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Synthesis and Optical Characterization of a Novel Benzofuran-Based Molecule: 3-Amino-2-Pinacolone Benzofuran

Yıl 2025, Cilt: 15 Sayı: 2, 145 - 161, 31.12.2025
https://doi.org/10.37094/adyujsci.1810288
https://izlik.org/JA85UJ78PH

Öz

In the present study, a novel benzofuran-based compound, 3-amino-2-pinacolone benzofuran (APBF), was synthesized in high yield via the aldol condensation of 2-hydroxybenzonitrile with 1-chloropinacolone in the presence of potassium carbonate and acetonitrile. The structure of APBF was confirmed by FTIR and 1H, 13C-NMR spectroscopic analyses, which clearly defined its spectral characteristics. The UV–Vis absorption properties of APBF were comprehensively investigated to elucidate its photophysical behavior. Intense absorption bands were observed corresponding to π→π* transitions within the conjugated benzofuran framework, while the red-shifted bands were attributed to n→π* transitions arising from the carbonyl and amino functional groups. The APBF molecule exhibited excellent optical transparency in the higher wavelength region. Some optical dispersion parameters, including the single-oscillator energy, dispersion energy, oscillator strength, and oscillator wavelength were determined from the dispersion analysis. The optical band gap was found to be 3.311 eV indicating potential suitability of APBF for electro-optical applications. The relatively low Urbach energy (0.035 eV) indicated a well-ordered molecular structure with minimal defect-induced disorder confirming the excellent optical quality of the present molecule.

