JSCS Vol 67, No. 10  

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J. Serb. Chem. Soc. 67 (10)639–646(2002)
UDC 546.27:549.261+546.76
JSCS-2985
Short communication

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SHORT COMMUNICATION
Chemical composition and antimicrobial action of the ethanol extracts of
Salvia pratensis L., Salvia glutinosa L. and Salvia aethiopis L.

DRAGAN T. VELICKOVIC, NOVICA V. RANDJELOVIC*, MIHAILO S. RISTIC**, ANDRIJA A. SMELCEROVIC*** and ANA S. VELICKOVIC****

AD “Zdravlje” Pharmaceutical and Chemical Industry, Vlajkova St. 199, YU-16000 Leskovac,
*Faculty of Technology, Bulevar Oslobodjenja St. 124, YU-16000 Leskovac,
**Institue for Medicinal Plants Research “Dr. Josif Pancic”, Tadeusa Koscuska St. 1, YU-11000 Belgrade,
***Chemical Industry “Nevena”, Djordja Stamenkovica St. bb., YU-16000 Leskovac, and
****Medical Center “Mosa Pijade”, Department of General Practice, Rade Koncara St. 2, YU-16000 Leskovac, Yugoslavia

(Received 1 April, revised 27 May 2002)
Abstract: In this paper the chemical composition and antimicrobial action of the extracts from the flower, leaf and stem of Salvia pratensis L., Salvia glutinosa L. and Salvia aethiopis L. were investigated. The investigated extracts mostly contain monoterpenes to a high degree, except the flower extract of S. pratensis and the leaf extract of S. glutinosa where sesquiterpenes were found in great amounts. Diterpenes were found only in the extracts of S. aethiopis. All these extracts contained 1,8-cineole (to the highest degree (19.1 %) in the stem extract of S. glutinosa) and beta-caryophyllene (to the highest degree (7.0 %) in the flower extract of S. pratensis). The antimicrobial activities of the extracts were determined by the diffusion and dilution method.

Keywords: Salvia pratensis, Salvia glutinosa, Salvia aethiopis, Lamiaceae, extracts, chemical composition, antimicrobial activity.


J. Serb. Chem. Soc. 67 (10)647–651(2002)
UDC 54-12+539.2+512.546.1
JSCS-2986
Original scientific paper

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Upgrading the Wiener index

EDUARDO A. CASTRO, IVAN GUTMAN*, DAMIAN MARINO and PABLO PERUZZO

CEQUINOR, Departamento de Quimica, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, C. C. 962, La Plata 1900, Argentina and
*Faculty of Science, University of Kragujevac, P. O. Box 60, YU-34000 Kragujevac, Yugoslavia

(Received 18 June 2002)
The Wiener index W is the oldest molecular-graph-based structure-descriptor. It is defined as the sum of the distances of all pairs of vertices of the molecular graph G, where the distance is the number of edges in the shortest path connecting the respective vertices, and where G is the hydrogen-depleted molecular graph. This seemingly very simple topological index could be "upgraded" (a) by using as the distance the sum of the bond lengths along the shortest path, or (b) by using the Euclidean distance between the respective pairs of atoms. Each of these "upgraded" Wiener indices could be computed either (a) for the hydrogen-depleted or (b) for the hydrogen-filled molecular graph. We provide examples showing that none of the modifications (aa), (ab), (ba), (bb) yields better results than the ordinary Wiener index, and that there is a very good linear correlation between W and its "upgraded" variants.

Keywords: Wiener index, topological index, 3D-structure descriptors, chemical graph theory, QSPR, QSAR.


