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Journal articles on the topic 'Ferrocenecarboxaldehyde'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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1

Sun, Longfei, Xiaohua Zhang, Wenyang Wang, and Jinhua Chen. "Carbon nanotube–ionic liquid composite gel based high-performance bioanode for glucose/O2 biofuel cells." Analytical Methods 7, no. 12 (2015): 5060–66. http://dx.doi.org/10.1039/c5ay00863h.

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2

Huang, Guo-sheng, Qing-bao Song, and Yong-xiang Ma. "METAL COMPLEXES OF FERROCENECARBOXALDEHYDE 2,4-DICHLOROBENZOYLHYDRAZONE." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 31, no. 2 (2001): 297–302. http://dx.doi.org/10.1081/sim-100002048.

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3

Niazimbetova, Zukhra I., Dennis H. Evans, Ilia A. Guzei, Christopher D. Incarvito, and Arnold L. Rheingold. "Cathodically Promoted Addition of Nitroalkanes to Ferrocenecarboxaldehyde." Journal of The Electrochemical Society 146, no. 4 (1999): 1492–95. http://dx.doi.org/10.1149/1.1391792.

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4

Jia, Jian Hong, Hua Qing Dong, Yu Jin Li, Wei Jian Sheng, and Jian Rong Gao. "One-Pot Process for Preparation of Ferrocenylethene Derivatives via Solvent-Free Wittig Reaction." Advanced Materials Research 476-478 (February 2012): 1218–21. http://dx.doi.org/10.4028/www.scientific.net/amr.476-478.1218.

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One-pot process for preparation ferrocenylethene derivatives by solvent-free Wittig Reaction of ferrocenecarboxaldehyde, alcohol, triphenylphosphonium bromide, and NaOH without the synthesis of phosphorus ylides was reported. The ferrocenylethene products obtained had an 80% yield with NaOH as the base at room temperature for 30 to 90 minutes.

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5

El-Hussieny, Marwa, Hisham Abdallah A. Yosef, Mohamed R. H. Mahran, and Nabila M. Ibrahim. "Reactions of ferrocenyl chalcones with hydrazines and active methylene compounds." Heterocyclic Communications 22, no. 2 (2016): 69–77. http://dx.doi.org/10.1515/hc-2016-0006.

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AbstractClaisen-Schmidt condensation of ferrocenecarboxaldehyde (2b) with 2-acetylfuran (4) yielded (E)-3-ferrocenyl-1-(2-furyl)prop-2-en-1-one (E-5) together with 1,5-di(2-furyl)-3-ferrocenylpentane-1,5-dione (6). Reactions of the ferrocenyl chalcones 3a,b and 5 with hydrazine hydrate, phenyl hydrazine, ethyl acetoacetate, ethyl cyanoacetate and malononitrile, were also studied. Possible reaction mechanisms were discussed and structures of the new products were unambiguously characterized by common analytical and spectroscopic methods.

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6

Ren, Qun Xiang, Tian Hao Chi, Ying Ying Sun, Li Feng, and Ming Yang Ma. "Preparation of Ferrocene Functionalized Multiwall Carbon Nanotube Nanocomposites and its Electrochemical Behavior." Applied Mechanics and Materials 401-403 (September 2013): 667–70. http://dx.doi.org/10.4028/www.scientific.net/amm.401-403.667.

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Ferrocenecarboxaldehyde (FcCHO) was covalently bound onto the multi-wall carbon nanotubes functionalized with amino groups (AMWNTs) to achieve Fc-AMWNTs conjugate. The cyclic voltammetry were used to characterize the nanocomposites. Here, Fc-AMWNTs were applied to construct glucose biosensors with IO4--oxidized glucose oxidase (IO4--oxidized GOx) through the covalent assembly method without any cross-linker. The presence of both ferrocene as mediator of electron transfer and MWNTs as conductor enhanced greatly the electrocatalytic response toward the glucose. Furthermore, our enzyme electrodes

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7

Subramanian, Ranga, Chandana Karunatilaka, Riley O. Schock, Brian J. Drouin, Paul A. Cassak, and Stephen G. Kukolich. "Determination of structural parameters for ferrocenecarboxaldehyde using Fourier transform microwave spectroscopy." Journal of Chemical Physics 123, no. 5 (2005): 054317. http://dx.doi.org/10.1063/1.1993593.

