Pfendt, Lidija B.

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  • Pfendt, Lidija B. (6)
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The chemical characteristics of soil which determine phosphorus partitioning in highly calcareous soils

Topalović, Ana; Pfendt, Lidija B.; Perovic, Natalija; Đorđević, Dragana S.; Trifunović, Snežana S.; Pfendt, Petar A.

(Serbian Chemical Soc, Belgrade, 2006)

TY  - JOUR
AU  - Topalović, Ana
AU  - Pfendt, Lidija B.
AU  - Perovic, Natalija
AU  - Đorđević, Dragana S.
AU  - Trifunović, Snežana S.
AU  - Pfendt, Petar A.
PY  - 2006
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/819
AB  - Phosphorus fractions from three highly calcareous soils (average, 24.9 +/- 4.8 %CO32-) from sampling sites with a Mediterranean climate were isolated by sequential extraction. In order to provide a more reliable basis for the definition of the obtained P-fractions, principal component analysis was applied and from the chemical characteristics of the 14 investigated soils, those characteristics which define at he content and association features of the P-fractions were assessed. The soils are characterized by a relatively high pH (8.0-8.2) and by significantly differing contents of organic mater, acid-soluble Mg and total P. These differences affected the various association features of the P-fraction with the soil constituents. The NH4F-P fraction (isolated with 0.5 M NH4F, pH 8.2) is defined by the contents of the main metals of the oxide-hydroxide-clay associations (Al, Fe, Mn) or by the the redox potential (Eh) of Mn. The accumulation of NaOH-phosphorus (extractable with 0.1 M NaOH) depended on the constituents of the oxide hydroxide-clay association, the humic substances and Eh-related factors. In those soils in which NaOH-P is defined by the oxide-hydroxide-clay association, the participation of Fe as a bridge-forming metal is proposed. The main part of total P, i.e., Delta P = TP - (NH4F-P + NaOH-P) is defined by the status of Mn- and Fe-humic complexes or by the concentration of hydroxyl-ions.
AB  - Iz tri visoko-krečnjačka zemljišta (prosečni sadržaj CO 3 2- 24.9 ± 4.8%, pH 8.0 - 8.2), sa lokacija sa sredozemnom klimom, izolovane su frakcije fosfora sekvencijalnom ekstrakcijom. U cilju obezbeđivanja pouzdanije osnove za definisanje dobijenih frakcijafosfora (P-frakcija), primenjena je analiza principalne komponente (PC-analiza). Među 14 hemijskih karakteristika zemljišta, izdvojene su one koje definišu sadržaj pojedinih P-frakcija i prirodu njihove asocijacije sa sastojcima zemljišta. Frakcija NH 4-P (izolovana sa 0,5M NH 4F, pH = 8,2) definisana je sadržajem glavnih metala oksidne-hidroksidne-glinene asocijacije (Al, Fe, Mn) ili Eh-statusom izraženim sadržajem Mn. Akumulacija NaOH-P (ekstrahovanog sa 0,1 M NaOH) zavisila je od sastojaka oksidne-hidroksidne-glinene asocijacije, od huminskih supstanci i od faktora koji stoje u vezi sa Eh. U onim zemljištima u kojima je NaOH-P definisana sastojcima oksidne-hidroksidne-glinene asocijacije, pretpostavljeno je vezivanje fosfora preko Fe-mostova. Glavna količina fosfora ∆P = TP - (NH 4F-P + NaOH-P), u pojedinim zemljištima definisana je ili statusom Mn- i Fe-huminskih kompleksa, ili pH-vrednošću.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - The chemical characteristics of soil which determine phosphorus partitioning in highly calcareous soils
T1  - Hemijske karakteristike visoko-krečnjačkih zemljišta koje određuju raspodelu fosfora
VL  - 71
IS  - 11
SP  - 1219
EP  - 1236
DO  - 10.2298/JSC0611219T
ER  - 
@article{
author = "Topalović, Ana and Pfendt, Lidija B. and Perovic, Natalija and Đorđević, Dragana S. and Trifunović, Snežana S. and Pfendt, Petar A.",
year = "2006",
