Konrad Seppelt

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Konrad Seppelt (2018) Seppelt, Konrad.jpg
Konrad Seppelt (2018)

Konrad Seppelt (born September 2, 1944 in Leipzig) [1] is a academic author, professor and former vice president of the Free University Berlin.

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Publications

Scientific publications

A random selection of Prof Seppelt's publications:

Related Research Articles

In chemistry, noble gas compounds are chemical compounds that include an element from the noble gases, group 18 of the periodic table. Although the noble gases are generally unreactive elements, many such compounds have been observed, particularly involving the element xenon.

In organometallic chemistry, acetylide refers to chemical compounds with the chemical formulas MC≡CH and MC≡CM, where M is a metal. The term is used loosely and can refer to substituted acetylides having the general structure RC≡CM. Acetylides are reagents in organic synthesis. The calcium acetylide commonly called calcium carbide is a major compound of commerce.

<span class="mw-page-title-main">Phosphorus pentachloride</span> Chemical compound

Phosphorus pentachloride is the chemical compound with the formula PCl5. It is one of the most important phosphorus chlorides/oxychlorides, others being PCl3 and POCl3. PCl5 finds use as a chlorinating reagent. It is a colourless, water-sensitive solid, although commercial samples can be yellowish and contaminated with hydrogen chloride.

<span class="mw-page-title-main">Xenon hexafluoride</span> Chemical compound

Xenon hexafluoride is a noble gas compound with the formula XeF6. It is one of the three binary fluorides of xenon that have been studied experimentally, the other two being XeF2 and XeF4. All known are exergonic and stable at normal temperatures. XeF6 is the strongest fluorinating agent of the series. It is a colorless solid that readily sublimes into intensely yellow vapors.

<span class="mw-page-title-main">Fluoroantimonic acid</span> Chemical compound

Fluoroantimonic acid is a mixture of hydrogen fluoride and antimony penta­fluoride, containing various cations and anions. This mixture is a superacid that, in terms of corrosiveness, is trillions of times stronger than 100% sulfuric acid in terms of its protonating ability measured by Hammett function. It even protonates some hydro­carbons to afford pentacoordinate carbo­cations. Like its precursor hydrogen fluoride, it attacks glass, but can be stored in containers lined with PTFE (Teflon) or PFA.

<span class="mw-page-title-main">Molybdenum(V) chloride</span> Chemical compound

Molybdenum(V) chloride is the inorganic compound with the empirical formula MoCl5. This dark volatile solid is used in research to prepare other molybdenum compounds. It is moisture-sensitive and soluble in chlorinated solvents.

<span class="mw-page-title-main">Selenium tetrafluoride</span> Chemical compound

Selenium tetrafluoride (SeF4) is an inorganic compound. It is a colourless liquid that reacts readily with water. It can be used as a fluorinating reagent in organic syntheses (fluorination of alcohols, carboxylic acids or carbonyl compounds) and has advantages over sulfur tetrafluoride in that milder conditions can be employed and it is a liquid rather than a gas.

<span class="mw-page-title-main">Gold compounds</span>

Gold compounds are compounds by the element gold (Au). Although gold is the most noble of the noble metals, it still forms many diverse compounds. The oxidation state of gold in its compounds ranges from −1 to +5, but Au(I) and Au(III) dominate its chemistry. Au(I), referred to as the aurous ion, is the most common oxidation state with soft ligands such as thioethers, thiolates, and organophosphines. Au(I) compounds are typically linear. A good example is Au(CN)−2, which is the soluble form of gold encountered in mining. The binary gold halides, such as AuCl, form zigzag polymeric chains, again featuring linear coordination at Au. Most drugs based on gold are Au(I) derivatives.

<span class="mw-page-title-main">Tetraxenonogold(II)</span> Chemical compound

Tetraxenonogold(II), gold tetraxenide(II) or AuXe2+
4
is a cationic complex with a square planar configuration of atoms. It is found in the compound AuXe2+
4
(Sb
2
F
11
)
2
(tetraxenonogold undecafluorodiantimonate), which exists in triclinic and tetragonal crystal modifications. The AuXe2+
4
ion is stabilised by interactions with the fluoride atoms of the counterion. The Au−Xe bond length is 274 pm (2.74 Å). Tetraxenonogold(II) is unusual in that it is a coordination complex of xenon, which is weakly basic. It is also unusual in that it contains gold in the +2 oxidation state. It can be produced by reduction of AuF3 by xenon in the presence of fluoroantimonic acid. The salt crystallises at low temperature. Four xenon atoms bond with the gold(II) ion to make this complex.