J. Serb. Chem. Soc. 67(10)653–659(2002)
UDC 546.663+542.913+66.061
JSCS-2987
Original scientific paper

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Extraction of Tb(III) with N,N,N’,N’-tetrabutylmalonamide

SUN GUOXIN, CUI YU**, JIANG RUNTIAN, XU RONGQI and SUN SIXIU**

Institute of Chemistry and Environmental Engineering, Jinan University, Jinan, 250022, P. R. China,
*Institute of Chemical Engineering, Jinan University, Jinan, 250022, P. R. China, and
**Institute of Chemistry, Shandong University, Jinan, 250100, P. R. China

(Received 15 April, revised 25 June 2002)
The study on the extraction and separation of rare earths with new extractants is important in rare earth hydrometallurgy and nuclear fuel reprocessing. In this work, a new synthesis method of N,N,N’,N’-tetrabutylmalonamide (TBMA) is described with a yield higher than 80 %. The extraction behavior of TBMA employing n-hexane-20 % n-octanol, benzene and toluene as diluents toward Tb(III) was investigated. The effect of the concentrations of nitric acid, lithium nitrate and extractant as well as the temperature on the extraction distribution ratio was studied in different diluents. The stoichiometry of the extracted species of Tb(III) conforms to Tb(NO3)3·3TBMA. An attempt was made to determine the structure of the extracted species from IR and mol conductance data.

Keywords: synthesis, N,N,N’,N’-tetrabutylmalonamide, extraction, Tb(III), diluent, structure.


J. Serb. Chem. Soc. 67(10)661–667(2002)
UDC 547.56+547.632.5:543.23
JSCS-2988
Original scientific paper

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A kinetic method for the determination of phenol

SNEZANA S. MITIC and VALENTINA V. ZIVANOVIC

Faculty of Sciences and Mathematics, Department of Chemistry, University of Nis, Visegradska 33, P.O.Box 224, YU-18000 Nis, Yugoslavia

(Received 21 March 2001, Revised 1 July 2002)
A kinetic method for the determination of phenol is proposed. The method is based on the inhibiting effect of phenol on the Mn(II) catalysis of the oxidation of malachite green with potassium periodate. The reaction rate was followed spectrophotometrically at 615 nm. Kinetic expression for the reaction in the presence and absence of phenol are postulated. The optimal experimental conditions for the determination of phenol were established and phenol was determined in concentrations from 30.0 to 188.0 ng/cm3 with a relative standard deviation of 5.5 %. The lower detecton limit is 7.8 ng/cm3. The effects of certain foreign ions upon the reaction rate were determined for the assessment of the selectivity of the method. The method was applied for the determination of phenol in tap and river water.

Keywords: phenol kinetic determination, malachite green oxidation, potassium periodate.


J. Serb. Chem. Soc. 67(10)669–676(2002)
UDC 546.72+543.48:556
JSCS-2989
Original scientific paper

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Spectrophotometric determination of trace iron(III) in natural water after its preconcentration with a chelating resin

ZENOVIA MOLDOVAN and ELEONORA-ANA NEAGU*

University of Bucharest, Faculty of Chemistry, Department of Analytical Chemistry, 4-12 Regina Elisabeta Blvd., 703461-Bucharest, Romania and
*Institute of Rare and Nonferrous Metals, 102 Biruintei Blvd., Bucharest, Romania

(Received 2 February, revised 17 May 2002)
A method for the determination of Fe(III) at trace levels is described. Thus, prior to the spectrophotometric determination, a preconcentration of the trace amounts of iron(III) using a chelate forming resin is proposed. A strong base anion-exchange resin (Dowex 2X4) loaded with Ferron (7-iodo-8-hydroxyquinoline-5-sulphonic acid) was used for Fe(III) preconcentration, at pH 2.2. After desorption with 5 % ascorbic acid in 0.5 M HCl, the analyte (converted from Fe(III) to Fe(II) was determined spectrophotometrically at 510 nm as Fe(II)-o-phenanthroline complex. The accuracy of the proposed method was verified by comparing the obtained results with those obtained using AAS with the standard addition method. The sensitivity of the spectrophotometric method (after preconcentration) was 0.01 mg Fe(III)/ml. The recovery for iron(III) at the 7 mg/l level was 97 %.

Keywords: iron(III), Ferron, chelating resin, preconcentration, spectrophotometric determination.


