TY  - JOUR
AU  - Pavlović, Miomir G.
AU  - Kindlova, Š.
AU  - Roušar, Ivo
PY  - 1992
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4735
AB  - It is shown that the critical overpotential of dendritic growth initiation increases with increasing copper concentration under identical hydrodynamic conditions, as well as with increasing rotation speed to the rde (rotating disc electrode).
PB  - Elsevier
T2  - Electrochimica Acta
T1  - The initiation of dendritic growth of electrodeposited copper on a rotating disc electrode with changing copper concentration and diffusion layer thickness
VL  - 37
IS  - 1
SP  - 23
EP  - 27
DO  - 10.1016/0013-4686(92)80006-8
ER  - 

@article{
author = "Pavlović, Miomir G. and Kindlova, Š. and Roušar, Ivo",
year = "1992",
abstract = "It is shown that the critical overpotential of dendritic growth initiation increases with increasing copper concentration under identical hydrodynamic conditions, as well as with increasing rotation speed to the rde (rotating disc electrode).",
publisher = "Elsevier",
journal = "Electrochimica Acta",
title = "The initiation of dendritic growth of electrodeposited copper on a rotating disc electrode with changing copper concentration and diffusion layer thickness",
volume = "37",
number = "1",
pages = "23-27",
doi = "10.1016/0013-4686(92)80006-8"
}

Pavlović, M. G., Kindlova, Š.,& Roušar, I.. (1992). The initiation of dendritic growth of electrodeposited copper on a rotating disc electrode with changing copper concentration and diffusion layer thickness. in Electrochimica Acta
Elsevier., 37(1), 23-27.
https://doi.org/10.1016/0013-4686(92)80006-8

Pavlović MG, Kindlova Š, Roušar I. The initiation of dendritic growth of electrodeposited copper on a rotating disc electrode with changing copper concentration and diffusion layer thickness. in Electrochimica Acta. 1992;37(1):23-27.
doi:10.1016/0013-4686(92)80006-8 .

Pavlović, Miomir G., Kindlova, Š., Roušar, Ivo, "The initiation of dendritic growth of electrodeposited copper on a rotating disc electrode with changing copper concentration and diffusion layer thickness" in Electrochimica Acta, 37, no. 1 (1992):23-27,
https://doi.org/10.1016/0013-4686(92)80006-8 . .

TY  - JOUR
AU  - Miodragović, Zoran
AU  - Jokić, Aleksandar M.
AU  - Pfendt, Petar A.
PY  - 1992
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4737
AB  - Fulvic acids (FAs) from the whole Quaternary sequence (to a depth of 26 m) of the alluvial sediment of the Sava river (taken from a site in Novi Beograd, Belgrade, Yugoslavia) were investigated with the aim of examining the effect of the environment (clay or sand) on their characteristics. Characterization of the FAs was carried out by correlating the results obtained by various instrumental techniques (u.v.-vis. and i.r. spectroscopy, fluorimetry). Differences were noticed between the FAs, depending on whether they originated from sand or clay, which indicates that the hydrogeological environment represents an important factor in determining their characteristics, though the role of the precursor material may be significant. FAs found in clay layers are less aliphatic, have a greater non-aliphatic hydroxyl group content and exhibit more similar fluorescence ntensities compared to FAs originating from sand. The greater mutual similarities of the clay FAs in comparison to those from sands is a result of diagenesis occurring in a more "closed" system.
PB  - Elsevier
T2  - Organic Geochemistry
T1  - Fulvic acid characterization in an alluvial sediment sequence: differences between clay and sand environments
VL  - 18
IS  - 4
SP  - 481
EP  - 487
DO  - 10.1016/0146-6380(92)90111-A
ER  - 

@article{
author = "Miodragović, Zoran and Jokić, Aleksandar M. and Pfendt, Petar A.",
year = "1992",
abstract = "Fulvic acids (FAs) from the whole Quaternary sequence (to a depth of 26 m) of the alluvial sediment of the Sava river (taken from a site in Novi Beograd, Belgrade, Yugoslavia) were investigated with the aim of examining the effect of the environment (clay or sand) on their characteristics. Characterization of the FAs was carried out by correlating the results obtained by various instrumental techniques (u.v.-vis. and i.r. spectroscopy, fluorimetry). Differences were noticed between the FAs, depending on whether they originated from sand or clay, which indicates that the hydrogeological environment represents an important factor in determining their characteristics, though the role of the precursor material may be significant. FAs found in clay layers are less aliphatic, have a greater non-aliphatic hydroxyl group content and exhibit more similar fluorescence ntensities compared to FAs originating from sand. The greater mutual similarities of the clay FAs in comparison to those from sands is a result of diagenesis occurring in a more "closed" system.",
publisher = "Elsevier",
journal = "Organic Geochemistry",
title = "Fulvic acid characterization in an alluvial sediment sequence: differences between clay and sand environments",
volume = "18",
number = "4",
pages = "481-487",
doi = "10.1016/0146-6380(92)90111-A"
}

Miodragović, Z., Jokić, A. M.,& Pfendt, P. A.. (1992). Fulvic acid characterization in an alluvial sediment sequence: differences between clay and sand environments. in Organic Geochemistry
Elsevier., 18(4), 481-487.
https://doi.org/10.1016/0146-6380(92)90111-A

Miodragović Z, Jokić AM, Pfendt PA. Fulvic acid characterization in an alluvial sediment sequence: differences between clay and sand environments. in Organic Geochemistry. 1992;18(4):481-487.
doi:10.1016/0146-6380(92)90111-A .

Miodragović, Zoran, Jokić, Aleksandar M., Pfendt, Petar A., "Fulvic acid characterization in an alluvial sediment sequence: differences between clay and sand environments" in Organic Geochemistry, 18, no. 4 (1992):481-487,
https://doi.org/10.1016/0146-6380(92)90111-A . .

TY  - JOUR
AU  - Pfendt, Petar A.
AU  - Polić, Predrag
AU  - Krsmanović, V. D.
AU  - Vitorović, Dragomir K.
PY  - 1990
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4736
AB  - An attempt was made to distinguish metal-organic matter interactions in two types of sulfate-reducing environments, mild (MR) and strong sulfate-reducing (SR), in the Aleksinac oil shale deposit (Oligocene-Miocene). Samples from the MR group show (all differences are statistically highly significant): lower organic matter content, compared with the SR group, higher O/C and N/C ratios (0.147 ± 0.054 and 0.041 ± 0.014, respectively, compared with 0.125 ± 0.031 and 0.035 ± 0.008, respectively, in the SR group), and higher Cu, Zn, Pb, Cr, Mo and Co contents than in the SR group. Statistically significant correlations between metals, the N/C and the SiO2/Al2O3 ratio in the MR group only, represent a record of highly interdependent processes of organic-metal-silicate interactions which had been occurring in the mild sulfate-reducing conditions during oil shale formation.
PB  - Elsevier
T2  - Organic Geochemistry
T1  - Metal-organic matter interactions in the formation of an oil shale deposit
VL  - 16
IS  - 1-3
SP  - 621
EP  - 629
DO  - 10.1016/0146-6380(90)90075-B
ER  - 

