TY  - JOUR
AU  - Vučković, Gordana
AU  - Tanasković, Slađana B.
AU  - Antonijević-Nikolić, Mirjana
AU  - Živković-Radovanović, Vukosava
AU  - Gojgić-Cvijović, Gordana
PY  - 2009
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/504
AB  - Four new air-stable mixed-ligand Co(II) complexes having the general formula [Co2(Y)tpmc]Z3×q(H2O/CH3CN) (HY = N-methylglycine/N,N-dimethylglycine, Z = - 4BF , qH2O=4 or 3; HY=S-norvaline/S-valine Z=-ClO4 , qCH3CN = 0.5; qH2O = 0.5; tpmc = N,N',N'',N'''-tetrakis(2-pyridylmethyl)- -1,4,8,11-tetraazacyclotetradecane) were prepared. The composition, some physical and chemical properties and their tentative geometries were evaluated based on elemental analysis (C, H, N), conductometric and magnetic measurements, spectroscopic data (UV/Vis, IR) and cyclic voltammetry. The data were compared with earlier described analogous complexes containing the macrocyclic ligand and aliphatic aminocarboxylates. It is assumed that all complexes are binuclear with an exo coordination mode of the octaazamacrocyclic pendant ligand in the boat conformation. In addition, two -N-(CH2)2-N- portions of the cyclam ring within the tpmc ligand and Co(II) ions in the high-spin state are most probably bridged via oxygen atoms from the anion of the aminocarboxylate/derivatives, whereas nitrogen atoms rest uncoordinated. In all cases, a combined chelate-bridged coordination is proposed as the most probable. The complexes were electrochemically stable in the potential range -1.0 to 1.0 V. They were also preliminary assayed toward some microorganisms together with the ligands, starting simple salts and solvents as test substances. In some cases, certain antimicrobial activity of the complexes was detected.
AB  - Dobijena su četiri nova mešovito-ligandna kompleksa Co(II), stabilna na vazduhu, opšte formule [Co2(Y)tpmc]Z3×q(H2O/CH3CN) (HY = N-metilglicin/N,N-dimetilglicin, Z=-4BF , qH2O=4 ili 3); HY = S-norvalin/S-valin, Z=-ClO4, qCH3CN=0,5; qH2O=0,5; tpmc= N,N',N'',N'''-tetrakis(2-piridilmetil)-1,4,8,11-tetraazaciklotetradekan). Sastav, neka fizička i hemijska svojstva i njihove približne geometrije su izvedene na osnovu elementalne analize (C, H, N), konduktometrijskih i magnetnih merenja, spektroskopskih podataka (UV/Vis, IR) odnosno ciklične voltametrije. Podaci su upoređeni sa ranije opisanim analogim kompleksima koji sadrže makrociklični ligand i alifatične aminokarboksilate. Pretpostavljeno je da su svi kompleksi dinuklearni sa egzo koordinacijom pendantnog oktaazamakrocikla u konformaciji lađe. Pored dva -N-(CH2)2-N- dela ciklamovog prstena unutar tpmc-a, joni visoko-spinskog Co(II) su najverovatnije premošćeni angažovanjem kiseonikovih atoma sa anjona aminokarboksilata/derivata, dok atomi azota ostaju nekoordinovani. Za sve komplekse predložen je kombinovani helatno-mostovni način vezivanja. Kompleksi su bili elektrohemijski stabilni u opsegu potencijala -1,0 do 1,0 V. Oni su preliminarno testirani na mikroorganizme zajedno sa ligandima, polaznim prostim solima i rastvaračima kao test supstancama. U nekim slučajevima je nađena izvesna antimikrobna aktivnost kompleksa.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - A study of novel cobalt(II) octaazamacrocyclic complexes with aminocarboxylates or their derivatives
T1  - Proučavanje novih kompleksa kobalta(II) sa oktaazamakrociklom i aminokarboksilatima ili njihovim derivatima
VL  - 74
IS  - 6
SP  - 629
EP  - 640
DO  - 10.2298/JSC0906629V
ER  - 

