TY  - DATA
AU  - Mitrović, Aleksandra D.
AU  - Stevanović, Jelena
AU  - Milčić, Miloš K.
AU  - Zekić, Andrijana
AU  - Stanković, Dalibor
AU  - Chen, Shigui
AU  - Bađić, Jovica D.
AU  - Milić, Dragana
AU  - Maslak, Veselin
PY  - 2015
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3369
PB  - Royal Soc Chemistry, Cambridge
T2  - RSC Advances
T1  - Supplementary material for the article: Mitrović, A.; Stevanović, J.; Milčić, M.; Žekić, A.; Stanković, D.; Chen, S.; Badjić, J. D.; Milić, D.; Maslak, V. Fulleropyrrolidine Molecular Dumbbells Act as Multi-Electron-Acceptor Triads. Spectroscopic, Electrochemical, Computational and Morphological Characterizations. RSC Advances 2015, 5 (107), 88241–88248. https://doi.org/10.1039/c5ra16309a
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3369
ER  - 

@misc{
author = "Mitrović, Aleksandra D. and Stevanović, Jelena and Milčić, Miloš K. and Zekić, Andrijana and Stanković, Dalibor and Chen, Shigui and Bađić, Jovica D. and Milić, Dragana and Maslak, Veselin",
year = "2015",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "RSC Advances",
title = "Supplementary material for the article: Mitrović, A.; Stevanović, J.; Milčić, M.; Žekić, A.; Stanković, D.; Chen, S.; Badjić, J. D.; Milić, D.; Maslak, V. Fulleropyrrolidine Molecular Dumbbells Act as Multi-Electron-Acceptor Triads. Spectroscopic, Electrochemical, Computational and Morphological Characterizations. RSC Advances 2015, 5 (107), 88241–88248. https://doi.org/10.1039/c5ra16309a",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3369"
}

Mitrović, A. D., Stevanović, J., Milčić, M. K., Zekić, A., Stanković, D., Chen, S., Bađić, J. D., Milić, D.,& Maslak, V.. (2015). Supplementary material for the article: Mitrović, A.; Stevanović, J.; Milčić, M.; Žekić, A.; Stanković, D.; Chen, S.; Badjić, J. D.; Milić, D.; Maslak, V. Fulleropyrrolidine Molecular Dumbbells Act as Multi-Electron-Acceptor Triads. Spectroscopic, Electrochemical, Computational and Morphological Characterizations. RSC Advances 2015, 5 (107), 88241–88248. https://doi.org/10.1039/c5ra16309a. in RSC Advances
Royal Soc Chemistry, Cambridge..
https://hdl.handle.net/21.15107/rcub_cherry_3369

Mitrović AD, Stevanović J, Milčić MK, Zekić A, Stanković D, Chen S, Bađić JD, Milić D, Maslak V. Supplementary material for the article: Mitrović, A.; Stevanović, J.; Milčić, M.; Žekić, A.; Stanković, D.; Chen, S.; Badjić, J. D.; Milić, D.; Maslak, V. Fulleropyrrolidine Molecular Dumbbells Act as Multi-Electron-Acceptor Triads. Spectroscopic, Electrochemical, Computational and Morphological Characterizations. RSC Advances 2015, 5 (107), 88241–88248. https://doi.org/10.1039/c5ra16309a. in RSC Advances. 2015;.
https://hdl.handle.net/21.15107/rcub_cherry_3369 .

Mitrović, Aleksandra D., Stevanović, Jelena, Milčić, Miloš K., Zekić, Andrijana, Stanković, Dalibor, Chen, Shigui, Bađić, Jovica D., Milić, Dragana, Maslak, Veselin, "Supplementary material for the article: Mitrović, A.; Stevanović, J.; Milčić, M.; Žekić, A.; Stanković, D.; Chen, S.; Badjić, J. D.; Milić, D.; Maslak, V. Fulleropyrrolidine Molecular Dumbbells Act as Multi-Electron-Acceptor Triads. Spectroscopic, Electrochemical, Computational and Morphological Characterizations. RSC Advances 2015, 5 (107), 88241–88248. https://doi.org/10.1039/c5ra16309a" in RSC Advances (2015),
https://hdl.handle.net/21.15107/rcub_cherry_3369 .