@article{
author = "Pfendt, Petar A. and Polić, Predrag and Krsmanović, V. D. and Vitorović, Dragomir K.",
year = "1990",
abstract = "An attempt was made to distinguish metal-organic matter interactions in two types of sulfate-reducing environments, mild (MR) and strong sulfate-reducing (SR), in the Aleksinac oil shale deposit (Oligocene-Miocene). Samples from the MR group show (all differences are statistically highly significant): lower organic matter content, compared with the SR group, higher O/C and N/C ratios (0.147 ± 0.054 and 0.041 ± 0.014, respectively, compared with 0.125 ± 0.031 and 0.035 ± 0.008, respectively, in the SR group), and higher Cu, Zn, Pb, Cr, Mo and Co contents than in the SR group. Statistically significant correlations between metals, the N/C and the SiO2/Al2O3 ratio in the MR group only, represent a record of highly interdependent processes of organic-metal-silicate interactions which had been occurring in the mild sulfate-reducing conditions during oil shale formation.",
publisher = "Elsevier",
journal = "Organic Geochemistry",
title = "Metal-organic matter interactions in the formation of an oil shale deposit",
volume = "16",
number = "1-3",
pages = "621-629",
doi = "10.1016/0146-6380(90)90075-B"
}

Pfendt, P. A., Polić, P., Krsmanović, V. D.,& Vitorović, D. K.. (1990). Metal-organic matter interactions in the formation of an oil shale deposit. in Organic Geochemistry
Elsevier., 16(1-3), 621-629.
https://doi.org/10.1016/0146-6380(90)90075-B

Pfendt PA, Polić P, Krsmanović VD, Vitorović DK. Metal-organic matter interactions in the formation of an oil shale deposit. in Organic Geochemistry. 1990;16(1-3):621-629.
doi:10.1016/0146-6380(90)90075-B .

Pfendt, Petar A., Polić, Predrag, Krsmanović, V. D., Vitorović, Dragomir K., "Metal-organic matter interactions in the formation of an oil shale deposit" in Organic Geochemistry, 16, no. 1-3 (1990):621-629,
https://doi.org/10.1016/0146-6380(90)90075-B . .

TY  - JOUR
AU  - Adžić, Radoslav R.
AU  - Štrbac, Svetlana
AU  - Anastasijević, Nikola A.
PY  - 1989
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4215
AB  - Oxide formation and oxygen reduction on gold have been investigated with single crystal electrode surfaces of various orientations. Both reactions show sensitivity to the surface orientation, presence of steps, their density and orientation. The initial stages of oxide formation can be correlated with calculated relative surface energy. Anions exert a pronounced effect on oxide formation. The activity for oxygen reduction can be correlated with the same surface property except for Au(100). Structural effect from this particular plane outweighs the electronic effects. No correlation for alkaline solutions was found. Rotating ring-disc measurements show no hydrogen peroxide generation Au(100) in the presence of almost neutral AuOH-(1 - λ)on the surface. This makes it the most active electrocatalyst for oxygen reduction in alkaline solutions. At more negative potentials (no AuOH on the surface) a series mechanism up to the peroxide stage is operative. The Au(311) plane also shows a high activity dependent on AuOH-(1 - λ). Data for both reactions clearly demonstrate that each crystallographic orientation gives an electrode surface with distinct electrochemical properties.
PB  - Elsevier
T2  - Materials Chemistry and Physics
T1  - Electrocatalysis of oxygen on single crystal gold electrodes
VL  - 22
IS  - 3-4
SP  - 349
EP  - 375
DO  - 10.1016/0254-0584(89)90005-9
ER  - 

@article{
author = "Adžić, Radoslav R. and Štrbac, Svetlana and Anastasijević, Nikola A.",
year = "1989",
abstract = "Oxide formation and oxygen reduction on gold have been investigated with single crystal electrode surfaces of various orientations. Both reactions show sensitivity to the surface orientation, presence of steps, their density and orientation. The initial stages of oxide formation can be correlated with calculated relative surface energy. Anions exert a pronounced effect on oxide formation. The activity for oxygen reduction can be correlated with the same surface property except for Au(100). Structural effect from this particular plane outweighs the electronic effects. No correlation for alkaline solutions was found. Rotating ring-disc measurements show no hydrogen peroxide generation Au(100) in the presence of almost neutral AuOH-(1 - λ)on the surface. This makes it the most active electrocatalyst for oxygen reduction in alkaline solutions. At more negative potentials (no AuOH on the surface) a series mechanism up to the peroxide stage is operative. The Au(311) plane also shows a high activity dependent on AuOH-(1 - λ). Data for both reactions clearly demonstrate that each crystallographic orientation gives an electrode surface with distinct electrochemical properties.",
publisher = "Elsevier",
journal = "Materials Chemistry and Physics",
title = "Electrocatalysis of oxygen on single crystal gold electrodes",
volume = "22",
number = "3-4",
pages = "349-375",
doi = "10.1016/0254-0584(89)90005-9"
}

Adžić, R. R., Štrbac, S.,& Anastasijević, N. A.. (1989). Electrocatalysis of oxygen on single crystal gold electrodes. in Materials Chemistry and Physics
Elsevier., 22(3-4), 349-375.
https://doi.org/10.1016/0254-0584(89)90005-9

Adžić RR, Štrbac S, Anastasijević NA. Electrocatalysis of oxygen on single crystal gold electrodes. in Materials Chemistry and Physics. 1989;22(3-4):349-375.
doi:10.1016/0254-0584(89)90005-9 .

Adžić, Radoslav R., Štrbac, Svetlana, Anastasijević, Nikola A., "Electrocatalysis of oxygen on single crystal gold electrodes" in Materials Chemistry and Physics, 22, no. 3-4 (1989):349-375,
https://doi.org/10.1016/0254-0584(89)90005-9 . .

TY  - JOUR
AU  - Marković, Nenad M.
AU  - Marinković, N. S.
AU  - Adžić, Radoslav R.
PY  - 1988
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4201
AB  - The adsorption of hydrogen and sulphuric acid anions has been studied on single-crystal platinum stepped surfaces from the [110] zone. Both processes depend on the orientation of the electrode surface. The multiple states of hydrogen adsorption can be correlated with the nature and density of the adsorption sites. There is a negligible effect of adsorbate-adsorbate interaction. The voltammetric profiles are in a wide potential range determined by bisulphate and sulphate adsorption/desorption. A sharp peak found in voltammetry is associated with hydrogen adsorption in the step sites, composed of the (100)-(111) step-terrace combination, concurrent with sulphate desorption. Bisulphates and sulphates are strongly adsorbed in the trigonal sites in the step, which can be formed from the steps and terraces of different orientations from this zone. The exact position of the adsorbed hydrogen atoms and anions is discussed. A comparison with the adsorption in HClO4 is given for some surfaces.
PB  - Elsevier
T2  - Journal of Electroanalytical Chemistry
T1  - Electrosorption of hydrogen and sulphuric acid anions on single-crystal platinum stepped surfaces. Part I. The [110] zone
VL  - 241
IS  - 1-2
SP  - 309
EP  - 328
DO  - 10.1016/0022-0728(88)85134-9
ER  - 

@article{
author = "Marković, Nenad M. and Marinković, N. S. and Adžić, Radoslav R.",
year = "1988",
abstract = "The adsorption of hydrogen and sulphuric acid anions has been studied on single-crystal platinum stepped surfaces from the [110] zone. Both processes depend on the orientation of the electrode surface. The multiple states of hydrogen adsorption can be correlated with the nature and density of the adsorption sites. There is a negligible effect of adsorbate-adsorbate interaction. The voltammetric profiles are in a wide potential range determined by bisulphate and sulphate adsorption/desorption. A sharp peak found in voltammetry is associated with hydrogen adsorption in the step sites, composed of the (100)-(111) step-terrace combination, concurrent with sulphate desorption. Bisulphates and sulphates are strongly adsorbed in the trigonal sites in the step, which can be formed from the steps and terraces of different orientations from this zone. The exact position of the adsorbed hydrogen atoms and anions is discussed. A comparison with the adsorption in HClO4 is given for some surfaces.",
publisher = "Elsevier",
journal = "Journal of Electroanalytical Chemistry",
title = "Electrosorption of hydrogen and sulphuric acid anions on single-crystal platinum stepped surfaces. Part I. The [110] zone",
volume = "241",
number = "1-2",
pages = "309-328",
doi = "10.1016/0022-0728(88)85134-9"
}