abstract = "Phosphorus fractions from three highly calcareous soils (average, 24.9 +/- 4.8 %CO32-) from sampling sites with a Mediterranean climate were isolated by sequential extraction. In order to provide a more reliable basis for the definition of the obtained P-fractions, principal component analysis was applied and from the chemical characteristics of the 14 investigated soils, those characteristics which define at he content and association features of the P-fractions were assessed. The soils are characterized by a relatively high pH (8.0-8.2) and by significantly differing contents of organic mater, acid-soluble Mg and total P. These differences affected the various association features of the P-fraction with the soil constituents. The NH4F-P fraction (isolated with 0.5 M NH4F, pH 8.2) is defined by the contents of the main metals of the oxide-hydroxide-clay associations (Al, Fe, Mn) or by the the redox potential (Eh) of Mn. The accumulation of NaOH-phosphorus (extractable with 0.1 M NaOH) depended on the constituents of the oxide hydroxide-clay association, the humic substances and Eh-related factors. In those soils in which NaOH-P is defined by the oxide-hydroxide-clay association, the participation of Fe as a bridge-forming metal is proposed. The main part of total P, i.e., Delta P = TP - (NH4F-P + NaOH-P) is defined by the status of Mn- and Fe-humic complexes or by the concentration of hydroxyl-ions., Iz tri visoko-krečnjačka zemljišta (prosečni sadržaj CO 3 2- 24.9 ± 4.8%, pH 8.0 - 8.2), sa lokacija sa sredozemnom klimom, izolovane su frakcije fosfora sekvencijalnom ekstrakcijom. U cilju obezbeđivanja pouzdanije osnove za definisanje dobijenih frakcijafosfora (P-frakcija), primenjena je analiza principalne komponente (PC-analiza). Među 14 hemijskih karakteristika zemljišta, izdvojene su one koje definišu sadržaj pojedinih P-frakcija i prirodu njihove asocijacije sa sastojcima zemljišta. Frakcija NH 4-P (izolovana sa 0,5M NH 4F, pH = 8,2) definisana je sadržajem glavnih metala oksidne-hidroksidne-glinene asocijacije (Al, Fe, Mn) ili Eh-statusom izraženim sadržajem Mn. Akumulacija NaOH-P (ekstrahovanog sa 0,1 M NaOH) zavisila je od sastojaka oksidne-hidroksidne-glinene asocijacije, od huminskih supstanci i od faktora koji stoje u vezi sa Eh. U onim zemljištima u kojima je NaOH-P definisana sastojcima oksidne-hidroksidne-glinene asocijacije, pretpostavljeno je vezivanje fosfora preko Fe-mostova. Glavna količina fosfora ∆P = TP - (NH 4F-P + NaOH-P), u pojedinim zemljištima definisana je ili statusom Mn- i Fe-huminskih kompleksa, ili pH-vrednošću.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "The chemical characteristics of soil which determine phosphorus partitioning in highly calcareous soils, Hemijske karakteristike visoko-krečnjačkih zemljišta koje određuju raspodelu fosfora",
volume = "71",
number = "11",
pages = "1219-1236",
doi = "10.2298/JSC0611219T"
}
Topalović, A., Pfendt, L. B., Perovic, N., Đorđević, D. S., Trifunović, S. S.,& Pfendt, P. A.. (2006). The chemical characteristics of soil which determine phosphorus partitioning in highly calcareous soils. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 71(11), 1219-1236.
https://doi.org/10.2298/JSC0611219T
Topalović A, Pfendt LB, Perovic N, Đorđević DS, Trifunović SS, Pfendt PA. The chemical characteristics of soil which determine phosphorus partitioning in highly calcareous soils. in Journal of the Serbian Chemical Society. 2006;71(11):1219-1236.
doi:10.2298/JSC0611219T .
Topalović, Ana, Pfendt, Lidija B., Perovic, Natalija, Đorđević, Dragana S., Trifunović, Snežana S., Pfendt, Petar A., "The chemical characteristics of soil which determine phosphorus partitioning in highly calcareous soils" in Journal of the Serbian Chemical Society, 71, no. 11 (2006):1219-1236,
https://doi.org/10.2298/JSC0611219T . .
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Protolytic equilibria in homogeneous and heterogeneous systems of ketoconazole and its direct spectrophotometric determination in tablets

Vojic, MP; Popović, Gordana V.; Sladić, Dušan; Pfendt, Lidija B.

