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Progress in Chemistry 2015, Vol. 27 Issue (6): 704-743 DOI: 10.7536/PC150172 Previous Articles   Next Articles

• Supramolecular Chemistry Issue •

Current Researches and Applications of Perylene Compounds

Wang Hui1, Ponmani Jeyakkumar1, Sangaraiah Nagarajan1, Meng Jiangping*2, Zhou Chenghe*1   

  1. 1. Key Laboratory of Applied Chemistry of Chongqing Municipality, Institute of Bioorganic & Medicinal Chemistry, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China;
    2. Chongqing Key Laboratory of Environmental Materials & Remediation Technologies, College of Materials and Chemical Engineering, Chongqing University of Arts and Sciences, Chongqing 402160, China
  • Received: Revised: Online: Published:
  • Contact: 10.7536/PC150172 E-mail:mengjp2006@163.com;zhouch@swu.edu.cn
  • Supported by:
    The work was supported by the National Natural Science Foundation of China(No. 21172181, 21372186)(International(Regional)Cooperation and Exchange Program)(No. 81450110095), the Natural Science Foundation of Chongqing(No. CSTC2012jjB10026, CSTC2012jjA10153), and the Specialized Research Fund for the Doctoral Program of Higher Education of China(SRFDP 20110182110007).
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Perylene compounds possess a large π-conjugated system and are easy to be chemically modified by various functional groups. These unique structural characteristics endow with favourable physical and chemical properties as well as special functions, and enable perylene compounds to have a wide range of potential applications in the fields of material science, supramolecular chemistry, biology, pharmacy, medicine and so on. In particular, perylene-based organic photoelectric materials have been widely investigated and many important achievements have been made. More recently, more and more effort has been dedicated to other possible applications of perylene compounds, and the relative research has been expanded to many fields, especially the biomedical research has become an increasingly active emerging field, and attracted wide attention in recent years. Combining with our researches and referring other works from literatures in five years, this paper for the first time systematically reviewed the recent advance in the current research and development of perylene compounds in the fields of material, biological and medical sciences including organic optoelectronic materials, nanomaterials, biomedicinal photosensitizers, fluorescent labeling and imaging agents, drug carriers, artificial diagnostic agents, artificial ion receptors and molecular probes. This review mainly focused on strengthening the effects of structures on properties and applications. At last the perspectives of the foreseeable future are also presented.

Contents
1 Introduction
2 Perylene compounds as organic optoelectronic materials
2.1 Perylene compounds as organic solar cells materials
2.2 Perylene compounds as optoelectronic information materials
3 Perylene compounds as organic nanomaterials
4 Perylene comounds as biomedicine photosensitizers
5 Perylene comounds as fluorescent labling and imaging agents
6 Perylene comounds as drug carriers
7 Perylene comounds as artificial diagnostic agents
8 Perylene comounds as artificial ion receptors
8.1 Perylene comounds as artificial cationic receptors
8.2 Perylene comounds as artificial anion receptors
9 Perylene comounds as molecular probes
10 Conclusion and outlook

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[1] D'Souza F, Kadish K M. Handbook of Carbon Nano Materials. Singapore:World Scientific, 2011. 30.
[2] Geng Y, Li H B, Wu S X, Su Z M. J. Mater. Chem., 2012, 22: 20840.
[3] Zhang X, Zhan C L, Zhang X L, Yao J N. Tetrahedron, 2013, 69: 8155.
[4] Fuini J F, Surampudi A B, Penick M A, Mahindaratne M P D, Negrete G R, Brancaleon L. Dyes Pigments, 2011, 88: 204.
[5] Robb M J, Newton B, Fors B P, Hawker C J. J. Org. Chem., 2014, 79: 6360.
[6] Jimenez E Á, Lin M J, Burschka C, Becker J, Settels V, Engels B, Würthner F. Chem. Sci., 2014, 5: 608.
[7] Avlasevich Y, Li C, Müllen K. J. Mater. Chem., 2010, 20: 3814.
[8] Armstrong N R, Wang W N, Alloway D M, Placencia D, Ratcliff E, Brumbach M. Macromol. Rapid Commun., 2009, 30: 717.
[9] Segura J L, Herrera H, Bäuerle P. J. Mater. Chem., 2012, 22: 8717.
[10] Zhang W Q, Zhou X H, Xie Z Q, Yang B, Liu L L, Ma Y G. Chem. Commun., 2013, 49: 11560.
[11] Biedermann F, Elmalem E, Ghosh I, Nau W M, Scherman O A. Angew. Chem. Int. Ed., 2012, 51: 7739.
[12] Li Y J, Liu T F, Liu H B, Tian M Z, Li Y L. Acc. Chem. Res., 2014, 47: 1186.
[13] Suzuki S, Kozaki M, Nozakib K, Okada K. J. Photoch. Photobio. C, 2011, 12: 269.
[14] Tahir M, Sayyad M H, Wahab F, Aziz F, Shahid M, Munawar M A. Physica. B, 2013, 426: 6.
[15] Zhan X W, Facchetti A, Barlow S, Marks T J, Ratner M A, Wasielewski M R, Marder S R. Adv. Mater., 2011, 23: 268.
[16] Huang C, Barlow S, Marder S R. J. Org. Chem., 2011, 76: 2386.
[17] Hasegawa M, Iyoda M. Chem. Soc. Rev., 2010, 39: 2420.
[18] Baumgärtel T, Rehm S, Würthnerb F, von Borczyskowski C, Graaf H. Appl. Surf. Sci., 2014, 318: 51.
[19] 王丽华(Wang L H), 江山(Jiang S), 张志君(Zhang Z J), 张衡益(Zhang H Y), 刘育(Liu Y). 高等学校化学学报(Chemical Journal of Chinese Universities), 2013, 34(9): 2108.
[20] Cui X N, Charaf-Eddin A, Wang J S, Le-Guennic B, Zhao J Z, Jacquemin D. J. Org. Chem., 2014, 79: 2038.
[21] Zhang J F, An F F, Li Y A, Zheng C J, Yang Y L, Zhang X J, Zhang X H. Chem. Commun., 2013, 49: 8072.
[22] Davies M, Jung C, Wallis P, Schnitzler T, Li C, Müllen K, Bräuchle C. ChemPhysChem, 2011, 12: 1588.
[23] Wilson J N, Kool E T. Org. Biomol. Chem., 2006, 4: 4265.
[24] Zhou C B, Li W Y, Chen J, Yang M D, Li Y, Zhu J T, Yu C. Analyst, 2014, 139: 1057.
[25] Yang Y T, Yin C X, Huo F J, Chao J B, Zhang Y B. Sensor Actuat. B Chem., 2014, 204: 402.
[26] Kozma E, Catellani M. Dyes Pigments, 2013, 98: 160.
[27] Würthner F. Chem. Commun., 2004, 14: 1564.
[28] Soh N, Ueda T. Talanta, 2011, 85: 1233.
[29] Görl D, Zhang X, Würthner F. Angew. Chem. Int. Ed., 2012, 51: 6328.
[30] Li C, Henrike W. Adv. Mater., 2012, 24: 613.
[31] Chen L, Li C, Müllen K. J. Mater. Chem. C, 2014, 2: 1938.
[32] Jiang B P, Guo D S, Liu Y. Prog. Chem., 2013, 25: 869.
