Heterodinuclear CuIIPbII and CuIIMII (M = Mn, Fe, Co, Ni, Cu, Zn) Complexes of Macrocycles with Dissimilar 4- and 5-Coordination Sites: Synthesis, Structures, and Properties

Hisashi Ōkawa, Jun Nishio, Masaaki Ohba, Makoto Tadokoro, Naohide Matsumoto, Masayuki Koikawa, Sigeo Kida, David E. Fenton

研究成果: ジャーナルへの寄稿記事

157 引用 (Scopus)

抄録

Heterodinucleating macrocycles with two 2,6-bis(iminomethyl)-4-methylphenolate entities combined through two lateral chains, -(CH2)2- and -(CH2)mNH(CH2)m-(m = 2,3), at the imino nitrogens have been prepared as CuIIPbII complexes of the formula [CuPb(L)]XY (L2− = L1 for m = 2 and L2 for m = 3; XY = (C1O4)2, (NO3)(PF6), (AcO)(BPh4)). [CuPb(L1)](AcO)(BPh4)·DMF crystallizes in the monoclinic crystal system, space group P21/n, with Z = 4, a = 18.890(3) Å, b = 19.968(3) Å, c = 12.704(2) Å, β = 91.61(1)°, and F= 4790(1) Å3. The refinement converges with R = 0.0697 and Rw = 0.0863 for 4945 reflections with |F| > 3σ-(|Fo|). The crystal consists of a dimeric cation {CuPb(L1)(Ac)}22+ bridged by acetate groups, tetraphenylborate ions, and DMF molecules. The Cu is located at the 4-coordination site formed with the ethylene chain and assumes a planar environment. The Pb is at the 5-coordination site formed with the -(CH2)2NH(CH2)2- chain and assumes an eight-coordinate structure also involving three acetate oxygen atoms. The Cu- -Pb separation, bridged by two phenolic oxygens, is 3.577(2) Å. In the crystal, the dimeric cations further interact through out-of-plane bonding between the {CUN2O2} entities forming a column along the a axis. The [CuPb(Ll)]XY complexes react with metal(II) sulfates to form a series of CuIIMII complexes, [CuM(L1)]XY (M = Mn, Fe, Co, Ni, Cu, Zn). [CuMn(L1)](AcO)(BPh4) crystallizes in the monoclinic space group P21/n, with Z = 4, a = 17.508(8) Å, b = 15.539(5) Å, c = 16.515(5) Å, β= 106.30(3)°, and V = 4312(3) Å3. The refinement converges with R = 0.0689 and Rw = 0.0563 for 2935 reflections with |Fo| > 3σ(|Fo|). The Cu(II) and Mn(II) ions reside at the 4- and 5-coordination sites of the macrocycle, respectively, and the acetate group bridges the two metal ions providing a nearly square-pyramidal geometry for the Cu and a highly distorted six-coordinate environment for the Mn. The Cu-Mn separation is 3.122(2) Å. The cryomagnetic investigations (4.2–300 K) for the CuMn, CuFe, CuCo, CuNi, and CuCu complexes reveal the operation of an antiferromagnetic spin-exchange interaction within each molecule. The cyclic voltammograms of the CuM complexes show Cu(II)/Cu(I) reduction near −0.8 V (vs SCE) and oxidation at the ligand center near +1.3 V. The oxidation of the Fe(II) of the CuFe complex occurs at +0.64 V whereas the Mn(II) ion of the CuMn complex and the Co(II) ion of the CuCo complex are hardly oxidized.

