Synthesis and characterization of ruthenium(II)-pyridylamine complexes with catechol pendants as metal binding sites

Takahiko Kojima, Norihisa Hirasa, Daisuke Noguchi, Tomoya Ishizuka, Soushi Miyazaki, Yoshihito Shiota, Kazunari Yoshizawa, Shunichi Fukuzumi

研究成果: ジャーナルへの寄稿記事

10 引用 (Scopus)

抄録

A novel tris(2-pyridylmethyl)amine (TPA) derivate having two catechol moieties linked by amide linkages at the 6-positions of two pyridyl groups was synthesized. The ligand, N,N-bis[6-{3,4-(dihydroxy)benzamide}-2-pyridyl-methyl]- N-(2-pyridylmethyl)amine (Cat2-TPA; L2), and its precursor, N,N-bis[6-{3,4-bis(benzyloxy)-benzamide}-2-pyridyl-methyl]-N-(2-pyridylmethyl) -amine ((Bn2Cat)2-TPA; L1), formed stable ruthenium(II) complexes, [RuCl(L2)]PF6 (2) and [RuCl(L1)]PF6 (1), respectively. The crystal structure of [RuCl(L2)]Cl (2′) was determined by X-ray crystallography to show two isomers in terms of the orientation of one catechol moiety. In complex 2, the ligand bearing catechols acts as a pentadentate ligand involving coordination of one of the amide oxygen atoms in addition to that of the tetradentate TPA moiety and two metal-free catechol moieties as metal-binding sites. The coordination of L2 results in the preorganization of the two catechols to converge them to undergo intramolecular π-π interactions. The 1H NMR spectrum of 2 in DMSO-d 6 revealed that only one isomer was present in the solution. This selective formation could be ascribed to the formation of an intramolecular hydrogen-bonding network among the hydroxyl groups of the catechol moieties, as suggested by X-ray analysis. This intramolecular hydrogen bonding could differentiate the pKa values of the hydroxy groups of the catechol moieties into three kinds, as indicated by spectroscopic titration with tetramethylammonium hydroxide (TMAOH) in DMF. The complexation of 2 with other metal ions was also examined. The reaction of 2 with [Cu(NO3) 2(TMEDA)] (TMEDA = N,N,N′,N′-tetramethylethylenediamine) in methanol allowed us to observe the selective formation of a binuclear complex, [RuCl(L22-){Cu(TMEDA)}]PF6 (3), which was characterized by ESI-MS, UV-vis, and ESR spectroscopies. Its ESR spectrum in methanol suggested that the coordination of the Cu(II)-TMEDA unit to the converged catechol moieties would be different from conventional κ2-O,O′:η2-coordination: it exhibits a novel bridging coordination mode, bis-κ1-O:η1- coordination, to form the binuclear Ru(II)-Cu(II) complex.

元の言語英語
ページ(範囲)3737-3745
ページ数9
ジャーナルInorganic Chemistry
49
発行部数8
DOI
出版物ステータス出版済み - 4 19 2010

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Ruthenium
ruthenium
Metals
Binding Sites
synthesis
Catechols
metals
amines
Ligands
Amides
Isomers
amides
ligands
Amines
Paramagnetic resonance
Methanol
Hydrogen bonds
Bearings (structural)
isomers
methyl alcohol

All Science Journal Classification (ASJC) codes

  • Physical and Theoretical Chemistry
  • Inorganic Chemistry

これを引用

Synthesis and characterization of ruthenium(II)-pyridylamine complexes with catechol pendants as metal binding sites. / Kojima, Takahiko; Hirasa, Norihisa; Noguchi, Daisuke; Ishizuka, Tomoya; Miyazaki, Soushi; Shiota, Yoshihito; Yoshizawa, Kazunari; Fukuzumi, Shunichi.

:: Inorganic Chemistry, 巻 49, 番号 8, 19.04.2010, p. 3737-3745.

