These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: Preparation and reactivity of diazoalkane complexes of ruthenium stabilised by an indenyl ligand.
    Author: Albertin G, Antoniutti S, Castro J, Dottorello G.
    Journal: Dalton Trans; 2015 May 21; 44(19):9289-303. PubMed ID: 25913868.
    Abstract:
    Diazoalkane complexes [Ru(η(5)-C9H7)(N2CAr1Ar2)(PPh3)L]BPh4 (1-3) [L = PPh3, P(OMe)3, P(OEt)3; Ar1 = Ar2 = Ph; Ar1 = Ph, Ar2 = p-tolyl; Ar1Ar2 = C12H8 fluorenyl] were prepared by allowing chloro-complexes [RuCl(η(5)-C9H7)(PPh3)L] to react with an excess of diazoalkane in ethanol. Complexes 1-3 reacted with ethylene CH2=CH2 (1 atm) and maleic anhydride [ma, CH=CHCO(O)CO] to afford η(2)-alkene complexes [Ru(η(5)-C9H7)(η(2)-CH2=CH2)(PPh3)L]BPh4 (4, 5) and [Ru(η(5)-C9H7){η(2)-CH=CHCO(O)CO}(PPh3)L]BPh4 (7). Further, complexes 1-3 underwent cycloaddition with acrylonitrile CH2=C(H)CN, giving 1H-pyrazoline derivatives [Ru(η(5)-C9H7){η(1)-N=C(CN)CH2C(Ar1Ar2)NH}(PPh3)L]BPh4 (6). Treatment of diazoalkane complexes 1-3 with acetylene CH[triple bond, length as m-dash]CH under mild conditions (1 atm, room temperature) led to dipolar cycloaddition, affording 3H-pyrazole complexes [Ru(η(5)-C9H7)-{η(1)-N=NC(Ar1Ar2)CH=CH}(PPh3)L]BPh4 (8), whereas reaction with terminal alkynes RC≡CH (R = Ph, p-tolyl, Bu(t)) gave vinylidene derivatives [Ru(η(5)-C9H7){=C=C(H)R}(PPh3)L]BPh4 (9). The latter reacted with nucleophiles such as amines and alcohols to give amino- and alkoxy-carbene derivatives [Ru(η(5)-C9H7){=C(NHPr(n))(CH2Ph)}(PPh3)L]BPh4 (11) and [Ru(η(5)-C9H7){=C(CH3)(OEt)}(PPh3)L]BPh4 (10), respectively. In addition, complexes 9 reacted with phenylhydrazine to afford nitrile derivatives [Ru(η(5)-C9H7)(N[triple bond, length as m-dash]CCH2R)(PPh3)L]BPh4 (12) and phenylamine, whereas the reaction with water led to hydrolysis of the alkyne and formation of carbonyl complexes [Ru(η(5)-C9H7)(CO)(PPh3)L]BPh4 (13). Lastly, treatment of vinylidene complexes with the phosphines PPh3 and P(OMe)3 afforded alkenylphosphonium derivatives [Ru(η(5)-C9H7){C(H)=C(R)PPh3}(PPh3)L]BPh4 (14) and [Ru(η(5)-C9H7){C(R)=C(H)P(OMe)3}(PPh3)L]BPh4 (15), respectively. Compound [Ru(η(5)-C9H7){C(H)=C(H)PPh3}(PPh3)L]BPh4 (16) was also prepared. The complexes were characterised by spectroscopy (IR and NMR) and X-ray crystal structure determinations of [Ru(η(5)-C9H7){N2C(C12H8)}(PPh3){P(OEt)3}]BPh4 (3c), [Ru(η(5)-C9H7){=C=C(H)Ph}(PPh3){P(OEt)3}]BPh4 (9d) and [Ru(η(5)-C9H7){C(H)=C(Ph)PPh3}(PPh3){P(OEt)3}]BPh4 (14d).
    [Abstract] [Full Text] [Related] [New Search]