元の言語英語
ページ(範囲)2949-2957
ページ数9
ジャーナルInorganic Chemistry
32
発行部数13
DOI
出版物ステータス出版済み - 1 1 1993

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Ions
acetates
Acetates
synthesis
Crystals
Cations
ions
Tetraphenylborate
Oxygen
crystals
cations
Oxidation
oxidation
Molecules
spin exchange
Exchange interactions
Sulfates
Metal ions
molecules
sulfates

All Science Journal Classification (ASJC) codes

  • Physical and Theoretical Chemistry
  • Inorganic Chemistry

これを引用

Heterodinuclear CuIIPbII and CuIIMII (M = Mn, Fe, Co, Ni, Cu, Zn) Complexes of Macrocycles with Dissimilar 4- and 5-Coordination Sites : Synthesis, Structures, and Properties. / Ōkawa, Hisashi; Nishio, Jun; Ohba, Masaaki; Tadokoro, Makoto; Matsumoto, Naohide; Koikawa, Masayuki; Kida, Sigeo; Fenton, David E.

:: Inorganic Chemistry, 巻 32, 番号 13, 01.01.1993, p. 2949-2957.

研究成果: ジャーナルへの寄稿記事

Ōkawa, Hisashi ; Nishio, Jun ; Ohba, Masaaki ; Tadokoro, Makoto ; Matsumoto, Naohide ; Koikawa, Masayuki ; Kida, Sigeo ; Fenton, David E. / Heterodinuclear CuIIPbII and CuIIMII (M = Mn, Fe, Co, Ni, Cu, Zn) Complexes of Macrocycles with Dissimilar 4- and 5-Coordination Sites : Synthesis, Structures, and Properties. :: Inorganic Chemistry. 1993 ; 巻 32, 番号 13. pp. 2949-2957.
@article{0a4450efbf534337bf68aab85c85b5b0,
title = "Heterodinuclear CuIIPbII and CuIIMII (M = Mn, Fe, Co, Ni, Cu, Zn) Complexes of Macrocycles with Dissimilar 4- and 5-Coordination Sites: Synthesis, Structures, and Properties",
abstract = "Heterodinucleating macrocycles with two 2,6-bis(iminomethyl)-4-methylphenolate entities combined through two lateral chains, -(CH2)2- and -(CH2)mNH(CH2)m-(m = 2,3), at the imino nitrogens have been prepared as CuIIPbII complexes of the formula [CuPb(L)]XY (L2− = L1 for m = 2 and L2 for m = 3; XY = (C1O4)2, (NO3)(PF6), (AcO)(BPh4)). [CuPb(L1)](AcO)(BPh4)·DMF crystallizes in the monoclinic crystal system, space group P21/n, with Z = 4, a = 18.890(3) {\AA}, b = 19.968(3) {\AA}, c = 12.704(2) {\AA}, β = 91.61(1)°, and F= 4790(1) {\AA}3. The refinement converges with R = 0.0697 and Rw = 0.0863 for 4945 reflections with |F| > 3σ-(|Fo|). The crystal consists of a dimeric cation {CuPb(L1)(Ac)}22+ bridged by acetate groups, tetraphenylborate ions, and DMF molecules. The Cu is located at the 4-coordination site formed with the ethylene chain and assumes a planar environment. The Pb is at the 5-coordination site formed with the -(CH2)2NH(CH2)2- chain and assumes an eight-coordinate structure also involving three acetate oxygen atoms. The Cu- -Pb separation, bridged by two phenolic oxygens, is 3.577(2) {\AA}. In the crystal, the dimeric cations further interact through out-of-plane bonding between the {CUN2O2} entities forming a column along the a axis. The [CuPb(Ll)]XY complexes react with metal(II) sulfates to form a series of CuIIMII complexes, [CuM(L1)]XY (M = Mn, Fe, Co, Ni, Cu, Zn). [CuMn(L1)](AcO)(BPh4) crystallizes in the monoclinic space group P21/n, with Z = 4, a = 17.508(8) {\AA}, b = 15.539(5) {\AA}, c = 16.515(5) {\AA}, β= 106.30(3)°, and V = 4312(3) {\AA}3. The refinement converges with R = 0.0689 and Rw = 0.0563 for 2935 reflections with |Fo| > 3σ(|Fo|). The Cu(II) and Mn(II) ions reside at the 4- and 5-coordination sites of the macrocycle, respectively, and the acetate group bridges the two metal ions providing a nearly square-pyramidal geometry for the Cu and a highly distorted six-coordinate environment for the Mn. The Cu-Mn separation is 3.122(2) {\AA}. The cryomagnetic investigations (4.2–300 K) for the CuMn, CuFe, CuCo, CuNi, and CuCu complexes reveal the operation of an antiferromagnetic spin-exchange interaction within each molecule. The cyclic voltammograms of the CuM complexes show Cu(II)/Cu(I) reduction near −0.8 V (vs SCE) and oxidation at the ligand center near +1.3 V. The oxidation of the Fe(II) of the CuFe complex occurs at +0.64 V whereas the Mn(II) ion of the CuMn complex and the Co(II) ion of the CuCo complex are hardly oxidized.",
author = "Hisashi Ōkawa and Jun Nishio and Masaaki Ohba and Makoto Tadokoro and Naohide Matsumoto and Masayuki Koikawa and Sigeo Kida and Fenton, {David E.}",
year = "1993",
month = "1",
day = "1",
doi = "10.1021/ic00065a025",
language = "English",
volume = "32",
pages = "2949--2957",
journal = "Inorganic Chemistry",
issn = "0020-1669",
publisher = "American Chemical Society",
number = "13",