Kaynakça

  • [1] Hillemane, V., Anil Kumar, N.V., The oxygen-containing fused heterocyclic compounds, IntechOpen, 2020, doi:10.5772/intechopen.88026.
  • [2] Currie, B.M., Neyt-Galetti, N.C., Olivier, T., Van der Merwe, P., Dibokwane, L.S., Reinhardt, A.M., et al., Synthesis of an 8-membered oxygen-containing benzo-fused heterocycle using flow technologies – an exercise in undertaking research with sustainability as a driver, RSC Sustainability, 3, 1356–1365, 2024.
  • [3] Izzotti, A., Pulliero, A., The effects of environmental chemical carcinogens on the microRNA machinery, International Journal of Hygiene and Environmental Health, 217, 601–627, 2014.
  • [4] Kanzouai, Y., Chalkha, M., Hadni, H., Laghmari, M., Bouzammit, R., Nakkabi, A., et al., , G., Design, synthesis, in-vitro and in-silico studies of chromone‐isoxazoline conjugates as anti‐bacterial agents, Journal of Molecular Structure, 1293, 136205, 2023.
  • [5] Kurt, A., Kaya, M., Koca, M., Synthesis and characterization of coumarin derived surface active monomer, Adıyaman University Journal of Science, 6, 110–121, 2016.
  • [6] Kurt, A., Avcı, H.İ., Koca, M., Synthesis and characterization of a novel isocoumarin derived polymer and its thermal decomposition kinetics, Macedonian Journal of Chemistry and Chemical Engineering, 37, 173–184, 2018.
  • [7] Mushtaq, A., Zahoor, A.F., Ahmad, S., Saif, M.J., Ul Haq, A., Khan, S.G., et al., A comprehensive review on benzofuran synthesis featuring innovative and catalytic strategies, ACS Omega, 9, 20728–20752, 2024.
  • [8] Koca, M., Kurt, A., Kırılmış, C., Aydoğdu, Y., Synthesis, characterization and thermal degradation of novel poly(2-(5-bromo benzofuran-2-yl)-2-oxoethyl methacrylate), Polymer Engineering and Science, 52, 323–330, 2012.
  • [9] Dhameliya, T.M., Donga, H.A., Vaghela, P.V., Panchal, B.G., Sureja, D.K., Bodiwala, K.B., et al., A decennary update on applications of metal nanoparticles (MNPs) in the synthesis of nitrogen- and oxygen-containing heterocyclic scaffolds, RSC Advances, 10, 32740–32820, 2020.
  • [10] Borissov, A., Maurya, Y.K., Moshniaha, L., Wong, W.-S., Zyla-Karwowska, M., Stepien, M., Recent advances in heterocyclic nanographenes and other polycyclic heteroaromatic compounds, Chemical Reviews, 122, 565–788, 2022.
  • [11] Osati, S., Safari, N., Kalate Bojdi, M., Saeed Hosseiny Davarani, S., Electrosynthesis of novel π-extended benzofuran derivatives of porphyrincatecholes, Journal of Electroanalytical Chemistry, 655, 120–127, 2011.
  • [12] Yilmaz, A., Koca, M., Boga, M., Kurt, A., Ozturk, T., Synthesis of novel oxime and benzofuran chemical frameworks possessing potent anticholinesterase activity: a SAR study related to Alzheimer disease, ChemistrySelect, 8, e202302058, 2023.
  • [13] Yilmaz, A., Koca, M., Ercan, S., Acar, O.Ö., Boga, M., Sen, A., et al., Amelioration potential of synthetic oxime chemical cores against multiple sclerosis and Alzheimer’s diseases: evaluation in aspects of in silico and in vitro experiments, Journal of Molecular Structure, 1318, 139193, 2024.
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  • [20] Ibrahim, N., Moussallem, C., Allain, M., Segut, O., Gohier, F., Frère, P., Exploring the electronic properties of extended benzofuran-cyanovinyl derivatives obtained from lignocellulosic and carbohydrate platforms raw materials, ChemPlusChem, 86, 475–482, 2021.
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  • [24] Sharifi, A., Abaee, M.S., Tavakkoli, A., et al., An efficient and general procedure for room-temperature synthesis of benzofurans under solvent-free conditions using KF/Al2O3, Journal of the Iranian Chemical Society, 5, S113–S117, 2008.
  • [25] Leow, M.L., Chin, H.L., Yu, P.S., Pasunooti, K.K., Tay, R.X., Zhang, D., et al., Benzofuran-based estrogen receptor α modulators as anti-cancer therapeutics: in silico and experimental studies, Current Medicinal Chemistry, 20, 2820–2837, 2013.
  • [26] Abdelhafez, O.M., Abedelatif, N.A., Badria, F.A., DNA binding, antiviral activities and cytotoxicity of new furochromone and benzofuran derivatives, Archives of Pharmacal Research, 34, 1623–1632, 2011.
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  • [28] Shi, M., He, Y., Sun, Y., Fang, D., Miao, J., Ali, M.U., et al., Bis(diphenylamino)-benzo[4,5]thieno[3,2-b]benzofuran as hole transport material for highly efficient RGB organic light-emitting diodes with low efficiency roll-off and long lifetime, Organic Electronics, 84, 105793, 2020.
  • [29] Gao, Y., Saparbaev, A., Zhang, Y., Yang, R., Guo, F., Yang, Y., et al., Efficient polymer solar cells based on poly(thieno[2,3-f]benzofuran-co-thienopyrroledione) with a high open circuit voltage exceeding 1 V, Dyes and Pigments, 146, 543–550, 2017.
  • [30] Deng, G., Xu, H., Huang, H., Jiang, J., Kun, J., Zhang, X., et al., Synthesis and properties study of a novel nonlinear optical chromophore containing benzo[b]furan moiety based on julolidine, Journal of Molecular Structure, 1196, 439–443, 2019.
  • [31] Calikyilmaz, E., Karaoglu, G., Demir, M., Şahin, O., Ulgut, B., Akdag, A., et al., Intramolecular through-space charge transfer between benzofuran and ynone groups on a naphthalene spacer, Chemical Communications, 60, 550–553, 2024.
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Benzofuran Temelli Yeni Bir Molekülün Sentezi ve Optik Karakterizasyonu: 3-Amino-2-Pinakolon Benzofuran

