Relationship between the bite size of diphosphine ligands and tetrahedral distortions of "square-planar" nickel(II) complexes

Stabilization of nickel(I) and palladium(I) complexes using diphosphine ligands with large bites

Alex Miedaner, Daniel L DuBois, Daniel L. DuBois

Research output: Contribution to journalArticle

102 Citations (Scopus)

Abstract

Nickel and palladium complexes of the type [M(L2)2](BF4)2 and [M(L2)(L2′)](BF4)2 (where L2 and L2′ are diphosphine ligands) have been synthesized. The lowest energy electronic absorption band for the nickel complexes decreases in energy as the bite size of the diphosphine ligand increases. Similarly, the half-wave potentials for the Ni(II/I) and Pd(II/0) couples become more positive as the bite size increases. Structural studies of [Ni(dppm)2](BF4)2 (where dppm is bis(diphenylphosphino)methane) and [Ni-(dppb)2](PF6)2 (where dppb is 1,2-bis(diphenylphosphino) benzene) show that increasing the bite size of the diphosphine ligands results in larger tetrahedral distortions. [Ni(dppm)2](BF4)2 (C50H44B2F8NiP4) crystallizes in the monoclinic space group P21/n with a = 11.158 (10) Å, b = 17.43 (2) Å, c = 12.849 (11) Å, β = 111.38 (7)°, V = 3228 Å3, and Z = 2. The structure was refined to R = 0.155 and Rw = 0.201 for 1005 independent reflections with Fo > 6σ(Fo). [Ni(dppb)2](PF6)2 (C74H64F12NiP6) crystallizes in space group P1 with a = 11.359 (6) Å, b = 13.960 (5) Å, c = 21.297(7) Å, α = 84.69 (3)°, β = 84.79 (4)°, γ = 78.96(3)°, V = 3298 (2) Å3, and Z = 2. The structure was refined to R = 0.072 and Rw = 0.085 for 2333 independent reflections with Fo > 6σ(Fo). The tetrahedral distortion observed for [Ni(dppb)2](PF6)2 was modeled by using extended Hückel calculations. These calculations indicate that the observed distortion may have an electronic as well as a steric component. The calculations also allow rationalization of the electronic absorption spectra, electrochemical data, and the stability of the Ni(I) and Pd(I) complexes [Ni(dppp)2](BF4) (where dppp is 1,3-bis(diphenylphosphino)propane) and [Pd(dppx)2](BF4) (where dppx is α,α′-bis(diphenylphosphino)-o-xylene). Complexes containing the ligand dppm have a marked tendency to become five-coordinate, as indicated by the structural determination of [Ni(dppm)2(CH3CN)](PF6)2. The latter complex (C59H55F12NNiP6) crystallizes in space group P4/m with a = 19.363 (4) Å, c = 15.526 (4) Å, V = 5822 (2) Å3, and Z = 4. The structure was refined to R = 0.048 and Rw = 0.062 for 3470 independent reflections with Fo > 6σ(Fo).

Original languageEnglish
Pages (from-to)417-427
Number of pages11
JournalInorganic Chemistry
Volume30
Issue number3
Publication statusPublished - 1991

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Palladium
Nickel
palladium
Stabilization
stabilization
nickel
Ligands
ligands
Absorption spectra
Methane
absorption spectra
xylene
electronics
propane
electronic spectra
tendencies
methane
benzene
energy