TY  - JOUR
AU  - Mitrović, Aleksandra D.
AU  - Stevanović, Jelena
AU  - Milčić, Miloš K.
AU  - Zekić, Andrijana
AU  - Stanković, Dalibor
AU  - Chen, Shigui
AU  - Bađić, Jovica D.
AU  - Milić, Dragana
AU  - Maslak, Veselin
PY  - 2015
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1984
AB  - We synthesized three dumbbell-like compounds 2a-c, each containing two C-60 groups at the periphery and pyromellitic diimide (PMDI) in the middle, and examined their electronic as well as assembly characteristics with both experimental and computational methods. Cyclic voltammetry (CV) measurements revealed that each of three electron-accepting (AAA) triads could accommodate up to eight electrons. Computational studies (density functional theory, DFT) of 2a-c at PBEPBE/6-311G(d, p) level of theory, with B3LYP/6-31G(d) optimized geometries, revealed that HOMO-LUMO energy gaps are similar to those of the model compound [6,6]-phenyl-C-61-butyric acid methyl ester (PCBM). Compounds 2a-c were also found to assemble into vesicles and nanoparticles on the copper grid (100-300 nm, TEM), while giving more sizeable aggregates after a deposition on the glass (SEM,  gt  5 mm). Understanding the packing of 2a-c on various solid substrates, as well as the assembly characteristics in general, is important for tuning the properties and fabrication of electronic/optical devices. On the basis of the results of conformational analysis (MM and DFT calculations), we deduced that different alkyl spacers in 2a-c ought to play a role in pi-pi interactions between the aromatic components of the triad to guide the packing and therefore morphology of the material.
PB  - Royal Soc Chemistry, Cambridge
T2  - RSC Advances
T1  - Fulleropyrrolidine molecular dumbbells act as multi-electron-acceptor triads. Spectroscopic, electrochemical, computational and morphological characterizations
VL  - 5
IS  - 107
SP  - 88241
EP  - 88248
DO  - 10.1039/c5ra16309a
ER  - 

@article{
author = "Mitrović, Aleksandra D. and Stevanović, Jelena and Milčić, Miloš K. and Zekić, Andrijana and Stanković, Dalibor and Chen, Shigui and Bađić, Jovica D. and Milić, Dragana and Maslak, Veselin",
year = "2015",
abstract = "We synthesized three dumbbell-like compounds 2a-c, each containing two C-60 groups at the periphery and pyromellitic diimide (PMDI) in the middle, and examined their electronic as well as assembly characteristics with both experimental and computational methods. Cyclic voltammetry (CV) measurements revealed that each of three electron-accepting (AAA) triads could accommodate up to eight electrons. Computational studies (density functional theory, DFT) of 2a-c at PBEPBE/6-311G(d, p) level of theory, with B3LYP/6-31G(d) optimized geometries, revealed that HOMO-LUMO energy gaps are similar to those of the model compound [6,6]-phenyl-C-61-butyric acid methyl ester (PCBM). Compounds 2a-c were also found to assemble into vesicles and nanoparticles on the copper grid (100-300 nm, TEM), while giving more sizeable aggregates after a deposition on the glass (SEM,  gt  5 mm). Understanding the packing of 2a-c on various solid substrates, as well as the assembly characteristics in general, is important for tuning the properties and fabrication of electronic/optical devices. On the basis of the results of conformational analysis (MM and DFT calculations), we deduced that different alkyl spacers in 2a-c ought to play a role in pi-pi interactions between the aromatic components of the triad to guide the packing and therefore morphology of the material.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "RSC Advances",
title = "Fulleropyrrolidine molecular dumbbells act as multi-electron-acceptor triads. Spectroscopic, electrochemical, computational and morphological characterizations",
volume = "5",
number = "107",
pages = "88241-88248",
doi = "10.1039/c5ra16309a"
}

Mitrović, A. D., Stevanović, J., Milčić, M. K., Zekić, A., Stanković, D., Chen, S., Bađić, J. D., Milić, D.,& Maslak, V.. (2015). Fulleropyrrolidine molecular dumbbells act as multi-electron-acceptor triads. Spectroscopic, electrochemical, computational and morphological characterizations. in RSC Advances
Royal Soc Chemistry, Cambridge., 5(107), 88241-88248.
https://doi.org/10.1039/c5ra16309a

Mitrović AD, Stevanović J, Milčić MK, Zekić A, Stanković D, Chen S, Bađić JD, Milić D, Maslak V. Fulleropyrrolidine molecular dumbbells act as multi-electron-acceptor triads. Spectroscopic, electrochemical, computational and morphological characterizations. in RSC Advances. 2015;5(107):88241-88248.
doi:10.1039/c5ra16309a .

