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Preparation and reactivity of diazoalkane complexes of ruthenium stabilised by an indenyl ligand†
Gabriele Albertin,Stefano Antoniutti,Jesús Castro,Gianluca Dottorello
Dalton Transactions Pub Date : 04/27/2015 00:00:00 , DOI:10.1039/C5DT00755K
Abstract

Diazoalkane complexes [Ru(η5-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(η5-C9H7)(PPh3)L] to react with an excess of diazoalkane in ethanol. Complexes 1–3 reacted with ethylene CH2[double bond, length as m-dash]CH2 (1 atm) and maleic anhydride [ma, CH[double bond, length as m-dash]CHCO(O)CO] to afford η2-alkene complexes [Ru(η5-C9H7)(η2-CH2[double bond, length as m-dash]CH2)(PPh3)L]BPh4 (4, 5) and [Ru(η5-C9H7){η2-CH[double bond, length as m-dash]CHCO(O)CO}(PPh3)L]BPh4 (7). Further, complexes 1–3 underwent cycloaddition with acrylonitrile CH2[double bond, length as m-dash]C(H)CN, giving 1H-pyrazoline derivatives [Ru(η5-C9H7){η1-N[double bond, length as m-dash]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(η5-C9H7)-{η1-N[double bond, length as m-dash]NC(Ar1Ar2)CH[double bond, length as m-dash]CH}(PPh3)L]BPh4 (8), whereas reaction with terminal alkynes RC[triple bond, length as m-dash]CH (R = Ph, p-tolyl, But) gave vinylidene derivatives [Ru(η5-C9H7){[double bond, length as m-dash]C[double bond, length as m-dash]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(η5-C9H7){[double bond, length as m-dash]C(NHPrn)(CH2Ph)}(PPh3)L]BPh4 (11) and [Ru(η5-C9H7){[double bond, length as m-dash]C(CH3)(OEt)}(PPh3)L]BPh4 (10), respectively. In addition, complexes 9 reacted with phenylhydrazine to afford nitrile derivatives [Ru(η5-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(η5-C9H7)(CO)(PPh3)L]BPh4 (13). Lastly, treatment of vinylidene complexes 9 with the phosphines PPh3 and P(OMe)3 afforded alkenylphosphonium derivatives [Ru(η5-C9H7){C(H)[double bond, length as m-dash]C(R)PPh3}(PPh3)L]BPh4 (14) and [Ru(η5-C9H7){C(R)[double bond, length as m-dash]C(H)P(OMe)3}(PPh3)L]BPh4 (15), respectively. Compound [Ru(η5-C9H7){C(H)[double bond, length as m-dash]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(η5-C9H7){N2C(C12H8)}(PPh3){P(OEt)3}]BPh4 (3c), [Ru(η5-C9H7){[double bond, length as m-dash]C[double bond, length as m-dash]C(H)Ph}(PPh3){P(OEt)3}]BPh4 (9d) and [Ru(η5-C9H7){C(H)[double bond, length as m-dash]C(Ph)PPh3}(PPh3){P(OEt)3}]BPh4 (14d).

Graphical abstract: Preparation and reactivity of diazoalkane complexes of ruthenium stabilised by an indenyl ligand
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