ASJC Scopus subject areas

  • Inorganic Chemistry

Cite this

@article{dd5b8586df0e4ce99195652d77a08418,
title = "Relationship between the bite size of diphosphine ligands and tetrahedral distortions of {"}square-planar{"} nickel(II) complexes: Stabilization of nickel(I) and palladium(I) complexes using diphosphine ligands with large bites",
abstract = "Nickel and palladium complexes of the type [M(L2)2](BF4)2 and [M(L2)(L2′)](BF4)2 (where L2 and L2′ are diphosphine ligands) have been synthesized. The lowest energy electronic absorption band for the nickel complexes decreases in energy as the bite size of the diphosphine ligand increases. Similarly, the half-wave potentials for the Ni(II/I) and Pd(II/0) couples become more positive as the bite size increases. Structural studies of [Ni(dppm)2](BF4)2 (where dppm is bis(diphenylphosphino)methane) and [Ni-(dppb)2](PF6)2 (where dppb is 1,2-bis(diphenylphosphino) benzene) show that increasing the bite size of the diphosphine ligands results in larger tetrahedral distortions. [Ni(dppm)2](BF4)2 (C50H44B2F8NiP4) crystallizes in the monoclinic space group P21/n with a = 11.158 (10) {\AA}, b = 17.43 (2) {\AA}, c = 12.849 (11) {\AA}, β = 111.38 (7)°, V = 3228 {\AA}3, and Z = 2. The structure was refined to R = 0.155 and Rw = 0.201 for 1005 independent reflections with Fo > 6σ(Fo). [Ni(dppb)2](PF6)2 (C74H64F12NiP6) crystallizes in space group P1 with a = 11.359 (6) {\AA}, b = 13.960 (5) {\AA}, c = 21.297(7) {\AA}, α = 84.69 (3)°, β = 84.79 (4)°, γ = 78.96(3)°, V = 3298 (2) {\AA}3, and Z = 2. The structure was refined to R = 0.072 and Rw = 0.085 for 2333 independent reflections with Fo > 6σ(Fo). The tetrahedral distortion observed for [Ni(dppb)2](PF6)2 was modeled by using extended H{\"u}ckel calculations. These calculations indicate that the observed distortion may have an electronic as well as a steric component. The calculations also allow rationalization of the electronic absorption spectra, electrochemical data, and the stability of the Ni(I) and Pd(I) complexes [Ni(dppp)2](BF4) (where dppp is 1,3-bis(diphenylphosphino)propane) and [Pd(dppx)2](BF4) (where dppx is α,α′-bis(diphenylphosphino)-o-xylene). Complexes containing the ligand dppm have a marked tendency to become five-coordinate, as indicated by the structural determination of [Ni(dppm)2(CH3CN)](PF6)2. The latter complex (C59H55F12NNiP6) crystallizes in space group P4/m with a = 19.363 (4) {\AA}, c = 15.526 (4) {\AA}, V = 5822 (2) {\AA}3, and Z = 4. The structure was refined to R = 0.048 and Rw = 0.062 for 3470 independent reflections with Fo > 6σ(Fo).",
author = "Alex Miedaner and DuBois, {Daniel L} and DuBois, {Daniel L.}",
year = "1991",
language = "English",
volume = "30",
pages = "417--427",
journal = "Inorganic Chemistry",
issn = "0020-1669",
publisher = "American Chemical Society",
number = "3",

}

TY - JOUR

T1 - Relationship between the bite size of diphosphine ligands and tetrahedral distortions of "square-planar" nickel(II) complexes

T2 - Stabilization of nickel(I) and palladium(I) complexes using diphosphine ligands with large bites

AU - Miedaner, Alex

AU - DuBois, Daniel L

AU - DuBois, Daniel L.