Marković, N. M., Marinković, N. S.,& Adžić, R. R.. (1988). Electrosorption of hydrogen and sulphuric acid anions on single-crystal platinum stepped surfaces. Part I. The [110] zone. in Journal of Electroanalytical Chemistry
Elsevier., 241(1-2), 309-328.
https://doi.org/10.1016/0022-0728(88)85134-9

Marković NM, Marinković NS, Adžić RR. Electrosorption of hydrogen and sulphuric acid anions on single-crystal platinum stepped surfaces. Part I. The [110] zone. in Journal of Electroanalytical Chemistry. 1988;241(1-2):309-328.
doi:10.1016/0022-0728(88)85134-9 .

Marković, Nenad M., Marinković, N. S., Adžić, Radoslav R., "Electrosorption of hydrogen and sulphuric acid anions on single-crystal platinum stepped surfaces. Part I. The [110] zone" in Journal of Electroanalytical Chemistry, 241, no. 1-2 (1988):309-328,
https://doi.org/10.1016/0022-0728(88)85134-9 . .

TY  - JOUR
AU  - Anastasijević, Nikola A.
AU  - Vešović, V. B.
AU  - Adžić, Radoslav R.
PY  - 1987
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4210
AB  - A general scheme of oxygen reduction is given and analysis of the disk-ring measurements is performed. Expressions for the diagnostic criteria for such a scheme have been derived and their implications are discussed. The existence of superoxide and oxygen ions and the interaction of the series and direct paths have been assumed in postulating the scheme. Also, all the electrochemical reactions involved only one-electron exchange. The possibilities and limitations of the disk-ring measurements in the mechanistic study of oxygen reduction are discussed together with a re-evaluation of some well-accepted criteria which are shown to be misleading. New definitions and terminology for different pathways of O2 reduction are proposed.
PB  - Elsevier
T2  - Journal of Electroanalytical Chemistry
T1  - Determination of the kinetic parameters of the oxygen reduction reaction using the rotating ring-disk electrode. Part I. Theory
VL  - 229
IS  - 1-2
SP  - 305
EP  - 316
DO  - 10.1016/0022-0728(87)85148-3
ER  - 

@article{
author = "Anastasijević, Nikola A. and Vešović, V. B. and Adžić, Radoslav R.",
year = "1987",
abstract = "A general scheme of oxygen reduction is given and analysis of the disk-ring measurements is performed. Expressions for the diagnostic criteria for such a scheme have been derived and their implications are discussed. The existence of superoxide and oxygen ions and the interaction of the series and direct paths have been assumed in postulating the scheme. Also, all the electrochemical reactions involved only one-electron exchange. The possibilities and limitations of the disk-ring measurements in the mechanistic study of oxygen reduction are discussed together with a re-evaluation of some well-accepted criteria which are shown to be misleading. New definitions and terminology for different pathways of O2 reduction are proposed.",
publisher = "Elsevier",
journal = "Journal of Electroanalytical Chemistry",
title = "Determination of the kinetic parameters of the oxygen reduction reaction using the rotating ring-disk electrode. Part I. Theory",
volume = "229",
number = "1-2",
pages = "305-316",
doi = "10.1016/0022-0728(87)85148-3"
}

Anastasijević, N. A., Vešović, V. B.,& Adžić, R. R.. (1987). Determination of the kinetic parameters of the oxygen reduction reaction using the rotating ring-disk electrode. Part I. Theory. in Journal of Electroanalytical Chemistry
Elsevier., 229(1-2), 305-316.
https://doi.org/10.1016/0022-0728(87)85148-3

Anastasijević NA, Vešović VB, Adžić RR. Determination of the kinetic parameters of the oxygen reduction reaction using the rotating ring-disk electrode. Part I. Theory. in Journal of Electroanalytical Chemistry. 1987;229(1-2):305-316.
doi:10.1016/0022-0728(87)85148-3 .

Anastasijević, Nikola A., Vešović, V. B., Adžić, Radoslav R., "Determination of the kinetic parameters of the oxygen reduction reaction using the rotating ring-disk electrode. Part I. Theory" in Journal of Electroanalytical Chemistry, 229, no. 1-2 (1987):305-316,
https://doi.org/10.1016/0022-0728(87)85148-3 . .

TY  - JOUR
AU  - Adžić, Radoslav R.
AU  - Avramov Ivić, Milka
PY  - 1986
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4312
AB  - Ethylene glycol is a potential fuel of practical interest whose electrooxidation has not been studied in detail. This is a complex reaction whose mechanism is far from being understood. It is quite clear, however, that some kind of strongly bound intermediate is formed in the oxidation of ethylene glycol on platinum. This is indicated also by the effects of foreign metal adatoms covering a part of the Pt surface. Thus, pronounced catalytic effects of Pb, Tl and Bi have been observed in alkaline solutions and these are partly based on a suppression of formation and/or adsorption of strongly bound intermediates. In this work the oxidation of ethylene glycol on gold single crystals with the (100), (110) and (111) orientations has been studied with the aim of investigating whether there is structural sensitivity in this reaction. Structural sensitivity, as well as the role of AuOH species formed on surfaces, could be of interest for both electrocatalysis and catalysis.
PB  - Elsevier
T2  - Journal of Catalysis
T1  - Structural effects in electrocatalysis: Oxidation of ethylene glycol on single crystal gold electrodes in alkaline solutions
VL  - 101
IS  - 2
SP  - 532
EP  - 535
DO  - 10.1016/0021-9517(86)90282-4
ER  - 

@article{
author = "Adžić, Radoslav R. and Avramov Ivić, Milka",
year = "1986",
abstract = "Ethylene glycol is a potential fuel of practical interest whose electrooxidation has not been studied in detail. This is a complex reaction whose mechanism is far from being understood. It is quite clear, however, that some kind of strongly bound intermediate is formed in the oxidation of ethylene glycol on platinum. This is indicated also by the effects of foreign metal adatoms covering a part of the Pt surface. Thus, pronounced catalytic effects of Pb, Tl and Bi have been observed in alkaline solutions and these are partly based on a suppression of formation and/or adsorption of strongly bound intermediates. In this work the oxidation of ethylene glycol on gold single crystals with the (100), (110) and (111) orientations has been studied with the aim of investigating whether there is structural sensitivity in this reaction. Structural sensitivity, as well as the role of AuOH species formed on surfaces, could be of interest for both electrocatalysis and catalysis.",
publisher = "Elsevier",
journal = "Journal of Catalysis",
title = "Structural effects in electrocatalysis: Oxidation of ethylene glycol on single crystal gold electrodes in alkaline solutions",
volume = "101",
number = "2",
pages = "532-535",
doi = "10.1016/0021-9517(86)90282-4"
}

Adžić, R. R.,& Avramov Ivić, M.. (1986). Structural effects in electrocatalysis: Oxidation of ethylene glycol on single crystal gold electrodes in alkaline solutions. in Journal of Catalysis
Elsevier., 101(2), 532-535.
https://doi.org/10.1016/0021-9517(86)90282-4

Adžić RR, Avramov Ivić M. Structural effects in electrocatalysis: Oxidation of ethylene glycol on single crystal gold electrodes in alkaline solutions. in Journal of Catalysis. 1986;101(2):532-535.
doi:10.1016/0021-9517(86)90282-4 .

