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Metal complexes classification

Table 2-2 Oxidative addition reactions on transition metal complexes classification of the adding compounds... Table 2-2 Oxidative addition reactions on transition metal complexes classification of the adding compounds...
Macropolycyclic ligands, 2,942 classification, 2,917 metal complexes binding sites, 2, 922 cavity size, 2,924 chirality, 2, 924 conformation, 2,923 dimensionality, 2, 924 electronic effects, 2, 922 shaping groups, 2,923 structural effects, 2,922 molecular cation complexes, 2,947 molecular neutral complexes, 2,952 multidentate, 2,915-953 nomenclature, 2,920 Macro tetrolide actins metal complexes, 2,973 Macrotricycles anionic complexes, 2,951 cylindrical... [Pg.157]

Busch DH (2005) First Considerations Principles, Classification, and History. 249 in press Bussiere G, Beaulac R, Belisle H, Lescop C, Luneau D, Rey P, Reber C (2004) Excited States and Optical Spectroscopy of Nitronyl Nitroxides and Their Lanthanide and Transition Metal Complexes. 241 97-118 Cadierno V, see Majoral J-P (2002) 220 53-77 Camara M, see Chhabra SR (2005) 240 279-315 Caminade A-M, see Majoral J-P (2003) 223 111-159 CantriU SJ, see Arico F (2005) 249 in press... [Pg.255]

This is the most common route, the reagent being a metal compound/solvent combination. Typical conditions call for the metal salt (e.g., acetate) in a buffer system (e.g., NaOAc/AcOH) and a co-solvent such as chloroform. Generally the reaction mixture is refluxed until the metal complex spectrum (see Section 9.22.5.6 and Table 4) is fully developed. Metal acetylacetonates and metal phenoxides have also been employed. The topic has been reviewed in detail by Buchler,51 who has also summarized the history and classification of metal complexes of this series, and the mechanisms of metalation.52... [Pg.955]

It is only for reasons of simplified classification that the pigments which are described in this section, like azomethine metal complex pigments (Sec. 2.10.1.2), are listed in Chapter 2. Actually, rather than being azo pigments, these are azo methine and methine pigments, which in the classification system adopted in this book are formally located between azo pigments and polycyclic pigments. [Pg.401]

The basic classification of nucleophilic substitutions is founded on the consideration that when a new metal complex is formed through the breaking of a coordination bond with the first ligand (or water) and the formation of a new coordination bond with the second ligand, the rupture and formation of the two bonds can occur to a greater or lesser extent in a synchronons manner. When the mpture and the formation of the bonds occur in a synchronous way, the mechanism is called substitution nucleophilic bimolecular (in symbols Sn2). On the other extreme, when the rupture of the first bond precedes the formation of the new one, the mechanism is called substitution nucleophilic unimolecular (in symbols SnI). Mechanisms Sn2 and SnI are only limiting cases, and an entire range of intermediate situations exists. [Pg.219]

Jhe classification of metal complex reactions as 14 labile and 11 inert by Taube (121) was based essentially on literature of qualitative observations. In the last decade or so this situation has changed dramatically, as even a cursory examination of the Tables will show. [Pg.54]

D. Symmetry Classification of Interaction in Arene-Metal Complex 42... [Pg.1]

Cyclodextrins classification, 920 Cyclohexane-1,2-diamine metal complexes, 34 C.yclohexanc-l,2-dione monooxime metal complexes, 273 Cyclohexane-1,3,5-triamine metal complexes, 50 Cyclohexanone oxime... [Pg.1076]


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See also in sourсe #XX -- [ Pg.464 ]




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