Aryl complexes properties

Homoleptic germylenes, preparation and properties, 3, 773 Homoleptic lanthanide(II) alkyl compounds, properties, 4, 4 Homoleptic manganese aryl complexes, preparation, 5, 816 Homoleptic manganese isonitrilates, preparation, 5, 773—774 Homoleptic molybdenum complexes, preparation and characteristics, 5, 514... 

Metal-Containing Tridentate Formazans. Formazans substituted with OH or COOH in the 2-position of the N1- or Ns-aryl group have the same complexing properties as 2-hydroxy- (or carboxy)-2-aminodiarylazo dyes. Similarly, they also form 1 1 complexes with four-coordinate metals, and 1 2 complexes with six-coordinate metals. Being N ligands formazans react more readily with cobalt salts than with chromium salts. The mostly blue 1 2 cobalt(m) complexes of type 34 [72] and the mostly gray-blue complexes of type 35 [73] are known. 

The superior donor properties of amino groups over alkoxy substituents causes a higher electron density at the metal centre resulting in an increased M-CO bond strength in aminocarbene complexes. Therefore, the primary decarbo-nylation step requires harsher conditions moreover, the CO insertion generating the ketene intermediate cannot compete successfully with a direct electro-cyclisation of the alkyne insertion product, as shown in Scheme 9 for the formation of indenes. Due to that experience amino(aryl)carbene complexes are prone to undergo cyclopentannulation. If, however, the donor capacity of the aminocarbene ligand is reduced by N-acylation, benzannulation becomes feasible [22]. 

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