English
往期目录
新闻公告
More
化学进展 2006, Vol. 18 Issue (06): 698-706 前一篇   后一篇

• 综述与评论 •

二芳基乙烯类化合物用作光开关的最新研究*

龚涛;冯嘉春;韦玮**;黄维**   

  1. 复旦大学先进材料实验室 先进光子材料与器件国家重点实验室 上海 200433
  • 收稿日期:2005-06-01 修回日期:2006-02-01 出版日期:2006-06-24 发布日期:2006-06-24
  • 通讯作者: 韦玮；黄维
下载PDF ( 2469 ) 引用
导出

Recent Progress in Diarylethene as a Photoswitching Unit

Tao Gong;Jiachun Feng;Wei Wei**; Wei Huang**   

  1. Lab of Advanced Materials, Key Laboratory of Advanced Photonics Materials and Devices,Fudan University, Shanghai 200433,China 
  • Received:2005-06-01 Revised:2006-02-01 Online:2006-06-24 Published:2006-06-24
  • Contact: Wei Wei; Wei Huang
本文在综述二芳基乙烯类化合物各种性能的基础上，重点介绍了二芳基乙烯类化合物作为荧光光控开关、荧光共振能量转移、光致变色电开关、光致变色磁开关、光致变色液晶开关和多功能光致变色开关的最新发展动态，以及二芳基乙烯类化合物的形态对光开关性能的影响。最后对未来光存储材料的研究趋势作了展望。
关键词： 二芳基乙烯, 有机光致变色, 光存储, 分子开关
Based on summarizing diversified performance of the diarylethene compounds, this review has a closer look of properties that can be photoswitched by using diarylethenes as a photoswitching of fluorescence, fluorescence resonance energy transfer, photoswitching of electrical conductivity, magnetism, liquid crystal and muti-addressable photochromic switches. The effect of the modality of the diarylethene compounds on the property of photoswitching is also introduced. Some future research topics of optical storage materials are discussed.
Key words: diarylethenes, organic photochromism, optical storage, molecular switches

中图分类号: 

()

