Synthesis, structure, and thermal behavior of discrete Co(II), Ag(I), and Pd(II) complexes with 2,3-bis(2-pyridyl)quinoxaline. Insight into coordination modes

Ok Sang Jung; Sung Ho Park; Yun Ju Kim; Young A. Lee; Ho G. Jang; Uk Lee

doi:10.1016/S0020-1693(00)00346-7

Synthesis, structure, and thermal behavior of discrete Co(II), Ag(I), and Pd(II) complexes with 2,3-bis(2-pyridyl)quinoxaline. Insight into coordination modes

Ok Sang Jung, Sung Ho Park, Yun Ju Kim, Young A. Lee, Ho G. Jang, Uk Lee

College of Science

Research output: Contribution to journal › Article

23 Citations (Scopus)

Abstract

The reactions of 2,3-bis(2-pyridyl)quinoxaline (bpq) with CoCl₂·6H₂O, Ag(CH₃CN)₄)BF₄, and PdCl₂(C₆H₅CN)₂ produce [CoCl₂(bpq)]₂·2CHCl₃, [Ag(bpq)CH₃CN]₂(BF₄)₂· 2CH₃CN, and [PdCl₂(bpq)], respectively. All the products are discrete 1:1 (metal:bpq) adducts, where the chelation mode of the bpq is dependent upon the metal atoms. The structure of [CoCl₂(bpq)]₂·2CHCl₃ is a centrosymmetric Cl-bridged four-membered dimer, [Co₂Cl₂], in which the bpq is bonded to the cobalt(II) atom in an anisobidentate mode with the nitrogen donors of pyridine and pyrazine rings. For [Ag(bpq)CH₃CN]₂(BF₄)₂· 2CH₃CN, each bpq ligand connects two tetrahedral silver(I) ions in a tridentate mode, resulting in a cationic cyclic dimer. The structure of [PdCl₂(bpq)] approximates to a molecular rocking chair with an isobidentate bpq through the nitrogen donors of 2-pyridyl rings. The compounds exhibit significant and characteristic relationships between the structures and their thermal properties. For [CoCl₂(bpq)]₂·2CHCl₃, the solvate chloroform molecules are safely contained up to 144°C, but drastically evaporate above this temperature. The striking feature of [Ag(bpq)CH₃CN]₂(BF₄)₂· 2CH₃CN is that the skeletal cyclic dimer is basically retained after dissociation of the coordinated acetonitriles in the solid state.

Original language	English
Pages (from-to)	93-99
Number of pages	7
Journal	Inorganica Chimica Acta
Volume	312
Issue number	1-2
DOIs	https://doi.org/10.1016/S0020-1693(00)00346-7
Publication status	Published - 2001 Jan 29

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Keywords

2,3-Bis(2-pyridyl)quinoxaline complexes
Crystal structures
Thermal properties

ASJC Scopus subject areas

Physical and Theoretical Chemistry
Inorganic Chemistry
Materials Chemistry

Cite this

Jung, O. S., Park, S. H., Kim, Y. J., Lee, Y. A., Jang, H. G., & Lee, U. (2001). Synthesis, structure, and thermal behavior of discrete Co(II), Ag(I), and Pd(II) complexes with 2,3-bis(2-pyridyl)quinoxaline. Insight into coordination modes. Inorganica Chimica Acta, 312(1-2), 93-99. https://doi.org/10.1016/S0020-1693(00)00346-7

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title = "Synthesis, structure, and thermal behavior of discrete Co(II), Ag(I), and Pd(II) complexes with 2,3-bis(2-pyridyl)quinoxaline. Insight into coordination modes",

abstract = "The reactions of 2,3-bis(2-pyridyl)quinoxaline (bpq) with CoCl2·6H2O, Ag(CH3CN)4)BF4, and PdCl2(C6H5CN)2 produce [CoCl2(bpq)]2·2CHCl3, [Ag(bpq)CH3CN]2(BF4)2· 2CH3CN, and [PdCl2(bpq)], respectively. All the products are discrete 1:1 (metal:bpq) adducts, where the chelation mode of the bpq is dependent upon the metal atoms. The structure of [CoCl2(bpq)]2·2CHCl3 is a centrosymmetric Cl-bridged four-membered dimer, [Co2Cl2], in which the bpq is bonded to the cobalt(II) atom in an anisobidentate mode with the nitrogen donors of pyridine and pyrazine rings. For [Ag(bpq)CH3CN]2(BF4)2· 2CH3CN, each bpq ligand connects two tetrahedral silver(I) ions in a tridentate mode, resulting in a cationic cyclic dimer. The structure of [PdCl2(bpq)] approximates to a molecular rocking chair with an isobidentate bpq through the nitrogen donors of 2-pyridyl rings. The compounds exhibit significant and characteristic relationships between the structures and their thermal properties. For [CoCl2(bpq)]2·2CHCl3, the solvate chloroform molecules are safely contained up to 144°C, but drastically evaporate above this temperature. The striking feature of [Ag(bpq)CH3CN]2(BF4)2· 2CH3CN is that the skeletal cyclic dimer is basically retained after dissociation of the coordinated acetonitriles in the solid state.",

