Interconversion between Polymeric and Monomeric Forms of Oxovanadium(IV) Complexes with Tetradentate Schiff Base Ligands Derived from (R,R)-2,4-Pentanediamine

Ryuichi Kasahara, Masanobu Tsuchimoto, Shigeru Ohba, Kiyohiko Nakajima, Hiroyuki Ishida, Masaaki Kojima

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Abstract

New tetradentate Schiff base-oxovanadium(IV) complexes, [VO{3-Xsal-(R,R)-2,4-ptn}] (H2{3-Xsal(R,F)-2,4-ptn}: N,N'-di-3-Xsalicylidene-(R,R)-2,4-pentanediamine; X = EtO (ethoxy), MeO (methoxy), and H) were prepared and characterized. Only an orange polymeric form was obtained for the 3-methoxy and nonsubstituted (X = H) complexes. Both orange polymeric (1) and green monomeric (2) crystals were obtained for the 3-ethoxy substituted complex. X-ray structure analyses of 1 and 2 were carried out. Crystal data: [VO{3-EtOsal-(R,R)-2,4-ptn}]·H2O (1), VO6N2C23H30, orthorhombic, P212121, a = 13.764(4) Å,b = 21.544(4) Å, c = 7.682(5) Å, Z = 4; [VO{3-EtOsal-(R,R)-2,4-ptn}] (2), VO5N2C23H28, orthorhombic, P212121, a = 10.393(2) Å, b = 22.278(2) Å, c = 9.886(2) A, Z = 4. The orange crystals (1) have water of crystallization, and the complexes take a polynuclear linear chain structure (⋯V==O⋯V=O⋯) with a six-membered N-N chelate ring in a chair form. The green crystals (2) have no water of crystallization, and the complexes take a mononuclear square-pyramidal structure with a six-membered N-N chelate ring in a flattened boat form. Upon heating at 170 °C for 10 min, orange 1 turned to green 2, which reverted to orange 1 by suspension in water-acetonitrile. Mechanism of the interconversion between the polymeric and monomeric forms is discussed on the basis of their crystal structures.

Original languageEnglish
Pages (from-to)7661-7665
Number of pages5
JournalInorganic Chemistry
Volume35
Issue number26
Publication statusPublished - 1996

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Schiff Bases
imines
Ligands
Crystals
ligands
Crystallization
chelates
crystals
Water
crystallization
water
rings
boats
Boats
seats
acetonitrile
Suspensions
Crystal structure
Heating
X rays

ASJC Scopus subject areas

  • Inorganic Chemistry

Cite this

Interconversion between Polymeric and Monomeric Forms of Oxovanadium(IV) Complexes with Tetradentate Schiff Base Ligands Derived from (R,R)-2,4-Pentanediamine. / Kasahara, Ryuichi; Tsuchimoto, Masanobu; Ohba, Shigeru; Nakajima, Kiyohiko; Ishida, Hiroyuki; Kojima, Masaaki.

In: Inorganic Chemistry, Vol. 35, No. 26, 1996, p. 7661-7665.

Research output: Contribution to journalArticle

Kasahara, Ryuichi ; Tsuchimoto, Masanobu ; Ohba, Shigeru ; Nakajima, Kiyohiko ; Ishida, Hiroyuki ; Kojima, Masaaki. / Interconversion between Polymeric and Monomeric Forms of Oxovanadium(IV) Complexes with Tetradentate Schiff Base Ligands Derived from (R,R)-2,4-Pentanediamine. In: Inorganic Chemistry. 1996 ; Vol. 35, No. 26. pp. 7661-7665.
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title = "Interconversion between Polymeric and Monomeric Forms of Oxovanadium(IV) Complexes with Tetradentate Schiff Base Ligands Derived from (R,R)-2,4-Pentanediamine",
abstract = "New tetradentate Schiff base-oxovanadium(IV) complexes, [VO{3-Xsal-(R,R)-2,4-ptn}] (H2{3-Xsal(R,F)-2,4-ptn}: N,N'-di-3-Xsalicylidene-(R,R)-2,4-pentanediamine; X = EtO (ethoxy), MeO (methoxy), and H) were prepared and characterized. Only an orange polymeric form was obtained for the 3-methoxy and nonsubstituted (X = H) complexes. Both orange polymeric (1) and green monomeric (2) crystals were obtained for the 3-ethoxy substituted complex. X-ray structure analyses of 1 and 2 were carried out. Crystal data: [VO{3-EtOsal-(R,R)-2,4-ptn}]·H2O (1), VO6N2C23H30, orthorhombic, P212121, a = 13.764(4) {\AA},b = 21.544(4) {\AA}, c = 7.682(5) {\AA}, Z = 4; [VO{3-EtOsal-(R,R)-2,4-ptn}] (2), VO5N2C23H28, orthorhombic, P212121, a = 10.393(2) {\AA}, b = 22.278(2) {\AA}, c = 9.886(2) A, Z = 4. The orange crystals (1) have water of crystallization, and the complexes take a polynuclear linear chain structure (⋯V==O⋯V=O⋯) with a six-membered N-N chelate ring in a chair form. The green crystals (2) have no water of crystallization, and the complexes take a mononuclear square-pyramidal structure with a six-membered N-N chelate ring in a flattened boat form. Upon heating at 170 °C for 10 min, orange 1 turned to green 2, which reverted to orange 1 by suspension in water-acetonitrile. Mechanism of the interconversion between the polymeric and monomeric forms is discussed on the basis of their crystal structures.",
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T1 - Interconversion between Polymeric and Monomeric Forms of Oxovanadium(IV) Complexes with Tetradentate Schiff Base Ligands Derived from (R,R)-2,4-Pentanediamine

