Veselinović, Dragan S.

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  • Veselinović, Dragan S. (12)
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Author's Bibliography

Radioaktivnost u mahovinama i lišajevima sakupljenim 2015. godine u NP Đerdap

Čučulović, Ana; Čučulović, Rodoljub; Nestorović, Saša; Veselinović, Dragan S.

(Београд : Институт за нуклеарне науке "Винча" : Друштво за заштиту од зрачења Србије и Црне Горе, 2017)

TY  - CONF
AU  - Čučulović, Ana
AU  - Čučulović, Rodoljub
AU  - Nestorović, Saša
AU  - Veselinović, Dragan S.
PY  - 2017
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/8261
UR  - https://plus.sr.cobiss.net/opac7/bib/245691404
UR  - http://dzz.org.rs/wp-content/uploads/2013/06/Zbornik_XXIX_Simpozijum_DZZ_SCG_Srebrno_jezero_2.pdf
AB  - U radu su prikazani nivoi aktivnosti prirodnih radionuklida (40K, 226Ra, 232Th, 238U) i
veštački proizvedenog 137Cs u uzorcima mahovina (28) i lišajeva (17) sakupljenim na
teritoriji Nacionalnog parka Đerdap u maju 2015. godine. U svim uzorcima mahovina i
lišajeva utvrđeno je prisustvo radionuklida. Dobijeni rezultati upućuju na zaključak da
su mahovine i lišajevi dobri biomonitori i bioindikatori radiozagađenja životne sredine,
kao i da je neophodno pratiti nivoe aktivnosti radionuklida u njima zbog mogućeg
radijacionog rizika organizama koji ih koriste za ishranu ili upotrebljavaju za neku
drugu svrhu.
AB  - Activity levels of natural (40K, 226Ra, 232Th, 238U) and artificially produced 137Cs
radionuclides in moss (28) and lichen (17) samples collected on the territory of the
Djerdap national park in May 2015 are presented in this work. Radionuclide presence
was established in all moss and lichen samples. The obtained results indicate that moss
and lichen are good bioindicators of radio-pollution of the environment. It is necessary
to monitor activity levels of radionuclides in moss and lichen due to possible radiation
risks of organisms consuming them as food or using them for other purposes.
PB  - Београд : Институт за нуклеарне науке "Винча" : Друштво за заштиту од зрачења Србије и Црне Горе
C3  - 29. симпозијум ДЗЗСЦГ : зборник радова
T1  - Radioaktivnost u mahovinama i lišajevima sakupljenim 2015. godine u NP Đerdap
T1  - Radioactivity in moss and lichen collected in 2015 from NP Djerdap
SP  - 99
EP  - 107
ER  - 
@conference{
author = "Čučulović, Ana and Čučulović, Rodoljub and Nestorović, Saša and Veselinović, Dragan S.",
year = "2017",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/8261, https://plus.sr.cobiss.net/opac7/bib/245691404, http://dzz.org.rs/wp-content/uploads/2013/06/Zbornik_XXIX_Simpozijum_DZZ_SCG_Srebrno_jezero_2.pdf",
abstract = "U radu su prikazani nivoi aktivnosti prirodnih radionuklida (40K, 226Ra, 232Th, 238U) i
veštački proizvedenog 137Cs u uzorcima mahovina (28) i lišajeva (17) sakupljenim na
teritoriji Nacionalnog parka Đerdap u maju 2015. godine. U svim uzorcima mahovina i
lišajeva utvrđeno je prisustvo radionuklida. Dobijeni rezultati upućuju na zaključak da
su mahovine i lišajevi dobri biomonitori i bioindikatori radiozagađenja životne sredine,
kao i da je neophodno pratiti nivoe aktivnosti radionuklida u njima zbog mogućeg
radijacionog rizika organizama koji ih koriste za ishranu ili upotrebljavaju za neku
drugu svrhu., Activity levels of natural (40K, 226Ra, 232Th, 238U) and artificially produced 137Cs
radionuclides in moss (28) and lichen (17) samples collected on the territory of the
Djerdap national park in May 2015 are presented in this work. Radionuclide presence
was established in all moss and lichen samples. The obtained results indicate that moss
and lichen are good bioindicators of radio-pollution of the environment. It is necessary
to monitor activity levels of radionuclides in moss and lichen due to possible radiation
risks of organisms consuming them as food or using them for other purposes.",
publisher = "Београд : Институт за нуклеарне науке "Винча" : Друштво за заштиту од зрачења Србије и Црне Горе",
journal = "29. симпозијум ДЗЗСЦГ : зборник радова",
title = "Radioaktivnost u mahovinama i lišajevima sakupljenim 2015. godine u NP Đerdap, Radioactivity in moss and lichen collected in 2015 from NP Djerdap",
pages = "99-107"
}
Čučulović, A., Čučulović, R., Nestorović, S.,& Veselinović, D. S. (2017). Radioactivity in moss and lichen collected in 2015 from NP Djerdap.
29. симпозијум ДЗЗСЦГ : зборник радова
Београд : Институт за нуклеарне науке "Винча" : Друштво за заштиту од зрачења Србије и Црне Горе., 99-107.
Čučulović A, Čučulović R, Nestorović S, Veselinović DS. Radioactivity in moss and lichen collected in 2015 from NP Djerdap. 29. симпозијум ДЗЗСЦГ : зборник радова. 2017;:99-107
Čučulović Ana, Čučulović Rodoljub, Nestorović Saša, Veselinović Dragan S., "Radioactivity in moss and lichen collected in 2015 from NP Djerdap" 29. симпозијум ДЗЗСЦГ : зборник радова (2017):99-107

Natural radionuclide uptake by mosses in eastern Serbia in 2008-2013

Cuculovic, Ana; Cuculovic, Rodoljub; Sabovljevic, Marko; Radenković, Mirjana; Veselinović, Dragan S.

(2016)