}

TY - JOUR

T1 - Heterodinuclear CuIIPbII and CuIIMII (M = Mn, Fe, Co, Ni, Cu, Zn) Complexes of Macrocycles with Dissimilar 4- and 5-Coordination Sites

T2 - Synthesis, Structures, and Properties

AU - Ōkawa, Hisashi

AU - Nishio, Jun

AU - Ohba, Masaaki

AU - Tadokoro, Makoto

AU - Matsumoto, Naohide

AU - Koikawa, Masayuki

AU - Kida, Sigeo

AU - Fenton, David E.

PY - 1993/1/1

Y1 - 1993/1/1

N2 - Heterodinucleating macrocycles with two 2,6-bis(iminomethyl)-4-methylphenolate entities combined through two lateral chains, -(CH2)2- and -(CH2)mNH(CH2)m-(m = 2,3), at the imino nitrogens have been prepared as CuIIPbII complexes of the formula [CuPb(L)]XY (L2− = L1 for m = 2 and L2 for m = 3; XY = (C1O4)2, (NO3)(PF6), (AcO)(BPh4)). [CuPb(L1)](AcO)(BPh4)·DMF crystallizes in the monoclinic crystal system, space group P21/n, with Z = 4, a = 18.890(3) Å, b = 19.968(3) Å, c = 12.704(2) Å, β = 91.61(1)°, and F= 4790(1) Å3. The refinement converges with R = 0.0697 and Rw = 0.0863 for 4945 reflections with |F| > 3σ-(|Fo|). The crystal consists of a dimeric cation {CuPb(L1)(Ac)}22+ bridged by acetate groups, tetraphenylborate ions, and DMF molecules. The Cu is located at the 4-coordination site formed with the ethylene chain and assumes a planar environment. The Pb is at the 5-coordination site formed with the -(CH2)2NH(CH2)2- chain and assumes an eight-coordinate structure also involving three acetate oxygen atoms. The Cu- -Pb separation, bridged by two phenolic oxygens, is 3.577(2) Å. In the crystal, the dimeric cations further interact through out-of-plane bonding between the {CUN2O2} entities forming a column along the a axis. The [CuPb(Ll)]XY complexes react with metal(II) sulfates to form a series of CuIIMII complexes, [CuM(L1)]XY (M = Mn, Fe, Co, Ni, Cu, Zn). [CuMn(L1)](AcO)(BPh4) crystallizes in the monoclinic space group P21/n, with Z = 4, a = 17.508(8) Å, b = 15.539(5) Å, c = 16.515(5) Å, β= 106.30(3)°, and V = 4312(3) Å3. The refinement converges with R = 0.0689 and Rw = 0.0563 for 2935 reflections with |Fo| > 3σ(|Fo|). The Cu(II) and Mn(II) ions reside at the 4- and 5-coordination sites of the macrocycle, respectively, and the acetate group bridges the two metal ions providing a nearly square-pyramidal geometry for the Cu and a highly distorted six-coordinate environment for the Mn. The Cu-Mn separation is 3.122(2) Å. The cryomagnetic investigations (4.2–300 K) for the CuMn, CuFe, CuCo, CuNi, and CuCu complexes reveal the operation of an antiferromagnetic spin-exchange interaction within each molecule. The cyclic voltammograms of the CuM complexes show Cu(II)/Cu(I) reduction near −0.8 V (vs SCE) and oxidation at the ligand center near +1.3 V. The oxidation of the Fe(II) of the CuFe complex occurs at +0.64 V whereas the Mn(II) ion of the CuMn complex and the Co(II) ion of the CuCo complex are hardly oxidized.

