55 research outputs found
Reactivity Studies of [(thf)<sub>2</sub>Mg{μ-C(CH<sub>3</sub>)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>C(CH<sub>3</sub>)<sub>2</sub>}]<sub>2</sub>: Scrambling Reactions and Diverse Reactions with Dichlorophenylphosphane
In
THF solution [{(thf)<sub>2</sub>Mg{μ-C(CH<sub>3</sub>)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>(CH<sub>3</sub>)<sub>2</sub>C}}<sub>2</sub>] (<b>1</b>) exchanges the alkanediide ligand with [{(thf)<sub>2</sub>Mg{μ-CH<sub>2</sub>)<sub>5</sub>}}<sub>2</sub>] in an
equilibrium leading to the formation of [{(thf)<sub>2</sub>Mg}<sub>2</sub>{μ-C(CH<sub>3</sub>)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>C(CH<sub>3</sub>)<sub>2</sub>}{μ-(CH<sub>2</sub>)<sub>5</sub>}] (<b>2</b>). Depending on the crystallization temperature,
homoleptic <b>1</b> or heteroleptic <b>2</b> crystallizes
from THF solutions, verifying a temperature-dependent Schlenk equilibrium.
Irradiation of a solution of <b>1</b> in [D<sub>8</sub>]THF
with UV light yields magnesium hydride and alkene via a β-hydride
elimination reaction. In a metathetical approach dichlorophenylphosphane reacts with <b>1</b> in THF to give the intermediate “PhP(Cl){C(CH<sub>3</sub>)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>(CH<sub>3</sub>)<sub>2</sub>CMgCl” (<b>3-MgCl</b>), which forms three subsequent
products. In order to ease handling and characterization of these
compounds, hydrolysis and oxidation with sulfur has been performed.
This product mixture was separated by column chromatography, yielding
the chlorophosphane sulfide [Ph(S)P(Cl){C(CH<sub>3</sub>)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>(CH<sub>3</sub>)<sub>2</sub>CH)}] (<b>3-S</b>), the cyclic phosphane sulfide [Ph(S)P{C(CH<sub>3</sub>)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>(CH<sub>3</sub>)<sub>2</sub>C)}] (<b>4-S</b>), and the cyclic 1,1-diphosphane disulfide
[{(Ph(S)P}<sub>2</sub>{μ-C(CH<sub>3</sub>)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>(CH<sub>3</sub>)<sub>2</sub>C}] (<b>6-S<sub>2</sub></b>). Furthermore, traces of the acyclic 1,1-diphosphane
disulfides [{PhP(S)(C(CH<sub>3</sub>)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>CH(CH<sub>3</sub>)<sub>2</sub>)}{PhP(S)(C(CH<sub>3</sub>)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>C(CH<sub>3</sub>)(CH<sub>2</sub>)}] (<b>8-S<sub>2</sub></b>) and <i>meso</i>-[{Ph(S)P(C(CH<sub>3</sub>)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>(CH<sub>3</sub>)<sub>2</sub>CH)}<sub>2</sub>] (<b>7-S<sub>2</sub></b>) have also
been isolated. Compounds <b>6</b>–<b>8</b> represent
the phosphorus-containing products of indirect Grignard reductions
Reactivity Studies of [(thf)<sub>2</sub>Mg{μ-C(CH<sub>3</sub>)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>C(CH<sub>3</sub>)<sub>2</sub>}]<sub>2</sub>: Scrambling Reactions and Diverse Reactions with Dichlorophenylphosphane
In
THF solution [{(thf)<sub>2</sub>Mg{μ-C(CH<sub>3</sub>)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>(CH<sub>3</sub>)<sub>2</sub>C}}<sub>2</sub>] (<b>1</b>) exchanges the alkanediide ligand with [{(thf)<sub>2</sub>Mg{μ-CH<sub>2</sub>)<sub>5</sub>}}<sub>2</sub>] in an
equilibrium leading to the formation of [{(thf)<sub>2</sub>Mg}<sub>2</sub>{μ-C(CH<sub>3</sub>)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>C(CH<sub>3</sub>)<sub>2</sub>}{μ-(CH<sub>2</sub>)<sub>5</sub>}] (<b>2</b>). Depending on the crystallization temperature,
homoleptic <b>1</b> or heteroleptic <b>2</b> crystallizes
from THF solutions, verifying a temperature-dependent Schlenk equilibrium.
