Academic literature on the topic 'Copper NHC complexes'

I shall now describe a special case of the Lewis acid–base reactions I introduced in Reaction 9. I showed there that a Lewis acid is a species that can accept a lone pair from another incoming species and form a bond to it, that a Lewis base is a species that provides that lone pair, and that the result of this sharing is a complex of the two species joined together by a chemical bond. The important special case I would like to share with you here is when the Lewis acid is a metal atom or ion, especially but not necessarily one drawn from the d-block of the periodic table (a ‘transition metal’). The d-block consists of the elements that make up the skinny central rectangle of the periodic table. They include important constructional metals, such as iron, nickel, and copper, and also the chemically aloof ‘noble’ metals gold, platinum, and silver. The Lewis base that I focus on will be a molecule or ion that also has an independent existence in the wild, such as water, H2O, or ammonia, NH3. In most cases the complex consists of the central metal atom or ion with up to six Lewis bases clustering around it. In this context, the Lewis bases are known as ‘ligands’ (from the Latin for ‘bound’) and I shall use that term here. I don’t want you to think that I am embarking on stratospherically esoteric material again. These metal complexes are hugely important in many aspects of the everyday world. For instance, chlorophyll is a complex of magnesium and is responsible for capturing the energy of the Sun for photosynthesis (Reaction 26). There is hardly a more important molecule. One that comes close in importance is haemoglobin, an elaborate complex of iron, which ensures that oxygen reaches all your cells and keeps you alive. Many pigments are complexes, so your life is decorated and made more colourful by them. Some pharmaceuticals are complexes based on platinum, so one day, perhaps even now, you might be kept alive by one of these artificial complexes.

An oxidase catalyzes the oxidation of a substrate by O2 without incorporating an oxygen atom into the product. A monooxygenase catalyzes oxidation by O2 with incorporation of one oxygen atom into the product, and oxidation by a dioxygenase proceeds with incorporation of both atoms of O2 into the product. These reactions generally require an organic or metallic coenzyme, with few exceptions, notably urate oxidase. Mechanisms of action of phenylalanine hydroxylase, galactose oxidase, and ascorbate oxidase are provided in chapter 4 in connection with the introduction of metallic coenzymes. In this chapter, we present cases of well-studied coenzyme and metal-dependent oxidases and oxygenases, and we consider one example of an oxidase that does not require a cofactor. Biochemical diversity may be a characteristic of oxidases, which include flavoproteins, heme proteins, copper proteins, and quinoproteins. The actions of copper and topaquinone-dependent amine oxidases are presented in chapter 3, and in chapter 4, two copper-dependent oxidases are discussed. In this chapter, we discuss flavin-dependent oxidases, a mononuclear iron oxidase, and a cofactor-independent oxidase. Flavin-dependent oxidases catalyze the reaction of O2 with an alcohol or amine to produce the corresponding carbonyl compound and H2O2. Examples include glucose oxidase, which produces gluconolactone and H2O2 from glucose and O2 according to. A D-Amino acid oxidase (EC 1.4.3.3) catalyzes a formally similar reaction to produce an α-keto acid from the corresponding α-D-amino acid. The oxidation of an amino acid by an oxidase produces ammonium ion in addition to hydrogen peroxide and the ketoacid, and so it is formally more complex. It proceeds in the three phases described in, the reduction of FAD to FADH2 by the amino acid, hydrolysis of the resultant α-iminoacid to the corresponding α-ketoacid and NH4, and oxidation of FADH2 by O2 to form H2O2. D-Amino acid oxidase is a thoroughly studied example of a flavoprotein oxidase. The enzyme is a 84-kDa homodimer containing one molecule of FAD per subunit. The mechanisms of the hydrolysis of imines and of the oxidation of dihydroflavins are discussed in chapters 1 and 3.

Abstract The significance of materialized prototypes from CAD generated mechanical parts has been recognized since more than a decade. Despite the ever increasing quality and speed of graphical visualization methods, solid 3D hard copies from designs remain essential for certain stages in the creation process. Especially during the phase of conceptual geometric design, when alternative shape proposals must be quickly judged, automatic, fast and inexpensive production of replica is of importance. However, for such a kind of prototyping in conjunction with CAD, traditional methods based on CAM a