AB - Heterodinucleating macrocycles with two 2,6-bis(iminomethyl)-4-methylphenolate entities combined through two lateral chains, -(CH2)2- and -(CH2)mNH(CH2)m-(m = 2,3), at the imino nitrogens have been prepared as CuIIPbII complexes of the formula [CuPb(L)]XY (L2− = L1 for m = 2 and L2 for m = 3; XY = (C1O4)2, (NO3)(PF6), (AcO)(BPh4)). [CuPb(L1)](AcO)(BPh4)·DMF crystallizes in the monoclinic crystal system, space group P21/n, with Z = 4, a = 18.890(3) Å, b = 19.968(3) Å, c = 12.704(2) Å, β = 91.61(1)°, and F= 4790(1) Å3. The refinement converges with R = 0.0697 and Rw = 0.0863 for 4945 reflections with |F| > 3σ-(|Fo|). The crystal consists of a dimeric cation {CuPb(L1)(Ac)}22+ bridged by acetate groups, tetraphenylborate ions, and DMF molecules. The Cu is located at the 4-coordination site formed with the ethylene chain and assumes a planar environment. The Pb is at the 5-coordination site formed with the -(CH2)2NH(CH2)2- chain and assumes an eight-coordinate structure also involving three acetate oxygen atoms. The Cu- -Pb separation, bridged by two phenolic oxygens, is 3.577(2) Å. In the crystal, the dimeric cations further interact through out-of-plane bonding between the {CUN2O2} entities forming a column along the a axis. The [CuPb(Ll)]XY complexes react with metal(II) sulfates to form a series of CuIIMII complexes, [CuM(L1)]XY (M = Mn, Fe, Co, Ni, Cu, Zn). [CuMn(L1)](AcO)(BPh4) crystallizes in the monoclinic space group P21/n, with Z = 4, a = 17.508(8) Å, b = 15.539(5) Å, c = 16.515(5) Å, β= 106.30(3)°, and V = 4312(3) Å3. The refinement converges with R = 0.0689 and Rw = 0.0563 for 2935 reflections with |Fo| > 3σ(|Fo|). The Cu(II) and Mn(II) ions reside at the 4- and 5-coordination sites of the macrocycle, respectively, and the acetate group bridges the two metal ions providing a nearly square-pyramidal geometry for the Cu and a highly distorted six-coordinate environment for the Mn. The Cu-Mn separation is 3.122(2) Å. The cryomagnetic investigations (4.2–300 K) for the CuMn, CuFe, CuCo, CuNi, and CuCu complexes reveal the operation of an antiferromagnetic spin-exchange interaction within each molecule. The cyclic voltammograms of the CuM complexes show Cu(II)/Cu(I) reduction near −0.8 V (vs SCE) and oxidation at the ligand center near +1.3 V. The oxidation of the Fe(II) of the CuFe complex occurs at +0.64 V whereas the Mn(II) ion of the CuMn complex and the Co(II) ion of the CuCo complex are hardly oxidized.

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