JSCS Vol 72, No. 2

Whole issue - PDF (1.238 KB WinZip file)

 

J. Serb. Chem. Soc. 72 (2) 89–100 (2007)

UDC 551.583:531.3+536.7:546.33'135+547.292–38, JSCS–3538, doi: 10.2298/JSC0702089M; Original scientific paper

 

Kinetic study of the reaction between sodium chloroacetate and potassium ethylxanthogenate

MILUTIN MILOSAVLJEVIC, ALEKSANDAR MARINKOVIC, BOBAN CEKOVIC* and SLAVICA RAZIC**

Faculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, P. O. Box 3503, Belgrade, Serbia

*Military Technical Institute, Belgrade, Serbia

**Faculty of Pharmacy, University of Belgrade, P. O. Box 146, 11000 Belgrade, Serbia

 

(Received 1 August, revised 7 December 2005)

The reaction kinetics of the synthesis of sodium ethyl xanthogeneacetate from potassium ethylxanthogenate and sodium chloroacetate in distilled water as the reaction medium at 25, 30, 35 and 40 °C, were investigated. The obtained reaction mixture was a complex system which demanded the use of two methods for the kinetic measurements. The reaction was followed using the conductrometric and UV/Vis spectrophotometric method with equimolar initial concentrations of the reactants and under pseudo-first order conditions with respect to one of the reactants. The rate constants of the pseudo-first order and second order reactions were calculated from the data. On the basis of the reaction constants, the activation parAMeters were calculated and are discussed.

 

Keywords: kinetic rate, rate constant, sodium ethyl xanthogeneacetate, thermodynAMic parAMeters.

Full Article - PDF 127 KB

J. Serb.Chem. Soc. 72 (2) 101–107 (2007)

UDC 547.216'466.1+547.466.23'466.1:615.281, JSCS–3539, doi: 10.2298/JSC0702101D; Original scientific paper

 

First total synthesis and biological evaluation of halolitoralin A

RAJIV DAHIYA and DEVENDER PATHAK

Rajiv Academy For Pharmacy, Chattikara, Mathura, India

 

(Received 2 February 2006)

A new potent bioactive alanine-rich cyclic hexapeptide halolitoralin A(8), which was previously isolated from the marine sediment-derived bacterial strain Halobacillus litoralis YS3016, has been synthesized by the solution phase technique. All the coupling reactions were performed at room temperature utilizing dicyclohexylcarbodiimide (DCC) as the coupling reagent and N-methylmorpholine (NMM) as the base. The structure of the peptide was characterized by IR, 1H-NMR, 13C-NMR, FAB MS spectral data, as well as elemental analysis and DSC. The synthesized cyclopeptide was also screened for its antimicrobial and anthelmintic activities and found to exhibit potent antifungal activity against the pathogenic fungi Candida albicans and Trichophyton mentagrophytes along with potent antibacterial activity against the grAM negative bacteria Pseudomonas aeruginosa and Escherichia coli. GrAM negative bacteria were found to be more sensitive than grAM positive bacteria towards the newly synthesized peptide. In addition, the peptide was also found to exhibit moderate anthelmintic activity against the earthworms Megascoplex konkanensis and Eudrilus sp.

 

Keywords: halolitoralin A, cyclic hexapeptide, alanine-rich peptide, antimicrobial activity, anthelmintic activity.

Full Article - PDF 107 KB

J. Serb. Chem. Soc. 72 (2) 109–117 (2007)

UDC 542.913+547.853/.854:615.281, JSCS–3540, 10.2298/JSC0702109V; Original scientific paper

 

Microwave assisted synthesis and antimicrobial activity of some novel pyrimidine derivatives

S. J. VAGHASIA and V. H. SHAH

Department of Chemistry, Saurashtra University, Rajkot-360 005, India

 

(Received 7 December 2005, revised 19. August 2006)