(Serbian Chemical Soc, Belgrade, 2005)

TY  - JOUR
AU  - Vojic, MP
AU  - Popović, Gordana V.
AU  - Sladić, Dušan
AU  - Pfendt, Lidija B.
PY  - 2005
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/687
AB  - The acid-base equilibria of a diprotic, slightly hydrosoluble base ketoconazole were studied in homogeneous and heterogeneous water systems. The determinations were performed at 25 degreesC at a constant ionic strength of 0.1 M (NaCl). The acidity constant K,,, was determined by potentiometric (pK(a1) 3.20) and spectrophotometric (pK(al) 3.26) methods. A pK(a2) constant of 6.10 was obtained based on the equilibrium constants pK(s0) 4.84 and pK(s1) -1.26, determined in a heterogeneous ketoconazole system. The obtained values of the constants served to calculate the solubility and the distribution of the equilibrium forms of ketoconazole as a function of pH. On the basis of the distribution of the equilibrium forms of ketoconazole, a spectrophotometric method for the determination of its content in commercial tablets was developed. The determinations were performed at 225 nm in 0.1 M HCl. The method is simple and rapid and enables the direct spectrophotometric determination of the content of ketoconazole without previous isolation.
AB  - Proučene su kiselinsko-bazne ravnoteže u homogenom i heterogenom vodenom sistemu ketokonazola, diprotične teško rastvorne baze. Određivanja su vršena na temperaturi 25ºC i pri konstantnoj jonskoj sili 0,1M(NaCl). Kiselinska konstantaKa1 određena je potenciometrijski (pKa1 3,20) i spektrofotometrijski (pKa1 3,26). Konstanta pKa2 6,10 izračunata je iz ravnotežnih konstanti određenih u heterogenom sistemu: pKs0 4,84 i pKs1 -1,26. Na osnovu dobijenih vrednosti za konstante izračunata je rastvorljivost i raspodela ravnotežnih oblika ketokonazola u funkciji pH. Na bazi raspodele ravnotežnih oblika ketokonazola predložena je spektrofotometrijska metoda za njegovo određivanje u komercijalnim tabletama. Određivanja su vršena na talasnoj dužini 225 nm u 0,1M HCl.Metoda je jednostavna i brza, i omogućava direktno spektrofotometrijsko određivanje ketokonazola, bez prethodnog izolovanja.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Protolytic equilibria in homogeneous and heterogeneous systems of ketoconazole and its direct spectrophotometric determination in tablets
T1  - Protolitičke ravnoteže u homogenom i heterogenom sistemu ketokonazola i njegovo direktno spektrofotometrijsko određivanje u tabletama
VL  - 70
IS  - 1
SP  - 67
EP  - 78
DO  - 10.2298/JSC0501067V
ER  - 
@article{
author = "Vojic, MP and Popović, Gordana V. and Sladić, Dušan and Pfendt, Lidija B.",
year = "2005",
abstract = "The acid-base equilibria of a diprotic, slightly hydrosoluble base ketoconazole were studied in homogeneous and heterogeneous water systems. The determinations were performed at 25 degreesC at a constant ionic strength of 0.1 M (NaCl). The acidity constant K,,, was determined by potentiometric (pK(a1) 3.20) and spectrophotometric (pK(al) 3.26) methods. A pK(a2) constant of 6.10 was obtained based on the equilibrium constants pK(s0) 4.84 and pK(s1) -1.26, determined in a heterogeneous ketoconazole system. The obtained values of the constants served to calculate the solubility and the distribution of the equilibrium forms of ketoconazole as a function of pH. On the basis of the distribution of the equilibrium forms of ketoconazole, a spectrophotometric method for the determination of its content in commercial tablets was developed. The determinations were performed at 225 nm in 0.1 M HCl. The method is simple and rapid and enables the direct spectrophotometric determination of the content of ketoconazole without previous isolation., Proučene su kiselinsko-bazne ravnoteže u homogenom i heterogenom vodenom sistemu ketokonazola, diprotične teško rastvorne baze. Određivanja su vršena na temperaturi 25ºC i pri konstantnoj jonskoj sili 0,1M(NaCl). Kiselinska konstantaKa1 određena je potenciometrijski (pKa1 3,20) i spektrofotometrijski (pKa1 3,26). Konstanta pKa2 6,10 izračunata je iz ravnotežnih konstanti određenih u heterogenom sistemu: pKs0 4,84 i pKs1 -1,26. Na osnovu dobijenih vrednosti za konstante izračunata je rastvorljivost i raspodela ravnotežnih oblika ketokonazola u funkciji pH. Na bazi raspodele ravnotežnih oblika ketokonazola predložena je spektrofotometrijska metoda za njegovo određivanje u komercijalnim tabletama. Određivanja su vršena na talasnoj dužini 225 nm u 0,1M HCl.Metoda je jednostavna i brza, i omogućava direktno spektrofotometrijsko određivanje ketokonazola, bez prethodnog izolovanja.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Protolytic equilibria in homogeneous and heterogeneous systems of ketoconazole and its direct spectrophotometric determination in tablets, Protolitičke ravnoteže u homogenom i heterogenom sistemu ketokonazola i njegovo direktno spektrofotometrijsko određivanje u tabletama",
volume = "70",
number = "1",
pages = "67-78",
doi = "10.2298/JSC0501067V"
}
Vojic, M., Popović, G. V., Sladić, D.,& Pfendt, L. B.. (2005). Protolytic equilibria in homogeneous and heterogeneous systems of ketoconazole and its direct spectrophotometric determination in tablets. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 70(1), 67-78.
https://doi.org/10.2298/JSC0501067V
Vojic M, Popović GV, Sladić D, Pfendt LB. Protolytic equilibria in homogeneous and heterogeneous systems of ketoconazole and its direct spectrophotometric determination in tablets. in Journal of the Serbian Chemical Society. 2005;70(1):67-78.
doi:10.2298/JSC0501067V .
Vojic, MP, Popović, Gordana V., Sladić, Dušan, Pfendt, Lidija B., "Protolytic equilibria in homogeneous and heterogeneous systems of ketoconazole and its direct spectrophotometric determination in tablets" in Journal of the Serbian Chemical Society, 70, no. 1 (2005):67-78,
https://doi.org/10.2298/JSC0501067V . .
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Study on protolytic equilibria of lorazepam and oxazepam by UV and NMR spectroscopy

