Sintesis, Karakterisasi, dan Potensi Pengaplikasian Kompleks Koordinasi Zn(II) sebagai Sensor Fluoresensi
Main Article Content
Abstract
Peningkatan aktivitas industri telah mendorong meningkatnya pencemaran lingkungan oleh ion logam berat, sehingga diperlukan metode analisis yang sensitif, selektif, dan efisien. Sensor fluoresensi berbasis senyawa kompleks logam menjadi alternatif yang menjanjikan dibandingkan metode konvensional seperti AAS dan FTIR yang memiliki keterbatasan biaya dan portabilitas. Jurnal review ini membahas pengembangan dan potensi kompleks koordinasi Zn(II)–8-hidroksikuinolin sebagai sensor fluoresensi, dengan fokus pada aspek sintesis, karakterisasi, mekanisme fluoresensi, serta aplikasinya. Ion Zn(II) dipilih karena konfigurasi elektron d¹⁰ yang bersifat non-quenching, stabil, relatif tidak toksik, dan ramah lingkungan. Ligan 8-hidroksikuinolin berperan sebagai ligan bidentat melalui atom nitrogen dan oksigen, membentuk khelat stabil yang meningkatkan intensitas fluoresensi melalui mekanisme chelation-enhanced fluorescence (CHEF). Review ini menunjukkan bahwa variasi pelarut mempengaruhi efisiensi pembentukan kompleks, yang dibuktikan melalui karakterisasi FTIR dan AAS. Berbagai studi juga mengonfirmasi aplikasi kompleks Zn(II)–8-hidroksikuinolin dalam sensor ion logam, material fluoresen, sistem polimer, hingga aplikasi biomedis dan OLED. Dengan demikian, kompleks ini memiliki potensi besar sebagai material sensor fluoresensi yang sensitif, selektif, dan berkelanjutan
Downloads
Article Details
Issue
Section

This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
References
Abendrot, M., Checinska, L., Kusz, J., Lisowska, K., Zawadzka, K., Felczak, A., & Kalinowska-Lis, U. (2020). Zinc(II) Complexes with Amino Acids for Potential Use in Dermatology: Synthesis, Crystal Structures, and Antibacterial Activity 2 ,. Molecules, 25(Ii), 951. https://pmc.ncbi.nlm.nih.gov/articles/PMC7070670/pdf/molecules-25-00951.pdf
Asmorowati, D. S., Azmi, K. U., & Sumarti, S. (2025). Optimization of the AAS Method with Variations in Air Speed, Wavelength, and Light Current. Indonesian Journal of Chemical Science, 14(2).
Bronson, R., Montalti, M., Prodi, L., Zaccheroni, N., Lamb, R., Dalley, N., Izatt, R., Bradshaw, J., & Savage, P. (2004). Origins of “on—off” Fluorescent Behavior of 8-Hydroxyquinoline Containing Chemosensors. Tetrahedron, 60, 11139–11144. https://doi.org/10.1016/j.tet.2004.08.062
Chen, Y., & Zhang, W. (2021). Synthesis, Characterization and Fluorescence Property of a New Zinc(II) Complex Based on 2,6-Bis(imino)pyridyl Ligand. Journal of Chemical Crystallography, 51(1), 132–138. https://doi.org/10.1007/s10870-020-00828-3
Cipurković, A., Horozić, E., Marić, S., Mekić, L., & Junuzović, H. (2021). Metal Complexes with 8-Hydroxyquinoline : Synthesis and In Vitro Antimicrobial Activity. 1–10. https://doi.org/10.4236/ojapps.2021.111001
Côrte-Real, L., Pósa, V., Martins, M., Colucas, R., May, N. V., Fontrodona, X., Romero, I., Mendes, F., Reis, C. P., Gaspar, M. M., Pessoa, J. C., Enyedy, E. A., & Correia, I. (2023). Cu ( II ) and Zn ( II ) Complexes of New 8 ‑ Hydroxyquinoline Schiff Bases : Investigating Their Structure , Solution Speciation , and Anticancer Potential. Inorganic Chemistry, 62, 11466–11486. https://doi.org/10.1021/acs.inorgchem.3c01066
Dash, A. C., & Dash, N. (1987). Effect of Solvent on the Reactions. 83(8), 2505–2514.
