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Indonesian Journal of Chemistry

ijc
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Published by Universitas Gadjah Mada

ISSN : 14119420 EISSN : 24601578 DOI : -

Core Subject : Science, Engineering,

Chemical Engineering, Chemistry & Bioengineering Chemistry

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).

Arjuna Subject : -

Articles 1,981 Documents

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STRUCTURE OF IRIDIUM(III) HYDRATION BASED ON AB INITIO QUANTUM MECHANICAL CHARGE FIELD MOLECULAR DYNAMICS SIMULATIONS Ponco Iswanto; Ria Armunanto; Harno D. Pranowo
Indonesian Journal of Chemistry Vol 10, No 3 (2010)
Publisher : Universitas Gadjah Mada

Structural properties of Iridium(III) hydration have been studied based on an ab initio Quantum Mechanical Charge Field (QMCF) Molecular Dynamics (MD) Simulations. The most chemical-relevant region was treated by ab initio calculation at Hartree-Fock level. For the remaining region was calculated by Molecular Mechanics method. LANL2DZ ECP and DZP Dunning basis sets were applied to Ir3+ ion and water, respectively. The average distance of Ir-O in the first hydration shell is 2.03 Å. The QMCF MD Simulation can detect only one complex structure with coordination number of 6 in the first hydration shell. Bond angle analysis shows that Ir3+ ion hydration in the first hydration shell has octahedral structure.

IDENTIFICATION AND ANTIOXIDANT ACTIVITY TEST OF SOME COMPOUNDS FROM METHANOL EXTRACT PEEL OF BANANA (Musa paradisiaca Linn.) Sri Atun; Retno Arianingrum; Sri Handayani; Rudyansah Rudyansah; Mary Garson
Indonesian Journal of Chemistry Vol 7, No 1 (2007)
Publisher : Universitas Gadjah Mada

The objective of these research was measured activity as antioxidant some compounds in methanol extracts of peel of banana (Musa paradisiaca Linn.), isolated some compounds which had activities as antioxidant, and determined this structure. Method of this study was extracted powdered peel of banana with methanol at room temperature. Extract was concentrated in vaccuo and then successively was partitioned with n-hexane, chloroform, etyl acetate, and buthanol. Antioxidant test from each fractions was measured by hydroxyl radical scavenger test with Fenton reaction method. The result of this study showed activity each fractions as hydroxyl radical scavenger activity of chloroform, etyl acetate, and buthanol fraction were IC50 693.15; 2347.40; and 1071.14 mg/mL respectively. The isolation of secondary metabolite compounds from chloroform fraction obtained two isolate compounds. Identification by spectroscopy IR, MS, 1H and 13C NMR one and two dimension showed that the compounds are 5,6,7,4'-tetrahidroxy-3,4-flavan-diol and a new compound cyclohexenon derivative (2-cyclohexene-1-on-2,4,4-trimethyl-3-O-2'-hydroxypropyl ether).

SYNTHESIS AND REACTIONS OF 1-(4’-BROMOPHENACYL)-3-(4’-BROMO-PHENYL)-4,6-DIMETHOXYINDOLE Jumina Jumina
Indonesian Journal of Chemistry Vol 5, No 2 (2005)
Publisher : Universitas Gadjah Mada

1-Phenacyl-3-aryl-4,6-dimethoxyindoles 2b and 2c were obtained in good yields respectively through cyclization of N,N-diphenacylaniline 1b and 1c in trifluoroacetic acid. However, instead of giving pyrroloindole 3c, treatment of phenacylindole 2c with polyphosphoric acid afforded indolizine 5 in 42% yield. Phenacylindole 2c reacts with the Vilsmeier aroylation reagent consisted of a mixture of phosphoryl chloride and p-chloro-N,N-dimethylbenzamide to give 2-aroylindole 6 (32%) and pyrroloindole 7 (22%). When treated with sodium borohydride, phenacylindole 2c gave alcohol 8 in 83% yield. Nonetheless, treatment of alcohol 8 with either p-toluenesulfonic acid in glacial acetic acid or boron trifluoride etherate in benzene did not give the desired dihydropyrroloindole 12. Instead, the reactions afforded respectively acetyl ester 9 and indole 10 in 56% and 63% yield.