Adžić, Radoslav R., Avramov Ivić, Milka, "Structural effects in electrocatalysis: Oxidation of ethylene glycol on single crystal gold electrodes in alkaline solutions" in Journal of Catalysis, 101, no. 2 (1986):532-535,
https://doi.org/10.1016/0021-9517(86)90282-4 . .

TY  - JOUR
AU  - Amblès, André
AU  - Đordjević, Mirjana V.
AU  - Vitorović, Dragomir K.
PY  - 1985
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4505
AB  - In order to obtain evidence on the relationship between kerogen structural types and the quantity and nature of their oxidation products, the products of a multistage (13 step) alkaline permanganate degradation of type-III kerogen from a sample of the Mannville shale, Canada, have been studied in detail. High yield of oxidation products was obtained, 81.89% based on original kerogen: 0.61% neutrals and bases, 4.82% of ether-soluble acids, and 76.46% of precipitated ether-insoluble acids. The ether-soluble acids and the soluble acids produced by further controlled permanganate degradation of precipitated acids were found to consist of different mono- and polycarboxylic, partly alkyl-substituted, aromatic acids as major oxidation products (over 90%). Saturated unbranched mono- and dicarboxylic acids were found in small concentrations. In this way a typical aromatic structure of type-III kerogen was confirmed. The structure of the examined kerogen is probably largely alkyl-substituted and cross-linked by relatively short chains or bridges.
PB  - Elsevier
T2  - Chemical Geology
T1  - Multistage alkaline permanganate degradation of a type-III kerogen
VL  - 48
IS  - 1-4
SP  - 305
EP  - 312
DO  - 10.1016/0009-2541(85)90055-5
ER  - 

@article{
author = "Amblès, André and Đordjević, Mirjana V. and Vitorović, Dragomir K.",
year = "1985",
abstract = "In order to obtain evidence on the relationship between kerogen structural types and the quantity and nature of their oxidation products, the products of a multistage (13 step) alkaline permanganate degradation of type-III kerogen from a sample of the Mannville shale, Canada, have been studied in detail. High yield of oxidation products was obtained, 81.89% based on original kerogen: 0.61% neutrals and bases, 4.82% of ether-soluble acids, and 76.46% of precipitated ether-insoluble acids. The ether-soluble acids and the soluble acids produced by further controlled permanganate degradation of precipitated acids were found to consist of different mono- and polycarboxylic, partly alkyl-substituted, aromatic acids as major oxidation products (over 90%). Saturated unbranched mono- and dicarboxylic acids were found in small concentrations. In this way a typical aromatic structure of type-III kerogen was confirmed. The structure of the examined kerogen is probably largely alkyl-substituted and cross-linked by relatively short chains or bridges.",
publisher = "Elsevier",
journal = "Chemical Geology",
title = "Multistage alkaline permanganate degradation of a type-III kerogen",
volume = "48",
number = "1-4",
pages = "305-312",
doi = "10.1016/0009-2541(85)90055-5"
}

Amblès, A., Đordjević, M. V.,& Vitorović, D. K.. (1985). Multistage alkaline permanganate degradation of a type-III kerogen. in Chemical Geology
Elsevier., 48(1-4), 305-312.
https://doi.org/10.1016/0009-2541(85)90055-5

Amblès A, Đordjević MV, Vitorović DK. Multistage alkaline permanganate degradation of a type-III kerogen. in Chemical Geology. 1985;48(1-4):305-312.
doi:10.1016/0009-2541(85)90055-5 .

Amblès, André, Đordjević, Mirjana V., Vitorović, Dragomir K., "Multistage alkaline permanganate degradation of a type-III kerogen" in Chemical Geology, 48, no. 1-4 (1985):305-312,
https://doi.org/10.1016/0009-2541(85)90055-5 . .

TY  - JOUR
AU  - Lorenc, Ljubinka B.
AU  - Bondarenko, Lidija
AU  - Mihailović, Milhailo Lj.
PY  - 1985
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4514
AB  - Thermal decomposition of steroidal 5α,8α-peroxides (such as 1) resulted in bisfragmentation of the C(5)-C(10) and C(8)-C(9) bonds, and elimination of acetic acid, to produce a new type of bicyclic compounds, namely 5,10;8,9-diseco-steroid derivatives (such as 2). some chemical transformations of product 2 are described.
PB  - Elsevier
T2  - Tetrahedron Letters
T1  - Transformation of steroidal 5α,8α-peroxides to the 14-membered ring containing 5,10;8,9-diseco-steroid derivatives
VL  - 26
IS  - 3
SP  - 389
EP  - 392
DO  - 10.1016/S0040-4039(01)80825-X
ER  - 

@article{
author = "Lorenc, Ljubinka B. and Bondarenko, Lidija and Mihailović, Milhailo Lj.",
year = "1985",
abstract = "Thermal decomposition of steroidal 5α,8α-peroxides (such as 1) resulted in bisfragmentation of the C(5)-C(10) and C(8)-C(9) bonds, and elimination of acetic acid, to produce a new type of bicyclic compounds, namely 5,10;8,9-diseco-steroid derivatives (such as 2). some chemical transformations of product 2 are described.",
publisher = "Elsevier",
journal = "Tetrahedron Letters",
title = "Transformation of steroidal 5α,8α-peroxides to the 14-membered ring containing 5,10;8,9-diseco-steroid derivatives",
volume = "26",
number = "3",
pages = "389-392",
doi = "10.1016/S0040-4039(01)80825-X"
}

Lorenc, L. B., Bondarenko, L.,& Mihailović, M. Lj.. (1985). Transformation of steroidal 5α,8α-peroxides to the 14-membered ring containing 5,10;8,9-diseco-steroid derivatives. in Tetrahedron Letters
Elsevier., 26(3), 389-392.
https://doi.org/10.1016/S0040-4039(01)80825-X

Lorenc LB, Bondarenko L, Mihailović ML. Transformation of steroidal 5α,8α-peroxides to the 14-membered ring containing 5,10;8,9-diseco-steroid derivatives. in Tetrahedron Letters. 1985;26(3):389-392.
doi:10.1016/S0040-4039(01)80825-X .

Lorenc, Ljubinka B., Bondarenko, Lidija, Mihailović, Milhailo Lj., "Transformation of steroidal 5α,8α-peroxides to the 14-membered ring containing 5,10;8,9-diseco-steroid derivatives" in Tetrahedron Letters, 26, no. 3 (1985):389-392,
https://doi.org/10.1016/S0040-4039(01)80825-X . .