Yıl 2025, Cilt: 15 Sayı: 2, 145 - 161, 31.12.2025
https://doi.org/10.37094/adyujsci.1810288
https://izlik.org/JA85UJ78PH

Öz

Bu çalışmada, yeni bir benzofuran yapılı bileşik olan 3-amino-2-pinakolon benzofuran (APBF) bileşiği, potasyum karbonat ve asetonitril varlığında 2-hidroksibenzonitril ile 1-kloropinakolonun aldol kondenzasyonu yoluyla yüksek verimle sentezlendi. FTIR ile 1H ve 13C-NMR spektroskopik analizleri, APBF bileşiğinin yapısını doğrulamış ve karakteristik spektral özelliklerini açık bir şekilde ortaya koymuştur. UV–Vis absorpsiyon özellikleri ayrıntılı olarak incelenmiş ve bileşiğin fotofiziksel davranışı aydınlatılmıştır. Gözlenen güçlü absorpsiyon bantlarının, konjuge benzofuran iskeletindeki π→π* geçişlerinden kaynaklandığı; kırmızı dalga boyuna kaymış bantların ise karbonil ve amino fonksiyonel gruplarına ait n→π* geçişlerinden kaynaklandığı belirlenmiştir. APBF molekülü, yüksek dalga boyu bölgesinde mükemmel optik geçirgenlik sergilemiştir. Dağılım analizlerinden osilatör enerjisi, dağılım enerjisi, osilatör şiddeti ve osilatör dalga boyu gibi optik dağılım parametreleri belirlenmiştir. Optik bant aralığı 3.311 eV olarak bulunmuş olup, APBF molekülünün elektro-optik uygulamalar için potansiyel bir aday olabileceğini göstermektedir. Ayrıca, nispeten düşük Urbach enerjisi (0.035 eV), kusur kaynaklı düzensizliklerin oldukça az olduğu, iyi düzenlenmiş bir moleküler yapıya işaret etmektedir ve mevcut molekülün yüksek optik kalitesini doğrulamaktadır.