The synthesis of thiazolo [5,4-d]pyrimidines can be achieved from different 5-thiazolidinones, 2-butyl-1H-imidazole-5-carbaldehyde and thiourea using microwave irradiation within 5 min. The structures of the products were supported by FTIR, PMR and mass spectral data. The in vitro antimicrobial activity of the synthesized thiazolo [5,4-d]pyrimidines 1a-j, having substituents at the 1- and 3-positions, were determined by the cup-plate method against several standard strains chosen to define the spectrum and potency of the new compounds. The antimicrobial activities of the thiazolo [5,4-d]pyrimidines 1a-j are compared with those of known chosen standard drugs, viz. AMpicillin, chlorAMphenicol, ciprofloxacin, norfloxacin and griseofulvin.

 

Keywords: microwave irradiation, thiazolo [5,4-d]pyrimidines, antimicrobial activity.

Full Article - PDF 99 KB

J. Serb. Chem. Soc. 72 (2) 119–127 (2007)

UDC 542.913+667.281.2:677.042.4:579–188, JSCS–3541, 10.2298/JSC0702119D; Original scientific paper

 

Synthesis and application of new mordent and disperse azo dyes based on 2,4-dihydroxybenzophenone

BHARAT C. DIXIT, HITENDRAM. PATEL and DHIRUBHAI J. DESAI

Department of Chemistry, V. P. &AMp; R. P. T. P. Science College, Vallabh Vidyanagar-388120, Gujarat, India

 

(Received 2 December 2005, revised 20 April 2006)

Novel mordent and disperse azo dyes were prepared by the coupling of various diazo solutions of aromatic AMines with 2,4-ihydroxybenzophenone. The resultant dyes were characterized by elemental analyses as well as IR and NMR spectral studies. The UV-visible spectral data have also been  iscussed in terms of structural property relationship. The dyeing assessment of all the dyeswas evaluated on wool and polyester textile fibers. The dyeing of chrome treated (i.e., chrome mordented) wool and polyesters was also monitored. The results show that a better hue was obtained on mordented fibers. The results of the anti-bacterial properties of the chrome dyes revealed that the toxicity of these dyes against bacteria is fairly good.

 

Keywords: disperse dye,mordent dye, UVabsorber, dyeing, antimicrobial activity.

Full Article - PDF 98 KB

J. Serb. Chem. Soc. 72 (2) 129–132 (2007)

UDC 547.82.004.14+66.094.3:661.183.7, JSCS–3542, doi: 10.2298/JSC0702129A; Short communication

 

SHORT COMMUNICATION

The use of pyridinium fluorochromate (PFC) supported on TriSyl silica gel for oxidation reactions

FATMA AYDIN and ERSAN TURUNC*

Canakkale Onsekiz Mart University, Department of Chemistry, 17020, Canakkale, Turkey

*Mersin University, Department of Chemistry, 33342, Mersin, Turkey

 

(Received 23 March, revised 19 May 2006)

Pyridinium fluorochromate supported on TriSyl silicas was prepared by co-adsorption. The supported reagent was used in equimolar quantity to oxidise some organic compounds with good yields and complete selectivity. These procedures are mild, efficient, safe and the work-ups are very convenient.

 

Keywords: oxidation, pyridinium fluorochromate (PFC), TriSyl silicas.

Full Article - PDF 69 KB

J. Serb. Chem. Soc. 72 (2) 133–138 (2007)

UDC 582.936:549.25+549.328.1, JSCS–3543, doi: 10.2298/JSC0702133R; Original scientific paper

 

Content of heavymetals in Gentiana lutea L. roots and galenic forms

DRAGOJA RADANOVIC, SVETLANA ANTIC-MLADENOVIC*, MIODRAG JAKOVLJEVIC* and MIRJANA KRESOVIC*

Institute for Medicinal Plants Research "Dr Josif Pancic", Tadeusa Koscuska 1, 11000 Belgrade, Serbia

*Faculty of Agriculture, Nemanjina 6, 11080 Belgrade-Zemun, Serbia

 

(Received 24 March, revised 10 May 2006)

