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    Please use this identifier to cite or link to this item: http://tkuir.lib.tku.edu.tw:8080/dspace/handle/987654321/25150


    Title: Preparative, structural, and physical studies of TTM-TTF complexes with Qmnt a quinone-type acceptor fused with sulfur-containing heterocycles
    Other Titles: Qmnt(一種銜合含硫雜環的Quinono類電子受體)與TTM-TTF之錯合物的製備、結構和物性研究
    Authors: 李榮熹;Lee, Jung-Si;Chang, Kevin;王文竹;Wang, Wen-jwu;Lee, Gene-Hsiang
    Contributors: 淡江大學化學學系
    Date: 1995-03-15
    Issue Date: 2009-12-01
    Publisher: Lausanne: Elsevier S.A.
    Abstract: The 2:3 complex of tetrakis(methylthio)tetrathiafulvalene (TTM-TTF) and the acceptor 5,10-dihydro-5,1-dioxobenzo- [1,2-b:4,5-b′]bis[1,4]dithiin-2,3,7,8-tetracarbonitrile (Qmnt), a p-benzoquinone derivative fused with sulfur-containing heterocycles, was prepared as powder by mixing equi-molar TTM-TTF and Qmnt in hot acetonitrile. Slow evaporation of dilute acetonitrile solution of [TTM-TTF]2[Qmnt]3 yielded needle-like crystals of [TTM-TTF][Qmnt]. The 1:1 complex crystallizes in the triclinic space group P1, with a=7.114(4),b=10.434(3), c=11.305(3)A, α=106.83(3), β=103.03(3), γ=96.82(3)•, Z=1. The TTM-TTF and Qmnt molecules are stacking alternately along the α axis, with their long molecular axes nearly perpendicular to each other. The room-temperature DC conductivity (compressed pellet) of [TTM-TTF]2[Qmnt]3 is 0.22 S cm−1 with Ea=0.14 eV, and that of [TTM-TTF][Qmnt] is 1.5 × 10−5S cm−1 with Ea=0.36 eV
    Relation: Synthetic metals 70(1-3), pp.1221-1222
    DOI: 10.1016/0379-6779(94)02827-L
    Appears in Collections:[化學學系暨研究所] 期刊論文

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