An unusual [4 + 2] fusion strategy to forge meso-N/O-heteroarene-fused (quinoidal) porphyrins with intense near-infrared Q-bands. Issue 30 (25th June 2019)
- Record Type:
- Journal Article
- Title:
- An unusual [4 + 2] fusion strategy to forge meso-N/O-heteroarene-fused (quinoidal) porphyrins with intense near-infrared Q-bands. Issue 30 (25th June 2019)
- Main Title:
- An unusual [4 + 2] fusion strategy to forge meso-N/O-heteroarene-fused (quinoidal) porphyrins with intense near-infrared Q-bands
- Authors:
- Li, Chengming
Zhu, Lei
Liang, Wenbo
Su, Rongchuan
Yin, Jiangliang
Hu, Yanmei
Lan, Yu
Wu, Di
You, Jingsong - Abstract:
- Abstract : Divergent synthesis of meso-N / O -heteroarene-fused (quinoidal) porphyrins was established via rhodium-catalyzed β-C–H activation/annulation of quinoidal porphyrins with alkynes. Abstract : Here we present a divergent synthesis of brand-new types of meso-N / O -heteroarene-fused (quinoidal) porphyrins through Rh-catalyzed β-C–H activation/annulation of 5, 15-dioxoporphyrins and dioxime derivatives with alkynes, in which the synthetic disconnections are difficult to access through the commonly used intramolecular cyclization strategy. Using the O -methyl oxime as a traceless oxidizing directing group, the meso-N -embedded pyridine-fused anti -quinoidal porphyrin3 and pyridinium-fused cation4 are formed with controllable chemoselectivity and complete anti -selectivity. Replacing the exocyclic oxime with a carbonyl group delivers the pyran-fused porphyrin5, achieving structural conversion from a quinoidal conformation to a stable porphyrin macrocycle. Further oxidation of the expanded dimer5ea gives the oxonium6, which exhibits intense near-infrared (NIR) Q-bands up to 1300 nm. Theoretical studies demonstrate that the incorporation of a heteroatom at the meso -position enables more effective π-extension, resulting in a 22π aromatic ( vs. 18π aromatic) character of pyran-fused porphyrins ( syn / anti -5aa ). Compared with the commercially available methylene blue (MB ), syn -5al exhibits a better ability ( Φ Δ = 0.61) to sensitize singlet oxygen ( 1 O2 ) whenAbstract : Divergent synthesis of meso-N / O -heteroarene-fused (quinoidal) porphyrins was established via rhodium-catalyzed β-C–H activation/annulation of quinoidal porphyrins with alkynes. Abstract : Here we present a divergent synthesis of brand-new types of meso-N / O -heteroarene-fused (quinoidal) porphyrins through Rh-catalyzed β-C–H activation/annulation of 5, 15-dioxoporphyrins and dioxime derivatives with alkynes, in which the synthetic disconnections are difficult to access through the commonly used intramolecular cyclization strategy. Using the O -methyl oxime as a traceless oxidizing directing group, the meso-N -embedded pyridine-fused anti -quinoidal porphyrin3 and pyridinium-fused cation4 are formed with controllable chemoselectivity and complete anti -selectivity. Replacing the exocyclic oxime with a carbonyl group delivers the pyran-fused porphyrin5, achieving structural conversion from a quinoidal conformation to a stable porphyrin macrocycle. Further oxidation of the expanded dimer5ea gives the oxonium6, which exhibits intense near-infrared (NIR) Q-bands up to 1300 nm. Theoretical studies demonstrate that the incorporation of a heteroatom at the meso -position enables more effective π-extension, resulting in a 22π aromatic ( vs. 18π aromatic) character of pyran-fused porphyrins ( syn / anti -5aa ). Compared with the commercially available methylene blue (MB ), syn -5al exhibits a better ability ( Φ Δ = 0.61) to sensitize singlet oxygen ( 1 O2 ) when irradiated with a 680 nm laser beam, and has potential as a photodynamic therapy (PDT) photosensitizer in the body's therapeutic window (650–900 nm). … (more)
- Is Part Of:
- Chemical science. Volume 10:Issue 30(2019)
- Journal:
- Chemical science
- Issue:
- Volume 10:Issue 30(2019)
- Issue Display:
- Volume 10, Issue 30 (2019)
- Year:
- 2019
- Volume:
- 10
- Issue:
- 30
- Issue Sort Value:
- 2019-0010-0030-0000
- Page Start:
- 7274
- Page End:
- 7280
- Publication Date:
- 2019-06-25
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/SC ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9sc01596e ↗
- Languages:
- English
- ISSNs:
- 2041-6520
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3151.490000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 11304.xml