TY  - JOUR
AU  - Vitorović, Dragomir K.
AU  - Đorđević, Mirjana V.
AU  - Amblès, André
AU  - Jacquesy, Jean Claude
PY  - 1984
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4476
AB  - The products of a 27-step alkaline permanganate degradation of a type II kerogen from a sample of Toarcian shale, Paris Basin, have been studied. The high yield of oxidation products consisted of 1.86% neutrals and bases, 24.48% ether-soluble acids, and 45.95% precipitated, ether-insoluble acids, based on weight of original kerogen. The ether-soluble acids and the soluble products of further permanganate degradation of precipitated acids were found to consist mostly of saturated unbranched C6-C22 α,ω-dicarboxylic and C9-C25 monocarboxylic acids. Significant amounts of aromatic monocarboxylic, dicarboxylic and tricarboxylic acids were also found. Alkane tri- and tetracarboxylic acids were obtained in small concentration.
PB  - Elsevier
T2  - Organic Geochemistry
T1  - Multistage alkaline permanganate degradation of a type II kerogen
VL  - 5
IS  - 4
SP  - 259
EP  - 265
DO  - 10.1016/0146-6380(84)90013-5
ER  - 

@article{
author = "Vitorović, Dragomir K. and Đorđević, Mirjana V. and Amblès, André and Jacquesy, Jean Claude",
year = "1984",
abstract = "The products of a 27-step alkaline permanganate degradation of a type II kerogen from a sample of Toarcian shale, Paris Basin, have been studied. The high yield of oxidation products consisted of 1.86% neutrals and bases, 24.48% ether-soluble acids, and 45.95% precipitated, ether-insoluble acids, based on weight of original kerogen. The ether-soluble acids and the soluble products of further permanganate degradation of precipitated acids were found to consist mostly of saturated unbranched C6-C22 α,ω-dicarboxylic and C9-C25 monocarboxylic acids. Significant amounts of aromatic monocarboxylic, dicarboxylic and tricarboxylic acids were also found. Alkane tri- and tetracarboxylic acids were obtained in small concentration.",
publisher = "Elsevier",
journal = "Organic Geochemistry",
title = "Multistage alkaline permanganate degradation of a type II kerogen",
volume = "5",
number = "4",
pages = "259-265",
doi = "10.1016/0146-6380(84)90013-5"
}

Vitorović, D. K., Đorđević, M. V., Amblès, A.,& Jacquesy, J. C.. (1984). Multistage alkaline permanganate degradation of a type II kerogen. in Organic Geochemistry
Elsevier., 5(4), 259-265.
https://doi.org/10.1016/0146-6380(84)90013-5

Vitorović DK, Đorđević MV, Amblès A, Jacquesy JC. Multistage alkaline permanganate degradation of a type II kerogen. in Organic Geochemistry. 1984;5(4):259-265.
doi:10.1016/0146-6380(84)90013-5 .

Vitorović, Dragomir K., Đorđević, Mirjana V., Amblès, André, Jacquesy, Jean Claude, "Multistage alkaline permanganate degradation of a type II kerogen" in Organic Geochemistry, 5, no. 4 (1984):259-265,
https://doi.org/10.1016/0146-6380(84)90013-5 . .

TY  - JOUR
AU  - Popov, Konstantin I.
AU  - Maksimović, Miodrag D.
AU  - Stevanović, Rade M.
AU  - Krstajić, Nedeljko V.
PY  - 1984
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4433
AB  - The effect of a pulsating current on the microthrowing power of metal deposits in the early stage of deposition was investigated by scanning electron microscopy. It is shown that at the same average current density the microthrowing power of metal deposits increases rapidly with increasing pause-to-pulse ratio.
PB  - Elsevier
T2  - Surface Technology
T1  - Fundamental aspects of pulsating current metal electrodeposition VIII: The effect of pause-to-pulse ratio on microthrowing power of metal deposition
VL  - 22
IS  - 2
SP  - 155
EP  - 158
DO  - 10.1016/0376-4583(84)90051-7
ER  - 

@article{
author = "Popov, Konstantin I. and Maksimović, Miodrag D. and Stevanović, Rade M. and Krstajić, Nedeljko V.",
year = "1984",
abstract = "The effect of a pulsating current on the microthrowing power of metal deposits in the early stage of deposition was investigated by scanning electron microscopy. It is shown that at the same average current density the microthrowing power of metal deposits increases rapidly with increasing pause-to-pulse ratio.",
publisher = "Elsevier",
journal = "Surface Technology",
title = "Fundamental aspects of pulsating current metal electrodeposition VIII: The effect of pause-to-pulse ratio on microthrowing power of metal deposition",
volume = "22",
number = "2",
pages = "155-158",
doi = "10.1016/0376-4583(84)90051-7"
}

Popov, K. I., Maksimović, M. D., Stevanović, R. M.,& Krstajić, N. V.. (1984). Fundamental aspects of pulsating current metal electrodeposition VIII: The effect of pause-to-pulse ratio on microthrowing power of metal deposition. in Surface Technology
Elsevier., 22(2), 155-158.
https://doi.org/10.1016/0376-4583(84)90051-7

Popov KI, Maksimović MD, Stevanović RM, Krstajić NV. Fundamental aspects of pulsating current metal electrodeposition VIII: The effect of pause-to-pulse ratio on microthrowing power of metal deposition. in Surface Technology. 1984;22(2):155-158.
doi:10.1016/0376-4583(84)90051-7 .

Popov, Konstantin I., Maksimović, Miodrag D., Stevanović, Rade M., Krstajić, Nedeljko V., "Fundamental aspects of pulsating current metal electrodeposition VIII: The effect of pause-to-pulse ratio on microthrowing power of metal deposition" in Surface Technology, 22, no. 2 (1984):155-158,
https://doi.org/10.1016/0376-4583(84)90051-7 . .

TY  - JOUR
AU  - Popov, Konstantin I.
AU  - Maksimović, Miodrag D.
AU  - Simičić, M.V.
AU  - Krstajić, Nedeljko V.
PY  - 1984
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4470
AB  - It is shown that spongy deposits are obtained under d.c. conditions and that compact deposits are obtained in pulsating current (PC) deposition with high pause-to-pulse ratios at the same average current density and deposition time. This is explained by an increased nucleation rate in PC deposition.
PB  - Elsevier
T2  - Surface Technology
T1  - Fundamental aspects of pulsating current metal electrodeposition IX: The prevention of spongy deposit formation on inert substrates
VL  - 22
IS  - 2
SP  - 159
EP  - 164
DO  - 10.1016/0376-4583(84)90052-9
ER  - 

@article{
author = "Popov, Konstantin I. and Maksimović, Miodrag D. and Simičić, M.V. and Krstajić, Nedeljko V.",
year = "1984",
abstract = "It is shown that spongy deposits are obtained under d.c. conditions and that compact deposits are obtained in pulsating current (PC) deposition with high pause-to-pulse ratios at the same average current density and deposition time. This is explained by an increased nucleation rate in PC deposition.",
publisher = "Elsevier",
journal = "Surface Technology",
title = "Fundamental aspects of pulsating current metal electrodeposition IX: The prevention of spongy deposit formation on inert substrates",
volume = "22",
number = "2",
pages = "159-164",
doi = "10.1016/0376-4583(84)90052-9"
}

Popov, K. I., Maksimović, M. D., Simičić, M.V.,& Krstajić, N. V.. (1984). Fundamental aspects of pulsating current metal electrodeposition IX: The prevention of spongy deposit formation on inert substrates. in Surface Technology
Elsevier., 22(2), 159-164.
https://doi.org/10.1016/0376-4583(84)90052-9

Popov KI, Maksimović MD, Simičić M, Krstajić NV. Fundamental aspects of pulsating current metal electrodeposition IX: The prevention of spongy deposit formation on inert substrates. in Surface Technology. 1984;22(2):159-164.
doi:10.1016/0376-4583(84)90052-9 .

Popov, Konstantin I., Maksimović, Miodrag D., Simičić, M.V., Krstajić, Nedeljko V., "Fundamental aspects of pulsating current metal electrodeposition IX: The prevention of spongy deposit formation on inert substrates" in Surface Technology, 22, no. 2 (1984):159-164,
https://doi.org/10.1016/0376-4583(84)90052-9 . .