[33] Li S W, Yang H L, Dong Z P, Guo S J, Zhao J H, Gou G L, Ren R, Huang J W, Jin J, Ma J T. Catal. Sci. Technol., 2013, 3: 2303.
[34] 张天慧(Zhang T H), 朴玲钰(Piao L Y), 赵谡玲(Zhao S L), 徐征(Xu Z), 杨磊(Yang L), 刘祥志(Liu X Z), 鞠思婷(Ju S T). 有机化学(Chinese Journal of Organic Chemistry), 2011, 31(2): 260.
[35] Quintana J A, Villalvilla J M, de la Pena A, Segura J L, Diaz-Garcia M A. J. Phys. Chem. C, 2014, 118: 26577.
[36] Lin Y Z, Wang Y F, Wang J Y, Hou J H, Li Y F, Zhu D B, Zhan X W. Adv. Mater., 2014, 26: 5137.
[37] Lu Z H, Zhang X, Zhan C L, Jiang B, Zhang X L, Chen L L, Yao J N. Phys. Chem. Chem. Phys., 2013, 15: 11375.
[38] 刘艳姣(Liu Y J), 刘菁(Liu Q), 张林骅(Zhang L H), 方俊锋(Fang J F), 张文俊(Zhang W J), 刘治田(Liu Z T). 有机化学(Chinese Journal of Organic Chemistry), 2014, 34(5): 1021.
[39] Perrin L, Hudhomme P. Eur. J. Org. Chem., 2011, 2011: 5427.
[40] Chou W Y, Chang J, Yen C T, Lin Y S, Tang F C, Liu S J, Cheng H L, Hsu S L C, Chen J S. Phys. Chem. Chem. Phys., 2012, 14: 5284.
[41] Jeong S, Han Y S, Kwon Y, Choi M S, Cho G, Kim K S, Kim Y. Synthetic. Met., 2010, 160: 2109.
[42] Zhang Y D, Wang H L, Xiao Y, Wang L G, Shi D Q, Cheng C H. ACS Appl. Mater. Inter., 2013, 5: 11093.
[43] Zang L, Che Y K, Moore J S. Acc. Chem. Res., 2008, 41: 1596.
[44] Yagai S, Seki T, Murayama H, Wakikawa Y, Ikoma T, Kikkawa Y, Karatsu T, Kitamura A, Honsho Y, Seki S. Small, 2010, 6: 2731.
[45] Tang Y D, Zhang J Q, Zhang S L, Geng R X, Zhou C H. Chin. J. Chem., 2012, 30: 1831.
[46] Zhang S L, Damu G L V, Zhang L, Geng R X, Zhou C H. Eur. J. Med. Chem., 2012, 55: 164.
[47] 耿蓉霞(Geng R X), 周成合(Zhou C H). 有机化学(Chinese Journal of Organic Chemistry), 2008, 28(1): 163.
[48] Zhang S L, Zhang L, Wen Q M, Geng R X, Zhou C H. Acta Crystallogr. Sect. E, 2012, 68: o1752.
[49] Hildebrandt A, Lang H. Organometallics, 2013, 32: 5640.
[50] Liu X, Cai P, Chen D C, Chen J W, Su S J, Cao Y. Sci. China Chem., 2014, 57: 973.
[51] Singh R, Giussani E, Mróz M M, Fonzo F D, Fazzi D, Cabanillas-González J, Oldridge L, Vaenas N, Kontos A G, Falaras P, Grimsdale A C, Jacob J, Müllen K, Keivanidis P E. Org. Electron., 2014, 15: 1347.
[52] Banerjee S, Veale E B, Phelan C M, Murphy S A, Tocci G M, Gillespie L J, Frimannsson D O, Kelly J M, Gunnlaugsson T. Chem. Soc. Rev., 2013, 42: 1601.
[53] Lv J S, Peng X M, Babu B K, Zhou C H. Bioorg. Med. Chem. Lett., 2014, 24: 308.
[54] Damu G L V, Wang Q P, Zhang H Z, Zhang Y Y, Lv J S, Zhou C H. Sci. China Chem., 2013, 56: 952.
[55] Zhang Y Y, Zhou C H. Bioorg. Med. Chem. Lett., 2011, 21: 4349.
[56] Cheriya R T, Mallia A R, Hariharan M. Energy Environ. Sci., 2014, 7: 1661.
[57] Kozma E, Kotowski D, Luzzati S, Catellani M, Bertini F, Famulari A, Raos G. RSC Adv., 2013, 3: 9185.
[58] Kozma E, Kotowski D, Catellani M, Luzzati S, Famulari A, Bertini F. Dyes Pigments, 2013, 99: 329.
[59] 孟江平(Meng J P), 卢一卉(Lu Y H), 海力且木 ·依不那音(Halqam I), 周成合(Zhou C H). 中国生化药物杂志(Chinese Journal of Biochemical Pharmaceutics), 2008, 29(6): 418.
[60] 李硕(Li S), 向清祥(Xiang Q X), 陈稼轩(Chen J X), 周成合(Zhou C H). 化学研究与应用(Chemical Research and Application), 2009, 21(10): 1375.
[61] Peng X M, Cai G X, Zhou C H. Curr. Top. Med. Chem., 2013, 13: 1963.
[62] Zhou C H, Zhang H Z. ZL 2012101519967,2014.
[63] Zhou C H, Yu K G, Meng J P, Fang B, Luo Y, Zhang F F, Li T Q, Li J. ZL 2007100927898,2012.
[64] Zhou C H, Fang B, Gan L L. ZL 200810070036.1,2011.
[65] Zhou C H, Chang J J, Zhang Y Y. ZL 201110355875.X,2013.
[66] 周成合(Zhou C H), 蔡桂鑫(Cai G X), 耿蓉霞(Geng R X), 吕劲松(Lv J S). 基础药物化学(General Medincal Chemistry). 北京: 科学出版社(Beijing: Science Press), 2014. 122.
[67] 孟江平(Meng J P), 徐强(Xu Q), 宋仲容(Song Z R), 凌立新(Ling L X), 周成合(Zhou C H). 中国抗生素杂志(Chinese Journal of Antibiotics), 2012, 36(2): 81.
[68] Damu G L V, Cui S F, Peng X M, Wen Q M, Cai G X, Zhou C H. Bioorg. Med. Chem. Lett., 2014, 24: 3605.
[69] Zhang H Z, Cui S F, Nagarajan S, Rasheed S, Cai G X, Zhou C H. Tetrahedron Lett., 2014, 55: 4105.
[70] Zhang H Z, Lin J M, Rasheed S, Zhou C H. Sci. China Chem., 2014, 57: 807.
[71] Song S, Han H, Kim Y, Lee B H, Park S H, Jin Y, Kim I, Lee K, Suh H. Sol. Energ. Mat. Sol. C, 2011, 95: 1838.
[72] Budagumpi S, Haque R A, Salman A W. Coordin. Chem. Rev., 2012, 256: 1787.
[73] Dinçalp H, Çimen O, Ameri T, Brabec C J, I çli S. Spectrochim. Acta Part A, 2014, 128: 197.
[74] Rajaram S, Shivanna R, Kandappa S K, Narayan K S. J. Phys. Chem. Lett., 2012, 3: 2405.
[75] Shivanna R, Shoaee S, Dimitrov S, Kandappa S K, Rajaram S, Durrant J R, Narayan K S. Energy Environ. Sci., 2014, 7: 435.
