Thermal dehydrogenation reacton of [N,N'-bis(3-ethoxysalicylidene)-1,2- diphenyl-1,2-ethanediaminato]nickel(II) with [VO(salen)]NO3 in the solid state

Gakuse Hoshina, Masanobu Tsuchimoto, Shigeru Ohba

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Abstract

A dehydrogenation reaction of the red-brown powder of [Ni(3-EtOsal-meso- stien)] (H2(3-EtOsal-meso-stien) = N,N'-bis(3-ethoxysalicylidene)- (R,S)(S,R)-1,2-diphenyl-1,2-ethanediamine) did not occur by heating solely in the air up to 210 °C. However, the reaction occurred upon heating together with [VO(salen)] (H2(salen) = N,N'-disalicylidene-1,2-ethane-diamine) in the air at 190 °C, and a red powder of [Ni(3-EtOsalton)] (H2(3-EtOsalton) =N,N'-bis(3-ethoxysalicylidene)- 1,2-diphenyl-1,2-ethenediamine) was obtained. The dehydrogenation reaction could also be carried out under Ar at 160 °C by mixing with [VO(salen)]NO3. These facts revealed that the oxidants in solid state dehydrogenation in air are the V(v) species originating from the v(IV)=O complex. The crystal structures of [Ni(3-EtOsal- meso-stien)]-CH3CN-H2O, (1); [Ni(3-EtOsal-rac-stien)] · 0.5H2O, (2); and [Ni(3-EtOsalton)] · CH3OH · 1.33H2O, (3) were determined by X-ray analyses. [Ni(3-EtOsalton)] was prepared in a dioxane solution of [Ni(3- EtOsalstien)] using DDQ (2,3-dichloro-5,6-dicyano-1,4- benzoquinone) as an oxidant. The rac complex, [Ni(3-EtOsal-rac-stien)] (H2(3-EtOsal-rac-stien) = N,N'-bis(3-ethoxy-salicylidene)-(R,R)(S,S)-1,2-diphenyl-1,2-ethanediamine), is less reactive in dehydrogenation than the meso in the solid state as well as in solution. The molecular structures in (1) and (2) indicate that the benzylic H atoms are sterically protected by phenyl groups in the rac complex, but are exposed to the oxidant in the meso complex.

Original languageEnglish
Pages (from-to)369-374
Number of pages6
JournalBulletin of the Chemical Society of Japan
Volume73
Issue number2
DOIs
Publication statusPublished - 2000 Feb

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ethylenediamine
Dehydrogenation
Nickel
Oxidants
Powders
Air
Heating
Molecular structure
Crystal structure
X rays
Atoms
disalicylaldehyde ethylenediamine
Hot Temperature
diphenyl

ASJC Scopus subject areas

  • Chemistry(all)

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Thermal dehydrogenation reacton of [N,N'-bis(3-ethoxysalicylidene)-1,2- diphenyl-1,2-ethanediaminato]nickel(II) with [VO(salen)]NO3 in the solid state. / Hoshina, Gakuse; Tsuchimoto, Masanobu; Ohba, Shigeru.

In: Bulletin of the Chemical Society of Japan, Vol. 73, No. 2, 02.2000, p. 369-374.

Research output: Contribution to journalArticle

@article{68e9ad7c4d2140f7a6ede929ffde1975,
title = "Thermal dehydrogenation reacton of [N,N'-bis(3-ethoxysalicylidene)-1,2- diphenyl-1,2-ethanediaminato]nickel(II) with [VO(salen)]NO3 in the solid state",
abstract = "A dehydrogenation reaction of the red-brown powder of [Ni(3-EtOsal-meso- stien)] (H2(3-EtOsal-meso-stien) = N,N'-bis(3-ethoxysalicylidene)- (R,S)(S,R)-1,2-diphenyl-1,2-ethanediamine) did not occur by heating solely in the air up to 210 °C. However, the reaction occurred upon heating together with [VO(salen)] (H2(salen) = N,N'-disalicylidene-1,2-ethane-diamine) in the air at 190 °C, and a red powder of [Ni(3-EtOsalton)] (H2(3-EtOsalton) =N,N'-bis(3-ethoxysalicylidene)- 1,2-diphenyl-1,2-ethenediamine) was obtained. The dehydrogenation reaction could also be carried out under Ar at 160 °C by mixing with [VO(salen)]NO3. These facts revealed that the oxidants in solid state dehydrogenation in air are the V(v) species originating from the v(IV)=O complex. The crystal structures of [Ni(3-EtOsal- meso-stien)]-CH3CN-H2O, (1); [Ni(3-EtOsal-rac-stien)] · 0.5H2O, (2); and [Ni(3-EtOsalton)] · CH3OH · 1.33H2O, (3) were determined by X-ray analyses. [Ni(3-EtOsalton)] was prepared in a dioxane solution of [Ni(3- EtOsalstien)] using DDQ (2,3-dichloro-5,6-dicyano-1,4- benzoquinone) as an oxidant. The rac complex, [Ni(3-EtOsal-rac-stien)] (H2(3-EtOsal-rac-stien) = N,N'-bis(3-ethoxy-salicylidene)-(R,R)(S,S)-1,2-diphenyl-1,2-ethanediamine), is less reactive in dehydrogenation than the meso in the solid state as well as in solution. The molecular structures in (1) and (2) indicate that the benzylic H atoms are sterically protected by phenyl groups in the rac complex, but are exposed to the oxidant in the meso complex.",
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T1 - Thermal dehydrogenation reacton of [N,N'-bis(3-ethoxysalicylidene)-1,2- diphenyl-1,2-ethanediaminato]nickel(II) with [VO(salen)]NO3 in the solid state