TY  - JOUR
AU  - Popov, Konstantin I.
AU  - Maksimović, Miodrag D.
AU  - Totovski, Dimitri Ć.
AU  - Nakić, Vjekoslav M.
PY  - 1983
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4420
AB  - The equivalent electrical resistance of a cell with plane parallel electrodes is described by a simple mathematical model. The limits of this model were determined experimentally. The relation between the overpotential at the edge and at the middle of the electrode is established. The causes of dendrite occurrence at the edge of the electrode in galvanostatic cadmium deposition are discussed.
PB  - Elsevier
T2  - Surface Technology
T1  - Some aspects of current density distribution in electrolytic cells I: Dendritic growth of cadmium at the cathode edge in galvanostatic electrodeposition
VL  - 19
IS  - 2
SP  - 173
EP  - 180
DO  - 10.1016/0376-4583(83)90067-5
ER  - 

@article{
author = "Popov, Konstantin I. and Maksimović, Miodrag D. and Totovski, Dimitri Ć. and Nakić, Vjekoslav M.",
year = "1983",
abstract = "The equivalent electrical resistance of a cell with plane parallel electrodes is described by a simple mathematical model. The limits of this model were determined experimentally. The relation between the overpotential at the edge and at the middle of the electrode is established. The causes of dendrite occurrence at the edge of the electrode in galvanostatic cadmium deposition are discussed.",
publisher = "Elsevier",
journal = "Surface Technology",
title = "Some aspects of current density distribution in electrolytic cells I: Dendritic growth of cadmium at the cathode edge in galvanostatic electrodeposition",
volume = "19",
number = "2",
pages = "173-180",
doi = "10.1016/0376-4583(83)90067-5"
}

Popov, K. I., Maksimović, M. D., Totovski, D. Ć.,& Nakić, V. M.. (1983). Some aspects of current density distribution in electrolytic cells I: Dendritic growth of cadmium at the cathode edge in galvanostatic electrodeposition. in Surface Technology
Elsevier., 19(2), 173-180.
https://doi.org/10.1016/0376-4583(83)90067-5

Popov KI, Maksimović MD, Totovski DĆ, Nakić VM. Some aspects of current density distribution in electrolytic cells I: Dendritic growth of cadmium at the cathode edge in galvanostatic electrodeposition. in Surface Technology. 1983;19(2):173-180.
doi:10.1016/0376-4583(83)90067-5 .

Popov, Konstantin I., Maksimović, Miodrag D., Totovski, Dimitri Ć., Nakić, Vjekoslav M., "Some aspects of current density distribution in electrolytic cells I: Dendritic growth of cadmium at the cathode edge in galvanostatic electrodeposition" in Surface Technology, 19, no. 2 (1983):173-180,
https://doi.org/10.1016/0376-4583(83)90067-5 . .

TY  - JOUR
AU  - Milosavljević, Slobodan
AU  - Jeremić, Dragoslav
AU  - Mihailović, Milhailo Lj.
AU  - Wehrli, Felix W.
PY  - 1981
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4421
AB  - Unambiguous signal assignments in the 13C spectra of monodeuterated cyclooctanones derived from the lead tetraacetate or silver oxide/bromine oxidations of the corresponding 1‐monodeutero‐alcohols have been obtained from deuterium‐induced 13C isotope shifts and geminal and vicinal 13C-2H spin‐spin coupling constants. The label in the ketones is shown to be in position 5.
PB  - Wiley
T2  - Organic Magnetic Resonance
T1  - Deuterium‐induced 13C nuclear magnetic resonance isotope shifts and 13C-2H couplings for signal assignments and determination of deuteration site in cyclooctanone
VL  - 17
IS  - 4
SP  - 299
EP  - 300
DO  - 10.1002/mrc.1270170415
ER  - 

@article{
author = "Milosavljević, Slobodan and Jeremić, Dragoslav and Mihailović, Milhailo Lj. and Wehrli, Felix W.",
year = "1981",
abstract = "Unambiguous signal assignments in the 13C spectra of monodeuterated cyclooctanones derived from the lead tetraacetate or silver oxide/bromine oxidations of the corresponding 1‐monodeutero‐alcohols have been obtained from deuterium‐induced 13C isotope shifts and geminal and vicinal 13C-2H spin‐spin coupling constants. The label in the ketones is shown to be in position 5.",
publisher = "Wiley",
journal = "Organic Magnetic Resonance",
title = "Deuterium‐induced 13C nuclear magnetic resonance isotope shifts and 13C-2H couplings for signal assignments and determination of deuteration site in cyclooctanone",
volume = "17",
number = "4",
pages = "299-300",
doi = "10.1002/mrc.1270170415"
}

Milosavljević, S., Jeremić, D., Mihailović, M. Lj.,& Wehrli, F. W.. (1981). Deuterium‐induced 13C nuclear magnetic resonance isotope shifts and 13C-2H couplings for signal assignments and determination of deuteration site in cyclooctanone. in Organic Magnetic Resonance
Wiley., 17(4), 299-300.
https://doi.org/10.1002/mrc.1270170415

Milosavljević S, Jeremić D, Mihailović ML, Wehrli FW. Deuterium‐induced 13C nuclear magnetic resonance isotope shifts and 13C-2H couplings for signal assignments and determination of deuteration site in cyclooctanone. in Organic Magnetic Resonance. 1981;17(4):299-300.
doi:10.1002/mrc.1270170415 .

Milosavljević, Slobodan, Jeremić, Dragoslav, Mihailović, Milhailo Lj., Wehrli, Felix W., "Deuterium‐induced 13C nuclear magnetic resonance isotope shifts and 13C-2H couplings for signal assignments and determination of deuteration site in cyclooctanone" in Organic Magnetic Resonance, 17, no. 4 (1981):299-300,
https://doi.org/10.1002/mrc.1270170415 . .

TY  - JOUR
AU  - Lorenc, Ljubinka B.
AU  - Juranić, Ivan O.
AU  - Mihailović, Milhailo Lj.
PY  - 1977
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4598
AB  - U.v. irradiation of the steroidal isoxazolidines 5α,10α-imino- oxy-5(10 → 1βH)abeo-5α-cholestan-3β-olacetate (1a) and the corresponding N-methyl and N-acetyl derivatives (1b) and (1c) in various solvents in the presence of oxygen, gave the nitro products (2), (3), and (4) and the azoxy products (5) and (6); a mechanism involving exciplex formation followed by proton transfer from isoxazolidine to molecular oxygen is proposed.
PB  - Royal Society of Chemistry
T2  - Journal of the Chemical Society, Chemical Communications
T1  - Photochemically induced oxidation of some steroidal isoxazolidines by molecular oxygen
IS  - 21
SP  - 749
EP  - 751
DO  - 10.1039/C39770000749
ER  - 

@article{
author = "Lorenc, Ljubinka B. and Juranić, Ivan O. and Mihailović, Milhailo Lj.",
year = "1977",
abstract = "U.v. irradiation of the steroidal isoxazolidines 5α,10α-imino- oxy-5(10 → 1βH)abeo-5α-cholestan-3β-olacetate (1a) and the corresponding N-methyl and N-acetyl derivatives (1b) and (1c) in various solvents in the presence of oxygen, gave the nitro products (2), (3), and (4) and the azoxy products (5) and (6); a mechanism involving exciplex formation followed by proton transfer from isoxazolidine to molecular oxygen is proposed.",
publisher = "Royal Society of Chemistry",
journal = "Journal of the Chemical Society, Chemical Communications",
title = "Photochemically induced oxidation of some steroidal isoxazolidines by molecular oxygen",
number = "21",
pages = "749-751",
doi = "10.1039/C39770000749"
}

Lorenc, L. B., Juranić, I. O.,& Mihailović, M. Lj.. (1977). Photochemically induced oxidation of some steroidal isoxazolidines by molecular oxygen. in Journal of the Chemical Society, Chemical Communications
Royal Society of Chemistry.(21), 749-751.
https://doi.org/10.1039/C39770000749

Lorenc LB, Juranić IO, Mihailović ML. Photochemically induced oxidation of some steroidal isoxazolidines by molecular oxygen. in Journal of the Chemical Society, Chemical Communications. 1977;(21):749-751.
doi:10.1039/C39770000749 .

