6-(3,4-dicyanophenylthio)-hexylthiophene-2-carboxylate | 960596-72-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 6-(3,4-dicyanophenylthio)-hexylthiophene-2-carboxylate
• CAS: 960596-72-9
• 化学式: C₁₉H₁₈N₂O₂S₂
• 分子量: 370.496
• InChiKey: WMEBWBURFNGRSF-UHFFFAOYSA-N

反应信息

• 作为反应物：
  描述：

  6-(3,4-dicyanophenylthio)-hexylthiophene-2-carboxylate 、 2,9,16,23-tetrakis-(6-(thiophene-2-carboxylate)-hexylthio)phthalocyanine 、 copper dichloride 以 further solvent(s) 为溶剂， 以18.56%的产率得到2,9,16,23-tetrakis-(6-(thiophene-2-carboxylate)-hexylthio)phthalocyaninato copper(II)
  参考文献：
  名称：

  Metal-ion sensing and aggregation studies on reactive phthalocyanines bearing soft-metal receptor moieties; synthesis, spectroscopy and electrochemistry

  摘要：

  Tetrasubstituted metal-free {2H[Pc(S(CH2)(6)OCOC4H3S)(4)]} and copperphthalocyanine {Cu[Pc(S(CH2)(6)OCOC4H3S)(4)]}, bearing thiophene-2-carboxylate-hexylthio moieties, have been prepared as isomeric mixtures via cyclo-tetramerization. Both new compounds have been characterized by elemental analysis, FTIR, H-1 and C-13 NMR, MS (Maldi-TOF) and UV-Vis spectral data, The cation binding abilities of the functional phthalocyanines with Ag-I, Pd-II, Hg-II, Pb-II and Cd-II are evaluated by a monomer-oligomer formation technique with U-V-Vis spectroscopy. Spectroscopic properties of the complexes were affected strongly by the electron-donating sulfanyl units on the periphery. Cyclic voltammetry and differential pulse voltammetry studies show that both compounds give up to three ligand based reduction processes and one ligand-based oxidation process having diffusion-controlled one electron transfer properties. (C) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.poly.2007.07.042