Popović, Gordana V.; Sladić, Dušan; Stefanovic, VM; Pfendt, Lidija B.

(Pergamon-Elsevier Science Ltd, Oxford, 2003)

TY  - JOUR
AU  - Popović, Gordana V.
AU  - Sladić, Dušan
AU  - Stefanovic, VM
AU  - Pfendt, Lidija B.
PY  - 2003
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/549
AB  - Protolytic equilibria in homogeneous and heterogeneous systems of lorazepam and oxazepam, which are sparingly soluble ampholytes from the class of 1,4-benzodiazepines, were studied at 25 degreesC and ionic strength of 0.1 M. Acidity constants and equilibrium constants in a heterogeneous system were determined. On the basis of the analysis of the corresponding C-13- and H-1-NMR spectra, deprotonation site in the molecules of the investigated compounds was predicted. Finally, the correlation between chemical shifts in the H-1-NMR spectra and the acidity of the amide proton of 1,4-benzodiazepines was established. (C) 2003 Elsevier Science B.V. All rights reserved.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Journal of Pharmaceutical and Biomedical Analysis
T1  - Study on protolytic equilibria of lorazepam and oxazepam by UV and NMR spectroscopy
VL  - 31
IS  - 4
SP  - 693
EP  - 699
DO  - 10.1016/S0731-7085(02)00686-6
ER  - 
@article{
author = "Popović, Gordana V. and Sladić, Dušan and Stefanovic, VM and Pfendt, Lidija B.",
year = "2003",
abstract = "Protolytic equilibria in homogeneous and heterogeneous systems of lorazepam and oxazepam, which are sparingly soluble ampholytes from the class of 1,4-benzodiazepines, were studied at 25 degreesC and ionic strength of 0.1 M. Acidity constants and equilibrium constants in a heterogeneous system were determined. On the basis of the analysis of the corresponding C-13- and H-1-NMR spectra, deprotonation site in the molecules of the investigated compounds was predicted. Finally, the correlation between chemical shifts in the H-1-NMR spectra and the acidity of the amide proton of 1,4-benzodiazepines was established. (C) 2003 Elsevier Science B.V. All rights reserved.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Journal of Pharmaceutical and Biomedical Analysis",
title = "Study on protolytic equilibria of lorazepam and oxazepam by UV and NMR spectroscopy",
volume = "31",
number = "4",
pages = "693-699",
doi = "10.1016/S0731-7085(02)00686-6"
}
Popović, G. V., Sladić, D., Stefanovic, V.,& Pfendt, L. B.. (2003). Study on protolytic equilibria of lorazepam and oxazepam by UV and NMR spectroscopy. in Journal of Pharmaceutical and Biomedical Analysis
Pergamon-Elsevier Science Ltd, Oxford., 31(4), 693-699.
https://doi.org/10.1016/S0731-7085(02)00686-6
Popović GV, Sladić D, Stefanovic V, Pfendt LB. Study on protolytic equilibria of lorazepam and oxazepam by UV and NMR spectroscopy. in Journal of Pharmaceutical and Biomedical Analysis. 2003;31(4):693-699.
doi:10.1016/S0731-7085(02)00686-6 .
Popović, Gordana V., Sladić, Dušan, Stefanovic, VM, Pfendt, Lidija B., "Study on protolytic equilibria of lorazepam and oxazepam by UV and NMR spectroscopy" in Journal of Pharmaceutical and Biomedical Analysis, 31, no. 4 (2003):693-699,
https://doi.org/10.1016/S0731-7085(02)00686-6 . .
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Protolytic equilibria of bromazepam

Pfendt, Lidija B.; Popović, Gordana V.; Damjanović, Tatjana Ž.; Sladić, Dušan

(Serbian Chemical Soc, Belgrade, 2002)