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author = "Jung, {Ok Sang} and Park, {Sung Ho} and Kim, {Yun Ju} and Lee, {Young A.} and Jang, {Ho G.} and Uk Lee",

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T1 - Synthesis, structure, and thermal behavior of discrete Co(II), Ag(I), and Pd(II) complexes with 2,3-bis(2-pyridyl)quinoxaline. Insight into coordination modes

AU - Jung, Ok Sang

AU - Park, Sung Ho

AU - Kim, Yun Ju

AU - Lee, Young A.

AU - Jang, Ho G.

AU - Lee, Uk

PY - 2001/1/29

Y1 - 2001/1/29

N2 - The reactions of 2,3-bis(2-pyridyl)quinoxaline (bpq) with CoCl2·6H2O, Ag(CH3CN)4)BF4, and PdCl2(C6H5CN)2 produce [CoCl2(bpq)]2·2CHCl3, [Ag(bpq)CH3CN]2(BF4)2· 2CH3CN, and [PdCl2(bpq)], respectively. All the products are discrete 1:1 (metal:bpq) adducts, where the chelation mode of the bpq is dependent upon the metal atoms. The structure of [CoCl2(bpq)]2·2CHCl3 is a centrosymmetric Cl-bridged four-membered dimer, [Co2Cl2], in which the bpq is bonded to the cobalt(II) atom in an anisobidentate mode with the nitrogen donors of pyridine and pyrazine rings. For [Ag(bpq)CH3CN]2(BF4)2· 2CH3CN, each bpq ligand connects two tetrahedral silver(I) ions in a tridentate mode, resulting in a cationic cyclic dimer. The structure of [PdCl2(bpq)] approximates to a molecular rocking chair with an isobidentate bpq through the nitrogen donors of 2-pyridyl rings. The compounds exhibit significant and characteristic relationships between the structures and their thermal properties. For [CoCl2(bpq)]2·2CHCl3, the solvate chloroform molecules are safely contained up to 144°C, but drastically evaporate above this temperature. The striking feature of [Ag(bpq)CH3CN]2(BF4)2· 2CH3CN is that the skeletal cyclic dimer is basically retained after dissociation of the coordinated acetonitriles in the solid state.

AB - The reactions of 2,3-bis(2-pyridyl)quinoxaline (bpq) with CoCl2·6H2O, Ag(CH3CN)4)BF4, and PdCl2(C6H5CN)2 produce [CoCl2(bpq)]2·2CHCl3, [Ag(bpq)CH3CN]2(BF4)2· 2CH3CN, and [PdCl2(bpq)], respectively. All the products are discrete 1:1 (metal:bpq) adducts, where the chelation mode of the bpq is dependent upon the metal atoms. The structure of [CoCl2(bpq)]2·2CHCl3 is a centrosymmetric Cl-bridged four-membered dimer, [Co2Cl2], in which the bpq is bonded to the cobalt(II) atom in an anisobidentate mode with the nitrogen donors of pyridine and pyrazine rings. For [Ag(bpq)CH3CN]2(BF4)2· 2CH3CN, each bpq ligand connects two tetrahedral silver(I) ions in a tridentate mode, resulting in a cationic cyclic dimer. The structure of [PdCl2(bpq)] approximates to a molecular rocking chair with an isobidentate bpq through the nitrogen donors of 2-pyridyl rings. The compounds exhibit significant and characteristic relationships between the structures and their thermal properties. For [CoCl2(bpq)]2·2CHCl3, the solvate chloroform molecules are safely contained up to 144°C, but drastically evaporate above this temperature. The striking feature of [Ag(bpq)CH3CN]2(BF4)2· 2CH3CN is that the skeletal cyclic dimer is basically retained after dissociation of the coordinated acetonitriles in the solid state.

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KW - Thermal properties

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10.1016/S0020-1693(00)00346-7