Lithium halides solid state structures

Lande assumed that in the solid state structures of the lithium halides, LiX, the anions were in contact with one another (see diagram 5.1 and Figure 5.15a with the accompanying discussion). Lande took half of each anion-anion distance to be the radius of that anion, and then obtained fu+ by substituting into equation 5.6 values of rx and the measured internuclear Li—X distances. 

Experimentally, x values for gaseous lithium halides were determined as early as 1949 by molecular beam resonance experiments In solution, the quadrupolar interaction of ethyUithium and of t-butyllithium were investigated in 1964 . It was found that tetrameric and hexameric aggregates have different interactions. In the solid state x of tetrameric methyl- and ethyUithium was determined in 1965 and 1966 , and for lithium formate in 1972 . However, it was not untU Jackman started his investigations of lithium enolates and phenoxides in solution that the quadrupolar interaction was used in a systematic fashion to obtain structural information . 

Later, Tieke reported the UV- and y-irradiation polymerization of butadiene derivatives crystallized in perovskite-type layer structures [21,22]. He reported the solid-state polymerization of butadienes containing aminomethyl groups as pendant substituents that form layered perovskite halide salts to yield erythro-diisotactic 1,4-trans polymers. Interestingly, Tieke and his coworker determined the crystal structure of the polymerized compounds of some derivatives by X-ray diffraction [23,24]. From comparative X-ray studies of monomeric and polymeric crystals, a contraction of the lattice constant parallel to the polymer chain direction by approximately 8% is evident. Both the carboxylic acid and aminomethyl substituent groups are in an isotactic arrangement, resulting in diisotactic polymer chains. He also referred to the y-radiation polymerization of molecular crystals of the sorbic acid derivatives with a long alkyl chain as the N-substituent [25]. More recently, Schlitter and Beck reported the solid-state polymerization of lithium sorbate [26]. However, the details of topochemical polymerization of 1,3-diene monomers were not revealed until very recently. 

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