TY  - JOUR
AU  - Pfendt, Lidija B.
AU  - Popović, Gordana V.
AU  - Damjanović, Tatjana Ž.
AU  - Sladić, Dušan
PY  - 2002
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/484
AB  - The protolytic equilibria of bromazepam, an ampholyte sparingly soluble in water, in homogeneous and heterogeneous systems were studied in the pH range 0-14 at 25 degreesC and at ionic strength of 0.1 mol/dm(3) (NaCl). On the basis of C-13-NMR spectra, the protonation site was predicted - in acidic media the pyridine nitrogen of bormazepam is protonated. The acidity constants of bromazepam were determined spectrophotometrically (pK(a1) 2.83 and pK(a2) 11.60) and potentiometrically (pk(a1) 2.99). In the heterogeneous system the following equilibrium constants were determined: K-s0 = [HA] (pK(s0) 3.44), K-s1 = [H(2)A(+)]/[H3O+] (pK(s1) 0.61), and K-s2 = [A(-)][H3O+] (pK(s2) 15.04).
AB  - Proučavane su protolitičke ravnoteže bromazepama, amfolita iz klase 1,4-benzodiazepina, slabo rastvornog u vodi. Ispitivanja su vršena u homogenom i heterogenom sistemu u pH intervalu 0–14, na temperaturi 25ºC i pri jonskoj sili 0,1 mol/dm3 (NaCl). Na osnovu 13C-NMR spektara pretpostavljeno je da do protonovanja u molekulu bromazepama dolazi na piridinskom atomu azota. Kiselinske konstante određene su spektrofotometrijski (pKa1 2.83 and pKa2 11.60) i potenciometrijski (pKa1 2,99). U heterogenom sistemu određene su sledeće ravnotežne konstante Ks0 =[HA](pKs0 3.44), Ks1=[H2A+]/[H3O+](pKs1 0.61), and Ks2 =[A-][H3O+](pKs2 15.04).
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Protolytic equilibria of bromazepam
T1  - Protolitičke ravnoteže bromazepama
VL  - 67
IS  - 3
SP  - 187
EP  - 195
DO  - 10.2298/JSC0203187P
ER  - 
@article{
author = "Pfendt, Lidija B. and Popović, Gordana V. and Damjanović, Tatjana Ž. and Sladić, Dušan",
year = "2002",
abstract = "The protolytic equilibria of bromazepam, an ampholyte sparingly soluble in water, in homogeneous and heterogeneous systems were studied in the pH range 0-14 at 25 degreesC and at ionic strength of 0.1 mol/dm(3) (NaCl). On the basis of C-13-NMR spectra, the protonation site was predicted - in acidic media the pyridine nitrogen of bormazepam is protonated. The acidity constants of bromazepam were determined spectrophotometrically (pK(a1) 2.83 and pK(a2) 11.60) and potentiometrically (pk(a1) 2.99). In the heterogeneous system the following equilibrium constants were determined: K-s0 = [HA] (pK(s0) 3.44), K-s1 = [H(2)A(+)]/[H3O+] (pK(s1) 0.61), and K-s2 = [A(-)][H3O+] (pK(s2) 15.04)., Proučavane su protolitičke ravnoteže bromazepama, amfolita iz klase 1,4-benzodiazepina, slabo rastvornog u vodi. Ispitivanja su vršena u homogenom i heterogenom sistemu u pH intervalu 0–14, na temperaturi 25ºC i pri jonskoj sili 0,1 mol/dm3 (NaCl). Na osnovu 13C-NMR spektara pretpostavljeno je da do protonovanja u molekulu bromazepama dolazi na piridinskom atomu azota. Kiselinske konstante određene su spektrofotometrijski (pKa1 2.83 and pKa2 11.60) i potenciometrijski (pKa1 2,99). U heterogenom sistemu određene su sledeće ravnotežne konstante Ks0 =[HA](pKs0 3.44), Ks1=[H2A+]/[H3O+](pKs1 0.61), and Ks2 =[A-][H3O+](pKs2 15.04).",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Protolytic equilibria of bromazepam, Protolitičke ravnoteže bromazepama",