An experimental field for the cultivated production of Gentiana lutea L. was established five years ago at the Suvobor Mountain, Serbia. Soil analysis of this area revealed the occurrence of high pseudo-total (Ni – 1270 mg/kg, Cr – 423 mg/kg, Co – 385 mg/kg) and available (especially Ni – 133 mg/kg) heavy metals contents in the soil. Hence, the aim of this research was to evaluate the quality of Gentiana lutea L. – roots and galenic forms (liquid extract in 70 % ethanol, spissum and siccum) produced from the roots, because, for most plants, heavy metals accumulate in the root tissue. The AMounts of Ni and Cr found in the analyzed roots were very high (54 mg/kg and 14 mg/kg, respectively). The efficiency of ethanol in extracting heavy metals from the roots varied depending on the particular element. The highest efficiency was obtained for Ni (41.3 %), then for Cd (39.5 %), Pb (37.0%) and Co (30.4 %). According to this, a potential hazard exists for humans, if gentian's galenic forms are produced from the raw material with high heavy metals contents. It is concluded that quality control of the raw material must be carried out before further utilization of gentian.

 

Keywords: gentian, root, ethanol extract, nickel, chromium.

Full Article - PDF 93 KB

J. Serb. Chem. Soc. 72 (2) 139–150(2007)

UDC 678.84.004.14+542.913+678.073/.074, JSCS–3544, doi: 10.2298/JSC0702139A; Original scientific paper

 

Application of reactive siloxane prepolymers for the synthesis of thermoplastic poly(ester–siloxane)s and poly(ester–ether–siloxane)s

VESNA V. ANTIC, MARIJA V. VUCKOVIC and JASNA DJONLAGIC*

Institute of Chemistry, Technology and Metallurgy, Center of Chemistry-Department of Polymeric Materials, Studentski trg 12–16, 11000 Belgrade, Serbia

*Faculty of Technology of Metallurgy, Karnegijeva 4, 11000 Belgrade, Serbia

 

Thermoplastic poly(ester–siloxane)s (TPES) and poly(ester–ether–siloxane) s, (TPEES), based on poly(butylene terephthalate) (PBT) as the hard segment and different siloxane-prepolymers as the soft segments, were prepared. The TPES and TPEES were synthesized by catalyzed two-step transesterification from dimethyl terephthalate, (DMT), 1,4-butanediol, (BD) and a siloxane-prepolymer. Incorporation of dicarboxypropyl- or disilanol-terminated poly(dimethylsiloxane)s (PDMS) into the polar poly(butylene terephthalate) chains resulted in rather inhomogeneous TPES copolymers, which was a consequence of a prononuced phase separation of the polar and non-polar reactants during synthesis. Two concepts were employed to avoid or reduce phase separation: 1) the use of siloxane-containing triblock prepolymers with hydrophilic terminal blocks, such as ethylene oxide (EO), poly(propylene oxide) (PPO) or poly(caprolactone) (PLC) when the terminal blocks serve as a compatibilizer between the extremely non-polar PDMS and the polar DMT and BD, and 2) the use of a high-boiling solvent (1,2,4-trichlorobenzene) during the first phase of the reaction. Homogeneity was significantly improved in the case of copolymers based on PCL–PDMS–PCL.

 

Keywords: thermoplastic elastomers, poly(ester–siloxane)s, poly(ester–ether–siloxane)s, phase separation, compatibility.

Full Article - PDF 123 KB

J. Serb. Chem. Soc. 72 (2) 151–157 (2007)

UDC 539.193+546.11:536.722:543.2, JSCS–3545, doi: 10.2298/JSC0702151P; Original scientific paper

 

Evaluation of the intrAMolecular hydrogen bond enthalpy by means of specialized quantum chemical methods

ALEXEI N. PANKRATOV and ALEXEI V. SHALABAY

Department of Chemistry, N. G. Chernyshevskii Saratov State University, 83 Astrakhanaskaya Street, Saratov 410012, Russia

 

(Received 17 Febryary, revised 14 April 2006)

By means of the MNDO/H, I-MNDO, MNDO/HB andMNDO/Mmethods, the values of the enthalpy of intrAMolecular hydrogen bond (IHB) formation for series of substances have been computed. The applicability of these methods for a semi-quantitative estimation of the IHB enthalpy in compounds with a planar quasicycle has been shown.