[76] Jiang W, Ye L, Li X G, Xiao C Y, Tan F, Zhao W C, Hou J H, Wang Z H. Chem. Commun., 2014, 50: 1024.
[77] 胡小链(Hu X L), 施敏敏(Shi M M), 左立见(Zuo L J), 傅磊(Fu L), 戴树洌(Dai S L), 陈红征(Chen H Z). 化学学报(Acta Chimica Sinica), 2011, 69(6): 673.
[78] Zhong Y, Trinh M T, Chen R S, Wang W, Khlyabich P P, Kumar B, Xu Q Z, Nam C Y, Sfeir M Y, Black C, Steigerwald M L, Loo Y L, Xiao S X, Ng F, Zhu X Y, Nuckolls C. J. Am. Chem. Soc., 2014, 136: 15215.
[79] Zhang X, Lu Z, Ye L, Zhan C, Hou J, Zhang S, Jiang B, Zhao Y, Huang J, Liu Y, Shi Q, Yao J. Adv. Mater., 2013, 25: 5791.
[80] Huang J H, Wang X, Zhang X, Niu Z X, Lu Z H, Jiang B, Sun Y X, Zhan C L, Yao J N. ACS Appl. Mater. Inter., 2014, 6: 3853.
[81] Jiang B, Zhang X, Zhan C L, Lu Z H, Huang J H, Ding X L, He S G, Yao J N. Polym. Chem., 2013, 4: 4631.
[82] 徐业伟(Xu Y W), 朱方华(Zhu F H), 张林(Zhang L). 材料导报(Materials Review), 2010, 24(21): 79.
[83] Jaggi M, Blum C, Marti B S, Liu S X, Leutwyler S, Decurtins S. Org. Lett., 2010, 12: 1344.
[84] Matsushima T, Matsuo H, Yamamoto T, Nakao A, Murata H. Sol. Energ. Mat. Sol. C., 2014, 123: 81.
[85] Sim B R, Kim B G, Lee J K, Do J Y. Thin Solid Films, 2011, 519: 8091.
[86] Ito S, Hiroto S, Shinokubo H. Org. Lett., 2013, 15: 3110.
[87] 刘震(Liu Z), 徐丰(Xu F), 严大东(Yan D D). 化学学报(Acta Chimica Sinica), 2014, 72(2): 171.
[88] Kim Y, Lim E. Polymers, 2014, 6: 382.
[89] Liaw D J, Wang K L, Huang Y C, Lee K R, Lai J Y, Ha C S. Prog. Polym. Sci., 2012, 37: 907.
[90] Liu W, Tkachov R, Komber H, Senkovskyy V, Schubert M, Wei Z, Facchetti A, Neher D, Kiriy A. Polym. Chem., 2014, 5: 3404.
[91] 叶怀英(Ye H Y), 李文(Li W), 李维实(Li W S). 有机化学(Chinese Journal of Organic Chemistry), 2012, 32(2): 266.
[92] 张飞飞(Zhang F F), 周成合(Zhou C H), 颜建平(Yan J P). 有机化学(Chinese Journal of Organic Chemistry), 2010, 30(6): 783.
[93] Sherer C, Snape T J. Eur. J. Med. Chem., 2014, doi.org/10.1016/j.ejmech.2014.11.007
[94] Zhou C H, Zhang F F. ZL 200910104628.5,2014.
[95] 颜建平(Yan J P), 周成合(Zhou C H), 吉庆刚(Ji Q G), 耿蓉霞(Geng R X). 国际药学研究杂志(International Journal of Pharmaceutical Research), 2011, 38(2): 118.
[96] Zhang F F, Gan L L, Zhou C H. Bioorg. Med. Chem. Lett., 2010, 20: 1881.
[97] Li J L, Grimsdale A C. Chem. Soc. Rev., 2010, 39: 2399.
[98] Jiang H J, Sun J, Zhang J L. Curr. Org. Chem., 2012, 16: 2014.
[99] Lellouche J P, Koner R R, Ghosh S. Rev. Chem. Eng., 2013, 29: 413.
[100] Jung I H, Lo W Y, Jang J, Chen W, Zhao D L, Landry E S, Lu L Y, Talapin D V, Yu L P. Chem. Mater., 2014, 26: 3450.
[101] Yuan M C, Su M H, Chiu M Y, Wei K H. J. Polym. Sci. Pol. Chem., 2010, 48: 1298.
[102] Fu W X, He C, Jiang S D, Chen Z Z, Zhang J T, Li Z B, Yan S K, Zhang R B. Macromolecules, 2011, 44: 203.
[103] Kim J H, Song C E, Kang I N, Shind W S, Hwang D H. Chem. Commun., 2013, 49: 3248.
[104] Jin S H, Ban T, Park J, Gal Y S, Lee A J W. Mol. Cryst. Liq. Cryst., 2013, 578: 95.
[105] Kozma E, Kotowski D, Bertini F, Luzzati S, Catellani M. Polymer, 2010, 51: 2264.
[106] Zhou Y, Yan Q F, Zheng Y Q, Wang J Y, Zhao D H, Pei J. J. Mater. Chem. A, 2013, 1: 6609.
[107] Liu Y, Larsen-Olsen T T, Zhao X G, Andreasen B, Søndergaard R R, Helgesenb M, Norrman K, Jørgense M, Krebs F C, Zhan X W. Sol. Energ. Mat. Sol. C., 2013, 112: 157.
[108] Raj M R, Anandan S, Solomon R V, Venuvanalingam P, Iyer S S K, Ashokkumar M. J. Photoch. Photobio. A, 2012, 247: 52.
[109] Raj M R, Ramkumar S, Anandan S. RSC Adv., 2013, 3: 5108.
[110] 和平(He P), 李在房(Li Z F), 侯秋飞(Hou Q F), 王艳玲(Wang Y L). 有机化学(Chinese Journal of Organic Chemistry), 2013, 33(2): 288.
[111] Kim J H, Kim H U, Mi D, Jin S H, Shin W S, Yoon S C, Kang I N, Hwang D H. Macromolecules, 2012, 45: 2367.
[112] Bu L, Guo X Y, Yu B, Fu Y Y, Qu Y, Xie Z Y, Yan D H, Geng Y H, Wang F S. Polymer, 2011, 52: 4253.
[113] 徐长志(Xu C Z), 肖斌(Xiao B), 柳清菊(Liu Q J). 材料导报(Materials Review), 2014, 28(7): 149.
[114] Vercelli B, Zotti G. ACS Appl. Mater. Inter., 2012, 4: 3233.
[115] Flamigni L, Zanelli A, Langhals H, Böck B. Photochem. Photobiol. Sci., 2013, 12: 2137.
[116] Imahori H, Umeyama T, Ito S. Acc Chem. Res., 2009, 42: 1809.
[117] Kodama K, Kobayashi A, Hirose T. Tetrahedron Lett., 2013, 54: 5514.
[118] Dinçalp H, ?evki K, ?çli S. Dyes Pigments, 2010, 86: 32.
[119] Bullock J E, Vagnini M T, Ramanan C, Co D T, Wilson T M, Dicke J W, Marks T J, Wasielewski M R. J. Phys. Chem. B, 2010, 114: 1794.
[120] Warnan J, Gardner J, Pleux L L, Petersson J, Pellegrin Y, Blart E, Hammarstrom L, Odobel F. J. Phys. Chem. C., 2014, 118: 103.