TY  - JOUR
AU  - Cuculovic, Ana
AU  - Cuculovic, Rodoljub
AU  - Sabovljevic, Marko
AU  - Radenković, Mirjana
AU  - Veselinović, Dragan S.
PY  - 2016
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/1114
AB  - The results of the study on natural radionuclide content in 102 samples of the moss species randomly collected in 20082013 at 30 locations of eastern Serbia are presented in the paper. The activity concentration values of U-238, Ra-226, Th-232, K-40, and Be-7 determined by gamma spectrometry were within the intervals: U-238 (1.1-50) Bq kg(-1), Ra-226 (1.1-41) Bq kg(-1), Th-232 (1.4-28) Bq kg(-1), K-40 (64-484) Bq kg(-1) and Be-7 (88-227) Bq kg(-1), not standing out of the average data reported for this region. The distribution of the obtained data for Ra-226, Th-232, and U-238 activity concentration in the analysed mosses has shown values up to 10 Bq kg(-1) with frequencies 47.1 %, 54.9 % and 48.0 %, respectively. The obtained activity concentration values of primordial K-40 and cosmogenic radionuclide Be-7 were up to 500 Bq kg(-1) and about 90 % of all the results for Be-7 uptake by mosses were in the 200-250 Bq kg(-1) concentration range.
T2  - Arhiv za higijenu rada i toksikologiju
T1  - Natural radionuclide uptake by mosses in eastern Serbia in 2008-2013
VL  - 67
IS  - 1
SP  - 31
EP  - 37
DO  - 10.1515/aiht-2016-67-2695
ER  - 
@article{
author = "Cuculovic, Ana and Cuculovic, Rodoljub and Sabovljevic, Marko and Radenković, Mirjana and Veselinović, Dragan S.",
year = "2016",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/1114",
abstract = "The results of the study on natural radionuclide content in 102 samples of the moss species randomly collected in 20082013 at 30 locations of eastern Serbia are presented in the paper. The activity concentration values of U-238, Ra-226, Th-232, K-40, and Be-7 determined by gamma spectrometry were within the intervals: U-238 (1.1-50) Bq kg(-1), Ra-226 (1.1-41) Bq kg(-1), Th-232 (1.4-28) Bq kg(-1), K-40 (64-484) Bq kg(-1) and Be-7 (88-227) Bq kg(-1), not standing out of the average data reported for this region. The distribution of the obtained data for Ra-226, Th-232, and U-238 activity concentration in the analysed mosses has shown values up to 10 Bq kg(-1) with frequencies 47.1 %, 54.9 % and 48.0 %, respectively. The obtained activity concentration values of primordial K-40 and cosmogenic radionuclide Be-7 were up to 500 Bq kg(-1) and about 90 % of all the results for Be-7 uptake by mosses were in the 200-250 Bq kg(-1) concentration range.",
journal = "Arhiv za higijenu rada i toksikologiju",
title = "Natural radionuclide uptake by mosses in eastern Serbia in 2008-2013",
volume = "67",
number = "1",
pages = "31-37",
doi = "10.1515/aiht-2016-67-2695"
}
Cuculovic, A., Cuculovic, R., Sabovljevic, M., Radenković, M.,& Veselinović, D. S. (2016). Natural radionuclide uptake by mosses in eastern Serbia in 2008-2013.
Arhiv za higijenu rada i toksikologiju, 67(1), 31-37.
https://doi.org/10.1515/aiht-2016-67-2695
Cuculovic A, Cuculovic R, Sabovljevic M, Radenković M, Veselinović DS. Natural radionuclide uptake by mosses in eastern Serbia in 2008-2013. Arhiv za higijenu rada i toksikologiju. 2016;67(1):31-37
Cuculovic Ana, Cuculovic Rodoljub, Sabovljevic Marko, Radenković Mirjana, Veselinović Dragan S., "Natural radionuclide uptake by mosses in eastern Serbia in 2008-2013" Arhiv za higijenu rada i toksikologiju, 67, no. 1 (2016):31-37,
https://doi.org/10.1515/aiht-2016-67-2695 .
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Lišajevi-bioindikatori radioaktivnog zagađenja životne sredine

Čučulović, Ana; Čučulović, Rodoljub; Nestorović, Saša; Veselinović, Dragan S.

(Београд : Институт за нуклеарне науке "Винча", Лабораторија за заштиту од зрачења и заштиту животне средине : Друштво за заштиту од зрачења Србије и Црне Горе, 2016)

TY  - CHAP
AU  - Čučulović, Ana
AU  - Čučulović, Rodoljub
AU  - Nestorović, Saša
AU  - Veselinović, Dragan S.
PY  - 2016
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/8241
UR  - http://www.vbs.rs/scripts/cobiss?command=DISPLAY&base=99999&rid=226685452&fmt=11&lani=sc
UR  - http://dzz.org.rs/wp-content/uploads/2013/06/30-godina-Cernobilja-monografija-1.pdf
AB  - Tkivo lišajeva odražava elementarni sastav životne sredine, pa su oni dobri
bioindikatori i biomonitori zagađenja životne sredine, jer nemaju formiran koren,
list, stablo, kutikulu i stome, a vodu i mineralne materije upijaju celom površinom
talusa. Nivoi aktivnosti 137Cs u lišajevima BiH 1985. godine bili su od 397 do 696
Bq/kg. Srednji nivo aktivnosti 137Cs u lišajevima vrste Evernia prunastri u prvoj
polovini 1987. godine je bio 10161 Bq/kg, odnosno, 13610 Bq/kg u drugoj polovini
iste godine, a u lišajevima vrste Cetraria islandica je u drugoj polovini 1987.
godine bio 10392 Bq/kg. U periodu 1986-2015. godina, nivoi aktivnosti 137Cs u
ispitivanim uzorcima lišajeva opadaju. Srednji nivo aktivnosti 137Cs u lišajevima
vrste Hypogimnia physodes sakupljenim 2010. godine u NP Đerdap bio je 150
Bq/kg, a 2015. godine 128 Bq/kg. Nivoi aktivnosti 137Cs su u nivoima pre akcidenta
u Černobilju (1986. god), tj. novih zagađenja ovim izotopom nije bilo.
AB  - Lichen tissue reflects the elementary composition of the environment. They are
good bioindicators and biomonitors of environment pollution as they do not have
a formed root, leaves, trunk, cuticula and stoma and they absorb water and
minerals with the whole thallus surface. The activity levels of 137Cs in lichen in
BiH in 1985 were from 397 to 696 Bq/kg. The average activity level of 134+137Cs
in lichen of the Evernia prunastri species in the first half of 1987 was 10161
Bq/kg, and 13610 Bq/kg in the second half of the same year. In lichen of the
Cetraria islandicaspecies in the second half of 1987 the activity level was 10392
Bq/kg. In the period 1986-2015 the activity levels of 137Cs in investigated lichen
samples decreased. The average activity level of 137Cs in Hypogimnia
physodeslichen species collected in 2010 in NP Djerdap was 150 Bq/kg, while in
2015 it was 128 Bq/kg. Activity levels of 137Cs have dropped to levels before the
Chernobyl accident so no new pollutions with this isotope have occurred.
PB  - Београд : Институт за нуклеарне науке "Винча", Лабораторија за заштиту од зрачења и заштиту животне средине : Друштво за заштиту од зрачења Србије и Црне Горе
T2  - Чернобиљ : 30 година после : монографија
T1  - Lišajevi-bioindikatori radioaktivnog zagađenja životne sredine
T1  - Lichen - bioindicators of radioactive pollution of the environment
SP  - 241
EP  - 255
ER  - 
@article{
author = "Čučulović, Ana and Čučulović, Rodoljub and Nestorović, Saša and Veselinović, Dragan S.",
year = "2016",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/8241, http://www.vbs.rs/scripts/cobiss?command=DISPLAY&base=99999&rid=226685452&fmt=11&lani=sc, http://dzz.org.rs/wp-content/uploads/2013/06/30-godina-Cernobilja-monografija-1.pdf",
abstract = "Tkivo lišajeva odražava elementarni sastav životne sredine, pa su oni dobri
bioindikatori i biomonitori zagađenja životne sredine, jer nemaju formiran koren,
list, stablo, kutikulu i stome, a vodu i mineralne materije upijaju celom površinom
talusa. Nivoi aktivnosti 137Cs u lišajevima BiH 1985. godine bili su od 397 do 696
Bq/kg. Srednji nivo aktivnosti 137Cs u lišajevima vrste Evernia prunastri u prvoj
polovini 1987. godine je bio 10161 Bq/kg, odnosno, 13610 Bq/kg u drugoj polovini
iste godine, a u lišajevima vrste Cetraria islandica je u drugoj polovini 1987.
godine bio 10392 Bq/kg. U periodu 1986-2015. godina, nivoi aktivnosti 137Cs u
ispitivanim uzorcima lišajeva opadaju. Srednji nivo aktivnosti 137Cs u lišajevima
vrste Hypogimnia physodes sakupljenim 2010. godine u NP Đerdap bio je 150
Bq/kg, a 2015. godine 128 Bq/kg. Nivoi aktivnosti 137Cs su u nivoima pre akcidenta
u Černobilju (1986. god), tj. novih zagađenja ovim izotopom nije bilo., Lichen tissue reflects the elementary composition of the environment. They are
good bioindicators and biomonitors of environment pollution as they do not have
a formed root, leaves, trunk, cuticula and stoma and they absorb water and
minerals with the whole thallus surface. The activity levels of 137Cs in lichen in
BiH in 1985 were from 397 to 696 Bq/kg. The average activity level of 134+137Cs
in lichen of the Evernia prunastri species in the first half of 1987 was 10161
Bq/kg, and 13610 Bq/kg in the second half of the same year. In lichen of the
Cetraria islandicaspecies in the second half of 1987 the activity level was 10392
Bq/kg. In the period 1986-2015 the activity levels of 137Cs in investigated lichen
samples decreased. The average activity level of 137Cs in Hypogimnia
physodeslichen species collected in 2010 in NP Djerdap was 150 Bq/kg, while in
2015 it was 128 Bq/kg. Activity levels of 137Cs have dropped to levels before the
Chernobyl accident so no new pollutions with this isotope have occurred.",
publisher = "Београд : Институт за нуклеарне науке "Винча", Лабораторија за заштиту од зрачења и заштиту животне средине : Друштво за заштиту од зрачења Србије и Црне Горе",
journal = "Чернобиљ : 30 година после : монографија",
title = "Lišajevi-bioindikatori radioaktivnog zagađenja životne sredine, Lichen - bioindicators of radioactive pollution of the environment",
pages = "241-255"
}
Čučulović, A., Čučulović, R., Nestorović, S.,& Veselinović, D. S. (2016). Lichen - bioindicators of radioactive pollution of the environment.
Чернобиљ : 30 година после : монографија
Београд : Институт за нуклеарне науке "Винча", Лабораторија за заштиту од зрачења и заштиту животне средине : Друштво за заштиту од зрачења Србије и Црне Горе., 241-255.
Čučulović A, Čučulović R, Nestorović S, Veselinović DS. Lichen - bioindicators of radioactive pollution of the environment. Чернобиљ : 30 година после : монографија. 2016;:241-255
Čučulović Ana, Čučulović Rodoljub, Nestorović Saša, Veselinović Dragan S., "Lichen - bioindicators of radioactive pollution of the environment" Чернобиљ : 30 година после : монографија (2016):241-255