J. Serb. Chem. Soc. 67(10)677–684(2002)
UDC 546.562+547.57:543
JSCS-2990
Original scientific paper

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Cu(II) complexes with a pendant octaazamacrocycle and m-bonded aromatic carboxylates

GORDANA VUCKOVIC, MIRJANA ANTONIJEVIC* and DEJAN POLETI**

Faculty of Chemistry, University of Belgrade, P. O. Box 158, YU-11001 Belgrade
*High School for Chemistry and Technology, YU-15000 Sabac and
**Department of General and Inorganic Chemistry, Faculty of Technology and Metallurgy, Karnegijeva, 4, YU-11000 Belgrade, Yugoslavia

(Received 20 March 2002)
Three new cationic mixed-ligand Cu(II) complexes with N,N’,N’’,N’’’-tetrakis(2-pyridylmethyl)-1,4,8,11-tetraazacyclotetradecane (tpmc) and bridging aromatic mono- or dicarboxylate ligands were prepared. Elemental analysis, conductometric and magnetic measurements, as well as electronic and IR spectroscopy were employed for their characteriization. It is proposed that the complexes [Cu2(C6H5COO)tpmc](CIO4)3MeOH and [Cu2(Hpht)tpmc](CIO4)3H2O (H2pht = phthalic acid) are binuclear with m-coordination of the carboxylate monoanions. The third complex, [Cu4ipht(tpmc)2](CIO4)6NaClO42MeCN (H2ipht = isophthalic acid) is one of the rare tetranuclear Cu(II)-tpmc complexes with an aromatic dicarboxylate ion bridging two Cu2tpmc units. This was also confirmed by preliminary results of the determination of the crystal structure.

Keywords: copper(II) complexes, octaazamacrocycle, benzoate, phthalate, isophthalate.


J. Serb. Chem. Soc. 67(10)685–696(2002)
UDC 546.663+542.913+66.061
JSCS-2991
Original scientific paper

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Study of the ability of self-assembled N-vinylcarbazole monolayers to protect copper against corrosion

CHUN-TAO WANG*, SHEN-HAO CHEN*,**, HOU-YI MA*, LAN HUA* and NAI-XING WANG*

*Department of Chemistry, Shandong University, Jinan 250100, P. R. China and
**State Key Laboratory for Corrosion and Protection, Shenyang 110015, P. R. China

(Received 17 January, revised 28 June 2002)
N-Vinylcarbazole (NVC) monolayers were self-assembled on copper surfaces. The electrochemical properties of the copper surfaces modified by NVC self-assembled monolayers (SAMs) were investigated using polarization and electrochemical impedance spectroscopic (EIS) methods. The polarization measurements indicated that the NVC SAMs could reduce the rates of the anodic and cathodic reaction on the surface of copper electrodes in 0.5 mol dm-3 NaCl solution. The EIS results showed the NVC formed a closely packed film that was able to inhibit copper corrosion. X-Ray photoelectron spectroscopy (XPS) analysis of the copper samples and atomic adsorption analysis of the solution showed that the copper surfaces were covered by NVC SAMs, and the adsorption of NVC on the copper surfaces was accompanied with dissolution of Cu into the solution.

Keywords: self-assembled monolayers, N-vinylcarbazole, copper, EIS, XPS.


J. Serb. Chem. Soc. 67(10)697–707(2002)
UDC 546.27:549.261+546.76
JSCS-2992
Original scientific paper

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The effect of boron on the amount and type of carbides in chromium white irons

STANKA M. TOMOVIC-PETROVIC, SRDJAN V. MARKOVIC* and SLAVICA ZEC**

Institute “Kirilo Savic”, Vojvode Stepe 51, YU-11000 Belgrade,
*Faculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, YU-11000 Belgrade and
**Vinca Institute for Nuclear Science, P. O. Box 522, YU-11000 Belgrade, Yugoslavia

(Received  23 August 2000,  revised 15 June 2002)
The effect of boron, in the amounts of 0.26, 0.39, and 0.59 wt.%, on the volume fraction and structure of carbides in Cr white irons was examined. It was demonstrated that the addition of boron can change the microstructural characteristics of white iron containing about 13 wt.% Cr. With increasing boron content, the volume fractions of M3C carbide increase, but the volume fracton of M7C3 carbide remains unchanged. The addition of boron tends to produce hard borides and/or borocarbides. It also prevents the formation of pearlite, which results in alloys possessing good wear resistance.

Keywords: chromium white iron, boron, carbides, borocarbide.


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