Application of the boron center for the design of a covalently bonded closely spaced triad of porphyrin-fullerene mediated by dipyrromethane. Issue 19 (26th April 2017)

• Record Type: Journal Article
• Authors: Gao, Di; Aly, Shawkat M.; Karsenti, Paul-Ludovic; Brisard, Gessie; Harvey, Pierre D.
• Is Part Of: Dalton transactions. Volume 46:Issue 19(2017)
• Page Start: 6278
• Page End: 6290
• Publication Date: 2017-04-26
• Subjects: Chemistry, Inorganic -- Periodicals; Chemistry, Physical and theoretical -- Periodicals; Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/c7dt00472a
• Languages: English
• ISSNs: 1477-9226

Abstract

Abstract : Charge separation stabilization is achieved by placing porphyrin and C60 at the two ends of central BODIPY. Abstract : Two novel triads had been designed through covalent bond connection of the boron dipyrromethane (BODIPY), free base porphyrin (H2P) or zinc(ii ) porphyrin (ZnP) and N -methyl-2-phenyl-3, 4-fulleropyrrolidine (C60 ) mediated by BODIPY. This closely spaced triad arrangement where porphyrin and fullerene are placed apart is anticipated to stabilize charge separation by separating the two radicals from each other. Two model polyads were synthesized with BODIPY and H2P or ZnP to investigate interaction between the two chromophores. Photo-excitation of the BODIPY triggered an efficient singlet energy transfer where the rates are found to be ∼10 10 –10 11 s −1 . For triads with C60 fast electron transfer was confirmed by the detection of the C60 ˙ − signature from femtosecond transient absorption (fs-TA) in ∼0.4–3 ps. The charge recombination is estimated to be in the nanosecond window. This indicates the convenience of this arrangement for stabilizing the charge-separated state.