Kaynakça

  • [1] Hillemane, V., Anil Kumar, N.V., The oxygen-containing fused heterocyclic compounds, IntechOpen, 2020, doi:10.5772/intechopen.88026.
  • [2] Currie, B.M., Neyt-Galetti, N.C., Olivier, T., Van der Merwe, P., Dibokwane, L.S., Reinhardt, A.M., et al., Synthesis of an 8-membered oxygen-containing benzo-fused heterocycle using flow technologies – an exercise in undertaking research with sustainability as a driver, RSC Sustainability, 3, 1356–1365, 2024.
  • [3] Izzotti, A., Pulliero, A., The effects of environmental chemical carcinogens on the microRNA machinery, International Journal of Hygiene and Environmental Health, 217, 601–627, 2014.
  • [4] Kanzouai, Y., Chalkha, M., Hadni, H., Laghmari, M., Bouzammit, R., Nakkabi, A., et al., , G., Design, synthesis, in-vitro and in-silico studies of chromone‐isoxazoline conjugates as anti‐bacterial agents, Journal of Molecular Structure, 1293, 136205, 2023.
  • [5] Kurt, A., Kaya, M., Koca, M., Synthesis and characterization of coumarin derived surface active monomer, Adıyaman University Journal of Science, 6, 110–121, 2016.
  • [6] Kurt, A., Avcı, H.İ., Koca, M., Synthesis and characterization of a novel isocoumarin derived polymer and its thermal decomposition kinetics, Macedonian Journal of Chemistry and Chemical Engineering, 37, 173–184, 2018.
  • [7] Mushtaq, A., Zahoor, A.F., Ahmad, S., Saif, M.J., Ul Haq, A., Khan, S.G., et al., A comprehensive review on benzofuran synthesis featuring innovative and catalytic strategies, ACS Omega, 9, 20728–20752, 2024.
  • [8] Koca, M., Kurt, A., Kırılmış, C., Aydoğdu, Y., Synthesis, characterization and thermal degradation of novel poly(2-(5-bromo benzofuran-2-yl)-2-oxoethyl methacrylate), Polymer Engineering and Science, 52, 323–330, 2012.
  • [9] Dhameliya, T.M., Donga, H.A., Vaghela, P.V., Panchal, B.G., Sureja, D.K., Bodiwala, K.B., et al., A decennary update on applications of metal nanoparticles (MNPs) in the synthesis of nitrogen- and oxygen-containing heterocyclic scaffolds, RSC Advances, 10, 32740–32820, 2020.
  • [10] Borissov, A., Maurya, Y.K., Moshniaha, L., Wong, W.-S., Zyla-Karwowska, M., Stepien, M., Recent advances in heterocyclic nanographenes and other polycyclic heteroaromatic compounds, Chemical Reviews, 122, 565–788, 2022.
  • [11] Osati, S., Safari, N., Kalate Bojdi, M., Saeed Hosseiny Davarani, S., Electrosynthesis of novel π-extended benzofuran derivatives of porphyrincatecholes, Journal of Electroanalytical Chemistry, 655, 120–127, 2011.
  • [12] Yilmaz, A., Koca, M., Boga, M., Kurt, A., Ozturk, T., Synthesis of novel oxime and benzofuran chemical frameworks possessing potent anticholinesterase activity: a SAR study related to Alzheimer disease, ChemistrySelect, 8, e202302058, 2023.
  • [13] Yilmaz, A., Koca, M., Ercan, S., Acar, O.Ö., Boga, M., Sen, A., et al., Amelioration potential of synthetic oxime chemical cores against multiple sclerosis and Alzheimer’s diseases: evaluation in aspects of in silico and in vitro experiments, Journal of Molecular Structure, 1318, 139193, 2024.
  • [14] Khanam, H., Shamsuzzaman, Bioactive benzofuran derivatives: a review, European Journal of Medicinal Chemistry, 97, 483–504, 2015.
  • [15] Krawczyk, P., Modulation of benzofuran structure as a fluorescent probe to optimize linear and nonlinear optical properties and biological activities, Journal of Molecular Modeling, 26, 272, 2020.
  • [16] Huang, P., Du, J., Biewer, M.C., Stefan, M.C., Developments of furan and benzodifuran semiconductors for organic photovoltaics, Journal of Materials Chemistry A, 3, 6244–6257, 2015.
  • [17] Patel, P., Vishakha, S.R., , Asati, V., Kurmi, B.D., Verma, S.K., Gupta, G.D., et al., Furan and benzofuran derivatives as privileged scaffolds as anticancer agents: SAR and docking studies (2010 to till date), Journal of Molecular Structure, 1299, 137098, 2024.
