CobaltMaghrebV1, PascalFrancis, Curation, bibRecord, 000205

Synthesis, Characterization and Electrochemical Behavior of CoII, NiII and CdII Complexes with N202 Donor Ligands Derived from 4,4'-Diaminobiphenyl and 2-Hydroxybenzaldehyde or 2,4-Dihydroxybenzaldehyde

Identifieur interne : 000205 ( PascalFrancis/Curation ); précédent : 000204; suivant : 000206

Synthesis, Characterization and Electrochemical Behavior of CoII, NiII and CdII Complexes with N202 Donor Ligands Derived from 4,4'-Diaminobiphenyl and 2-Hydroxybenzaldehyde or 2,4-Dihydroxybenzaldehyde

Auteurs : Lakhdar Sibous [Algérie] ; Embarek Bentouhami [Algérie] ; Amor Maïza [Algérie] ; Gilles M. Bouet [France] ; MUSTAYEEN AHMED KHAN [France]

Source :

Journal of solution chemistry [ 0095-9782 ] ; 2010.

RBID : Pascal:10-0289681

Descripteurs français

Pascal (Inist)
- Synthèse, Caractérisation, Electrochimie, Complexe de cobalt, Cobalt II, Complexe de nickel, Nickel II, Complexe de cadmium, Cadmium II, Voltammétrie cyclique, Condensation, Base Schiff, Chlorure.
Wicri :
- topic : Condensation.

English descriptors

KwdEn :
- Cadmium II, Cadmium complex, Characterization, Chlorides, Cobalt II, Cobalt complex, Condensation, Cyclic voltammetry, Electrochemistry, Nickel II, Nickel complex, Schiff base, Synthesis.

Abstract

The condensation of 2-hydroxybenzaldehyde or 2,4-dihydroxybenzaldehyde with 4,4'-diaminobiphenyl in absolute EtOH in a molar ratio 2:1 gave, respectively, the Schiff base ligands H₂L1 or H₂L2. The bases served as tetradentate ligands to coordinate Co^II, Ni^II and Co^II chlorides, leading to complexes where the metal:ligand ratio is 2:1. All of the compounds were characterized by elemental analysis, infrared, electronic and mass spectroscopy, ¹H-n.m.r. and d.s.c. The cyclic voltammograms of the ligands and their complexes in DMF are discussed.

