Volume-12, Issue-5, May 2026
1. Analysis of the Evolution and Influencing Factors of the Global Zirconium Ore Trade Pattern Based on Complex Networks
Authors: Li Kang
Keywords: global zirconium ore trade; complex networks; international trade networks; QAP analysis; influencing factors.
Page No: 01-14
Abstract
This paper examines the evolution of the global zirconium ore trade network using a matrix of bilateral trade relationships from 2014 to 2023, selecting 2014, 2017, 2020, and 2023 as cross-sectional years. Focusing on the countries that account for the top 80% of the global zirconium ore trade volume, this study employs the Quadratic Assignment Procedure (QAP) to systematically analyze the key factors driving trade volumes and their temporal evolution across four dimensions: economic scale, factor endowments, geographical distance, and institutional quality. The study yields four main findings: (1) Overall, the network exhibits the characteristic of "expanding in scale but becoming increasingly sparse." While the number of participating countries has increased, network density and centrality have declined, and the network’s small-world properties have weakened under the influence of external shocks. (2) Trade flows are highly concentrated with a shifting center of gravity. China has emerged as a major transshipment hub with strong resource allocation capabilities, acting as the primary core of the network, while emerging hubs exemplified by the Netherlands have concurrently risen. (3) The community structure has evolved toward multipolarity and regionalization. It has gradually restructured from an early tripolar structure centered around China, Italy, and South Africa into a more decentralized multipolar configuration anchored by China, Spain, and South Africa, accompanied by frequent shifts in regional sub-centers. (4) The trade-driving mechanisms are characterized by a combination of economic complementarity and resource endowment orientation. QAP regression analysis reveals that differences in per capita GDP and urbanization levels are the primary positive drivers of bilateral trade. Furthermore, the zirconium ore trade has transcended the geographical distance and linguistic-cultural barriers typical of traditional gravity models, demonstrating the hallmark features of cross-regional, long-distance allocation. Conversely, disparities in government effectiveness and significant differences in economic size constitute barriers to trade.
Keywords: global zirconium ore trade; complex networks; international trade networks; QAP analysis; influencing factors.
References
- Cheng, J., Yi, J., & Wu, Q. (2021). Carbon neutrality, strategic emerging industry development and critical mineral management. China Population, Resources and Environment, 31(9), 135-142.
- Wang, A., & Yuan, X. (2022). Thoughts on the security of China's strategic critical mineral resources under the background of great power competition. Bulletin of Chinese Academy of Sciences, 37(11), 1550-1559.
- Zhang, S., Wang, Z., Li, Y., Mo, X., Dong, Q., Chen, C., ... Wang, Y. (2022). List, application and global pattern of critical minerals in China. Conservation and Utilization of Mineral Resources, 42(5), 138-168.
- Perks, C., & Mudd, G. (2019). Titanium, zirconium resources and production: A state of the art literature review. Ore Geology Reviews, 107, 629-646.
- Greenblatt, J. B., Brown, N. R., Slaybaugh, R., Wilks, T., Stewart, E., & McCoy, S. T. (2017). The future of low-carbon electricity. Annual Review of Environment and Resources, 42(1), 289-316.
- Xiong, X., Zeng, X., Zhang, Z., Pell, R., Matsubae, K., & Hu, Z. (2023). China's recycling potential of large-scale public transport vehicles and its implications. Communications Engineering, 2(1), 56.
- Zhu, X., Geng, Y., Gao, Z., Tian, X., Xiao, S., & Houssini, K. (2023). Investigating zirconium flows and stocks in China: A dynamic material flow analysis. Resources Policy, 80, 103139.
- Fahad, M., Waqar, A., & Kim, B. (2024). Effective-performance of inorganic and organic (barium zirconium titanate/polyvinylidene fluoride) piezoelectric composite for energy harvesting and self-powered smart IoT-based electronics. Journal of Alloys and Compounds, 985, 174033.
- Yu, S., Duan, H., & Cheng, J. (2021). An evaluation of the supply risk for China's strategic metallic mineral resources. Resources Policy, 70, 101891.
- Hayes, S. M., & McCullough, E. A. (2018). Critical minerals: A review of elemental trends in comprehensive criticality studies. Resources Policy, 59, 192-199.