  • [18] Mandado, M., Otero, N., Mosquera, R.A., Local aromaticity study of heterocycles using n-center delocalization indices: the role of aromaticity on the relative stability of position isomers, Tetrahedron, 62, 12204–12210, 2006.
  • [19] Kurt, A., Koca, M., Optical properties of poly(2-(5-bromo benzofuran-2-yl)-2-oxoethyl methacrylate)/organoclay nanocomposites, The Arabian Journal for Science and Engineering, 40, 2975–2984, 2015.
  • [20] Ibrahim, N., Moussallem, C., Allain, M., Segut, O., Gohier, F., Frère, P., Exploring the electronic properties of extended benzofuran-cyanovinyl derivatives obtained from lignocellulosic and carbohydrate platforms raw materials, ChemPlusChem, 86, 475–482, 2021.
  • [21] Sharma, U., Naveen, T., Maji, A., Manna, S., Maiti, D., Palladium-catalyzed synthesis of benzofurans and coumarins from phenols and olefins, Angewandte Chemie, 52, 12669–12673, 2013.
  • [22] Devi, A.P., Dhingra, N., Chundawat, R.S., Ameta, K.L., Green synthesis of 2-benzylidene-1-benzofuran-3-ones and in vitro neuraminidase study using molecular docking, SAR and QSAR in Environmental Research, 33, 499–512, 2022.
  • [23] Gopinathan, A., Aneeja, T.A., Abdulla, A.C.M., Recent advances in the microwave assisted synthesis of benzofuran and indole derivatives, Heterocycles, 103, 65, 2021.
  • [24] Sharifi, A., Abaee, M.S., Tavakkoli, A., et al., An efficient and general procedure for room-temperature synthesis of benzofurans under solvent-free conditions using KF/Al2O3, Journal of the Iranian Chemical Society, 5, S113–S117, 2008.
  • [25] Leow, M.L., Chin, H.L., Yu, P.S., Pasunooti, K.K., Tay, R.X., Zhang, D., et al., Benzofuran-based estrogen receptor α modulators as anti-cancer therapeutics: in silico and experimental studies, Current Medicinal Chemistry, 20, 2820–2837, 2013.
  • [26] Abdelhafez, O.M., Abedelatif, N.A., Badria, F.A., DNA binding, antiviral activities and cytotoxicity of new furochromone and benzofuran derivatives, Archives of Pharmacal Research, 34, 1623–1632, 2011.
  • [27] Khodarahmi, G., Asadi, P., Hassanzadeh, F., Khodarahmi, E., Benzofuran as a promising scaffold for the synthesis of antimicrobial and antibreast cancer agents: a review, Journal of Research in Medical Sciences, 20, 1094–1104, 2015.
  • [28] Shi, M., He, Y., Sun, Y., Fang, D., Miao, J., Ali, M.U., et al., Bis(diphenylamino)-benzo[4,5]thieno[3,2-b]benzofuran as hole transport material for highly efficient RGB organic light-emitting diodes with low efficiency roll-off and long lifetime, Organic Electronics, 84, 105793, 2020.
  • [29] Gao, Y., Saparbaev, A., Zhang, Y., Yang, R., Guo, F., Yang, Y., et al., Efficient polymer solar cells based on poly(thieno[2,3-f]benzofuran-co-thienopyrroledione) with a high open circuit voltage exceeding 1 V, Dyes and Pigments, 146, 543–550, 2017.
  • [30] Deng, G., Xu, H., Huang, H., Jiang, J., Kun, J., Zhang, X., et al., Synthesis and properties study of a novel nonlinear optical chromophore containing benzo[b]furan moiety based on julolidine, Journal of Molecular Structure, 1196, 439–443, 2019.
  • [31] Calikyilmaz, E., Karaoglu, G., Demir, M., Şahin, O., Ulgut, B., Akdag, A., et al., Intramolecular through-space charge transfer between benzofuran and ynone groups on a naphthalene spacer, Chemical Communications, 60, 550–553, 2024.
  • [32] Kurt, A., Yılmaz, P., Thermal decomposition kinetics of benzofuran derived polymer/organosilicate nanocomposites, Kuwait Journal of Science, 43, 172–184, 2016.
  • [33] Wang, D., Dou, K., Cui, W., Li, F., Jing, X., Yu, L., et al., VOC enhancement of thienobenzofuran and benzotriazole backboned photovoltaic polymer by side chain sulfuration or fluoridation, Dyes and Pigments, 184, 108775, 2021.
  • [34] Trofimov, F.A., Lelyak, G.F., Shevchenko, L.I., Grinev, A.N., Condensation of salicylnitrile with some α-halo carbonyl compounds, Chemistry of Heterocyclic Compounds, 10, 1016–1018, 1974.