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8

Bhaswati, Bhattacharyya, and Dhara Kaliprasanna. "Highly efficient, mild, one pot synthesis of 2-substituted benzimidazoles, benzothiazoles and pyridoimidazoles promoted by N-iodosuccinimide." Journal of Indian Chemical Society Vol. 90, Oct 2013 (2013): 1749–59. https://doi.org/10.5281/zenodo.5791892.

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Department of Chemistry, Hooghly Mohsin College, Hooghly-712 101, West Bengal, India Department of Chemistry, University College of Science & Technology, University of Calcutta, Kolkata-700 009, India <em>E-mail </em>: kali.dhara@gmail.com <em>Manuscript received 07 June 2013, accepted 13 June 2013</em> A common and highly efficient metal-free route for the synthesis of 2-substituted benzimidazoles, benzothiazoles and pyridoimidazoles from suitable 1,2-difunctionalised aromatic compounds and various aromatic and aliphatic aldehydes and ferrocenecarboxaldehyde was developed using N-iodosucc

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9

Štěpnička, Petr, and Tomáš Baše. "Preparation and structures of 1′-(diphenylphosphino)ferrocenecarboxaldehyde and {1′-(diphenylphosphino)ferrocenyl}methanol." Inorganic Chemistry Communications 4, no. 11 (2001): 682–87. http://dx.doi.org/10.1016/s1387-7003(01)00298-2.

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10

Xu, C., H. Cai, P. He, and Y. Fang. "Ferrocenecarboxaldehyde labeled DNA probe for the study on DNA damage and protection." Fresenius' Journal of Analytical Chemistry 367, no. 6 (2000): 593–95. http://dx.doi.org/10.1007/s002160000414.

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11

Lewkowski, Jarosław. "The unusual stereochemical behaviour of ferrocenecarboxaldehyde in reaction with chiral alkylammonium hypophosphite." Journal of Organometallic Chemistry 681, no. 1-2 (2003): 225–27. http://dx.doi.org/10.1016/s0022-328x(03)00620-x.

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12

Xiong, Guo Xuan, Hai Qing Huang, and Chuo Yang. "A Novel Poly(Ferrocenyl-Schiff Base) and its Charge Transfer Complex with Iodine." Advanced Materials Research 97-101 (March 2010): 634–37. http://dx.doi.org/10.4028/www.scientific.net/amr.97-101.634.

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A ferrocenyl Schiff base monomer was synthesized through the condensation of ferrocenecarboxaldehyde and phenylenediamine under neutral conditions, and then been used to produce copolymer materials with terephthaloyl chloride monomer by the Friedel-Crafts method. The model compound and copolymer of a novel poly(ferrocene-Schiff base) and their charge transfer complex with iodine was successful obtained, their structures been characterized by 1H-NMR spectra, infrared spectra, and ultraviolet spectra. In addition, the effects of iodine doping degree on its structure was studied, the electrical m

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13

Cooke, Graeme, Helen M. Palmer, and Olaf Schulz. "Novel Ferrocene Derivatives From Precursors Derived From Alumina-Catalysed Knoevenagel Reactions of Ferrocenecarboxaldehyde." Synthesis 1995, no. 11 (1995): 1415–18. http://dx.doi.org/10.1055/s-1995-4125.

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14

Kivrak, Arif, and Metin Zora. "Efficient one-pot synthesis of cyanoferrocene from ferrocenecarboxaldehyde using NH2OH·HCl/KI/ZnO/CH3CN system." Journal of Organometallic Chemistry 692, no. 11 (2007): 2346–49. http://dx.doi.org/10.1016/j.jorganchem.2007.02.002.

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15

Li, Hao, Hin-Soon Cheng, Ai-Hua Seow, and Teck-Peng Loh. "Diastereoselective allylation of planar chiral substituted ferrocenecarboxaldehyde: an efficient entry to chiral ferrocenyl ligands." Tetrahedron Letters 48, no. 12 (2007): 2209–11. http://dx.doi.org/10.1016/j.tetlet.2007.01.065.

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16

Enders, Dieter, René Lochtman, and Gerhard Raabe. "Enantioselective Synthesis of 1-Ferrocenylalkylamines via 1,2-Addition of Organolithium Compounds to Ferrocenecarboxaldehyde-SAMP-Hydrazone." Synlett 1996, no. 02 (1996): 126–28. http://dx.doi.org/10.1055/s-1996-5345.