Desorption of Metals from Cetraria Islandica (L.) Ach. Lichen Using Solutions Simulating Acid Rain

Cuculovic, Ana A.; Pavlović, Mirjana S.; Savović, Jelena; Veselinović, Dragan S.

(2014)

TY  - JOUR
AU  - Cuculovic, Ana A.
AU  - Pavlović, Mirjana S.
AU  - Savović, Jelena
AU  - Veselinović, Dragan S.
PY  - 2014
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/5859
AB  - Desorption of metals K, Al, Ca, Mg, Fe, Ba, Zn, Mn, Cu and Sr from Cetraria islandica (L.) with solutions whose composition was similar to that of acid rain, was investigated. Desorption of metals from the lichen was performed by five successive desorption processes. Solution mixtures containing H2SO4, HNO3 and H2SO4-HNO3 were used for desorption. Each solution had three different pH values: 4.61, 5.15 and 5.75, so that the desorptions were performed with nine different solutions successively five times, always using the same solution volume. The investigated metals can be divided into two groups. One group was comprised of K, Ca and Mg, which were desorbed in each of the five desorption processes at all pH values used. The second group included Al, Fe, Zn, Ba, Mn and Sr; these were not desorbed in each individual desorption and not at all pH values, whereas Cu was not desorbed at all under any circumstances. Using the logarithmic dependence of the metal content as a function of the desorption number, it was found that potassium builds two types of links and is connected with weaker links in lichen. Potassium is completely desorbed, 80% in the first desorption, and then gradually in the following desorptions. Other metals are linked with one weaker link (desorption 1-38%) and with one very strong link (desorption below the metal detection limit).
T2  - Archives of biological sciences
T1  - Desorption of Metals from Cetraria Islandica (L.) Ach. Lichen Using Solutions Simulating Acid Rain
VL  - 66
IS  - 1
SP  - 273
EP  - 284
DO  - 10.2298/ABS1401273C
ER  - 
@article{
author = "Cuculovic, Ana A. and Pavlović, Mirjana S. and Savović, Jelena and Veselinović, Dragan S.",
year = "2014",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/5859",
abstract = "Desorption of metals K, Al, Ca, Mg, Fe, Ba, Zn, Mn, Cu and Sr from Cetraria islandica (L.) with solutions whose composition was similar to that of acid rain, was investigated. Desorption of metals from the lichen was performed by five successive desorption processes. Solution mixtures containing H2SO4, HNO3 and H2SO4-HNO3 were used for desorption. Each solution had three different pH values: 4.61, 5.15 and 5.75, so that the desorptions were performed with nine different solutions successively five times, always using the same solution volume. The investigated metals can be divided into two groups. One group was comprised of K, Ca and Mg, which were desorbed in each of the five desorption processes at all pH values used. The second group included Al, Fe, Zn, Ba, Mn and Sr; these were not desorbed in each individual desorption and not at all pH values, whereas Cu was not desorbed at all under any circumstances. Using the logarithmic dependence of the metal content as a function of the desorption number, it was found that potassium builds two types of links and is connected with weaker links in lichen. Potassium is completely desorbed, 80% in the first desorption, and then gradually in the following desorptions. Other metals are linked with one weaker link (desorption 1-38%) and with one very strong link (desorption below the metal detection limit).",
journal = "Archives of biological sciences",
title = "Desorption of Metals from Cetraria Islandica (L.) Ach. Lichen Using Solutions Simulating Acid Rain",
volume = "66",
number = "1",
pages = "273-284",
doi = "10.2298/ABS1401273C"
}
Cuculovic, A. A., Pavlović, M. S., Savović, J.,& Veselinović, D. S. (2014). Desorption of Metals from Cetraria Islandica (L.) Ach. Lichen Using Solutions Simulating Acid Rain.
Archives of biological sciences, 66(1), 273-284.
https://doi.org/10.2298/ABS1401273C
Cuculovic AA, Pavlović MS, Savović J, Veselinović DS. Desorption of Metals from Cetraria Islandica (L.) Ach. Lichen Using Solutions Simulating Acid Rain. Archives of biological sciences. 2014;66(1):273-284
Cuculovic Ana A., Pavlović Mirjana S., Savović Jelena, Veselinović Dragan S., "Desorption of Metals from Cetraria Islandica (L.) Ach. Lichen Using Solutions Simulating Acid Rain" Archives of biological sciences, 66, no. 1 (2014):273-284,
https://doi.org/10.2298/ABS1401273C .
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Antioxidant activity of propolis extracts from Serbia: A polarographic approach

Potkonjak, Nebojša I.; Veselinović, Dragan S.; Novaković, Miroslav M.; Gorjanovic, Stanislava Z.; Pezo, Lato; Sužnjevicć, Desanka Ž.