[121] Sao C N, Onken K, Saragi T P I, Fuhrmann-Lieker T, Salbeck J. Synthetic. Met., 2012, 162: 888.
[122] Dinçalp H, A?kar Z, Zafer C, ? çli S. Dyes Pigments, 2011, 91: 182.
[123] Keerthi A, Liu Y, Wang Q, Valiyaveettil S. Chem. Eur. J., 2012, 18: 11669.
[124] Niu H J, Luo J, Wen J, Wu W J, Mu J S, Wang C, Bai X D, Wang, W. J. App. Polym. Sci., 2012, 125: 200.
[125] Wonneberger H, Pschirer N, Bruder I, Sch-eboom J, Ma C Q, Erk P, Li C, Bäuerle P, Müllen K.. Chem. Asian J., 2011, 6: 1744.
[126] Neubauer A, Szarko J M, Bartelt A F, Eichberger R, Hannappel T. J. Phys. Chem. C, 2011, 115: 5683.
[127] Gibson E A, Pleux L L, Fortage J, Pellegrin Y, Blart E, Odobel F, Hagfeldt A, Gerrit Boschloo G. Langmuir, 2012, 28: 6485.
[128] Albert-Seifried S, Finlayson C E, Laquai F, Friend R H, Swager T M, Kouwer P H J, Jurí D?ek M, Kitto H J, Valster S, Nolte R J M, Rowan A E. Chem. Eur. J., 2010, 16: 10021.
[129] Besur S, Hou W H, Schmeltzer P, Bonkovsky H L. Metabolites, 2014, 4: 977.
[130] Ogawa K, Kobuke Y. Nonlinear Optics. New York: Wiley, 2012, 340.
[131] Shu M, Kuo S, Wang Y, Jiang Y, Liu Y T, Gallo R L, Huang C M. P Curr. Med. Chem., 2013, 20: 562.
[132] 于克贵(Yu K G), 周成合(Zhou C H), 李东红(Li D H). 中国药学杂志(Chinese Pharmaceutical Journal), 2008, 43(7): 481.
[133] Li D H, Diao J L, Gui K Y, Zhou C H. Chin. Chem. Lett., 2007, 18: 1331.
[134] 于克贵(Yu K G), 周成合(Zhou C H), 李东红(Li D H). 化学研究与应用(Chemical Research and Application), 2007, 19(12): 1296.
[135] Ishihara S, Labuta J, Rossom W V, Ishikawa D, Minami K, Hill J P, Ariga K. Phys. Chem. Chem. Phys., 2014, 16: 9713.
[136] Angaridis P A, Lazarides T, Coutsolelos A C. Polyhedron, 2014, 82: 19.
[137] Jiao C J, Zu N N, Huang K W, Wang P, Wu J S. Org. Lett., 2011, 13: 3652.
[138] Jiao C J, Huang K W, Chi C Y, Wu J H. J. Org. Chem., 2011, 76: 661.
[139] Panda D K, Goodson F S, Ray S, Lowell R, Saha S. Chem. Commun., 2012, 48: 8775.
[140] Lee C W, Lu H P, Reddy N M, Lee H W, Diau E W G, Yeh C Y. Dyes Pigments, 2011, 91: 317.
[141] Luo J, Xu M F, Li R Z, Huang K W, Jiang C Y, Qi Q B, Zeng W D, Zhang J, Chi C Y, Wang P, Wu J S. J. Am. Chem. Soc., 2014, 136: 265.
[142] Benjamin W E, Veit D R, Perkins M J, Bain E, Scharnhorst K, McDowall S, Patrick D L, Gilbertson J D. Chem. Mater., 2014, 26: 1291.
[143] Schiphorst J T, Kendhale A M, Debije M G, Menelaou C, Herz L M, Schenning A P H J. Chem. Mater., 2014, 26: 3876.
[144] Debije M G, Menelaou C, Herz L M, Schenning A P H J. Adv. Opt. Mater., 2014, 2: 687.
[145] Stopel M H W, Blum C, Subramaniam V. J. Phys. Chem. Lett., 2014, 5: 3259.
[146] Sanguineti A, Sassi M, Turrisi R, Ruffo R, Vaccaro G, Meinardi F, Beverina L. Chem. Commun., 2013, 49: 1618.
[147] Haines C, Chen M, Ghiggino K P. Sol. Energ. Mat. Sol. C., 2012, 105: 287.
[148] Sukul P K, Datta A, Malik S. Chem. Eur. J., 2014, 20: 3019.
[149] Funahashi M, Sonoda A. Dalton Trans., 2013, 42: 15987.
[150] Keivanidis P E, Laquai F, Howard I A, Friend R H. Adv. Funct. Mater., 2011, 21: 1355.
[151] Bednorza M, Matt G J, G?owacki E D, Fromherz T F, Brabec C J, Scharber M C, Sitter H, Sariciftci N S. Org. Electron., 2013, 14: 1344.
[152] Susarova D K, Troshin P A, Hglinger D, Koeppe R, Babenko S D, Lyubovskaya R N, Razumov V F, Sariciftci N S. Sol. Energ Mat. Sol. C., 2010, 94: 803.
[153] Lin H T, Wu Y S, Cao X Q, Fu H B. J. Phys. Chem. C, 2012, 116: 21657.
[154] Yu A D, Kurosawa T, Ueda M, Chen W C. J. Polym. Sci. Pol. Chem., 2014, 52: 139.
[155] Chou Y H, You N H, Kurosawa T, Lee W Y, Higashihara T, Ueda M, Chen W C. Macromolecules, 2012, 45: 6946.
[156] Chiu Y C, Liu C L, Lee W Y, Chen Y G, Kakuchi T, Che W C. NPG Asia Mater., 2013, 5: e35.
[157] Chiu Y C, Chen T Y, Chen Y G, Satoh T, Kakuchi T, Chen W C. ACS Appl. Mater. Inter., 2014, 6 (15): 12780.
[158] Guo Y L, Zhang J, Yu G, Zheng J, Zhang L, Zhao Y, Wen Y G, Liu Y Q. Org. Electron., 2012, 13: 1969.
[159] Sanchez R S, Gras-Charles R, Bourdelande J L, Guirado G, Hernando J. J. Phys. Chem. C, 2012, 116: 7164.
[160] Berberich M, Natali M, Spenst P, Chiorboli C, Scandola F, Würthner F. Chem. Eur. J., 2012, 18: 13651.
[161] Fukaminato T, Doi T, Tamaoki N, Okuno K, Ishibashi Y, Miyasaka H, Irie M. J. Am. Chem. Soc., 2011, 133: 4984.
[162] 马锋(Ma F), 王世荣(Wang S R), 郭俊杰(Guo J J), 李祥高(Li X G). 有机化学(Chinese Journal of Organic Chemistry), 2012, 32(3): 497.
[163] Kim D K, Oh J D, Shin E S, Seo H S, Choi J H. J. Appl. Phys., 2014, 115: 164503/1.
[164] Ma L C, Guo Y L, Wen Y G, Liu Y Q, Zhan X W. Appl. Phy. Lett., 2013, 103: 203303/1.
[165] Gsänger M, Oh J H, Könemann M, Höffken H W, Krause A M, Bao Z N, Würthner F. Angew. Chem. Int. Ed., 2010, 49: 740.
[166] Ting H W, Che S Y, Huang T C, Wei J H, Yew T R. ChemPhysChem, 2011, 12: 871.