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17

Fisher, Steven P., Rafael Ramos, Ryan H. Groeneman, John W. Kenney, and Eric W. Reinheimer. "Supramolecular interactions within a dual organometallic adduct based upon trimeric perfluoro-ortho-phenylenemercury and ferrocenecarboxaldehyde." Journal of Organometallic Chemistry 848 (October 2017): 239–42. http://dx.doi.org/10.1016/j.jorganchem.2017.08.005.

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18

COOKE, G., H. M. PALMER, and O. SCHULZ. "ChemInform Abstract: Novel Ferrocene Derivatives from Precursors Derived from Alumina- Catalyzed Knoevenagel Reactions of Ferrocenecarboxaldehyde." ChemInform 27, no. 10 (2010): no. http://dx.doi.org/10.1002/chin.199610240.

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19

Lasri, Jamal, Magda M. Aly, Naser Eltaher Eltayeb, and Bandar A. Babgi. "Synthesis of symmetrical and asymmetrical azines from hydrazones and/or ferrocenecarboxaldehyde as potential antimicrobial–antitumor agents." Journal of Molecular Structure 1164 (July 2018): 1–8. http://dx.doi.org/10.1016/j.molstruc.2018.03.030.

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20

Yao, Jiayu, Jian Wang, Zhongzhou Zhang, Fei Chen, and Yuhong Liu. "Ferrocenecarboxaldehyde modified terephthalaldehyde-phenolic resin: A comprehensive study on the synthesis, curing behavior, and pyrolysis process." Polymer 278 (June 2023): 125993. http://dx.doi.org/10.1016/j.polymer.2023.125993.

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21

Tajimi, Naomasa, Hikaru Sano, Kuniaki Murase, Kyung-Hwang Lee, and Hiroyuki Sugimura. "Thermal Immobilization of Ferrocene Derivatives on (111) Surface of n-Type Silicon: Parallel between Vinylferrocene and Ferrocenecarboxaldehyde." Langmuir 23, no. 6 (2007): 3193–98. http://dx.doi.org/10.1021/la062674e.

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22

Qin, Pei-yu, Wei Feng, Rui Wang та ін. "Theoretical investigation on the mechanism of ferrocenecarboxaldehyde-catalyzed direct β-alkylation of 1-phenylethanol with benzyl alcohol". Polyhedron 111 (червень 2016): 179–84. http://dx.doi.org/10.1016/j.poly.2016.03.031.

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23

ENDERS, D., R. LOCHTMAN, and G. RAABE. "ChemInform Abstract: Enantioselective Synthesis of 1-Ferrocenylalkylamines via 1,2-Addition of Organolithium Compounds to Ferrocenecarboxaldehyde-SAMP-Hydrazone." ChemInform 27, no. 25 (2010): no. http://dx.doi.org/10.1002/chin.199625177.

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24

Ashraf, Hashim, Ayesha Qamar, and Nikhil Maheshwari. "Attenuation of hexaconazole induced oxidative stress by folic acid, malic acid and ferrocenecarboxaldehyde in an invertebrate model Bombyx mori." Heliyon 8, no. 12 (2022): e12577. http://dx.doi.org/10.1016/j.heliyon.2022.e12577.

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25

Tice, Nathan C., Sean Parkin, and John P. Selegue. "Synthesis, characterization and crystal structures of boron-containing intermediates in the reductive amination of ferrocenecarboxaldehyde to a bis(ferrocenylmethyl) amine." Journal of Organometallic Chemistry 692, no. 4 (2007): 791–800. http://dx.doi.org/10.1016/j.jorganchem.2006.10.015.

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26

Herrick, Richard S., Christopher J. Ziegler, Melissa Precopio, Kerianne Crandall, Janet Shaw, and Ronald M. Jarret. "Synthesis of tungsten compounds with Schiff base ligands prepared from ferrocenecarboxaldehyde: Observation of the migration of an imine double bond." Journal of Organometallic Chemistry 693, no. 4 (2008): 619–24. http://dx.doi.org/10.1016/j.jorganchem.2007.11.046.

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27

Perchikov, Roman N., Daria V. Provotorova, Anna S. Kharkova, et al. "Bioanalytical System for Determining the Phenol Index Based on Pseudomonas putida BS394(pBS216) Bacteria Immobilized in a Redox-Active Biocompatible Composite Polymer “Bovine Serum Albumin–Ferrocene–Carbon Nanotubes”." Polymers 14, no. 24 (2022): 5366. http://dx.doi.org/10.3390/polym14245366.

