxidation with DDQ. Attempts at extending this synthesis to a push–pull quinoidal/cumulenic porphyrin dimer were not successful. The crystal structures of the quinoidal porphyrins indicate that there is no significant contribution from singlet biradical or zwitterionic resonance forms. The crystal structure of an ethyne-linked porphyrin dimer shows that the torsion angle between the porphyrin units is only about 3°, in keeping with crystallographic results on related compounds, but contrasting with the torsion angle of about 35° predicted by computational studies. The free-base quinoidal porphyrin monomers form tightly π-stacked layer structures, despite their curved geometries and bulky aryl substituents. |
| spellingShingle | Smith, M Blake, I Clegg, W Anderson, H Push–pull quinoidal porphyrins |
| title | Push–pull quinoidal porphyrins |
| title_full | Push–pull quinoidal porphyrins |
| title_fullStr | Push–pull quinoidal porphyrins |
| title_full_unstemmed | Push–pull quinoidal porphyrins |
| title_short | Push–pull quinoidal porphyrins |
| title_sort | push pull quinoidal porphyrins |
| work_keys_str_mv | AT smithm pushpullquinoidalporphyrins AT blakei pushpullquinoidalporphyrins AT cleggw pushpullquinoidalporphyrins AT andersonh pushpullquinoidalporphyrins |