The design and synthesis of porphyrin/oligiothiophene hybrid monomers

被引:24
作者
Collis, GE
Campbell, WM
Officer, DL
Burrell, AK
机构
[1] Los Alamos Natl Lab, Los Alamos, NM 87545 USA
[2] Massey Univ, Nanomat Res Ctr, Palmerston North, New Zealand
关键词
D O I
10.1039/b502517f
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In an effort to build effective photovoltaic cells based on porphyrin-functionalised polythiophenes we have focused on synthetic routes to three monomer types. By controlling the geometric structure of the monomer, oxidation of these materials should produce polymers with different architectural structures, and as a result, different opto-electronic properties. Employing Wittig protocols allowed access to monomers in which the porphyrin moiety is connected to the beta-position of the thiophene via an alkene linkage. In addition, monomers were constructed using porphyrin condensation methods to afford alpha-thiophene meso-substituted porphryins. Another set of monomers was also prepared via porphyrin condensation routes, but instead utilising beta-formylthiophenes. By utilising different formyloligothiophenes we were able to generate a series of monomers that can be used to control the loading of the porphyrin in the polythiophene matrix.
引用
收藏
页码:2075 / 2084
页数:10
相关论文
共 77 条
[1]  
Alder A. D., 1967, J ORG CHEM, V32, P476
[2]   5,15-BIS(8-QUINOLYL)OCTAETHYLPORPHYRIN AND -BIS(2-PYRIDYL)OCTAETHYLPORPHYRIN - PREPARATION, STABILITIES OF ATROPISOMERS, AND METAL-ION BINDING-PROPERTIES [J].
AOYAMA, Y ;
KAMOHARA, T ;
YAMAGISHI, A ;
TOI, H ;
OGOSHI, H .
TETRAHEDRON LETTERS, 1987, 28 (19) :2143-2146
[3]   CONJUGATED MACROCYCLES RELATED TO THE PORPHYRINS .3. ACID-CATALYZED CONDENSATIONS OF THIOPHENECARBOXALDEHYDES WITH A DIPYRRYLMETHANE [J].
ARMIGER, YLST ;
LASH, TD .
JOURNAL OF HETEROCYCLIC CHEMISTRY, 1992, 29 (02) :523-527
[4]   PYRROMETHANES AND PORPHYRINS THEREFROM [J].
ARSENAULT, GP ;
BULLOCK, E ;
MACDONALD, SF .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1960, 82 (16) :4384-4389
[5]   Modification of electrodes with porphyrin-functionalised conductive polymers [J].
Ballarin, B ;
Masiero, S ;
Seeber, R ;
Tonelli, D .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1998, 449 (1-2) :173-180
[6]   Electrochemical synthesis and characterisation of polythiophene conducting polymers functionalised by metal-containing porphyrin residue [J].
Ballarin, B ;
Seeber, R ;
Tassi, L ;
Tonelli, D .
SYNTHETIC METALS, 2000, 114 (03) :279-285
[7]   Investigation of atropisomerism in ortho-substituted tetraphenylporphyrins: An experimental module involving synthesis, chromatography, and NMR spectroscopy [J].
Beeston, RF ;
Stitzel, SE ;
Rhea, MA .
JOURNAL OF CHEMICAL EDUCATION, 1997, 74 (12) :1468-1471
[8]   Meso-tetrathienylporphyrins:: electrochemical and axial ligation properties [J].
Bhyrappa, P ;
Bhavana, P .
CHEMICAL PHYSICS LETTERS, 2001, 349 (5-6) :399-404
[9]   Efficient synthesis of free-base 2-formyl-5,10,15,20-tetraarylporphyrins, their reduction and conversion to [(porphyrin-2-yl)methyl]phosphonium salts [J].
Bonfantini, EE ;
Burrell, AK ;
Campbell, WM ;
Crossley, MJ ;
Gosper, JJ ;
Harding, MM ;
Officer, DL ;
Reid, DCW .
JOURNAL OF PORPHYRINS AND PHTHALOCYANINES, 2002, 6 (11-12) :708-719
[10]   Effect of LiF/metal electrodes on the performance of plastic solar cells [J].
Brabec, CJ ;
Shaheen, SE ;
Winder, C ;
Sariciftci, NS ;
Denk, P .
APPLIED PHYSICS LETTERS, 2002, 80 (07) :1288-1290