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The possibility of using the microorganisms Pseudomonas sp. 7p-81, Pseudomonas putida BS394(pBS216), Rhodococcus erythropolis s67, Rhodococcus pyridinivorans 5Ap, Rhodococcus erythropolis X5, Rhodococcus pyridinivorans F5 and Pseudomonas veronii DSM 11331T as the basis of a biosensor for the phenol index to assess water environments was studied. The adaptation of microorganisms to phenol during growth was carried out to increase the selectivity of the analytical system. The most promising microorganisms for biosensor formation were the bacteria P. putida BS394(pBS216). Cells were immobilized i

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28

Mendoza-Morales, William O., Esteban Rodríguez, Aliana González, et al. "Synthesis, Structure, Electrochemistry, and In Vitro Anticancer and Anti-Migratory Activities of (Z)- and (E)-2-Substituted-3-Ferrocene-Acrylonitrile Hybrids and Their Derivatives." Molecules 30, no. 13 (2025): 2835. https://doi.org/10.3390/molecules30132835.

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In this study, a series of (Z)- and (E)-2-substituted-3-ferrocene-acrylonitrile derivatives were synthesized, characterized, and evaluated in vitro for their anticancer and anti-migration properties. The compounds were synthesized via the Knoevenagel condensation of the appropriate benzyl cyanide or benzoyl acetonitrile with ferrocenecarboxaldehyde 1, producing isolated yields of 99 to 23%. The structures of the compounds were analyzed using IR, 1H NMR, 13C{1H} NMR, GC-MS, and UV/Vis spectroscopic methods. Single-crystal X-ray diffraction analysis of representative compounds 21, 27, and 29 dem

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29

Lasri, Jamal, Abeer S. Elsherbiny, Naser Eltaher Eltayeb, Matti Haukka, and Mohamed E. El-Hefnawy. "Synthesis and characterization of ferrocene-based Schiff base and ferrocenecarboxaldehyde oxime and their adsorptive removal of methyl blue from aqueous solution." Journal of Organometallic Chemistry 866 (July 2018): 21–26. http://dx.doi.org/10.1016/j.jorganchem.2018.04.004.

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30

Houlton, Andrew, John R. Miller, Jack Silver, et al. "Molecular materials for non-linear optics. Second harmonic generation and the crystal and molecular structure of the 4-nitrophenylimine of ferrocenecarboxaldehyde." Inorganica Chimica Acta 205, no. 1 (1993): 67–70. http://dx.doi.org/10.1016/s0020-1693(00)87356-9.

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31

Mousa, Aya Osama, Cheng-Hsin Chuang, Shiao-Wei Kuo, and Mohamed Gamal Mohamed. "Strategic Design and Synthesis of Ferrocene Linked Porous Organic Frameworks toward Tunable CO2 Capture and Energy Storage." International Journal of Molecular Sciences 24, no. 15 (2023): 12371. http://dx.doi.org/10.3390/ijms241512371.

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This work focuses on porous organic polymers (POPs), which have gained significant global attention for their potential in energy storage and carbon dioxide (CO2) capture. The study introduces the development of two novel porous organic polymers, namely FEC-Mel and FEC-PBDT POPs, constructed using a simple method based on the ferrocene unit (FEC) combined with melamine (Mel) and 6,6′-(1,4-phenylene)bis(1,3,5-triazine-2,4-diamine) (PBDT). The synthesis involved the condensation reaction between ferrocenecarboxaldehyde monomer (FEC-CHO) and the respective aryl amines. Several analytical methods

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32

Juan, Prakash Naskar, Biswas Chiranjan, Chanda Sumana, Z. Slawin A.M., and Bhattacharya Rahul. "A ferrocene tagged novel organic moiety Synthesis, crystal structure and electrochemical aspects." Journal of Indian Chemical Society Vol. 87, Oct 2010 (2010): 1159–65. https://doi.org/10.5281/zenodo.5804819.