[ 1 ] Eigler D M, Lutz C P , Rudge W E. Nature , 1991 , 352 : 600 —603
[ 2 ] Tian H , Yang S J . Chem. Sov. Rev. , 2004 , 33 : 85 —97
[ 3 ] Irie M, Fukaminato T , Sasaki T , et al . Nature , 2002 , 420 :759 —760
[ 4 ] 樊美公(Fan M G) . 化学进展(Progress in Chemistry) , 1997 ,9 : 170 —178
[ 5 ] Yokoyama Y. Chem. Rev. , 2000 , 100 : 1717 —1739
[ 6 ] Berkovie G, Krongauz V , Weiss V. Chem. Rev. , 2000 , 100 :1741 —1753
[ 7 ] John C C , Robert J G. Organic Photochromic and Termochromic Compound. NY: Plenum Press , 1999. 11 —83
[ 8 ] Huang K, Qiu H J , Wan M X. Macromolecules , 2002 , 35 :8653 —8655
[ 9 ] Irie M. Chem. Rev. , 2000 , 100 : 1685 —1716
[10] Matsuda K, Irie M. J . Photochem. Photobiol . C: Photochem.Rev. , 2004 , 5 : 169 —182
[11] Wigglesworth T J , Myles A J , Branda N R. Eur. J . Org.Chem. , 2005 , 7 , 1233 —1238
[12] Irie M, Uchida K. Bull . Chem. Soc. Jpn. , 1998 , 71 : 985 —996.
[13] Irie M, Yamaguchi T , Nakazumi H , et al . Bull . Chem. Soc.Jpn. , 1999 , 72 : 1139 —1142.
[14] Nokamura S , Irie M. J . Org. Chem. , 1988 , 53 : 6136 —6138
[15] Gilat S L , Kawai S H , Lehn J M. Chem. Eur. J . , 1995 , 1 :275 —284
[16] Kobatake S , Uchida K, Tsuchida E , et al . Chem. Lett . , 2000 ,11 : 1340 —1341
[17] 钟少峰(Zhong S F) , 余海洋(Yu H Y) . 感光科学与光化学(Photographic Science and Photochemistry) , 2003 , 21 : 200 —211
[18] Irie M, Sakemura K, Okinaka M, et al . J . Org. Chem. , 1995 ,60 : 8305 —8309
[19] Uchida K, Tsuchida E , Aoi Y, et al . Chem. Lett . , 1999 , 1 :63 —64
[20] Stellacci F , Bertarelli C , Toscano F , et al . Adv. Mater. , 1999 ,11 : 292 —295
[21] Takeshita M, Kato N , Kawauchi S , et al . J . Org. Chem. , 1998 ,63 : 9306 —9313
[22] Hossain M K, Takeshita M, Yamato T. Tetrahedron Lett . , 2005 ,46 : 431 —433
[23] Miyasaka H , Nobuto T , Iiayal A , et al . Chem. Phys. Lett . ,1997 , 269 : 281 —285
[24] Ern J , Bens A T , Bock A , et al . J . Lumin. , 1998 , 76/77 :90 —94
[25] Irie M, Eriguchi T , Takada T , et al . Tetrahedron , 1997 , 53 :12263 —12271
[26] Irie M, Miyatake O , Uchida K, et al . J . Am. Chem. Soc. ,1994 , 116 : 9894 —9900
[27] Kawai S H , Gilat S L , Ponsinet R , et al . Chem. Eur. J . , 1995 ,1 : 285 —293
[28] Yamaguchi T , Uchida K, Irie M. J . Am. Chem. Soc. , 1997 ,119 : 6066 —6071
[29] Stllacci F , Bertarelli C , Toscano F , et al . Chem. Phys. Lett . ,1999 , 320 : 563 —570
[30] Miyasaka H , Murakami M, Itaya A , et al . J . Am. Chem. Soc. ,2001 , 123 : 753 —754
[31] Murakami M, Miyasaka H , Okada T , et al . J . Am. Chem.Soc. , 2004 , 126 : 14764 —14772
[32] Irie M, Ishida H , Tsujioka T. Jpn. J . Appl . Phys. , 1999 , 38 :6114 —6117
[33] Tsujioka T , Irie M. Jpn. J . Appl . Phys. Part 1 , 1999 , 38 :4100 —4104
[34] Takeshita M, Irie M. Chem. Lett . , 1998 , 11 : 1123 —1124
[35] Tsivgoulis G M, Lehn J M. Chem. Eur. J . , 1996 , 2 : 1399 —1406
