L. Cheng et Nj. Coville, SYNTHESIS AND SOLID-STATE ISOMERIZATION-REACTIONS OF DIAG-(ETA(5)-C5H4R)RE(CO)(L)X-2 AND LAT-(ETA(5)-C5H4R)RE(CO)(L)X-2, Journal of organometallic chemistry, 556(1-2), 1998, pp. 111-118
Reaction of diag- or lat- (i.e. trans or cis)(eta(5)-C5H4R)Re(CO)(2)X-
2 (R = Me, t-Bu, SiMe3; X = Br, I) with isocyanides, phosphites and tr
iphenyl phosphine proceeded rapidly at room temperature (r.t.) in the
presence of Me3NO to give (eta(5)-C5H4R)Re(CO)(L)X-2 (L = CNC6H3Me2, P
(OMe)(3), P((OPr)-Pr-i)(3), P(OPh)(3), PPH3) in good yields (typically
> 75%) with the diagonal isomer as the dominant ( > 90%) product. The
diag-(eta(5)-C5H4R)Re(CO)(L)X-2 isomer were readily converted into th
e lateral isomer in excellent yield (> 70%) by directly heating solid
diag-(eta(5)-C5H4R)Re(CO)(L)X-2 under nitrogen below its melting point
. Solution phase isomerisation in CHCl3 or C6D6 (r.t., visible light i
rradiation) also proceeded from the diag to the lat isomer. The solid-
state reaction between diag-(eta(5)-C5H4Me)Re(CO)[P(OPh)(3)]Br-2 and e
xcess NaI surprisingly gave diag-(eta(5)-C5H4Me)Re(CO)(2)I-2 in quanti
tative yield, revealing both Re-P and Re-Br bond cleavage. The new com
plexes, diag- and lat-(eta(5)-C5H4R)Re(CO)(L)X-2, have been fully char
acterized by elemental analysis and IR and NMR spectroscopy. (C) 1998
Elsevier Science S.A. All rights reserved.