Investigating the role of corrole as an excitation energy relay in light-induced processes in closely connected N,N'-bis( biphenyl-4-yl) aniline functionalized corrole donor-acceptor dyad

被引:0
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作者
Chuncha, Vijaykumar [1 ]
Balahoju, Shivaprasad Achary [2 ]
Dutta, Snigdha [1 ]
Giribabu, Lingamallu [2 ,3 ]
Chitta, Raghu [1 ,4 ]
机构
[1] Natl Inst Technol Warangal, Dept Chem, Artificial Photosynth Lab, Hanamkonda, Telangana, India
[2] CSIR Indian Inst Chem Technol, Polymers & Funct Mat Div, Hyderabad 500007, Telangana, India
[3] Acad Sci & Innovat Res, Ghaziabad, India
[4] Natl Inst Technol Warangal, Dept Chem, Artificial Photosynth Lab, Hanamkonda 506004, Telangana, India
关键词
corrole; N; N'-Bis(; biphenyl-4-yl); aniline; photo-induced energy transfer; photosynthetic antenna-reaction center model; INTRAMOLECULAR CHARGE-TRANSFER; SENSITIZED SOLAR-CELLS; PHOTOINDUCED ELECTRON-TRANSFER; ZINC PORPHYRIN; PHOTOPHYSICAL PROPERTIES; TRIPHENYLAMINE; FULLERENE; SYSTEMS; CONVERSION; STATE;
D O I
10.1111/php.13939
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A photosynthetic antenna-reaction center model, BBA-PFCor comprised of N,N'-bis( biphenyl-4- yl) aniline (BBA) covalently functionalized to bis(pentafluoro)corrole moiety has been prepared and the contribution of the BBA as the photoinduced energy transfer antenna was investigated. UV-visible studies have shown that integrating the electron-rich BBA chromophore into the corrole core has broadened the soret band of the corrole moiety with the absorption spanning from 300 to 700 nm. Electrochemical studies, in corroboration with the computational calculations, revealed that, BBA moiety can act as an electron reservoir and, in the excited state, it would transfer the excited energy to the corrole moiety in the dyad. Steady-state fluorescence studies have demonstrated that, upon photoexcitation of the BBA moiety of BBA-PFCor at 310nm in solvents of varied polarity, the BBA emission centered at 400 nm was observed to be quenched, with the concomitant appearance of the corrole emission from 500 to 700 nm, indicating the happening of photoinduced energy transfer (PEnT) from (1)BBA* to corrole moiety. Parallel control experiments involving the excitation of the corrole moiety at 410 nm did not result in the diminishing of the corrole emission, suggesting that the quenching of the BBA emission in BBA-PFCor is majorly due to intramolecular PEnT from (1)BBA* to corrole moiety leading to the formation of singlet excited corrole, that is, (1)BBA*-PFCor -> BBA(-1)PFCor*. The free energy changes of PEnT, Delta G(EnT), were found to be thermodynamically feasible in all the solvents used for the study. Parallel time-resolved fluorescence studies were congruent with the steady-state fluorescence results and provided further evidence for the occurrence of ultrafast PEnT from (1)BBA* -> corrole in the dyad with the rates of energy transfer (k(EnT)) of similar to 10(8) s(-1).
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页码:1041 / 1054
页数:14
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