(2012)

TY  - JOUR
AU  - Potkonjak, Nebojša I.
AU  - Veselinović, Dragan S.
AU  - Novaković, Miroslav M.
AU  - Gorjanovic, Stanislava Z.
AU  - Pezo, Lato
AU  - Sužnjevicć, Desanka Ž.
PY  - 2012
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/5101
AB  - Antioxidant activity (AO) of commercial propolis extracts (PEs), available on Serbian market, was determined by direct current (DC) polarography. Polarographic anodic current of 5.0 mmol L-1 alkaline solution of H2O2 was recorded at potentials of mercury dissolution. Decrease of the current was plotted against the volume of gradually added PEs. The volume of PE causing 20% current decrease was determined from the linear part of the plot. Antioxidant activity was expressed in H2O2 equivalent (HPEq), representing the volume of PE that corresponds to 1.0 mmol L-1 H2O2 decrease. Resulting HPEq ranged between 1.71 +/- 0.11 and 8.00 +/- 0.18 mu L. Range of 1,1-dipheny1-2-picryl hydrazyl (DPPH) radical scavenging activity was from 0.093 +/- 0.004% to 0.346 +/- 0.006%. Total phenolic content (TCP) of PE with superior AO activity was 5.31 +/- 0.05%g GAE, while the extract with the lowest activity contained 1.45 +/- 0.02%g GAE. Antioxidant activity, determined by polarographic method, was correlated with DPPH scavenging activity (R-2 = 0.991) and TCP (R-2 = 0.985). Validity of obtained results was further confirmed using ANOVA and post hoc Tukey HSD test. (C) 2012 Elsevier Ltd. All rights reserved.
T2  - Food and Chemical Toxicology
T1  - Antioxidant activity of propolis extracts from Serbia: A polarographic approach
VL  - 50
IS  - 10
SP  - 3614
EP  - 3618
DO  - 10.1016/j.fct.2012.07.029
ER  - 
@article{
author = "Potkonjak, Nebojša I. and Veselinović, Dragan S. and Novaković, Miroslav M. and Gorjanovic, Stanislava Z. and Pezo, Lato and Sužnjevicć, Desanka Ž.",
year = "2012",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/5101",
abstract = "Antioxidant activity (AO) of commercial propolis extracts (PEs), available on Serbian market, was determined by direct current (DC) polarography. Polarographic anodic current of 5.0 mmol L-1 alkaline solution of H2O2 was recorded at potentials of mercury dissolution. Decrease of the current was plotted against the volume of gradually added PEs. The volume of PE causing 20% current decrease was determined from the linear part of the plot. Antioxidant activity was expressed in H2O2 equivalent (HPEq), representing the volume of PE that corresponds to 1.0 mmol L-1 H2O2 decrease. Resulting HPEq ranged between 1.71 +/- 0.11 and 8.00 +/- 0.18 mu L. Range of 1,1-dipheny1-2-picryl hydrazyl (DPPH) radical scavenging activity was from 0.093 +/- 0.004% to 0.346 +/- 0.006%. Total phenolic content (TCP) of PE with superior AO activity was 5.31 +/- 0.05%g GAE, while the extract with the lowest activity contained 1.45 +/- 0.02%g GAE. Antioxidant activity, determined by polarographic method, was correlated with DPPH scavenging activity (R-2 = 0.991) and TCP (R-2 = 0.985). Validity of obtained results was further confirmed using ANOVA and post hoc Tukey HSD test. (C) 2012 Elsevier Ltd. All rights reserved.",
journal = "Food and Chemical Toxicology",
title = "Antioxidant activity of propolis extracts from Serbia: A polarographic approach",
volume = "50",
number = "10",
pages = "3614-3618",
doi = "10.1016/j.fct.2012.07.029"
}
Potkonjak, N. I., Veselinović, D. S., Novaković, M. M., Gorjanovic, S. Z., Pezo, L.,& Sužnjevicć, D. Ž. (2012). Antioxidant activity of propolis extracts from Serbia: A polarographic approach.
Food and Chemical Toxicology, 50(10), 3614-3618.
https://doi.org/10.1016/j.fct.2012.07.029
Potkonjak NI, Veselinović DS, Novaković MM, Gorjanovic SZ, Pezo L, Sužnjevicć DŽ. Antioxidant activity of propolis extracts from Serbia: A polarographic approach. Food and Chemical Toxicology. 2012;50(10):3614-3618
Potkonjak Nebojša I., Veselinović Dragan S., Novaković Miroslav M., Gorjanovic Stanislava Z., Pezo Lato, Sužnjevicć Desanka Ž., "Antioxidant activity of propolis extracts from Serbia: A polarographic approach" Food and Chemical Toxicology, 50, no. 10 (2012):3614-3618,
https://doi.org/10.1016/j.fct.2012.07.029 .
22
23
25

Metal extraction from Cetraria islandica (L.) Ach. lichen using low pH solutions

Cuculovic, Ana A.; Pavlović, Mirjana S.; Veselinović, Dragan S.; Miljanić, Šćepan S.

(2008)