[167] Liu C M, Xiao C Y, Li Y, Hu W P, Li Z B, Wang Z H. Chem. Commun., 2014, 50: 12462.
[168] Arulkashmir A, Jain B, John J C, Roy K, Krishnamoorthy K. Chem. Commun., 2014, 50: 326.
[169] Tsai H Y, Chang C W, Chen K Y. Tetrahedron Lett., 2014, 55: 884.
[170] Jeon H G, Yokota Y, Hattori J, Oguma N, Hirata N, Suzuki T, Ichikawa M. Appl. Phys. Express., 2012, 5: 041602/1.
[171] Fang B, Zhou C H, Rao X C. Eur. J. Med. Chem., 2010, 45: 4388.
[172] Lee I L, Li S R, Chen K F, Ku P J, Singh A S, Kuo H T, Wen Y S, Chu C W, Su S S. Eur. J. Org. Chem., 2012, 2012: 2906.
[173] An N S, Shi Y A, Feng J Q, Li D P, Gao J, Chen Y L, Li X Y. Org. Electron., 2013, 14: 1197.
[174] Zhang J H, Tan L, Jiang W, Hua W P, Wang Z H. J. Mater. Chem. C, 2013, 1: 3200.
[175] Oh J H, Lee W Y, Noe T, Chen W C, Könemann M, Bao Z N. J. Am. Chem. Soc., 2011, 133: 4204.
[176] Ortiz R P, Herrera H, Blanco R, Huang H, Facchetti A, Marks T J, Zheng Y, Segura J L. J. Am. Chem. Soc., 2010, 132: 8440.
[177] Zhao X G, Ma L C, Zhang L, Wen Y G, Chen J M, Shuai Z G, Liu Y Q, Zhan X W. Macromolecules, 2013, 46: 2152.
[178] Zhou W Y, Wen Y G, Ma L C, Liu Y Q, Zhan X W. Macromolecules, 2012, 45: 4115.
[179] Pron A, Reghu R R, Rybakiewicz R, Cybulski H, Djurado D, Grazulevicius J V, Zagorska M, Kulszewicz-Bajer I, Verilhac J M. J. Phys. Chem. C., 2011, 115: 15008.
[180] Jiang W, Zhou Y, Geng H, Jiang S D, Yan S K, Hu W P, Wang Z H, Shuai Z G, Pei J. J. Am. Chem. Soc., 2011, 133: 1.
[181] Cormier R A, Gregg B A. RSC Adv., 2014, 4: 2368.
[182] Maiti D K, Bhattacharjee R, Datta A, Banerjee A. J. Phys. Chem. C, 2013, 117: 23178.
[183] Llewellyn B A, Slater A G, Goretzki G, Easun T L, Sun X Z, Davies E S, Argent S P, Lewis W, Beeby A, George M W, Champness N R. Dalton T., 2014, 43: 85.
[184] Pärs M, Gräf K, Bauer P, Thelakkat M, Köhler J. Appl. Phys. Lett., 2013, 103: 221115/1.
[185] Schmidt R, Pärs M, Weller T, Thelakkat M, Köhler J. Appl. Phys. Lett., 2014, 104: 013304/1.
[186] Tan W J, Li X, Zhang J J, Tian H. Dyes Pigments, 2011, 89: 260.
[187] 崔胜峰(Cui S F), 周成合(Zhou C H), 耿蓉霞(Geng R X), 吉庆刚(Ji Q G). 中国生化药物杂志(Chinese Journal of Biochemical Pharmaceutics), 2012, 33(3): 311.
[188] 崔胜峰(Cui S F), 王艳(Wang Y), 吕敬松(Lv J S), Damu G L V, 周成合(Zhou C H). 中国科学: 化学(Scientia Sinica Chimica), 2012, 42(8): 1105.
[189] Lin Y Z, Fan H J, Li Y F, Zhan X W. Adv. Mater., 2012, 24: 3087.
[190] Zhu L J, Jiao C J, Dao H, Xia, D H, Wu J S. Tetrahedron Lett., 2011, 52: 6411.
[191] Dubey R K, Niemi M, Kaunisto K, Stranius K, Efimov A, Tkachenko N V, Lemmetyinen H. Inorg. Chem., 2013, 52: 9761.
[192] Chu X B, Guan M, Zhang Y, Li Y Y, Liu X F, Zeng Y P. RSC Adv., 2013, 3: 9509.
[193] Hu B, Zhang Y J, Lv X J, Ouyang M, Fu Z Y, Zhang C. Opt. Mater., 2012, 34: 1529.
[194] Xu L H, Su C, Zhang C, Ma C N. Synthetic Me.t, 2011, 161: 1856.
[195] Wang H, Xie H L, Liang Y, Feng L L, Cheng X Y, Lu H F, Feng S Y. J. Mater. Chem. C, 2013, 1: 5367.
[196] Choi J, Sakong C, Choi J H, Yoon C, Jae Pil Kim, J P. Dyes Pigments, 2011, 90: 82.
[197] Sakong C, Kim Y D, Choi J H, Yoon C, Kim J P. Dyes Pigments, 2011, 88: 166.
[198] Choi J, Lee W, Sakong C, Yuk S B, Park J S, Kim J P. Dyes Pigments, 2012, 94: 34.
[199] Islam M R, Sundararajan P R. Phys. Chem. Chem. Phys., 2013, 15: 21058.
[200] Mahata K, Frischmann P D, Wurthner F. J. Am. Chem. Soc., 2013, 135: 15656.
[201] Fennel F, Wolter S, Xie Z Q, Plotz P A, Kuhn O, Wurthner F, Lochbrunner S. J. Am. Chem. Soc., 2013, 135: 18722.
[202] Chen S, Jacobs D L, Xu J K, Li Y X, Wang C Y, Zang L. RSC Adv., 2014, 4: 48486.
[203] Boobalan G, Imran P K M, Nagarajan S. Spectrochim. Acta A, 2013, 113: 340.
[204] Kim B J, Yu H, Oh J H, Kang M S, Cho J H. J. Phys. Chem. C, 2013, 117: 10743.
[205] Datar A, Balakrishnan K, Zang L. Chem. Commun., 2013, 49: 6894.
[206] Wei J J, Jin L, Wan K, Zhou C H. Bull. Korean Chem. Soc., 2011, 32: 229.
[207] Bai S, Debnath S, Javid N, Frederix P W J M, Fleming S, Pappas C, Ulijn R V. Langmuir, 2014, 30: 7576.
[208] Huang Y W, Wang J H, Wei Z X. Chem. Commun., 2014, 50: 8343.
[209] Hu J C, Kuang W F, Deng K, Zou W J, Huang Y W, Wei Z X, Faul C F J. Adv. Funct. Mater., 2012, 22: 4149.
[210] Huang Y W, Wang J C, Zhai H Y, Zhu L Y, Wei Z X. Soft Matter., 2014, 10: 7920.
[211] Xue C M, Birel O, Gao M, Zhang S, Dai L M, Urbas A, Li Q. J. Phys. Chem. C, 2012, 116: 10396.
[212] Santosh G, Shirman E, Weissman H, Shimoni E, Pinkas I, Rudich Y, Rybtchinski B. J. Phys. Chem. B, 2010, 114: 14389.
[213] Zhang J, You S S, Yan S K, Müllen K, Yang W T, Yin M Z. Chem. Commun., 2014, 50: 7511.
