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INDONESIA
Indonesian Journal of Chemistry
ISSN : 14119420     EISSN : 24601578     DOI : -
Indonesian Journal of Chemistry is an International, peer-reviewed, open access journal that publishes original research articles, review articles, as well as short communication in all areas of chemistry including applied chemistry. The journal is accredited by The Ministry of Research, Technology and Higher Education (RISTEKDIKTI) No : 21/E/KPT/2018 (in First Rank) and indexed in Scopus since 2012. Since 2018 (Volume 18), Indonesian Journal of Chemistry publish four issues (numbers) annually (February, May, August and November).
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Articles 25 Documents
Search results for , issue "Vol 22, No 1 (2022)" : 25 Documents clear
Synthesis of SO42–/ZrO2 Solid Acid and Na2O/ZrO2 Solid Base Catalysts Using Hydrothermal Method for Biodiesel Production from Low-Grade Crude Palm Oil Sri Setyaningsih; Maisari Utami; Akhmad Syoufian; Eddy Heraldy; Nasih Widya Yuwono; Karna Wijaya
Indonesian Journal of Chemistry Vol 22, No 1 (2022)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.65404

Abstract

Biodiesel is a renewable energy source that can be produced through esterification as well as transesterification reactions. This work presents a series of zirconia catalysts synthesized by hydrothermal method on various concentrations in acidic (H2SO4 0.3, 0.5, and 0.7 M) and basic (NaOH 1, 2, 3, and 4 M) solution to get a catalyst with the highest acidity or basicity. Characterizations of the catalysts were performed by FTIR, XRD, SEM-EDX, surface area analysis, acidity, and basicity test. The most active acid catalyst activity was evaluated for the esterification of low-grade crude palm oil (LGCPO), while the solid base catalyst was utilized for the transesterification reaction. The solid acid catalyst of 0.7 M SO42–/ZrO2 60 °C; 24 h was denoted as the most active acid catalyst with a total acidity of 1.86 mmol g–1, while 4 M Na2O/ZrO2 60 °C; 24 h catalyst was considered as the solid base catalyst with the highest total basicity of 3.75 ± 0.12 mmol g–1. The optimized acid catalyst exhibited a 31 times higher acidity than commercial ZrO2. The concentration of free fatty acids (FFA) decreased to 68.87% in the esterification reaction. The solid base catalyst of 4 M Na2O/ZrO2 60 °C; 24 h successfully converted LGCPO into biodiesel by 68.55% through a transesterification reaction.
Novel Benzo[f]coumarin Derivatives as Probable Acetylcholinesterase Inhibitors: Synthesis, In Vitro, and In Silico Studies for Evaluation of Their Anti-AChE Activity Zaizafoon Nabeel; Qassim Abdul-Hussein Jaber; Nabeel Abed Abdul-Rida
Indonesian Journal of Chemistry Vol 22, No 1 (2022)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.65663

Abstract

Novel benzo[f]coumarin derivatives bearing pyrimidine unit were successfully synthesized. The target is to develop novel acetylcholinesterase inhibitors. The benzo[f]coumarin chalcone 4 was prepared via Claisen-Schmidt condensation between 3-acetyl-5,6-benzocoumarin and 4-hydroxybenzaldehyde in the alkaline medium. Then, the cyclocondensation of chalcone 4 with urea, thiourea, and guanidine HCl in the presence of glacial acetic acid led to the formation of various pyrimidines. Structures of the newly synthesized compounds were characterized by FT-IR, 1H-NMR, 13C-NMR spectra, and elemental analysis. The acetylcholinesterase (AChE) inhibitory activity tests were carried out using Ellman's assay and donepezil as a reference drug. The biological activity results revealed that the derivatives 6 and 7 inhibit AChE activity in healthy samples showed that the greater inhibition percentage was found respectively at concentrations of 10–4 and 10–10 M while low inhibition percentage was obtained at 10–12 and 10–4 M. AChE showed inhibition constant Ki in the range of 10–4-10–12 M in the presence of maximum and minimum inhibitor concentrations, probably due to variant types of inhibition from non and uncompetitive. In addition, molecular modeling simulations of targeted compounds revealed their mechanism of action as potent inhibitors for the AChE enzyme.
Development of an Analytical Method for Kasugamycin Residue in Herbal Medicine, Achyranthes japonica Nakai Jeong Yoon Choi; Hun Ju Ham; Min-woo Kim; Abd Elaziz Sulieman Ahmed Ishag; Jang-Hyun Hur
Indonesian Journal of Chemistry Vol 22, No 1 (2022)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.65970

