Electro-inorganic synthesis: a convergent paired electrochemical synthesis and voltammetric studies of copper(II)-2-aminophenol derivatives

Abstract Electrochemical reduction of 2-nitrophenol and 5-methyl-2-nitrophenol has been studied in water/ethanol mixture using cyclic voltammetry and controlled-potential coulometry. Our voltammetric data indicate the formation of 2-aminophenol ($ HL^{I} $) and 5-methyl-2-aminophenol ($ HL^{II} $),...
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Gespeichert in:

Autor*in:	Nematollahi, D. [verfasserIn] Gomar, F. [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2012

Schlagwörter:	2-Aminophenol 2-Nitrophenol Copper(II)-2-aminophenol complex Electrochemical synthesis Cyclic voltammetry

Übergeordnetes Werk:	Enthalten in: Journal of the Iranian Chemical Society - Tehran, 2004, 9(2012), 5 vom: 04. Mai, Seite 693-704
Übergeordnetes Werk:	volume:9 ; year:2012 ; number:5 ; day:04 ; month:05 ; pages:693-704

Links:	Volltext

DOI / URN:	10.1007/s13738-012-0082-7

Katalog-ID:	SPR032219245

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520			\|a Abstract Electrochemical reduction of 2-nitrophenol and 5-methyl-2-nitrophenol has been studied in water/ethanol mixture using cyclic voltammetry and controlled-potential coulometry. Our voltammetric data indicate the formation of 2-aminophenol ($ HL^{I} $) and 5-methyl-2-aminophenol ($ HL^{II} $), respectively. Also, the electrochemical synthesis of copper(II) complex of 2-aminophenols has been carried out using copper metal as a sacrificial anode and lead metal as a cathode in water/ethanol (50/50 v/v). The electrochemical synthesis of copper(II)-2-aminophenols consists of a multi-step such as (a) cathodic reduction of 2-nitrophenols to related 2-aminophenols, (b) generation of $ Cu^{2+} $ from copper anode, (c) complexation of 2-aminophenols with $ Cu^{2+} $. In this work, we have proposed a mechanism for the electrode process. Some parameters such as electrode material, current density, electricity passed and temperature, were also systematically studied. The convergent paired electrochemical synthesis of copper(II) complex of 2-aminophenols has been successfully performed in a one-pot process, under constant current condition in an undivided cell, in a good yield and purity. Also, the electrochemical behavior of copper(II)-2-aminophenol complex was studied and the stability constant of copper(I)-2-aminophenol complex was evaluated using cyclic voltammetry.
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allfields	10.1007/s13738-012-0082-7 doi (DE-627)SPR032219245 (SPR)s13738-012-0082-7-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Nematollahi, D. verfasserin aut Electro-inorganic synthesis: a convergent paired electrochemical synthesis and voltammetric studies of copper(II)-2-aminophenol derivatives 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Electrochemical reduction of 2-nitrophenol and 5-methyl-2-nitrophenol has been studied in water/ethanol mixture using cyclic voltammetry and controlled-potential coulometry. Our voltammetric data indicate the formation of 2-aminophenol ($ HL^{I} $) and 5-methyl-2-aminophenol ($ HL^{II} $), respectively. Also, the electrochemical synthesis of copper(II) complex of 2-aminophenols has been carried out using copper metal as a sacrificial anode and lead metal as a cathode in water/ethanol (50/50 v/v). The electrochemical synthesis of copper(II)-2-aminophenols consists of a multi-step such as (a) cathodic reduction of 2-nitrophenols to related 2-aminophenols, (b) generation of $ Cu^{2+} $ from copper anode, (c) complexation of 2-aminophenols with $ Cu^{2+} $. In this work, we have proposed a mechanism for the electrode process. Some parameters such as electrode material, current density, electricity passed and temperature, were also systematically studied. The convergent paired electrochemical synthesis of copper(II) complex of 2-aminophenols has been successfully performed in a one-pot process, under constant current condition in an undivided cell, in a good yield and purity. Also, the electrochemical behavior of copper(II)-2-aminophenol complex was studied and the stability constant of copper(I)-2-aminophenol complex was evaluated using cyclic voltammetry. 2-Aminophenol (dpeaa)DE-He213 2-Nitrophenol (dpeaa)DE-He213 Copper(II)-2-aminophenol complex (dpeaa)DE-He213 Electrochemical synthesis (dpeaa)DE-He213 Cyclic voltammetry (dpeaa)DE-He213 Gomar, F. verfasserin aut Enthalten in Journal of the Iranian Chemical Society Tehran, 2004 9(2012), 5 vom: 04. Mai, Seite 693-704 (DE-627)515979767 (DE-600)2244820-2 1735-2428 nnns volume:9 year:2012 number:5 day:04 month:05 pages:693-704 https://dx.doi.org/10.1007/s13738-012-0082-7 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_165 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 9 2012 5 04 05 693-704