- Silveira, J. W., & Resende, M. (2020). Competition in the international niobium market: A residual demand approach. Resources Policy, 65, 101564.
- Giese, E. C. (2022). Strategic minerals: Global challenges post-COVID-19. The Extractive Industries and Society, 12, 101113.
- Zhou, X., Zhang, H., Zheng, S., & Xing, W. (2022). The global recycling trade for twelve critical metals: Based on trade pattern and trade quality analysis. Sustainable Production and Consumption, 33, 831-845.
- Chen, W., Wang, L., & Jiang, Y. (2024). Spatiotemporal evolution and resilience characteristics of the global lithium resource trade network. Economic Geography, 44(10), 1-11.
- Li, Y., Zuo, Z., Cheng, J., & Xu, D. (2024). Evolutionary characteristics and structural dependence determinants of global lithium trade network: An industry chain perspective. Resources Policy, 99, 105381.
- Li, Y., Huang, J., Zeng, A., & Zhang, H. (2024). Trade risk transmission of global cobalt industrial chain based on multi-layer network. Resources Policy, 98, 105338.
- Yu, Y., Ma, D., & Zhu, W. (2023). Resilience assessment of international cobalt trade network. Resources Policy, 83, 103636.
- Zhang, H., Huang, X., Zhang, Y., & Wang, X. (2024). Demand shortage risk propagation mechanism in the multi-layer trade network of the global tungsten industry chain. Resources Science, 46(5), 948-959.
- Zheng, X., Li, H., Liu, X., Wang, X., Zhang, Y., Tang, Q., & Ren, B. (2025). Supply risk propagation in international trade networks of the tungsten industry chain. Humanities and Social Sciences Communications, 12(1), 54.
- Zhang, X., Wang, Q., Dang, N., Li, Y., Zhang, F., Zhang, Q., ... Xu, R. (2025). Evolutionary pattern and influencing factors of foreign trade in China's nickel industry chain. China Mining Magazine, 34(2), 232-243.
- Chen, W., Jiang, Y., & Liu, Z. (2025). Evolution and resilience of the global nickel resource trade network. World Regional Studies, 34(1), 1-15.
- Liao, Q., Xie, L., Han, J., & Zhang, X. (2025). Evolution of the global rare earth metal trade network pattern and supply crisis propagation. China Mining Magazine, 34(6), 26-37.
- Guo, Q., & Wang, Y. (2024). Rare earth trade dependence network structure and its impact on trade prices: An industry chain perspective. Resources Policy, 91, 104930.
- Lee, W., Fonseca, M. V. A., Qursillananda, Y., Koet, M., & Lee, S. (2026). Changes in international copper ore trading relationships due to the impact of COVID-19 pandemic: Based on social network analysis. Resources Policy, 112, 105794.
- Xiao, Q., & Li, J. (2022). Evolutionary characteristics of the spatial pattern of the global rice trade network and its enlightenment to China. Chinese Journal of Agricultural Resources and Regional Planning, 43(12), 1-8.
- Liu, Y., & Liu, H. (2024). Dynamic evolution and driving factors of the international oil trade network. Resources Science, 46(9), 1852-1866.
- Wang, X. Y., Chen, B., & Song, Y. (2025). Dynamic change of international arms trade network structure and its influence mechanism. International Journal of Emerging Markets, 20(2), 660-677.
- Guo, Y., Zhao, B., & Zhang, H. (2023). The impact of the Belt and Road Initiative on the natural gas trade: A network structure dependence perspective. Energy, 263, 125912.
- Gephart, J. A., Rovenskaya, E., Dieckmann, U., Pace, M. L., & Brännström, Å. (2016). Vulnerability to shocks in the global seafood trade network. Environmental Research Letters, 11(3), 035008.
- Luo, F., Liu, W., Xu, M., Liu, Q., & Wang, J. (2025). Evolution characteristics and invulnerability simulation analysis of global zirconium ore trade network. Frontiers in Earth Science, 12, 1496579.
2. Real-Time Environmental Data Collector with Energy Harvesting and Intelligent Sensing for Marine Applications
Authors: Dr Heng Kok Hui John Gerard; Yew Zi Hon
Keywords: Underwater data collector, vertical profiler, energy harvesting, real-time environmental data, ocean acoustics, CTD sensors.
