Synthesis and Characterization of rGO@ZnO Nanocomposites for Esterification of Acetic Acid.

In the present work, the aim is to synthesize reduced graphene oxide (rGO) and zinc:reduced graphene oxide composite catalysts (ZnO:rGO) for esterification of acetic acid with -heptanol. The physical and chemical characteristics of the rGO and rGO-metal oxide composite catalysts such as textural surface characteristics, surface morphology, thermal stability, functional groups, and elemental analysis were studied. The surface areas of rGO, ZnO, and ZnO were recorded, respectively, at 31.

Migratory insertion of [B(C6F5)2] into C-H bonds: CO promoted transfer of the boryl fragment.

The reaction of (eta(5)-C5H5)Fe(CO)2B(C6F5)2 with CO has been shown to proceed via ligand substitution at the metal with accompanying transfer of the boryl fragment (via C-H insertion) to the Cp ring, thereby generating the zwitterion [eta(5)-C5H4B(C6F5)2H]Fe(CO)3 in quantitative yield.

Reactivity of the bis(pentafluorophenyl)boranes ClB(C6F5)2 and [HB(C6F5)2]n towards late transition metal reagents.

The reactivities of the highly electrophilic boranes ClB(C(6)F(5))(2) (1) and [HB(C(6)F(5))(2)](n) (2) towards a range of organometallic reagents featuring metals from Groups 7-10 have been investigated. Salt elimination chemistry is observed 1 between and the nucleophilic anions eta(5)-C(5)R(5))Fe(CO)(2)](-)(R = H or Me) and [Mn(CO)(5)](-), leading to the generation of the novel boryl complexes (eta(5)-C(5)R(5))Fe(CO)(2)B(C(6)F(5))(2)[R = H (3) or Me (4)] and (OC)(5)MnB(C(6)F(5))(2) (5). Such systems are designed to probe the extent to which the strongly sigma-donor boryl ligand can also act as a pi-acceptor; a variety of spectroscopic, structural and computational probes imply that even with such strongly electron withdrawing boryl substituents, the pi component of the metal-boron linkage is a relatively minor one.