Irradiation of a solution of <b>1</b> in [D<sub>8</sub>]THF
with UV light yields magnesium hydride and alkene via a β-hydride
elimination reaction. In a metathetical approach dichlorophenylphosphane reacts with <b>1</b> in THF to give the intermediate “PhP(Cl){C(CH<sub>3</sub>)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>(CH<sub>3</sub>)<sub>2</sub>CMgCl” (<b>3-MgCl</b>), which forms three subsequent
products. In order to ease handling and characterization of these
compounds, hydrolysis and oxidation with sulfur has been performed.
This product mixture was separated by column chromatography, yielding
the chlorophosphane sulfide [Ph(S)P(Cl){C(CH<sub>3</sub>)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>(CH<sub>3</sub>)<sub>2</sub>CH)}] (<b>3-S</b>), the cyclic phosphane sulfide [Ph(S)P{C(CH<sub>3</sub>)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>(CH<sub>3</sub>)<sub>2</sub>C)}] (<b>4-S</b>), and the cyclic 1,1-diphosphane disulfide
[{(Ph(S)P}<sub>2</sub>{μ-C(CH<sub>3</sub>)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>(CH<sub>3</sub>)<sub>2</sub>C}] (<b>6-S<sub>2</sub></b>). Furthermore, traces of the acyclic 1,1-diphosphane
disulfides [{PhP(S)(C(CH<sub>3</sub>)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>CH(CH<sub>3</sub>)<sub>2</sub>)}{PhP(S)(C(CH<sub>3</sub>)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>C(CH<sub>3</sub>)(CH<sub>2</sub>)}] (<b>8-S<sub>2</sub></b>) and <i>meso</i>-[{Ph(S)P(C(CH<sub>3</sub>)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>(CH<sub>3</sub>)<sub>2</sub>CH)}<sub>2</sub>] (<b>7-S<sub>2</sub></b>) have also
been isolated. Compounds <b>6</b>–<b>8</b> represent
the phosphorus-containing products of indirect Grignard reductions
Trimethylsilylmethylcalcium Iodide, an Easily Accessible Grignard-Type Reagent of a Heavy Alkaline Earth Metal
The
direct synthesis of iodomethyltrimethylsilane with calcium
and magnesium in ether yields the corresponding ether adducts [(thf)<sub>4</sub>Ca(I)(CH<sub>2</sub>SiMe<sub>3</sub>)] (<b>1a</b>) and
[(Et<sub>2</sub>O)<sub>2</sub>Mg(I)(CH<sub>2</sub>SiMe<sub>3</sub>)] (<b>2a</b>). The 1,4-dioxane method allows shifting the
Schlenk equilibrium toward bis(trimethylsilylmethyl)magnesium <b>2b</b>. After substitution of ligated thf ligands by tetrahydropyran
(thp) crystalline [(thp)<sub>4</sub>Ca(I)(CH<sub>2</sub>SiMe<sub>3</sub>)] (<b>1b</b>) can be isolated. The Ca–C and Ca–I
bond lengths of 252.7(3) and 319.11(3) pm represent characteristic
values. Steric repulsion between ligated thp ligands and the rather
bulky trimethylsilylmethyl group widens the Ca–C–Si
angle to 131.19(14)°. NMR data and quantum chemical studies support
that hyperconjugative effects might be operative, leading to a shortened
Si–C bond of this Ca–C–Si fragment
Solution Stability of Organocalcium Compounds in Ethereal Media
Organocalcium compounds (post-Grignard
reagents) of the type [Ca(R)(X)(L)<sub><i>n</i></sub>] are
very reactive and able to degrade ethers
with α- and β-deprotonation as possible first reaction
step. In this systematic study, the durability of phenyl-, α-naphthyl-,
and 1,2-dihydronaphth-4-ylcalcium derivatives in cyclic ethers such
as tetrahydrofuran (THF), tetrahydropyran (THP), and α-methyltetrahydrofuran
(Me-THF) is investigated. The temperature, solvent, and the nature
of the second anionic ligand X [iodide, bis(trimethylsilyl)amide,
α-naphthyl] significantly influence the durability of their
ethereal solutions