Abstract

This study developed a suitable analytical method for kasugamycin residues in Achyranthes japonica using LC/MS/MS equipped with an amide column for polar substances. Extraction and cleanup processes were done at pH 4.5–5. Purification efficiency was assessed and confirmed step by step by selecting silica, hydrophilic-lipophilic balance (HLB), strong cation exchange (SCX), and double (HLB and SCX) cleanup SPE cartridges. The results indicated that silica SPE cartridge exhibited overloading tendency, while HLB SPE cartridge had low cleaning efficiency. Among SPE cartridges used, double cleanup and SCX were found sufficient with respective matrix effects of –15% and +14%, respectively. The LOD and LOQ were 0.008 ng and 0.04 mg/kg, respectively. The correlation coefficient (R2) was higher than 0.99, recovery rate ranges were 86.3–97.2%, and the RSD was below 8.8%. All methods are consistent with the Codex guidelines criteria. This study developed an appropriate LC/MS/MS analytical method for kasugamycin residue analysis in A. japonica with optimized, efficient extraction and purification conditions using a single SCX SPE cartridge, which is simple and time-efficient. In addition, the HLB and SCX SPE cartridges of the double cleanup methods were identified as primary methods that can be applied for the cleanup of other medicinal herbs.
Preparation and Characterization of New Tetra-Dentate N2O2 Schiff Base with Some of Metal Ions Complexes Naser Shaalan; Waleed Madhloom Khalaf; Shatha Mahdi
Indonesian Journal of Chemistry Vol 22, No 1 (2022)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.66118

Abstract

This study describes preparation a new series of tetra-dentate N2O2 dinuclear complexes Cr(III), Co(II)and Cu(II) of the Schiff base 2-[5-(2-hydroxy-phenyl)-1,3,4-thiadiazol-2-ylimino]-methyl-naphthalen-1-ol], (LH2) derived from 1-hydroxy-naphthalene-2-carbaldehyde with 2-amino-5-(2-hydroxy-phenyl)-1,3,4-thiadiazole. These ligands were characterized by FT-IR, UV-Vis, Mass spectra, elemental analysis, and 1H-NMR. All prepared complexes have been characterized by conductance measurement, magnetic susceptibility, electronic spectra, infrared spectrum, thermal Analysis (TGA), and metal analysis by atomic absorption. The stoichiometry of metal to ligand, magnetic susceptibility, and electronic spectra measurements show an octahedral geometry for all (Cr3+, Co2+, Cu2+) complexes. Conductivity measurement shows that the prepared (Co2+, Cu2+) complexes were nonelectrolyte except (Cr3+). Studying the extraction efficiency such as ligand concentration, temperature and incubation time, centrifuge time, amount of surfactant were evaluated and optimized. The linear range of ions Cr(III), Co(II) and Cu(II) with ligand (0.2–3, 0.2–4, 0.2–3, µg mL–1), each individually, and relative standard deviation (0.15%, 0.34%, 0.46%). The successful method was applied for the determination of trace metal ions in the wastewater.
Synthesis of Mn-Doped Fe-MOFs with Different Ratios and Its Application for Photocatalytic Degradation of Rhodamine B Dye Kim Ngan Thi Tran; Thuy Bich Tran; Sy Trung Do; Kim Oanh Thi Nguyen; Tan Van Lam
Indonesian Journal of Chemistry Vol 22, No 1 (2022)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.67742