 

Keywords: intrAMolecular hydrogen bond, enthalpy, quantum chemical evaluation, organic compounds with a planar quasicycle.

Full Article - PDF 83 KB

J. Serb. Chem. Soc. 72 (2) 159–164 (2007)

UDC 530.19*Rydberg:530.19*BuckinghAM:531.64, JSCS– 3546, doi: 10.2298/JSC0702159L; Original scientific paper

 

Relationship and discrepancies between the Extended-Rydberg and the Generalized BuckinghAM potential energy functions

TEIK-CHENG LIM

Faculty of Engineering, Nanoscience and Nanotechnology Initiative, 9 Engineering Drive 1,National University of Singapore, S 117576, Republic of Singapore

 

(Received 22 December 2005, revised 10 April 2006)

This paper relates the interatomic energy according to the Exdended-Rydberg and the Generalized BuckinghAM potential functions by applying a Maclaurin series expansion on the latter and thereafter comparing it with the former. In so doing, the plotted curves of these two functions not only show equal curvature at the equilibrium state, but also reveal a discrepancy for the finite distortion. It is shown that, when equated at equilibrium, the Generalized BuckinghAM gives a lower energy in comparison to the Extended-Rydberg at finite bond compression and stretching. However, the energy difference diminishes when the interatomic distance exceeds twice that at equilibrium. Due to such discrepancies upon comparative normalization, it would be beneficial for computational chemists to select the appropriate potential function for the purpose of conservative molecular modeling.

 

Keywords: Extended-Rydberg, Generalized BuckinghAM, interatomic energy, Maclaurin series, potential functions

Full Article - PDF 89 KB

J. Serb. Chem. Soc. 72 (2) 165–181 (2007)

UDC 66.087+546.92:547.261+66.094.3, JSCS–3547, doi: 10.2298/JSC0702165T; Original scientific paper

 

Effect of glassy carbon properties on the electrochemical deposition of platinum nano-catalyst and its activity for methanol oxidation

SANJA TERZIC, DUSAN TRIPKOVIC, VLADISLAVA M. JOVANOVIC, AMALIJA TRIPKOVIC and ANDRZEJ KOWAL*

ICTM – Institute of Electrochemistry, University of Belgrade, Njegoseva 12, P. O. Box 473, 11000 Belgrade, Serbia

*Institute of Catalysis and Surface Chemistry, Polish Academy of Science, Krakow, Niezapominajek 8, 30–239, Poland

 

(Received 31 January, revised 15 March 2006)

The effects of the properties of glassy carbon on the deposition of platinum particles and the electrocatalytic activity of platinum supported on glassy carbon (GC/Pt) for methanol oxidation in alkaline and acidic solutions were studied. Platinum was potentiostatically deposited on two glassy carbon sAMples, thermally treated at different temperatures, which were either polished or anodicaly polarised in acid (GCOX-AC/Pt) and in alkali (GCOX-AL/Pt). Anodic polarisation of glassy carbon, either in alkaline or acidic solution, enhances the activity of both types of GC/Pt electrodes for methanol oxidation. The activity of the catalysts follows the change in the properties of the glassy carbon support upon anodic treatment. The specific activity of the GCOX-AL/Pt electrode for this reaction in alkali is increased only a few times in comparison with the activity of the GC/Pt one. On the other hand, the specific activity of the GCOX-AC/Pt electrode for methanol oxidation in acid is about one order of magnitude higher than that of the GC/Pt electrode. The role of the substrate on the properties of catalyst is discussed in detail.

 

Keywords: glassy carbon support, platinu catalyst, electrochemical properties, methanol electrooxidation, scanning tunneling microscopy (STM).