@article{
author = "Vučković, Gordana and Tanasković, Slađana B. and Antonijević-Nikolić, Mirjana and Živković-Radovanović, Vukosava and Gojgić-Cvijović, Gordana",
year = "2009",
abstract = "Four new air-stable mixed-ligand Co(II) complexes having the general formula [Co2(Y)tpmc]Z3×q(H2O/CH3CN) (HY = N-methylglycine/N,N-dimethylglycine, Z = - 4BF , qH2O=4 or 3; HY=S-norvaline/S-valine Z=-ClO4 , qCH3CN = 0.5; qH2O = 0.5; tpmc = N,N',N'',N'''-tetrakis(2-pyridylmethyl)- -1,4,8,11-tetraazacyclotetradecane) were prepared. The composition, some physical and chemical properties and their tentative geometries were evaluated based on elemental analysis (C, H, N), conductometric and magnetic measurements, spectroscopic data (UV/Vis, IR) and cyclic voltammetry. The data were compared with earlier described analogous complexes containing the macrocyclic ligand and aliphatic aminocarboxylates. It is assumed that all complexes are binuclear with an exo coordination mode of the octaazamacrocyclic pendant ligand in the boat conformation. In addition, two -N-(CH2)2-N- portions of the cyclam ring within the tpmc ligand and Co(II) ions in the high-spin state are most probably bridged via oxygen atoms from the anion of the aminocarboxylate/derivatives, whereas nitrogen atoms rest uncoordinated. In all cases, a combined chelate-bridged coordination is proposed as the most probable. The complexes were electrochemically stable in the potential range -1.0 to 1.0 V. They were also preliminary assayed toward some microorganisms together with the ligands, starting simple salts and solvents as test substances. In some cases, certain antimicrobial activity of the complexes was detected., Dobijena su četiri nova mešovito-ligandna kompleksa Co(II), stabilna na vazduhu, opšte formule [Co2(Y)tpmc]Z3×q(H2O/CH3CN) (HY = N-metilglicin/N,N-dimetilglicin, Z=-4BF , qH2O=4 ili 3); HY = S-norvalin/S-valin, Z=-ClO4, qCH3CN=0,5; qH2O=0,5; tpmc= N,N',N'',N'''-tetrakis(2-piridilmetil)-1,4,8,11-tetraazaciklotetradekan). Sastav, neka fizička i hemijska svojstva i njihove približne geometrije su izvedene na osnovu elementalne analize (C, H, N), konduktometrijskih i magnetnih merenja, spektroskopskih podataka (UV/Vis, IR) odnosno ciklične voltametrije. Podaci su upoređeni sa ranije opisanim analogim kompleksima koji sadrže makrociklični ligand i alifatične aminokarboksilate. Pretpostavljeno je da su svi kompleksi dinuklearni sa egzo koordinacijom pendantnog oktaazamakrocikla u konformaciji lađe. Pored dva -N-(CH2)2-N- dela ciklamovog prstena unutar tpmc-a, joni visoko-spinskog Co(II) su najverovatnije premošćeni angažovanjem kiseonikovih atoma sa anjona aminokarboksilata/derivata, dok atomi azota ostaju nekoordinovani. Za sve komplekse predložen je kombinovani helatno-mostovni način vezivanja. Kompleksi su bili elektrohemijski stabilni u opsegu potencijala -1,0 do 1,0 V. Oni su preliminarno testirani na mikroorganizme zajedno sa ligandima, polaznim prostim solima i rastvaračima kao test supstancama. U nekim slučajevima je nađena izvesna antimikrobna aktivnost kompleksa.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "A study of novel cobalt(II) octaazamacrocyclic complexes with aminocarboxylates or their derivatives, Proučavanje novih kompleksa kobalta(II) sa oktaazamakrociklom i aminokarboksilatima ili njihovim derivatima",
volume = "74",
number = "6",
pages = "629-640",
doi = "10.2298/JSC0906629V"
}

Vučković, G., Tanasković, S. B., Antonijević-Nikolić, M., Živković-Radovanović, V.,& Gojgić-Cvijović, G.. (2009). A study of novel cobalt(II) octaazamacrocyclic complexes with aminocarboxylates or their derivatives. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 74(6), 629-640.
https://doi.org/10.2298/JSC0906629V

Vučković G, Tanasković SB, Antonijević-Nikolić M, Živković-Radovanović V, Gojgić-Cvijović G. A study of novel cobalt(II) octaazamacrocyclic complexes with aminocarboxylates or their derivatives. in Journal of the Serbian Chemical Society. 2009;74(6):629-640.
doi:10.2298/JSC0906629V .