[214] Islam M R, Sundararajan P R. Eur. Polym. J., 2013, 49: 2042.
[215] Zhou Z Y, Brusso J L, Holdcroft S. Chem. Mater., 2010, 22: 2287.
[216] Du F F, Tian J, Wang H, Liu B, Jin B K, Bai R K. Macromolecules, 2012, 45: 3086.
[217] Ie Y, Sakurai T, Jinnai S, Karakawa M, Okuda A, Mori S, Aso Y. Chem. Commun., 2013, 49: 8386.
[218] Liu H B, Zuo Z C, Guo Y B, Li Y J, Li Y L. Angew. Chem. Int. Ed., 2010, 49: 2705.
[219] Lambrecht J, Saragi T P I, Onken K, Salbeck J. ACS Appl. Mater. Inter., 2011, 3: 1809.
[220] Xie Z Q, Stepanenko V, Radacki K, Würthner F. Chem. Eur. J., 2012, 18: 7060.
[221] Sun K, Li Y, Fu W X. Chem. Commun., 2013, 49: 9212.
[222] Zhou C H, Wang Y. Curr. Med. Chem., 2012, 19: 239.
[223] 王艳(Wang Y), 周成合(Zhou C H). 中国科学: 化学(Scientia Sinica Chimica), 2011, 41(9): 1429.
[224] 万昆(Wan K), 张奕奕(Zhang Y Y), 周成合(Zhou C H), 周向东(Zhou X D), 耿蓉霞(Geng R X), 吉庆刚(Ji Q G). 中国抗生素杂志(Chinese Journal of Antibiotics), 2012, 36(1): 8.
[225] 魏金建(Wei J J), 王艳(Wang Y), 王宪龙(Wang X L), 周成合(Zhou C H), 吉庆刚(Ji Q G). 中国药学杂志(Chinese Pharmaceutical Journal), 2011, 46(7): 481.
[226] 白雪(Bai X), 周成合(Zhou C H), 米佳丽(Mi J L). 化学研究与应用(Chemical Research and Application), 2007, 19(7): 721.
[227] 朱永和(Zhu Y H), 王振荣(Wang Z R), 李布青(Li B Q). 农药大典(Encyclopedia Agricultural Chemincals). 北京: 中国三峡出版社(Beijing: China Three Gorges Publishing House), 2006, 788.
[228] Astruc D, Liang L Y, Rapakousiou A, Ruiz J. Acc. Chem. Res., 2012, 45: 630.
[229] Jur?cek M, Kouwer P H J, Rowan A E. Chem. Commun., 2011, 47: 8740.
[230] Zhang H Z, Damu G L V, Cai G X, Zhou C H. Curr. Org. Chem., 2014, 18: 359.
[231] Wang Q P, Zhang J Q, Damu G L V, Wan K, Zhang H Z, Zhou C H. Sci. China Chem., 2012, 55: 2134.
[232] Wang X L, Wan K, Zhou C H. Eur. J. Med. Chem., 2010, 45: 4631.
[233] Wan K, Zhou C H. Bull. Korean Chem. Soc., 2010, 31: 2003.
[234] Luo Y, Lu Y H, Gan L L, Zhou C H, Wu J, Geng R X, Zhang Y Y. Arch. Pharm., 2009, 342: 386.
[235] Ustinov A, Weissman H, Shirman E, Pinkas I, Zuo X B, Rybtchinski B. J. Am. Chem. Soc., 2011, 133: 16201.
[236] Dinçalp H, K?z?lok Š? çli S. J. Fluoresc., 2014, 24: 917.
[237] Nagai K, Abe T, Kaneyasu Y, Yasuda Y, Kimishima I, Iyoda T, Imaya H. ChemSusChem, 2011, 4: 727.
[238] Dincalp H, K?z?lok S, Birel Ö H, ? çli S. J. Photoch. Photobio. A, 2012, 235: 40.
[239] 于克贵(Yu K G), 刘建仓(Liu J C), 周成合(Zhou C H), 刁俊林(Diao J L), 胥婷(Xu T), 李东红(Li D H). 中国药物化学杂志(Chinese Journal of Medicinal Chemistry), 2008, 18(6): 414.
[240] Zhou X Q, Liu D Z, Wang T Y, Hua X X, Guo J F, Weerasingheb K C, Wang L C, Li W. J. Photoch. Photobio. A, 2014, 274: 57.
[241] Wu Y S, Zhen Y G, Ma Y C, Zheng R H, Wang Z H, Fu H B. J. Phys. Chem. Lett., 2010, 1: 2499.
[242] Liu Y F, Zhao J Z. Chem. Commun., 2012, 48: 3751.
[243] Yang Z, Yuan Y, Jiang R C, Fu N, Lu X M, Tian C C, Hu W B, Fan Q L, Huang W. Polym. Chem., 2014, 5: 1372.
[244] Aigner D, Dmitriev R I, Borisov S M, Papkovsky D B, Klimant I. J. Mater. Chem. B, 2014, 2: 6792.
[245] Zill A T, Licha K, Haag R, Zimmerman S C. New J. Chem., 2012, 36: 419.
[246] Wang K R, An H W, Rong R X, Cao Z R, Li X L. Macromol. Rapid Commun., 2014, 35: 727.
[247] Yang S K, Shi X H, Park S, Doganay S, Ha T, Zimmerman S C. J. Am. Chem. Soc., 2011, 133: 9964.
[248] Heek T, Würthner F, Haag R. Dyes Chem. Eur. J., 2013, 19: 10911.
[249] Heek T, Nikolaus J, Schwarzer R, Fasting C, Welker P, Licha K, Herrmann A, Haag R. Bioconjugate Chem., 2013, 24: 153.
[250] Battagliarin G, Davies M, Mackowiak S, Li C, Müllen K. ChemPhysChem, 2012, 13: 923.
[251] 米佳丽(Mi J L), 吴俊(Wu J), 周成合(Zhou C H). 华西药学杂志(West China Journal of Pharmaceutical Sciences), 2008, 23(1): 84.
[252] 米佳丽(Mi J L), 周成合(Zhou C H), 白雪(Bai X). 中国抗生素杂志(Chinese Journal of Antibiotics), 2007, 32(10): 587.
[253] Shi Y, Zhou C H. Bioorg. Med. Chem. Lett., 2011, 21: 956.
[254] Cui S F, Ren Y, Zhang S L, Peng X M, Damu G L V, Geng R X, Zhou C H. Bioorg. Med. Chem. Lett., 2013, 23: 3267.
[255] Wang Y, Damu G L V, Lv J S, Geng R X, Yang D C, Zhou C H. Bioorg. Med. Chem. Lett., 2012, 22: 5363.
[256] Langhals H, Pust T. Eur. J. Org. Chem., 2010, 16: 3140.
[257] Yang X C, Chai M Y, Zhu Y, Yang W T, Xu F J. J. Mater. Chem., 2012, 22: 7806.
[258] Zhang Y Y, Mi J L, Zhou C H, Zhou X D. Eur. J. Med. Chem., 2011, 46: 4391.
[259] Zhang S L, Chang J J, Damu G L V, Geng R X, Zhou C H. Med. Chem. Commun., 2013, 4: 839.
[260] 王宪龙(Wang X L), 甘淋玲(Gan L L), 闫聪彦(Yan C Y), 周成合(Zhou C H). 中国科学: 化学(Scientia Sinica Chimica), 2011, 41(3): 451.