POLYMORPHIC TRANSFORMATION OF TITANIUM DIOXIDE CAUSED BY HEAT TREATMENT OF PROTONIC LEPIDOCROCITE TITANATE Hari Sutrisno; Sunarto Sunarto
Indonesian Journal of Chemistry Vol 10, No 2 (2010)
Publisher : Universitas Gadjah Mada

The polymorphic phases of titanium dioxide were successfully prepared by heat treatments of protonic lepidocrocite titanate, H0.54Ti1.8650.135O4·0.5H2O at various temperatures. The prepared powders were characterized with EDX (Energy Dispersive X-ray), Scanning Electron Microscopy (SEM), X-rays Diffractometer (XRD), Raman Spectroscopy, and High Resolution Transmission Electron Microscopy (HRTEM). The effect of calcination temperature on the phase structure and morphology of the heated samples was investigated. The research indicated that the protonic titanate, H0.54Ti1.8650.135O4·0.5H2O ( = vacancy), lost the interlayer water by being heated up to 200 °C to produce a dehydrated phase, H0.54Ti1.8650.135O4. Above 300 °C, the dehydrated phase, H0.54Ti1.8650.135O4, completely transformed to TiO2(B) and anatase was obtained as pure phase at 600 °C. The phase transformed as the following process: H0.54Ti1.8650.135O4·0.5H2O ® H0.54Ti1.8650.135O4·0.25H2 ® H0.54Ti1.8650.135O4 ® TiO2(B) ® TiO2-anatase.

INTERACTION BETWEEN Li+ CATION WITH CROWN ETHERS OF Bz15C5, DBz16C5 AND DBz18C6: MOLECULAR MODELING BASE ON MNDO/d SEMIEMPIRICAL METHOD Harno Dwi Pranowo; Chairil Anwar
Indonesian Journal of Chemistry Vol 3, No 1 (2003)
Publisher : Universitas Gadjah Mada

The aim of this research is to find information about the substituent effect to the structure of crown ether benzo-15-crown-5 (Bz15C5), dibenzo-16-crown-5 (DBz16C5) and dibenzo-18-crown-6 (DBz18C6), and also crown ether selectivity to coordinate a Li+ metal cation. The presence of substituent could change the conformations flexibility of crown ether during interact with metal cation. In this research semi empirical MNDO/d method was used for calculations. Firstly, geometry optimization was conducted to crown ethers structure using MNDO/d methods. The next steps were running the geometry optimization of complexes between cation Li+ with crown ethers. Data were produced from these calculation are the parameter of crown ether structures, structures of the complexes, and the binding energy of the cation-crown ethers. The presence of electron-withdrawing substituents decreased the binding energy while that of electron-donating one increase the binding energy (value of ΔE more negative). The substituents which are increase the degree of symmetry of the cation-crown ether complexes could give the increase of crown ether selectivity to bind the cation. Selectivity of crown ether to bind the cation depends on the structural match between ionic radii of crown ether cavity (the ion-cavity size concept). Bz15C5 what has higher selectivity to bind Li+ than DBz16C5 and DBz18C6.

THE EXTRACTION OF NICKEL(II) AND COPPER(II) USING LIQUID MEMBRANE EMULSION TECHNIQUE Pirim Setiarso; Selvi Purwanti N.
Indonesian Journal of Chemistry Vol 6, No 2 (2006)
Publisher : Universitas Gadjah Mada

Research on the extraction of Nickel(II) and Copper(II) using liquid membrane emulsion technique has been conducted. The purpose of this research is to know the influence of pH, extraction time and presence of competed metals (Ni2+ in Cu2+ and vice versa) toward the membrane extraction capability. In this research, 84 mL of Ni2+ and Cu2+ with concentration of 100 ppm, each, was extracted using pH variation (4.0, 4.5, 5.0, 5.5, 6.0). The optimum pH will be used to obtain the time of equilibrium and influence of the competed ions. Time variations (15, 20, 25, 30, 35 minute) were used with the concentration of the competed ions of 20, 40, 60, 80, 100 ppm. The percentage of ions extracted was analyzed by Atomic Absorption Spectrometry. The result shows that the optimum pH was 5.0 for extracting 79.3137 % Cu2+ and 50.3448 % Ni2+. Time of equilibrium was 30 minutes for extracting 85.4117 % Cu2+ and 53.7691 % Ni2+. The presence of Ni2+ influenced Cu2+ extracted and vice versa.