Page No: 15-18
Abstract
Underwater data collectors are devices designed to acquire information from beneath the ocean surface, providing valuable insight to subsurface conditions that are hard to measure by conventional surface instruments such as buoys and ship-based sensors.
The proposed data collector is optimized for Singapore waters and integrates an expanded sensor suite, including conductivity, temperature, and depth (CTD) sensors, a hydrophone, and an echosounder. The system is designed with a reduced size and weight (0.9 m length, 10.2 kg) compared to current underwater data collectors such as Argo floats (Argo: 1.3 m length, 40 kg) and has an extended deployment time of 10 years (~3500 profiles, assuming daily profiling), compared to 3–5 years (~100–200 profiles at 10-day cycles) for Argo systems. This extended operational lifespan is enabled by rechargeable batteries and solar energy harvesting.
The system architecture includes a buoyancy engine for depth control, sensor integration for data acquisition, power system design, and solar energy harvesting. The resulting data collector is lightweight, man-portable, and readily deployable. The sensor suite includes conductivity, temperature and depth sensors for inferring sound velocity of the ocean waters at that location and depth, an echosounder for determining seabed depth, and a hydrophone to listen to the ocean soundscape and for underwater sound pollution monitoring. Experimental validation demonstrates accurate sensor measurements, stable depth control, and effective solar energy harvesting, with example quantitative results provided in Section V.
The system is intended for the collection of oceanographic data, with an emphasis on real-time measurements of ocean conditions (data transmitted upon each surfacing). The enhanced data collector will facilitate oceanographic research by providing real-time data on ocean conditions, sound pollution monitoring and sediment movement information.
Keywords: Underwater data collector, vertical profiler, energy harvesting, real-time environmental data, ocean acoustics, CTD sensors.
References
- Asakawa, K., Watari, K., Ohuchi, H., Nakamura, M., Hyakudome, T., & Ishihara, Y. (2016). Buoyancy engine developed for underwater gliders. Advanced Robotics, *30*(1), 41–49. https://doi.org/10.1080/01691864.2015.1102647
- Erbe, C., Duncan, A., & Vigness-Raposa, K. J. (2022). Introduction to sound propagation under water. Springer.
- GO-BGC | Global Ocean Biogeochemistry Array. (2023, August). *GO-SHIP IO5: CTD casting | Describing one cycle of CTD casting* [Video]. https://www.go-bgc.org/expedition/indian-2023/ctd-casting
- Gould, J., Roemmich, D., Wijffels, S., Freeland, H., Ignaszewsky, M., Jianping, X., Pouliquen, S., Desaubies, Y., Send, U., Radhakrishnan, K., Takeuchi, K., Kim, K., Danchenkov, M., Sutton, P., King, B., Owens, B., & Riser, S. (2004). Argo profiling floats bring new era of in situ ocean observations. Eos, Transactions American Geophysical Union, *85*(19), 185–192.
- Intergovernmental Oceanographic Commission. (2010). The international thermodynamic equation of seawater – 2010: Calculation and use of thermodynamic properties. United Nations Educational, Scientific and Cultural Organization.
- International Electrotechnical Commission. (2021). *IEC 61215-2: Terrestrial photovoltaic (PV) modules – Design qualification and type approval – Part 2: Test procedures*.https://cdn.standards.iteh.ai/samples/101269/e9c169bfdf004586a8c0cf8bf9e2a625/IEC-61215-2-2021.pdf
- Mézo, T. L., Maillot, G. L., Ropert, T., Jaulin, L., Ponte, A., & Zerr, B. (2020). Design and control of a low-cost autonomous profiling float. Mechanics & Industry, *21*(5), Article 511.https://doi.org/10.1051/meca/2020037
- Saeed Al-Ali, A. G. O. M. M. (2025). A review of solar photovoltaic technologies: Developments, challenges, and future perspectives. Energy Conversion and Management: X, *27*, Article 101057. https://doi.org/10.1016/j.ecmx.2025.101057
- Wong, A. P. S., Wijffels, S. E., Riser, S. C., Pouliquen, S., Hosoda, S., Roemmich, D., Gilson, J., Johnson, G. C., Martini, K., Murphy, D. J., Scanderbeg, M., Bhaskar, T. V. S. U., Buck, J. J. H., Merceur, F., & Carval, T. (2020). Argo data 1999–2019: Two million temperature-salinity profiles and subsurface velocity observations from a global array of profiling floats. Frontiers in Marine Science, *7*, Article 700. https://doi.org/10.3389/fmars.2020.00700
- Yu, Y., Yang, Q., Ji, F., & Zhou, W. (2025). Research advances in energy management and harvesting technologies for autonomous profiling floats. Frontiers in Marine Science, *12*, Article 1598701. https://doi.org/10.3389/fmars.2025.1598701.