spelling	10.1007/s13738-012-0082-7 doi (DE-627)SPR032219245 (SPR)s13738-012-0082-7-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Nematollahi, D. verfasserin aut Electro-inorganic synthesis: a convergent paired electrochemical synthesis and voltammetric studies of copper(II)-2-aminophenol derivatives 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Electrochemical reduction of 2-nitrophenol and 5-methyl-2-nitrophenol has been studied in water/ethanol mixture using cyclic voltammetry and controlled-potential coulometry. Our voltammetric data indicate the formation of 2-aminophenol ($ HL^{I} $) and 5-methyl-2-aminophenol ($ HL^{II} $), respectively. Also, the electrochemical synthesis of copper(II) complex of 2-aminophenols has been carried out using copper metal as a sacrificial anode and lead metal as a cathode in water/ethanol (50/50 v/v). The electrochemical synthesis of copper(II)-2-aminophenols consists of a multi-step such as (a) cathodic reduction of 2-nitrophenols to related 2-aminophenols, (b) generation of $ Cu^{2+} $ from copper anode, (c) complexation of 2-aminophenols with $ Cu^{2+} $. In this work, we have proposed a mechanism for the electrode process. Some parameters such as electrode material, current density, electricity passed and temperature, were also systematically studied. The convergent paired electrochemical synthesis of copper(II) complex of 2-aminophenols has been successfully performed in a one-pot process, under constant current condition in an undivided cell, in a good yield and purity. Also, the electrochemical behavior of copper(II)-2-aminophenol complex was studied and the stability constant of copper(I)-2-aminophenol complex was evaluated using cyclic voltammetry. 2-Aminophenol (dpeaa)DE-He213 2-Nitrophenol (dpeaa)DE-He213 Copper(II)-2-aminophenol complex (dpeaa)DE-He213 Electrochemical synthesis (dpeaa)DE-He213 Cyclic voltammetry (dpeaa)DE-He213 Gomar, F. verfasserin aut Enthalten in Journal of the Iranian Chemical Society Tehran, 2004 9(2012), 5 vom: 04. Mai, Seite 693-704 (DE-627)515979767 (DE-600)2244820-2 1735-2428 nnns volume:9 year:2012 number:5 day:04 month:05 pages:693-704 https://dx.doi.org/10.1007/s13738-012-0082-7 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_165 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 9 2012 5 04 05 693-704
allfields_unstemmed	10.1007/s13738-012-0082-7 doi (DE-627)SPR032219245 (SPR)s13738-012-0082-7-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Nematollahi, D. verfasserin aut Electro-inorganic synthesis: a convergent paired electrochemical synthesis and voltammetric studies of copper(II)-2-aminophenol derivatives 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Electrochemical reduction of 2-nitrophenol and 5-methyl-2-nitrophenol has been studied in water/ethanol mixture using cyclic voltammetry and controlled-potential coulometry. Our voltammetric data indicate the formation of 2-aminophenol ($ HL^{I} $) and 5-methyl-2-aminophenol ($ HL^{II} $), respectively. Also, the electrochemical synthesis of copper(II) complex of 2-aminophenols has been carried out using copper metal as a sacrificial anode and lead metal as a cathode in water/ethanol (50/50 v/v). The electrochemical synthesis of copper(II)-2-aminophenols consists of a multi-step such as (a) cathodic reduction of 2-nitrophenols to related 2-aminophenols, (b) generation of $ Cu^{2+} $ from copper anode, (c) complexation of 2-aminophenols with $ Cu^{2+} $. In this work, we have proposed a mechanism for the electrode process. Some parameters such as electrode material, current density, electricity passed and temperature, were also systematically studied. The convergent paired electrochemical synthesis of copper(II) complex of 2-aminophenols has been successfully performed in a one-pot process, under constant current condition in an undivided cell, in a good yield and purity. Also, the electrochemical behavior of copper(II)-2-aminophenol complex was studied and the stability constant of copper(I)-2-aminophenol complex was evaluated using cyclic voltammetry. 2-Aminophenol (dpeaa)DE-He213 2-Nitrophenol (dpeaa)DE-He213 Copper(II)-2-aminophenol complex (dpeaa)DE-He213 Electrochemical synthesis (dpeaa)DE-He213 Cyclic voltammetry (dpeaa)DE-He213 Gomar, F. verfasserin aut Enthalten in Journal of the Iranian Chemical Society Tehran, 2004 9(2012), 5 vom: 04. Mai, Seite 693-704 (DE-627)515979767 (DE-600)2244820-2 1735-2428 nnns volume:9 year:2012 number:5 day:04 month:05 pages:693-704 https://dx.doi.org/10.1007/s13738-012-0082-7 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_165 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 9 2012 5 04 05 693-704
