用户名: 密码: 验证码:
A α-cyanostilbene-modified Schiff base as efficient turn-on fluorescent chemosensor for Zn 2 +
详细信息    查看全文
  • 作者:AIXIANG DING ; FANG TANG ; TAO WANG ; XUTANG TAO
  • 关键词:Fluorescence sensor ; Schiff base ; α ; cyanostilbene ; chelation ; enhanced fluorescence effect ; zinc ion.
  • 刊名:Journal of Chemical Sciences
  • 出版年:2015
  • 出版时间:March 2015
  • 年:2015
  • 卷:127
  • 期:3
  • 页码:375-382
  • 全文大小:2,006 KB
  • 参考文献:1.Carter K P, You ng A M and Palmer A E 2014 Chem. Rev. doi: 10.-021/?cr400546e
    2.Liu T and Liu S Y 2011 Anal. Chem. 83 2775
    3.Carter R E, Weiss J H and Shuttleworth C W 2010 Neuroreport 21 1060
    4.Maret W, Jacob C, Vallee B L and Fisher E H 1999 Proc. Natl. Acad. Sci. 96 1936
    5.An J M, Yan M H, Yang Z Y, Li T R and Zhou Q X 2013 Dyes Pigments 99 1
    6.Kong L, Chen Y, Ye W B and Zhao L, Song B 2013 Sens. Actuators B 177 218
    7.Zhang Y, Guo X F, Zheng L, Jia L H and Qian X H 2013 J. Photochem. Photobiol. A 257 20
    8.Liu X J, Zhang N, Zhou J, Chang T J, Fang C L and Shangguan D H 2013 Analyst 138 901
    9.Safin D A, Babashkina M G and Garcia Y 2013 Dalton Trans. 42 1969
    10.Goswami S, Das A K, Aich K, Manna A, Maity S, Khanra K and Bhattacharyya N 2013 Analyst 138 4593
    11.Jiao S Y, Peng L L, Li K, Xie Y M, Ao M Z, Wang X and Yu X Q 2013 Analyst 138 5762
    12.Du J, Huang Z, Yu X Q and Pu L 2013 Chem. Commun. 49 5399
    13.Mikata Y, Sato Y, Takeuchi S, Kuroda Y, Konno H and Iwatsuki S 2013 Dalton Trans. 42 9688
    14.Wang L, Qin W W and Liu W S 2010 Inorg. Chem. Commun. 13 1122
    15.Helal A and Kim H S 2013 Spectrochim. Acta 105 273
    16.Kumar M, Kumar N and Bhalla V 2013 Chem. Commun. 49 877
    17.Ingale S A and Seela F 2012 J. Org. Chem. 77 9352
    18.Pearce D A, Jotterand N, Carrico I S and Imperiali B 2001 J. Am. Chem. Soc. 123 5160
    19.Zhang Y, Guo X F, Si W X, Jia L H and Qian X H 2008 Org. Lett. 10 473
    20.Ding Y B, Xie Y S, Li X, Hill J P, Zhang W B and Zhu W H 2011 Chem. Commun. 47 5431
    21.Thirupathi P and Lee K H 2013 Bioorg. Med. Chem. Lett. 23 6811
    22.Tong A J, Dong H and Li L D 2002 Anal. Chim. Acta 46 31
    23.Xu Z C. Qian X H, Cui J N and Zhang R 2006 Tetrahedron 62 10117
    24.Nolan E M and Lippard S J 2004 Inorg. Chem. 43 8310
    25.Aoki S, Kagata D, Shiro M, Takeda K and Kimura E 2004 J. Am. Chem. Soc. 126 13377
    26.Wang P F, Hong Z R, Xie Z Y, Tong S, Wong O, Lee C S, Wong N, Hung L and Lee S 2003 Chem. Commun. 1664
    27.Yu T Z, Zhang K, Zhao Y L, Yang C H, Zhang H, Qian L, Fan D W, Dong W K, Chen L L and Qiu Y Q 2008 Inorg. Chim. Acta 361 233
    28.Xie Y Z, Shan G G, Li P, Zhou Z Y and Su Z M 2013 Dyes Pigments 96 467
    29.Navarro M, Castro W, Martíznez A and Delgado R A S 2011 J. Inorg. Biochem. 105 276
    30.Mishra A P, Mishra R K and Pandey M D 2011 Russ. J. Inorg. Chem. 56 1757
    31.Aziz A A A, Badr I H A and El-Syaed I S A 2012 Spectrochim. Acta A 97 388
    32.Wang S C, Men G W, Zhao L Y, Hou Q F and Jiang S M 2010 Sens. Actuators B 145 826
    33.Zang L B, Shang H G, Wei D Y and Jiang S M 2013 Sens. Actuators B 185 389
    34.Hiseh W H, Wan C F, Liao D J and Wu A T 2012 Tetrahedron Lett. 53 5848
    35.Ding C X, He C H and Xie Y S 2013 Chinese Chem. Lett. 24 463
    36.Liu S B, Bi C F, Fan Y H, Zhao Y, Zhang P F, Luo Q D and Zhang D M 2011 Inorg. Chem. Commun. 14 1297
