E. Lindner et al., STOICHIOMETRIC AND CATALYTIC REACTIONS OF THE POLYSILOXANE-BOUND (ETHER-PHOSPHINE)RHODIUM(I) COMPLEX [CLRH(PO)(P-SIMILAR-TO-O)] IN INTERPHASES, Chemistry, 3(11), 1997, pp. 1833-1845
The reaction of four equivalents of the monomeric trimethoxysilyl(T)-f
unctionalized ether-phosphine ligand CyP(CH2CH2OCH3)(CH2)(3)SiR3 (R =
OMe [1a(T-0)], Me [1b]) with [{mu-ClRh(COE)(2)}(2)] yielded the monome
ric pseudo 14 electron rhodium(I) complexes [CIRh(PO)(P similar to O)]
(2a(T-0)(2), 2b). For the sol-gel process the complex 2 a(TO), was pr
otected by introduction of the volatile, reversibly binding ligand pyr
idine. Thus, the monomeric compound 2a(TO), was co-condensed with two
and eight equivalents of the co-condensation agent MeSi(OMe)(2)(CH2)(6
)(MeO)(2)SiMe (D-0-C-6- D-0) to give the polysiloxane-bound congeners
2(T-n)(2)(D-i-C-6-D-i)(y) (y = 2 and 8, respectively; i = 0 - 2; n = 0
- 3). The polysiloxane-bound complex 2(T-n)(2)-(D-i-C-6-D-i)(2) was t
reated with a variety of small molecules in the gas/solid and liquid/s
olid interphases. It was shown that a facile cleavage of the Rh - O bo
nd in the ether - phosphine chelate occurred even in the solid state.
The reaction of 2(T-n)(2) (D-i-C-6-D-i)(2) with carbon monoxide, carbo
n disulfide, and diphenylacetylene resulted in the irreversible coordi
nation of the molecule to the metal. In the presence of pyridine, the
polysiloxane-bound complex 2(T-n)(2)(D-i-C-6-D-i)(2) oxidatively added
hydrogen to give the octahedrally configurated complex [ClRhH2(Py)(P
similar to O)(2)] [6(T-n)(2)(D-i-C-6-D-i)(2)]. Treatment of dry 2(T-n)
(2)(D-i-C-6-D-i)(2) with ethene led to the reversible formation of the
corresponding complex. Although the materials display low surface are
as, at least 75% of the rhodium centers within the matrix are accessib
le to the rather bulky tolan molecules. The complexes 2(T-n)(2)(D-i-C-
6-D-i)(y) (y = 2, 8) show high activities and selectivities in the hyd
rogenation of tolan. The conversion was found to depend markedly on th
e amount of co-condensate D-0-C-6-D-0 and on the polarity of the solve
nt. The polysiloxane-bound complexes 2(T-n)(2)(D-i-C-6-D-i)(y) are mor
e active than their monomeric congener 2a(T-0)(2).