S. Mihan et al., HYDROCARBON-BRIDGED METAL-COMPLEXES .39. CHEMISTRY OF PENTACARBONYL-RHENIUM-ACETYLIDES, Journal of organometallic chemistry, 541(1-2), 1997, pp. 423-439
Hydrocarbon-bridged Metal Complexes, XXXIX. Chemistry of Pentacarbonyl
-rhenium-acetylides. As a by-product in the preparation of (OC)(5)Re-C
=C-Re(CO)(5) (1) from [(OC)(5)Re(mu-eta(1):eta(2)-C=CH)Re(O)(5)]BF4 an
d K[KBEt3] the new fluxional hydride-bridged cluster (OC)(5)Re-C=C-Re(
CO)(4)[HRe(CO)(4)] (2) is obtained. (OC)(5)Mn-C=C-Mn(CO)(5) (4) is ava
ilable from [(OC)(5)Mn(eta(1):eta(2)-C=CH)Mn(CO)(5)]BF4 (3) and K[HBEt
3]. Reaction of 1 with Me3O+BF4- gives the sigma,pi-bridged complex [(
OC)(5)Re(mu-eta(1):eta(2)-C=CMe)Re(CO)(5)]BF4 (5). The alkynyl complex
(OC)(5)Re-C=C-SiMe3 (6) can be prepared by reaction of Na[Re(CO)(5)]
with 1-tosyl-2-trimethylsilyl-ethyne. The reaction of tosylethyne with
Na[Re(CO)(5)] affords (OC)(5)Re-C=CH (7) and (OC)(5)Re-C(H)=C(H)(tosy
l) (9). Complex 7 is also formed by cleavage of the Me3Si group from 6
. (OC)(5)ReOSO2CF3 reacts with Li(en)C=CH to give the chelate carbamoy
l complex (OC)(4) ReNH2CH2CH2NHCO (8). Elimination of CO from (OC)(5)R
e-C=C-Re(CO)(5) gives the tetrameric sigma,pi-acetylide-bridged cluste
r [(OC)(5)Re-C=C-Re(CO)(4)](2) (11). Similarly, [Me3Si-C=C-Re(CO)(4)](
2) (12) is formed from Me3Si-Re(CO)(5). The structures of 2, 9, 11 and
12 were determined by X-ray diffraction. As by-products from the ther
molysis of 1 and 7, [Re(CO)(3)OH](4) . 4H(2)O and [(OC)(3)ReOH](4).4(O
C)(5)ReCOCH3 were obtained. (C) 1997 Elsevier Science S.A.