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Open-shell lanthanide(II+) or -(III+) complexes bearing σ-silyl and silylene ligands: synthesis, structure, and bonding analysis.

Zitz R, Arp H, Hlina J, Walewska M, Marschner C, Szilvási T, Blom B, Baumgartner J - Inorg Chem (2015)

Bottom Line: Density functional theory calculations were carried out for complexes 2a-2d, 5, and 6 to elucidate the bonding situation between the Ln(II+) or Ln(III+) centers and Si.In particular, a decrease in the Mayer bond order (MBO) of the Ln-Si bond is observed in the series 2a-2d in moving from the lighter to the heavier lanthanides (Tm = 0.53, Ho = 0.62, Tb = 0.65, and Gd = 0.75), which might indicate decreasing covalency in the Ln-Si bond.In accordance with the long bond lengths observed experimentally in complexes 5 and 6, comparatively low MBOs were determined for both silylene complexes (5, 0.24; 6, 0.25) .

View Article: PubMed Central - PubMed

Affiliation: †Institut für Anorganische Chemie, Technische Universität Graz, Stremayrgasse 9, 8010 Graz, Austria.

ABSTRACT
Complexes featuring lanthanide (Ln)-Si bonds represent a highly neglected research area. Herein, we report a series of open-shell Ln(II+) and Ln(III+) complexes bearing σ-bonded silyl and base-stabilized N-heterocyclic silylene (NHSi) ligands. The reactions of the Ln(III+) complexes Cp3Ln (Ln = Tm, Ho, Tb, Gd; Cp = cyclopentadienide) with the 18-crown-6 (18-cr-6)-stabilized 1,4-oligosilanyl dianion [(18-cr-6)KSi(SiMe3)2SiMe2SiMe2Si(SiMe3)2K(18-cr-6)] (1) selectively afford the corresponding metallacyclopentasilane salts [Cp2Ln({Si(SiMe3)2SiMe2}2)](-)[K2(18-cr-6)2Cp](+) [Ln = Tm (2a), Ho (2b), Tb (2c), Gd (2d)]. Complexes 2a-2d represent the first examples of structurally characterized Tm, Ho, Tb, and Gd complexes featuring Ln-Si bonds. Strikingly, the analogous reaction of 1 with the lighter element analogue Cp3Ce affords the acyclic product [Cp3CeSi(SiMe3)2SiMe2SiMe2Si(SiMe3)2-Cp3Ce](2-)2[K(18-cr-6)](+) (3) as the first example of a complex featuring a Ce-Si bond. In an alternative synthetic approach, the aryloxy-functionalized benzamidinato NHSi ligand Si(OC6H4-2-tBu){(NtBu)2CPh} (4a) and the alkoxy analogue Si(OtBu){(NtBu)2CPh} (4b) were reacted with Cp*2Sm(OEt2), affording, by OEt2 elimination, the corresponding silylene complexes, both featuring Sm(II+) centers: Cp*2Sm ← :Si(O-C6H4-2-tBu){(NtBu)2CPh} (6) and Cp*2Sm ← :Si(OtBu){(NtBu)2CPh} (5). Complexes 5 and 6 are the first four-coordinate silylene complexes of any f-block element to date. All complexes were fully characterized by spectroscopic means and by single-crystal X-ray diffraction analysis. In the series 2a-2d, a linear correlation was observed between the Ln-Si bond lengths and the covalent radii of the corresponding Ln metals. Moreover, in complexes 5 and 6, notably long Sm-Si bonds are observed, in accordance with a donor-acceptor interaction between Si and Sm [5, 3.4396(15) Å; 6, 3.3142(18) Å]. Density functional theory calculations were carried out for complexes 2a-2d, 5, and 6 to elucidate the bonding situation between the Ln(II+) or Ln(III+) centers and Si. In particular, a decrease in the Mayer bond order (MBO) of the Ln-Si bond is observed in the series 2a-2d in moving from the lighter to the heavier lanthanides (Tm = 0.53, Ho = 0.62, Tb = 0.65, and Gd = 0.75), which might indicate decreasing covalency in the Ln-Si bond. In accordance with the long bond lengths observed experimentally in complexes 5 and 6, comparatively low MBOs were determined for both silylene complexes (5, 0.24; 6, 0.25) .