Lorenc, Ljubinka B., Juranić, Ivan O., Mihailović, Milhailo Lj., "Photochemically induced oxidation of some steroidal isoxazolidines by molecular oxygen" in Journal of the Chemical Society, Chemical Communications, no. 21 (1977):749-751,
https://doi.org/10.1039/C39770000749 . .

TY  - JOUR
AU  - Vorkapić, L. Ž.
AU  - Drozić, D. M.
AU  - Despić, Aleksandar R.
PY  - 1974
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4654
AB  - Corrosion of pure and amalgamated zinc in pure concentrated KOH solutions was investigated using two methods: (a) galvanostatic measurements of the kinetics of hydrogen evolution with electrodic assessment of corrosion properties of the system, and (b) volumetric measurement of the hydrogen evolution reflecting directly the rate of corrosion. The latter was followed as a function of time during 150 hr. It was found that the corrosion rate varies considerably with time and was suggested that different factors control the initial and the steady-state corrosion. The initial corrosion rate increases with increasing KOH concentration which is indicative of the chemical mechanism of hydrogen evolution. The change of the corrosion rate with time and the steady-state corrosion rate can be explained in terms of formation of an impermeable ZnO film at the surface. In such a case the concentration dependence of the corrosion rate is inverse with time, which explains some results reported in literature. The amalgamated zinc surface gives complex galvanostatic transients which indicate a new phase formation in the process of initiation of hydrogen evolution, which could pertain to some solid potassium-zinc-mercury alloy.
PB  - IOP Publishing
T2  - Journal of Electrochemical Society
T1  - Corrosion of Pure and Amalgamated Zinc in Concentrated Alkali Hydroxide Solutions
VL  - 121
IS  - 11
SP  - 1385
EP  - 1392
DO  - 10.1149/1.2401695
ER  - 

@article{
author = "Vorkapić, L. Ž. and Drozić, D. M. and Despić, Aleksandar R.",
year = "1974",
abstract = "Corrosion of pure and amalgamated zinc in pure concentrated KOH solutions was investigated using two methods: (a) galvanostatic measurements of the kinetics of hydrogen evolution with electrodic assessment of corrosion properties of the system, and (b) volumetric measurement of the hydrogen evolution reflecting directly the rate of corrosion. The latter was followed as a function of time during 150 hr. It was found that the corrosion rate varies considerably with time and was suggested that different factors control the initial and the steady-state corrosion. The initial corrosion rate increases with increasing KOH concentration which is indicative of the chemical mechanism of hydrogen evolution. The change of the corrosion rate with time and the steady-state corrosion rate can be explained in terms of formation of an impermeable ZnO film at the surface. In such a case the concentration dependence of the corrosion rate is inverse with time, which explains some results reported in literature. The amalgamated zinc surface gives complex galvanostatic transients which indicate a new phase formation in the process of initiation of hydrogen evolution, which could pertain to some solid potassium-zinc-mercury alloy.",
publisher = "IOP Publishing",
journal = "Journal of Electrochemical Society",
title = "Corrosion of Pure and Amalgamated Zinc in Concentrated Alkali Hydroxide Solutions",
volume = "121",
number = "11",
pages = "1385-1392",
doi = "10.1149/1.2401695"
}

Vorkapić, L. Ž., Drozić, D. M.,& Despić, A. R.. (1974). Corrosion of Pure and Amalgamated Zinc in Concentrated Alkali Hydroxide Solutions. in Journal of Electrochemical Society
IOP Publishing., 121(11), 1385-1392.
https://doi.org/10.1149/1.2401695

Vorkapić LŽ, Drozić DM, Despić AR. Corrosion of Pure and Amalgamated Zinc in Concentrated Alkali Hydroxide Solutions. in Journal of Electrochemical Society. 1974;121(11):1385-1392.
doi:10.1149/1.2401695 .

Vorkapić, L. Ž., Drozić, D. M., Despić, Aleksandar R., "Corrosion of Pure and Amalgamated Zinc in Concentrated Alkali Hydroxide Solutions" in Journal of Electrochemical Society, 121, no. 11 (1974):1385-1392,
https://doi.org/10.1149/1.2401695 . .

TY  - JOUR
AU  - Mićović, Vukić M.
AU  - Stojčić, S.
AU  - Bralović, M.
AU  - Mladenović, Slobodan
AU  - Jeremić, Dragoslav
AU  - Stefanović, Milutin
PY  - 1969
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4586
AB  - Unbranched α,ω-diols are mainly converted by means of lead tetra-acetate in refluxing benzene to the corresponding ethers of di-α-tetrahydrofuryl, di-α-tetrahydropyryl and/or α-tetrahydrofuryl-α′-tetrahydropyryl type. Thus, 1,6-hexanediol affords cis-1,4-dioxaperhydropentalene (Ia) in 15·2% yield; 1,7-heptanediol affords 1,6-dioxaspiro[4.4]nonane (II) in 29·2% yield; 1,8-octanediol cyclizes to 1,6-dioxaspiro[4.5]decane (IIIa) in 39·3% yield; 1,9-nonanediol affords a mixture of di-α-tetrahydrofurylmethane (IV, 33·2%), 2-(α-tetrahydrofuryl)α′-tetrahydropyran (IVa, 3·7%) and 1,7-di-oxaspiro[5.5]undecane (IVb, 3·3%); 1,10-decanediol is oxidized to a mixture of 1,2-di-α-tetrahydrofurylethane (V, 27·2%), and threo- and erythro-α-tetrahydrofuryl-α′-tetrahydropyrylmethanes (Va, 4·3%); and 1,11-undecanediol affords, as main product, 1,3-di-α-tetrahydrofurylpropane (VI) in 40·1% yield, together with small amounts of four other ethers which were not identified.
PB  - Elsevier
T2  - Tetrahedron
T1  - The reaction of lead tetra-acetate with some unbranched α,ω-diols
VL  - 25
IS  - 5
SP  - 985
EP  - 993
DO  - 10.1016/S0040-4020(01)82671-5
ER  - 