THE EFFECT OF HYDROGEL DRESSING COPOLYMER POLI(VINYLPIRROLIDONE) (PVP) - k- CARRAGEENAN PREPARED BY RADIATION AND HEALING TIMES ON THE RADIUS REDUCTIONS BURN INJURIED OF WISTAR WHITE RAT Erizal Erizal
Indonesian Journal of Chemistry Vol 8, No 2 (2008)
Publisher : Universitas Gadjah Mada

The pre-clinical study of poly (vinyl pirrolidone) (PVP)-k- carrageenan hydrogel has been carried out. The aim of this study is to investigate the effect of hydrogel for healing burn injuried in the rats. The hydrogels were prepared by g-irradiation of aqueous solutions of 15 wt.-% PVP and 2 wt.-% k- carrageenan at a sterilization dose of 25 kGy. The physico-chemical properties of hydrogels were investigated. The results showed that the hydrogels suitable as candidate for wound dressing with gel fraction of 90 ± 5 (%), the water absorption was 4500 ± 55 (w/w), the water content was 83 ± 2 (%), tensile strength was 1,5 ± 0,1 kg/cm2 and adhesiveness was 0. The effect of the hydrogel as wound dressing was evaluated by attaching to a burn of the back skin of rats as a function of time observation. Advantages of the hydrogel were slightly faster rate of reducing radius diameter of injured burn skin, easy removal without damage to renewed skin.

THERMO-RESPONSIVE HYDROGEL OF POLI VINYL ALCOHOL (PVA) - CO- N- ISOPROPYL ACRYLAMIDE (NIPAAM) PREPARED BY –γ RADIATION AS A MATRIX PUMPING/ON-OFF SYSTEM Erizal Erizal; Rahayu C Rahayu C
Indonesian Journal of Chemistry Vol 9, No 1 (2009)
Publisher : Universitas Gadjah Mada

Interpenetrating networks (IPN) crosslinked polymer of polyvinyl alcohol (PVA) containing copolymer N-isopropylacryalmide (NIPAAm) were fabricated by radiation technique and characterized in terms of their aqueous swelling and critical behaviour. The influence of irradiation dose (> 10 kGy) and PVA concentration (5-15%wt ) on the gel fraction and swelling properties were investigated. With an increase of -γ irradiation dosage, the gel fraction of hydrogels was inclined to increase but the swelling behaviour decreased markedly. The incorporation of PVA into NIPAAm by irradiation led a significant increase in swelling capability when comparing to the pure homopolymer (NIPAAm) hydrogels. In addition, the shrinking rate upon heating was significantly improved if the PVA content in poly(PVA-co-NIPAAm) hydrogels was less than 15% wt%. at temperature exceeding the collapsed transition point, all copolymer gels collapsed to a state of nearly complete dehydration. Based on its swelling-deswelling properties in the repeated application, the hydrogels are stable and showed a behaviour as matrix pumping system/on-off. The hydrogels would have potential applications in chemistry, pharmacy, and health care purposes.

THE OPTIMIZATION OF ENZYMATIC SYNTHESIS FOR LAUROYL-N-METHYL GLUCAMIDE SURFACTANTS Zuhrina Masyithah; Seri Bima Sembiring; Zul Alfian; Tjahjono Herawan
Indonesian Journal of Chemistry Vol 11, No 3 (2011)
Publisher : Universitas Gadjah Mada

The optimization of enzymatic synthesis for lauroyl-N-methyl glucamide surfactants is studied. The fraction of palm kernel oil namely lauric acid (AL) was amidificationed with N-methyl glucamine (MGL) to produce lauroyl-N-methyl glucamide. Study was carried out by using immobilized lipase from Candida antarctica (Novozyme 435®), and tert-amylalcohol as a solvent. Response Surface Methodology (RSM) based on a five level, three variable design was employed, firstly, for studying the interactive effect of various parameters on the reaction, and secondly, for the optimization. The reaction parameters observed were Novozyme concentration, substrate molar ratio, and temperature. Simultaneously increasing Novozyme concentration, substrate molar ratio, and temperature improves the reaction yield and the effect of temperature is noted more significant. The expected optimum condition was at molar ratio MGL:AL 1:1, the Novozyme concentration of 8% and the reaction temperature of 50-55 °C. The reactions at the optimum condition produce the convertion of lauric acid of 64.5% and yield of 96.5%. With the optimization procedure the higher alkyl glucamide yield was achieved.

SYNTHESIS OF SAFRYL KETONE FROM SAFROLE Hanoch J Sohilait; Hardjono Sastrohamidjojo; Sabirin Matsjeh; J Stuart Grossert
Indonesian Journal of Chemistry Vol 4, No 1 (2004)
Publisher : Universitas Gadjah Mada

Synthesis of safryl ketone from safrole has been achieved through conversion of allyl group to secondary alcohol, followed by oxidation with PCC-Al2O3. The oxymecuration-demercuration reaction of safrole with HgSO4-NaBH4 yields safryl alcohol (66.38%) and the oxidation of safryl alcohol with PCC-Al2O3 yields safryl ketone (62.92%). The structure elucidation of these products was conducted using Fourier Transformed Infra Red Spectroscopy (FTIR), Proton-Nuclear Magnetic Resonance (1H-NMR) and Mass Spectroscopy (MS).

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