WELL-DEFINED OLIGO(PYRROLE-2,5-DIYL)S BY THE ULLMANN REACTION

被引:60
作者
GROENENDAAL, L [1 ]
PEERLINGS, HWI [1 ]
VANDONGEN, JLJ [1 ]
HAVINGA, EE [1 ]
VEKEMANS, JAJM [1 ]
MEIJER, EW [1 ]
机构
[1] EINDHOVEN UNIV TECHNOL,ORGAN CHEM LAB,5600 MB EINDHOVEN,NETHERLANDS
关键词
D O I
10.1021/ma00105a015
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The Ullmann coupling reaction has been used to polymerize N-t-BOC-2,5-dibromopyrrole into well-defined oligo(pyrrole-2,5-diyl)s. After optimization of the reaction conditions, i.e. using 1 wt equiv of Cu-bronze in DMF at 100 degrees C for 1 h, oligomers up to 25 repeating pyrrole units are obtained. Starting from 5,5'- and 5,5''-dibrominated N-t-BOC protected bi- and terpyrrole as monomers, the polymerization is slower and a lower degree of polymerization is observed, yielding oligomers with an even lower molecular weight than those resulting from N-t-BOC-2,5-dibromopyrrole. The first 20 oligomers of poly(N-t-BOC-pyrrole) have been isolated by preparative HPLC. Characterization of the individual oligomers shows that they ah are hydrogen terminated and possess a perfect 2,5-linkage: oligo(pyrrole-2,5-diyl)s. The isolated oligomers have been used to study the optical and electrical properties of the oligomers as a function of chain length.
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页码:116 / 123
页数:8
相关论文
共 51 条
  • [1] SAPPHYRINS - NOVEL AROMATIC PENTAPYRROLIC MACROCYCLES
    BAUER, VJ
    CLIVE, DLJ
    DOLPHIN, D
    PAINE, JB
    HARRIS, FL
    KING, MM
    LODER, J
    WANG, SWC
    WOODWARD, RB
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1983, 105 (21) : 6429 - 6436
  • [2] SYNTHESIS AND STRUCTURAL CHARACTERIZATION OF ALKYL OLIGOTHIOPHENES - THE 1ST ISOMERICALLY PURE DIALKYLSEXITHIOPHENE
    BAUERLE, P
    PFAU, F
    SCHLUPP, H
    WURTHNER, F
    GAUDL, KU
    CARO, MB
    FISCHER, P
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1993, (03): : 489 - 494
  • [3] SELECTIVE SYNTHESIS OF ALPHA-SUBSTITUTED OLIGOTHIOPHENES
    BAUERLE, P
    WURTHNER, F
    GOTZ, G
    EFFENBERGER, F
    [J]. SYNTHESIS-STUTTGART, 1993, (11): : 1099 - 1103
  • [4] THEORETICAL STUDY OF THE ELECTRICAL PROPERTIES OF BIPHENYLENE POLYMERS: PREDICTION OF NEW HIGHLY CONDUCTING POLYMER COMPLEXES.
    Bredas, J.L.
    Baughman, R.H.
    [J]. Journal of polymer science. Part B, Polymer letters, 1983, 21 (06): : 475 - 479
  • [5] SYNTHESIS OF LOW-BANDGAP ZWITTERIONIC AND PLANAR CONJUGATED PYRROLE-DERIVED POLYMERS - REVERSIBLE OPTICAL ABSORPTIONS FROM THE W TO THE NEAR-IR
    BROCKMANN, TW
    TOUR, JM
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (16) : 7435 - 7436
  • [6] CONVENIENT SYNTHETIC EQUIVALENTS OF 2-LITHIOPYRROLE AND 2,5-DILITHIOPYRROLE
    CHEN, W
    CAVA, MP
    [J]. TETRAHEDRON LETTERS, 1987, 28 (48) : 6025 - 6026
  • [7] Chen W., 1991, ORG SYNTH, V70, P151
  • [8] ELECTROCHEMICAL COUPLING OF DIALKYLATED SEXITHIOPHENE
    DELABOUGLISE, D
    HMYENE, M
    HOROWITZ, G
    YASSAR, A
    GARNIER, F
    [J]. ADVANCED MATERIALS, 1992, 4 (02) : 107 - 110
  • [9] ULLMANN SYNTHESIS OF BIARYLS 1945-1963
    FANTA, PE
    [J]. CHEMICAL REVIEWS, 1964, 64 (06) : 613 - &
  • [10] THE ULLMANN SYNTHESIS OF BIARYLS
    FANTA, PE
    [J]. CHEMICAL REVIEWS, 1946, 38 (01) : 139 - 196