研究成果: ジャーナルへの寄稿記事

Kojima, Takahiko ; Hirasa, Norihisa ; Noguchi, Daisuke ; Ishizuka, Tomoya ; Miyazaki, Soushi ; Shiota, Yoshihito ; Yoshizawa, Kazunari ; Fukuzumi, Shunichi. / Synthesis and characterization of ruthenium(II)-pyridylamine complexes with catechol pendants as metal binding sites. :: Inorganic Chemistry. 2010 ; 巻 49, 番号 8. pp. 3737-3745.
@article{25ce3660943646d6ab54f8cf14af42b7,
title = "Synthesis and characterization of ruthenium(II)-pyridylamine complexes with catechol pendants as metal binding sites",
abstract = "A novel tris(2-pyridylmethyl)amine (TPA) derivate having two catechol moieties linked by amide linkages at the 6-positions of two pyridyl groups was synthesized. The ligand, N,N-bis[6-{3,4-(dihydroxy)benzamide}-2-pyridyl-methyl]- N-(2-pyridylmethyl)amine (Cat2-TPA; L2), and its precursor, N,N-bis[6-{3,4-bis(benzyloxy)-benzamide}-2-pyridyl-methyl]-N-(2-pyridylmethyl) -amine ((Bn2Cat)2-TPA; L1), formed stable ruthenium(II) complexes, [RuCl(L2)]PF6 (2) and [RuCl(L1)]PF6 (1), respectively. The crystal structure of [RuCl(L2)]Cl (2′) was determined by X-ray crystallography to show two isomers in terms of the orientation of one catechol moiety. In complex 2, the ligand bearing catechols acts as a pentadentate ligand involving coordination of one of the amide oxygen atoms in addition to that of the tetradentate TPA moiety and two metal-free catechol moieties as metal-binding sites. The coordination of L2 results in the preorganization of the two catechols to converge them to undergo intramolecular π-π interactions. The 1H NMR spectrum of 2 in DMSO-d 6 revealed that only one isomer was present in the solution. This selective formation could be ascribed to the formation of an intramolecular hydrogen-bonding network among the hydroxyl groups of the catechol moieties, as suggested by X-ray analysis. This intramolecular hydrogen bonding could differentiate the pKa values of the hydroxy groups of the catechol moieties into three kinds, as indicated by spectroscopic titration with tetramethylammonium hydroxide (TMAOH) in DMF. The complexation of 2 with other metal ions was also examined. The reaction of 2 with [Cu(NO3) 2(TMEDA)] (TMEDA = N,N,N′,N′-tetramethylethylenediamine) in methanol allowed us to observe the selective formation of a binuclear complex, [RuCl(L22-){Cu(TMEDA)}]PF6 (3), which was characterized by ESI-MS, UV-vis, and ESR spectroscopies. Its ESR spectrum in methanol suggested that the coordination of the Cu(II)-TMEDA unit to the converged catechol moieties would be different from conventional κ2-O,O′:η2-coordination: it exhibits a novel bridging coordination mode, bis-κ1-O:η1- coordination, to form the binuclear Ru(II)-Cu(II) complex.",
author = "Takahiko Kojima and Norihisa Hirasa and Daisuke Noguchi and Tomoya Ishizuka and Soushi Miyazaki and Yoshihito Shiota and Kazunari Yoshizawa and Shunichi Fukuzumi",
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T1 - Synthesis and characterization of ruthenium(II)-pyridylamine complexes with catechol pendants as metal binding sites

