Electrochemical examination of mixed-ligand cobalt(III) complexes with tetraazamacrocyclic ligand and heterocyclic dithiocarbamates
Abstract
Electrochemical stability of eight complexes of the general formula [co 111 Rdtc(1-8)cyclam](ClO 4 ) 2 , where cyclam=1,4,8,11-tetraazacyclotetradecane and Rdtc - (1-8)=4-morpholine (Morphdtc), 4-thiomorpholine (Timdtc), 4-piperazine (Pzdtc), N-methyl piperazine (N-Mepzdtc), piperidine (Pipdtc), 2-, 3- or 4-methylpiperidine (2-, 3- or 4-Mepipdtc) dithiocarbamates, respectively, were studied. The substances were examined in aqueous NaClO 4 solution and nonaqueous LiClO 4 in CH 3 CN solution by cyclic voltammetry. In aqueous solution, macrocyclic ligand cyclam is characterized by the anodic peak at 0.95 V. The Rdtc - ligands have two anodic peaks, one in the region 0.25-0.30 V and the other in the 0.78-0.95 V region. Absence of these anodic peaks in the case of the complexes indicates that coordination to cobalt(III) stabilizes both cyclam and Rdtc - ligands, but reversible peaks in the range -0.68 to -0.78 V support the Co(III) redox reaction. In nonaqueous solutions cyclam has one anod...ic peak at 1.75 V. The ligands with heteroatom in the ring (Morphdtc, Timdtc, Pzdtc, N-Mepzdtc) have two anodic peaks, while the other four ligands (Pipdtc, 2-, 3- and 4-Mepipdtc) have only one anodic peak. In nonaqueous solution again, coordination to Co(III) ion stabilizes the Rdtc - ligands and contrary to aqueous solution no Co(III) redox reaction occurs, indicating a greater stability of the complexes in this media. Finally, the electrochemical results are compared with spectroscopic data obtained previously.
Keywords:
Aqueous solution / binding kinetics / Cobalt(III) complexes / complex formation / cyclam / cyclam derivative / Cyclic voltammetry / dithiocarbamic acid derivative / electrochemical analysis / Glassy carbon / heterocyclic compound / ligand binding / macrocyclic compound / molecular stability / Nonaqueous solution / oxidation reduction reaction / piperidine derivative / review / spectroscopy / thiomorpholine derivativeSource:
Electroanalysis, 2001, 13, 13, 1129-1135Publisher:
- Wiley-VCH Verlag GmbH
Funding / projects:
- Ministry of Science and Technology of the Republic Serbia (Project 02E35)
- Ministry of Science and Technology of the Republic Serbia (Project 02E20)
DOI: 10.1002/1521-4109(200109)13:13<1129::AID-ELAN1129>3.0.CO;2-K
ISSN: 1040-0397
Scopus: 2-s2.0-0034797910
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Institution/Community
IHTMTY - JOUR AU - Jovanović, Vladislava M. AU - Babić-Samardžija, Ksenija AU - Sovilj, Sofija P. PY - 2001 UR - https://cer.ihtm.bg.ac.rs/handle/123456789/3656 AB - Electrochemical stability of eight complexes of the general formula [co 111 Rdtc(1-8)cyclam](ClO 4 ) 2 , where cyclam=1,4,8,11-tetraazacyclotetradecane and Rdtc - (1-8)=4-morpholine (Morphdtc), 4-thiomorpholine (Timdtc), 4-piperazine (Pzdtc), N-methyl piperazine (N-Mepzdtc), piperidine (Pipdtc), 2-, 3- or 4-methylpiperidine (2-, 3- or 4-Mepipdtc) dithiocarbamates, respectively, were studied. The substances were examined in aqueous NaClO 4 solution and nonaqueous LiClO 4 in CH 3 CN solution by cyclic voltammetry. In aqueous solution, macrocyclic ligand cyclam is characterized by the anodic peak at 0.95 V. The Rdtc - ligands have two anodic peaks, one in the region 0.25-0.30 V and the other in the 0.78-0.95 V region. Absence of these anodic peaks in the case of the complexes indicates that coordination to cobalt(III) stabilizes both cyclam and Rdtc - ligands, but reversible peaks in the range -0.68 to -0.78 V support the Co(III) redox reaction. In nonaqueous solutions cyclam has one anodic peak at 1.75 V. The