<span class="mw-page-title-main">Rhenium pentachloride</span> Chemical compound

Rhenium pentachloride is an inorganic compound of chlorine and rhenium. The compound has the formula Re2Cl10 but it is usually referred to as rhenium pentachloride. It is a red-brown solid.

<span class="mw-page-title-main">Arsenic pentachloride</span> Chemical compound

Arsenic pentachloride is a chemical compound of arsenic and chlorine. This compound was first prepared in 1976 through the UV irradiation of arsenic trichloride, AsCl3, in liquid chlorine at −105 °C. AsCl5 decomposes at around −50 °C. The structure of the solid was finally determined in 2001. AsCl5 is similar to phosphorus pentachloride, PCl5 in having a trigonal bipyramidal structure where the equatorial bonds are shorter than the axial bonds (As-Cleq = 210.6 pm, 211.9 pm; As-Clax= 220.7 pm).

<span class="mw-page-title-main">Difluorophosphate</span> Chemical compound

Difluorophosphate or difluorodioxophosphate or phosphorodifluoridate is an anion with formula PO2F−2. It has a single negative charge and resembles perchlorate and monofluorosulfonate in shape and compounds. These ions are isoelectronic, along with tetrafluoroaluminate, phosphate, orthosilicate, and sulfate. It forms a series of compounds. The ion is toxic to mammals as it causes blockage to iodine uptake in the thyroid. However it is degraded in the body over several hours.

<span class="mw-page-title-main">Werner Urland</span> German chemist (born 1944)

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.

<span class="mw-page-title-main">Transition metal alkyl complexes</span> Coordination complex

Transition metal alkyl complexes are coordination complexes that contain a bond between a transition metal and an alkyl ligand. Such complexes are not only pervasive but are of practical and theoretical interest.

Karl Wieghardt is a German inorganic chemist and emeritus director of the Max Planck Institute for Chemical Energy Conversion in Mülheim. He was active in the preparation and detailed characterization of models for iron and manganese metalloenzymes, metal complexes of noninnocent ligands, and magnetic interactions in polynuclear metal complexes.

<span class="mw-page-title-main">Transition metal chloride complex</span> Coordination complex

In chemistry, a transition metal chloride complex is a coordination complex that consists of a transition metal coordinated to one or more chloride ligand. The class of complexes is extensive.

Sulfidostannates, or thiostannates are chemical compounds containing anions composed of tin linked with sulfur. They can be considered as stannates with sulfur substituting for oxygen. Related compounds include the thiosilicates, and thiogermanates, and by varying the chalcogen: selenostannates, and tellurostannates. Oxothiostannates have oxygen in addition to sulfur. Thiostannates can be classed as chalcogenidometalates, thiometallates, chalcogenidotetrelates, thiotetrelates, and chalcogenidostannates. Tin is almost always in the +4 oxidation state in thiostannates, although a couple of mixed sulfides in the +2 state are known,

<span class="mw-page-title-main">Transition metal ether complex</span>

In chemistry, a transition metal ether complex is a coordination complex consisting of a transition metal bonded to one or more ether ligand. The inventory of complexes is extensive. Common ether ligands are diethyl ether and tetrahydrofuran. Common chelating ether ligands include the glymes, dimethoxyethane (dme) and diglyme, and the crown ethers. Being lipophilic, metal-ether complexes often exhibit solubility in organic solvents, a property of interest in synthetic chemistry. In contrast, the di-ether 1,4-dioxane is generally a bridging ligand.

<span class="mw-page-title-main">Seleninyl fluoride</span> Chemical compound

Seleninyl fluoride is an oxyfluoride of selenium with the chemical formula SeOF2.

Bromosyl trifluoride is an inorganic compound of bromine, fluorine, and oxygen with the chemical formula BrOF3.

References

  1. "The Robert A. Welch Foundation Research Bulletin" (51). 1988: 26.{{cite journal}}: Cite journal requires |journal= (help)