Mixed-ligand molecular paneling: Dodecanuclear cuboctahedral coordination cages based on a combination of edge-bridging and face-capping ligands

N.K. Al-Rasbi, I.S. Tidmarsh, S.P. Argent, H. Adams, L.P. Harding, M.D. Ward

Research output: Contribution to journalArticle

65 Citations (Scopus)

Abstract

Reaction of a tris-bidentate ligand L1 (which can cap one triangular face of a metal polyhedron), a bis-bidentate ligand L2 (which can span one edge of a metal polyhedron), and a range of M2+ ions (M = Co, Cu, Cd), which all have a preference for six coordination geometry, results in assembly of the mixed-ligand polyhedral cages [M12(μ3-L1)4(μ-L2)12]24+. When the components are combined in the correct proportions [M2+:L1:L2 = 3:1:3] in MeNO2, this is the sole product. The array of 12 M2+ cations has a cuboctahedral geometry, containing six square and eight triangular faces around a substantial central cavity; four of the eight M3 triangular faces (every alternate one) are capped by a ligand L1, with the remaining four M3 faces having a bridging ligand L2 along each edge in a cyclic helical array. Thus, four homochiral triangular {M3(L2)3}6+ helical units are connected by four additional L1 ligands to give the mixed-ligand cuboctahedral array, a topology which could not be formed in any homoleptic complex of this type but requires the cooperation of two different types of ligand. The complex [Cd3(L2)3(ClO4)4(MeCN)2(H2O)2](ClO4)2, a trinuclear triple helicate in which two sites at each Cd(II) are occupied by monodentate ligands (solvent or counterions), was also characterized and constitutes an incomplete fragment of the dodecanuclear cage comprising one triangular {M3(L2)3}6+ face which has not yet reacted with the ligands L1. 1H NMR and electrospray mass spectrometric studies show that the dodecanuclear cages remain intact in solution; the NMR studies show that the Cd12 cage has four-fold (D2) symmetry, such that there are three independent Cd(II) environments, as confirmed by a 113Cd NMR spectrum. These mixed-ligand cuboctahedral complexes reveal the potential of using combinations of face-capping and edge-bridging ligands to extend the range of accessible topologies of polyhedral coordination cages.
LanguageEnglish
Pages11641-11649
Number of pages9
JournalJournal of the American Chemical Society
Volume130
Issue number35
DOIs
Publication statusPublished - Aug 2008

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Ligands
Nuclear magnetic resonance
Metals
Topology
Geometry
Cations
Positive ions
Ions

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title = "Mixed-ligand molecular paneling: Dodecanuclear cuboctahedral coordination cages based on a combination of edge-bridging and face-capping ligands",
abstract = "Reaction of a tris-bidentate ligand L1 (which can cap one triangular face of a metal polyhedron), a bis-bidentate ligand L2 (which can span one edge of a metal polyhedron), and a range of M2+ ions (M = Co, Cu, Cd), which all have a preference for six coordination geometry, results in assembly of the mixed-ligand polyhedral cages [M12(μ3-L1)4(μ-L2)12]24+. When the components are combined in the correct proportions [M2+:L1:L2 = 3:1:3] in MeNO2, this is the sole product. The array of 12 M2+ cations has a cuboctahedral geometry, containing six square and eight triangular faces around a substantial central cavity; four of the eight M3 triangular faces (every alternate one) are capped by a ligand L1, with the remaining four M3 faces having a bridging ligand L2 along each edge in a cyclic helical array. Thus, four homochiral triangular {M3(L2)3}6+ helical units are connected by four additional L1 ligands to give the mixed-ligand cuboctahedral array, a topology which could not be formed in any homoleptic complex of this type but requires the cooperation of two different types of ligand. The complex [Cd3(L2)3(ClO4)4(MeCN)2(H2O)2](ClO4)2, a trinuclear triple helicate in which two sites at each Cd(II) are occupied by monodentate ligands (solvent or counterions), was also characterized and constitutes an incomplete fragment of the dodecanuclear cage comprising one triangular {M3(L2)3}6+ face which has not yet reacted with the ligands L1. 1H NMR and electrospray mass spectrometric studies show that the dodecanuclear cages remain intact in solution; the NMR studies show that the Cd12 cage has four-fold (D2) symmetry, such that there are three independent Cd(II) environments, as confirmed by a 113Cd NMR spectrum. These mixed-ligand cuboctahedral complexes reveal the potential of using combinations of face-capping and edge-bridging ligands to extend the range of accessible topologies of polyhedral coordination cages.",
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Mixed-ligand molecular paneling : Dodecanuclear cuboctahedral coordination cages based on a combination of edge-bridging and face-capping ligands. / Al-Rasbi, N.K.; Tidmarsh, I.S.; Argent, S.P.; Adams, H.; Harding, L.P.; Ward, M.D.

