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Pentamethylcyclopentadienyl
1,2,3,4,5-Pentamethylcyclopentadiene is a cyclic diene with the formula C5Me5H (Me = CH3). 1,2,3,4,5-Pentamethylcyclopentadiene is the precursor to the ligand ''1,2,3,4,5-pentamethylcyclopentadienyl'', which is often denoted Cp* (C5Me5) and read as "C P star", the "star" signifying the five methyl groups radiating from the core of the ligand. In contrast to less-substituted cyclopentadiene derivatives, Cp*H is not prone to dimerization. Synthesis Pentamethylcyclopentadiene is commercially available. It was first prepared from tiglaldehyde via 2,3,4,5-tetramethylcyclopent-2-enone. Alternatively, 2-butenyllithium adds to ethyl acetate followed by acid-catalyzed dehydrocyclization: Organometallic derivatives Cp*H is a precursor to organometallic compounds containing the ligand, commonly called Cp*−. Some representative reactions leading to such Cp*–metal complexes follow: :Cp*H + C4H9Li → Cp*Li + C4H10 :Cp*Li + TiCl4 → Cp*TiCl3 + LiCl Some Cp* co ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Hexamethyl Dewar Benzene
Dewar benzene (also spelled ''dewarbenzene'') or bicyclo .2.0exa-2,5-diene is a bicyclic isomer of benzene with the molecular formula C6H6. The compound is named after James Dewar who included this structure in a list of possible C6H6 structures in 1869. However, he did not propose it as the structure of benzene, and in fact he supported the correct structure previously proposed by August Kekulé in 1865. Structure and properties Unlike benzene, Dewar benzene is not flat because the carbons where the rings join are bonded to four atoms rather than three. These carbons tend toward tetrahedral geometry, and the two cyclobutene rings make an angle where they are ''cis''- fused to each other. The compound has nevertheless considerable strain energy and reverts to benzene with a chemical half-life of two days. This thermal conversion is relatively slow because it is symmetry forbidden based on orbital symmetry arguments. Synthesis The compound itself was first synthesized in 1962 as a ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Decamethylferrocene
Decamethylferrocene or bis(pentamethylcyclopentadienyl)iron(II) is a chemical compound with formula or . It is a sandwich compound, whose molecule has an iron(II) cation attached by coordination bonds between two pentamethylcyclopentadienyl anions (, ). It can also be viewed as a derivative of ferrocene, with a methyl group replacing each hydrogen atom of its cyclopentadienyl rings. The name and formula are often abbreviated to DmFc, or . This compound is a yellow crystalline solid that is used in chemical laboratories as a weak reductant. The iron(II) core is easily oxidized to iron(III), yielding the monovalent cation decamethylferrocenium, and even to higher oxidation states. Preparation Decamethylferrocene is prepared in the same manner as ferrocene from pentamethylcyclopentadiene. This method can be used to produce other decamethylcyclopentadienyl sandwich compounds. :2 Li(C5Me5) + FeCl2 → Fe(C5Me5)2 + 2 LiCl The product can be purified by sublimation. has stagg ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Pentamethylcyclopentadienyl Rhodium Dichloride Dimer
Pentamethylcyclopentadienyl rhodium dichloride dimer is an organometallic compound with the formula C5(CH3)5RhCl2)sub>2, commonly abbreviated p*RhCl2sub>2 This dark red air-stable diamagnetic solid is a reagent in organometallic chemistry. Structure and preparation The compound has idealized C2h symmetry. Each metal centre is pseudo-octahedral. The compound is prepared by the reaction of rhodium trichloride trihydrate and pentamethylcyclopentadiene in hot methanol, from which the product precipitates: :2 Cp*H + 2 RhCl3(H2O)3 -> ce \text/chem> p*RhCl2sub>2 + 2 HCl + 6 H2O It was first prepared by the reaction of hydrated rhodium trichloride with hexamethyl Dewar benzene Reactions Reductive carbonylation gives p*Rh(CO)2 The Rh-'' μ''-Cl bonds are labile and cleave en route to a variety of adducts of the general formula Cp*RhCl2L. Treatment with silver ions in polar coordinating solvents cause ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Rhodium(III) Chloride
Rhodium(III) chloride refers to inorganic compounds with the formula RhCl3(H2O)''n'', where ''n'' varies from 0 to 3. These are diamagnetic solids featuring octahedral Rh(III) centres. Depending on the value of ''n'', the material is either a dense brown solid or a soluble reddish salt. The soluble trihydrated (n = 3) salt is widely used to prepare compounds used in homogeneous catalysis, notably for the industrial production of acetic acid and hydroformylation. Structures Aqueous solutions of RhCl3(H2O)3 have been characterized by 103Rh NMR spectroscopy, which shows the presence of several species. The proportions of which change with time and depend on the concentration of chloride. The relative distribution of these species determines the colour of the solutions, which can range from yellow (the hexaaquo ion) to "raspberry-red". Some of these species are h(H2O)6sup>3+, hCl(H2O)5sup>2+, ''cis''- and ''trans''- hCl2(H2O)4sup>+, and hCl3(H2O)3 Individual ions have been separ ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Pentamethylcyclopentadienyl Iridium Dichloride Dimer