AU - Kasahara, Ryuichi

AU - Tsuchimoto, Masanobu

AU - Ohba, Shigeru

AU - Nakajima, Kiyohiko

AU - Ishida, Hiroyuki

AU - Kojima, Masaaki

PY - 1996

Y1 - 1996

N2 - New tetradentate Schiff base-oxovanadium(IV) complexes, [VO{3-Xsal-(R,R)-2,4-ptn}] (H2{3-Xsal(R,F)-2,4-ptn}: N,N'-di-3-Xsalicylidene-(R,R)-2,4-pentanediamine; X = EtO (ethoxy), MeO (methoxy), and H) were prepared and characterized. Only an orange polymeric form was obtained for the 3-methoxy and nonsubstituted (X = H) complexes. Both orange polymeric (1) and green monomeric (2) crystals were obtained for the 3-ethoxy substituted complex. X-ray structure analyses of 1 and 2 were carried out. Crystal data: [VO{3-EtOsal-(R,R)-2,4-ptn}]·H2O (1), VO6N2C23H30, orthorhombic, P212121, a = 13.764(4) Å,b = 21.544(4) Å, c = 7.682(5) Å, Z = 4; [VO{3-EtOsal-(R,R)-2,4-ptn}] (2), VO5N2C23H28, orthorhombic, P212121, a = 10.393(2) Å, b = 22.278(2) Å, c = 9.886(2) A, Z = 4. The orange crystals (1) have water of crystallization, and the complexes take a polynuclear linear chain structure (⋯V==O⋯V=O⋯) with a six-membered N-N chelate ring in a chair form. The green crystals (2) have no water of crystallization, and the complexes take a mononuclear square-pyramidal structure with a six-membered N-N chelate ring in a flattened boat form. Upon heating at 170 °C for 10 min, orange 1 turned to green 2, which reverted to orange 1 by suspension in water-acetonitrile. Mechanism of the interconversion between the polymeric and monomeric forms is discussed on the basis of their crystal structures.

AB - New tetradentate Schiff base-oxovanadium(IV) complexes, [VO{3-Xsal-(R,R)-2,4-ptn}] (H2{3-Xsal(R,F)-2,4-ptn}: N,N'-di-3-Xsalicylidene-(R,R)-2,4-pentanediamine; X = EtO (ethoxy), MeO (methoxy), and H) were prepared and characterized. Only an orange polymeric form was obtained for the 3-methoxy and nonsubstituted (X = H) complexes. Both orange polymeric (1) and green monomeric (2) crystals were obtained for the 3-ethoxy substituted complex. X-ray structure analyses of 1 and 2 were carried out. Crystal data: [VO{3-EtOsal-(R,R)-2,4-ptn}]·H2O (1), VO6N2C23H30, orthorhombic, P212121, a = 13.764(4) Å,b = 21.544(4) Å, c = 7.682(5) Å, Z = 4; [VO{3-EtOsal-(R,R)-2,4-ptn}] (2), VO5N2C23H28, orthorhombic, P212121, a = 10.393(2) Å, b = 22.278(2) Å, c = 9.886(2) A, Z = 4. The orange crystals (1) have water of crystallization, and the complexes take a polynuclear linear chain structure (⋯V==O⋯V=O⋯) with a six-membered N-N chelate ring in a chair form. The green crystals (2) have no water of crystallization, and the complexes take a mononuclear square-pyramidal structure with a six-membered N-N chelate ring in a flattened boat form. Upon heating at 170 °C for 10 min, orange 1 turned to green 2, which reverted to orange 1 by suspension in water-acetonitrile. Mechanism of the interconversion between the polymeric and monomeric forms is discussed on the basis of their crystal structures.

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