Literature DB >> 14746498

Role of the spacer in the singlet-singlet energy transfer mechanism (Förster vs Dexter) in cofacial bisporphyrins.

Sébastien Faure1, Christine Stern, Roger Guilard, Pierre D Harvey.   

Abstract

The cofacial bisporphyrins H4DPS (DPS = 4,6-bis[5-(2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrinyl)]dibenzothiophene), H4DPO (DPO = 4,6-bis[5-(2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrinyl)]dibenzofuran), H4DPX (DPX = 4,5-bis[5-(2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrinyl)]-9,9-dimethylxanthene), H4DPA (DPA = 1,8-bis[5-(2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrinyl)]anthracene), and H4DPB (DPB = 1,8-bis[5-(2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrinyl)]biphenylene) have been monometalated by Zn(OAc)2.2H2O and by GaCl3 to explore the singlet-singlet energy transfer from the photoexcited metal porphyrin center to the linked free base porphyrin. The spectroscopic (UV-vis and fluorescence) and photophysical properties (fluorescence lifetimes, tauF, and quantum yields, phiF) have been investigated at 298 and 77 K in degassed 2-MeTHF for the donor-acceptor systems, (Zn)H2DPS, (Zn)H2DPO, (Zn)H2DPA, (Zn)H2DPX, and (Zn)H2DPB, as well as for the bis-zinc complexes, (Zn)2DPS, (Zn)2DPO, (Zn)2DPX, and (Zn)2DPB, respectively, and the monoporphyrin derivatives, H2P, (Zn)P, and (Ga-OMe)P (P2- = 5-phenyl-2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrin-dianion). The singlet-singlet energy transfer rate constants (KET) were obtained using KET = (1/tauF -1/tauFo), where tauFo is the fluorescence lifetime of the corresponding bis-zinc(II) systems (or (Zn)P and (Ga-OMe)P) where no energy transfer occurs. The tauF value for three bis-zinc(II) compounds varies from 1.69 to 2.01 ns and is 1.84 (at 298 K) and 3.20 ns (at 77 K) for (Ga-OMe)P. In the donor-acceptor bismacrocycles, depending on the spacer and the temperature, the fluorescence lifetimes decrease down to 50-240 ps. The KET values range from approximately 4 to approximately 21 (ns(-1)) and have been analyzed considering both the Förster and the Dexter mechanisms. Using the C(meso)-C(meso) distance parameters in the calculations, the Förster and Dexter mechanisms operate for DPS and DPO, and for DPA, DPX, and DPB spacer systems, respectively. The limit distance where one mechanism dominates over the other is estimated to be around 5-6 A.

Entities:  

Year:  2004        PMID: 14746498     DOI: 10.1021/ja0379823

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  4 in total

1.  Discrepancy between experimental and theoretical excitation transfer rates in LH2 bacteriochlorophyll-protein complexes of purple bacteria.

Authors:  A Y Borisov
Journal:  Eur Biophys J       Date:  2007-07-13       Impact factor: 1.733

2.  Supramolecular allosteric cofacial porphyrin complexes.

Authors:  Christopher G Oliveri; Nathan C Gianneschi; SonBinh T Nguyen; Chad A Mirkin; Charlotte L Stern; Zdzislaw Wawrzak; Maren Pink
Journal:  J Am Chem Soc       Date:  2006-12-20       Impact factor: 15.419

3.  Selective anion binding by a cofacial binuclear zinc complex of a Schiff-base pyrrole macrocycle.

Authors:  Aline M J Devoille; Patricia Richardson; Nathan L Bill; Jonathan L Sessler; Jason B Love
Journal:  Inorg Chem       Date:  2011-03-10       Impact factor: 5.165

4.  Dimeric Corrole Analogs of Chlorophyll Special Pairs.

Authors:  Vinay K Sharma; Atif Mahammed; Amir Mizrahi; Maryann Morales; Natalia Fridman; Harry B Gray; Zeev Gross
Journal:  J Am Chem Soc       Date:  2021-05-20       Impact factor: 16.383

  4 in total

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