3. Conventional Route for Synthesis of Novel Heterocyclic 2-(Substituted-2-oxo-2H-chromen-3-yl)-3-(4-(2-(substituted-phenyl)-4,5-diphenyl-4,5-dihydro-1H-imidazol-1-yl)phenyl)-2-methylthiazolidin-4-one Derivatives and Their Antimicrobial Activity
Authors: Tandrani Ghosh; Sadhana Sing; Rishi kumar Vishnoi; Krishna Srivastavaa
Keywords: Benzil, thioglycolic acid, coumarin, acetoacetic ester, substituted salicylaldehyde, benzene-1,4-diamine, acetic acid.
Page No: 19-28
Abstract
Conventional routes were achieved for the synthesis of methylthiazolidin-4-one derivatives starting through reaction of substituted salicylaldehyde and acetoacetic ester, which gives acetyl-coumarin. Upon further reaction with benzene-1,4-diamine, it was converted into imine, subsequently cyclized into a thiazole-amine in the presence of thioglycolic acid. The final derivatives were cyclized by a three-component one-pot reaction of amine, substituted aldehyde, and ketone, yielding 2-(8-fluoro-2-oxo-2H-chromen-3-yl)-3-(4-(2-(4-hydroxy-3-methoxyphenyl)-4,5-diphenyl-4,5-dihydro-1H-imidazol-1-yl)phenyl)-2-methylthiazolidin-4-one derivatives. The structures of the novel synthesized derivatives were established by elemental analysis, UV, FT-IR, ¹H-NMR, and mass spectra. The obtained derivatives displayed excellent to moderate antimicrobial activity.
Keywords: Benzil, thioglycolic acid, coumarin, acetoacetic ester, substituted salicylaldehyde, benzene-1,4-diamine, acetic acid.
References
- Abbas, S. Y., Abd El-Aziz, M. M., Awad, S. M., & Mohamed, M. S. (2023). Synthesis and evaluation of antipyrine derivatives bearing a thiazole moiety as antibacterial and antifungal agents. Synthetic Communications, *53*(21), 1812–1822. https://doi.org/10.1080/00397911.2023.2248306
- Al-Ghamdi, H. A., Almughem, F. A., Alshabibi, M. A., Alsharif, A. A., & Almaghrabi, M. (2024). Synthesis and biological evaluation of novel imidazole derivatives as antimicrobial agents. Biomolecules, *14*(9), Article 1198. https://doi.org/10.3390/biom14091198
- Asif, M. (2017). A mini review: Biological significances of nitrogen hetero atom containing heterocyclic compounds. International Journal of Bioorganic Chemistry, *2*(4), 146–152.
- Aslam, K., Khosa, M. K., Jahan, N., & Nosheen, S. (2010). Synthesis and application of coumarin. Pakistan Journal of Pharmaceutical Sciences, *23*(4), 449–454.
- Bhatnagar, A., & Pemawat, G. (2023). An overview on synthetic routes of anti-inflammatory active scaffolds including thiazole and thiazolidine cores. Phosphorus, Sulfur, and Silicon and the Related Elements, *198*(7), 554–565. https://doi.org/10.1080/10426507.2023.2189253
- Gandioso, A., Palau, M., Bresolí-Obach, R., Galán, A., Rovira, A., & Nonell, S. (2018). High photostability in nonconventional coumarins with far-red/NIR emission through azetidinyl substitution. The Journal of Organic Chemistry, *83*(19), 11519–11531.
