2
3
4
5
L. Wang, X. He, Y. Guo, J. Xu and S. Shao, Org. Biomol. Chem., 2011,
, 752–757.
J. Kang, M. Choi, J. Y. Kwon, E. Yeol and J. Yoon, J. Org. Chem., 2002,
7, 4384–4386.
R. Martinez, A. Espinosa, A. Tarraga and P. Molina, Tetrahedron, 2008,
4, 2184–2191.
(a) P. Kaur, S. Kaur and K. Singh, Tetrahedron Lett., 2007, 48, 7191–
193; (b) P. Kaur, S. Kaur, A. Mahajan and K. Singh, Inorg. Chem.
12 I. A. Koval, P. Gamez, C. Belle, K. Selmeczi and J. Reedijk, Chem. Soc.
Rev., 2006, 35, 814–840.
13 (a) K. J. Barnham, C. L. Masters and A. I. Bush, Nat. Rev. Drug Discov-
ery, 2004, 3, 205–214; (b) E. Gaggelli, H. Kozlowski, D. Valensin and
G. Valensin, Chem. Rev., 2006, 106, 1995–2044; (c) E. Madsen and
J. D. Gitlin, Annu. Rev. Neurosci., 2007, 30, 317–337.
9
6
6
14 A. K. Jain, R. K. Singh, S. Jain and J. Raisoni, Transition Met. Chem.,
2007, 33, 243–249.
7
Commun., 2008, 11, 626–629; (c) P. Kaur, S. Kaur and K. Singh, Inorg.
Chem. Commun., 2009, 12, 978–981; (d) P. Kaur, D. Sareen, S. Kaur and
K. Singh, Inorg. Chem. Commun., 2009, 12, 272–275; (e) P. Kaur and
D. Sareen, Dyes Pigm., 2011, 88, 296–300; (f) P. Kaur, S. Kaur,
Y. Kasetti, P. V. Bharatam and K. Singh, Talanta, 2010, 83, 644–650;
15 S. L. Belli and A. Zirino, Anal. Chem., 1993, 65, 2583–2589.
16 A. P. de Silva, H. Q. N. Gunaratne and C. P. McCoy, Nature, 1993, 364,
42–44.
17 (a) A. P. de Silva, H. Q. N. Gunaratne and C. P. McCoy, J. Am. Chem.
Soc., 1997, 119, 7891–7892; (b) A. Credi, V. Balzani, S. J. Langford and
J. F. Stoddart, J. Am. Chem. Soc., 1997, 119, 2679–2681; (c) A. P. de
Silva, I. M. Dixon, H. Q. N. Gunaratne, T. Gunnlaugsson,
P. R. S. Maxwell and T. E. Rice, J. Am. Chem. Soc., 1999, 121, 1393–
1394; (d) A. P. de Silva and N. D. McClenaghan, J. Am. Chem. Soc.,
2000, 122, 3965–3966; (e) A. Saghatelian, N. H. Volcker, K.
M. Guckian, V. S. Y. Lin and M. R. Ghadiri, J. Am. Chem. Soc., 2003,
125, 346–347; (f) K. K. Upadhyay, A. Kumar, R. K. Mishra, T. M. Fyles,
S. Upadhyay and K. Thapliyal, New J. Chem., 2010, 34, 1862–1866;
(g) J. Wang and C.-S. Ha, Analyst, 2010, 135, 1214–1218; (h) M. Suresh,
A. Ghosh and A. Das, Chem. Commun., 2008, 3906–3908.
(g) P. Kaur, D. Sareen and K. Singh, Talanta, 2011, 83, 1695–1700;
(h) P. Kaur, S. Kaur and K. Singh, Talanta, 2011, 84, 947–951;
(i) P. Kaur, M. Kaur and K. Singh, Talanta, 2011, 85, 1050–1055;
( j) P. Kaur, S. Kaur, K. Singh, P. R. Sharma and T. Kaur, Dalton Trans.,
2
011, 40, 10818–10821.
6
(a) E. M. Nolan and S. J. Lippard, Chem. Rev., 2008, 108, 3443–3480;
(
(
b) D. T. Quang and J. S. Kim, Chem. Rev., 2010, 110, 6280–6301;
c) Z.-Q. Guo, W.-Q. Chen and X.-M. Duan, Org. Lett., 2010, 12, 2202–
2
205; (d) K. L. Ciesienski, L. M. Hyman, S. Derisavifard and
K. J. Franz, Inorg. Chem., 2010, 49, 6808–6810; (e) L. Huang, F. Chen,
P. Xi, G. Xie, Z. Li, Y. Shi, M. Xu, H. Liu, Z. Ma, D. C. Bai and
Z. Z. Zeng, Dyes Pigm., 2011, 90, 265–268; (f) Y.-C. Hsieh, J.-L. Chir,
S.-T. Yang, S.-J. Chen, C.-H. Hu and A.-T. Wu, Carbohydr. Res., 2011,
18 (a) K. Kurack, C. Trieflinger, A. Kovalchuck and J. Daub, Chem.–Eur. J.,
2007, 13, 8998–9003; (b) S. Wang, G. Men, L. Zhao, Q. Hou and
S. Jiang, Sens. Actuators, B, 2010, 145, 826–831.
3
46, 978–981; (g) L. Tang, F. Li, M. Liu and R. N. Kumar, Spectrochim.