AU - Hoshina, Gakuse

AU - Tsuchimoto, Masanobu

AU - Ohba, Shigeru

PY - 2000/2

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N2 - A dehydrogenation reaction of the red-brown powder of [Ni(3-EtOsal-meso- stien)] (H2(3-EtOsal-meso-stien) = N,N'-bis(3-ethoxysalicylidene)- (R,S)(S,R)-1,2-diphenyl-1,2-ethanediamine) did not occur by heating solely in the air up to 210 °C. However, the reaction occurred upon heating together with [VO(salen)] (H2(salen) = N,N'-disalicylidene-1,2-ethane-diamine) in the air at 190 °C, and a red powder of [Ni(3-EtOsalton)] (H2(3-EtOsalton) =N,N'-bis(3-ethoxysalicylidene)- 1,2-diphenyl-1,2-ethenediamine) was obtained. The dehydrogenation reaction could also be carried out under Ar at 160 °C by mixing with [VO(salen)]NO3. These facts revealed that the oxidants in solid state dehydrogenation in air are the V(v) species originating from the v(IV)=O complex. The crystal structures of [Ni(3-EtOsal- meso-stien)]-CH3CN-H2O, (1); [Ni(3-EtOsal-rac-stien)] · 0.5H2O, (2); and [Ni(3-EtOsalton)] · CH3OH · 1.33H2O, (3) were determined by X-ray analyses. [Ni(3-EtOsalton)] was prepared in a dioxane solution of [Ni(3- EtOsalstien)] using DDQ (2,3-dichloro-5,6-dicyano-1,4- benzoquinone) as an oxidant. The rac complex, [Ni(3-EtOsal-rac-stien)] (H2(3-EtOsal-rac-stien) = N,N'-bis(3-ethoxy-salicylidene)-(R,R)(S,S)-1,2-diphenyl-1,2-ethanediamine), is less reactive in dehydrogenation than the meso in the solid state as well as in solution. The molecular structures in (1) and (2) indicate that the benzylic H atoms are sterically protected by phenyl groups in the rac complex, but are exposed to the oxidant in the meso complex.

AB - A dehydrogenation reaction of the red-brown powder of [Ni(3-EtOsal-meso- stien)] (H2(3-EtOsal-meso-stien) = N,N'-bis(3-ethoxysalicylidene)- (R,S)(S,R)-1,2-diphenyl-1,2-ethanediamine) did not occur by heating solely in the air up to 210 °C. However, the reaction occurred upon heating together with [VO(salen)] (H2(salen) = N,N'-disalicylidene-1,2-ethane-diamine) in the air at 190 °C, and a red powder of [Ni(3-EtOsalton)] (H2(3-EtOsalton) =N,N'-bis(3-ethoxysalicylidene)- 1,2-diphenyl-1,2-ethenediamine) was obtained. The dehydrogenation reaction could also be carried out under Ar at 160 °C by mixing with [VO(salen)]NO3. These facts revealed that the oxidants in solid state dehydrogenation in air are the V(v) species originating from the v(IV)=O complex. The crystal structures of [Ni(3-EtOsal- meso-stien)]-CH3CN-H2O, (1); [Ni(3-EtOsal-rac-stien)] · 0.5H2O, (2); and [Ni(3-EtOsalton)] · CH3OH · 1.33H2O, (3) were determined by X-ray analyses. [Ni(3-EtOsalton)] was prepared in a dioxane solution of [Ni(3- EtOsalstien)] using DDQ (2,3-dichloro-5,6-dicyano-1,4- benzoquinone) as an oxidant. The rac complex, [Ni(3-EtOsal-rac-stien)] (H2(3-EtOsal-rac-stien) = N,N'-bis(3-ethoxy-salicylidene)-(R,R)(S,S)-1,2-diphenyl-1,2-ethanediamine), is less reactive in dehydrogenation than the meso in the solid state as well as in solution. The molecular structures in (1) and (2) indicate that the benzylic H atoms are sterically protected by phenyl groups in the rac complex, but are exposed to the oxidant in the meso complex.

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