@article{
author = "Mićović, Vukić M. and Stojčić, S. and Bralović, M. and Mladenović, Slobodan and Jeremić, Dragoslav and Stefanović, Milutin",
year = "1969",
abstract = "Unbranched α,ω-diols are mainly converted by means of lead tetra-acetate in refluxing benzene to the corresponding ethers of di-α-tetrahydrofuryl, di-α-tetrahydropyryl and/or α-tetrahydrofuryl-α′-tetrahydropyryl type. Thus, 1,6-hexanediol affords cis-1,4-dioxaperhydropentalene (Ia) in 15·2% yield; 1,7-heptanediol affords 1,6-dioxaspiro[4.4]nonane (II) in 29·2% yield; 1,8-octanediol cyclizes to 1,6-dioxaspiro[4.5]decane (IIIa) in 39·3% yield; 1,9-nonanediol affords a mixture of di-α-tetrahydrofurylmethane (IV, 33·2%), 2-(α-tetrahydrofuryl)α′-tetrahydropyran (IVa, 3·7%) and 1,7-di-oxaspiro[5.5]undecane (IVb, 3·3%); 1,10-decanediol is oxidized to a mixture of 1,2-di-α-tetrahydrofurylethane (V, 27·2%), and threo- and erythro-α-tetrahydrofuryl-α′-tetrahydropyrylmethanes (Va, 4·3%); and 1,11-undecanediol affords, as main product, 1,3-di-α-tetrahydrofurylpropane (VI) in 40·1% yield, together with small amounts of four other ethers which were not identified.",
publisher = "Elsevier",
journal = "Tetrahedron",
title = "The reaction of lead tetra-acetate with some unbranched α,ω-diols",
volume = "25",
number = "5",
pages = "985-993",
doi = "10.1016/S0040-4020(01)82671-5"
}

Mićović, V. M., Stojčić, S., Bralović, M., Mladenović, S., Jeremić, D.,& Stefanović, M.. (1969). The reaction of lead tetra-acetate with some unbranched α,ω-diols. in Tetrahedron
Elsevier., 25(5), 985-993.
https://doi.org/10.1016/S0040-4020(01)82671-5

Mićović VM, Stojčić S, Bralović M, Mladenović S, Jeremić D, Stefanović M. The reaction of lead tetra-acetate with some unbranched α,ω-diols. in Tetrahedron. 1969;25(5):985-993.
doi:10.1016/S0040-4020(01)82671-5 .

Mićović, Vukić M., Stojčić, S., Bralović, M., Mladenović, Slobodan, Jeremić, Dragoslav, Stefanović, Milutin, "The reaction of lead tetra-acetate with some unbranched α,ω-diols" in Tetrahedron, 25, no. 5 (1969):985-993,
https://doi.org/10.1016/S0040-4020(01)82671-5 . .

TY  - JOUR
AU  - Mihailović, Milhailo Lj.
AU  - Bošnjak, Jovan
AU  - Maksimović, Z.
AU  - Čeković, Živorad M.
AU  - Lorenc, Ljubinka B.
PY  - 1966
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4656
AB  - Factors influencing the relative rates of the homolytic and heterolytic processes in the lead tetra-acetate oxidation of unbranched primary and secondary aliphatic alcohols have been investigated, with a view to determine the conditions giving optimal yields of cyclic ethers or carbonyl compounds.
PB  - Elsevier
T2  - Tetrahedron
T1  - Lead tetra-acetate oxidation of saturated aliphatic alcohols-V. Factors influencing the formation of cyclic ethers and carbonyl compounds
VL  - 22
IS  - 3
SP  - 955
EP  - 963
DO  - 10.1016/0040-4020(66)80070-4
ER  - 

@article{
author = "Mihailović, Milhailo Lj. and Bošnjak, Jovan and Maksimović, Z. and Čeković, Živorad M. and Lorenc, Ljubinka B.",
year = "1966",
abstract = "Factors influencing the relative rates of the homolytic and heterolytic processes in the lead tetra-acetate oxidation of unbranched primary and secondary aliphatic alcohols have been investigated, with a view to determine the conditions giving optimal yields of cyclic ethers or carbonyl compounds.",
publisher = "Elsevier",
journal = "Tetrahedron",
title = "Lead tetra-acetate oxidation of saturated aliphatic alcohols-V. Factors influencing the formation of cyclic ethers and carbonyl compounds",
volume = "22",
number = "3",
pages = "955-963",
doi = "10.1016/0040-4020(66)80070-4"
}

Mihailović, M. Lj., Bošnjak, J., Maksimović, Z., Čeković, Ž. M.,& Lorenc, L. B.. (1966). Lead tetra-acetate oxidation of saturated aliphatic alcohols-V. Factors influencing the formation of cyclic ethers and carbonyl compounds. in Tetrahedron
Elsevier., 22(3), 955-963.
https://doi.org/10.1016/0040-4020(66)80070-4

Mihailović ML, Bošnjak J, Maksimović Z, Čeković ŽM, Lorenc LB. Lead tetra-acetate oxidation of saturated aliphatic alcohols-V. Factors influencing the formation of cyclic ethers and carbonyl compounds. in Tetrahedron. 1966;22(3):955-963.
doi:10.1016/0040-4020(66)80070-4 .

Mihailović, Milhailo Lj., Bošnjak, Jovan, Maksimović, Z., Čeković, Živorad M., Lorenc, Ljubinka B., "Lead tetra-acetate oxidation of saturated aliphatic alcohols-V. Factors influencing the formation of cyclic ethers and carbonyl compounds" in Tetrahedron, 22, no. 3 (1966):955-963,
https://doi.org/10.1016/0040-4020(66)80070-4 . .

TY  - JOUR
AU  - Mihailović, Milhailo Lj.
AU  - Čeković, Živorad M.
AU  - Jeremić, Dragoslav
PY  - 1965
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4628
AB  - The lead tetraacetate oxidation of saturated aliphatic alcohols, with structures which do not permit 1,5-cyclization, gave tetrahydropyran derivatives in yields not exceeding 16%. The formation of a small amount of the rearranged ether, 2-ethyl-2-methyltetrahydrofuran, from 4,4-dimethyl-1-pentanol indicates that the cyclization reaction proceeds via an intermediate with carbonium ion character.
PB  - Elsevier
T2  - Tetrahedron
T1  - Lead tetraacetate oxidation of saturated aliphatic alcohols-IV. The formation of six-membered cyclic ethers
VL  - 21
IS  - 10
SP  - 2813
EP  - 2821
DO  - 10.1016/S0040-4020(01)98366-8
ER  - 

@article{
author = "Mihailović, Milhailo Lj. and Čeković, Živorad M. and Jeremić, Dragoslav",
year = "1965",
abstract = "The lead tetraacetate oxidation of saturated aliphatic alcohols, with structures which do not permit 1,5-cyclization, gave tetrahydropyran derivatives in yields not exceeding 16%. The formation of a small amount of the rearranged ether, 2-ethyl-2-methyltetrahydrofuran, from 4,4-dimethyl-1-pentanol indicates that the cyclization reaction proceeds via an intermediate with carbonium ion character.",
publisher = "Elsevier",
journal = "Tetrahedron",
title = "Lead tetraacetate oxidation of saturated aliphatic alcohols-IV. The formation of six-membered cyclic ethers",
volume = "21",
number = "10",
pages = "2813-2821",
doi = "10.1016/S0040-4020(01)98366-8"
}

Mihailović, M. Lj., Čeković, Ž. M.,& Jeremić, D.. (1965). Lead tetraacetate oxidation of saturated aliphatic alcohols-IV. The formation of six-membered cyclic ethers. in Tetrahedron
Elsevier., 21(10), 2813-2821.
https://doi.org/10.1016/S0040-4020(01)98366-8

Mihailović ML, Čeković ŽM, Jeremić D. Lead tetraacetate oxidation of saturated aliphatic alcohols-IV. The formation of six-membered cyclic ethers. in Tetrahedron. 1965;21(10):2813-2821.
doi:10.1016/S0040-4020(01)98366-8 .

Mihailović, Milhailo Lj., Čeković, Živorad M., Jeremić, Dragoslav, "Lead tetraacetate oxidation of saturated aliphatic alcohols-IV. The formation of six-membered cyclic ethers" in Tetrahedron, 21, no. 10 (1965):2813-2821,
https://doi.org/10.1016/S0040-4020(01)98366-8 . .