19 P. Gans, A. Sabatini and A. Vacca, Talanta, 1996, 43, 1739–1753.
Acta, Part A, 2011, 78, 1168–1172; (h) P. Mahato, A. Ghosh, S. Saha,
S. Mishra, S. K. Mishra and A. Das, Inorg. Chem., 2010, 49, 11485–
A o
20 Detection limit (DL) is given as DL = (0.03×RSDB)/(χ /c ), where
RSDB (relative standard deviation of the background expressed as a
percent) is the sensitivity (the slope of the calibration curve of intensity
11492; (i) Y. Li, S. He, Y. Lu and X. Zeng, Org. Biomol. Chem., 2011, 9,
2
606–2609; ( j) Y. Zhou, X.-Y. You, Y. Fang, J.-Y. Li, K. Liu and C. Yao,
A
versus composition), χ is the net analyte signal (i.e. signal above back-
Org. Biomol. Chem., 2010, 8, 4819–4822.
ground) and c is the composition of the element in the sample
o
7
8
D. W. Boening, Chemosphere, 2000, 40, 1335–1351.
21 (a) L. R. Naik, H. M. S. Kumar, S. R. Inamdar and N. N. Math, Spec-
trosc. Lett., 2005, 38, 645–659; (b) S. Jayaraman and A. S. Verkman,
Biophys. Chem., 2000, 85, 49–57; (c) A. L. Koner, P. P. Mishra, S. Jha
and A. Dutta, J. Photochem. Photobiol., A, 2005, 170, 21–26.
22 (a) M. Yu, M. Shi, Z. Chen, F. Li, X. Li, Y. Gao, J. Xu, H. Yang,
Z. Zhou, T. Yi and C. Huang, Chem.–Eur. J., 2008, 14, 6892–6900;
(b) G.-K. Li, Z.-X. Xu, C.-F. Chen and Z.-T. Huang, Chem. Commun.,
2008, 1774–1776; (c) Z.-C. Wen, R. Yang, H. He and Y.-B. Jiang, Chem.
Commun., 2006, 106–108.
23 G. T. Cheek and R. F. Nelson, J. Org. Chem., 1978, 43, 1230–1232.
24 T.-L. Ho, Chem. Rev., 1975, 75, 1–20.
25 (a) M. A. Omary, R. M. Kassab, M. R. Haneline, O. Elbjeirami and
F. P. Gabbai, Inorg. Chem., 2003, 42, 2176–2178; (b) C. Burress,
O. Elbjeirami, M. A. Omary and F. P. Gabbai, J. Am. Chem. Soc., 2005,
127, 12166–12167.
(a) W. F. Fitzgerald, C. H. Lamborg and C. R. Hammerschmidt, Chem.
Rev., 2007, 107, 641–662; (b) M. Nendza, T. Herbst, C. Kussatz and
A. Gies, Chemosphere, 1997, 35, 1875–1885; (c) A. Renzoni, F. Zino
and E. Franchi, Environ. Res., 1998, 77, 68–72; (d) J. M. Llobet,
G. Falco, C. Casas, A. Teixido and J. L. Damingo, J. Agric. Food Chem.,
2
003, 51, 838–842.
E. K. Silbergeld, I. A. Silva and J. F. Nyland, Toxicol. Appl. Pharmacol.,
005, 207, 282–292.
0 (a) M. Q. Zhang, Y. C. Zhu and R. W. Deng, China Ambio., 2002, 31,
82–484; (b) G. Westphal and E. Hallier, Lancet, 2003, 361, 698–699;
c) M. Harada, S. Nakachi, K. Tasaka, S. Sakashita, K. Muta,
K. Yanagida, R. Doi, T. Kazaki and H. Ohno, Sci. Total Environ., 2001,
69, 183–187.
1 (a) C. Andreini, L. Banci, I. Bertini and A. Rosato, J. Proteome Res.,
008, 7, 209–216; (b) E. L. Que, D. W. Domaille and C. J. Chang, Chem.
Rev., 2008, 108, 1517–1549; (c) E. D. Harris, J. Trace Elem. Exp. Med.,
001, 14, 207–210.
9
2
1
4
(
2
1
2
26 E. Coronado, J. R. Galan-Mascaros, C. Marti-Gastaldo, E. Palomares,
J. R. Durrant, R. Vilar, M. Gratzel and M. K. Nazeeruddin, J. Am. Chem.
Soc., 2005, 127, 12351–12356.
2
This journal is © The Royal Society of Chemistry 2012
Org. Biomol. Chem., 2012, 10, 1497–1501 | 1501