TY  - JOUR
AU  - Cuculovic, Ana A.
AU  - Pavlović, Mirjana S.
AU  - Veselinović, Dragan S.
AU  -  Miljanić, Šćepan S.
PY  - 2008
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/3434
AB  - Extraction of metals (K, Al, Ca, Mg, Fe, Cu, Ba, Zn, Mn and Sr) from dry Cetraria islandica (L.) Ach. lichen was performed using solutions similar to acid rain (solution A - H2SO4-HNO3-(NH4)(2)SO4 and solution B - H2SO4-HNO3-(NH4)(2)SO4-NH4NO3). The pH values of these solutions were 2.00, 2.58, 2.87, 3.28, and 3.75. Five consecutive extractions were performed with each solution. In all solutions, the extracted metal content, except Cu and Ca, was the highest in the first extract. The highest percentage of the metals desorbed in the first extraction was obtained using solutions with low pH values, 2.00, 2.58, and 2.87. The iowest percentage in the first extraction was obtained using solutions with pH 3.28 and pH 3.75, indicating influence of the H+ ion on the extraction. According to the results obtained, the investigated metals form two groups. The first group includes K, Al, Ca, Mg, and Fe. They were extracted in each of the five extractions at each of the pH values. The second group includes Ba, Zn, Mn, Cu, and Sr, which were not all extracted at each pH value. The first group yielded three types of extraction curves when the logarithms of extracted metal amounts were plotted as a function of the number of successive extractions. These effects indicate that three different positions (centres) of metal ion accumulation exist in the lichen (due to sorption, complex formation, or other processes present in the tissues).
T2  - Journal of the Serbian Chemical Society
T1  - Metal extraction from Cetraria islandica (L.) Ach. lichen using low pH solutions
VL  - 73
IS  - 4
SP  - 405
EP  - 413
DO  - 10.2298/JSCO804405C
ER  - 
@article{
author = "Cuculovic, Ana A. and Pavlović, Mirjana S. and Veselinović, Dragan S. and  Miljanić, Šćepan S.",
year = "2008",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/3434",
abstract = "Extraction of metals (K, Al, Ca, Mg, Fe, Cu, Ba, Zn, Mn and Sr) from dry Cetraria islandica (L.) Ach. lichen was performed using solutions similar to acid rain (solution A - H2SO4-HNO3-(NH4)(2)SO4 and solution B - H2SO4-HNO3-(NH4)(2)SO4-NH4NO3). The pH values of these solutions were 2.00, 2.58, 2.87, 3.28, and 3.75. Five consecutive extractions were performed with each solution. In all solutions, the extracted metal content, except Cu and Ca, was the highest in the first extract. The highest percentage of the metals desorbed in the first extraction was obtained using solutions with low pH values, 2.00, 2.58, and 2.87. The iowest percentage in the first extraction was obtained using solutions with pH 3.28 and pH 3.75, indicating influence of the H+ ion on the extraction. According to the results obtained, the investigated metals form two groups. The first group includes K, Al, Ca, Mg, and Fe. They were extracted in each of the five extractions at each of the pH values. The second group includes Ba, Zn, Mn, Cu, and Sr, which were not all extracted at each pH value. The first group yielded three types of extraction curves when the logarithms of extracted metal amounts were plotted as a function of the number of successive extractions. These effects indicate that three different positions (centres) of metal ion accumulation exist in the lichen (due to sorption, complex formation, or other processes present in the tissues).",
journal = "Journal of the Serbian Chemical Society",
title = "Metal extraction from Cetraria islandica (L.) Ach. lichen using low pH solutions",
volume = "73",
number = "4",
pages = "405-413",
doi = "10.2298/JSCO804405C"
}
Cuculovic, A. A., Pavlović, M. S., Veselinović, D. S.,&  Miljanić, Š. S. (2008). Metal extraction from Cetraria islandica (L.) Ach. lichen using low pH solutions.
Journal of the Serbian Chemical Society, 73(4), 405-413.
https://doi.org/10.2298/JSCO804405C
Cuculovic AA, Pavlović MS, Veselinović DS,  Miljanić ŠS. Metal extraction from Cetraria islandica (L.) Ach. lichen using low pH solutions. Journal of the Serbian Chemical Society. 2008;73(4):405-413
Cuculovic Ana A., Pavlović Mirjana S., Veselinović Dragan S.,  Miljanić Šćepan S., "Metal extraction from Cetraria islandica (L.) Ach. lichen using low pH solutions" Journal of the Serbian Chemical Society, 73, no. 4 (2008):405-413,
https://doi.org/10.2298/JSCO804405C .
8

Chiral ligand-exchange chromatography as the screening method for proposed modifications in exametazime synthesis to enhance diastereoselectivity

Nikolić, Nadežda S.; Veselinović, Dragan S.; Vladimirov, Sote; Karljiković-Rajić, Katarina; Lingeman, H

(2004)

TY  - JOUR
AU  - Nikolić, Nadežda S.
AU  - Veselinović, Dragan S.
AU  - Vladimirov, Sote
AU  - Karljiković-Rajić, Katarina
AU  - Lingeman, H
PY  - 2004
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/2714
AB  - Tc-99m(V)-d,l-HM-PAO complex is well-known radiopharmaceutical for regional cerebral blood flow imaging. The proposed modifications in exametazime, hexamethylpropyleneamine oxime (HM-PAO) (4,8-diaza-3,6,6,9-tetramethylundecane-2,10-dione bisoxime) synthesis, for reduction of intermediary reactant diiminebisoxime (DI) (4,8-diaza-3,6,6,9-tetramethylundecane-3,8-diene-2,10-dione bisoxime) concerned two reductants (NaBH4 and KBH4), two solvents (ethanol and 2-propanol), and three mole ratios of reactant/reductants (1:1, 1:1.5, and 1:2). The simultaneous analysis of diastereo-enantiomeric HM-PAO content, as well as the content of starting DI, in different reduction mixtures were pet-formed using chiral ligand-exchange chromatography (CLEC). The separation of the samples of investigated reduction mixtures, obtained in the second step of HM-PAO synthesis, has been accomplished by using an achiral sorbent (RP- 18) and a chiral mobile phase (CMP) containing copper(II) complex with N,N-ditnethyl-L-phenylalanine (L-DM-PhA) as initial complex for CLEC. With 12 different reduction conditions, the obtained ratios of diastereoisomers d,l-HM-PAO: mesa-HM-PAO varied from 69.2:30.8 to 15.9:84.1, in comparison to the reduction in routine synthesis of HM-PAO which gives an equal mixture of diastereoisomers. The ternary mixed complexes formation recorded spectrophotometrically on addition of HM-PAO or DI to the mobile phase with binary complex Cu(L-DM-PhA)(2), due to the evidence of bathochromic shift of 46 nm for lambda(max) with significant difference in absorptivity contributes to separation mechanism. (C) 2003 Elsevier B.V. All rights reserved.
T2  - Journal of Pharmaceutical and Biomedical Analysis
T1  - Chiral ligand-exchange chromatography as the screening method for proposed modifications in exametazime synthesis to enhance diastereoselectivity
VL  - 34
IS  - 2
SP  - 285
EP  - 293
DO  - 10.1016/S0731-7085(03)00551-X
ER  - 
@article{
author = "Nikolić, Nadežda S. and Veselinović, Dragan S. and Vladimirov, Sote and Karljiković-Rajić, Katarina and Lingeman, H",
year = "2004",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/2714",
abstract = "Tc-99m(V)-d,l-HM-PAO complex is well-known radiopharmaceutical for regional cerebral blood flow imaging. The proposed modifications in exametazime, hexamethylpropyleneamine oxime (HM-PAO) (4,8-diaza-3,6,6,9-tetramethylundecane-2,10-dione bisoxime) synthesis, for reduction of intermediary reactant diiminebisoxime (DI) (4,8-diaza-3,6,6,9-tetramethylundecane-3,8-diene-2,10-dione bisoxime) concerned two reductants (NaBH4 and KBH4), two solvents (ethanol and 2-propanol), and three mole ratios of reactant/reductants (1:1, 1:1.5, and 1:2). The simultaneous analysis of diastereo-enantiomeric HM-PAO content, as well as the content of starting DI, in different reduction mixtures were pet-formed using chiral ligand-exchange chromatography (CLEC). The separation of the samples of investigated reduction mixtures, obtained in the second step of HM-PAO synthesis, has been accomplished by using an achiral sorbent (RP- 18) and a chiral mobile phase (CMP) containing copper(II) complex with N,N-ditnethyl-L-phenylalanine (L-DM-PhA) as initial complex for CLEC. With 12 different reduction conditions, the obtained ratios of diastereoisomers d,l-HM-PAO: mesa-HM-PAO varied from 69.2:30.8 to 15.9:84.1, in comparison to the reduction in routine synthesis of HM-PAO which gives an equal mixture of diastereoisomers. The ternary mixed complexes formation recorded spectrophotometrically on addition of HM-PAO or DI to the mobile phase with binary complex Cu(L-DM-PhA)(2), due to the evidence of bathochromic shift of 46 nm for lambda(max) with significant difference in absorptivity contributes to separation mechanism. (C) 2003 Elsevier B.V. All rights reserved.",
journal = "Journal of Pharmaceutical and Biomedical Analysis",
title = "Chiral ligand-exchange chromatography as the screening method for proposed modifications in exametazime synthesis to enhance diastereoselectivity",
volume = "34",
number = "2",
pages = "285-293",
doi = "10.1016/S0731-7085(03)00551-X"
}
Nikolić, N. S., Veselinović, D. S., Vladimirov, S., Karljiković-Rajić, K.,& Lingeman, H. (2004). Chiral ligand-exchange chromatography as the screening method for proposed modifications in exametazime synthesis to enhance diastereoselectivity.
Journal of Pharmaceutical and Biomedical Analysis, 34(2), 285-293.
https://doi.org/10.1016/S0731-7085(03)00551-X
Nikolić NS, Veselinović DS, Vladimirov S, Karljiković-Rajić K, Lingeman H. Chiral ligand-exchange chromatography as the screening method for proposed modifications in exametazime synthesis to enhance diastereoselectivity. Journal of Pharmaceutical and Biomedical Analysis. 2004;34(2):285-293
Nikolić Nadežda S., Veselinović Dragan S., Vladimirov Sote, Karljiković-Rajić Katarina, Lingeman H, "Chiral ligand-exchange chromatography as the screening method for proposed modifications in exametazime synthesis to enhance diastereoselectivity" Journal of Pharmaceutical and Biomedical Analysis, 34, no. 2 (2004):285-293,
https://doi.org/10.1016/S0731-7085(03)00551-X .
2
2
2

