Dimetallic Imido Complexes of Molybdenum and
Tungsten with Bridged Bis(η<sup>5</sup>-cyclopentadienyl) Ligands.
Molecular Structure of
[(MoO)<sub>2</sub>(μ-N<i><sup>t</sup></i>Bu)<sub>2</sub>{μ-(η<sup>5</sup>-C<sub>5</sub>H<sub>4</sub>)<sub>2</sub>SiMe<sub>2</sub>}]
Francisco Amor
Pilar Gómez-Sal
Ernesto de Jesús
Avelino Martín
Ana I. Pérez
Pascual Royo
Amelio Vázquez de Miguel
10.1021/om950943i.s001
https://acs.figshare.com/articles/journal_contribution/Dimetallic_Imido_Complexes_of_Molybdenum_and_Tungsten_with_Bridged_Bis_sup_5_sup_-cyclopentadienyl_Ligands_Molecular_Structure_of_MoO_sub_2_sub_-N_i_sup_t_sup_i_Bu_sub_2_sub_-_sup_5_sup_-C_sub_5_sub_H_sub_4_sub_sub_2_sub_SiMe_sub_2_sub_/3776979
New imido and oxo dimetallic complexes of Mo and W with the
monobridged or dibridged
bis(cyclopentadienyl) ligands Cp<sup>1</sup>Cp or
Cp<sup>2</sup>Cp [Cp<sup>1</sup>Cp =
(η<sup>5</sup>-C<sub>5</sub>H<sub>4</sub>)<sub>2</sub>SiMe<sub>2</sub>,
Cp<sup>2</sup>Cp = (η<sup>5</sup>-C<sub>5</sub>H<sub>3</sub>)<sub>2</sub>(SiMe<sub>2</sub>)<sub>2</sub>]
have been synthesized. The Cp<sup>2</sup>Cp complexes have
been obtained as both
<i>cis</i> and <i>trans</i> isomers which differ in the
stereodisposition of the two metal fragments with
respect to the Cp<sup>2</sup>Cp system, the stereochemistry being
unchanged in all the reactions
described. Addition of H<sub>2</sub>N<i><sup>t</sup></i>Bu
to
[(MCl<sub>4</sub>)<sub>2</sub>(μ-Cp<i><sup>n</sup></i>Cp)]
(M = Mo, <i>n</i> = 1, <b>2a</b>; <i>n</i> = 2,
<b>2b</b>; M = W,
<i>n</i> = 2, <b>2c</b>) affords the imido M(V) complexes
[{M(N<i><sup>t</sup></i>Bu)Cl<sub>2</sub>}<sub>2</sub>(μ-Cp<i><sup>n</sup></i>Cp)]
(<b>4a−c</b>). Complexes
<b>4a,c</b> are oxidized by PCl<sub>5</sub> to give
[{M(N<i><sup>t</sup></i>Bu)Cl<sub>3</sub>}<sub>2</sub>(μ-Cp<i><sup>n</sup></i>Cp)]
(<b>5a,c</b>). Both <b>4a</b> and <b>5a</b>
afford
[{MoCl(μ-N<i><sup>t</sup></i>Bu)}<sub>2</sub>(μ-Cp<sup>1</sup>Cp)]
(<b>6</b>) by reduction with sodium amalgam. The differences
found
between this reaction and the related reductions of the mononuclear Cp
analogues are
discussed. Reaction of <b>6</b> with HgO affords the oxo
complex
[{MoO(μ-N<i><sup>t</sup></i>Bu)}<sub>2</sub>(μ-Cp<sup>1</sup>Cp)]
(<b>7</b>).
[(MoOCl)<sub>2</sub>(μ-O)(μ-Cp<sup>2</sup>Cp)]
(<b>3</b>) is obtained by reaction of
[{Mo(CO)<sub>3</sub>Cl}<sub>2</sub>(μ-Cp<sup>2</sup>Cp)]
with CH<sub>3</sub>NO<sub>2</sub> or bubbling air through a THF solution of
<i>cis</i>-[(MoCl<sub>4</sub>)<sub>2</sub>(μ-Cp<sup>2</sup>Cp)].
The molecular
structure of <b>7</b> has been determined by a single-crystal X-ray
analysis.
1996-04-16 00:00:00
PCl 5
Complexes 4
Cp analogues
sodium amalgam
THF solution
trans isomers
Cp 2 Cp complexes
2 SiMe 2
Molecular Structure
Cp 2 Cp system
C 5 H 3
C 5 H 4
metal fragments
CH 3
Cp 1 Cp
SiMe 2
oxo dimetallic complexes
H 2 N t Bu
Cp 2 Cp
Dimetallic Imido Complexes