Abstract

Recent trends in environmental remediation have shifted to the use of metal-organic framework (MOF) composites due to their unique structural properties. It is still challenging to diversify MOFs photocatalysts to fulfill application to treat toxic organic pigments. In this study, Fe-MOF bimetallic materials were synthesized by doping Mn2+ ions at different ratios. The structural and morphological characteristics of the materials were analyzed by XRD, UV-Vis, FT-IR, SEM, and UV-Vis DRS methods. Mn/Fe-MOF bimetallic organic framework materials were used to evaluate the photocatalytic degradation of Rhodamine B (RhB) dyes. The results show that, under the same experimental conditions, the RhB degradation efficiency of Mn/Fe-MOF is enhanced than that of the pristine Fe-MOF catalyst under the influence of visible light. After 120 min, the RhB solution was decomposed to 91.78% by combining 0.1 Mn/Fe-MOF, H2O2, and visible light irradiation. At the same time, the presence of H2O2 in the reaction system also showed a strong impact on the efficiency of RhB degradation. The activity from the two metal centers of Mn/Fe-MOF contributes to the formation of a unique structure and composition that can be used as a photocatalyst for colored wastewater treatment.
Synthesis and Docking Study of 2–Aryl-4,5-diphenyl-1H-imidazole Derivatives as Lead Compounds for Antimalarial Agent Ika Septiana; Bambang Purwono; Chairil Anwar; Beta Achromi Nurohmah; Jufrizal Syahri
Indonesian Journal of Chemistry Vol 22, No 1 (2022)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.67777

Abstract

Series of 2-aryl-4,5-diphenyl-1H-imidazole derivatives of 2-(4-hydroxy-3-methoxyphenyl)-4,5-diphenyl-1H-imidazole (1), 2-(4,5-dimethoxyphenyl)-4,5-diphenyl-1H-imidazole (2) and 2-(4-methoxyphenyl)-4,5-diphenyl-1H-imidazole (3) were produced and evaluated for their in vitro antimalarial activities against the chloroquine-sensitive Plasmodium falciparum 3D7 strain. A molecular docking study was also carried out against the crystal protein of Plasmodium falciparum dihydrofolate reductase-thymidylate synthase (PfDHFR-TS) (PDB ID: 1J3I.pdb) to predict the interaction between the compounds and protein. The physicochemical and pharmacokinetic parameters were computationally performed to predict the parameters of the absorption, distribution, metabolism, excretion, and toxicity (ADMET). Imidazoles were synthesized from aryl aldehyde derivatives with benzyl and ammonium acetate in glacial acetic acid using microwave-assisted-organic synthesis. Compounds 1, 2, and 3 were produced in 64.33, 50.56, and 70.55% yields, respectively. The IC50 of compounds 1, 2, and 3 against chloroquine-sensitive Plasmodium falciparum 3D7 strain was found to be 1.14, 5.28, and 2.42 µM, respectively. The molecular docking study agreed with the in vitro data by showing the lowest CDOCKER energy for compound 1 (-47.48 kcal/mol), followed by 3 (-43.79 kcal/mol) and 2 (-41.47 kcal/mol). The physicochemical and pharmacokinetic parameters showed that imidazoles 1, 2, and 3 obeyed Lipinski rules of five to propose as lead compounds for the antimalarial agents.
On the Mechanical and Thermal Properties of Poly(Vinyl Alcohol) – Alginate Composite Yarn Reinforced with Nanocellulose from Oil Palm Empty Fruit Bunches Ainul Maghfirah; Farah Fahma; Nurmalisa Lisdayana; Muchammad Yunus; Ahmad Kusumaatmaja; Grandprix Thomryes Marth Kadja
Indonesian Journal of Chemistry Vol 22, No 1 (2022)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.67881

Abstract

PVA-alginate hydrogel is a promising material for use in biomedical applications due to its desirable characteristics: biocompatible, durable, non-toxic, and low cost. However, the low gel strength of this composite limits its use in biomedical applications. This study aims to develop enhanced mechanical and thermal properties of poly(vinyl alcohol) PVA-alginate composite yarn by adding nanocellulose isolated from the sustainable oil palm empty fruit bunches (OPEFBs). The PVA-alginate composite yarns reinforced with nanocellulose were prepared with various nanocellulose contents (1 wt.%, 2 wt.%, and 5 wt.%). The composite's tensile strength exhibited an increasing trend with the addition of nanocellulose, while the elongation at break showed the opposite trend. Moreover, it was demonstrated that the composite's thermal degradation shifts to higher temperatures with the addition of nanocellulose. The observed activation energies for the thermal degradation calculated using the Coats-Redfern method exhibited a significant increment for the composites reinforced with nanocellulose. These results show that the addition of nanocellulose into the PVA-alginate matrix enhances the chemical and thermal properties of the resulting hydrogel. All these improvements have resulted from more abundant and robust hydrogen bonds generated by the nanocellulose presence.
Molecular interactions of Andrographis paniculata Burm. f. Active Compound with Nuclear Receptor (CAR and PXR): An In Silico Assessment Approach Elza Sundhani; Agung Endro Nugroho; Arief Nurrochmad; Endang Lukitaningsih
Indonesian Journal of Chemistry Vol 22, No 1 (2022)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.67981