ligands with heteroatom in the ring (Morphdtc, Timdtc, Pzdtc, N-Mepzdtc) have two anodic peaks, while the other four ligands (Pipdtc, 2-, 3- and 4-Mepipdtc) have only one anodic peak. In nonaqueous solution again, coordination to Co(III) ion stabilizes the Rdtc - ligands and contrary to aqueous solution no Co(III) redox reaction occurs, indicating a greater stability of the complexes in this media. Finally, the electrochemical results are compared with spectroscopic data obtained previously. PB - Wiley-VCH Verlag GmbH T2 - Electroanalysis T1 - Electrochemical examination of mixed-ligand cobalt(III) complexes with tetraazamacrocyclic ligand and heterocyclic dithiocarbamates VL - 13 IS - 13 SP - 1129 EP - 1135 DO - 10.1002/1521-4109(200109)13:13<1129::AID-ELAN1129>3.0.CO;2-K ER -
@article{ author = "Jovanović, Vladislava M. and Babić-Samardžija, Ksenija and Sovilj, Sofija P.", year = "2001", abstract = "Electrochemical stability of eight complexes of the general formula [co 111 Rdtc(1-8)cyclam](ClO 4 ) 2 , where cyclam=1,4,8,11-tetraazacyclotetradecane and Rdtc - (1-8)=4-morpholine (Morphdtc), 4-thiomorpholine (Timdtc), 4-piperazine (Pzdtc), N-methyl piperazine (N-Mepzdtc), piperidine (Pipdtc), 2-, 3- or 4-methylpiperidine (2-, 3- or 4-Mepipdtc) dithiocarbamates, respectively, were studied. The substances were examined in aqueous NaClO 4 solution and nonaqueous LiClO 4 in CH 3 CN solution by cyclic voltammetry. In aqueous solution, macrocyclic ligand cyclam is characterized by the anodic peak at 0.95 V. The Rdtc - ligands have two anodic peaks, one in the region 0.25-0.30 V and the other in the 0.78-0.95 V region. Absence of these anodic peaks in the case of the complexes indicates that coordination to cobalt(III) stabilizes both cyclam and Rdtc - ligands, but reversible peaks in the range -0.68 to -0.78 V support the Co(III) redox reaction. In nonaqueous solutions cyclam has one anodic peak at 1.75 V. The ligands with heteroatom in the ring (Morphdtc, Timdtc, Pzdtc, N-Mepzdtc) have two anodic peaks, while the other four ligands (Pipdtc, 2-, 3- and 4-Mepipdtc) have only one anodic peak. In nonaqueous solution again, coordination to Co(III) ion stabilizes the Rdtc - ligands and contrary to aqueous solution no Co(III) redox reaction occurs, indicating a greater stability of the complexes in this media. Finally, the electrochemical results are compared with spectroscopic data obtained previously.", publisher = "Wiley-VCH Verlag GmbH", journal = "Electroanalysis", title = "Electrochemical examination of mixed-ligand cobalt(III) complexes with tetraazamacrocyclic ligand and heterocyclic dithiocarbamates", volume = "13", number = "13", pages = "1129-1135", doi = "10.1002/1521-4109(200109)13:13<1129::AID-ELAN1129>3.0.CO;2-K" }
Jovanović, V. M., Babić-Samardžija, K.,& Sovilj, S. P.. (2001). Electrochemical examination of mixed-ligand cobalt(III) complexes with tetraazamacrocyclic ligand and heterocyclic dithiocarbamates. in Electroanalysis Wiley-VCH Verlag GmbH., 13(13), 1129-1135. https://doi.org/10.1002/1521-4109(200109)13:13<1129::AID-ELAN1129>3.0.CO;2-K
Jovanović VM, Babić-Samardžija K, Sovilj SP. Electrochemical examination of mixed-ligand cobalt(III) complexes with tetraazamacrocyclic ligand and heterocyclic dithiocarbamates. in Electroanalysis. 2001;13(13):1129-1135. doi:10.1002/1521-4109(200109)13:13<1129::AID-ELAN1129>3.0.CO;2-K .
Jovanović, Vladislava M., Babić-Samardžija, Ksenija, Sovilj, Sofija P., "Electrochemical examination of mixed-ligand cobalt(III) complexes with tetraazamacrocyclic ligand and heterocyclic dithiocarbamates" in Electroanalysis, 13, no. 13 (2001):1129-1135, https://doi.org/10.1002/1521-4109(200109)13:13<1129::AID-ELAN1129>3.0.CO;2-K . .