PY - 1991

Y1 - 1991

N2 - Nickel and palladium complexes of the type [M(L2)2](BF4)2 and [M(L2)(L2′)](BF4)2 (where L2 and L2′ are diphosphine ligands) have been synthesized. The lowest energy electronic absorption band for the nickel complexes decreases in energy as the bite size of the diphosphine ligand increases. Similarly, the half-wave potentials for the Ni(II/I) and Pd(II/0) couples become more positive as the bite size increases. Structural studies of [Ni(dppm)2](BF4)2 (where dppm is bis(diphenylphosphino)methane) and [Ni-(dppb)2](PF6)2 (where dppb is 1,2-bis(diphenylphosphino) benzene) show that increasing the bite size of the diphosphine ligands results in larger tetrahedral distortions. [Ni(dppm)2](BF4)2 (C50H44B2F8NiP4) crystallizes in the monoclinic space group P21/n with a = 11.158 (10) Å, b = 17.43 (2) Å, c = 12.849 (11) Å, β = 111.38 (7)°, V = 3228 Å3, and Z = 2. The structure was refined to R = 0.155 and Rw = 0.201 for 1005 independent reflections with Fo > 6σ(Fo). [Ni(dppb)2](PF6)2 (C74H64F12NiP6) crystallizes in space group P1 with a = 11.359 (6) Å, b = 13.960 (5) Å, c = 21.297(7) Å, α = 84.69 (3)°, β = 84.79 (4)°, γ = 78.96(3)°, V = 3298 (2) Å3, and Z = 2. The structure was refined to R = 0.072 and Rw = 0.085 for 2333 independent reflections with Fo > 6σ(Fo). The tetrahedral distortion observed for [Ni(dppb)2](PF6)2 was modeled by using extended Hückel calculations. These calculations indicate that the observed distortion may have an electronic as well as a steric component. The calculations also allow rationalization of the electronic absorption spectra, electrochemical data, and the stability of the Ni(I) and Pd(I) complexes [Ni(dppp)2](BF4) (where dppp is 1,3-bis(diphenylphosphino)propane) and [Pd(dppx)2](BF4) (where dppx is α,α′-bis(diphenylphosphino)-o-xylene). Complexes containing the ligand dppm have a marked tendency to become five-coordinate, as indicated by the structural determination of [Ni(dppm)2(CH3CN)](PF6)2. The latter complex (C59H55F12NNiP6) crystallizes in space group P4/m with a = 19.363 (4) Å, c = 15.526 (4) Å, V = 5822 (2) Å3, and Z = 4. The structure was refined to R = 0.048 and Rw = 0.062 for 3470 independent reflections with Fo > 6σ(Fo).

AB - Nickel and palladium complexes of the type [M(L2)2](BF4)2 and [M(L2)(L2′)](BF4)2 (where L2 and L2′ are diphosphine ligands) have been synthesized. The lowest energy electronic absorption band for the nickel complexes decreases in energy as the bite size of the diphosphine ligand increases. Similarly, the half-wave potentials for the Ni(II/I) and Pd(II/0) couples become more positive as the bite size increases. Structural studies of [Ni(dppm)2](BF4)2 (where dppm is bis(diphenylphosphino)methane) and [Ni-(dppb)2](PF6)2 (where dppb is 1,2-bis(diphenylphosphino) benzene) show that increasing the bite size of the diphosphine ligands results in larger tetrahedral distortions. [Ni(dppm)2](BF4)2 (C50H44B2F8NiP4) crystallizes in the monoclinic space group P21/n with a = 11.158 (10) Å, b = 17.43 (2) Å, c = 12.849 (11) Å, β = 111.38 (7)°, V = 3228 Å3, and Z = 2. The structure was refined to R = 0.155 and Rw = 0.201 for 1005 independent reflections with Fo > 6σ(Fo). [Ni(dppb)2](PF6)2 (C74H64F12NiP6) crystallizes in space group P1 with a = 11.359 (6) Å, b = 13.960 (5) Å, c = 21.297(7) Å, α = 84.69 (3)°, β = 84.79 (4)°, γ = 78.96(3)°, V = 3298 (2) Å3, and Z = 2. The structure was refined to R = 0.072 and Rw = 0.085 for 2333 independent reflections with Fo > 6σ(Fo). The tetrahedral distortion observed for [Ni(dppb)2](PF6)2 was modeled by using extended Hückel calculations. These calculations indicate that the observed distortion may have an electronic as well as a steric component. The calculations also allow rationalization of the electronic absorption spectra, electrochemical data, and the stability of the Ni(I) and Pd(I) complexes [Ni(dppp)2](BF4) (where dppp is 1,3-bis(diphenylphosphino)propane) and [Pd(dppx)2](BF4) (where dppx is α,α′-bis(diphenylphosphino)-o-xylene). Complexes containing the ligand dppm have a marked tendency to become five-coordinate, as indicated by the structural determination of [Ni(dppm)2(CH3CN)](PF6)2. The latter complex (C59H55F12NNiP6) crystallizes in space group P4/m with a = 19.363 (4) Å, c = 15.526 (4) Å, V = 5822 (2) Å3, and Z = 4. The structure was refined to R = 0.048 and Rw = 0.062 for 3470 independent reflections with Fo > 6σ(Fo).

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M3 - Article

VL - 30

SP - 417

EP - 427

JO - Inorganic Chemistry

JF - Inorganic Chemistry

SN - 0020-1669

IS - 3

ER -