Vučković, Gordana, Tanasković, Slađana B., Antonijević-Nikolić, Mirjana, Živković-Radovanović, Vukosava, Gojgić-Cvijović, Gordana, "A study of novel cobalt(II) octaazamacrocyclic complexes with aminocarboxylates or their derivatives" in Journal of the Serbian Chemical Society, 74, no. 6 (2009):629-640,
https://doi.org/10.2298/JSC0906629V . .

TY  - JOUR
AU  - Vučković, Gordana
AU  - Tanasković, Slađana B.
AU  - Rychlewska, Urszula
AU  - Radanović, Dušanka
AU  - Mroziñski, Jerzy
AU  - Korabik, Maria
PY  - 2007
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4250
AB  - A novel binuclear Co(II) complex, [Co2(Cl)2tpmc](BF4)2 (tpmc = N,N′,N″,N‴-tetrakis(2-pyridylmethyl)-1,4,8,11-tetraaz acyclotetradecane), was prepared and structurally characterized by X-ray diffraction analysis at low temperature. The complex crystallizes in P21/c space group of the monoclinic crystal system, and its crystals are isomorphic with those of [Cu2(Br)2tpmc](ClO4)2 complex. In the crystal structure the complex cations [Co2(Cl)2tpmc]2+ are settled around the inversion centres. Cobalt(II) is exo coordinated with four macrocyclic N atoms, and Cl- supplements the fifth coordination site. Based on the index of trigonality, the coordination polyhedron formed around Co(II) ion is described as distorted trigonal bipyramid. Two metal centres are at a distance of 5.710 Å. This is the first Co(II) complex for which X-ray analysis confirmed a chair conformation of tpmc ligand. IR, EPR (X-band) and UV/VIS absorption and reflectance spectra, molar conductivities and magnetic measurements (SQUID) are used to study the investigated complex. A comparative structural analysis with some of the described Co(II) and Cu(II) complexes of analogous geometries and type of pendant azamacrocyclic ligands was also done.
PB  - Elsevier
T2  - Journal of Molecular Structure
T1  - Preparation, characterization and X-ray analysis of [Co2(Cl)2tpmc](BF4)2. Comparative structural analysis with the complexes having analogous geometries and ligands
VL  - 827
IS  - 1-3
SP  - 80
EP  - 87
DO  - 10.1016/j.molstruc.2006.05.009
ER  - 

@article{
author = "Vučković, Gordana and Tanasković, Slađana B. and Rychlewska, Urszula and Radanović, Dušanka and Mroziñski, Jerzy and Korabik, Maria",
year = "2007",
abstract = "A novel binuclear Co(II) complex, [Co2(Cl)2tpmc](BF4)2 (tpmc = N,N′,N″,N‴-tetrakis(2-pyridylmethyl)-1,4,8,11-tetraaz acyclotetradecane), was prepared and structurally characterized by X-ray diffraction analysis at low temperature. The complex crystallizes in P21/c space group of the monoclinic crystal system, and its crystals are isomorphic with those of [Cu2(Br)2tpmc](ClO4)2 complex. In the crystal structure the complex cations [Co2(Cl)2tpmc]2+ are settled around the inversion centres. Cobalt(II) is exo coordinated with four macrocyclic N atoms, and Cl- supplements the fifth coordination site. Based on the index of trigonality, the coordination polyhedron formed around Co(II) ion is described as distorted trigonal bipyramid. Two metal centres are at a distance of 5.710 Å. This is the first Co(II) complex for which X-ray analysis confirmed a chair conformation of tpmc ligand. IR, EPR (X-band) and UV/VIS absorption and reflectance spectra, molar conductivities and magnetic measurements (SQUID) are used to study the investigated complex. A comparative structural analysis with some of the described Co(II) and Cu(II) complexes of analogous geometries and type of pendant azamacrocyclic ligands was also done.",
publisher = "Elsevier",
journal = "Journal of Molecular Structure",
title = "Preparation, characterization and X-ray analysis of [Co2(Cl)2tpmc](BF4)2. Comparative structural analysis with the complexes having analogous geometries and ligands",
volume = "827",
number = "1-3",
pages = "80-87",
doi = "10.1016/j.molstruc.2006.05.009"
}