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Department of Chemistry, Jadavpur University, Kolkata-700 032, India <em>E-mail:</em> jpnaskar@hotmail.com Fax : 91-33-24146223 Kalikamala Vidyapith for Girls, 124, Raja R .L. Mitra Road, Kolkata-700 010, India School of Chemistry, University of St. Andrews, Fife, KY16 9ST, UK lndian Chemical Society, 92, Acharya Prafulla Chandra Road, Kolkata-700 009, India <em>E-mail:</em> hllrahul@yahoo.com <em>Manuscript received 26 November 2009, revised 28 January 2010, accepted 19 March 2010</em> Reaction of 2-(2-aminoethyl)pyridine (L) with ferrocenecarboxaldehyde (FCAL) in toluene gives rise to LH, th

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33

Fukuda, Tsutomu, Akihiro Takehara, Naoto Haniu, and Masatomo Iwao. "Synthesis of chiral primary 1-ferrocenylalkylamines via highly diastereoselective addition of organolithium compounds to ferrocenecarboxaldehyde imine derived from (S)-2-methoxy-1-phenylethylamine." Tetrahedron: Asymmetry 11, no. 20 (2000): 4083–91. http://dx.doi.org/10.1016/s0957-4166(00)00398-0.

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34

Kimura, Takayuki, Ryohei Shoda, Nobukazu Taniguchi, Ken Kamikawa та Motokazu Uemura. "Asymmetric synthesis of β-amino alcohol by reductive cross-coupling of planar chiral ferrocenecarboxaldehyde with N-tosyl ferrocenylideneamine, and its application to asymmetric reaction". Inorganica Chimica Acta 357, № 6 (2004): 1829–35. http://dx.doi.org/10.1016/j.ica.2003.12.030.

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35

Taniguchi, Nobukazu, and Motokazu Uemura. "Stereoselective pinacol coupling of planar chiral (benzaldehyde)Cr(CO)3, (benzaldimine)Cr(CO)3, ferrocenecarboxaldehyde and (dienal)Fe(CO)3 complexes with samarium diiodide." Tetrahedron 54, no. 42 (1998): 12775–88. http://dx.doi.org/10.1016/s0040-4020(98)00778-9.

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36

Fukuda, Tsutomu, Akihiro Takehara, Naoto Haniu, and Masatomo Iwao. "ChemInform Abstract: Synthesis of Chiral Primary 1-Ferrocenylalkylamines via Highly Diastereoselective Addition of Organolithium Compounds to Ferrocenecarboxaldehyde Imine Derived from (S)-2-Methoxy-1-phenylethylamine." ChemInform 32, no. 12 (2001): no. http://dx.doi.org/10.1002/chin.200112177.

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37

TANIGUCHI, N., and M. UEMURA. "ChemInform Abstract: Stereoselective Pinacol Coupling of Planar Chiral (Benzaldehyde)Cr(CO)3, (Benzaldimine)Cr(CO)3, Ferrocenecarboxaldehyde, and (Dienal)Fe(CO)3 Complexes with Samarium Diiodide." ChemInform 30, no. 5 (2010): no. http://dx.doi.org/10.1002/chin.199905038.

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38

Kharkova, Anna S., Anastasia S. Medvedeva, Lyubov S. Kuznetsova, et al. "A “2-in-1” Bioanalytical System Based on Nanocomposite Conductive Polymers for Early Detection of Surface Water Pollution." Polymers 16, no. 10 (2024): 1431. http://dx.doi.org/10.3390/polym16101431.

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This work proposes an approach to the formation of receptor elements for the rapid diagnosis of the state of surface waters according to two indicators: the biochemical oxygen demand (BOD) index and toxicity. Associations among microorganisms based on the bacteria P. yeei and yeast S. cerevisiae, as well as associations of the yeasts O. polymorpha and B. adeninivorans, were formed to evaluate these indicators, respectively. The use of nanocomposite electrically conductive materials based on carbon nanotubes, biocompatible natural polymers—chitosan and bovine serum albumin cross-linked with fer

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39

Riant, Olivier, Odile Samuel, Timo Flessner, Stephan Taudien, and Henri B. Kagan. "An Efficient Asymmetric Synthesis of 2-Substituted Ferrocenecarboxaldehydes." Journal of Organic Chemistry 62, no. 20 (1997): 6733–45. http://dx.doi.org/10.1021/jo970075u.

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40

García, Jasón, Albert Moyano, and Malgorzata Rosol. "An efficient, general synthesis of racemic 2-substituted ferrocenecarboxaldehydes." Tetrahedron 63, no. 9 (2007): 1907–12. http://dx.doi.org/10.1016/j.tet.2007.01.003.