No MeSH data available.


Molecular structure of 6 (thermal ellipsoid plot drawn at the 30% probability level).All hydrogen atoms are omitted for clarity. Bond lengths (Å)and angles (deg): Sm1–Si1 3.3142(18), Si1–O1 1.683(7),Si1–N1 1.865(7), Si1–N2 1.872(7); O1–Si1–N196.8(3), O1–Si1–N2 100.0(3), N1–Si1–N269.7(3), O1–Si1–Sm1 125.2(2), N1–Si1–Sm1107.9(2), N2–Si1–Sm1 134.2(2).
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fig6: Molecular structure of 6 (thermal ellipsoid plot drawn at the 30% probability level).All hydrogen atoms are omitted for clarity. Bond lengths (Å)and angles (deg): Sm1–Si1 3.3142(18), Si1–O1 1.683(7),Si1–N1 1.865(7), Si1–N2 1.872(7); O1–Si1–N196.8(3), O1–Si1–N2 100.0(3), N1–Si1–N269.7(3), O1–Si1–Sm1 125.2(2), N1–Si1–Sm1107.9(2), N2–Si1–Sm1 134.2(2).

Mentions: Compound 5 (Figure 5) crystallized in the monoclinicspace group P2(1)/n, 6 (Figure 6) in orthorhombic P2(1)2(1)2(1), and 7 (Figure 7) in triclinic P1̅ with two benzene moleculesand two additional ones on special positions in the unit cell. TheSm–Si distance for the samarium silylene synthesized by Evanset al.21 is 3.192 Å. The Sm–Sidistances for our compounds are with 3.440 Å for 5, 3.314 Å for 6, and 3.299 Å for 7 substantially longer, suggesting a weaker interaction.


Open-shell lanthanide(II+) or -(III+) complexes bearing σ-silyl and silylene ligands: synthesis, structure, and bonding analysis.

Zitz R, Arp H, Hlina J, Walewska M, Marschner C, Szilvási T, Blom B, Baumgartner J - Inorg Chem (2015)

Molecular structure of 6 (thermal ellipsoid plot drawn at the 30% probability level).All hydrogen atoms are omitted for clarity. Bond lengths (Å)and angles (deg): Sm1–Si1 3.3142(18), Si1–O1 1.683(7),Si1–N1 1.865(7), Si1–N2 1.872(7); O1–Si1–N196.8(3), O1–Si1–N2 100.0(3), N1–Si1–N269.7(3), O1–Si1–Sm1 125.2(2), N1–Si1–Sm1107.9(2), N2–Si1–Sm1 134.2(2).
© Copyright Policy
Related In: Results  -  Collection

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Show All Figures
getmorefigures.php?uid=PMC4389698&req=5

fig6: Molecular structure of 6 (thermal ellipsoid plot drawn at the 30% probability level).All hydrogen atoms are omitted for clarity. Bond lengths (Å)and angles (deg): Sm1–Si1 3.3142(18), Si1–O1 1.683(7),Si1–N1 1.865(7), Si1–N2 1.872(7); O1–Si1–N196.8(3), O1–Si1–N2 100.0(3), N1–Si1–N269.7(3), O1–Si1–Sm1 125.2(2), N1–Si1–Sm1107.9(2), N2–Si1–Sm1 134.2(2).
Mentions: Compound 5 (Figure 5) crystallized in the monoclinicspace group P2(1)/n, 6 (Figure 6) in orthorhombic P2(1)2(1)2(1), and 7 (Figure 7) in triclinic P1̅ with two benzene moleculesand two additional ones on special positions in the unit cell. TheSm–Si distance for the samarium silylene synthesized by Evanset al.21 is 3.192 Å. The Sm–Sidistances for our compounds are with 3.440 Å for 5, 3.314 Å for 6, and 3.299 Å for 7 substantially longer, suggesting a weaker interaction.