Diana, R., & Panunzi, B. (2020). The Role of Zinc ( II ) Ion in Fluorescence Tuning of Tridentate Pincers : A Review. Molecules, 25.
Fakhruddin, M. M., & Dyah, P. (2024). Kajian Pemanfaatan Tailing Pengolahan Emas Untuk Pembuatan Batako Sebagai Aplikasi Zero Waste Material Di PT Global Minerallium Corporindo Kecamatan Batu Sopang Provinsi Kalimantan Timur. Jurnal Penelitian Rumpun Ilmu Teknik (JUPRIT), 3(1), 149–166.
Gao, B., Fang, L., Zhang, R., & Men, J. (2013). Synthesis and luminescence properties of polymeric complexes of Cu(II), Zn(II) and Al(III) with 8-hydroxyquinoline side group-containing polysulfone. Synthetic Metals, 165, 27–34. https://doi.org/https://doi.org/10.1016/j.synthmet.2012.12.031
Heredia-moya, J., Fiallos-ayala, A., & Cevallos-vallejo, A. (2025). Phenylthiadiazole-Based Schiff Base Fluorescent Chemosensor for the Detection of Al 3 + and Zn 2 + Ions. Chemistry, 7, 1–16.
Hermawati, E. S., Suhartana, & Taslimah. (2016). Jurnal Kimia Sains dan Aplikasi Sintesis dan Karakterisasi Senyawa Kompleks Zn ( II ) -8-. Jurnal Kimia Sains Dan Aplikasi, 19(3), 94–98.
Hu, Y., Du, L., & Yang, J. (2020). A highly sensitive and selective chemosensors for detection of Zn2+ and its application in live cell imaging. Inorganica Chimica Acta, 509, 119675. https://doi.org/https://doi.org/10.1016/j.ica.2020.119675
Huang, Q., Hu, T., Changlu, Z., Jin, B., & Peng, R. (2022). New approach to synthesis Zinc(II)-(8-hydroxyquinoline) complex and its luminescent property. Optical Materials, 134, 113163. https://doi.org/10.1016/j.optmat.2022.113163
Jabłońska-Wawrzycka, A., Rogala, P., Czerwonka, G., & Hodorowicz, M. (2025). Chloride and Acetonitrile Ruthenium ( IV ) Complexes : Crystal Architecture , Chemical Characterization , Antibiofilm Activity , and Bioavailability in Biological Systems. Molecules, 30(3), 1–28.
Kamel, R. M., El, S. S., Maram, S., & Soliman, M. A. A. M. H. A. (2024). Eco-friendly Fluorescent Sensor for Sensitive and Selective Detection of Zn 2 + and Fe 3 + Ions : Applications in Human Hair Samples. Journal of Fluorescence, 35(6), 4213–4224. https://doi.org/10.1007/s10895-024-03798-3
Khan, M., Izhar, D. U., Madiha, A., Huma, M., Batool, F., Jan, M., & Fayaz, M. (2025). Global Research journal of Natural Science and Technology ( Grjnst ) Synthesis and characterization of Cu ( II ), Zn ( II ), Cd ( II ), and Mn ( II ) Complexes with heterocyclic N-donor ligands and carboxylic acid derivatives and their antibacterial activ. Global Research Journal of Natural Science and Technology (Grjnst), 3(4). https://doi.org/10.53762/grjnst.03.04.22
Kong, M., Xing, F., & Zhu, S. (2022). A new tripodal 8-hydroxyquinoline as a high sensitivity fluorescence sensor for Zn(II) in ethanol and its two morphology in solid. Inorganic Chemistry Communications, 141, 109530. https://doi.org/https://doi.org/10.1016/j.inoche.2022.109530
Li, Y., Zhang, M., Wang, Y., Guan, L., Zhao, D., Hao, X., & Guo, Y. (2024). A Zn ( II ) Coordination Polymer for Fluorescent Turn-Off. Molecules, 29(2943). https://doi.org/10.3390/molecules29122943
Manna, D., Lo, R., Miriyala, V. M., Nachtigallová, D., Trávníček, Z., & Hobza, P. (2024). Impact of dielectric constant of solvent on the formation of transition metal-ammine complexes. Journal of Computational Chemistry, 45(4), 204–209. https://doi.org/10.1002/jcc.27230
