Geometrically homogenous series of covalently linked zinc/free-base porphyrin dimers of varying length;: Design, synthesis and characterization

被引:11
作者
Ljungdahl, Thomas [1 ]
Pettersson, Karin
Albinsson, Bo
Martensson, Jerker
机构
[1] Chalmers Univ Technol, Dept Chem & Biol Engn Organ Chem, S-41296 Gothenburg, Sweden
[2] Chalmers Univ Technol, Dept Chem & Biol Engn Phys Chem, S-41296 Gothenburg, Sweden
关键词
bridge-mediated coupling; cross-coupling; donor-acceptor systems; porphyrin;
D O I
10.1002/ejoc.200600240
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Singlet excitation energy transfer, SEET, can be mediated by a bridge, connecting an energy donor and acceptor, via a superexchange mechanism. The mediation efficiency depends on the energy difference between the first excited states of the donor and the bridge, Delta E-DB, as well as the donor-acceptor distance, R-DA, We have previously constructed a series of donor-bridge-acceptor, D-B-A, systems that allowed us to study how SEET depends on Delta E-DB. To expand this study into a second dimension, the distance dependence, a new series of D-B-A systems were constructed. This series was based on the same zinc/free-base porphyrin couple as the donor-acceptor pair in the previous series. Their relative orientation was also retained. In contrast to our first series, the bridges in the latter were of varying length. The bridges were oligo(phenyleneethynylene)phenylene (OPE) structures and the length was systematically changed by increasing the number of phenyleneethynylene units from 1 to 4. To obtain high quality samples, the D-B-A systems were assembled by a building block approach where the zinc and free-base porphyrins Were introduced separately using Heck alkyrrylations. The performance of the OPE structure as a mediator and scaffold is discussed in terms of singlet excited state energies and flexibility. For the first time, when combining the topical D-B A systems with our previous subset, a homogeneous series of D-B-A systems has been synthesized that allows for studies of both the distance dependence and the energy difference dependence of SEET. (c) Wiley-VCH Verlag GmbH & Co.
引用
收藏
页码:3087 / 3096
页数:10
相关论文
共 29 条
[1]   SYNTHESIS OF A CYCLIC PORPHYRIN TRIMER WITH A SEMI-RIGID CAVITY [J].
ANDERSON, HL ;
SANDERS, JKM .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1989, (22) :1714-1715
[2]   Triplet energy transfer in porphyrin dimers:: Comparison between π- and σ-chromophore bridged systems [J].
Andréasson, J ;
Kajanus, J ;
Mårtensson, J ;
Albinsson, B .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (40) :9844-9845
[3]   Energy transfer in rigid Ru(II)/Os(II) dinuclear complexes with biscyclometalating bridging ligands containing a variable number of phenylene units [J].
Barigelletti, F ;
Flamigni, L ;
Guardigli, M ;
Juris, A ;
Beley, M ;
ChodorowskiKimmes, S ;
Collin, JP ;
Sauvage, JP .
INORGANIC CHEMISTRY, 1996, 35 (01) :136-142
[4]   Molecular dynamics of covalently-linked multi-porphyrin arrays [J].
BothnerBy, AA ;
Dadok, J ;
Johnson, TE ;
Lindsey, JS .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (44) :17551-17557
[5]   Excited-state energy transfer processes in phenylene- and biphenylene-linked and directly-linked Zinc(II) and free-base hybrid diporphyrins [J].
Cho, HS ;
Jeong, DH ;
Yoon, MC ;
Kim, YH ;
Kim, YR ;
Kim, D ;
Jeoung, SC ;
Kim, SK ;
Aratani, N ;
Shinmori, H ;
Osuka, A .
JOURNAL OF PHYSICAL CHEMISTRY A, 2001, 105 (17) :4200-4210
[6]   A highly selective synthesis of diarylethynes and their oligomers by a palladium-catalyzed Sonogashira coupling reaction under phase transfer conditions [J].
Chow, HF ;
Wan, CW ;
Low, KH ;
Yeung, YY .
JOURNAL OF ORGANIC CHEMISTRY, 2001, 66 (05) :1910-1913
[7]   A THEORY OF SENSITIZED LUMINESCENCE IN SOLIDS [J].
DEXTER, DL .
JOURNAL OF CHEMICAL PHYSICS, 1953, 21 (05) :836-850
[8]  
ENG MP, IN PRESS J PHYS CHEM
[9]   ENERGIEWANDERUNG UND FLUORESZENZ [J].
FORSTER, T .
NATURWISSENSCHAFTEN, 1946, 33 (06) :166-175
[10]  
Harriman A, 2000, ANGEW CHEM INT EDIT, V39, P4287, DOI 10.1002/1521-3773(20001201)39:23<4287::AID-ANIE4287>3.0.CO