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Wolfgang Kaim | |
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| Born | 13 May 1951 Bad Vilbel, Germany |
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| Fields | Chemistry |
Wolfgang Kaim (born 13 May 1951 in Bad Vilbel, Germany) is a German chemist who held the chair of coordination chemistry at the University of Stuttgart. He is co-author of the internationally recognized book, Bioinorganic Chemistry [1] which was awarded with the Literature Award of the German Chemical Industry.
Kaim studied chemistry and physics at the University of Frankfurt and the University of Konstanz. His diploma thesis in physical organic chemistry was supervised by E. Daltrozzo (1974). He started working on main group radicals in Hans Bock's group at the University of Frankfurt, where he earned his PhD in 1978. After a post-doctoral year with F. A. Cotton at Texas A&M University, supported by a postdoctoral Liebig Fellowship, he completed his habilitation for inorganic chemistry in 1982 ("Coordination Chemistry of Reduced Heterocycles"). Kaim continued his independent research career at the University of Frankfurt with a Winnacker Fellowship followed by a Heisenberg Fellowship. In 1987 he moved to the University of Stuttgart to take up a chaired position for coordination chemistry until 2019.
Kaim is an adjunct professor at the Northern Illinois University (USA), and has been visiting professor at the Sun Yat-sen University in Guangzhou (China), guest professor at the Universidad de Chile in Santiago (Chile), the University of Concepción (Chile) and the Indian Institute of Technology Bombay (India). [2]
He has been the advisor of more than 70 PhD students.
In 2014 he was awarded the Alfred Stock Memorial Prize by the Gesellschaft Deutscher Chemiker (GDCh). In the same year he received the L. F. Leloir Award from Argentina.
Kaim's interdisciplinary research covers the areas of radical stabilization by metal coordination ('non-innocent ligands'), coenzyme models, the extension of mixed-valence chemistry, electron transfer effects on M-C and M-H bonds, the crystallization of new organic radicals and the electron transfer properties of boron compounds, as well as spectroelectrochemistry in the IR, UV/VIS/near-infrared regions as spectroscopic probes for electron transfer sites and the consequences of electron transfer or charge transfer on structure and bonding, EPR spectroscopy as a less common but highly useful methodology and CV (cyclic voltammetry).
He is the co-author of more than 700 publications in peer-reviewed journals. [3]
Inorganic chemistry deals with synthesis and behavior of inorganic and organometallic compounds. This field covers chemical compounds that are not carbon-based, which are the subjects of organic chemistry. The distinction between the two disciplines is far from absolute, as there is much overlap in the subdiscipline of organometallic chemistry. It has applications in every aspect of the chemical industry, including catalysis, materials science, pigments, surfactants, coatings, medications, fuels, and agriculture.
In coordination chemistry, a ligand is an ion or molecule with a functional group that binds to a central metal atom to form a coordination complex. The bonding with the metal generally involves formal donation of one or more of the ligand's electron pairs, often through Lewis bases. The nature of metal–ligand bonding can range from covalent to ionic. Furthermore, the metal–ligand bond order can range from one to three. Ligands are viewed as Lewis bases, although rare cases are known to involve Lewis acidic "ligands".
Plastocyanin is a copper-containing protein that mediates electron-transfer. It is found in a variety of plants, where it participates in photosynthesis. The protein is a prototype of the blue copper proteins, a family of intensely blue-colored metalloproteins. Specifically, it falls into the group of small type I blue copper proteins called "cupredoxins".
Bioinorganic chemistry is a field that examines the role of metals in biology. Bioinorganic chemistry includes the study of both natural phenomena such as the behavior of metalloproteins as well as artificially introduced metals, including those that are non-essential, in medicine and toxicology. Many biological processes such as respiration depend upon molecules that fall within the realm of inorganic chemistry. The discipline also includes the study of inorganic models or mimics that imitate the behaviour of metalloproteins.
Inner sphere complex is a type of surface complex that refers to the surface chemistry changing a water-surface interface to one without water molecules bridging a ligand to the metal ion. Formation of inner sphere complexes occurs when ions bind directly to the surface with no intervening water molecules. These types of surface complexes are restricted to ions that have a high affinity for surface sites and include specifically adsorbed ions that can bind to the surface through covalent bonding.
Dithiolene metal complexes are complexes containing 1,2-dithiolene ligands. 1,2-Dithiolene ligands, a particular case of 1,2-dichalcogenolene species along with 1,2-diselenolene derivatives, are unsaturated bidentate ligand wherein the two donor atoms are sulfur. 1,2-Dithiolene metal complexes are often referred to as "metal dithiolenes", "metallodithiolenes" or "dithiolene complexes". Most molybdenum- and tungsten-containing proteins have dithiolene-like moieties at their active sites, which feature the so-called molybdopterin cofactor bound to the Mo or W.
Tetracyanoquinodimethane (TCNQ) is the organic compound with the formula (NC)2CC6H4C(CN)2. This cyanocarbon, a relative of para-quinone, is an electron acceptor that is used to prepare charge transfer salts, which are of interest in molecular electronics.