  • [35] Nadeem, M.Y., Ahmed, W., Optical properties of ZnS thin films, Turkish Journal of Physics, 24, 651–659, 2000.
  • [36] Nosidlak, N., Dulian, P., Mierzwiński, D., Jaglarz, J., The determination of the electronic parameters of thin amorphous organic films by ellipsometric and spectrophotometric study, Coatings, 10, 980, 2020.
  • [37] Jung, J., Dinescu, A., Emission pathway switching by solvent polarity: facile synthesis of benzofuran-bipyridine derivatives and turn-on fluorescence probe for zinc ions, Tetrahedron Letters, 58, 358–361, 2017.
  • [38] Zidan, H.M., Abu-Elnader, M., Structural and optical properties of pure PMMA and metal chloride-doped PMMA films, Physica B: Condensed Matter, 355, 308–317, 2005.
  • [39] Kurt, A., Influence of AlCl₃ on the optical properties of new synthesized 3-armed poly(methyl methacrylate) films, Turkish Journal of Chemistry, 34, 67–69, 2010.
  • [40] Kurt, A., Koca, M., Blending of poly(ethyl methacrylate) with poly(2-hydroxy-3-phenoxypropyl methacrylate): thermal and optical properties, The Arabian Journal for Science and Engineering, 39, 5413–5420, 2014.
  • [41] Watanabe, I., Morikawa, K., Samitsu, S., Mori, H., High refractive index copolymers from aromatic heterocycle-based vinyl sulfides and phthalimide/maleimide derivatives, Macromolecular Chemistry and Physics, 224, 2300289, 2023.
  • [42] Fu, M.-C., Ueda, M., Ando, S., Higashihara, T., Development of novel triazine-based poly(phenylene sulfide)s with high refractive index and low birefringence, ACS Omega, 5, 5134–5141, 2020.
  • [43] Koca, M., Kurt, A., Investigation of optical properties of a novel pyrazole containing polymer poly(1,3-diphenyl-1H-pyrazol-5-yl methacrylate) thin film, Russian Journal of Physical Chemistry A, 96, 2967–2973, 2022.
  • [44] Kurt, A., Koca, M., Blending of poly(methyl methacrylate) with poly(1,3-diphenyl-1H-pyrazol-5-yl methacrylate): investigation of its optical properties, Adıyaman University Journal of Science, 12, 177–192, 2022.
  • [45] Tauc, J., Optical properties of non-crystalline solids, in: F. Abeles (Ed.), Optical Properties of Solids, North-Holland, Amsterdam, 1972, 277–313.
  • [46] Koca, M., Dagdelen, F., Aydoğdu, Y., Thermal and optical properties of benzofuran-2-yl 3-phenyl-3-methylcyclobutyl thiosemicarbazone, Materials Letters, 58, 2901–2905, 2004.
  • [47] Abdo, J., Ayoub, A., Ibrahim, N., Allain, M., Frère, P., Tuning the solid state luminescence of benzofuran-cyanostilbenes by functionalization with electron donors or acceptors, ChemPlusChem, 88, e202300402, 2023.
  • [48] Urbach, F., The long-wavelength edge of photographic sensitivity and of the electronic absorption of solids, Physical Review, 92, 1324–1324, 1953.
  • [49] Zhang, C., Mahadevan, S., Yuan, J., Ho, J.K.W., Gao, Y., Liu, W., et al., Unraveling Urbach tail effects in high-performance organic photovoltaics: dynamic vs static disorder, ACS Energy Letters, 7, 1971–1979, 2022.
  • [50] Wemple, S.H., DiDomenico, M., Behavior of the electronic dielectric constant in covalent and ionic materials, Physical Review B, 3, 1338–1351, 1971.
  • [51] Wemple, S.H., Refractive-index behavior of amorphous semiconductors and glasses, Physical Review B, 7, 3767–3777, 1973.
  • 52] Veena, G., Lobo, B., Dispersive parameters of oxidized PVA-PVP blend films, Turkish Journal of Physics, 43, 337–354, 2019.
  • [53] El-Ghamaz, N.A., Ghoneim, M.M., El-Sonbati, A.Z., Diab, M.A., El-Bindary, A.A., Abd El-Kader, M.K., Synthesis and optical properties studies of antipyrine derivatives thin films, Journal of Saudi Chemical Society, 21, S339–S348, 2017.
  • [54] Wemple, S.H., DiDomenico, M., Oxygen-octahedra ferroelectrics. I. Theory of electro-optical and nonlinear optical effects, Journal of Applied Physics, 40, 720–734, 1969.
Toplam 54 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Fiziksel Organik Kimya, Organik Kimyasal Sentez
Bölüm Araştırma Makalesi
Yazarlar