A01	`01`	`1`		`@0 0095-9782`
A02	`01`			`@0 JSLCAG`
A03		`1`		`@0 J. solution chem.`
A05				`@2 39`
A06				`@2 4`
A08	`01`	`1`	`ENG`	`@1 Synthesis, Characterization and Electrochemical Behavior of Co^II, Ni^II and Cd^II Complexes with N₂0₂ Donor Ligands Derived from 4,4'-Diaminobiphenyl and 2-Hydroxybenzaldehyde or 2,4-Dihydroxybenzaldehyde`
A11	`01`	`1`		`@1 SIBOUS (Lakhdar)`
A11	`02`	`1`		`@1 BENTOUHAMI (Embarek)`
A11	`03`	`1`		`@1 MAÏZA (Amor)`
A11	`04`	`1`		`@1 BOUET (Gilles M.)`
A11	`05`	`1`		`@1 MUSTAYEEN AHMED KHAN`
A14	`01`			`@1 Département de Génie des Procédés, Faculté des Sciences de l'Ingénieur, Université Ferhat Abbas @2 Sétif 19000 @3 DZA @Z 1 aut. @Z 2 aut. @Z 3 aut.`
A14	`02`			`@1 Chimie de Coordination, Faculté de Pharmacie, Université d'Angers, 16 Boulevard Daviers @2 49045 Angers @3 FRA @Z 4 aut. @Z 5 aut.`
A20				`@1 511-521`
A21				`@1 2010`
A23	`01`			`@0 ENG`
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A44				`@0 0000 @1 © 2010 INIST-CNRS. All rights reserved.`
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A64	`01`	`1`		`@0 Journal of solution chemistry`
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C01	`01`		`ENG`	@0 The condensation of 2-hydroxybenzaldehyde or 2,4-dihydroxybenzaldehyde with 4,4'-diaminobiphenyl in absolute EtOH in a molar ratio 2:1 gave, respectively, the Schiff base ligands H₂L1 or H₂L2. The bases served as tetradentate ligands to coordinate Co^II, Ni^II and Co^II chlorides, leading to complexes where the metal:ligand ratio is 2:1. All of the compounds were characterized by elemental analysis, infrared, electronic and mass spectroscopy, ¹H-n.m.r. and d.s.c. The cyclic voltammograms of the ligands and their complexes in DMF are discussed.
C02	`01`	`X`		`@0 001C01B`
C02	`02`	`X`		`@0 001C01H`
C03	`01`	`X`	`FRE`	`@0 Synthèse @5 01`
C03	`01`	`X`	`ENG`	`@0 Synthesis @5 01`
C03	`01`	`X`	`SPA`	`@0 Síntesis @5 01`
C03	`02`	`X`	`FRE`	`@0 Caractérisation @5 02`
C03	`02`	`X`	`ENG`	`@0 Characterization @5 02`
C03	`02`	`X`	`SPA`	`@0 Caracterización @5 02`
C03	`03`	`X`	`FRE`	`@0 Electrochimie @5 03`
C03	`03`	`X`	`ENG`	`@0 Electrochemistry @5 03`
C03	`03`	`X`	`SPA`	`@0 Electroquímica @5 03`
C03	`04`	`X`	`FRE`	`@0 Complexe de cobalt @5 04`
C03	`04`	`X`	`ENG`	`@0 Cobalt complex @5 04`
C03	`04`	`X`	`SPA`	`@0 Cobalto complejo @5 04`
C03	`05`	`X`	`FRE`	`@0 Cobalt II @2 NC @5 05`
C03	`05`	`X`	`ENG`	`@0 Cobalt II @2 NC @5 05`
C03	`05`	`X`	`SPA`	`@0 Cobalto II @2 NC @5 05`
C03	`06`	`X`	`FRE`	`@0 Complexe de nickel @5 06`
C03	`06`	`X`	`ENG`	`@0 Nickel complex @5 06`
C03	`06`	`X`	`SPA`	`@0 Níquel complejo @5 06`
C03	`07`	`X`	`FRE`	`@0 Nickel II @2 NC @5 07`
C03	`07`	`X`	`ENG`	`@0 Nickel II @2 NC @5 07`
C03	`07`	`X`	`SPA`	`@0 Niquel II @2 NC @5 07`
C03	`08`	`X`	`FRE`	`@0 Complexe de cadmium @5 08`
C03	`08`	`X`	`ENG`	`@0 Cadmium complex @5 08`
C03	`08`	`X`	`SPA`	`@0 Cadmio complejo @5 08`
C03	`09`	`X`	`FRE`	`@0 Cadmium II @2 NC @5 09`
C03	`09`	`X`	`ENG`	`@0 Cadmium II @2 NC @5 09`
C03	`09`	`X`	`SPA`	`@0 Cadmio II @2 NC @5 09`
C03	`10`	`X`	`FRE`	`@0 Voltammétrie cyclique @5 10`
C03	`10`	`X`	`ENG`	`@0 Cyclic voltammetry @5 10`
C03	`10`	`X`	`SPA`	`@0 Voltametría cíclica @5 10`
C03	`11`	`X`	`FRE`	`@0 Condensation @5 11`
C03	`11`	`X`	`ENG`	`@0 Condensation @5 11`
C03	`11`	`X`	`SPA`	`@0 Condensación @5 11`
C03	`12`	`X`	`FRE`	`@0 Base Schiff @5 12`
C03	`12`	`X`	`ENG`	`@0 Schiff base @5 12`
C03	`12`	`X`	`SPA`	`@0 Base Schiff @5 12`
C03	`13`	`X`	`FRE`	`@0 Chlorure @2 NA @5 13`
C03	`13`	`X`	`ENG`	`@0 Chlorides @2 NA @5 13`
C03	`13`	`X`	`SPA`	`@0 Cloruro @2 NA @5 13`
N21				`@1 186`
N44	`01`			`@1 OTO`
N82				`@1 OTO`