- Gupta, K., Sirbaiya, A. K., Kumar, V., & Rahman, M. A. (2022). Current perspective of synthesis of medicinally relevant benzothiazole based molecules: Potential for antimicrobial and anti-inflammatory activities. Mini-Reviews in Medicinal Chemistry, *22*(14), 1895–1935. https://doi.org/10.2174/1389557522666220217101805
- Gurav, S. S., Jadhav, S. R., Mali, S. N., Pawar, S. D., & Shinde, A. A. (2023). An efficient one-pot multicomponent Amberlite IR120(H) catalyzed microwave-assisted synthesis of 1,2,4,5-tetrasubstituted-1H-imidazoles: Plausible mechanism and antibacterial evaluation. Synthetic Communications, *53*(22), 2029–2040. https://doi.org/10.1080/00397911.2023.2267131
- Hemeda, L. R., El Hassab, M. A., Abdelgawad, M. A., Elsayed, Z. M., & Al-Warhi, T. (2023). Discovery of pyrimidine-tethered benzothiazole derivatives as novel anti-tubercular agents towards multi- and extensively drug resistant Mycobacterium tuberculosis. Journal of Enzyme Inhibition and Medicinal Chemistry, *38*(1), Article 2250575. https://doi.org/10.1080/14756366.2023.2250575
- Henary, M., Kananda, C., Rotolo, L., Savino, B., & Owens, E. A. (2020). Benefits and applications of microwave-assisted synthesis of nitrogen containing heterocycles in medicinal chemistry. RSC Advances, *10*, 14170–14197.
- Heravi, M., Sadjadi, S., Oskooie, H., Hekmat Shoar, R., & Bamoharram, F. F. (2008). The synthesis of coumarin-3-carboxylic acids and 3-acetyl-coumarin derivatives using heteropolyacids as heterogeneous and recyclable catalysts. Catalysis Communications, *9*(4), 470–474. https://doi.org/10.1016/j.catcom.2007.07.005
- Huang, W., Lu, Y., Yao, N., Li, Y., & Wang, S. (2024). A novel collapse strategy of zeolitic imidazole frameworks shell triggered by p-benzoquinone for the fluorescence monitoring α-glucosidase activity and screening natural anti-diabetes drug. Sensors and Actuators B: Chemical, *404*, Article 135234. https://doi.org/10.1016/j.snb.2023.135234
- Jun, J., Yang, S., Lee, J., Park, H., & Kim, H. (2023). Discovery of novel imidazole chemotypes as isoform-selective JNK3 inhibitors for the treatment of Alzheimer's disease. European Journal of Medicinal Chemistry, *245*, Article 114894. https://doi.org/10.1016/j.ejmech.2022.114894
- Mahesh, K. P., Swapnil, S. M., & Manikrao, M. S. (2001). Coumarin synthesis via Pechmann condensation in Lewis acidic chloroaluminate ionic liquid. Tetrahedron Letters, *42*(52), 9285–9287.
- Matos, M. J., Santana, L., Uriarte, E., & Borges, F. (2015). Coumarins—An important class of phytochemicals. In Phytochemicals: Isolation, characterisation and role in human health. InTech. https://doi.org/10.5772/59982
- Nagaraju, P., Reddy, P. N., Padmaja, P., & Ugale, V. G. (2021). Microwave-assisted synthesis of thiazole/benzothiazole fused pyranopyrimidine derivatives and evaluation of their biological activity. Letters in Organic Chemistry, *18*(1), 49–57. https://doi.org/10.2174/1570178617999200517130138
- Nandurkar, Y., Shinde, A., Bhoye, M. R., Pawar, S., & Pissurlenkar, R. R. S. (2023). Synthesis and biological screening of new 2-(5-aryl-1-phenyl-1H-pyrazol-3-yl)-4-aryl thiazole derivatives as potential antimicrobial agents. ACS Omega, *8*(9), 8743–8754. https://doi.org/10.1021/acsomega.2c08137
- O'Kennedy, R., & Thornes, R. D. (1997). Coumarins: Biology, applications and mode of action. Wiley.