Mitrović, Aleksandra D., Stevanović, Jelena, Milčić, Miloš K., Zekić, Andrijana, Stanković, Dalibor, Chen, Shigui, Bađić, Jovica D., Milić, Dragana, Maslak, Veselin, "Fulleropyrrolidine molecular dumbbells act as multi-electron-acceptor triads. Spectroscopic, electrochemical, computational and morphological characterizations" in RSC Advances, 5, no. 107 (2015):88241-88248,
https://doi.org/10.1039/c5ra16309a . .

TY  - JOUR
AU  - Kop, Tatjana
AU  - Bjelaković, Mira S.
AU  - Đordević, Jelena
AU  - Zekić, Andrijana
AU  - Milić, Dragana
PY  - 2015
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1998
AB  - Two different alpha,omega-diglicynes linked by linear polyoxaalkyl chains in the presence of formaldehyde underwent Prato reaction to the fullerene C-60. The shorter linker templated formation of only cis-bisadducts, while the longer one afforded a mixture of four bisadducts (all cis and the equatorial) and difullerene dumbbell compound. Their structures were confirmed by the extensive analysis of the spectral data and molecular symmetry, as well. All compounds expressed an ability to arrange into hierarchically ordered supramolecular aggregates, the form of which depended both on the addition pattern and the spacer structure. The attenuated electron-accepting affinity, examined by cyclic voltammetry was in agreement with diminished delocalization of the pi-electronic system. In addition, all compounds exerted a notable radical scavenging activity.
PB  - Royal Soc Chemistry, Cambridge
T2  - RSC Advances
T1  - Fulleropyrrolidines derived from dioxa- and trioxaalkyl-tethered diglycines
VL  - 5
IS  - 115
SP  - 94599
EP  - 94606
DO  - 10.1039/c5ra17392b
ER  - 

@article{
author = "Kop, Tatjana and Bjelaković, Mira S. and Đordević, Jelena and Zekić, Andrijana and Milić, Dragana",
year = "2015",
abstract = "Two different alpha,omega-diglicynes linked by linear polyoxaalkyl chains in the presence of formaldehyde underwent Prato reaction to the fullerene C-60. The shorter linker templated formation of only cis-bisadducts, while the longer one afforded a mixture of four bisadducts (all cis and the equatorial) and difullerene dumbbell compound. Their structures were confirmed by the extensive analysis of the spectral data and molecular symmetry, as well. All compounds expressed an ability to arrange into hierarchically ordered supramolecular aggregates, the form of which depended both on the addition pattern and the spacer structure. The attenuated electron-accepting affinity, examined by cyclic voltammetry was in agreement with diminished delocalization of the pi-electronic system. In addition, all compounds exerted a notable radical scavenging activity.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "RSC Advances",
title = "Fulleropyrrolidines derived from dioxa- and trioxaalkyl-tethered diglycines",
volume = "5",
number = "115",
pages = "94599-94606",
doi = "10.1039/c5ra17392b"
}

Kop, T., Bjelaković, M. S., Đordević, J., Zekić, A.,& Milić, D.. (2015). Fulleropyrrolidines derived from dioxa- and trioxaalkyl-tethered diglycines. in RSC Advances
Royal Soc Chemistry, Cambridge., 5(115), 94599-94606.
https://doi.org/10.1039/c5ra17392b

Kop T, Bjelaković MS, Đordević J, Zekić A, Milić D. Fulleropyrrolidines derived from dioxa- and trioxaalkyl-tethered diglycines. in RSC Advances. 2015;5(115):94599-94606.
doi:10.1039/c5ra17392b .

Kop, Tatjana, Bjelaković, Mira S., Đordević, Jelena, Zekić, Andrijana, Milić, Dragana, "Fulleropyrrolidines derived from dioxa- and trioxaalkyl-tethered diglycines" in RSC Advances, 5, no. 115 (2015):94599-94606,
https://doi.org/10.1039/c5ra17392b . .