[36] Yagi K, Soong C F , Irie M. J . Org. Chem. , 2001 , 66 : 5419 —5423
[37] Osuka A , Fujikane D , Shinmori H , et al . J . Org. Chem. ,2001 , 66 : 3913 —3923
[38] Kawai T , Sasaki T , Irie M. Chem. Commun. , 2001 , 8 : 711 —712
[39] Tian H , Chen B Z , Tu H Y, et al . Adv. Mater. , 2002 , 14 :918 —923
[40] Ern J , Bens A T , Martin H D , et al . J . Phys. Chem. A , 2001 ,105 : 1741 —1749
[41] Kim M S , Kawai T , Irie M. Chem. Lett . , 2001 , 7 : 702 —703
[42] Jukes R T F , Adamo V , Hartl F , et al . Inorg. Chem. , 2004 ,43 : 2779 —2792
[43] Giordano L , Jovin T M, Irie M, et al . J . Am. Chem. Soc. ,2002 , 124 : 7481 —7489
[44] Liddell P A , Koodis G, Moore A L , et al . J . Am. Chem. Soc. ,2002 , 124 : 7668 —7669
[45] Medvedeva D , Bobrovsky A , Boiko N , et al . Macromol . Rapid Commun. , 2005 , 26 : 177 —182
[46] Gilat S L , Kawai S H , Lehn J M. Chem. Eur. J . , 1995 , 1 :275 —284
[47] Kawai T , Kunitake T , Irie M. Chem. Lett . , 1999 , 9 : 905 —906
[48] Matsuda K, Irie M. J . Am. Chem. Soc. , 2000 , 122 : 7195 —7201
[49] Matsuda K, Matsuo M, Irie M. Chem. Lett . , 2001 , 5 : 436 —437
[50] Matsuda K, Matsuo M, Irie M. J . Org. Chem. , 2001 , 66 :8799 —8803
[51] Matsuda K, Irie M. J . Am. Chem. Soc. , 2001 , 123 : 9896 —9897
[52] Frigoli M, Mehl G H. ChemPhysChem, 2003 , 4 : 101 —103
[53] Chen S H , Chen H M P , Geng Y. et al . Adv. Mater. , 2003 ,15 : 1061 —1065
[54] Myles A J , Wigglesworth T J , Branda N R. Adv. Mater. , 2003 ,15 : 745 —748
[55] Higashiguchi K, Matsuda K, Irie M. Angew. Chem. Int . Ed. ,2003 , 42 : 3537 —3540
[56] Wang S , Li X C , Chen B Z , et al . Macromol . Chem. Phy. ,2004 , 205 : 1497 —1507
[57] Tian H , Chen B Z , Liu P H. Chem. Lett . , 2001 , 10 : 990 —991
[58] Irie M, Kobatake S , Horichi M. Science , 2001 , 291 : 1769 —1772
[59] Tian H , Tu H Y. Adv. Mater. , 2000 , 12 : 1597 —1600
[60] Cho H , Kim E. Macromolecules , 2002 , 35 : 8684 —8687
[61] Myles A J , Branda N R. Macromolecules , 2003 , 36 : 298 —303
[62] Wigglesworth T J , Branda N R. Adv. Mater. , 2004 , 16 : 123 —125
[1] 刘晓珺, 秦朗, 俞燕蕾. 胆甾相液晶螺旋方向的光调控[J]. 化学进展, 2023, 35(2): 247-262.
[2] 霍志铭, 李攻科*, 肖小华*. 有机光致变色材料在快速可视化检测中的应用[J]. 化学进展, 2017, 29(2/3): 252-261.
[3] 朱世琴, 李文龙, 朱为宏. 新型烯桥二芳基乙烯光致变色体系[J]. 化学进展, 2016, 28(7): 975-992.
[4] 邹祺, 张隽佶, 田禾*. 多功能二噻吩乙烯光致变色光分子开关材料[J]. 化学进展, 2012, (9): 1632-1645.
[5] 王延梅 王丽. 杯芳烃稀土配合物的光性能及应用*[J]. 化学进展, 2010, 22(0203): 427-432.
[6] 傅晓飞,孙伟,房晨婕,郭瑞,严纯华. 分子基逻辑材料*[J]. 化学进展, 2009, 21(05): 957-963.
[7] 文国涛,丁晓媛,刘磊,郭庆祥. 1,2-二芳基乙烯分子无损读取研究*[J]. 化学进展, 2005, 17(05): 826-838.
[8] 陈志敏,左霞,吴谊群. 高密度可录光盘存储材料:金属卟啉配合物*[J]. 化学进展, 2004, 16(05): 820-.
[9] 马文波,吴谊群,顾冬红,干福熹. 双光子吸收有机材料及其在三维数字光存储中的应用[J]. 化学进展, 2004, 16(04): 631-.
[10] 宋江莉,王秀芬. LCST类水凝胶开关效应的研究进展[J]. 化学进展, 2004, 16(01): 56-.
[11] 王煜,晋卫军. 用于识别金属离子的超分子荧光/磷光传感器*[J]. 化学进展, 2003, 15(03): 178-.
[12] 尹屹梅,林祥钦. 分子计算机的研究进展*[J]. 化学进展, 2001, 13(05): 337-.