In: Journal of the American Chemical Society, Vol. 130, No. 35, 08.2008, p. 11641-11649.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Mixed-ligand molecular paneling

T2 - Journal of the American Chemical Society

AU - Al-Rasbi, N.K.

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AU - Adams, H.

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AU - Ward, M.D.

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N2 - Reaction of a tris-bidentate ligand L1 (which can cap one triangular face of a metal polyhedron), a bis-bidentate ligand L2 (which can span one edge of a metal polyhedron), and a range of M2+ ions (M = Co, Cu, Cd), which all have a preference for six coordination geometry, results in assembly of the mixed-ligand polyhedral cages [M12(μ3-L1)4(μ-L2)12]24+. When the components are combined in the correct proportions [M2+:L1:L2 = 3:1:3] in MeNO2, this is the sole product. The array of 12 M2+ cations has a cuboctahedral geometry, containing six square and eight triangular faces around a substantial central cavity; four of the eight M3 triangular faces (every alternate one) are capped by a ligand L1, with the remaining four M3 faces having a bridging ligand L2 along each edge in a cyclic helical array. Thus, four homochiral triangular {M3(L2)3}6+ helical units are connected by four additional L1 ligands to give the mixed-ligand cuboctahedral array, a topology which could not be formed in any homoleptic complex of this type but requires the cooperation of two different types of ligand. The complex [Cd3(L2)3(ClO4)4(MeCN)2(H2O)2](ClO4)2, a trinuclear triple helicate in which two sites at each Cd(II) are occupied by monodentate ligands (solvent or counterions), was also characterized and constitutes an incomplete fragment of the dodecanuclear cage comprising one triangular {M3(L2)3}6+ face which has not yet reacted with the ligands L1. 1H NMR and electrospray mass spectrometric studies show that the dodecanuclear cages remain intact in solution; the NMR studies show that the Cd12 cage has four-fold (D2) symmetry, such that there are three independent Cd(II) environments, as confirmed by a 113Cd NMR spectrum. These mixed-ligand cuboctahedral complexes reveal the potential of using combinations of face-capping and edge-bridging ligands to extend the range of accessible topologies of polyhedral coordination cages.

AB - Reaction of a tris-bidentate ligand L1 (which can cap one triangular face of a metal polyhedron), a bis-bidentate ligand L2 (which can span one edge of a metal polyhedron), and a range of M2+ ions (M = Co, Cu, Cd), which all have a preference for six coordination geometry, results in assembly of the mixed-ligand polyhedral cages [M12(μ3-L1)4(μ-L2)12]24+. When the components are combined in the correct proportions [M2+:L1:L2 = 3:1:3] in MeNO2, this is the sole product. The array of 12 M2+ cations has a cuboctahedral geometry, containing six square and eight triangular faces around a substantial central cavity; four of the eight M3 triangular faces (every alternate one) are capped by a ligand L1, with the remaining four M3 faces having a bridging ligand L2 along each edge in a cyclic helical array. Thus, four homochiral triangular {M3(L2)3}6+ helical units are connected by four additional L1 ligands to give the mixed-ligand cuboctahedral array, a topology which could not be formed in any homoleptic complex of this type but requires the cooperation of two different types of ligand. The complex [Cd3(L2)3(ClO4)4(MeCN)2(H2O)2](ClO4)2, a trinuclear triple helicate in which two sites at each Cd(II) are occupied by monodentate ligands (solvent or counterions), was also characterized and constitutes an incomplete fragment of the dodecanuclear cage comprising one triangular {M3(L2)3}6+ face which has not yet reacted with the ligands L1. 1H NMR and electrospray mass spectrometric studies show that the dodecanuclear cages remain intact in solution; the NMR studies show that the Cd12 cage has four-fold (D2) symmetry, such that there are three independent Cd(II) environments, as confirmed by a 113Cd NMR spectrum. These mixed-ligand cuboctahedral complexes reveal the potential of using combinations of face-capping and edge-bridging ligands to extend the range of accessible topologies of polyhedral coordination cages.

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