Pentamethylcyclopentadienyl iridium dichloride dimer is an organometallic compound with the formula C5(CH3)5IrCl2)sub>2, commonly abbreviated p*IrCl2sub>2 This bright orange air-stable diamagnetic solid is a reagent in organometallic chemistry. Structure The compound has C2h symmetry. Each metal is pseudo-octahedral. The terminal and bridging Ir-Cl bonds have the lengths 2.39 and 2.45 Å, respectively. Preparation, reactions Pentamethylcyclopentadienyl iridium dichloride dimer was first prepared by the reaction of hydrated iridium trichloride with hexamethyl Dewar benzene. More conveniently, the compound is prepared by the reaction of hydrated iridium trichloride and pentamethylcyclopentadiene in hot methanol, from which the product precipitates :2 Cp*H + 2 IrCl3(H2O)3 → p*IrCl2sub>2 + 2 HCl + 6 H2O The Ir-'' μ''-Cl bonds are labile and can be cleaved to give a variety of adducts of the general formula Cp*IrCl2L. Such adducts undergo further substitution to ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Tuck-in Complex
In organometallic chemistry, a tuck-in complex usually refers to derivatives of Cp* ligands wherein a methyl group is deprotonated and the resulting methylene attaches to the metal. The C5–CH2–M angle is acute. The term "tucked in" was coined to describe derivatives of organotungsten complexes. Although most "tucked-in" complexes are derived from Cp* ligands, other pi-bonded rings undergo similar reactions. Scope and bonding The "tuck-in" process is related to ortho-metalation in the sense that it is an intramolecular cyclometalation. Tuck-in complexes derived from Cp* ligands are derivatives of tetramethylfulvene, sometimes abbreviated Me4Fv. A variety of complexes are known for Me4Fv and related ligands. In these complexes, the Fv can serve as a 4-electron or as a 6-electron ligand. Examples The original example proceeded via sequential loss of two equivalents of H2 from decamethyltungstocene dihydride, Cp*2WH2. The first dehydrogenation step affords a simple tuck- ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Lithium Chloride
Lithium chloride is a chemical compound with the formula Li Cl. The salt is a typical ionic compound (with certain covalent characteristics), although the small size of the Li+ ion gives rise to properties not seen for other alkali metal chlorides, such as extraordinary solubility in polar solvents (83.05 g/100 mL of water at 20 °C) and its hygroscopic properties. Chemical properties The salt forms crystalline hydrates, unlike the other alkali metal chlorides. Mono-, tri-, and pentahydrates are known. The anhydrous salt can be regenerated by heating the hydrates. LiCl also absorbs up to four equivalents of ammonia/mol. As with any other ionic chloride, solutions of lithium chloride can serve as a source of chloride ion, e.g., forming a precipitate upon treatment with silver nitrate: : LiCl + AgNO3 → AgCl + LiNO3 Preparation Lithium chloride is produced by treatment of lithium carbonate with hydrochloric acid. Anhydrous LiCl is prepared from the hydrate ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Chemical Communications
''ChemComm'' (or ''Chemical Communications''), formerly known as ''Journal of the Chemical Society D: Chemical Communications'' (1969–1971), ''Journal of the Chemical Society, Chemical Communications'' (1972–1995), is a peer-reviewed scientific journal published by the Royal Society of Chemistry. It covers all aspects of chemistry. In January 2012, the journal moved to publishing 100 issues per year. The current chair of the Editorial Board is Douglas Stephan (University of Toronto, Canada), while the executive editor is Richard Kelly. Abstracting and indexing The journal is abstracted and indexed in: * Chemical Abstracts * Science Citation Index * Current Contents/Physical, Chemical & Earth Sciences * Scopus * Index Medicus/MEDLINE/PubMed According to the ''Journal Citation Reports'', the journal has a 2021 impact factor of 6.065. See also * ''New Journal of Chemistry'' * ''Chemical Society Reviews'' * ''Chemical Science'' * ''RSC Advances ''RSC Advances'' is an online ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Iridium(III) Chloride
Iridium(III) chloride is the inorganic compound with the formula IrCl3. The anhydrous compound is relatively rare, but the related hydrate is useful for preparing other iridium compounds. The anhydrous salt is a dark green crystalline solid. More commonly encountered is the trihydrate IrCl3(H2O)3. Preparation Iridium is separated from the other platinum group metals as crystalline ammonium hexachloroiridate, (NH4)2 rCl6 which can be reduced to iridium metal in a stream of hydrogen. The spongy Ir thus produced reacts with chlorine at 300–400 °C to give iridium(III) chloride. Hydrated iridium trichloride is obtained by heating hydrated iridium(III) oxide with hydrochloric acid. Structure Like the related rhodium compound, IrCl3 adopts the structure seen for aluminium chloride. This is the monoclinic α polymorph. A rhombohedral β polymorph also exists. Both polymorphs have effectively the same anion lattice but differ in the octahedral interstices the iridium ions ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Angewandte Chemie
''Angewandte Chemie'' (, meaning "Applied Chemistry") is a weekly peer-reviewed scientific journal that is published by Wiley-VCH on behalf of the German Chemical Society (Gesellschaft Deutscher Chemiker). Publishing formats include feature-length reviews, short highlights, research communications, minireviews, essays, book reviews, meeting reviews, correspondences, corrections, and obituaries. This journal contains review articles covering all aspects of chemistry. According to the ''Journal Citation Reports'', the journal had a 2021 impact factor of 16.823. Editions The journal appears in two editions with separate volume and page numbering: a German edition, ''Angewandte Chemie'' ( (print), (online)), and a fully English-language edition, ''Angewandte Chemie International Edition'' ( (print), (online)). The editions are identical in content with the exception of occasional reviews of German-language books or German translations of IUPAC recommendations. Business model ''A ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