TY  - DATA
AU  - Kop, Tatjana
AU  - Bjelaković, Mira S.
AU  - Đordević, Jelena
AU  - Zekić, Andrijana
AU  - Milić, Dragana
PY  - 2015
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3370
PB  - Royal Soc Chemistry, Cambridge
T2  - RSC Advances
T1  - Supplementary material for the article:  Kop, T.; Bjelaković, M.; Dordević, J.; Žekić, A.; Milić, D. Fulleropyrrolidines Derived from Dioxa- and Trioxaalkyl-Tethered Diglycines. RSC Advances 2015, 5 (115), 94599–94606. https://doi.org/10.1039/c5ra17392b
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3370
ER  - 

@misc{
author = "Kop, Tatjana and Bjelaković, Mira S. and Đordević, Jelena and Zekić, Andrijana and Milić, Dragana",
year = "2015",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "RSC Advances",
title = "Supplementary material for the article:  Kop, T.; Bjelaković, M.; Dordević, J.; Žekić, A.; Milić, D. Fulleropyrrolidines Derived from Dioxa- and Trioxaalkyl-Tethered Diglycines. RSC Advances 2015, 5 (115), 94599–94606. https://doi.org/10.1039/c5ra17392b",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3370"
}

Kop, T., Bjelaković, M. S., Đordević, J., Zekić, A.,& Milić, D.. (2015). Supplementary material for the article:  Kop, T.; Bjelaković, M.; Dordević, J.; Žekić, A.; Milić, D. Fulleropyrrolidines Derived from Dioxa- and Trioxaalkyl-Tethered Diglycines. RSC Advances 2015, 5 (115), 94599–94606. https://doi.org/10.1039/c5ra17392b. in RSC Advances
Royal Soc Chemistry, Cambridge..
https://hdl.handle.net/21.15107/rcub_cherry_3370

Kop T, Bjelaković MS, Đordević J, Zekić A, Milić D. Supplementary material for the article:  Kop, T.; Bjelaković, M.; Dordević, J.; Žekić, A.; Milić, D. Fulleropyrrolidines Derived from Dioxa- and Trioxaalkyl-Tethered Diglycines. RSC Advances 2015, 5 (115), 94599–94606. https://doi.org/10.1039/c5ra17392b. in RSC Advances. 2015;.
https://hdl.handle.net/21.15107/rcub_cherry_3370 .

Kop, Tatjana, Bjelaković, Mira S., Đordević, Jelena, Zekić, Andrijana, Milić, Dragana, "Supplementary material for the article:  Kop, T.; Bjelaković, M.; Dordević, J.; Žekić, A.; Milić, D. Fulleropyrrolidines Derived from Dioxa- and Trioxaalkyl-Tethered Diglycines. RSC Advances 2015, 5 (115), 94599–94606. https://doi.org/10.1039/c5ra17392b" in RSC Advances (2015),
https://hdl.handle.net/21.15107/rcub_cherry_3370 .

TY  - JOUR
AU  - Bjelaković, Mira S.
AU  - Kop, Tatjana
AU  - Baošić, Rada
AU  - Zlatović, Mario
AU  - Zekić, Andrijana
AU  - Maslak, Veselin
AU  - Milić, Dragana
PY  - 2014
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1869
AB  - Four fullerosteroidal conjugates, previously confirmed to express two- to threefold better antioxidant activity in vitro than C-60, were subjected to additional studies, including electrochemical, theoretical, and morphological examination. All tested compounds underwent reversible, diffusion-controlled reductions. A notable influence of the solvent properties on the reduction potential, the level of aggregation, and the lowest unoccupied molecular orbital (LUMO) energy was observed. Theoretical calculations indicated that the energy gain obtained by an intermediate formation, together with compounds' polarizability, polarity, and lipophilicity contributed to the radical quenching capacity. Very large supramolecular aggregates of all fullerosteroidal esters with no hierarchical arrangement were observed in precipitated samples, while solvent induced self-assembling led to round nanoplates, which further arranged to flower-shaped hierarchically ordered architectures or uniformly distributed discoid particles. As in electrochemical studies, fine tuning of the aggregation level was achieved by the solvent.
PB  - Springer Wien, Wien
T2  - Monatshefte Fur Chemie
T1  - Electrochemical, theoretical, and morphological studies of antioxidant fullerosteroids
VL  - 145
IS  - 11
SP  - 1715
EP  - 1725
DO  - 10.1007/s00706-014-1287-5
ER  - 

