S2- and S1-states properties of zinc porphyrin polypeptides

被引:14
作者
Fujitsuka, Mamoru
Cho, Dae Won
Solladie, Nathalie
Troiani, Vincent
Qiu, Hongjin
Majima, Tetsuro
机构
[1] Osaka Univ, Inst Sci & Ind Res, SANKEN, Ibaraki, Osaka 5670047, Japan
[2] CNRS, Chim Coordinat Lab, Grp Synth Syst Porphyrin, F-31077 Toulouse 4, France
关键词
porphyrin; polypeptides; light harvesting system; S-2-excited state; singlet energy migration;
D O I
10.1016/j.jphotochem.2006.12.034
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
S-2- and S-1-states properties of zinc porphyrin polypeptides were investigated using various fast spectroscopic techniques. The B band of zinc porphyrin polypeptides showed broadening and shift to the longer wavelength side with the polymerization degree, indicating the interaction between the porphyrin units. The lifetime of S-2-fluorescence became shorter with increasing the polymerization degree. This phenomenon can be explained by applying the energy gap law to the S-2-S-1 internal conversion. From the picosecond transient absorption measurements, singlet singlet annihilation was confirmed, indicating the intrachain singlet energy migration in the polypeptides. The annihilation rate became faster with the polymerization degree because of the shorter distance between the zinc porphyrin units of longer polypeptides. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:346 / 350
页数:5
相关论文
共 43 条
[1]  
Aratani N, 2000, ANGEW CHEM INT EDIT, V39, P1458, DOI 10.1002/(SICI)1521-3773(20000417)39:8<1458::AID-ANIE1458>3.0.CO
[2]  
2-E
[3]   Novel porphyrinic peptides with assigned sequence of metallated chromophores, a further step towards redox switches [J].
Aubert, N ;
Troiani, V ;
Gross, M ;
Solladíe, N .
TETRAHEDRON LETTERS, 2002, 43 (46) :8405-8408
[4]   Excitation energy transport processes of porphyrin monomer, dimer, cyclic trimer, and hexamer probed by ultrafast fluorescence anisotropy decay [J].
Cho, HS ;
Rhee, H ;
Song, JK ;
Min, CK ;
Takase, M ;
Aratani, N ;
Cho, S ;
Osuka, A ;
Joo, T ;
Kim, D .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (19) :5849-5860
[5]  
Choi MS, 2001, ANGEW CHEM INT EDIT, V40, P3194, DOI 10.1002/1521-3773(20010903)40:17<3194::AID-ANIE3194>3.0.CO
[6]  
2-5
[7]   Helical polymer-anchored porphyrin nanorods [J].
de Witte, PAJ ;
Castriciano, M ;
Cornelissen, JJLM ;
Scolaro, LM ;
Nolte, RJM ;
Rowan, AE .
CHEMISTRY-A EUROPEAN JOURNAL, 2003, 9 (08) :1775-1781
[8]   Femtosecond study of exciton transport dynamics in (phthalocyaninato)polysiloxane [J].
Ern, J ;
Bock, A ;
Oddos-Marcel, L ;
Rengel, H ;
Wegner, G ;
Trommsdorff, HP ;
Kryschi, C .
JOURNAL OF PHYSICAL CHEMISTRY A, 1999, 103 (14) :2446-2450
[9]   Ethynyl porphyrins bridging bis(phosphine)platinum(II) centers: molecular models for conjugated organometallic porphyrin polymers [J].
Ferri, A ;
Polzonetti, G ;
Licoccia, S ;
Paolesse, R ;
Favretto, D ;
Traldi, P ;
Russo, MV .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1998, (23) :4063-4069
[10]   Fast exciton migration in porphyrin-functionalized polypeptides [J].
Fujitsuka, M ;
Hara, M ;
Tojo, S ;
Okada, A ;
Troiani, V ;
Solladié, N ;
Majima, T .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (01) :33-35