Cobalt(II) chloride complex formation in acetamide-calcium nitrate tetrahydrate melts

Savović, Jelena; Nikolic, R; Veselinović, Dragan S.

(2004)

TY  - JOUR
AU  - Savović, Jelena
AU  - Nikolic, R
AU  - Veselinović, Dragan S.
PY  - 2004
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/2788
AB  - The absorption spectra of Co(II) chloride complexes, containing variable concentrations of chloride ligand, in a molten mixture of 80 mol% acetamide-20 mol% calcium nitrate tetrahydrate, were studied at 313, 333, 353, and 363 K, in the wavelength range 400-800 nm. The melt contains three possible ligands (CH3CONH2, H2O, and NO3-) for competition with added chloride ligand. Addition of chloride caused a shift of the absorption maximum of octahedral cobalt( II) nitrate towards lower energies and pronounced changes in the shape of the initial spectrum of cobalt( II) nitrate. The effect of temperature changes on the molar absorption coefficient of the Co( II) species was dependent on the chloride concentration and was attributed to the structural changes occurring in the cobalt( II) species. The STAR and STAR FA programs were applied to identify the complex ionic species and to calculate the stability constants of Co( II) complexes formed in this solvent. The results indicate the highest probability of formation of the following complex species: Co(NO3)(4)(2-), Co(NO3)(2)Cl-2(2-), and CoCl42-. Stability constants of each complex were presented for the equilibria occurring at 313, 333, 353, and 363 K. Distribution of the Co( II) species was also calculated over the ranges of chloride concentration and temperature investigated.
T2  - Journal of Solution Chemistry
T1  - Cobalt(II) chloride complex formation in acetamide-calcium nitrate tetrahydrate melts
VL  - 33
IS  - 3
SP  - 287
EP  - 300
DO  - 10.1023/B:JOSL.0000035361.89473.a4
ER  - 
@article{
author = "Savović, Jelena and Nikolic, R and Veselinović, Dragan S.",
year = "2004",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/2788",
abstract = "The absorption spectra of Co(II) chloride complexes, containing variable concentrations of chloride ligand, in a molten mixture of 80 mol% acetamide-20 mol% calcium nitrate tetrahydrate, were studied at 313, 333, 353, and 363 K, in the wavelength range 400-800 nm. The melt contains three possible ligands (CH3CONH2, H2O, and NO3-) for competition with added chloride ligand. Addition of chloride caused a shift of the absorption maximum of octahedral cobalt( II) nitrate towards lower energies and pronounced changes in the shape of the initial spectrum of cobalt( II) nitrate. The effect of temperature changes on the molar absorption coefficient of the Co( II) species was dependent on the chloride concentration and was attributed to the structural changes occurring in the cobalt( II) species. The STAR and STAR FA programs were applied to identify the complex ionic species and to calculate the stability constants of Co( II) complexes formed in this solvent. The results indicate the highest probability of formation of the following complex species: Co(NO3)(4)(2-), Co(NO3)(2)Cl-2(2-), and CoCl42-. Stability constants of each complex were presented for the equilibria occurring at 313, 333, 353, and 363 K. Distribution of the Co( II) species was also calculated over the ranges of chloride concentration and temperature investigated.",
journal = "Journal of Solution Chemistry",
title = "Cobalt(II) chloride complex formation in acetamide-calcium nitrate tetrahydrate melts",
volume = "33",
number = "3",
pages = "287-300",
doi = "10.1023/B:JOSL.0000035361.89473.a4"
}
Savović, J., Nikolic, R.,& Veselinović, D. S. (2004). Cobalt(II) chloride complex formation in acetamide-calcium nitrate tetrahydrate melts.
Journal of Solution Chemistry, 33(3), 287-300.
https://doi.org/10.1023/B:JOSL.0000035361.89473.a4
Savović J, Nikolic R, Veselinović DS. Cobalt(II) chloride complex formation in acetamide-calcium nitrate tetrahydrate melts. Journal of Solution Chemistry. 2004;33(3):287-300
Savović Jelena, Nikolic R, Veselinović Dragan S., "Cobalt(II) chloride complex formation in acetamide-calcium nitrate tetrahydrate melts" Journal of Solution Chemistry, 33, no. 3 (2004):287-300,
https://doi.org/10.1023/B:JOSL.0000035361.89473.a4 .
15
15
15

Chiral ligand-exchange chromatography for diastereo-enantio separation of exametazime

Nikolić, Nadežda S.; Veselinović, Dragan S.; Vučina, Jurij L.; Lingeman, H; Karljiković-Rajić, Katarina

(2003)