@article{
author = "Bjelaković, Mira S. and Kop, Tatjana and Baošić, Rada and Zlatović, Mario and Zekić, Andrijana and Maslak, Veselin and Milić, Dragana",
year = "2014",
abstract = "Four fullerosteroidal conjugates, previously confirmed to express two- to threefold better antioxidant activity in vitro than C-60, were subjected to additional studies, including electrochemical, theoretical, and morphological examination. All tested compounds underwent reversible, diffusion-controlled reductions. A notable influence of the solvent properties on the reduction potential, the level of aggregation, and the lowest unoccupied molecular orbital (LUMO) energy was observed. Theoretical calculations indicated that the energy gain obtained by an intermediate formation, together with compounds' polarizability, polarity, and lipophilicity contributed to the radical quenching capacity. Very large supramolecular aggregates of all fullerosteroidal esters with no hierarchical arrangement were observed in precipitated samples, while solvent induced self-assembling led to round nanoplates, which further arranged to flower-shaped hierarchically ordered architectures or uniformly distributed discoid particles. As in electrochemical studies, fine tuning of the aggregation level was achieved by the solvent.",
publisher = "Springer Wien, Wien",
journal = "Monatshefte Fur Chemie",
title = "Electrochemical, theoretical, and morphological studies of antioxidant fullerosteroids",
volume = "145",
number = "11",
pages = "1715-1725",
doi = "10.1007/s00706-014-1287-5"
}

Bjelaković, M. S., Kop, T., Baošić, R., Zlatović, M., Zekić, A., Maslak, V.,& Milić, D.. (2014). Electrochemical, theoretical, and morphological studies of antioxidant fullerosteroids. in Monatshefte Fur Chemie
Springer Wien, Wien., 145(11), 1715-1725.
https://doi.org/10.1007/s00706-014-1287-5

Bjelaković MS, Kop T, Baošić R, Zlatović M, Zekić A, Maslak V, Milić D. Electrochemical, theoretical, and morphological studies of antioxidant fullerosteroids. in Monatshefte Fur Chemie. 2014;145(11):1715-1725.
doi:10.1007/s00706-014-1287-5 .

Bjelaković, Mira S., Kop, Tatjana, Baošić, Rada, Zlatović, Mario, Zekić, Andrijana, Maslak, Veselin, Milić, Dragana, "Electrochemical, theoretical, and morphological studies of antioxidant fullerosteroids" in Monatshefte Fur Chemie, 145, no. 11 (2014):1715-1725,
https://doi.org/10.1007/s00706-014-1287-5 . .

TY  - DATA
AU  - Mitrović, Aleksandra D.
AU  - Todorović, Nina
AU  - Zekić, Andrijana
AU  - Stanković, Dalibor
AU  - Milić, Dragana
AU  - Maslak, Veselin
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3549
PB  - Wiley-V C H Verlag Gmbh, Weinheim
T2  - European Journal of Organic Chemistry
T1  - Supplementary data for article: Mitrović, A. D.; Todorović, N.; Zekić, A.; Stanković, D.; Milić, D.; Maslak, V. Synthesis, Electrochemistry, and Hierarchical Self-Organization of Fulleropyrrolidine-Phthalimide Dyads. European Journal of Organic Chemistry 2013, No. 11, 2188–2193. https://doi.org/10.1002/ejoc.201201631
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3549
ER  - 

@misc{
author = "Mitrović, Aleksandra D. and Todorović, Nina and Zekić, Andrijana and Stanković, Dalibor and Milić, Dragana and Maslak, Veselin",
year = "2013",
publisher = "Wiley-V C H Verlag Gmbh, Weinheim",
journal = "European Journal of Organic Chemistry",
title = "Supplementary data for article: Mitrović, A. D.; Todorović, N.; Zekić, A.; Stanković, D.; Milić, D.; Maslak, V. Synthesis, Electrochemistry, and Hierarchical Self-Organization of Fulleropyrrolidine-Phthalimide Dyads. European Journal of Organic Chemistry 2013, No. 11, 2188–2193. https://doi.org/10.1002/ejoc.201201631",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3549"
}

Mitrović, A. D., Todorović, N., Zekić, A., Stanković, D., Milić, D.,& Maslak, V.. (2013). Supplementary data for article: Mitrović, A. D.; Todorović, N.; Zekić, A.; Stanković, D.; Milić, D.; Maslak, V. Synthesis, Electrochemistry, and Hierarchical Self-Organization of Fulleropyrrolidine-Phthalimide Dyads. European Journal of Organic Chemistry 2013, No. 11, 2188–2193. https://doi.org/10.1002/ejoc.201201631. in European Journal of Organic Chemistry
Wiley-V C H Verlag Gmbh, Weinheim..
https://hdl.handle.net/21.15107/rcub_cherry_3549

Mitrović AD, Todorović N, Zekić A, Stanković D, Milić D, Maslak V. Supplementary data for article: Mitrović, A. D.; Todorović, N.; Zekić, A.; Stanković, D.; Milić, D.; Maslak, V. Synthesis, Electrochemistry, and Hierarchical Self-Organization of Fulleropyrrolidine-Phthalimide Dyads. European Journal of Organic Chemistry 2013, No. 11, 2188–2193. https://doi.org/10.1002/ejoc.201201631. in European Journal of Organic Chemistry. 2013;.
https://hdl.handle.net/21.15107/rcub_cherry_3549 .