Vučković, G., Tanasković, S. B., Rychlewska, U., Radanović, D., Mroziñski, J.,& Korabik, M.. (2007). Preparation, characterization and X-ray analysis of [Co2(Cl)2tpmc](BF4)2. Comparative structural analysis with the complexes having analogous geometries and ligands. in Journal of Molecular Structure
Elsevier., 827(1-3), 80-87.
https://doi.org/10.1016/j.molstruc.2006.05.009

Vučković G, Tanasković SB, Rychlewska U, Radanović D, Mroziñski J, Korabik M. Preparation, characterization and X-ray analysis of [Co2(Cl)2tpmc](BF4)2. Comparative structural analysis with the complexes having analogous geometries and ligands. in Journal of Molecular Structure. 2007;827(1-3):80-87.
doi:10.1016/j.molstruc.2006.05.009 .

Vučković, Gordana, Tanasković, Slađana B., Rychlewska, Urszula, Radanović, Dušanka, Mroziñski, Jerzy, Korabik, Maria, "Preparation, characterization and X-ray analysis of [Co2(Cl)2tpmc](BF4)2. Comparative structural analysis with the complexes having analogous geometries and ligands" in Journal of Molecular Structure, 827, no. 1-3 (2007):80-87,
https://doi.org/10.1016/j.molstruc.2006.05.009 . .

TY  - JOUR
AU  - Sovilj, Sofija P.
AU  - Vučković, Gordana
AU  - Babić-Samardžija, Ksenija
AU  - Matsumoto, N.
AU  - Jovanović, Vladislava M.
AU  - Mrozinski, J.
PY  - 1999
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3672
AB  - A new dinuclear cobalt(II) complex, [Co2(ox)tpmc](ClO4)2 3H2O, (tpmc = N, N′, N″, N″′-tetrakis(2-pyridylmethyl)-1, 4, 8, 11-tetraazacyclotetradecane, ox2 -oxalate ion), has been synthesized and its crystal structure solved by single crystal X-ray diffraction studies. It crystallizes in the monoclinic system, space group P21, with a = 97558(8) A, b = 21.455(2) A, c - 21.241(2) A, β=100.069(8)°, V=4391.0(8) A3, Z =4,R = 0.083, Rw = 0.086. Its structure consists of two dinuclear, crystallographically unique molecules in which the oxalate ion bridges two cobalt(II) ions unsymmetrically. E:ach cobalt is hexa-coordinated with four macrocyclic nitrogens and two oxygens in an octahedral arrangement of an “em” coordination of a macrocyclic ligand. The third oxygen is simultaneously bonded to both cobalt ions and the last one remains uncoordinated, which is the unique way of oxalato ion coordination. Intramolecular antiferromagnetic coupling between the two cobalt(II) ions is observed and yielded J = -9.3 an−1, g - 5.64 and g = 1.21. The variable temperature (4.2-192 K) inagiietic susceptibility nieasureinents are interpreted on the basis of the spin lamiltonian H 25/9JSASB + goβHz(SAZ - SBZ). Cyclic voltanllnetiy suggests that the complex is electrochcmically stable up to the potential of the cobalt reduction.
PB  - Taylor and Francis
T2  - Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry
T1  - Synthesis, crystal structure, magnetic properties and cyclic voltammetry of the unsymmetric (μ-oxalato)-[N,N′,N″,N‴-tetrakis-(2-pyridylmethyl)-1,4,8, 11-tetraazacyclotetra-decane]dicobalt(II) perchlorate trihydrate
VL  - 29
IS  - 5
SP  - 785
EP  - 803
DO  - 10.1080/00945719909349487
ER  - 

