260548-62-7

Upstream product

• 288098-78-2 [(η5-Me5C5)Ru((NC4H9)2CC6H5)(η3-allyl)]PF6 

Downstream Products

• 288069-05-6 [(η5-Me5C5)Ru((NC4H9)2CC6H5)(η3-CH2C(CH3)CH2)]PF6 
• 288098-78-2 [(η5-Me5C5)Ru((NC4H9)2CC6H5)(η3-allyl)]PF6 
• 288069-03-4 [(η5-Me5C5)Ru((NC4H9)2CC6H5)(η3-allyl)]Cl 
• 260548-65-0 (eta.5-C₅Me₅)Ru(CO)((N-tBu)2CPh) 
• 389571-49-7 [Ru(II)(η5-C5Me5)(η-t-BuNC(Ph)N-t-Bu)(η2-CH2CHCH2OAc)] 
• 389608-57-5 [Ru(IV)(η3-CH2C(Me)CH2)(η5-C5Me5)(>eta.2-t-BuNC(Ph)N-t-Bu)]Cl 

Relevant academic research and scientific papers

Oxidative addition of allylic substrates to coordinatively unsaturated ruthenium compounds, [Ru(η5-C5Me5)(η-amidinate)]: Preparation, structure elucidation, and catalysis of novel ruthenium (IV)-η3-allyl complexes

Oxidative addition reactions of allylic halides, acetates, and carbonates with [Ru(η5-C5Me5)(η-amidinate)] [amidinate: iPrNC(Me)=NiPr (1a), 1BuNC(Ph)=N1Bu (1b)], which shows signs of coordinative unsaturation, gave novel cationic π-allyl ruthenium(IV) species. The compounds [Ru(η3-allyl)(η5-C5Mes)(η 2-amidinate)]+X- were isolated by anion exchange of the products (X = PF6, BF4, BPh4), and were characterized by spectroscopic analysis. The crystallography of two of the [Ru(η3-allyl)(η5-C5Mes)(η 2-amidinate)] +X- revealed a four-legged piano stool structure in which two nitrogen atoms in the amidinate ligand and two carbon atoms in the η3-allyl ligands occupy the positions of four legs; the orientation of the η3-allyl ligand was endo. Although cyclic voltammograms of the precursor, [Ru(η5-C5Me5)(η-amidinate)], indicated possible oxidative addition of organic halides other than allylic halides to [Ru(η5-C5Me5)(η-amidinate)], only allylic halides gave the corresponding Ru(IV) products. The importance of prior coordination of the carbon-carbon double bond of allylic substrates was evidenced by NMR observation of the intermediate in the reaction of 1a or 1b with allyl acetate. Addition of nucleophiles such as PhLi, dimethyl methylsodiomalonate, and piperidine to the [Ru(η3-allyl)(η5-C5Me 5)(η2-amidinate)]+X- gave rise to allylation of these nucleophiles and regeneration of [Ru(η5-C5Me5)(η-amidinate)]. The reactions of allyl methyl carbonate with nucleophiles were also achieved by catalysis of either [Ru(η5C5Me5)(η-amidinate)] or [Ru(η3-allyl)(η5-C5Me 5)(η2-amidinate)]+X-.

(η5-C5Me5)Ru(amidinate): Highly Reactive Ruthenium Complexes Formally Bearing 16 Valence Electrons Showing Signs of Coordinative Unsaturation

Novel coordinatively unsaturated ruthenium complexes, (η5-C5Me5)Ru(amidinate), were synthesized from [(η5-C5Me5)Ru(OMe)]2 and lithium amidinates, which exist as monomers in both