    37.Hosseini M, Vaezi Z, Ganjali M R, Faridbod F, Abkenar S D, Alizadeh K and Niasari M S 2010 Spectrochim. Acta A 5 978
    38.Udhayakumari D, Saravanamoorthy S, Ashok M and Velmathi S 2011 Tetrahedron Lett. 52 4631
    39.Paul B K, Kar S and Guchhait N 2011 J. Photochem. Photobio. A 220 153
    40.Li H Y, Gao S and Xi Z 2009 Inorg. Chem. Commun. 12 300
    41.An B K, Kwon S K, Jung S D and Park S Y 2002 J. Am. Chem. Soc. 124 14410
    42.Chung J W, You Y, Huh H S, An B K, Yoon S J, Kim S H, Lee S W and Park S Y 2009 J. Am. Chem. Soc. 131 8163
    43.Dou C D, Han L, Zhao S S, Zhang H Y and Wang Y 2011 J. Phys. Chem. Lett. 2 666
    44.Zhu L L and Zhao Y L 2013 J. Mater. Chem. C 1 1059
    45.Lim C K, Kim S, Kwon I C, Ahn C H and Park S Y 2009 Chem. Mater. 21 5819
    46.Jia W B, Yang P, Li J J, Yin Z M, Kong L, Lu H B, Ge Z S, Wu Y Z, Hao X P and Yang J X 2014 Poly. Chem. 5 2282
    47.Jia W B, Wang H W, Yang L M, Lu H B, Kong L, Tian Y P, Tao X T and Yang J X 2013 J. Mater. Chem. C 1 7092
    48.Gou C, Qin S H, Wu H Q, Wang Y, Luo J and Liu X Y 2011 Inorg. Chem. Commun. 14 1622
    49.Kim B, Yeom H R, Choi W Y, Kim J Y and Yang C 2012 Tetrahedron 68 6696
    50.Lu H B, Qiu L Z, Zhang G Y, Ding A X, Xu W B, Zhang G B, Wang X H, Kong L, Tian Y P and Yang J X 2014 J. Mater. Chem. C 2 1386
    51.Frisch M J G W T, Schlegel H B, Scuseria G E, Robb M A, Cheeseman J R, Scalmani G, Barone V, Mennucci B, Petersson G A, Nakatsuji H, Caricato M, Li X, Hratchian H P, Izmaylov A F, Bloino J, Zheng G J, Sonnenberg L, Hada M, Ehara M, Toyota K, Fukuda R, Hasegawa J, Ishida M, Nakajima T, Honda Y, Kitao O, Nakai H, Vreven T, Montgomery J A, Peralta Jr J E, Ogliaro F, Bearpark M, Heyd J J, Brothers E, Kudin K N, Staroverov V N, Kobayashi R, Normand J, Raghavachari K, Rendell A, Burant J C, Iyengar S, Tomasi S J, Cossi M, Rega N, Millam J M, Klene M, Knox J E, Cross J B, Bakken V, Adamo C, Jaramillo J, Gomperts R, Stratmann R E, Yazyev O, Austin A J, Cammi R, Pomelli C, Ochterski J W, Martin R L, Morokuma K, Zakrzewski V G, Voth G A, Salvador P, Dannenberg J J, Dapprich S, Daniels A D, Farkas O, Foresman J B, Ort
  • 作者单位:AIXIANG DING (1)
    FANG TANG (1)
    TAO WANG (1)
    XUTANG TAO (2)
    JIAXIANG YANG (1) (2)

    1. Department of Chemistry, Key Laboratory of Functional Inorganic Materials of Anhui Province, Anhui University, Hefei, 230039, P. R. China
    2. State Key Laboratory of Crystal Materials, Shandong University, Jinan, Shandong, 250100, P. R. China
  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Chemistry
    Chemistry
  • 出版者:Springer India
  • ISSN:0973-7103
文摘
A novel Schiff base derivative (Z)-3-(4-(hexyloxy)phenyl)-2-(4-((E)-2-hydroxybenzylidene amino)phenyl)acrylonitrile (L) was designed, synthesized and characterized. L was used as a Zn2+ selective, turn-on, fluorescent chemosensor with a detection limit of 0.1 μM in DMF. 1:1 stoichiometric complex formation of L wih Zn2+ was confirmed through fluorescent titration experiments and Job’s plot. The enhancement of fluorescence intensity of L with addition of Zn2+ is the consequence of the inhibited isomerization of the C=N bond, namely chelation-enhanced fluorescence (CHEF) effect.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700