K.F. O'Driscoll

Bio: K.F. O'Driscoll is an academic researcher from University of Waterloo. The author has contributed to research in topics: Sorption & Catalysis. The author has an hindex of 11, co-authored 22 publications receiving 339 citations.

Kinetics of pollutant sorption by biosorbents: review

Abstract: A review of the mechanisms of solute sorption onto various biosorbents has been performed. The mechanisms have been subdivided into reaction based systems and diffusion based systems and the literature has been reviewed in accordance with these two groups. The range of solute-sorbent systems reviewed include metal ions, dyestuffs and several organic substances in aqueous systems onto a wide range of biosorbents and mineral earths. Extensive tables are presented summarising isotherm types, sorption capacities, kinetic models which have been applied particularly to biosorbent systems but also to many other adsorbent materials.

The Coordination Chemistry of 2,2′:6′,2″-Terpyridine and Higher Oligopyridines

Abstract: Publisher Summary This chapter presents a discussion on the coordination chemistry of 2,2’: 6’, 2”-terpyridine and higher oligopyridines. The potentially terdentate ligand 2,2’: 6’, 2”-terpyridine presented, was first isolated by Morgan and Burstall as one of the numerous products from the reaction of pyridine with iron (III) chloride. There has been a considerable increase in the use of these ligands in recent years, prompted in part by the attractive photochemical and photophysical properties exhibited by complexes of the related ligands 2,2’-bipyridine and 1,10-phenanthroline. The chapter discusses stabilization of unusual complexes and states that low oxidation states are characterized by an excess of electron density at the metal atom; stabilization may be achieved by the use of ligands capable of reducing that electron density. One of the simplest ways to reduce the electron density is to design ligands with low-lying vacant orbitals of suitable symmetry for overlap with filled metal orbitals. This results in the transfer of electron density from the metal to the ligand (back-donation). In general, ligand nonbonding or π antibonding orbitals are of the correct symmetry for such overlap. The oligopyridines are ideally suited to such roles; they possess a filled highest occupied molecular orbital (HOMO) and a vacant lowest unoccupied molecular orbital (LUMO) of suitable energies for interaction with metal d orbitals. The chapter also discusses monodentate, bidentate, and bridging; terdentate and higher polydentate; cyclometallated, and others.