Photoinduced Electron Transfer in Clicked Ferrocene-BODIPY-Fullerene Conjugates

被引:0
作者
Rabah, Jad [1 ]
Fatima, Anam [2 ]
Fensterbank, Helene [1 ]
Wright, Karen [1 ]
Vallee, Anne [1 ]
Gueye, Maissa [1 ]
Burdzinski, Gotard [3 ]
Clavier, Gilles [4 ]
Miomandre, Fabien [4 ]
Pham, Julie [4 ]
Sliwa, Michel [5 ]
Meallet-Renault, Rachel [2 ]
Steenkeste, Karine [2 ]
Pino, Thomas [2 ]
Ha-Thi, Minh-Huong [2 ]
Allard, Emmanuel [1 ]
机构
[1] Univ Paris Saclay, Inst Lavoisier Versailles, UVSQ, CNRS, FR-78000 Versailles, France
[2] Univ Paris Saclay, Inst Sci Mol Orsay, CNRS, FR-91405 Orsay, France
[3] Adam Mickiewicz Univ, Fac Phys, Quantum Elec Lab, PL-61614, Poznan, Poland
[4] Univ Paris Saclay, PPSM, CNRS, ENS Paris Saclay, FR-91190 Gif Sur Yvette, France
[5] Univ Lille, CNRS, UMR 8516, Lab Spect Interact React & Environm, FR-59000 Lille, France
关键词
boron dipyrromethenes; CuAAC reaction; donor-acceptor systems; electron transfer; ferrocene; fullerenes; DONOR-ACCEPTOR; EXCITED-STATE; TRIPLET PHOTOSENSITIZERS; ENERGY; DERIVATIVES; CHEMISTRY; DYADS; C-60; CYCLOADDITION; WATER;
D O I
10.1002/hlca.202300039
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ferrocene-BODIPY (Fc-BDP) conjugates in which one or two ferrocene entities are linked to the beta-positions of the BODIPY core by an ethynyl bridge have been developed. These derivatives were easily and efficiently grafted onto a dual-clickable fullerene platform using CuAAC reactions, leading to a clickable Fc-BDP-C-60 triad and a clickable [Fc](2)-BDP-C-60 tetrad which can be used for further derivatization with complex structures. Due to the extended pi-conjugation and the presence of an intramolecular charge transfer band from Fc to BDP, all these conjugates display a broad absorption in the visible region, which is bathochromically shifted when two Fc are appended to the BDP core. Ultrafast multistep electron transfers leading to charge stabilization were demonstrated in the Fc-BDP-C-60 triad and [Fc](2)-BDP-C-60 tetrad by femtosecond transient absorption studies.
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页数:20
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