[261] Zhou J, Zhang J, Lai Y B, Zhou Z, Zhao Y, Wang H Y, Wang Z. New J. Chem., 2013, 37: 2983.
[262] Zhou C H, Gan L L, Zhang Y Y, Zhang F F, Wang G Z, Jin L, Geng R X. Sci. China Chem., 2009, 52: 415.
[263] Kim H, Kim Y, Lee J. Asian J. Pharm Sci., 2013, 8: 96.
[264] 周成合(Zhou C H), 张飞飞(Zhang F F), 甘淋玲(Gan L L), 张奕奕(Zhang Y Y), 耿蓉霞(Geng R X). 中国科学: 化学(Scientia Sinica Chimica), 2009, 39(3): 208.
[265] Yadav P, Soni G, Mahor A, Alok S I, Singh P P, Verma A. Inter. J. Pharm. Sci. Res., 2014, 5: 1152.
[266] Zhou C H, Zhang Y Y, Yan C Y, Wan K, Gan L L, Shi Y. Anti-Cancer Agents Med. Chem., 2010, 10: 371.
[267] Blechinger J, Herrmann R, Kiener D, García-García F J, Scheu C, Reller A, Bräuchle C. Small, 2010, 6: 2427.
[268] Jana A, Devi K S P, Maiti T K, Pradeep-Singh N D. J. Am. Chem. Soc., 2012, 134: 7656.
[269] Jana A, Nguyen K T, Li X, Zhu P C, Nguan S, Tan N S, Agren H, Zhao Y L. ACS Nano., 2014, 8: 5939.
[270] Peng L P, Nagarajan S, Rasheed S, Zhou C H. Med. Chem. Commun., 2015, 6: 222.
[271] Luo Y L, Kishore B, Kumar K V, Zhou C H, Cai G X. Sci. China Chem., 2015, 58: 483.
[272] Yang F, Zhang Y, Liang H. Inter. J. Mol. Sci., 2014, 15: 3580.
[273] Matsuda R, Kye S H, Anguizola J, Hage D S. Rev. Anal. Chem., 2014, 33: 79.
[274] Cui S F, Peng L P, Zhang H Z, Rasheed S, Kumar K V, Zhou C H. Eur. J. Med. Chem., 2014, 86: 318.
[275] Zhang H Z, Jeyakkumar P, Kumar K V, Zhou C H. New J. Chem., 2015, in press.
[276] Li J M, Li Y X, Shahzad S A, Chen J, Chen Y, Wang Y, Yang M D, Yu C. Chem. Commun., 2015, DOI: 10.1039/C4CC10381E.
[277] Kasera S, Walsh Z, Barrio J D, Scherman O A. Supramol. Chem., 2014, 26: 280.
[278] Feng X L, An Y X, Yao Z Y, Li C, Shi G Q. ACS Appl. Mater. Inter., 2012, 4: 614.
[279] Rao L, Dworkin J D, Nell W E, Bierbach U. J. Phys. Chem. B, 2011, 115: 13701.
[280] Rehm T H, Stojkovi M R, Rehm S, Skugor M, Piantanida I, Würthner F. Chem. Sci., 2012, 3: 3393.
[281] Fu T, Zhao X H, Bai H R, Zhao Z L, Hu R, Kong R M, Zhang X B, Tan W H, Yu R Q. Chem. Commun., 2013, 49: 6644.
[282] Ju E G, Yang X J, Lin Y H, Pu F, Ren J S, Qu X G. Chem. Commun., 2012, 48: 11662.
[283] Wang B, Yu C. Angew. Chem. Int. Ed., 2010, 49: 1485.
[284] Li M, Zhao C Q, Yang X J, Ren J S, Xu C, Qu X G. Small, 2013, 9: 52.
[285] Zhan L, Lian L J, Zhen S J, Li C M, Huang C Z. Analyst, 2013, 138: 825.
[286] Li W Y, Chen J, Jiao H P, Zhang Q F, Zhou H P, Yu C. Chem. Commun., 2012, 48: 10123.
[287] Jiao H P, Wang B, Chen J, Liao D L, Li W Y, Yu C. Chem. Commun., 2012, 48: 7862.
[288] Liao D L, Chen J, Zhou H P, Wang Y, Li Y X, Yu C. Anal. Chem., 2013, 85: 2667.
[289] Chen J, Jiao H P, Li W Y, Liao D L, Zhou H P, Yu C. Chem. Asian J., 2013, 8: 276.
[290] Bo F, Gao B X, Duan W F, Li H X, Liu H M, Bai Q Q. RSC Adv., 2013, 3: 17007.
[291] Kim S K, Sessler J L. Acc. Chem. Res., 2014, 47: 2525.
[292] Rajnish S, Navneet K, Subodh K. Tetrahedron, 2014, 70: 4285.
[293] 常娟娟(Chang J J), 王艳(Wang Y), 张慧珍(Zhang H Z), 周成合(Zhou C H), 耿蓉霞(Geng R X), 吉庆刚(Ji Q G). 高等学校化学学报(Chemical Journal of Chinese Universities), 2011, 32(9): 1970.
[294] 时园(Shi Y), 周成合(Zhou C H), 周向东(Zhou X D), 耿蓉霞(Geng R X), 吉庆刚(Ji Q G). 药学学报(Acta Pharmaceutica Sinica), 2011, 46(7): 798.
[295] 吴俊(Wu J), 米佳丽(Mi J L), 周成合(Zhou C H). 中国药学杂志(Chinese Pharmaceutical Journal), 2007, 42(6): 404.
[296] Zhang L, Kumar K V, Rasheed S, Geng R X, Zhou C H. Chem. Biol. Drug. Des., 2015, doi: 10.1111/cbdd.12532.
[297] 孟江平(Meng J P), 耿蓉霞(Geng R X), 周成合(Zhou C H), 甘淋玲(Gan L L), 吴俊(Wu J). 中国新药杂志(Chinese Journal of New Drugs), 2009, 16(16): 1505.
[298] Zhang H Z, Damu G L V, Cai G X, Zhou C H. Eur. J. Med. Chem., 2013, 64: 329.
[299] Li S, Chen J X, Xiang Q X, Zhang L Q, Zhou C H, Xie J Q, Yu L, Li F Z. Eur. J. Med. Chem., 2014, 84: 677.
[300] 甘淋玲(Gan L L), 蔡佳利(Cai J L), 周成合(Zhou C H). 中国药学杂志(Chinese Pharmaceutical Journal), 2009, 44(18): 1361.
[301] 蔡佳利(Cai J L), 卢一卉(Lu Y H), 甘淋玲(Gan L L), 张奕奕(Zhang Y Y), 周成合(Zhou C H). 中国抗生素杂志(Chinese Journal of Antibiotics), 2009, 34: 454.
[302] 甘淋玲(Gan L L), 卢一卉(Lu Y H), 周成合(Zhou C H). 中国生化药物杂志(Chinese Journal of Biochemical Pharmaceutics), 2009, 30(8): 127.
[303] Gan L L, Fang B, Zhou C H. Bull. Korean Chem. Soc., 2010, 31: 3684.
[304] Clapham D E T. Nature, 2003, 426: 517.
[305] Caudarella R, Vescini F, Buffa A, Rizzoli E, Ceccoli L, Francucci C M. J. Endocrinol. Investigat., 2011, 34: 13.