allfieldsGer	10.1007/s13738-012-0082-7 doi (DE-627)SPR032219245 (SPR)s13738-012-0082-7-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Nematollahi, D. verfasserin aut Electro-inorganic synthesis: a convergent paired electrochemical synthesis and voltammetric studies of copper(II)-2-aminophenol derivatives 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Electrochemical reduction of 2-nitrophenol and 5-methyl-2-nitrophenol has been studied in water/ethanol mixture using cyclic voltammetry and controlled-potential coulometry. Our voltammetric data indicate the formation of 2-aminophenol ($ HL^{I} $) and 5-methyl-2-aminophenol ($ HL^{II} $), respectively. Also, the electrochemical synthesis of copper(II) complex of 2-aminophenols has been carried out using copper metal as a sacrificial anode and lead metal as a cathode in water/ethanol (50/50 v/v). The electrochemical synthesis of copper(II)-2-aminophenols consists of a multi-step such as (a) cathodic reduction of 2-nitrophenols to related 2-aminophenols, (b) generation of $ Cu^{2+} $ from copper anode, (c) complexation of 2-aminophenols with $ Cu^{2+} $. In this work, we have proposed a mechanism for the electrode process. Some parameters such as electrode material, current density, electricity passed and temperature, were also systematically studied. The convergent paired electrochemical synthesis of copper(II) complex of 2-aminophenols has been successfully performed in a one-pot process, under constant current condition in an undivided cell, in a good yield and purity. Also, the electrochemical behavior of copper(II)-2-aminophenol complex was studied and the stability constant of copper(I)-2-aminophenol complex was evaluated using cyclic voltammetry. 2-Aminophenol (dpeaa)DE-He213 2-Nitrophenol (dpeaa)DE-He213 Copper(II)-2-aminophenol complex (dpeaa)DE-He213 Electrochemical synthesis (dpeaa)DE-He213 Cyclic voltammetry (dpeaa)DE-He213 Gomar, F. verfasserin aut Enthalten in Journal of the Iranian Chemical Society Tehran, 2004 9(2012), 5 vom: 04. Mai, Seite 693-704 (DE-627)515979767 (DE-600)2244820-2 1735-2428 nnns volume:9 year:2012 number:5 day:04 month:05 pages:693-704 https://dx.doi.org/10.1007/s13738-012-0082-7 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_165 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 9 2012 5 04 05 693-704
allfieldsSound	10.1007/s13738-012-0082-7 doi (DE-627)SPR032219245 (SPR)s13738-012-0082-7-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Nematollahi, D. verfasserin aut Electro-inorganic synthesis: a convergent paired electrochemical synthesis and voltammetric studies of copper(II)-2-aminophenol derivatives 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Electrochemical reduction of 2-nitrophenol and 5-methyl-2-nitrophenol has been studied in water/ethanol mixture using cyclic voltammetry and controlled-potential coulometry. Our voltammetric data indicate the formation of 2-aminophenol ($ HL^{I} $) and 5-methyl-2-aminophenol ($ HL^{II} $), respectively. Also, the electrochemical synthesis of copper(II) complex of 2-aminophenols has been carried out using copper metal as a sacrificial anode and lead metal as a cathode in water/ethanol (50/50 v/v). The electrochemical synthesis of copper(II)-2-aminophenols consists of a multi-step such as (a) cathodic reduction of 2-nitrophenols to related 2-aminophenols, (b) generation of $ Cu^{2+} $ from copper anode, (c) complexation of 2-aminophenols with $ Cu^{2+} $. In this work, we have proposed a mechanism for the electrode process. Some parameters such as electrode material, current density, electricity passed and temperature, were also systematically studied. The convergent paired electrochemical synthesis of copper(II) complex of 2-aminophenols has been successfully performed in a one-pot process, under constant current condition in an undivided cell, in a good yield and purity. Also, the electrochemical behavior of copper(II)-2-aminophenol complex was studied and the stability constant of copper(I)-2-aminophenol complex was evaluated using cyclic voltammetry. 2-Aminophenol (dpeaa)DE-He213 2-Nitrophenol (dpeaa)DE-He213 Copper(II)-2-aminophenol complex (dpeaa)DE-He213 Electrochemical synthesis (dpeaa)DE-He213 Cyclic voltammetry (dpeaa)DE-He213 Gomar, F. verfasserin aut Enthalten in Journal of the Iranian Chemical Society Tehran, 2004 9(2012), 5 vom: 04. Mai, Seite 693-704 (DE-627)515979767 (DE-600)2244820-2 1735-2428 nnns volume:9 year:2012 number:5 day:04 month:05 pages:693-704 https://dx.doi.org/10.1007/s13738-012-0082-7 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_165 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 9 2012 5 04 05 693-704