@article{
author = "Sovilj, Sofija P. and Vučković, Gordana and Babić-Samardžija, Ksenija and Matsumoto, N. and Jovanović, Vladislava M. and Mrozinski, J.",
year = "1999",
abstract = "A new dinuclear cobalt(II) complex, [Co2(ox)tpmc](ClO4)2 3H2O, (tpmc = N, N′, N″, N″′-tetrakis(2-pyridylmethyl)-1, 4, 8, 11-tetraazacyclotetradecane, ox2 -oxalate ion), has been synthesized and its crystal structure solved by single crystal X-ray diffraction studies. It crystallizes in the monoclinic system, space group P21, with a = 97558(8) A, b = 21.455(2) A, c - 21.241(2) A, β=100.069(8)°, V=4391.0(8) A3, Z =4,R = 0.083, Rw = 0.086. Its structure consists of two dinuclear, crystallographically unique molecules in which the oxalate ion bridges two cobalt(II) ions unsymmetrically. E:ach cobalt is hexa-coordinated with four macrocyclic nitrogens and two oxygens in an octahedral arrangement of an “em” coordination of a macrocyclic ligand. The third oxygen is simultaneously bonded to both cobalt ions and the last one remains uncoordinated, which is the unique way of oxalato ion coordination. Intramolecular antiferromagnetic coupling between the two cobalt(II) ions is observed and yielded J = -9.3 an−1, g - 5.64 and g = 1.21. The variable temperature (4.2-192 K) inagiietic susceptibility nieasureinents are interpreted on the basis of the spin lamiltonian H 25/9JSASB + goβHz(SAZ - SBZ). Cyclic voltanllnetiy suggests that the complex is electrochcmically stable up to the potential of the cobalt reduction.",
publisher = "Taylor and Francis",
journal = "Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry",
title = "Synthesis, crystal structure, magnetic properties and cyclic voltammetry of the unsymmetric (μ-oxalato)-[N,N′,N″,N‴-tetrakis-(2-pyridylmethyl)-1,4,8, 11-tetraazacyclotetra-decane]dicobalt(II) perchlorate trihydrate",
volume = "29",
number = "5",
pages = "785-803",
doi = "10.1080/00945719909349487"
}

Sovilj, S. P., Vučković, G., Babić-Samardžija, K., Matsumoto, N., Jovanović, V. M.,& Mrozinski, J.. (1999). Synthesis, crystal structure, magnetic properties and cyclic voltammetry of the unsymmetric (μ-oxalato)-[N,N′,N″,N‴-tetrakis-(2-pyridylmethyl)-1,4,8, 11-tetraazacyclotetra-decane]dicobalt(II) perchlorate trihydrate. in Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry
Taylor and Francis., 29(5), 785-803.
https://doi.org/10.1080/00945719909349487

Sovilj SP, Vučković G, Babić-Samardžija K, Matsumoto N, Jovanović VM, Mrozinski J. Synthesis, crystal structure, magnetic properties and cyclic voltammetry of the unsymmetric (μ-oxalato)-[N,N′,N″,N‴-tetrakis-(2-pyridylmethyl)-1,4,8, 11-tetraazacyclotetra-decane]dicobalt(II) perchlorate trihydrate. in Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry. 1999;29(5):785-803.
doi:10.1080/00945719909349487 .

Sovilj, Sofija P., Vučković, Gordana, Babić-Samardžija, Ksenija, Matsumoto, N., Jovanović, Vladislava M., Mrozinski, J., "Synthesis, crystal structure, magnetic properties and cyclic voltammetry of the unsymmetric (μ-oxalato)-[N,N′,N″,N‴-tetrakis-(2-pyridylmethyl)-1,4,8, 11-tetraazacyclotetra-decane]dicobalt(II) perchlorate trihydrate" in Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry, 29, no. 5 (1999):785-803,
https://doi.org/10.1080/00945719909349487 . .