TY  - JOUR
AU  - Nikolić, Nadežda S.
AU  - Veselinović, Dragan S.
AU  - Vučina, Jurij L.
AU  - Lingeman, H
AU  - Karljiković-Rajić, Katarina
PY  - 2003
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/2661
AB  - The diastereo-enantio separation of isomeric mixtures of exametazime (HM-PAO) by liquid chromatography is described using an achiral sorbent (RP-18). A chiral eluent with the initial complex of Cu(II) and the optically active selector N,N-dimethyl-l-phenylalanine (l-DM-PhA), based on the ligand-exchange principle, has been applied. The separation is based on the presence of the immobilized binary complex Cu(l-DM-PhA)(2) and formation of mixed ternary complex. The optimal mole ratio of Cu(II):l-DM-PhA is 1:4, the pH should be between 4.1 and 4.2 and up to 0.8 mM of triethylamine is added for column presaturation with the initial complex. The elution order has been defined using isolated l-HM-PAO via l-HM-PAO L(+)tartrate and tneso-HM-PAO obtained by repeated recrystallization from the isomeric mixture of HM-PAO. Complete resolution between all isomers (R-S from 2.14 to 3.91) and partial resolution for meso(EE)/l-HM-PAO (R-S = 0.83) has been obtained. This means that the proposed chiral ligand-exchange chromatography (CLEC) can be used for determination of the isomeric purity of HM-PAO. This as an alternative method for resolution measurements with chiral columns. (C) 2003 Elsevier B.V. All rights reserved.
T2  - Journal of Pharmaceutical and Biomedical Analysis
T1  - Chiral ligand-exchange chromatography for diastereo-enantio separation of exametazime
VL  - 32
IS  - 6
SP  - 1159
EP  - 1166
DO  - 10.1016/S0731-7085(03)00230-9
ER  - 
@article{
author = "Nikolić, Nadežda S. and Veselinović, Dragan S. and Vučina, Jurij L. and Lingeman, H and Karljiković-Rajić, Katarina",
year = "2003",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/2661",
abstract = "The diastereo-enantio separation of isomeric mixtures of exametazime (HM-PAO) by liquid chromatography is described using an achiral sorbent (RP-18). A chiral eluent with the initial complex of Cu(II) and the optically active selector N,N-dimethyl-l-phenylalanine (l-DM-PhA), based on the ligand-exchange principle, has been applied. The separation is based on the presence of the immobilized binary complex Cu(l-DM-PhA)(2) and formation of mixed ternary complex. The optimal mole ratio of Cu(II):l-DM-PhA is 1:4, the pH should be between 4.1 and 4.2 and up to 0.8 mM of triethylamine is added for column presaturation with the initial complex. The elution order has been defined using isolated l-HM-PAO via l-HM-PAO L(+)tartrate and tneso-HM-PAO obtained by repeated recrystallization from the isomeric mixture of HM-PAO. Complete resolution between all isomers (R-S from 2.14 to 3.91) and partial resolution for meso(EE)/l-HM-PAO (R-S = 0.83) has been obtained. This means that the proposed chiral ligand-exchange chromatography (CLEC) can be used for determination of the isomeric purity of HM-PAO. This as an alternative method for resolution measurements with chiral columns. (C) 2003 Elsevier B.V. All rights reserved.",
journal = "Journal of Pharmaceutical and Biomedical Analysis",
title = "Chiral ligand-exchange chromatography for diastereo-enantio separation of exametazime",
volume = "32",
number = "6",
pages = "1159-1166",
doi = "10.1016/S0731-7085(03)00230-9"
}
Nikolić, N. S., Veselinović, D. S., Vučina, J. L., Lingeman, H.,& Karljiković-Rajić, K. (2003). Chiral ligand-exchange chromatography for diastereo-enantio separation of exametazime.
Journal of Pharmaceutical and Biomedical Analysis, 32(6), 1159-1166.
https://doi.org/10.1016/S0731-7085(03)00230-9
Nikolić NS, Veselinović DS, Vučina JL, Lingeman H, Karljiković-Rajić K. Chiral ligand-exchange chromatography for diastereo-enantio separation of exametazime. Journal of Pharmaceutical and Biomedical Analysis. 2003;32(6):1159-1166
Nikolić Nadežda S., Veselinović Dragan S., Vučina Jurij L., Lingeman H, Karljiković-Rajić Katarina, "Chiral ligand-exchange chromatography for diastereo-enantio separation of exametazime" Journal of Pharmaceutical and Biomedical Analysis, 32, no. 6 (2003):1159-1166,
https://doi.org/10.1016/S0731-7085(03)00230-9 .
7
9
7

Physical-chemic caracterisation of osteoporotic bone.

Poštić, Srđan D.; Markovic, V; Veselinović, Dragan S.; Mirjanic, M; Zec, Slavica

(2002)

TY  - CONF
AU  - Poštić, Srđan D.
AU  - Markovic, V
AU  - Veselinović, Dragan S.
AU  - Mirjanic, M
AU  - Zec, Slavica
PY  - 2002
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/6344
C3  - Journal of Dental Research
T1  - Physical-chemic caracterisation of osteoporotic bone.
VL  - 81
SP  - B284
EP  - B284
ER  - 
@conference{
author = "Poštić, Srđan D. and Markovic, V and Veselinović, Dragan S. and Mirjanic, M and Zec, Slavica",
year = "2002",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/6344",
journal = "Journal of Dental Research",
title = "Physical-chemic caracterisation of osteoporotic bone.",
volume = "81",
pages = "B284-B284"
}
Poštić, S. D., Markovic, V., Veselinović, D. S., Mirjanic, M.,& Zec, S. (2002). Physical-chemic caracterisation of osteoporotic bone..
Journal of Dental Research, 81, B284-B284.
Poštić SD, Markovic V, Veselinović DS, Mirjanic M, Zec S. Physical-chemic caracterisation of osteoporotic bone.. Journal of Dental Research. 2002;81:B284-B284
Poštić Srđan D., Markovic V, Veselinović Dragan S., Mirjanic M, Zec Slavica, "Physical-chemic caracterisation of osteoporotic bone." Journal of Dental Research, 81 (2002):B284-B284
1

Uranium contents from bomb craters

Miljević, Nada R.; Marković, Mirjana; Todorović, Dragana; Cvijović, Mirjana R.; Golobočanin, Dušan D.; Orlić, Milan P.; Veselinović, Dragan S.

