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Carbon–beryllium Bond
Organoberyllium chemistry involves the synthesis and properties of organometallic compounds featuring the group 2 alkaline earth metal beryllium (Be). The area remains less developed relative to the chemistry of other main-group elements, because Be compounds are toxic and few applications have been found. Structure Homoleptic compounds The coordination number of Be in organoberyllium compounds ranges from two to four. Dimethylberyllium and dimethylmagnesium adopts the same structure. Diethylberyllium, however, does not structurally resemble diethylmagnesium (which has the same structure as dimethylmagnesium). This contrast is attributed to the small size of Be relative to its heavier congener Mg: Be is one of the smallest atoms on the periodic table. Dineopentylberyllium and many other dialkyl derivatives has been reported. The phenyl derivative is represented by trimeric Be3Ph6. A terphenyl derivative is known. With bulky aryl ligands three-coordination is observed, see . ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Crystal Structure Of A BePh2 Complex That Produce Dimers
A crystal or crystalline solid is a solid material whose constituents (such as atoms, molecules, or ions) are arranged in a highly ordered microscopic structure, forming a crystal lattice that extends in all directions. In addition, macroscopic single crystals are usually identifiable by their geometrical shape, consisting of flat faces with specific, characteristic orientations. The scientific study of crystals and crystal formation is known as crystallography. The process of crystal formation via mechanisms of crystal growth is called crystallization or solidification. The word ''crystal'' derives from the Ancient Greek word (), meaning both "ice" and "rock crystal", from (), "icy cold, frost". Examples of large crystals include snowflakes, diamonds, and table salt. Most inorganic solids are not crystals but polycrystals, i.e. many microscopic crystals fused together into a single solid. Polycrystals include most metals, rocks, ceramics, and ice. A third category of sol ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Beryllocene Conformation
Beryllocene is an organoberyllium compound with the chemical formula Be(C5H5)2, first prepared in 1959. The colorless substance can be crystallized from petroleum ether in the form of white needles at −60 °C and decomposes quickly upon contact with atmospheric oxygen and water. Preparation Beryllocene can be prepared by reacting beryllium chloride and sodium cyclopentadienide in benzene or diethyl ether: :\mathrm Properties Physical In contrast to the uncharged metallocenes of the transition metals V, Cr, Fe, Co, Ni, Ru and Os, which have a strictly symmetrical and therefore dipoleless structure, beryllocene has an electric dipole moment of 2.46 Debye (in benzene), or 2.24 Debye (in cyclohexane), indicating asymmetry of the molecule. In the IR spectrum there are signals at 1524, 1610, 1669, 1715 and 1733 cm−1, which also indicate that the structure does correspond to that of ferrocene. In contrast, the nuclear magnetic resonance spectrum shows only ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Beryllium
Beryllium is a chemical element; it has Symbol (chemistry), symbol Be and atomic number 4. It is a steel-gray, hard, strong, lightweight and brittle alkaline earth metal. It is a divalent element that occurs naturally only in combination with other elements to form minerals. Gemstones high in beryllium include beryl (Aquamarine (gemstone), aquamarine, emerald, red beryl) and chrysoberyl. It is a Abundance of the chemical elements#Universe, relatively rare element in the universe, usually occurring as a product of the spallation of larger atomic nuclei that have collided with cosmic rays. Within the cores of stars, beryllium is depleted as it is fused into heavier elements. Beryllium constitutes about 0.0004 percent by mass of Earth's crust. The world's annual beryllium production of 220 tons is usually manufactured by extraction from the mineral beryl, a difficult process because beryllium bonds strongly to oxygen. In structural applications, the combination of high flexural ri ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Group 2 Organometallic Chemistry