Copper proteins are proteins that contain one or more copper ions as prosthetic groups. Copper proteins are found in all forms of air-breathing life. These proteins are usually associated with electron-transfer with or without the involvement of oxygen (O2). Some organisms even use copper proteins to carry oxygen instead of iron proteins. A prominent copper proteins in humans is in cytochrome c oxidase (cco). The enzyme cco mediates the controlled combustion that produces ATP.
In chemistry, a (redox) non-innocent ligand is a ligand in a metal complex where the oxidation state is not clear. Typically, complexes containing non-innocent ligands are redox active at mild potentials. The concept assumes that redox reactions in metal complexes are either metal or ligand localized, which is a simplification, albeit a useful one.
Alan McLeod Sargeson FAA FRS was an Australian inorganic chemist.
Hiroshi Nishihara, born 21 March 1955, is a Japanese chemist and Professor of Chemistry at The University of Tokyo in Japan. Currently heading the department of Chemistry and Inorganic Chemistry Laboratory in The University of Tokyo, he is a distinguished professor, researcher and pioneer in the field of synthesis and electrochemistry of conductive metal complex polymers.
Werner Urland is a German chemist whose name is imprinted in the pioneering implementation of the Angular Overlap Model for the interpretation of optical and magnetic properties of rare-earth coordination compounds. This approach receives a renewed value in the context of the vogue around the lanthanide-based new materials, such as achieving magnets at molecular scale, or designing new phosphor materials.
Sally Anne Brooker is a New Zealand inorganic chemist. She has been a full professor at the University of Otago since 2006.
2-Picolylamine is an organic compound with the formula H2NCH2C5H4N. A colorless liquid, it is a common bidentate ligand and a precursor to more complex multidentate ligands such as tris(2-pyridylmethyl)amine. It is usually prepared by hydrogenation of 2-cyanopyridine. One such complex is Baratta's catalyst RuCl2(PPh3)2(ampy) (ampy = 2-picolylamine) for transfer hydrogenation. Salts of the complex [Fe(pyCH2NH2)3]2+ exhibit spin crossover behavior, whereby the complex switches from high to low spin configurations, depending on the temperature.
Spectroelectrochemistry (SEC) is a set of multi-response analytical techniques in which complementary chemical information is obtained in a single experiment. Spectroelectrochemistry provides a whole vision of the phenomena that take place in the electrode process. The first spectroelectrochemical experiment was carried out by Theodore Kuwana, PhD, in 1964.
Mixed valence complexes contain an element which is present in more than one oxidation state. Well-known mixed valence compounds include the Creutz–Taube complex, Prussian blue, and molybdenum blue. Many solids are mixed-valency including indium chalcogenides.
Connie C. Lu is a Taiwanese-American inorganic chemist and a professor of chemistry at the University of Bonn. She was previously a professor of chemistry at the University of Minnesota, Twin Cities. Lu's research focuses on the synthesis of novel bimetallic coordination complexes, as well as metal-organic frameworks. These molecules and materials are investigated for the catalytic conversion of small molecules like as N2 and CO2 into value-added chemicals like ammonia and methanol. Lu is the recipient of multiple awards for her research, including the National Science Foundation CAREER Award and the Sloan Research Fellowship in 2013, and an Early Career Award from the University of Minnesota's Initiative for Renewable Energy and the Environment in 2010.
Frances Ann Walker was an American chemist known for her work on heme protein chemistry. She was an elected fellow of the American Association for the Advancement of Science and the American Chemical Society.
Cerium compounds are compounds containing the element cerium (Ce), a lanthanide. Cerium exists in two main oxidation states, Ce(III) and Ce(IV). This pair of adjacent oxidation states dominates several aspects of the chemistry of this element. Cerium(IV) aqueous solutions may be prepared by reacting cerium(III) solutions with the strong oxidizing agents peroxodisulfate or bismuthate. The value of E⦵(Ce4+/Ce3+) varies widely depending on conditions due to the relative ease of complexation and hydrolysis with various anions, although +1.72 V is representative. Cerium is the only lanthanide which has important aqueous and coordination chemistry in the +4 oxidation state.
A magnesium(I) dimer is a molecular compound containing a magnesium to magnesium bond (Mg-Mg), giving the metal an apparent +1 oxidation state. Alkaline earth metals are commonly found in the +2-oxidation state, such as magnesium. The M2+ are considered as redox-inert, meaning that the +2 state is significant. However, recent advancements in main group chemistry have yielded low-valent magnesium (I) dimers, also given as Mg (I), with the first compound being reported in 2007. They can be generally represented as LMg-MgL, with L being a monoanionic ligand. For example, β-diketiminate, commonly referred to as Nacnac, is a useful chelate regarding these complexes. By tuning the ligand, the thermodynamics of the complex change. For instance, the ability to add substituents onto Nacnac can contribute to the steric bulk, which can affect reactivity and stability. As their discovery has grown, so has their usefulness. They are employed in organic and inorganic reduction reactions. It is soluble in a hydrocarbon solvent, like toluene, stoichiometric, selective, and safe.
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