Nguyen, T.-C.-T., Huynh, T.-K.-C., Truong, H. B., Nguyen, T.-H.-A., Nguyen, H., Ton, A.-K., Nguyen, V.-T., & Thi-Hong-No Nguyen, and T.-K. H. (2024). Rapid and Efficient Dual Detection Of Zn2+ Ions and Oxytetracycline Hydrochloride Using a Responsive Fluorescent “On-Off” Sensor Based on Simple Salen-Type Schiff Base Ligand. Chemistry – An Asian Journal, 19(23). https://doi.org/10.1002/asia.202400636
Paul, J. J., Sai, K., Ganesan, R., Jha, P., Venkata, K., Chandra, G., & Sindhu, S. (2025). Zinc based organic metal complexes for OLED applications. Synthetic Metals, 316(June 2025), 117980. https://doi.org/10.1016/j.synthmet.2025.117980
Payehghadr, M., & Hashemi, S. (2017). Solvent effect on complexation reactions. Journal of Inclusion Phenomena and Macrocyclic Chemistry, 89. https://doi.org/10.1007/s10847-017-0759-8
Prachayasittikul, V., Prachayasittikul, S., Ruchirawat, S., & Prachayasittikul, V. (2013). 8-Hydroxyquinolines : a review of their metal chelating properties and medicinal applications. Drug Design, Development and Therapy, 7, 1157–1178. https://doi.org/10.2147/DDDT.S49763
Rohini, Paul, K., & Luxami, V. (2020). 8-Hydroxyquinoline Fluorophore for Sensing of Metal Ions and Anions. THE CHEMICAL RECORD, 20(1), 1–45. https://doi.org/10.1002/tcr.202000082
Sari, N. W., Fajri, M., Terpadu, L., Unggul, U. E., Barat, J., & Jeruk, K. (2018). ANALISIS FITOKIMIA DAN GUGUS FUNGSI DARI EKSTRAK ETANOL PISANG Pendahuluan Metodologi Penelitian Waktu dan TempatPenelitian Alat dan Bahan Persiapan Sampel Ekstraksi Pemeriksaan Alkaloid Pemeriksaan Flavonoid. Indonesian Journal of Biotechnology and Biodiversity, 2(1), 30–34.
Silvia, L., Rosyidah, K. C., & Zainuri, M. (2013). Pengaruh Ion Doping Zn pada Sifat Kemagnetan Barium M-Heksaferit BaFe 12 − x Zn x O 19 berbasis Pasir Besi Tulungagung. JURNAL FISIKA DAN APLIKASINYA, 9(3), 121–124.
Singh, L. K., Karlo, T., & Pandey, A. (2014). Author ’ s personal copy Spectrochimica Acta Part A : Molecular and Biomolecular Spectroscopy Performance of fruit extract of Melastoma malabathricum L . as sensitizer in DSSCs. Spectrochimica Acta Part A : Molecular and Biomolecular Spectroscopy Performance of Fruit Extract of Melastoma Malabathricum L . as Sensitizer in DSSCs.
Tas, H., Namyslo, J. C., & Schmidt, A. (2021). RSC Advances Zn 2 + detection of a benzimidazole 8-. RSC Advances, 11(58), 36450–36458. https://doi.org/10.1039/D1RA05591G
Wang, D., Du, L.-H., Li, L., Yu-MengWei, TaoWang, Cheng, J., Du, B., Jia, Y., & Yu, B.-Y. (2023). Zn(II)-Based Mixed-Ligand-Bearing Coordination Polymers as Multi-Responsive Fluorescent Sensors for Detecting Dichromate, Iodide, Nitenpyram, and Imidacloprid. Polymers, 15(11). https://doi.org/10.3390/polym15112570
Wang, F., Peng, R., & Sha, Y. (2008). Selective dendritic fluorescent sensors for Zn(II). Molecules, 13(4), 922–930. https://doi.org/10.3390/molecules13040922
Wang, Y., Peng, X., Shi, J., Tang, X., Jiang, J., & Liu, W. (2012). Highly selective fluorescent chemosensor for Zn 2 + derived from inorganic-organic hybrid magnetic core / shell Fe 3 O 4 @ SiO 2 nanoparticles. Nanoscale Research Letters, 7(1), 1–13.