image:GOHRUQ.png, Magnesium anthracenide with three thf ligands. Group 2 organometallic chemistry refers to the organic compound, organic derivativess of any group 2 element. It is a subtheme to main group organometallic chemistry. By far the most common group 2 organometallic compounds are the magnesium-containing Grignard reagents which are widely used in organic chemistry. Other organometallic group 2 compounds are typically limited to academic interests. Characteristics As the group 2 elements (also referred to as the alkaline earth metals) contain two valence electrons, their chemistries have similarities group 12 element, group 12 organometallic compounds. Both readily assume a +2 oxidation states with higher and lower states being rare, and are less electronegative than carbon. However, as the group two elements (with the exception of beryllium) have considerably low electronegativity the resulting C-M bonds are more highly polarized and ionic bond, ionic-like, if not entirel ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Dimethylmercury
Dimethylmercury is an extremely toxic organomercury compound with the formula ( CH3)2 Hg. A volatile, flammable, dense and colorless liquid, dimethylmercury is one of the strongest known neurotoxins. Less than 0.1 mL is capable of inducing severe mercury poisoning resulting in death. Synthesis, structure, and reactions The compound was one of the earliest organometallics reported, reflecting its considerable stability. The compound was first prepared by George Buckton in 1857 by a reaction of methylmercury iodide with potassium cyanide: : 2 CH3HgI + 2 KCN → Hg(CH3)2 + 2 KI + (CN)2 + Hg Later, Edward Frankland discovered that it could be synthesized by treating sodium amalgam with methyl halides: : Hg + 2 Na + 2 CH3I → Hg(CH3)2 + 2 NaI It can also be obtained by alkylation of mercuric chloride with methyllithium: : HgCl2 + 2 LiCH3 → Hg(CH3)2 + 2 LiCl The molecule adopts a linear structure with Hg–C bond lengths of 2.083 Å. Reactivity and physical propert ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Simon Aldridge
Simon Aldridge FRS is a British chemist specialising in inorganic chemistry, with a particular focus on the chemistry of main group elements. He is currently a Professor of Chemistry at the University of Oxford and a Fellow and Tutor in Inorganic Chemistry at The Queen’s College, Oxford. His research has significantly contributed to the field of main group chemistry. Aldridge has been recognised with several awards, including a Fellowship of the Royal Society (FRS) in 2024. Early life and education Aldridge was born in Shrewsbury, United Kingdom. He studied chemistry at Jesus College, University of Oxford, earning a Bachelor of Arts degree with first-class honours in 1992. He went on to complete a Doctor of Philosophy (DPhil) in Inorganic Chemistry at Oxford in 1996, under the supervision of A.J. Downs. His doctoral thesis focused on the chemistry of volatile compounds of main group elements. Academic career Aldridge began his academic career as a Post-doctoral Associate a ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Cyclic Alkyl Amino Carbenes
Cyclic(alkyl)(amino) carbenes (CAACs) are a class of stable singlet carbene ligands that feature one amino and one sp3 alkyl group adjacent to the carbene carbon atom. CAACs are a subset of Persistent carbene, N-heterocyclic carbenes (NHCs) in which the replacement of an Amine, amino group on the "classical" diaminocarbene with a Saturated and unsaturated compounds, saturated carbon atom results in a carbene ligand that is both a better σ-donor and π-acceptor than classical NHCs. The lone pair on the nitrogen atoms in classical NHCs allows for π-donation from both nitrogen atoms, while substitution of one nitrogen with a carbon atom results in weaker π-donation from only one nitrogen substituent, thus making CAACs stronger π-acceptors and more electrophilic than classical NHCs. Like NHCs, CAACs have tunable Steric effects, steric and electronic properties that make them versatile Ligand#:~:text=In coordination chemistry, a ligand,to form a coordination complex., ligands in both ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Diazabutadiene
Diimines are organic compounds containing two imine (RCH=NR') groups. Common derivatives are 1,2-diimines and 1,3-diimines. These compounds are used as ligands, but they are also precursors to other organic compounds. Preparation Diimines are prepared by condensation reactions where a dialdehyde or diketone is treated with amine and water is eliminated. Many are derived from the condensation of 1,2-diketones and dialdehydes with amines, often anilines. The dialdehyde glyoxal is an especially common precursor. Similar methods are used to prepare Schiff bases and oximes. 1,2-Diimines The 1,2-diimines are also called α-diimines and 1,4-diazabutadienes. An example is glyoxal-bis(mesitylimine), a yellow solid that is synthesized by condensation of 2,4,6-trimethylaniline and glyoxal. 2,2'-Bipyridine is a 1,2-diimine. 1,2-Diketimines are “non-innocent ligands”, akin to the dithiolenes. : 1,3-Diimines For example, acetylacetone (2,4-pentanedione) and a primary alkyl- or ary ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Alkynyl