volume = "67",
number = "3",
pages = "187-195",
doi = "10.2298/JSC0203187P"
}
Pfendt, L. B., Popović, G. V., Damjanović, T. Ž.,& Sladić, D.. (2002). Protolytic equilibria of bromazepam. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 67(3), 187-195.
https://doi.org/10.2298/JSC0203187P
Pfendt LB, Popović GV, Damjanović TŽ, Sladić D. Protolytic equilibria of bromazepam. in Journal of the Serbian Chemical Society. 2002;67(3):187-195.
doi:10.2298/JSC0203187P .
Pfendt, Lidija B., Popović, Gordana V., Damjanović, Tatjana Ž., Sladić, Dušan, "Protolytic equilibria of bromazepam" in Journal of the Serbian Chemical Society, 67, no. 3 (2002):187-195,
https://doi.org/10.2298/JSC0203187P . .
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Identification of the diazepine ring opening site in the reaction of acidic hydrolysis of bromazepam

Popović, Gordana V.; Damjanović, Tatjana Ž.; Sladić, Dušan; Pfendt, Lidija B.

(2002)

TY  - CONF
AU  - Popović, Gordana V.
AU  - Damjanović, Tatjana Ž.
AU  - Sladić, Dušan
AU  - Pfendt, Lidija B.
PY  - 2002
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/129
C3  - Arhiv za farmaciju
T1  - Identification of the diazepine ring opening site in the reaction of acidic hydrolysis of bromazepam
T1  - Identifikacija mesta hidrolitičkog otvaranja diazepinskog prstena bromazepama u kiseloj sredini
VL  - 52
IS  - 4
SP  - 462
EP  - 463
UR  - https://hdl.handle.net/21.15107/rcub_cherry_129
ER  - 
@conference{
author = "Popović, Gordana V. and Damjanović, Tatjana Ž. and Sladić, Dušan and Pfendt, Lidija B.",
year = "2002",
journal = "Arhiv za farmaciju",
title = "Identification of the diazepine ring opening site in the reaction of acidic hydrolysis of bromazepam, Identifikacija mesta hidrolitičkog otvaranja diazepinskog prstena bromazepama u kiseloj sredini",
volume = "52",
number = "4",
pages = "462-463",
url = "https://hdl.handle.net/21.15107/rcub_cherry_129"
}
Popović, G. V., Damjanović, T. Ž., Sladić, D.,& Pfendt, L. B.. (2002). Identification of the diazepine ring opening site in the reaction of acidic hydrolysis of bromazepam. in Arhiv za farmaciju, 52(4), 462-463.
https://hdl.handle.net/21.15107/rcub_cherry_129
Popović GV, Damjanović TŽ, Sladić D, Pfendt LB. Identification of the diazepine ring opening site in the reaction of acidic hydrolysis of bromazepam. in Arhiv za farmaciju. 2002;52(4):462-463.
https://hdl.handle.net/21.15107/rcub_cherry_129 .
Popović, Gordana V., Damjanović, Tatjana Ž., Sladić, Dušan, Pfendt, Lidija B., "Identification of the diazepine ring opening site in the reaction of acidic hydrolysis of bromazepam" in Arhiv za farmaciju, 52, no. 4 (2002):462-463,
https://hdl.handle.net/21.15107/rcub_cherry_129 .

