Polymer-grafted and neat vanadium(V) complexes as functional mimics of haloperoxidases

The monobasic tridentate ONN donor ligand 1-(2-pyridylazo)-2-naphthol [Hpan (I)] reacts with [V1v0(acac)2] in dry methanol to yield the oxidovanadium(IV) complex 1VIv0(acac)(pan)1 (1). The dioxidovanadium(V) complex Pv0(pan))2(u-0)2] (2) is obtained by aerial oxidation of 1 in methanol. Complex 2 can also be prepared directly by reacting [V1v0(acac)2] with I followed by aerial oxidation in methanol. Treatment of 1 or 2 in methanol with H202 yields the oxidomonoperoxidovanadium(V) complex [Vv0(02)(pan)(Me0H)] (3). Reaction of imidazolomethylpolystyrene cross-linked with 5% divinylbenzene (PS-im) with 2 in DMF resulted in the formation of the polymer-grafted dioxidovanadium(V) complex PS-im[Vv02(pan)] (4). All these complexes are characterized by various spectroscopic techniques (IR, electronic, NMR (IH and 51V) and electron paramagnetic resonance (EPR)), thermal, field-emission scanning electron micrographs (FE-SEM) as well as energy dispersive X-ray (EDX) studies. The crystal and molecular structure of 3 has been determined, confirming the ONN binding mode of!. The polymer-grafted complex 4 has been used for the oxidative bromination of styrene, salicylaldehyde and trans-stilbene. Various parameters, such as amounts of catalyst, oxidant (aqueous 30% H202), KBr and aqueous 70% HC104 have been optimized to obtain the maximum oxidative bromination of the substrates. Under the optimized reaction conditions, styrene gave a maximum of 99% conversion after 2 h of reaction, with the main products having a selectivity order of: 1-phenylethane-1,2-diol (75%) > 2-bromo-1phenylethane-1-ol (20%) > 1,2-dibromo-1-phenylethane (1.2%). With nearly same conversion in same time, the oxidative bromination of salicylaldehyde gave three products with the selectivity order: 5-bromosalicylaldehyde > 2,4,6-tribromophenol > 3,5-dibromosalicylaldehyde. A maximum of 91% conversion of trans-stilbene has been obtained in 2 h of reaction time, where selectivity of the obtained reaction products varied in the order: 2,3-diphenyloxirane (trans-stilbene oxide) > 1,2-dibromo-1,2diphenylethane > 2-brorno-1,2-diphenylethanol. The catalytic activity of the non-polymer grafted complex 2 is lower than that of the polymer-grafted one. In addition, the recycling ability of the grafted complex makes it better over the neat complex. 0 2013 Elsevier Ltd. All rights reserved.