Mitrović, Aleksandra D., Todorović, Nina, Zekić, Andrijana, Stanković, Dalibor, Milić, Dragana, Maslak, Veselin, "Supplementary data for article: Mitrović, A. D.; Todorović, N.; Zekić, A.; Stanković, D.; Milić, D.; Maslak, V. Synthesis, Electrochemistry, and Hierarchical Self-Organization of Fulleropyrrolidine-Phthalimide Dyads. European Journal of Organic Chemistry 2013, No. 11, 2188–2193. https://doi.org/10.1002/ejoc.201201631" in European Journal of Organic Chemistry (2013),
https://hdl.handle.net/21.15107/rcub_cherry_3549 .

TY  - JOUR
AU  - Mitrović, Aleksandra D.
AU  - Todorović, Nina
AU  - Zekić, Andrijana
AU  - Stanković, Dalibor
AU  - Milić, Dragana
AU  - Maslak, Veselin
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1358
AB  - A series of novel fulleropyrrolidine-phthalimide dyads was synthesized and their electrochemical and self-assembly properties were investigated. Efficient synthesis of acceptor-acceptor dyads was performed under microwave irradiation. Fine-tuning of the second redox potentials in the dyads was achieved by varying the length of the aliphatic spacer (C-2 to C-12) between the fulleropyrrolidine and phthalimide moieties. Shape-shifting and supramolecular polymorphism were observed for these compounds during self-assembly.
PB  - Wiley-V C H Verlag Gmbh, Weinheim
T2  - European Journal of Organic Chemistry
T1  - Synthesis, Electrochemistry, and Hierarchical Self-Organization of Fulleropyrrolidine-Phthalimide Dyads
IS  - 11
SP  - 2188
EP  - 2193
DO  - 10.1002/ejoc.201201631
ER  - 

@article{
author = "Mitrović, Aleksandra D. and Todorović, Nina and Zekić, Andrijana and Stanković, Dalibor and Milić, Dragana and Maslak, Veselin",
year = "2013",
abstract = "A series of novel fulleropyrrolidine-phthalimide dyads was synthesized and their electrochemical and self-assembly properties were investigated. Efficient synthesis of acceptor-acceptor dyads was performed under microwave irradiation. Fine-tuning of the second redox potentials in the dyads was achieved by varying the length of the aliphatic spacer (C-2 to C-12) between the fulleropyrrolidine and phthalimide moieties. Shape-shifting and supramolecular polymorphism were observed for these compounds during self-assembly.",
publisher = "Wiley-V C H Verlag Gmbh, Weinheim",
journal = "European Journal of Organic Chemistry",
title = "Synthesis, Electrochemistry, and Hierarchical Self-Organization of Fulleropyrrolidine-Phthalimide Dyads",
number = "11",
pages = "2188-2193",
doi = "10.1002/ejoc.201201631"
}

Mitrović, A. D., Todorović, N., Zekić, A., Stanković, D., Milić, D.,& Maslak, V.. (2013). Synthesis, Electrochemistry, and Hierarchical Self-Organization of Fulleropyrrolidine-Phthalimide Dyads. in European Journal of Organic Chemistry
Wiley-V C H Verlag Gmbh, Weinheim.(11), 2188-2193.
https://doi.org/10.1002/ejoc.201201631

Mitrović AD, Todorović N, Zekić A, Stanković D, Milić D, Maslak V. Synthesis, Electrochemistry, and Hierarchical Self-Organization of Fulleropyrrolidine-Phthalimide Dyads. in European Journal of Organic Chemistry. 2013;(11):2188-2193.
doi:10.1002/ejoc.201201631 .

Mitrović, Aleksandra D., Todorović, Nina, Zekić, Andrijana, Stanković, Dalibor, Milić, Dragana, Maslak, Veselin, "Synthesis, Electrochemistry, and Hierarchical Self-Organization of Fulleropyrrolidine-Phthalimide Dyads" in European Journal of Organic Chemistry, no. 11 (2013):2188-2193,
https://doi.org/10.1002/ejoc.201201631 . .