Study of heterogeneous equilibria in saturated aqueous solutions of some 7-chloro-1,4-benzodiazepines

Pfendt, Lidija B.; Sladić, Dušan; Janjić, Tomislav J.; Popović, Gordana V.

(1990)

TY  - JOUR
AU  - Pfendt, Lidija B.
AU  - Sladić, Dušan
AU  - Janjić, Tomislav J.
AU  - Popović, Gordana V.
PY  - 1990
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/20
AB  - Acid-base equilibria in heterogeneous and homogeneous systems of some sparingly soluble benzodiazepines (diazepam, prazepam, chlordiazepoxide and medazepam) were investigated in aqueous solution and the corresponding equilibrium constants were determined by the application of pH-metric, spectrophotometric and solubility methods. The sites of protonation were predicted on the basis of the analysis of the corresponding carbon-13 nuclear magnetic resonance spectra. In addition, buffer characteristics of saturated aqueous solutions of these drugs in the presence of the solid phase were investigated and it was established that they possess a very high buffer capacity over a specific pH range.
T2  - Analyst
T1  - Study of heterogeneous equilibria in saturated aqueous solutions of some 7-chloro-1,4-benzodiazepines
VL  - 115
IS  - 4
SP  - 383
EP  - 387
DO  - 10.1039/an9901500383
ER  - 
@article{
author = "Pfendt, Lidija B. and Sladić, Dušan and Janjić, Tomislav J. and Popović, Gordana V.",
year = "1990",
abstract = "Acid-base equilibria in heterogeneous and homogeneous systems of some sparingly soluble benzodiazepines (diazepam, prazepam, chlordiazepoxide and medazepam) were investigated in aqueous solution and the corresponding equilibrium constants were determined by the application of pH-metric, spectrophotometric and solubility methods. The sites of protonation were predicted on the basis of the analysis of the corresponding carbon-13 nuclear magnetic resonance spectra. In addition, buffer characteristics of saturated aqueous solutions of these drugs in the presence of the solid phase were investigated and it was established that they possess a very high buffer capacity over a specific pH range.",
journal = "Analyst",
title = "Study of heterogeneous equilibria in saturated aqueous solutions of some 7-chloro-1,4-benzodiazepines",
volume = "115",
number = "4",
pages = "383-387",
doi = "10.1039/an9901500383"
}
Pfendt, L. B., Sladić, D., Janjić, T. J.,& Popović, G. V.. (1990). Study of heterogeneous equilibria in saturated aqueous solutions of some 7-chloro-1,4-benzodiazepines. in Analyst, 115(4), 383-387.
https://doi.org/10.1039/an9901500383
Pfendt LB, Sladić D, Janjić TJ, Popović GV. Study of heterogeneous equilibria in saturated aqueous solutions of some 7-chloro-1,4-benzodiazepines. in Analyst. 1990;115(4):383-387.
doi:10.1039/an9901500383 .
Pfendt, Lidija B., Sladić, Dušan, Janjić, Tomislav J., Popović, Gordana V., "Study of heterogeneous equilibria in saturated aqueous solutions of some 7-chloro-1,4-benzodiazepines" in Analyst, 115, no. 4 (1990):383-387,
https://doi.org/10.1039/an9901500383 . .
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