Bottom Line: Density functional theory calculations were carried out for complexes 2a-2d, 5, and 6 to elucidate the bonding situation between the Ln(II+) or Ln(III+) centers and Si.In particular, a decrease in the Mayer bond order (MBO) of the Ln-Si bond is observed in the series 2a-2d in moving from the lighter to the heavier lanthanides (Tm = 0.53, Ho = 0.62, Tb = 0.65, and Gd = 0.75), which might indicate decreasing covalency in the Ln-Si bond.In accordance with the long bond lengths observed experimentally in complexes 5 and 6, comparatively low MBOs were determined for both silylene complexes (5, 0.24; 6, 0.25) .

View Article: PubMed Central - PubMed

Affiliation: †Institut für Anorganische Chemie, Technische Universität Graz, Stremayrgasse 9, 8010 Graz, Austria.

ABSTRACT
Complexes featuring lanthanide (Ln)-Si bonds represent a highly neglected research area. Herein, we report a series of open-shell Ln(II+) and Ln(III+) complexes bearing σ-bonded silyl and base-stabilized N-heterocyclic silylene (NHSi) ligands. The reactions of the Ln(III+) complexes Cp3Ln (Ln = Tm, Ho, Tb, Gd; Cp = cyclopentadienide) with the 18-crown-6 (18-cr-6)-stabilized 1,4-oligosilanyl dianion [(18-cr-6)KSi(SiMe3)2SiMe2SiMe2Si(SiMe3)2K(18-cr-6)] (1) selectively afford the corresponding metallacyclopentasilane salts [Cp2Ln({Si(SiMe3)2SiMe2}2)](-)[K2(18-cr-6)2Cp](+) [Ln = Tm (2a), Ho (2b), Tb (2c), Gd (2d)]. Complexes 2a-2d represent the first examples of structurally characterized Tm, Ho, Tb, and Gd complexes featuring Ln-Si bonds. Strikingly, the analogous reaction of 1 with the lighter element analogue Cp3Ce affords the acyclic product [Cp3CeSi(SiMe3)2SiMe2SiMe2Si(SiMe3)2-Cp3Ce](2-)2[K(18-cr-6)](+) (3) as the first example of a complex featuring a Ce-Si bond. In an alternative synthetic approach, the aryloxy-functionalized benzamidinato NHSi ligand Si(OC6H4-2-tBu){(NtBu)2CPh} (4a) and the alkoxy analogue Si(OtBu){(NtBu)2CPh} (4b) were reacted with Cp*2Sm(OEt2), affording, by OEt2 elimination, the corresponding silylene complexes, both featuring Sm(II+) centers: Cp*2Sm ← :Si(O-C6H4-2-tBu){(NtBu)2CPh} (6) and Cp*2Sm ← :Si(OtBu){(NtBu)2CPh} (5). Complexes 5 and 6 are the first four-coordinate silylene complexes of any f-block element to date. All complexes were fully characterized by spectroscopic means and by single-crystal X-ray diffraction analysis. In the series 2a-2d, a linear correlation was observed between the Ln-Si bond lengths and the covalent radii of the corresponding Ln metals. Moreover, in complexes 5 and 6, notably long Sm-Si bonds are observed, in accordance with a donor-acceptor interaction between Si and Sm [5, 3.4396(15) Å; 6, 3.3142(18) Å]. Density functional theory calculations were carried out for complexes 2a-2d, 5, and 6 to elucidate the bonding situation between the Ln(II+) or Ln(III+) centers and Si. In particular, a decrease in the Mayer bond order (MBO) of the Ln-Si bond is observed in the series 2a-2d in moving from the lighter to the heavier lanthanides (Tm = 0.53, Ho = 0.62, Tb = 0.65, and Gd = 0.75), which might indicate decreasing covalency in the Ln-Si bond. In accordance with the long bond lengths observed experimentally in complexes 5 and 6, comparatively low MBOs were determined for both silylene complexes (5, 0.24; 6, 0.25) .

No MeSH data available.