Mono complexes magnesium

By using an alternate synthetic route, a mono(amidinate) magnesium complex was obtained. In this case, the Giignard reagent formed by treatment of the terphenyliodide with Mg was allowed to react directly with 1 equivalent of 1,3-diisopropylcarbodiimide, yielding the amidinate (Scheme 18). ... 

Two independent routes to magnesium amidinates containing very bulky terphenyl substituents have been developed, yielding both mono- and bis(amidinate) magnesium complexes. As shown in Scheme 17, the free amidine reacted cleanly with 0.5 equivalents of dibutylmagnesium in toluene to form the bis (amidinate) in moderate yield. The highly soluble compounds was recrystallized from hexanes as clear, colorless crystalline blocks. ... 

The successful utilization of alkoxo Zn- and Mg-tris(pyrazolyl) borate initiators in the lactide polymerization inspired the synthesis of sterically bulky B-diketiminates (BDls) (Fig. 5) and their zinc and magnesium derivatives [60-62]. Replacing the ancillary ligands resulted in the production of several mono- and dinuclear complexes of Mg" and Zn" 24-39 (Fig. 6), which demonstrated excellent catalytic activity for the polymerization of l- and rac-lactide [62-66]. 

Fio. 2. Proposed kinetic model for yeast inorganic pyrophosphatase. Here M represents Mg + but may also apply to any divalent cation with which the enzyme is active. In the rate equation A represents all mono-magnesium PPi complexes, B represents the di-magnesium complex, and I represents free PPi. Hydrogen ion equilibria are not considered. Kinetic runs were done at pH 7.4, 30° (9). Best values for kinetic constants were obtained from a computer program for nonlinear regression (9S). 

An alkaline pyrophosphatase from rat liver cytoplasm has been partially purified and characterized (24) the corresponding enzyme from mice is inhibited by Mg J+-ADP and free PPj, and free Mg2+ has been implicated as an allosteric activator (23). Partial heat inactivation results in loss of the apparent allosteric effects. Rat liver mitochondrial pyrophosphatase, which is inhibited by adenine nucleotides (36), appears to be bound to the inside of the inner mitochondrial membrane (37). This enzyme, after solubilization, has been separated into two fractions which have somewhat different specificity (24, 38). A pyrophosphatase strongly simulated by sulfhydryl reagents (39) has been partially purified from brain tissue (40). The mono-magnesium PPj complex appears to be the true substrate for this enzyme (41). Pynes and Younathan have purified a pyrophosphatase 1800-fold from human erythrocytes (43). The properties of this enzyme are strikingly similar to those of the yeast enzyme the major difference appears to be the more rigid substrate specificity of the erythrocyte enzyme in the presence of Znz. ... 

With Chiral Mono(oxazoline)/metal Complexes 2-(Tosylamino)phenyloxazoline can also be utilized as a chiral ligand for the enantioselective Diels-Alder addition of acryloyl oxazolidi-nones. The requisite chiral magnesium complex is derived from methylmagnesium iodide and this chiral ligand [38] (Eq. 8A.20). 

Phosphinimido trichloro complexes, with Ti(IV), 4, 361 Phosphinimines, magnesium halide reactions, 2, 88 0-Phosphinoalkoxo ligands, on mono-Cp Ti(IV) complexes, 4,487... 

Mono-n-cyclopentadienylmagnesium compounds have so far only been isolated in the form of adducts with oxygen or nitrogen bases. The bis-(tetrahydrofuran) complexes of cyclopentadienyl(phenyl)- and -(methyl)-magnesium have been synthesized by Whitesides and co-workers (96) according to Eq. (4). 

In 1998, the same group reported the synthesis of magnesium metallocene NHC complexes, in addition to metallocene NHC complexes of other group 2 elements.21 The adducts show an interesting trend in the nature of the metal-carbene bonds which increase as metal radii increase. The trends are reflected in both the solid state structures (metal-carbene bond length increases) and the NMR spectra (downfield shift of C2) of the adducts (Table 1). In addition to mono-NHC complexes, the heavier alkaline earth elements (Sr and Ba) are capable of forming stable bis-NHC adducts. 

Mono- and diammonium phosphate are used as solid fertilizers, whereas ammonium polyphosphate is mainly utilized in solution as a liquid fertilizer, since unlike the orthophosphates, it is very soluble and is more difficult to granulate than the orthophosphates. As a result of its complexing properties, it also keeps impurities (iron, aluminum, magnesium etc.) in solution. 

Mono-diene complexes of zirconocene and hafnocene have been prepared by two methods [129-131 ], viz the photochemical reaction of diphenylzirconocene in the presence of diene and the reaction of metallocene dichlorides with diene magnesium adduct. The structures and reactivity of s-cis-dicm complexes indicate that the metal-lacyclopentene (B) is the preferred canonical form. Complexes of the type Cp2Zr(j-/ra/25-1,3-diene), have been prepared they were the first examples of this mode of coordination (C). Insertion of unsaturated compounds into a diene coordinated to zirconocene results in regioselective C—C bond formation [132-136]. 

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