Removal of cytostatic platinum compounds and recovery of precious metal from aqueous wastestream

Over the last decades, a strong antropogenic increase in platinum concentrations in the environment is observed. While catalytic converters used in cars and industry contribute to elevated levels in vegetation and soils, hospitals intensely discard platinum from their effluents to surface waters. Since the discovery of its cytostatic properties by Rosenberg, cisplatin and other platinum coordinating compounds such as carboplatin and more recently oxaliplatin are extensively used in chemotherapy for cancer treatment. After ingestion and interaction with DNA, the drugs are biodegraded and excreted by patients through urine – either in hospital or at home - to remain mostly untreated. Biomaterials are ubiquitous distributed over the world and ready available with equal performance. They show a promising potential as sorbent for pollutants from wastewaters. The precious metal containing material can be separated from solution as a solid and be processed and valorised afterwards. In a screening step, several natural wood-based materials and dried microalgal biological flocs have been tested for their sorption efficiency towards cytostatic platinum compounds

Towards a typology of coordinating compounds in Turkish

https://www.degruyter.com/view/j/flin.2018.52.issue-2/flin-2018-0008/flin-2018-0008.xml?format=IN

The synthesis and characterization of new higher nuclearity arene-ruthenium-sulfur clusters : a thesis presented in partial fulfillment of the requirements for the degree of Master of Science in Chemistry at Massey University, New Zealand

This thesis describes a project investigating the synthesis and characterization of new higher nuclearity arene-ruthenium-sulfur clusters and arene-ruthenium-nitrogen complexes. The thesis is divided into four chapters, with the introduction in Chapter One. The synthesis and characterization of new higher nuclearity arene-ruthenium-sulfur clusters are described in Chapter Two. These include two novel clusters, [Ru₅S₄(cymene)₄](PF₆)₂, [Ru₄(S₂)(SO)(cymene)₄](PF₆)₂ and one known cluster, [Ru₃S₂(cymene)₃](PF₆)₂. The X-ray crystallographic structures of these three arene-ruthenium-sulfur clusters are discussed in detail including how the number of valence electrons influences the structure, how the solid state structure and single crystal structure effect each other and how the structures determine the chemical shifts and other characters of the clusters. The unusual signals of these three clusters on ¹H NMR spectra are discussed carefully. The mechanisms of formation of arene-ruthenium-sulfur clusters are described in detail. Some electrochemistry and calculations (quantum chemistry) are also involved. The synthesis and characterization of arene-ruthenium-nitrogen complexes are described in Chapter Three. These include two new mono-nuclear complexes, [RuCl₂(NH₃)(cymene)], [Ru(NH₃)₃(cymene)](PF₆)₂, one novel amide dimer [RuCl(NH₂)(cymene)]₂ and one known complex, [RuCl(NH₃)₂(cymene)]PF₆. The mechanisms of reactions in which they are formed are also discussed. In Chapter Four, the experimental data is presented. The X ray crystallography of [Ru₅S₄(cymene)₄](PF₆)₂, [Ru₄(S₂)(SO)(cymene)₄](PF₆)₂, [RuCl₂(NH₃)(cymene)] and [RuCl(NH₂)(cymene)]₂ is described in detail

Anion receptor chemistry: highlights from 2011 and 2012

This review covers advances in anion complexation in the years 2011 and 2012. The review covers both organic and inorganic systems and also highlights the applications to which anion receptors can be applied such as self-assembly and molecular architecture, sensing, catalysis and anion transport

Recent Advances in the Synthetic and Mechanistic Aspects of the Ruthenium-catalyzed Carbon-heteroatom Bond Forming Reactions of Alkenes and Alkynes

The group’s recent advances in catalytic carbon-to-heteroatom bond forming reactions of alkenes and alkynes are described. For the C–O bond formation reaction, a well-defined bifunctional ruthenium-amido catalyst has been successfully employed for the conjugate addition of alcohols to acrylic compounds. The ruthenium-hydride complex (PCy3)2(CO)RuHCl was found to be a highly effective catalyst for the regioselective alkyne-to-carboxylic acid coupling reaction in yielding synthetically useful enol ester products. Cationic ruthenium-hydride catalyst generated in-situ from (PCy3)2(CO)RuHCl/HBF4·OEt2 was successfully utilized for both the hydroamination and related C–N bond forming reactions of alkenes. For the C–Si bond formation reaction, regio- and stereoselective dehydrosilylation of alkenes and hydrosilylation of alkynes have been developed by using a well-defined ruthenium-hydride catalyst. Scope and mechanistic aspects of these carbon-to-heteroatom bond forming reactions are discussed