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Le document en format XML

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 Complexes with N<sub>2</sub>
0<sub>2</sub>
 Donor Ligands Derived from 4,4'-Diaminobiphenyl and 2-Hydroxybenzaldehyde or 2,4-Dihydroxybenzaldehyde</title>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Synthesis, Characterization and Electrochemical Behavior of Co<sup>II</sup>
, Ni<sup>II</sup>
 and Cd<sup>II</sup>
 Complexes with N<sub>2</sub>
0<sub>2</sub>
 Donor Ligands Derived from 4,4'-Diaminobiphenyl and 2-Hydroxybenzaldehyde or 2,4-Dihydroxybenzaldehyde</title>
<author><name sortKey="Sibous, Lakhdar" sort="Sibous, Lakhdar" uniqKey="Sibous L" first="Lakhdar" last="Sibous">Lakhdar Sibous</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Département de Génie des Procédés, Faculté des Sciences de l'Ingénieur, Université Ferhat Abbas</s1>
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<author><name sortKey="Bentouhami, Embarek" sort="Bentouhami, Embarek" uniqKey="Bentouhami E" first="Embarek" last="Bentouhami">Embarek Bentouhami</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Département de Génie des Procédés, Faculté des Sciences de l'Ingénieur, Université Ferhat Abbas</s1>
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</author>
<author><name sortKey="Maiza, Amor" sort="Maiza, Amor" uniqKey="Maiza A" first="Amor" last="Maïza">Amor Maïza</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Département de Génie des Procédés, Faculté des Sciences de l'Ingénieur, Université Ferhat Abbas</s1>
<s2>Sétif 19000</s2>
<s3>DZA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
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<author><name sortKey="Bouet, Gilles M" sort="Bouet, Gilles M" uniqKey="Bouet G" first="Gilles M." last="Bouet">Gilles M. Bouet</name>
<affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Chimie de Coordination, Faculté de Pharmacie, Université d'Angers, 16 Boulevard Daviers</s1>
<s2>49045 Angers</s2>
<s3>FRA</s3>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>France</country>
</affiliation>
</author>
<author><name sortKey="Mustayeen Ahmed Khan" sort="Mustayeen Ahmed Khan" uniqKey="Mustayeen Ahmed Khan" last="Mustayeen Ahmed Khan">MUSTAYEEN AHMED KHAN</name>
<affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Chimie de Coordination, Faculté de Pharmacie, Université d'Angers, 16 Boulevard Daviers</s1>
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<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
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<series><title level="j" type="main">Journal of solution chemistry</title>
<title level="j" type="abbreviated">J. solution chem.</title>
<idno type="ISSN">0095-9782</idno>
<imprint><date when="2010">2010</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cadmium II</term>
<term>Cadmium complex</term>
<term>Characterization</term>
<term>Chlorides</term>
<term>Cobalt II</term>
<term>Cobalt complex</term>
<term>Condensation</term>
<term>Cyclic voltammetry</term>
<term>Electrochemistry</term>
<term>Nickel II</term>
<term>Nickel complex</term>
<term>Schiff base</term>
<term>Synthesis</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Synthèse</term>
<term>Caractérisation</term>
<term>Electrochimie</term>
<term>Complexe de cobalt</term>
<term>Cobalt II</term>
<term>Complexe de nickel</term>
<term>Nickel II</term>
<term>Complexe de cadmium</term>
<term>Cadmium II</term>
<term>Voltammétrie cyclique</term>
<term>Condensation</term>
<term>Base Schiff</term>
<term>Chlorure</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Condensation</term>
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<front><div type="abstract" xml:lang="en">The condensation of 2-hydroxybenzaldehyde or 2,4-dihydroxybenzaldehyde with 4,4'-diaminobiphenyl in absolute EtOH in a molar ratio 2:1 gave, respectively, the Schiff base ligands H<sub>2</sub>
L1 or H<sub>2</sub>
L2. The bases served as tetradentate ligands to coordinate Co<sup>II</sup>
, Ni<sup>II</sup>
 and Co<sup>II</sup>
 chlorides, leading to complexes where the metal:ligand ratio is 2:1. All of the compounds were characterized by elemental analysis, infrared, electronic and mass spectroscopy, <sup>1</sup>
H-n.m.r. and d.s.c. The cyclic voltammograms of the ligands and their complexes in DMF are discussed.</div>
</front>
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<fA08 i1="01" i2="1" l="ENG"><s1>Synthesis, Characterization and Electrochemical Behavior of Co<sup>II</sup>
, Ni<sup>II</sup>
 and Cd<sup>II</sup>
 Complexes with N<sub>2</sub>
0<sub>2</sub>
 Donor Ligands Derived from 4,4'-Diaminobiphenyl and 2-Hydroxybenzaldehyde or 2,4-Dihydroxybenzaldehyde</s1>
</fA08>
<fA11 i1="01" i2="1"><s1>SIBOUS (Lakhdar)</s1>
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<fA11 i1="02" i2="1"><s1>BENTOUHAMI (Embarek)</s1>
</fA11>
<fA11 i1="03" i2="1"><s1>MAÏZA (Amor)</s1>
</fA11>
<fA11 i1="04" i2="1"><s1>BOUET (Gilles M.)</s1>
</fA11>
<fA11 i1="05" i2="1"><s1>MUSTAYEEN AHMED KHAN</s1>
</fA11>
