21 research outputs found

    Dual Coordination Modes of Ethylene-Linked NP2 Ligands in Cobalt(II) and Nickel(II) Iodides

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    Here we report the syntheses and crystal structures of a series of cobalt(II) and nickel(II) complexes derived from _RNP2 ligands (where R = OMe_(Bz), H_(Bz), Br_(Bz), Ph) bearing ethylene linkers between a single N and two P donors. The Co^(II) complexes generally adopt a tetrahedral configuration of general formula [(NP2)Co(I)_2], wherein the two phosphorus donors are bound to the metal center but the central N-donor remains unbound. We have found one case of structural isomerism within a single crystal structure. The Co^(II) complex derived from _(Bz)NP2 displays dual coordination modes: one in the tetrahedral complex [(_(Bz)NP2)Co(I)_2]; and the other in a square pyramidal variant, [(_(Bz)NP2)Co(I)_2]. In contrast, the Ni^(II) complexes adopt a square planar geometry in which the P(Et)N(Et)P donors in the ligand backbone are coordinated to the metal center, resulting in cationic species of formula [(_RNP2)Ni(I)]^+ with iodide as counterion. All Ni^(II) complexes exhibit sharp ^1H and ^(31)P spectra in the diamagnetic region. The Co^(II) complexes are high-spin (S = 3/2) in the solid state as determined by SQUID measurements from 4 to 300 K. Solution electron paramagnetic resonance (EPR) experiments reveal a high-spin/low-spin Co^(II) equilibrium that is dependent on solvent and ligand substituent

    From Lithium Bis(trimethylsilyl)amide with Cyanoamine into Triazine Compounds: Synthesis and Structures of Lithium 6-((Trimethylsilyl)amido)-2,4-bis(dimethylamino)[1,3,5]triazines and Their Manganese and Cobalt Complexes

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    Addition reactions of lithium bis­(trimethylsilyl)­amide with dimethylcyanamide lead to novel lithium salts of 6-((trimethylsilyl)­amido)-2,4-bis­(dimethylamino)­[1,3,5]­triazines [<b>L</b>Li­(<b>D</b>)]<sub>2</sub> (<b>L</b> = NC­(NMe<sub>2</sub>)­NC­(NMe<sub>2</sub>)­NC­(NSiMe<sub>3</sub>); <b>D</b> = Me<sub>2</sub>NCN (<b>1</b>), Et<sub>2</sub>O (<b>2</b>)) and to the Mn and Co complexes [<b>LL′</b>M] (<b>L′ </b>= N­{N­(SiMe<sub>3</sub>)­C­(NMe<sub>2</sub>)}<sub>2</sub>; M = Mn (<b>3</b>), Co (<b>4</b>)); the structures of crystalline <b>1</b>, <b>3</b>, and <b>4</b> are reported. Their formation involves trimethylsilyl shifts, ring formation, and unusual Me<sub>2</sub>NSiMe<sub>3</sub> elimination

    From Lithium Bis(trimethylsilyl)amide with Cyanoamine into Triazine Compounds: Synthesis and Structures of Lithium 6-((Trimethylsilyl)amido)-2,4-bis(dimethylamino)[1,3,5]triazines and Their Manganese and Cobalt Complexes

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    Addition reactions of lithium bis­(trimethylsilyl)­amide with dimethylcyanamide lead to novel lithium salts of 6-((trimethylsilyl)­amido)-2,4-bis­(dimethylamino)­[1,3,5]­triazines [<b>L</b>Li­(<b>D</b>)]<sub>2</sub> (<b>L</b> = NC­(NMe<sub>2</sub>)­NC­(NMe<sub>2</sub>)­NC­(NSiMe<sub>3</sub>); <b>D</b> = Me<sub>2</sub>NCN (<b>1</b>), Et<sub>2</sub>O (<b>2</b>)) and to the Mn and Co complexes [<b>LL′</b>M] (<b>L′ </b>= N­{N­(SiMe<sub>3</sub>)­C­(NMe<sub>2</sub>)}<sub>2</sub>; M = Mn (<b>3</b>), Co (<b>4</b>)); the structures of crystalline <b>1</b>, <b>3</b>, and <b>4</b> are reported. Their formation involves trimethylsilyl shifts, ring formation, and unusual Me<sub>2</sub>NSiMe<sub>3</sub> elimination

    From Lithium Bis(trimethylsilyl)amide with Cyanoamine into Triazine Compounds: Synthesis and Structures of Lithium 6-((Trimethylsilyl)amido)-2,4-bis(dimethylamino)[1,3,5]triazines and Their Manganese and Cobalt Complexes

    No full text
    Addition reactions of lithium bis­(trimethylsilyl)­amide with dimethylcyanamide lead to novel lithium salts of 6-((trimethylsilyl)­amido)-2,4-bis­(dimethylamino)­[1,3,5]­triazines [<b>L</b>Li­(<b>D</b>)]<sub>2</sub> (<b>L</b> = NC­(NMe<sub>2</sub>)­NC­(NMe<sub>2</sub>)­NC­(NSiMe<sub>3</sub>); <b>D</b> = Me<sub>2</sub>NCN (<b>1</b>), Et<sub>2</sub>O (<b>2</b>)) and to the Mn and Co complexes [<b>LL′</b>M] (<b>L′ </b>= N­{N­(SiMe<sub>3</sub>)­C­(NMe<sub>2</sub>)}<sub>2</sub>; M = Mn (<b>3</b>), Co (<b>4</b>)); the structures of crystalline <b>1</b>, <b>3</b>, and <b>4</b> are reported. Their formation involves trimethylsilyl shifts, ring formation, and unusual Me<sub>2</sub>NSiMe<sub>3</sub> elimination
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