- Olofson, A., Yakushijin, K., & Horne, D. A. (1998). Synthesis of marine sponge alkaloids oroidin, clathrodin and dispacamides: Preparation and transformation of 2-amino-4,5-dialkoxy-4,5-dihydroimidazolines from 2-aminoimidazoles. The Journal of Organic Chemistry, *63*(4), 1248–1253. https://doi.org/10.1021/jo9718298
- Othman, I. M. M., Alamshany, Z. M., Tashkandi, N. Y., Gad-Elkareem, M. A. M., & El-Naggar, M. (2022). Synthesis and biological evaluation of new derivatives of thieno-thiazole and dihydrothiazolo-thiazole scaffolds integrated with a pyrazoline nucleus as anticancer and multi-targeting kinase inhibitors. RSC Advances, *12*, 561–577. https://doi.org/10.1039/D1RA08055E
- Pawar, S., Karan, R., Rawal, R. K., & Gupta, P. K. (2024). Antimicrobial and antifungal evaluation of some novel thiazolidin-4-one scaffold bearing compounds. Letters in Applied NanoBioScience, *13*(4), Article 166. https://doi.org/10.33263/LIANBS134.166
- Pawar, S., Kumar, K., Gupta, M. K., & Rawal, R. K. (2021). Synthetic and medicinal perspective of fused-thiazoles as anticancer agents. Anti-Cancer Agents in Medicinal Chemistry, *21*(11), 1379–1402. https://doi.org/10.2174/1871520620666200728133017
- Petrou, A., Geronikaki, A., Kartsev, V., & Eleftheriou, P. (2023). N-Derivatives of (Z)-methyl 3-(4-oxo-2-thioxothiazolidin-5-ylidene)methyl)-1H-indole-2-carboxylates as antimicrobial agents—In silico and in vitro evaluation. Pharmaceuticals, *16*(1), Article 131. https://doi.org/10.3390/ph16010131
- Raghu, M. S., Pradeep Kumar, C. B., Yogesh Kumar, K., Prashanth, M. K., & Nagaraju, G. (2022). Design, synthesis and molecular docking studies of imidazole and benzimidazole linked ethionamide derivatives as inhibitors of InhA and antituberculosis agents. Bioorganic & Medicinal Chemistry Letters, *60*, Article 128604. https://doi.org/10.1016/j.bmcl.2022.128604
- Richaud, A., Barba-Behrens, N., & Méndez, F. (2011). Chemical reactivity of the imidazole: A semblance of pyridine and pyrrole? Organic Letters, *13*(5), 972–975. https://doi.org/10.1021/ol103011h
- Saliyeva, L., Holota, S., Grozav, A., & Lesyk, R. (2022). Synthesis and evaluation of antimicrobial and anti-inflammatory activity of 6-aryliden-2-methyl-2,3-dihydroimidazo[2,1-b][1,3]thiazoles. Biointerface Research in Applied Chemistry, *12*(1), 292–303. https://doi.org/10.33263/BRIAC121.292303
- Sattigeri, V. J., Soni, A., Singhal, S., & Pandya, S. (2005). Synthesis and antimicrobial activity of novel thiazolidinones. Arkivoc, *2005*(ii), 46–59.
- Shaabani, A., Ghadari, R., Rahmati, A., & Rezayan, A. H. (2009). Coumarin synthesis via Knoevenagel condensation reaction in 1,1,3,3-N,N,N′,N′-tetramethylguanidinium trifluoroacetate ionic liquid. Journal of the Iranian Chemical Society, *6*, 710–714. https://doi.org/10.1007/BF03246160
- Solo, P., Arockia Doss, M., & Prasanna, D. (2022). Designing and docking studies of imidazole-based drugs as potential inhibitors of myeloperoxidase mediated inflammation and oxidative stress. Biocatalysis and Agricultural Biotechnology, *43*, Article 102421. https://doi.org/10.1016/j.bcab.2022.102421
- Srivastava, K., Prakash, R., Singh, R. B., & Srivastava, A. (2023). Synthesis, characterization and antibacterial evaluation of novel β-lactam and thiazolidin-4-one derivatives having thiadiazinyl ring. Bulletin of Pharmaceutical Sciences, Assiut University, *46*(1), 203–216.