language	English
source	Enthalten in Journal of the Iranian Chemical Society 9(2012), 5 vom: 04. Mai, Seite 693-704 volume:9 year:2012 number:5 day:04 month:05 pages:693-704
sourceStr	Enthalten in Journal of the Iranian Chemical Society 9(2012), 5 vom: 04. Mai, Seite 693-704 volume:9 year:2012 number:5 day:04 month:05 pages:693-704
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	2-Aminophenol 2-Nitrophenol Copper(II)-2-aminophenol complex Electrochemical synthesis Cyclic voltammetry
dewey-raw	540
isfreeaccess_bool	false
container_title	Journal of the Iranian Chemical Society
authorswithroles_txt_mv	Nematollahi, D. @@aut@@ Gomar, F. @@aut@@
publishDateDaySort_date	2012-05-04T00:00:00Z
hierarchy_top_id	515979767
dewey-sort	3540
id	SPR032219245
language_de	englisch
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author	Nematollahi, D.
spellingShingle	Nematollahi, D. ddc 540 bkl 35.00 misc 2-Aminophenol misc 2-Nitrophenol misc Copper(II)-2-aminophenol complex misc Electrochemical synthesis misc Cyclic voltammetry Electro-inorganic synthesis: a convergent paired electrochemical synthesis and voltammetric studies of copper(II)-2-aminophenol derivatives
authorStr	Nematollahi, D.
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topic_title	540 ASE 35.00 bkl Electro-inorganic synthesis: a convergent paired electrochemical synthesis and voltammetric studies of copper(II)-2-aminophenol derivatives 2-Aminophenol (dpeaa)DE-He213 2-Nitrophenol (dpeaa)DE-He213 Copper(II)-2-aminophenol complex (dpeaa)DE-He213 Electrochemical synthesis (dpeaa)DE-He213 Cyclic voltammetry (dpeaa)DE-He213
topic	ddc 540 bkl 35.00 misc 2-Aminophenol misc 2-Nitrophenol misc Copper(II)-2-aminophenol complex misc Electrochemical synthesis misc Cyclic voltammetry
topic_unstemmed	ddc 540 bkl 35.00 misc 2-Aminophenol misc 2-Nitrophenol misc Copper(II)-2-aminophenol complex misc Electrochemical synthesis misc Cyclic voltammetry
topic_browse	ddc 540 bkl 35.00 misc 2-Aminophenol misc 2-Nitrophenol misc Copper(II)-2-aminophenol complex misc Electrochemical synthesis misc Cyclic voltammetry
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title	Electro-inorganic synthesis: a convergent paired electrochemical synthesis and voltammetric studies of copper(II)-2-aminophenol derivatives
ctrlnum	(DE-627)SPR032219245 (SPR)s13738-012-0082-7-e
title_full	Electro-inorganic synthesis: a convergent paired electrochemical synthesis and voltammetric studies of copper(II)-2-aminophenol derivatives
author_sort	Nematollahi, D.
journal	Journal of the Iranian Chemical Society
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author_browse	Nematollahi, D. Gomar, F.
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class	540 ASE 35.00 bkl
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author-letter	Nematollahi, D.
doi_str_mv	10.1007/s13738-012-0082-7
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title_sort	electro-inorganic synthesis: a convergent paired electrochemical synthesis and voltammetric studies of copper(ii)-2-aminophenol derivatives
title_auth	Electro-inorganic synthesis: a convergent paired electrochemical synthesis and voltammetric studies of copper(II)-2-aminophenol derivatives
abstract	Abstract Electrochemical reduction of 2-nitrophenol and 5-methyl-2-nitrophenol has been studied in water/ethanol mixture using cyclic voltammetry and controlled-potential coulometry. Our voltammetric data indicate the formation of 2-aminophenol ($ HL^{I} $) and 5-methyl-2-aminophenol ($ HL^{II} $), respectively. Also, the electrochemical synthesis of copper(II) complex of 2-aminophenols has been carried out using copper metal as a sacrificial anode and lead metal as a cathode in water/ethanol (50/50 v/v). The electrochemical synthesis of copper(II)-2-aminophenols consists of a multi-step such as (a) cathodic reduction of 2-nitrophenols to related 2-aminophenols, (b) generation of $ Cu^{2+} $ from copper anode, (c) complexation of 2-aminophenols with $ Cu^{2+} $. In this work, we have proposed a mechanism for the electrode process. Some parameters such as electrode material, current density, electricity passed and temperature, were also systematically studied. The convergent paired electrochemical synthesis of copper(II) complex of 2-aminophenols has been successfully performed in a one-pot process, under constant current condition in an undivided cell, in a good yield and purity. Also, the electrochemical behavior of copper(II)-2-aminophenol complex was studied and the stability constant of copper(I)-2-aminophenol complex was evaluated using cyclic voltammetry.
