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

被引:126
作者
Faure, S
Stern, C
Guilard, R
Harvey, PD
机构
[1] Univ Bourgogne, LIMSAG, UMR 5633, F-21100 Dijon, France
[2] Univ Sherbrooke, Dept Chim, Sherbrooke, PQ J1K 2R1, Canada
关键词
D O I
10.1021/ja0379823
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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), H(4)DPA(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).2H(2)O 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, tau(F), and quantum yields, Phi(F)) have been investigated at 298 and 77 K in clegassed 2-MeTHF for the donor-acceptor systems, (Zn)H2DPS, (Zn)H2DPO, (Zn)H(2)DPA, (Zn)H2DPX, and (Zn)H2DPB, as well as for the bis-zinc complexes, (Zn)(2)DPS, (Zn)(2)DPO, (Zn)(2)DPX, and (Zn)(2)DPB, 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 (K-ET) Were obtained using K-ET = (1/tau(F) - 1/tau(F)degrees), where tau(F)degrees is the fluorescence lifetime of the corresponding bis-zinc(II) systems (or (Zn)P and (Ga-OMe)P) where no energy transfer occurs. The tau(F) 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 similar to4 to similar to21 (ns(-1)) and have been analyzed considering both the Forster and the Dexter mechanisms. Using the C-meso-C-meso distance parameters in the calculations, the Forster 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.
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页码:1253 / 1261
页数:9
相关论文
共 60 条
[1]  
[Anonymous], PORPHYRIN HDB, DOI DOI 10.1016/B978-0-08-092392-5.50008-0
[2]  
Aratani N., 2002, J PHOTOCHEM PHOTOB C, V3, P25, DOI DOI 10.1016/S1389-5567(02)00003-5
[3]   Highly efficient triplet-triplet intramolecular energy transfer and enhanced intersystem crossing in rigidly linked copper(II) porphyrin-free base porphyrin hybrid dimers [J].
Asano-Someda, M ;
Kaizu, Y .
INORGANIC CHEMISTRY, 1999, 38 (10) :2303-2311
[4]   Fine tuning of the photophysical properties of cofacial diporphyrins via the use of different spacers [J].
Bolze, F ;
Gros, CP ;
Drouin, M ;
Espinosa, E ;
Harvey, PD ;
Guilard, R .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2002, 643 :89-97
[5]  
BOLZE F, 2001, THESIS U BOURGOGNE D
[6]  
BRANDES S, 1993, THESIS U BOURGOGNE D
[7]   Xanthene-bridged cofacial bisporphyrins [J].
Chang, CJ ;
Deng, YQ ;
Heyduk, AF ;
Chang, CK ;
Nocera, DG .
INORGANIC CHEMISTRY, 2000, 39 (05) :959-966
[8]   Structural, spectroscopic, and reactivity comparison of xanthene- and dibenzofuran-bridged cofacial bisporphyrins [J].
Chang, CJ ;
Baker, EA ;
Pistorio, BJ ;
Deng, YQ ;
Loh, ZH ;
Miller, SE ;
Carpenter, SD ;
Nocera, DG .
INORGANIC CHEMISTRY, 2002, 41 (12) :3102-3109
[9]   A convergent synthetic approach using sterically demanding aryldipyrrylmethanes for tuning the pocket sizes of cofacial bisporphyrins [J].
Chang, CJ ;
Deng, YQ ;
Peng, SM ;
Lee, GH ;
Yeh, CY ;
Nocera, DG .
INORGANIC CHEMISTRY, 2002, 41 (11) :3008-3016
[10]   Porphyrin architectures bearing functionalized xanthene spacers [J].
Chang, CJ ;
Yeh, CY ;
Nocera, DG .
JOURNAL OF ORGANIC CHEMISTRY, 2002, 67 (04) :1403-1406