Alkaline Earth Metal–Carbene Complexes with the Versatile Tridentate 2,6-Bis(3-mesitylimidazol-2-ylidene)pyridine Ligand
Diffusion
of 2,6-bis(3-mesitylimidazol-2-ylidene)pyridine (Car<sup>Mes</sup>PyCar<sup>Mes</sup>, <b>2</b>) into a solution of
CaI<sub>2</sub> in THF leads to microcrystalline [(Car<sup>Mes</sup>PyCar<sup>Mes</sup>)(thf)CaI<sub>2</sub>] (<b>3</b>), in one
case containing a few single crystals of the unique separated ion
pair [(Car<sup>Mes</sup>PyCar<sup>Mes</sup>)<sub>2</sub>(thf)Ca]I<sub>2</sub> (<b>4</b>) with four Ca–C bonds. However, isolation
of single-crystalline [(Car<sup>Mes</sup>PyCar<sup>Mes</sup>)(thf)CaI<sub>2</sub>] (<b>3</b>) succeeds via the addition of <b>2</b> to a solution of [(thf)<sub>5</sub>CaI]<sup>+</sup>[BPh<sub>4</sub>]<sup>−</sup> due to a subsequent dismutation. Two modifications
with the shapes of needles and cubes crystallize simultaneously. In
contrast to this finding, the reaction of [(thf)<sub>5</sub>CaI]<sup>+</sup>[AlPh<sub>4</sub>]<sup>−</sup> with <b>2</b> yields
solvent separated [(Car<sup>Mes</sup>PyCar<sup>Mes</sup>)(thf)<sub>2</sub>CaI]<sup>+</sup>[AlPh<sub>4</sub>]<sup>−</sup> (<b>5</b>). The Ca–C<sub>NHC</sub> bond lengths lie in a typical
range of Ca–C<sub>Aryl</sub> σ bonds and represent the
shortest Ca–C<sub>NHC</sub> bonds known to date. Soluble [(Car<sup>Mes</sup>PyCar<sup>Mes</sup>)(thf)Ca(NPh<sub>2</sub>)<sub>2</sub>] (<b>6</b>) can be prepared via a metathetical approach from <b>4</b> and KNPh<sub>2</sub> as well as via the addition of <b>2</b> to Ca(NPh<sub>2</sub>)<sub>2</sub> in tetrahydrofuran. The
bulkier amido ligands lead to elongated bonds between the calcium
center and the ligand <b>2</b>. Furthermore, the reactions of
MI<sub>2</sub> (M = Sr, Ba) with <b>2</b> yield [(Car<sup>Mes</sup>PyCar<sup>Mes</sup>)(thf)<sub>2</sub>MI<sub>2</sub>] (M = Sr (<b>7</b>), Ba (<b>8</b>))
Cobalt(II)-Based Single-Ion Magnets with Distorted Pseudotetrahedral [N<sub>2</sub>O<sub>2</sub>] Coordination: Experimental and Theoretical Investigations
The synthesis and magnetic properties
of cobalt(II) complexes with sterically demanding Schiff-base ligands
are reported. The compounds [Co(L<sup>Br</sup>)<sub>2</sub>] (<b>1</b>) and [Co(L<sup>Ph</sup>)<sub>2</sub>]·CH<sub>2</sub>Cl<sub>2</sub> (<b>2</b>·CH<sub>2</sub>Cl<sub>2</sub>)
are obtained by the reaction of cobalt(II) acetate with the ligands
HL<sup>Br</sup> and HL<sup>Ph</sup> in a dichloromethane/methanol
mixture. <b>1</b> and <b>2</b> crystallize in the space
groups <i>P</i>2<sub>1</sub>2<sub>1</sub>2 and <i>P</i>1̅, respectively. X-ray diffraction studies revealed mononuclear
constitution of both complexes. For <b>1</b>, relatively short
intermolecular Co–Co distances of 569 pm are observed. In compound <b>2</b>, a hydrogen-bonded dichloromethane molecule is present,
leading to a solvent aggregate with remarkable thermal stability for
which desolvation is taking place between 150 and 210 °C. Magnetic
measurements were performed to determine the zero-field-splitting
(ZFS) parameter <i>D</i> for both complexes. Frequency-dependent
susceptibility measurements revealed slow magnetic relaxation behavior
with spin-reversal barriers of 36 cm<sup>–1</sup> for <b>1</b> and 43 cm<sup>–1</sup> for <b>2</b> at an applied
external field of 400 Oe. This observation is related to an increasing
distortion of the pseudotetrahedral coordination geometry for complex <b>2</b>. These distortions can be decomposed in two major contributions.
