影像科学与光化学 ›› 1999, Vol. 17 ›› Issue (2): 168-171.DOI: 10.7517/j.issn.1674-0475.1999.02.168

• 研究简报 • 上一篇    下一篇

可溶性亚酞菁的合成,光谱及聚集性质的研究

王小兵, 唐代华, 甄珍, 张建成, 刘新厚   

  1. 中国科学院感光化学研究所, 北京 100101
  • 收稿日期:1998-07-07 修回日期:1998-09-21 出版日期:1999-05-20 发布日期:1999-05-20
  • 通讯作者: 王小兵
  • 基金资助:
    国家自然科学基金资助项目(批准号:29584003)

SYNTHESIS,SPECTRAL AND AGGREGATION PROPERTIES OF SOLUBLE SUBPHTHALOCYANINES

WANG Xiao-bing, TANG Dai-hua, ZHEN Zhen, ZHANG Jian-cheng, LIU Xin-hou   

  1. Institute of Photographic Chemistry, The Chinese Academy of Sciences, Beijing 100101, P.R.China
  • Received:1998-07-07 Revised:1998-09-21 Online:1999-05-20 Published:1999-05-20

摘要: 酞菁类化合物作为一类有机功能材料,如导体或半导体、气敏元件、电化学催化剂、电致变色及光致变色材料、光动力疗法的药物以及非线性光学材料等[1],已经受到化学家和材料学家们的关注.近几十年来,化学家们已经成功地合成出了带各种不同取代基和含有不同中心金属原子的酞菁或萘酞菁类化合物,并对它们的物化性质进行了广泛而深入的研究.

关键词: 亚酞菁, 合成, 吸收光谱, 聚集

Abstract: Novel soluble μ-pheny l-tri (2,2-dimethylpropoxy) subphthalocyaninatoboron and μ-phenyl-tri (tert-butyl)-subnaphthalocyaninatoboron were prepared in this paper, and their spectral and aggregation properties were also studied. Our results indicate that the maximum absorption wavelength of SubNc is about 80 nm higher than that of SubPc, but both of them are blue-shifted about 100 nm compared with corresponding phthalocyanine and naphthalocyanine. Also, we find out that SubPc is stable, but SubNc is unstable to light. In addition, no aggregation in their solution takes place since the great spatialhindrance from the axial phenyl ring precludes molecular aggregation.

Key words: subphthalocyanine, synthesis, electronic absorption spectra, aggregation