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Charge separation, charge recombination and intersystem crossing in orthogonal naphthalimide–perylene electron donor/acceptor dyad
We prepared an orthogonal electron donor/acceptor dyad ( NI–Py ) with perylene (Py) as electron donor and 4-aminonaphthalimide ( NI ) as an electron acceptor. The molecule adopts orthogonal geometry due to the steric hindrance exerted by the 4-amino substituents on the NI moiety. The photophysical p...
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Published in: | Photochemical & photobiological sciences 2021, Vol.20 (1), p.69-85 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | We prepared an orthogonal electron donor/acceptor dyad (
NI–Py
) with perylene (Py) as electron donor and 4-aminonaphthalimide (
NI
) as an electron acceptor. The molecule adopts orthogonal geometry due to the steric hindrance exerted by the 4-amino substituents on the NI moiety. The photophysical properties of dyad were studied by steady-state UV–Vis absorption and fluorescence spectroscopies, femtosecond/nanosecond transient absorption spectroscopies and DFT computations. Ground state interaction between the NI and Py units is negligible; however, charge separation occurs upon photoexcitation, indicated by the quenching of the fluorescence of the dyad in polar solvents, i.e. fluorescence quantum yield (
Φ
F
) is 61.9% in toluene and
Φ
F
= 0.2% in methanol. Spin–orbit-coupled charge transfer-induced intersystem crossing (SOCT-ISC) was confirmed by femtosecond transient absorption spectroscopy (charge separation takes 1.7 ps and charge recombination takes 6.9 ns, in CH
2
Cl
2
). Nanosecond transient absorption spectra indicated the formation of perylene-localized triplet state, and the triplet state lifetime (175 μs) is much longer than that accessed with the heavy atom effect (3-bromoperylene; 16 μs). The singlet oxygen quantum (
Φ
Δ
) yield of the dyad is 2.2% in hexane and 9.5% in dichloromethane. The low SOCT-ISC efficiency as compared to the previously reported analogue (
Φ
Δ
= 80%) is attributed to the mismatch of the
1
CT/T
n
state energies, and/or the orientation of the NI and Py units, i.e. orthogonal geometry is not sufficient for achieving efficient SOCT-ISC in compact electron donor/acceptor dyads.
Graphical abstract |
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ISSN: | 1474-905X 1474-9092 |
DOI: | 10.1007/s43630-020-00002-w |