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2,3-二甲氧羰基-6,7-二氰基四硫富瓦烯衍生物合成

Synthesis of dimethyl 2-(4,5-dicyano-1,3-dithiol-2-ylidene)-1,3-dithiole-4,5-dicarboxylate
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摘要 在亚磷酸三乙酯存在下,利用高度稀释技术,通过4,5-二氰基-1,3-二硫杂环戊烯-2-酮和4,5-二甲氧羰基-1,3-二硫环戊烯-2-硫酮的交叉偶联反应,成功地合成了关键前躯体二氰基四硫富瓦烯衍生物,用NMR、TOF-Ms和IR表征了其结构,并用循环伏安法和紫外吸收光谱初步评价了四硫富瓦烯衍生物的电化学性质和光物理性质。 With high dilution technique, cross-coupling reaction happens between 4,5-dicyano-1,3- dithiol-2-one(2) and dimethyl 2-thioxo-l,3-dithiole-4,5-dicarboxylate(3) in toluene to produce the asymmetrical diycano tetrathiafolvalene derivative (1) in the presence of triethyl phosphate. The structures are characterized by NMR, TOF-Ms and IR. Electrochemical and photo physical properties are evaluated with cyclic voltammograms and UV absorption spectrum.
出处 《长春工业大学学报》 CAS 2016年第4期323-327,共5页 Journal of Changchun University of Technology
基金 国家自然科学基金资助项目(21442004)
关键词 高度稀释 四硫富瓦烯 交叉偶联 合成 high dilution tetrathiafulvalene cross-coupling synthesis.
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参考文献9

  • 1Otsubo T, Ogura F. Cromled tetrathiafulva|ene de- rivativesl-J ~. Bull. Chem. Soc. Jpn., 1985, 58 ( 4 ) .. 1343-1344.
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二级参考文献7

  • 1Otsubo T, Ogura F. Cromled tetrathiafulvalene derivatives[J]. Bull. Chem. Soc. Jpn. , 1985,58 (4) : 1343-1344.
  • 2Hansen T K, Joergensen T, Stein P C, et al. Crown ether derivatives of tetrathiafulvalene[J]. J. Org. Chem. ,1992,57(24) :6403-6409.
  • 3Nieisen M B, Becher J. Two and three-dimensional tetrathiafulvalene macrocycles[J]. Liebigs Ann. Recueil, 1997,18 : 2177-2187.
  • 4Jeppesen J O, Becher J. Pyrrolo-tetrathiafulvalenes and their applications in molecular and supmmolecu- lar chemistry[J]. Eur. J. Org. Chem. ,2003,17: 3245-3266.
  • 5Jrgensen T, HansenK, Becher J. Tetrathiafulvalenes as building-blocks in supramolecular chem- istry[J]. Chem. Soc. Rev. ,1994,23(1):41-51.
  • 6Becher J, Brimert T, Jeppesen J O, et al. Tetrathiafulvaleno-annelated porphyrins [J]. Angew. Chem. lnt. Ed. ,2001,40(13) :2497-2500.
  • 7Hou Rui-bin, Li Bao, Zhong Ke-li, et al. Tetrakis ( tetrathiafulvalene-tetrathiacrown ether ) porphyrazine triads: synthesis photophysieal, and electrochemical properties[J]. Eur. J. Org. Chem., 2012,6 : 1138-1146.

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