Abstract

The study aims to analyze the potential Herb-Drug Interactions (HDIs) of the chemical compound in Andrographis paniculate Burm. f. against Constitutive Androstane Receptor (CAR) and Pregnane X Receptor (PXR). The 1XVP and 1SKX obtained from the Protein Data Bank (PDB) were used as the targeted protein. The molecular docking analysis was done using the Molecular Operating Environment (MOE) and molecular dynamics simulation using Gromacs. The results of the docking analysis showed that 14-Deoxy-11,12-didehydroandrographolide had the strongest binding energy (1XVP-21.0998 Å) with the Arene-H binding type on Tyr326 and Andrographidine A had the strongest binding energy (1SKX-24.7363 Å) with the Arene-H binding type on Trp299. While Andrographolide is the major component, it also has a high affinity for the two PDB IDs (1XVP-17.4044 Å and 1SKX-21.8881 Å). Based on the RMSD value, the radius of gyration (Rg), and MM/PBSA on molecular dynamic simulations, it shows that the ligand and protein complex as a whole can bind strongly to amino acid residues at the active site. The complex also has sufficient stability and good affinity. Therefore, this study can predict the mechanism in HDIs, especially in CYP 450 expression through the activation pathways of CAR and PXR receptors.
Simple One-Pot Synthesis of Sulfonic-Acid-Functionalized Silica for Effective Catalytic Esterification of Levulinic Acid Desinta Dwi Ristiana; Suyanta Suyanta; Nuryono Nuryono
Indonesian Journal of Chemistry Vol 22, No 1 (2022)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.68301

Abstract

Silica functionalized with sulfonic acid catalyst (SiO2−SO3H) was synthesized through a one-pot method and evaluated as the catalyst material for esterification of levulinic acid in an excess amount of ethanol. Sodium silicate solution was used as the silica source, and then a silane coupling agent, namely GPTMS, was used to incorporate the sulfonic group of 2-aminoethanesulfonic acid (AS) into the silica. Functionalization of AS using GPTMS in the slightly acidic condition has been successfully carried out based on the characterization with FTIR, SEM-EDX, and TGA measurements. Catalyst with the AS to SiO2 molar ratio of 5:6 (SiO2−SO3H(5)) showed the highest acid content (1.02 mmol g–1) and the highest conversion of levulinic acid (70%). The reaction followed pseudo-first-order with the rate constant of 0.00414 min–1. Catalyst material was regenerated by washing with alcohol and water, and the catalyst material can be reused at least for 3 cycles. From this study, the SiO2−SO3H produced from a green process is an effective catalyst to produce esters used in fuel additives.
Improving the Performance of Polymer Inclusion Membranes in Separation Process Using Alternative Base Polymers: A Review Fidelis Nitti; Odi Theofilus Edison Selan; Bosirul Hoque; David Tambaru; Muhammad Cholid Djunaidi
Indonesian Journal of Chemistry Vol 22, No 1 (2022)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.68311

Abstract

Polymer inclusion membrane (PIM) has recently evolved as an alternative separation technique to conventional solvent extraction as it eliminates the use of toxic solvents, reduces separation cost, and simplifies the separation process. PIM is the new generation of a liquid membrane made by casting solution containing liquid phases (extractant and plasticizer/modifier) and base polymers. Despite its better performance and stability in comparison to the previous types of liquid membranes, PIM's robustness for applications on an industrial scale is still considered insufficient mainly due to its limited stability in the long-term separation process. In recent years, different approaches have been devoted to improving the stability of PIM while maintaining its performance. This review aims to summarize and evaluate the current literature on the improvement of the performance of PIMs with particular focus on the use of alternative base polymers, including non-conventional linear homopolymers, copolymers, or cross-linking polymers. Furthermore, more emphasis is given to the composition, fabrication process, and application of the PIMs. Finally, the performance of the PIMs with the alternative base polymers in terms of extraction rate and long-term stability is presented and compared to the PIMs fabricated using their corresponding common base polymers.

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