<fA14 i1="01"><s1>Département de Génie des Procédés, Faculté des Sciences de l'Ingénieur, Université Ferhat Abbas</s1>
<s2>Sétif 19000</s2>
<s3>DZA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</fA14>
<fA14 i1="02"><s1>Chimie de Coordination, Faculté de Pharmacie, Université d'Angers, 16 Boulevard Daviers</s1>
<s2>49045 Angers</s2>
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<sZ>5 aut.</sZ>
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<fC01 i1="01" l="ENG"><s0>The condensation of 2-hydroxybenzaldehyde or 2,4-dihydroxybenzaldehyde with 4,4'-diaminobiphenyl in absolute EtOH in a molar ratio 2:1 gave, respectively, the Schiff base ligands H<sub>2</sub>
L1 or H<sub>2</sub>
L2. The bases served as tetradentate ligands to coordinate Co<sup>II</sup>
, Ni<sup>II</sup>
 and Co<sup>II</sup>
 chlorides, leading to complexes where the metal:ligand ratio is 2:1. All of the compounds were characterized by elemental analysis, infrared, electronic and mass spectroscopy, <sup>1</sup>
H-n.m.r. and d.s.c. The cyclic voltammograms of the ligands and their complexes in DMF are discussed.</s0>
</fC01>
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</fC02>
<fC02 i1="02" i2="X"><s0>001C01H</s0>
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<fC03 i1="01" i2="X" l="FRE"><s0>Synthèse</s0>
<s5>01</s5>
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<fC03 i1="01" i2="X" l="ENG"><s0>Synthesis</s0>
<s5>01</s5>
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<fC03 i1="01" i2="X" l="SPA"><s0>Síntesis</s0>
<s5>01</s5>
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<fC03 i1="02" i2="X" l="FRE"><s0>Caractérisation</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG"><s0>Characterization</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA"><s0>Caracterización</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE"><s0>Electrochimie</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG"><s0>Electrochemistry</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Electroquímica</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Complexe de cobalt</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Cobalt complex</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA"><s0>Cobalto complejo</s0>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE"><s0>Cobalt II</s0>
<s2>NC</s2>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG"><s0>Cobalt II</s0>
<s2>NC</s2>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Cobalto II</s0>
<s2>NC</s2>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE"><s0>Complexe de nickel</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Nickel complex</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Níquel complejo</s0>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE"><s0>Nickel II</s0>
<s2>NC</s2>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG"><s0>Nickel II</s0>
<s2>NC</s2>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA"><s0>Niquel II</s0>
<s2>NC</s2>
<s5>07</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE"><s0>Complexe de cadmium</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG"><s0>Cadmium complex</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA"><s0>Cadmio complejo</s0>
<s5>08</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE"><s0>Cadmium II</s0>
<s2>NC</s2>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG"><s0>Cadmium II</s0>
<s2>NC</s2>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA"><s0>Cadmio II</s0>
<s2>NC</s2>
<s5>09</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE"><s0>Voltammétrie cyclique</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG"><s0>Cyclic voltammetry</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA"><s0>Voltametría cíclica</s0>
<s5>10</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE"><s0>Condensation</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG"><s0>Condensation</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA"><s0>Condensación</s0>
<s5>11</s5>
</fC03>
<fC03 i1="12" i2="X" l="FRE"><s0>Base Schiff</s0>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG"><s0>Schiff base</s0>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA"><s0>Base Schiff</s0>
<s5>12</s5>
</fC03>
<fC03 i1="13" i2="X" l="FRE"><s0>Chlorure</s0>
<s2>NA</s2>
<s5>13</s5>
</fC03>
<fC03 i1="13" i2="X" l="ENG"><s0>Chlorides</s0>
<s2>NA</s2>
<s5>13</s5>
</fC03>
<fC03 i1="13" i2="X" l="SPA"><s0>Cloruro</s0>
<s2>NA</s2>
<s5>13</s5>
</fC03>
<fN21><s1>186</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
</fN44>
<fN82><s1>OTO</s1>
</fN82>
</pA>
</standard>
</inist>
</record>

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Synthesis, Characterization and Electrochemical Behavior of CoII, NiII and CdII Complexes with N202 Donor Ligands Derived from 4,4'-Diaminobiphenyl and 2-Hydroxybenzaldehyde or 2,4-Dihydroxybenzaldehyde

Synthesis, Characterization and Electrochemical Behavior of CoII, NiII and CdII Complexes with N202 Donor Ligands Derived from 4,4'-Diaminobiphenyl and 2-Hydroxybenzaldehyde or 2,4-Dihydroxybenzaldehyde

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