\ce \ce Acetylene \ce \ce \ce Propyne \ce \ce \ce \ce 1-Butyne In organic chemistry, an alkyne is an unsaturated hydrocarbon containing at least one carbon—carbon triple bond. The simplest acyclic alkynes with only one triple bond and no other functional groups form a homologous series with the general chemical formula . Alkynes are traditionally known as acetylenes, although the name ''acetylene'' also refers specifically to , known formally as ethyne using IUPAC nomenclature. Like other hydrocarbons, alkynes are generally hydrophobic. Structure and bonding In acetylene, the H–C≡C bond angles are 180°. By virtue of this bond angle, alkynes are rod-like. Correspondingly, cyclic alkynes are rare. Benzyne cannot be isolated. The C≡C bond distance of 118 picometers (for C2H2) is much shorter than the C=C distance in alkenes (132 pm, for C2H4) or the C–C bond in alkanes (153 pm). : The triple bond is very strong with a bond strength of 839 kJ/mol. The si ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Cyclopentadienide
Sodium cyclopentadienide is an organosodium compound with the formula C5H5Na. The compound is often abbreviated as NaCp, where Cp− is the cyclopentadienide anion. Sodium cyclopentadienide is a colorless solid, although samples often are pink owing to traces of oxidized impurities. Preparation The first salt of cyclopentadienide to be reported was potassium cyclopentadienide, prepared by Johannes Thiele. In 1901 there was not much interest in the topic. Sodium cyclopentadienyl is prepared by treating cyclopentadiene with sodium: : The conversion can be conducted by heating a suspension of molten sodium in dicyclopentadiene.Tarun K. Panda, Michael T. Gamer, Peter W. Roesky "An Improved Synthesis of Sodium and Potassium Cyclopentadienide" Organometallics, 2003, 22, 877–878. In former times, the sodium was provided in the form of "sodium wire" or "sodium sand", a fine dispersion of sodium prepared by melting sodium in refluxing xylene and rapidly stirring. Sodium hydride ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Beryllocene
Beryllocene is an organoberyllium compound with the chemical formula Be(C5H5)2, first prepared in 1959. The colorless substance can be crystallized from petroleum ether in the form of white needles at −60 °C and decomposes quickly upon contact with atmospheric oxygen and water. Preparation Beryllocene can be prepared by reacting beryllium chloride and sodium cyclopentadienide in benzene or diethyl ether: :\mathrm Properties Physical In contrast to the uncharged metallocenes of the transition metals V, Cr, Fe, Co, Ni, Ru and Os, which have a strictly symmetrical and therefore dipoleless structure, beryllocene has an electric dipole moment of 2.46 Debye (in benzene), or 2.24 Debye (in cyclohexane), indicating asymmetry of the molecule. In the IR spectrum there are signals at 1524, 1610, 1669, 1715 and 1733 cm−1, which also indicate that the structure does correspond to that of ferrocene. In contrast, the nuclear magnetic resonance spectrum shows only ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Beryllium Chloride
Beryllium chloride is an inorganic compound with the formula BeCl2. It is a colourless, hygroscopic solid that dissolves well in many polar solvents. Its properties are similar to those of aluminium chloride, due to beryllium's diagonal relationship with aluminium. Structure and synthesis Beryllium chloride is prepared by reaction of the metal with chlorine at high temperatures: :Be + Cl2 → BeCl2 BeCl2 can also be prepared by carbothermal reduction of beryllium oxide in the presence of chlorine.Cotton, F. A.; Wilkinson, G. (1980) ''Advanced Inorganic Chemistry'' John Wiley and Sons, Inc: New York, . BeCl2 can be prepared by treating beryllium with hydrogen chloride. Two forms ( polymorphs) of BeCl2 are known. Both structures consist tetrahedral Be2+ centers interconnected by doubly bridging chloride ligands. One form consist of edge-sharing polytetrahedra. The other form resembles zinc iodide with interconnected adamantane-like cages. In contrast, BeF2 is a 3-dimensional ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
