112681-79-5Relevant academic research and scientific papers
Synthesis, characterisation and cytotoxicity studies of ruthenium arene complexes bearing trichlorogermyl ligands
Deacon-Price, Connor,Romano, Dario,Riedel, Tina,Dyson, Paul J.,Blom, Burgert
, p. 513 - 520 (2019)
The synthesis of five half sandwich ruthenium(II) trichlorogermyl complexes of the type [(η6-Arene)Ru(PR3)Cl(GeCl3)] (PR3 = Phosphane and phosphite ligands; Arene = p-cymene or C6H5-OC
Electronic effects in mixed N-heterocyclic carbene/phosphite indenylidene ruthenium metathesis catalysts
Bidal, Yannick D.,Urbina-Blanco, César A.,Poater, Albert,Cordes, David B.,Slawin, Alexandra M.Z.,Cavallo, Luigi,Cazin, Catherine S.J.
supporting information, p. 11326 - 11337 (2019/08/07)
Five new complexes [RuCl2(SIMes)(Ind)(O-pXC5H4)] bearing different para-substituted triphenylphosphites (X = H, OCH3, CF3, Cl, SF5 and CN) were synthesised and used to study the effect of t
Synthesis and characterisation of [(η6-cymene)Ru(L)X 2] compounds: Single crystal X-ray structure of [(η6- cymene)Ru(P{OPh}3)Cl2] at 203 K
Hodson, Emma,Simpson, Stephen J.
, p. 2695 - 2707 (2008/10/09)
Treatment of the chloro bridged dimer {[(η6-cymene)RuCl] 2(μ-Cl)2} (1) with the donor molecules in hot hexane causes bridge splitting reactions that produce the monomeric compounds [(η6-cymene)Ru(L)Cl2]. Treatment of the chloro bridged dimer {[(η6-cymene)RuCl]2(μ-Cl)2} (1) with the donor molecules P(OPh)3, P(OMe)3, PPh 3, PMe3, CO, SMe2, CNtBu and CNTos in hot hexane causes bridge splitting reactions that produce the monomeric compounds [(η6-cymene)Ru(L)Cl2], (4)-(11), respectively. Use of the chiral isonitrile S(-)-α-methylbenzylisonitrile produced the corresponding complex 12. The diiodo analogues, 13-15, were prepared similarly from {[(η6-cymene)RuI]2(μ-I) 2} (3) for P(OPh)3, P(OMe)3 and PPh 3, respectively. Insertion of tin(II) chloride into both metal-chlorine bonds was observed for [(η6-cymene)Ru(P{OMe} 3)Cl2] (5), while only monosubstitution was observed for [(η6-cymene)Ru(PPh3)Cl2] (6). Halide abstraction in the presence of a substrate reaction has been used to prepare some selected cationic compounds which contain an asymmetric ligand environment. Reaction of {[(η6-cymene)RuCl]2(μ-Cl)2} with 1,2-bis(diphenylphosphino)-ethane under ionising conditions produced the cation [(η6-cymene)Ru(dppe)Cl]PF6 (20). Selected compounds have been examined by {13C-1H} heteronuclear correlation and {1H-1H} COSY and NOESY experiments. The structure of [(η6-cymene)Ru(P{OPh}3)Cl2] ? CH2Cl2 (4) has been determined at -70°C.