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41

RIANT, O., O. SAMUEL, T. FLESSNER, S. TAUDIEN, and H. B. KAGAN. "ChemInform Abstract: An Efficient Asymmetric Synthesis of 2-Substituted Ferrocenecarboxaldehydes." ChemInform 29, no. 8 (2010): no. http://dx.doi.org/10.1002/chin.199808156.

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42

Taniguchi, Nobukazu, та Motokazu Uemura. "Planar chiral C2-symmetric bisferrocenes: Stereoselective pinacol coupling of α-substituted ferrocenecarboxaldehydes". Tetrahedron Letters 39, № 30 (1998): 5385–88. http://dx.doi.org/10.1016/s0040-4039(98)01080-6.

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43

Cano, Juan, Angel Benito, Ramón Martínez-Máñez, et al. "Ferrocene containing chelating ligands 3. Synthesis, spectroscopic characterization, electrochemical behaviour and interaction with metal ions of new ligands obtained by condensation of ferrocenecarboxaldehyde with 2-amino-benzoic acid derivatives. Crystal structures of 2-ferrocenylmethylamino-5-methyl-benzoic acid and 2-bis(ferrocenylmethyl)ammonium-5-methyl-benzoic acid perchlorate." Inorganica Chimica Acta 231, no. 1-2 (1995): 45–56. http://dx.doi.org/10.1016/0020-1693(94)04318-p.

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44

Janowska, Izabela, and Janusz Zakrzewski. "Circular dichroism spectra of planar chiral 2-substituted ferrocenecarboxaldehydes and 2-ferrocenyl-1,1-dicyanoethylenes." Tetrahedron: Asymmetry 14, no. 21 (2003): 3271–73. http://dx.doi.org/10.1016/j.tetasy.2003.09.005.

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45

TANIGUCHI, N., та M. UEMURA. "ChemInform Abstract: Planar Chiral C2-Symmetric Bisferrocenes: Stereoselective Pinacol Coupling of α-Substituted Ferrocenecarboxaldehydes." ChemInform 29, № 42 (2010): no. http://dx.doi.org/10.1002/chin.199842170.

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46

Taniguchi, Nobukazu, та Motokazu Uemura. "Asymmetric Synthesis of β-Amino Alcohols by Cross-Pinacol Coupling of Planar Chiral Ferrocenecarboxaldehydes with Imines". Journal of the American Chemical Society 122, № 34 (2000): 8301–2. http://dx.doi.org/10.1021/ja000479v.

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47

Mamane, Victor. "The diastereoselective ortho-lithiation of Kagan’s ferrocenyl acetal. Generation and reactivity of chiral 2-substituted ferrocenecarboxaldehydes." Tetrahedron: Asymmetry 21, no. 9-10 (2010): 1019–29. http://dx.doi.org/10.1016/j.tetasy.2010.03.012.

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48

Mamane, Victor. "ChemInform Abstract: The diastereoselective ortho-Lithiation of Kagan′s Ferrocenyl Acetal. Generation and Reactivity of Chiral 2-Substituted Ferrocenecarboxaldehydes." ChemInform 41, no. 46 (2010): no. http://dx.doi.org/10.1002/chin.201046218.

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49

Li, Hao, Hin-Soon Cheng, Ai-Hua Seow, and Teck-Peng Loh. "Diastereoselective Allylation of Planar Chiral Substituted Ferrocenecarboxaldehyde: An Efficient Entry to Chiral Ferrocenyl Ligands." ChemInform 38, no. 27 (2007). http://dx.doi.org/10.1002/chin.200727150.

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50

Cinar, Seda, and Ozge Surucu. "Preparation of poly(5‐ferrocenyl‐dipyrromethane) as sensor for electrochemical removal of aluminum and barium ions in real water samples." Applied Organometallic Chemistry, July 29, 2024. http://dx.doi.org/10.1002/aoc.7657.

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In this work, 5‐ferrocenyl‐dipyrromethane (Fc‐DPM) synthesized from the pyrrole and ferrocenecarboxaldehyde condensation was electrochemically deposited on a gold (Au) electrode and used to remove metal ions found in rural waters. The structural analysis of Fc‐DPM was recorded by means of nuclear magnetic resonance (NMR) techniques. The Fc‐DPM was electrochemically coated on an indium tin oxide‐polyethylene terephthalate (ITO‐PET) surface, and the resulting Fc‐DPM/ITO‐PET was characterized using scanning electron microscopy (SEM)–energy dispersive X‐ray (EDX) analysis. The heavy metal and mine

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