abstractGer	Abstract Electrochemical reduction of 2-nitrophenol and 5-methyl-2-nitrophenol has been studied in water/ethanol mixture using cyclic voltammetry and controlled-potential coulometry. Our voltammetric data indicate the formation of 2-aminophenol ($ HL^{I} $) and 5-methyl-2-aminophenol ($ HL^{II} $), respectively. Also, the electrochemical synthesis of copper(II) complex of 2-aminophenols has been carried out using copper metal as a sacrificial anode and lead metal as a cathode in water/ethanol (50/50 v/v). The electrochemical synthesis of copper(II)-2-aminophenols consists of a multi-step such as (a) cathodic reduction of 2-nitrophenols to related 2-aminophenols, (b) generation of $ Cu^{2+} $ from copper anode, (c) complexation of 2-aminophenols with $ Cu^{2+} $. In this work, we have proposed a mechanism for the electrode process. Some parameters such as electrode material, current density, electricity passed and temperature, were also systematically studied. The convergent paired electrochemical synthesis of copper(II) complex of 2-aminophenols has been successfully performed in a one-pot process, under constant current condition in an undivided cell, in a good yield and purity. Also, the electrochemical behavior of copper(II)-2-aminophenol complex was studied and the stability constant of copper(I)-2-aminophenol complex was evaluated using cyclic voltammetry.
abstract_unstemmed	Abstract Electrochemical reduction of 2-nitrophenol and 5-methyl-2-nitrophenol has been studied in water/ethanol mixture using cyclic voltammetry and controlled-potential coulometry. Our voltammetric data indicate the formation of 2-aminophenol ($ HL^{I} $) and 5-methyl-2-aminophenol ($ HL^{II} $), respectively. Also, the electrochemical synthesis of copper(II) complex of 2-aminophenols has been carried out using copper metal as a sacrificial anode and lead metal as a cathode in water/ethanol (50/50 v/v). The electrochemical synthesis of copper(II)-2-aminophenols consists of a multi-step such as (a) cathodic reduction of 2-nitrophenols to related 2-aminophenols, (b) generation of $ Cu^{2+} $ from copper anode, (c) complexation of 2-aminophenols with $ Cu^{2+} $. In this work, we have proposed a mechanism for the electrode process. Some parameters such as electrode material, current density, electricity passed and temperature, were also systematically studied. The convergent paired electrochemical synthesis of copper(II) complex of 2-aminophenols has been successfully performed in a one-pot process, under constant current condition in an undivided cell, in a good yield and purity. Also, the electrochemical behavior of copper(II)-2-aminophenol complex was studied and the stability constant of copper(I)-2-aminophenol complex was evaluated using cyclic voltammetry.
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title_short	Electro-inorganic synthesis: a convergent paired electrochemical synthesis and voltammetric studies of copper(II)-2-aminophenol derivatives
url	https://dx.doi.org/10.1007/s13738-012-0082-7
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doi_str	10.1007/s13738-012-0082-7
up_date	2024-07-04T02:47:13.446Z
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Our voltammetric data indicate the formation of 2-aminophenol ($ HL^{I} $) and 5-methyl-2-aminophenol ($ HL^{II} $), respectively. Also, the electrochemical synthesis of copper(II) complex of 2-aminophenols has been carried out using copper metal as a sacrificial anode and lead metal as a cathode in water/ethanol (50/50 v/v). The electrochemical synthesis of copper(II)-2-aminophenols consists of a multi-step such as (a) cathodic reduction of 2-nitrophenols to related 2-aminophenols, (b) generation of $ Cu^{2+} $ from copper anode, (c) complexation of 2-aminophenols with $ Cu^{2+} $. In this work, we have proposed a mechanism for the electrode process. Some parameters such as electrode material, current density, electricity passed and temperature, were also systematically studied. 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Electro-inorganic synthesis: a convergent paired electrochemical synthesis and voltammetric studies of copper(II)-2-aminophenol derivatives

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