Driving high quantum yield NIR emission through proquinoidal linkage motifs in conjugated supermolecular arrays. Issue 31 (5th August 2020)
- Record Type:
- Journal Article
- Title:
- Driving high quantum yield NIR emission through proquinoidal linkage motifs in conjugated supermolecular arrays. Issue 31 (5th August 2020)
- Main Title:
- Driving high quantum yield NIR emission through proquinoidal linkage motifs in conjugated supermolecular arrays
- Authors:
- Viere, Erin J.
Qi, Wei
Stanton, Ian N.
Zhang, Peng
Therien, Michael J. - Abstract:
- Abstract : Incorporation of proquinoidal BTD building blocks into conjugated porphyrin oligomers minimizes the extent of excited-state structural relaxation relative to the ground-state conformation, elucidating new classes of impressive NIR fluorophores. Abstract : High quantum yield NIR fluorophores are rare. Factors that drive low emission quantum yields at long wavelength include the facts that radiative rate constants increase proportional to the cube of the emission energy, while nonradiative rate constants increase in an approximately exponentially with decreasing S0 –S1 energy gaps (in accordance with the energy gap law). This work demonstrates how the proquinoidal BTD building blocks can be utilized to minimize the extent of excited-state structural relaxation relative to the ground-state conformation in highly conjugated porphyrin oligomers, and shows that 4-ethynylbenzo[ c ][1, 2, 5]thiadiazole (E-BTD ) units that terminate meso -to- meso ethyne-bridged (porphinato)zinc (PZn n ) arrays, and 4, 7-diethynylbenzo[ c ][1, 2, 5]thiadiazole (E-BTD-E ) spacers that are integrated into the backbone of these compositions, elucidate new classes of impressive NIR fluorophores. We report the syntheses, electronic structural properties, and emissive characteristics of neoteric PZn-(BTD-PZn) n, PZn2 -(BTD-PZn2 ) n, and BTD-PZn n -BTD fluorophores. Absolute fluorescence quantum yield ( ϕ f ) measurements, acquired using a calibrated integrating-sphere-based measurement system,Abstract : Incorporation of proquinoidal BTD building blocks into conjugated porphyrin oligomers minimizes the extent of excited-state structural relaxation relative to the ground-state conformation, elucidating new classes of impressive NIR fluorophores. Abstract : High quantum yield NIR fluorophores are rare. Factors that drive low emission quantum yields at long wavelength include the facts that radiative rate constants increase proportional to the cube of the emission energy, while nonradiative rate constants increase in an approximately exponentially with decreasing S0 –S1 energy gaps (in accordance with the energy gap law). This work demonstrates how the proquinoidal BTD building blocks can be utilized to minimize the extent of excited-state structural relaxation relative to the ground-state conformation in highly conjugated porphyrin oligomers, and shows that 4-ethynylbenzo[ c ][1, 2, 5]thiadiazole (E-BTD ) units that terminate meso -to- meso ethyne-bridged (porphinato)zinc (PZn n ) arrays, and 4, 7-diethynylbenzo[ c ][1, 2, 5]thiadiazole (E-BTD-E ) spacers that are integrated into the backbone of these compositions, elucidate new classes of impressive NIR fluorophores. We report the syntheses, electronic structural properties, and emissive characteristics of neoteric PZn-(BTD-PZn) n, PZn2 -(BTD-PZn2 ) n, and BTD-PZn n -BTD fluorophores. Absolute fluorescence quantum yield ( ϕ f ) measurements, acquired using a calibrated integrating-sphere-based measurement system, demonstrate that these supermolecules display extraordinary ϕ f values that range from 10–25% in THF solvent, and between 28–36% in toluene solvent over the 700–900 nm window of the NIR. These studies underscore how the regulation of proquinoidal conjugation motifs can be exploited to drive excited-state dynamical properties important for high quantum yield long-wavelength fluorescence emission. … (more)
- Is Part Of:
- Chemical science. Volume 11:Issue 31(2020)
- Journal:
- Chemical science
- Issue:
- Volume 11:Issue 31(2020)
- Issue Display:
- Volume 11, Issue 31 (2020)
- Year:
- 2020
- Volume:
- 11
- Issue:
- 31
- Issue Sort Value:
- 2020-0011-0031-0000
- Page Start:
- 8095
- Page End:
- 8104
- Publication Date:
- 2020-08-05
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/SC ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d0sc03446k ↗
- 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:
- 13956.xml