By F. G. A. Stone, Robert West
Just about all branches of chemistry and fabric technology now interface with organometallic chemistry - the learn of compounds containing carbon-metal bonds. This generally acclaimed serial includes authoritative studies that deal with all features of organometallic chemistry, a box which has multiplied drastically because the book of quantity 1 in 1964. . offers an authoritative, definitive evaluation addressing all features of organometallic chemistry.. worthy to all researchers inside this energetic box and is a needs to for each sleek library of chemistry.. prime quality study e-book inside this swiftly constructing box.
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Additional info for Advances in Organometallic Chemistry
V. Ionization-resistant hexacoordinate complexes Ionization of 31–34 proceeds smoothly as long as one of the monodentate ligands is a carbon-ligand group. When both of the monodentate ligands are electron-withdrawing groups, or when the R substituent is an electron-withdrawing group, ionization is prevented (Eq. 5 is evident from the 29Si chemical shifts (Table XVII), which remain in the high-field region characteristic of hexacoordination, and is further confirmed by crystal structures. The crystal structures of two of these hexacoordinate complexes, the monotriflato 53g, in which the CF3 groups prevent ionization, and the ditriflato (54c) were determined and are depicted in Figs.
30–32, and selected bond lengths are listed in Table XX, along with data for the corresponding dimethylamino chelates for comparison. The remarkable differences are apparent immediately from the figures: the difluoro complex (64a) crystallized in the cis geometry, while the dichloro and dibromo 65b and 66a preferred the trans geometry. ð24Þ ð25Þ 54 DANIEL KOST AND INNA KALIKHMAN FIG. 30. 20 Reproduced with permission from Elsevier. FIG. 31. 20 Reproduced with permission from Elsevier. Hydrazide-Based Hypercoordinate Silicon Compounds 55 FIG.
Structural assignment of the latter was achieved by NMR-spectral comparison with two fully ionic analogs: the ammoniumtriflate salt 59(OTf) (Fig. 26), and the non-equilibrating 60 (Fig. 41 FIG. 26. 41 Reproduced with permission from the American Chemical Society. 48 DANIEL KOST AND INNA KALIKHMAN FIG. 27. Molecular structure of 60 in the crystal. 867(5). 41 Reproduced with permission from the American Chemical Society. 4), showing remarkable temperature dependence (Fig. 0 ppm, assigned to 58). The intensity ratio of these two signals is temperature dependent in a fully reversible fashion, such that at lower temperatures the relative population of the pentacoordinate species (59) increases.
Advances in Organometallic Chemistry by F. G. A. Stone, Robert West