- Srivastava, K., Srivastava, A., Tiwari, R. P., & Singh, R. (2023). A facile synthesis, characterization and biological evaluation of novel spiro-thiazolidinone and quinazolinone-thiazolidine derivatives. Indian Journal of Chemistry, 62B(7), 770–779. https://doi.org/10.56042/ijc.v62i7.3830
- Tratrat, C., Petrou, A., Geronikaki, A., Kartsev, V., & Eleftheriou, P. (2022). Thiazolidin-4-ones as potential antimicrobial agents: Experimental and in silico evaluation. Molecules, *27*(6), Article 1930. https://doi.org/10.3390/molecules27061930
- Tsay, S. C., Hwu, J. R., Singha, R., & Shieh, S. (2013). Coumarins hinged directly on benzimidazoles and their ribofuranosides to inhibit hepatitis C virus. European Journal of Medicinal Chemistry, *63*, 290–293. https://doi.org/10.1016/j.ejmech.2013.02.008
- Verma, A., Joshi, S., & Singh, D. (2013). Imidazole: Having versatile biological activities. Journal of Chemistry, *2013*, Article 329412. https://doi.org/10.1155/2013/329412
- Wan, Y., Hur, W., Cho, C. Y., Liu, Y., & Cravatt, B. F. (2004). Synthesis and target identification of hymenialdisine analogs. Chemistry & Biology, *11*(2), 247–259. https://doi.org/10.1016/j.chembiol.2004.01.015
- Wang, J., Long, S., Liu, Z., & Zhang, Q. (2023). Structure-activity relationship studies of thiazole agents with potential anti methicillin-resistance Staphylococcus aureus activity. Process Biochemistry, *132*, 13–29. https://doi.org/10.1016/j.procbio.2023.06.013
- Zhao, C., Qiao, X., Yi, Z., Guan, Q., & Li, W. (2020). Active centre and reactivity descriptor of a green single component imidazole catalyst for acetylene hydrochlorination. Physical Chemistry Chemical Physics, *22*, 2849–2857. https://doi.org/10.1039/C9CP06005G.
4. Synthesis, Characterization and Antimicrobial Activities of Novel Heterocycles 8-(3-Chloro-2-(2-hydroxy-3-nitrophenyl)-4-oxoazetidin-1-yl)-4-methylpyrano[2,3-b]phenothiazin-2(11H)-one and 8-(4-(2-(3-Bromo-2-hydroxyphenyl)-3-chloro-4-oxoazetidin-1-yl)phenyl)-4-methylpyrano[2,3-b]phenothiazin-2(11H)-one Derivatives
Authors: Ayushi Sahu; Dolly Kumari; Rishi Kumar Vishnoi; Krishna Srivastava
Keywords: Phenothiazinone, acetoacetic ester, coumarin, benzidine, benzene-1,4-diamine, salicylaldehyde.
Page No: 29-41
Abstract
A convenient protocol for the synthesis of oxoazetidinyl-phenothiazinone derivatives has been initiated with the reaction of resorcinol and acetoacetic ester to yield coumarin. In another reaction, Schiff bases were prepared by the condensation of substituted-salicylaldehyde with benzidine and substituted-salicylaldehyde with benzene-1,4-diamine, subsequently cyclized with chloroacetyl chloride to form β-lactam-amine. Further, the amine reacted with coumarin in the presence of ZnCl₂ to form prefinal derivatives. The interaction of biphenylyl-azetidin-2-one or phenyl-azetidin-2-one with sulphur powder and iodine afforded the final phenothiazinone derivatives. The structures of the synthesized derivatives were determined by elemental analysis, UV-visible, FT-IR, ¹H-NMR, and mass spectra. The obtained derivatives exhibited excellent to moderate antimicrobial activity.
Keywords: Phenothiazinone, acetoacetic ester, coumarin, benzidine, benzene-1,4-diamine, salicylaldehyde.
References
- Kumar A, Sharma R. Bioorg Med Chem. 2014;22:3806.
- Nalawade AK, Kolhe PV. Eur J Chem. 2023;4:4.
- Amaral L, Viveiros M, Molnar J, Kristiansen JE. Expert Opin Drug Metab Toxicol. 2008;4:1337.