One is the elongation effect described by the parameter ϵ<sub>T</sub>, which is the ratio of the averaged obtuse and acute bond
angles. The other effect is related to a twisting distortion of the
chelate coordination planes at the cobalt center. A comparison with
literature examples reveals that the elongation effect seems to govern
the overall magnetic behavior in pseudotetrahedral complexes with
two bidentate chelate ligands. Ab initio calculations for complexes <b>1</b> and <b>2</b> using the CASPT2 method show strong splitting
of the excited <sup>4</sup>T<sub>2</sub> term, which explains the
observed strong ZFS. Spin–orbit calculations with the RASSI-SO
method confirm the single-molecule-magnet behavior because only small
transversal elements are found for the lowest Kramers doublet for
both complexes
1,2-Bis(anilido)ethane Complexes of Calcium and Potassium: Synthesis, Structures, and Catalytic Activity
The metalation of
1,2-bis(anilino)ethane with excess KH leads to
the formation of the potassium complex [(thf)<sub>3</sub>K<sub>2</sub>{1,2-(PhN)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>}] (<b>1</b>). Complex <b>1</b> quantitatively reacts with anhydrous CaI<sub>2</sub> in THF yielding insoluble KI and dinuclear [(thf)<sub>5</sub>Ca<sub>2</sub>{1,2-(PhN)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>}<sub>2</sub>] (<b>2</b>) after crystallization from a mixture of
THF and hexane. Addition of <i>N</i>,<i>N</i>,<i>N′</i>,<i>N′′</i>,<i>N′′′</i>,<i>N′′′</i>-hexamethyltriethylenetetraamine (hmteta) yields [(hmteta)Ca{1,2-(PhN)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>}] (<b>3</b>). The complexes <b>1</b> and <b>2</b> proved to be inactive as catalysts in hydroamination reactions
of diphenylbutadiyne with secondary amines. However, a mixture of <b>1</b> and <b>2</b> (K:Ca ratio of 2:1) mediated the addition
of <i>N</i>-methyl-aniline and 1,2-bis(anilino)ethane to
one of the CC triple bonds of diphenylbutadiyne. Addition
of 18-crown-6 ether (18C6) leads to the formation of the sparingly
soluble potassium complex [{(18C6)K}<sub>2</sub>{1,2-(PhN)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>}] (<b>5</b>) and the insoluble calcium
complex [(18C6)Ca{1,2-(PhN)<sub>2</sub>C<sub>2</sub>H<sub>4</sub>}]
(<b>6</b>). The calciate-mediated hydroamination reaction is
regiocontrolled, but <i>E</i>- and <i>Z</i>-isomeric
addition products are observed, regardless of whether the reaction
is performed at daylight or in the dark. If toluene is used as solvent
for this s-block metal-mediated hydroamination catalysis, (<i>Z,Z</i>)-1,4,5,8,9,12-hexaphenyl-5,8-diazadodeca-3,9-diene-1,11-diyne
(<i>Z,Z</i>-<b>8</b>) precipitates, allowing isolation
and characterization of this isomer. In solution, this compound isomerizes
upon irradiation yielding an equilibrium between (<i>Z,Z</i>)-, (<i>E,Z</i>)- and (<i>E,E</i>)-isomers. The
determination of the crystal structures of (<i>Z,Z</i>)-
and (<i>E,E</i>)-1,4,5,8,9,12-hexaphenyl-5,8-diazadodeca-3,9-diene-1,11-diyne
unequivocally allows the assignment of the NMR parameters to specific
isomers
Cobalt(II)-Based Single-Ion Magnets with Distorted Pseudotetrahedral [N<sub>2</sub>O<sub>2</sub>] Coordination: Experimental and Theoretical Investigations
The synthesis and magnetic properties
of cobalt(II) complexes with sterically demanding Schiff-base ligands
are reported. The compounds [Co(L<sup>Br</sup>)<sub>2</sub>] (<b>1</b>) and [Co(L<sup>Ph</sup>)<sub>2</sub>]·CH<sub>2</sub>Cl<sub>2</sub> (<b>2</b>·CH<sub>2</sub>Cl<sub>2</sub>)
are obtained by the reaction of cobalt(II) acetate with the ligands
HL<sup>Br</sup> and HL<sup>Ph</sup> in a dichloromethane/methanol
mixture. <b>1</b> and <b>2</b> crystallize in the space
groups <i>P</i>2<sub>1</sub>2<sub>1</sub>2 and <i>P</i>1̅, respectively. X-ray diffraction studies revealed mononuclear
constitution of both complexes. For <b>1</b>, relatively short
intermolecular Co–Co distances of 569 pm are observed. In compound <b>2</b>, a hydrogen-bonded dichloromethane molecule is present,
leading to a solvent aggregate with remarkable thermal stability for
which desolvation is taking place between 150 and 210 °C. Magnetic
measurements were performed to determine the zero-field-splitting
(ZFS) parameter <i>D</i> for both complexes. Frequency-dependent
susceptibility measurements revealed slow magnetic relaxation behavior
with spin-reversal barriers of 36 cm<sup>–1</sup> for <b>1</b> and 43 cm<sup>–1</sup> for <b>2</b> at an applied
external field of 400 Oe. This observation is related to an increasing
distortion of the pseudotetrahedral coordination geometry for complex <b>2</b>. These distortions can be decomposed in two major contributions.
