TY - JOUR
T1 - Reactions of co-ordinated ligands. Part 49. Ligand-displacement and oxidative-addition reactions of [Ru{P(OMe)3}(η4-C4Ph 4)(η4-C5H6)]; crystal structures of [Ru(NCMe){P(OMe)3} (η3-C3H5)(η4-C 4Ph4)][SbF6] and...
AU - Crocker, Mark
AU - Green, Michael
AU - Nagle, Katherine R.
AU - Williams, David J.
PY - 1990
Y1 - 1990
N2 - Title full: Reactions of co-ordinated ligands. Part 49. Ligand-displacement and oxidative-addition reactions of [Ru{P(OMe)3}(η4-C4Ph 4)(η4-C5H6)]; crystal structures of [Ru(NCMe){P(OMe)3} (η3-C3H5)(η4-C 4Ph4)][SbF6] and [Ru{C(Ph)=C(Ph)C(η6-C6H5)=C(Ph)CH 2CH=CH2}{P(OMe)3}2][BF4]. Treatment of the ruthenium(0) complex [Ru{P(OMe)3}(η4-C4Ph 4)(η4-C5H6)] with isoprene or cyclohexa-1,3-diene results in the displacement of C5H6 and formation of compounds of the type [Ru{P(OMe)3}(η4-1,3-diene) (η4-C4Ph4)]. Although trans-penta-1,3-diene reacts similarly to give the η4-trans-penta-1,3-diene complex, the corresponding reaction with cis-penta-1,3-diene affords a mixture of both the trans- and cis-penta-1,3-diene ruthenium complexes. A possible mechanism for this reaction is discussed. Cyclopenta-1,3-diene is also displaced on treatment of [Ru{P(OMe)3}(η4-C4Ph 4)(η4-C5H6)] with allyl bromide or 2-methylallyl chloride to give respectively the ruthenium(II) species [RuBr{P(OMe)3}(η3-C3H 5)(η4-C4Ph4)] and [RuCl{P(OMe)3}(η3-2-MeC3H 4)(η4-C4Ph4)]. Reaction of these species with AgBF4 in acetonitrile affords the cations [Ru(NCMe){P(OMe)3}(η3-C3H 5)(η4-C4Ph4)][BF4] and [Ru(NCMe){P(OMe)3}(η3-2-MeC3H 4)(η4-C4Ph4)] [BF4]. The solid-state structure of the corresponding SbF6-, salt of the former cation was established by X-ray crystallography. The geometry of the molecule is that of a three-legged piano-stool, the allyl group adopting an endo configuration. Instead of the expected propeller configuration for the η4-tetraphenylcyclobutadiene ligand, two of the phenyl rings lie roughly coplanar with the C4 ring, while the other two are approximately perpendicular to it. Attempts to replace the acetonitrile ligand present in these species by P(OMe)3 failed, however when AgBF4 was added to an acetone solution of [RuBr{P(OMe)3}(η3-C3H 5)(η4-C4Ph4)] followed by addition of P(OMe)3 a yellow cationic species was obtained, which was shown by X-ray crystallography to be the ring-opened compound [Ru{C(Ph)=C(Ph)C(η6-C6H5)=C(Ph)CH 2CH=CH2}{P(OMe)3}2][BF4]. A mechanism is proposed for this unusual reaction.
AB - Title full: Reactions of co-ordinated ligands. Part 49. Ligand-displacement and oxidative-addition reactions of [Ru{P(OMe)3}(η4-C4Ph 4)(η4-C5H6)]; crystal structures of [Ru(NCMe){P(OMe)3} (η3-C3H5)(η4-C 4Ph4)][SbF6] and [Ru{C(Ph)=C(Ph)C(η6-C6H5)=C(Ph)CH 2CH=CH2}{P(OMe)3}2][BF4]. Treatment of the ruthenium(0) complex [Ru{P(OMe)3}(η4-C4Ph 4)(η4-C5H6)] with isoprene or cyclohexa-1,3-diene results in the displacement of C5H6 and formation of compounds of the type [Ru{P(OMe)3}(η4-1,3-diene) (η4-C4Ph4)]. Although trans-penta-1,3-diene reacts similarly to give the η4-trans-penta-1,3-diene complex, the corresponding reaction with cis-penta-1,3-diene affords a mixture of both the trans- and cis-penta-1,3-diene ruthenium complexes. A possible mechanism for this reaction is discussed. Cyclopenta-1,3-diene is also displaced on treatment of [Ru{P(OMe)3}(η4-C4Ph 4)(η4-C5H6)] with allyl bromide or 2-methylallyl chloride to give respectively the ruthenium(II) species [RuBr{P(OMe)3}(η3-C3H 5)(η4-C4Ph4)] and [RuCl{P(OMe)3}(η3-2-MeC3H 4)(η4-C4Ph4)]. Reaction of these species with AgBF4 in acetonitrile affords the cations [Ru(NCMe){P(OMe)3}(η3-C3H 5)(η4-C4Ph4)][BF4] and [Ru(NCMe){P(OMe)3}(η3-2-MeC3H 4)(η4-C4Ph4)] [BF4]. The solid-state structure of the corresponding SbF6-, salt of the former cation was established by X-ray crystallography. The geometry of the molecule is that of a three-legged piano-stool, the allyl group adopting an endo configuration. Instead of the expected propeller configuration for the η4-tetraphenylcyclobutadiene ligand, two of the phenyl rings lie roughly coplanar with the C4 ring, while the other two are approximately perpendicular to it. Attempts to replace the acetonitrile ligand present in these species by P(OMe)3 failed, however when AgBF4 was added to an acetone solution of [RuBr{P(OMe)3}(η3-C3H 5)(η4-C4Ph4)] followed by addition of P(OMe)3 a yellow cationic species was obtained, which was shown by X-ray crystallography to be the ring-opened compound [Ru{C(Ph)=C(Ph)C(η6-C6H5)=C(Ph)CH 2CH=CH2}{P(OMe)3}2][BF4]. A mechanism is proposed for this unusual reaction.
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U2 - 10.1039/DT9900002571
DO - 10.1039/DT9900002571
M3 - Article
AN - SCOPUS:51149213405
SN - 1472-7773
SP - 2571
EP - 2580
JO - Journal of the Chemical Society, Dalton Transactions
JF - Journal of the Chemical Society, Dalton Transactions
IS - 8
ER -