(2001)

TY  - JOUR
AU  - Miljević, Nada R.
AU  - Marković, Mirjana
AU  - Todorović, Dragana
AU  - Cvijović, Mirjana R.
AU  - Golobočanin, Dušan D.
AU  - Orlić, Milan P.
AU  - Veselinović, Dragan S.
PY  - 2001
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/8773
AB  - Depleted uranium (DU) is a by-product of uranium enrichment process and its use is very dangerous and harmful. We measured uranium concentration in the surface soil (0-5 cm depth) from bomb craters caused by cruise missiles in which DU might have been used as counterweights during NATO attack. Total uranium concentration and isotopic ratio were determined using y-spectrometry and inductively coupled plasma method. Obtained results were in the range 1.7 - 22 mg/kg dry soil that was comparable to the uranium values found in off-side locations of Serbian soils.
T2  - Journal of Environmental Protection and Ecology
T1  - Uranium contents from bomb craters
VL  - 2
IS  - 3
SP  - 642
EP  - 648
ER  - 
@article{
author = "Miljević, Nada R. and Marković, Mirjana and Todorović, Dragana and Cvijović, Mirjana R. and Golobočanin, Dušan D. and Orlić, Milan P. and Veselinović, Dragan S.",
year = "2001",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/8773",
abstract = "Depleted uranium (DU) is a by-product of uranium enrichment process and its use is very dangerous and harmful. We measured uranium concentration in the surface soil (0-5 cm depth) from bomb craters caused by cruise missiles in which DU might have been used as counterweights during NATO attack. Total uranium concentration and isotopic ratio were determined using y-spectrometry and inductively coupled plasma method. Obtained results were in the range 1.7 - 22 mg/kg dry soil that was comparable to the uranium values found in off-side locations of Serbian soils.",
journal = "Journal of Environmental Protection and Ecology",
title = "Uranium contents from bomb craters",
volume = "2",
number = "3",
pages = "642-648"
}
Miljević, N. R., Marković, M., Todorović, D., Cvijović, M. R., Golobočanin, D. D., Orlić, M. P.,& Veselinović, D. S. (2001). Uranium contents from bomb craters.
Journal of Environmental Protection and Ecology, 2(3), 642-648.
Miljević NR, Marković M, Todorović D, Cvijović MR, Golobočanin DD, Orlić MP, Veselinović DS. Uranium contents from bomb craters. Journal of Environmental Protection and Ecology. 2001;2(3):642-648
Miljević Nada R., Marković Mirjana, Todorović Dragana, Cvijović Mirjana R., Golobočanin Dušan D., Orlić Milan P., Veselinović Dragan S., "Uranium contents from bomb craters" Journal of Environmental Protection and Ecology, 2, no. 3 (2001):642-648

Preparation and molecular structure of the trans(O-6) isomer of dihydrogen (1,3-propanediamine-N,N-diacetato-N,N-di-3-propionato)copper(II) complex. The stereochemistry of copper(II)-EDTA-type complexes in relation to the structure of the ligand

Prelesnik, Bogdan V.; Radanovic, DD; Tomić, Zoran D.; Djurdjevic, P; Radanovic, DJ; Veselinović, Dragan S.

(1996)

TY  - JOUR
AU  - Prelesnik, Bogdan V.
AU  - Radanovic, DD
AU  - Tomić, Zoran D.
AU  - Djurdjevic, P
AU  - Radanovic, DJ
AU  - Veselinović, Dragan S.
PY  - 1996
UR  - http://vinar.vin.bg.ac.rs/handle/123456789/2005
AB  - The hexadentate complex [Cu(H(2)1,3-pddadp)]. 1.5H(2)O (1,3-pddadp = 1,3-propanediamine-N,N-diacetate-N,N-di-3-propionate ion) has been prepared and isolated and its molecular structure determined by the single crystal X-ray diffraction technique. The complex is a trans(O-6) isomer, in which the copper(II) ion is surrounded octahedrally by two nitrogen and four oxygen atoms of 1,3-pddadp with two protonated beta-alaninate rings in trans positions. The copper atom environment is a tetragonally elongated octahedron with tetragonality (T) 0.798. A comparison of structures of the copper(II)-edta-type complexes shows an expected variation in their stereochemistry, depending on the structure of the ligand. The 1,3-pddadp ligand encircles the Cu-II ion more favourably than the edta ligand, which is capable of forming five-membered chelate rings only. Some properties of the complex are also given. Copyright (C) 1996 Elsevier Science Ltd
T2  - Polyhedron
T1  - Preparation and molecular structure of the trans(O-6) isomer of dihydrogen (1,3-propanediamine-N,N-diacetato-N,N-di-3-propionato)copper(II) complex. The stereochemistry of copper(II)-EDTA-type complexes in relation to the structure of the ligand
VL  - 15
IS  - 21
SP  - 3761
EP  - 3770
DO  - 10.1016/0277-5387(96)00115-5
ER  - 
@article{
author = "Prelesnik, Bogdan V. and Radanovic, DD and Tomić, Zoran D. and Djurdjevic, P and Radanovic, DJ and Veselinović, Dragan S.",
year = "1996",
url = "http://vinar.vin.bg.ac.rs/handle/123456789/2005",
abstract = "The hexadentate complex [Cu(H(2)1,3-pddadp)]. 1.5H(2)O (1,3-pddadp = 1,3-propanediamine-N,N-diacetate-N,N-di-3-propionate ion) has been prepared and isolated and its molecular structure determined by the single crystal X-ray diffraction technique. The complex is a trans(O-6) isomer, in which the copper(II) ion is surrounded octahedrally by two nitrogen and four oxygen atoms of 1,3-pddadp with two protonated beta-alaninate rings in trans positions. The copper atom environment is a tetragonally elongated octahedron with tetragonality (T) 0.798. A comparison of structures of the copper(II)-edta-type complexes shows an expected variation in their stereochemistry, depending on the structure of the ligand. The 1,3-pddadp ligand encircles the Cu-II ion more favourably than the edta ligand, which is capable of forming five-membered chelate rings only. Some properties of the complex are also given. Copyright (C) 1996 Elsevier Science Ltd",
journal = "Polyhedron",
title = "Preparation and molecular structure of the trans(O-6) isomer of dihydrogen (1,3-propanediamine-N,N-diacetato-N,N-di-3-propionato)copper(II) complex. The stereochemistry of copper(II)-EDTA-type complexes in relation to the structure of the ligand",
volume = "15",
number = "21",
pages = "3761-3770",
doi = "10.1016/0277-5387(96)00115-5"
}
Prelesnik, B. V., Radanovic, D., Tomić, Z. D., Djurdjevic, P., Radanovic, D.,& Veselinović, D. S. (1996). Preparation and molecular structure of the trans(O-6) isomer of dihydrogen (1,3-propanediamine-N,N-diacetato-N,N-di-3-propionato)copper(II) complex. The stereochemistry of copper(II)-EDTA-type complexes in relation to the structure of the ligand.
Polyhedron, 15(21), 3761-3770.
https://doi.org/10.1016/0277-5387(96)00115-5
Prelesnik BV, Radanovic D, Tomić ZD, Djurdjevic P, Radanovic D, Veselinović DS. Preparation and molecular structure of the trans(O-6) isomer of dihydrogen (1,3-propanediamine-N,N-diacetato-N,N-di-3-propionato)copper(II) complex. The stereochemistry of copper(II)-EDTA-type complexes in relation to the structure of the ligand. Polyhedron. 1996;15(21):3761-3770
Prelesnik Bogdan V., Radanovic DD, Tomić Zoran D., Djurdjevic P, Radanovic DJ, Veselinović Dragan S., "Preparation and molecular structure of the trans(O-6) isomer of dihydrogen (1,3-propanediamine-N,N-diacetato-N,N-di-3-propionato)copper(II) complex. The stereochemistry of copper(II)-EDTA-type complexes in relation to the structure of the ligand" Polyhedron, 15, no. 21 (1996):3761-3770,
https://doi.org/10.1016/0277-5387(96)00115-5 .
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