Electrochemical and spectroscopical characterization of ferrocenyl chalcones

Journal of the Electrochemical Society

Volumn 157, Issue 8, 2010, Pages

  Cardona, Rocío A ^a   Hernández, Kenneth ^a   Pedró, Laura E ^a   Otao, Myrna R ^a   Montes, Ingrid ^a   Guadalupe, Ana R ^a  

^a UNIVERSITY OF PUERTO RICO   (Puerto Rico)

Author keywords

[No Author keywords available]

Indexed keywords

ABSORBANCES; ACETYLFERROCENE; AROMATIC SYSTEM; CHALCONES; DIFFUSION COEFFICIENTS; DIMERIC SPECIES; DIMETHYLANILINE; ELECTROCHEMICAL BEHAVIORS; ELECTRON-TRANSFER RATE CONSTANTS; FERROCENYL; FORMAL POTENTIAL; GOOD YIELD; NICHOLSON METHODS; NUMBER OF ELECTRONS; RECRYSTALLIZATIONS; UV REGION;

ALDEHYDES; ELECTROPOLYMERIZATION; OLIGOMERS; RATE CONSTANTS; ULTRAVIOLET SPECTROSCOPY;

CHEMICAL COMPOUNDS;

EID: 77954745691     PISSN: 00134651     EISSN: None     Source Type: Journal    
DOI: 10.1149/1.3439669     Document Type: Article

References (24)

1. S. M. Batterjee, M. I. Marzouk, M. E. Aazab, and M. A. El-Hashash, Appl. Organomet. Chem. AOCHEX 0268-2605, 17, 291 (2003). 10.1002/aoc.414
2. E. Coutouli-Argyropoulou, C. Sideris, and G. Kokkinidis, J. Organomet. Chem. JORCAI 0022-328X, 691, 3909 (2006). 10.1016/j.jorganchem.2006.05.045
3. P. Debroy and S. Roy, Coord. Chem. Rev. CCHRAM 0010-8545, 251, 203 (2007). 10.1016/j.ccr.2006.07.001
4. T. Ihara, Y. Maruo, S. Takenaka, and M. Takagi, Nucleic Acids Res. NARHAD 0305-1048, 24, 4273 (1996). 10.1093/nar/24.21.4273
5. T. S. Zatsepin, S. Y. Andreev, T. Hianik, and T. S. Oretskaya, Russ. Chem. Rev. RCRVAB 0036-021X, 72, 537 (2003). 10.1070/RC2003v072n06ABEH000807
6. C. M. Jewell, M. E. Hays, Y. Kondo, N. L. Abbott, and D. M. Lynn, J. Controlled Release JCREEC 0168-3659, 112, 129 (2006). 10.1016/j.jconrel.2006.01. 014
7. S. Mu, Synth. Met. SYMEDZ 0379-6779, 139, 287 (2003). 10.1016/S0379-6779(03)00167-X
8. J. -B. Raoof, R. Ojani, and A. Kiani, J. Electroanal. Chem. JECHES 0022-0728, 515, 45 (2001). 10.1016/S0022-0728(01)00642-8
9. I. Willner, V. Pardo-Yissar, E. Katz, and K. T. Ranjit, J. Electroanal. Chem. JECHES 0022-0728, 497, 172 (2001). 10.1016/S0022-0728(00)00455-1
10. A. Shah, A. M. Khan, R. Qureshi, F. L. Ansari, M. F. Nazar, and S. S. Shah, Int. J. Mol. Sci. IJMCFK 1422-0067, 9, 1424 (2008). 10.3390/ijms9081424
11. X. Wu, E. R. T. Tiekink, I. Kostetski, N. Kocherginsky, A. L. C. Tan, S. B. Khoo, P. Wilairat, and M. -L. Go, Eur. J. Pharm. Sci. EPSCED 0928-0987, 27, 175 (2006). 10.1016/j.ejps.2005.09.007
12. S. Tomá, A. Gáplovsky, and I. Pavlík, Monatsh. Chem., 116, 479 (1985). 10.1007/BF00798369 0026-9247
13. A. Shah, R. Qureshi, A. M. Khan, F. L. Ansari, and S. Ahmad, Bull. Chem. Soc. Jpn. BCSJA8 0009-2673, 82, 453 (2009). 10.1246/bcsj.82.453
14. S. J. Ji, S. Y. Wang, Z. L. Shen, and M. F. Zhou, Chin. Chem. Lett. CCLEE7 1001-8417, 14, 1246 (2003).
15. S. J. Ji, S. Y. Wang, and Z. L. Shen, Chin. Chem. Lett. CCLEE7 1001-8417, 14, 663 (2003).
16. E. Solčániová, S. Toma, and A. Fiedlerová, Org. Magn. Reson. ORMRBD 0030-4921, 14, 181 (1980). 10.1002/mrc.1270140307
17. See supplementary material at http://dx.doi.org/10.1149/1.3439669 (E-JESOAN-157-027008) for additional information.
18. P. T. Kissinger and W. R. Heineman, J. Chem. Educ. JCEDA8 0021-9584, 60, 702 (1983). 10.1021/ed060p702
19. J. E. Heffner, J. C. Raber, O. A. Moe, and C. T. Wigal, J. Chem. Educ. JCEDA8 0021-9584, 75, 365 (1998). 10.1021/ed075p365
20. B. M. Smith and J. March, March's Advanced Organic Chemistry: Reaction, Mechanism and Structure, 5th ed., pp. 368-375, John Wiley & Sons, New York (2001).
21. A. M. Bond, T. L. E. Henderson, D. R. Mann, T. F. Mann, W. Thormann, and C. G. Zoski, Anal. Chem. ANCHAM 0003-2700, 60, 1878 (1988). 10.1021/ac00169a008
22. N. Oyama, T. Ohsaka, and T. Shimizu, Anal. Chem. ANCHAM 0003-2700, 57, 1526 (1985). 10.1021/ac00285a008
23. M. Leclerc, J. Guay, and L. H. Dao, Macromolecules MAMOBX 0024-9297, 22, 649 (1989). 10.1021/ma00192a024
24. R. S. Nicholson, Anal. Chem. ANCHAM 0003-2700, 37, 1351 (1965). 10.1021/ac60230a016