One is the elongation effect described by the parameter ϵ<sub>T</sub>, which is the ratio of the averaged obtuse and acute bond
angles. The other effect is related to a twisting distortion of the
chelate coordination planes at the cobalt center. A comparison with
literature examples reveals that the elongation effect seems to govern
the overall magnetic behavior in pseudotetrahedral complexes with
two bidentate chelate ligands. Ab initio calculations for complexes <b>1</b> and <b>2</b> using the CASPT2 method show strong splitting
of the excited <sup>4</sup>T<sub>2</sub> term, which explains the
observed strong ZFS. Spin–orbit calculations with the RASSI-SO
method confirm the single-molecule-magnet behavior because only small
transversal elements are found for the lowest Kramers doublet for
both complexes
Concept for Enhancement of the Stability of Calcium-Bound Pyrazolyl-Substituted Methanides
Metalation
of bis(3-thiophen-2-ylpyrazol-1-yl)phenylmethane [<b>2</b>,
which is accessible from the reaction of bis(3-thien-2-ylpyrazol-1-yl)methanone
(<b>1</b>) with triphosgene] with [(thf)<sub>2</sub>Ca{N(SiMe<sub>3</sub>)<sub>2</sub>}<sub>2</sub>] in tetrahydrofuran and subsequent
crystallization from a mixture of toluene and 1,2-dimethoxyethane
yield [(dme)Ca{C(Pz<sup>th</sup>)<sub>2</sub>Ph}{N(SiMe<sub>3</sub>)<sub>2</sub>}] (<b>3</b>). The α,α-bis(3-thiophen-2-ylpyrazol-1-yl)benzyl
ligand exhibits a κ<sup>2</sup><i>N</i>,κ<i>C</i>-coordination mode with a Ca–C σ-bond length
of 262.8(2) pm. The crystalline compound is stable if air and moisture
is strictly excluded; however, in solution; this calcium complex slowly
degrades
Directed Ortho Calciation of 1,3-Bis(3-isopropylimidazol-2-ylidene)benzene
The deprotonation
of 1,3-bis(3-isopropylimidazol-2-ylidene)benzene
with Me<sub>3</sub>SiCH<sub>2</sub>CaX (X = Br, I) in tetrahydrofuran
(THF) yields the ether adducts of the corresponding 2,6-bis(3-isopropylimidazol-2-ylidene)phenylcalcium
halides (X = Br (<b>1</b>·2thf), I (<b>2</b>·2thf)).
The crystallization behavior of <b>2</b> can be improved via
substitution of ligated thf molecules by tetrahydropyran (thp) ligands,
leading to <b>2</b>·2thp. These heteroleptic complexes <b>1</b>·2thf and <b>2</b>·2thp show very small Ca–C<sub>ipso</sub> bond lengths to the ipso-carbon atoms of the aryl groups.
Calciation of 1,3-bis(3-isopropylimidazol-2-ylidene)benzene with Ca(CH<sub>2</sub>SiMe<sub>3</sub>)<sub>2</sub> in THP leads to the formation
of ether-free homoleptic bis[2,6-bis(3-isopropylimidazol-2-ylidene)phenyl]calcium (<b>3</b>). Intramolecular
steric strain causes an elongation of the Ca–C<sub>ipso</sub> bonds to the aryl groups. In all of these complexes, the Ca–C<sub>carbene</sub> distances are significantly larger than those to the
ipso-carbon atoms of the aryl groups
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