Full Article - PDF 239 KB

J. Serb. Chem. Soc. 72 (2) 183–192 (2007)

UDC 66.094.3–097:547.212:547.313.2+66.023, JSCS–3548, doi: 10.2298/JSC0702183B; Original scientific paper

 

An experimental study of the partial oxidation of ethane to ethylene in a shallow fluidized bed reactor

DANICA BRZIC, DESISLAVA AHCHIEVA*, MIRKO PEGLOW* and STEFAN HEINRICH*

Faculty of Technology and Metallurgy, Karnegijeva 4, 11000 Belgrade, Serbia

*Otto-von-Guericke-Universität Magdeburg, IAUT, Universitätsplatz 2, D-39106 Magdeburg, Germany

 

The partial catalytic oxidation of ethane to ethylene was investigated experimentally in a shallow fluidized bed. The performaces of two catalyst types, pure g‑Al2O3 and V2O5/ g-Al2O3 particles 1.8 mm in diAMeter, were analyzed. A pilot fluidized bed reactor with rectangular cross-section of 100mm´100mm was used. The experiments were carried out under atmospheric pressure in a dilute system under oxygen excess conditions. V2O5/g-Al2O3 showed good catalytic performances regarding ethylene selectivity. The influence of the temperature (in the range of 400–600 °C) and the contact time (in the range of 35 – 85 kg sm-3) on the conversion of ethane and the selectivity to ethylene was analyzed. The highest yield of ethylene was 18 %.

 

Keywords: catalytic oxidation of ethane, ethylene, shallow fluidized bed.

Full Article - PDF 116 KB

J. Serb. Chem. Soc. 72 (2) 193–204 (2007)

UDC 547.6+547.538.7:631.445.6(262)”322”Herceg Novi, JSCS–3549, doi: 10.2298/JSC0702193J; Original scientific paper

 

Summertime PAH assembly in Mediterranean air: the Herceg Novi sAMpling station as an exAMple

VLADIMIR Z. JOVANOVIC*, PETAR A. PFENDT*,**, and ANKA J. JOVANOVIC***

*Department of Materials and Metallurgy, ICTM, Njego{eva 12, 11000 Belgrade, Serbia

**Faculty of Chemistry, University of Belgrade, Studentski trg 12–16, 11000 Belgrade, Serbia

***Institute of Public Health of Belgrade, Bulevar Despota Stefana 54-a, 11000 Belgrade, Serbia

 

(Received 3 November, revised 14 December 2005)

The results of an analysis of the total suspended particles (TSP), total solvent organic extracts (TSOE), and polycyclic aromatic hydrocarbons (PAHs) in aerosol sAMples collected from the atmosphere of Herceg Novi from 17th June to 15th September in 1998 and 1999 are presented. The TSP and TSOE concentrations were determined by the standard gravimetric method, whereas the PAHs from the organic part of the aerosol were analysed by the GC-MS method. The difference found in the TSP and TSOE contents between the two consecutive years (before and after the bombing of Yugoslavia) was attributed to changes in the intensity and origin of emissions from dominant sources, specific to the summer period of this region. The content and nature of the PAHs identified in the sAMples of 1998 and 1999 were also different, indicating the significance of traffic as the source of PAHs, which was of significantly lower intensity in 1999 (immediately after the war) due to the lower influx of tourists. Factor analysis showed that the PAH distribution at the measuring site in 1999 was largely determined by meteorological parAMeters, mainly by the average daily temperature and wind direction. In 1998, the dominant impact on the PAH distribution was attributed to traffic, both local and from a wider region, without an explicit impact of meteorological parAMeters.

 

Keywords: PAHs, Mediterranean air polution, particulate matter, meteorological conditions, factor analysis.

Full Article - PDF 41 KB

Journal Home Page

 

Copyright &AMp; copy; SHD 2007.
March 19, 2007.
For more information contact: JSCS@tmf.bg.ac.yu