- Malmakova AE, Jones AM. Organics. 2025;6:46.
- Gershon S, Sakalis G, Bowers PA. J Clin Psychiatry. 1981;42:463.
- Kalkanidis M, Klonis N, Tilley L, Deady LW. Biochem Pharmacol. 2002;63:833.
- Kaatz GW, Moudgal VV, Seo SM, Kristiansen JE. Antimicrob Agents Chemother. 2003;47:719.
- Amaral L, Viveiros M, Kristiansen JE. Trop Med Int Health. 2001;6:1016.
- Al Zahrani NA, El-Shishtawy RM, Elaasser MM, Asiri AM. Molecules. 2020;25:4566.
- Sun-Waterhouse D, Chen J, Chuah C, Wibisono R, Melton LD, Laing WA, Ferguson LR, Skinner M. Int J Food Sci Nutr. 2009;60:251.
- Gwaram NS, Ali HM, Abdulla MA, Buckle MJC, Sukumaran SD, Chung LY, Othman R, Alhadi AA, Yehye WA, Hadi AHA. Molecules. 2012;17:2408.
- Gao S. Mini Rev Med Chem. 2010;10:550.
- Teixeira J, Silva T, Benfeito S, Gaspar A, Garrido J, Borges F. Eur J Med Chem. 2013;62:289.
- Liu N, Jin Z, Zhang J, Jin J. Invest New Drugs. 2018;37:188.
- Gao Y, Sun TY, Bai WF, Bai CG. Eur J Med Chem. 2019;183:111692.
- Luan Y, Liu J, Gao J, Wang J. Lett Drug Des Discov. 2019;17:57.
- Tlhapi D, Ramaite ID, Anokwuru CP, Van Ree T, Hoppe HC. Molecules. 2020;25:3781.
- Abramovič H, Grobin B, Ulrih NP, Cigić B. J Chem. 2018;2018:1.
- Pai Mangalore R, Peel TN, Udy AA, Peleg AY. J Antimicrob Chemother. 2023;78:2395.
- Wi YM, Choi JY, Lee DE, et al. Sci Rep. 2025;15:9785.
- Neu HC. Am J Med. 1985;79:2.
- Tooke CL, Hinchliffe P, Bragginton EC, et al. J Mol Biol. 2019;431:3472.
- Frère JM, Page MGP. Curr Opin Pharmacol. 2014;18:112.
- Pandey N, Cascella M. StatPearls. 2023.
- Bush K. Antimicrob Agents Chemother. 2018;62.
- Livermore DM. Clin Microbiol Rev. 1995;8:557.
- Karaiskos I, Galani I, Daikos GL, Giamarellou H. Antibiotics. 2025;14:528.
- Umar F, Chukwuekwe CP. Antimicrob Res New Insights. 2025.
- Srivastava K, Prakash R, Singh RB, Srivastava A, Vishnoi RK. Bull Pharm Sci Assiut Univ. 2023;46(1):203-216.
- Drăgan M, Stan CD, Iacob AT, Dragostin OM, Boancă M, Lupuşoru CE, Zamfir CL, Profire L. Processes. 2020;8(11):1-19.
- Drawz SM, Bonomo R. Clin Microbiol Rev. 2010;23(1):160-201.
- Fedorchenko TG, Lipunova GN, Shchepochkin AV, Tsmokalyuk AN, Slepukhin PA, Chupakhin ON. Mendeleev Commun. 2018;28(3):297-299.
- Mishra CB, Shalini S, Gusain S, Prakash A, Kumari J, Kumari S, Yadav AK, Lynn AM, Tiwari M. RSC Adv. 2020;10(30):17602-17619.
- Pang B, Wang M, Liu W. Nat Prod Rep. 2016;33(2):162-173.
- Agarwal N. Curr Chem Lett. 2021:119-138.
- Mishra I, Mishra R, Mujwar S, Chandra P, Sachan N. J Heterocyclic Chem. 2020;57:2304-2329.
- Vaidya A, Pathak D, Shah K. Chem Biol Drug Des. 2021;97:572-591.
- Singh PP, Bansal S, Rawat K, Pullabhotla VSR. Res J Chem Environ. 2021;25(5):48-61.
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