[306] Zhang S L, Chang J J, Damu G L V, Fang B, Zhou X D, Geng R X, Zhou C H. Bioorg. Med. Chem. Lett., 2013, 23: 1008.
[307] Dai L L, Zhang Z, Nagarajan S, Rasheed S, Zhou C H. Med. Chem. Commun., 2015, 6: 147.
[308] Schulze M, Steffen A, Wuerthner F. Angew. Chem. Int. Ed., 2015, 54: 1570.
[309] Aigner D, Sergey M B, Klimant I. Anal. Bioanal. Chem., 2011, 400: 2475.
[310] Georgiev N I, Sakr A R, Bojinov V B. Dyes Pigments, 2011, 91: 332.
[311] Zhang L, Peng X M, Damu G L V, Geng R X, Zhou C H. Med. Res. Rev., 2014, 34: 340.
[312] 蔡佳利(Cai J L), 李硕(Li S), 周成合(Zhou C H), 甘淋玲(Gan L L), 吴俊(Wu J). 中国新药杂志(Chinese Journal of New Drugs), 2009, 18(7): 598.
[313] Hu Y W, Han D X, Zhang Q X, Wu T S, Li F H, Niu L. Biosens. Bioelectron., 2012, 38: 396.
[314] Zhang W, Li F H, Hu Y W, Gan S Y, Han D X, Zhang Q X, Niu L. J. Mater. Chem. B, 2014, 2: 3142.
[315] Hu Y W, Wang K K, Zhang Q X, Li F H, Wu T S, Niu L. Biomaterials, 2012, 33: 1097.
[316] Zhong L N, Xing F F, Bai Y L, Zhao Y M, Zhu S R. Spectro. Chim. Acta A, 2013, 115: 370.
[317] Singh P, Mittal L S, Kumar S, Bhargava G, Kumar S. J. Fluoresc., 2014, 24: 909.
[318] Zhao Y J, Sun J J, Shi Z Q, Pan C C, Xu M Y. Luminescence, 2011, 26: 214.
[319] Liu Z H, Tonnele C, Battagliarin G, Li C, Gropeanu R A, Weil T, Surin M, Beljonne D, Lazzaroni R, Debliquy M, Renoirt J M, Mullen K. J. Phys. Chem. B, 2014, 118: 309.
[320] Liu X J, Zhang N, Zhou J, Chang T J, Fang C L, Shangguan D H. Analyst, 2013, 138: 901.
[321] Malkondu S. Tetrahedron, 2014, 70: 5580.
[322] Ramesh M, Lin H C, Chu C W. Biosens. Bioelectron., 2013, 42: 76.
[323] Lu X Y, Guo Z Q, Feng M X, Zhu W H. ACS Appl. Mater. Inter., 2012, 4: 3657.
[324] Han A, Liu X H, Prestwich G D, Zang L. J. Mater. Chem., 2012, 22: 478.
[325] Li J F, Wu Y Z, Song F Y, Wei G, Cheng Y X, Zhu C J. J. Mater. Chem., 2012, 22: 478
[326] Wang H X, Lang Y H, Wang H X, Lou J J, Guo H M, Li X Y. Tetrahedron, 2014, 70: 1997.
[327] Cai J J, Sessler J L. Chem. Soc. Rev., 2014, 43: 6198.
[328] Gale P A, Perez-Tomas R, Quesada R. Acc. Chem. Res., 2013, 46: 2801.
[329] Haridas V, Sahu S, Praveen Kumar P P, Sapala A R. RSC Adv., 2012, 2: 12594.
[330] Suk J M, Chae M K, Jeong K S.. Pure Appl. Chem., 2012, 84: 953.
[331] Chen Z J, Wang L M, Zou G, Zhang L, Zhang G J, Cai X F, Teng M S. Dyes Pigments, 2012, 94: 410.
[332] Wang Y F, Zhang L, Zhang G J, Wu Y, Wu S Y, Yu J J, Wang L M. Tetrahedron Lett., 2014, 55: 3218.
[333] Du F F, Bao Y Y, Liu B, Tian J, Li Q B, Bai R K. Chem. Commun., 2013, 49: 4631.
[334] Urmila B. J. Pharm. Res., 2012, 5: 4236.
[335] Peng X M, Damu G L V, Zhou C H. Curr. Pharm. Design., 2013, 19: 3884.
[336] Jia X T, Yang Y, Xu Y F, Qian X H. Pure Appl. Chem., 2014, 86: 1237.
[337] Breul A M, Hager M D, Schubert U S. Chem. Soc. Rev., 2013, 42: 5366.
[338] Nandhikonda P, Cao Z, Heagy M D. Rev. Fluoresc., 2011, 6: 303.
[339] Zhang L, Chang J J, Zhang S L, Damu G L V, Geng R X, Zhou C H. Bioorg. Med. Chem., 2013, 21: 4158.
[340] 方波(Fang B), 周成合(Zhou C H), 周向东(Zhou X D). 国际药学研究杂志(International Journal of Pharmaceutical Research), 2010, 37(2): 105.
[341] DiCesare N D, Lakowicz J R. J. Biomed. Optics., 2002, 7: 538.
[342] Yin B T, Yan C Y, Peng X M, Zhang S L, Rasheed S, Geng R X, Zhou C H. Eur. J. Med. Chem., 2014, 71: 148.
[343] 金磊(Jin L), 闫聪彦(Yan C Y), 甘淋玲(Gan L L), 周成合(Zhou C H). 中国生化药物杂志(Chinese Journal of Biochemical Pharmaceutics), 2010, 31(5): 358.
[344] 刘勇(Liu Y), 张峰(Zhang F), 邹林波(Zou L B), 蹇军友(Jian J Y), 鲍小平(Bao X P). 有机化学(Chinese Journal of Organic Chemistry), 2013, 33(12): 2485.
[345] Alarcón F, Báez M, Bravo M, Richter P, Escandar G M, Olivieri A C, Fuentes E. Talanta, 2013, 103: 361.
[346] Marcia M, Singh P, Hauke F, Maggini M, Hirsch A. Org. Biomol. Chem., 2014, 12: 7045.
[347] Flamigni L, Ventura B, Barbieri A, Langhals H, Wetzel F, Fuchs K, Walter A. Chem. Eur. J., 2010, 16: 13406.
[348] Peng H N, Ding L P, Liu T H, Chen X L, Li L, Yin S W, Fang Y. Chem. Asian J., 2012, 7: 1576.
[349] E Y, Ma X J, Zhang Y F, Zhang Y B, Duan R, Ji H W, Li J, Che Y K, Zhao J C. Chem. Commun., 2014, 50: 13596.
[350] Che Y K, Yang X M, Liu G L, Yu C, Ji H W, Zuo J M, Zhao J C, Zang L. J. Am. Chem. Soc., 2010, 132: 5743.
[351] Shin I S, Hirsch T, Ehrl B, Jang D H, Wolfbeis O S, Hong J I. Anal. Chem., 2012, 84: 9163.
[352] Xu L Q, Zhang B, Sun M, Hong L, Neoh K G, Kang E T, Fu G D. J. Mater. Chem. A, 2013, 1: 1207.
[353] Huang L M, Tam-Chang S W. J. Fluoresc., 2011, 21: 213.
[354] Tahir M, Sayyad M H, Clark J, Wahaba F, Aziz F, Shahid M, Munaward M A, Chaudry J A. Sensor Actuat. B Chem., 2014, 192: 565.
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