AU - Kojima, Takahiko

AU - Hirasa, Norihisa

AU - Noguchi, Daisuke

AU - Ishizuka, Tomoya

AU - Miyazaki, Soushi

AU - Shiota, Yoshihito

AU - Yoshizawa, Kazunari

AU - Fukuzumi, Shunichi

PY - 2010/4/19

Y1 - 2010/4/19

N2 - A novel tris(2-pyridylmethyl)amine (TPA) derivate having two catechol moieties linked by amide linkages at the 6-positions of two pyridyl groups was synthesized. The ligand, N,N-bis[6-{3,4-(dihydroxy)benzamide}-2-pyridyl-methyl]- N-(2-pyridylmethyl)amine (Cat2-TPA; L2), and its precursor, N,N-bis[6-{3,4-bis(benzyloxy)-benzamide}-2-pyridyl-methyl]-N-(2-pyridylmethyl) -amine ((Bn2Cat)2-TPA; L1), formed stable ruthenium(II) complexes, [RuCl(L2)]PF6 (2) and [RuCl(L1)]PF6 (1), respectively. The crystal structure of [RuCl(L2)]Cl (2′) was determined by X-ray crystallography to show two isomers in terms of the orientation of one catechol moiety. In complex 2, the ligand bearing catechols acts as a pentadentate ligand involving coordination of one of the amide oxygen atoms in addition to that of the tetradentate TPA moiety and two metal-free catechol moieties as metal-binding sites. The coordination of L2 results in the preorganization of the two catechols to converge them to undergo intramolecular π-π interactions. The 1H NMR spectrum of 2 in DMSO-d 6 revealed that only one isomer was present in the solution. This selective formation could be ascribed to the formation of an intramolecular hydrogen-bonding network among the hydroxyl groups of the catechol moieties, as suggested by X-ray analysis. This intramolecular hydrogen bonding could differentiate the pKa values of the hydroxy groups of the catechol moieties into three kinds, as indicated by spectroscopic titration with tetramethylammonium hydroxide (TMAOH) in DMF. The complexation of 2 with other metal ions was also examined. The reaction of 2 with [Cu(NO3) 2(TMEDA)] (TMEDA = N,N,N′,N′-tetramethylethylenediamine) in methanol allowed us to observe the selective formation of a binuclear complex, [RuCl(L22-){Cu(TMEDA)}]PF6 (3), which was characterized by ESI-MS, UV-vis, and ESR spectroscopies. Its ESR spectrum in methanol suggested that the coordination of the Cu(II)-TMEDA unit to the converged catechol moieties would be different from conventional κ2-O,O′:η2-coordination: it exhibits a novel bridging coordination mode, bis-κ1-O:η1- coordination, to form the binuclear Ru(II)-Cu(II) complex.

AB - A novel tris(2-pyridylmethyl)amine (TPA) derivate having two catechol moieties linked by amide linkages at the 6-positions of two pyridyl groups was synthesized. The ligand, N,N-bis[6-{3,4-(dihydroxy)benzamide}-2-pyridyl-methyl]- N-(2-pyridylmethyl)amine (Cat2-TPA; L2), and its precursor, N,N-bis[6-{3,4-bis(benzyloxy)-benzamide}-2-pyridyl-methyl]-N-(2-pyridylmethyl) -amine ((Bn2Cat)2-TPA; L1), formed stable ruthenium(II) complexes, [RuCl(L2)]PF6 (2) and [RuCl(L1)]PF6 (1), respectively. The crystal structure of [RuCl(L2)]Cl (2′) was determined by X-ray crystallography to show two isomers in terms of the orientation of one catechol moiety. In complex 2, the ligand bearing catechols acts as a pentadentate ligand involving coordination of one of the amide oxygen atoms in addition to that of the tetradentate TPA moiety and two metal-free catechol moieties as metal-binding sites. The coordination of L2 results in the preorganization of the two catechols to converge them to undergo intramolecular π-π interactions. The 1H NMR spectrum of 2 in DMSO-d 6 revealed that only one isomer was present in the solution. This selective formation could be ascribed to the formation of an intramolecular hydrogen-bonding network among the hydroxyl groups of the catechol moieties, as suggested by X-ray analysis. This intramolecular hydrogen bonding could differentiate the pKa values of the hydroxy groups of the catechol moieties into three kinds, as indicated by spectroscopic titration with tetramethylammonium hydroxide (TMAOH) in DMF. The complexation of 2 with other metal ions was also examined. The reaction of 2 with [Cu(NO3) 2(TMEDA)] (TMEDA = N,N,N′,N′-tetramethylethylenediamine) in methanol allowed us to observe the selective formation of a binuclear complex, [RuCl(L22-){Cu(TMEDA)}]PF6 (3), which was characterized by ESI-MS, UV-vis, and ESR spectroscopies. Its ESR spectrum in methanol suggested that the coordination of the Cu(II)-TMEDA unit to the converged catechol moieties would be different from conventional κ2-O,O′:η2-coordination: it exhibits a novel bridging coordination mode, bis-κ1-O:η1- coordination, to form the binuclear Ru(II)-Cu(II) complex.

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