Adnan Kurt 0000-0001-8516-6525

Murat Koca 0000-0002-9250-0293

Gönderilme Tarihi 24 Ekim 2025
Kabul Tarihi 14 Aralık 2025
Yayımlanma Tarihi 31 Aralık 2025
DOI https://doi.org/10.37094/adyujsci.1810288
IZ https://izlik.org/JA85UJ78PH
Yayımlandığı Sayı Yıl 2025 Cilt: 15 Sayı: 2

Kaynak Göster

APA Kurt, A., & Koca, M. (2025). Synthesis and Optical Characterization of a Novel Benzofuran-Based Molecule: 3-Amino-2-Pinacolone Benzofuran. Adıyaman University Journal of Science, 15(2), 145-161. https://doi.org/10.37094/adyujsci.1810288
AMA 1.Kurt A, Koca M. Synthesis and Optical Characterization of a Novel Benzofuran-Based Molecule: 3-Amino-2-Pinacolone Benzofuran. ADYU J SCI. 2025;15(2):145-161. doi:10.37094/adyujsci.1810288
Chicago Kurt, Adnan, ve Murat Koca. 2025. “Synthesis and Optical Characterization of a Novel Benzofuran-Based Molecule: 3-Amino-2-Pinacolone Benzofuran”. Adıyaman University Journal of Science 15 (2): 145-61. https://doi.org/10.37094/adyujsci.1810288.
EndNote Kurt A, Koca M (01 Aralık 2025) Synthesis and Optical Characterization of a Novel Benzofuran-Based Molecule: 3-Amino-2-Pinacolone Benzofuran. Adıyaman University Journal of Science 15 2 145–161.
IEEE [1]A. Kurt ve M. Koca, “Synthesis and Optical Characterization of a Novel Benzofuran-Based Molecule: 3-Amino-2-Pinacolone Benzofuran”, ADYU J SCI, c. 15, sy 2, ss. 145–161, Ara. 2025, doi: 10.37094/adyujsci.1810288.
ISNAD Kurt, Adnan - Koca, Murat. “Synthesis and Optical Characterization of a Novel Benzofuran-Based Molecule: 3-Amino-2-Pinacolone Benzofuran”. Adıyaman University Journal of Science 15/2 (01 Aralık 2025): 145-161. https://doi.org/10.37094/adyujsci.1810288.
JAMA 1.Kurt A, Koca M. Synthesis and Optical Characterization of a Novel Benzofuran-Based Molecule: 3-Amino-2-Pinacolone Benzofuran. ADYU J SCI. 2025;15:145–161.
MLA Kurt, Adnan, ve Murat Koca. “Synthesis and Optical Characterization of a Novel Benzofuran-Based Molecule: 3-Amino-2-Pinacolone Benzofuran”. Adıyaman University Journal of Science, c. 15, sy 2, Aralık 2025, ss. 145-61, doi:10.37094/adyujsci.1810288.
Vancouver 1.Adnan Kurt, Murat Koca. Synthesis and Optical Characterization of a Novel Benzofuran-Based Molecule: 3-Amino-2-Pinacolone Benzofuran. ADYU J SCI. 01 Aralık 2025;15(2):145-61. doi:10.37094/adyujsci.1810288