Publications by authors named "Kang-Long Wong"

The reactivity of the cerium(IV) oxo complex [(L)Ce(═O)(HO)]·MeC(O)NH (1; L = [CoCp{P(O)(OEt)}], where Cp = η-CH) toward electrophiles and Brønsted acids has been investigated. The treatment of 1 with acetic anhydride afforded the diacetate complex [Ce(L)(OCMe)] (2). The reaction of 1 with B(CF) yielded [Ce(L)(MeCONH)][B(CF)(OH)] (3), in which the [B(CF)(OH)] anions are H-bonded to the O-bound acetamide ligands.

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Heterometallic Ce(IV)/M (M = Mo(VI), Re(VII), V(V)) oxo clusters supported by the Kläui tripodal oxygen ligand [(η(5)-C5H5)Co{P(O)(OEt)2}3](-) (LOEt(-)) have been synthesized and structurally characterized, and the catalytic activity of the Ce(IV)/V(V) oxo cluster in the oxidation of thioanisoles has been studied. Treatment of [Ce(LOEt)Cl3] (1) with [Ag2MoO4] afforded the reported Ce(IV)/Mo(VI) cluster [H4(CeLOEt)6Mo9O38] (2), whereas that with [AgReO4] yielded the Ce(IV)/Re(VII) cluster [{LOEtCe(ReO4)2(H2O)(μ-ReO4)}2] (3) that contains an 8-membered Ce2Re2O4 ring. Treatment of 1 with [Ag3VO4] afforded the Ce(IV)/V(V) cluster [H2(CeLOEt)4(V[double bond, length as m-dash]O)4(μ4-O)(μ3-O)12] (4) containing a {Ce4V4O13} oxo-metallic core.

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Ruthenium thio- and seleno-nitrosyl complexes containing chelating sulfur and oxygen ligands have been synthesised and their de-chalcogenation reactions have been studied. The reaction of mer-[Ru(N)Cl3(AsPh3)2] with elemental sulfur and selenium in tetrahydrofuran at reflux afforded the chalcogenonitrosyl complexes mer-[Ru(NX)Cl3(AsPh3)2] [X = S (1), Se (2)]. Treatment of 1 with KN(R2PS)2 afforded trans-[Ru(NS)Cl{N(R2PS)2}2] [R = Ph (3), Pr(i) (4), Bu(t) (5)].

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A tetranuclear Ce(IV) oxo cluster compound containing the Kläui tripodal ligand [Co(η(5) -C5 H5 ){P(O)(OEt)2 }3 ](-) (LOEt (-) ) has been synthesized and its reactions with H2 O2 , CO2 , NO, and Brønsted acids have been studied. The treatment of [Ce(LOEt )(NO3 )3 ] with Et4 NOH in acetonitrile afforded the tetranuclear Ce(IV) oxo cluster [Ce4 (LOEt )4 O7 H2 ] (1) containing an adamantane-like {Ce4 (μ2 -O)6 } core with a μ4 -oxo ligand at the center. The reaction of 1 with H2 O2 resulted in the formation of the peroxo cluster [Ce4 (LOEt )4 (μ4 -O)(μ2 -O2 )4 (μ2 -OH)2 ] (2).

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