Structures of Solvent-Free, Monomeric LiCCH, NaCCH, and KCCH
Douglas B Grotjahn1, Aldo J Apponi2, Matthew A Brewster2
1Department of Chemistry, San Diego State University, 5500 Campanile Drive, San Diego, CA 92182-1030 (USA), Fax: (+1) 619-594-4634.
Abstract:
The simplest alkali metal acetylides MCCH were made in the gas phase for the first time (see drawing), and their bond lengths were determined by millimeter/submillimeter spectroscopy of their isotopomers. The M-C bond lengths rCM are the shortest known for organoalkali metal compounds. In the case of LiCCH, the experimentally determined Li-C distance of 1.888 Å has an estimated accuracy of ±0.0005 Å, which should allow a rigorous test of theoretical methods.
Related Concept Videos
Solvents
A...
Titration in Nonaqueous Solvents
Chemical Shift: Internal References and Solvent Effects
The internal reference compound generally used in NMR spectroscopy is tetramethylsilane (TMS). TMS is preferred because it is chemically inert, soluble in NMR solvents, and easily removable. Also, the highly shielded methyl protons in TMS yield an intense...
Structures of Solids
Structural Isomerism
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can...
Structure of Lipids


