Metal-nitrogen bonding nitrosyl complexes

In general, the metal-nitrogen bond orders of metal-nitrosyl complexes are larger (i.e., the M-N bonds are stronger) than the metal-carbon bond orders for the corresponding... 

Metal nitrosyls are the transition metal complexes of nitric oxide (NO) containing a metal-nitrogen bond. Roussin s red salt, Na2[Fe2(NO)4S2], and Roussin s black salt, Na[Fe4(NO)7S3], were the earliest known metallic nitrosyls. In line with the inclusion of metal carbonyl complexes under the category of organometaUic compounds, the metallic nitrosyl complexes are also recently included in organometaUic compounds. The nitric oxide cation is isoelectronic with carbon monoxide. Hence, there is quite a bit of resemblance in the chemistry of metaUic carbonyls and nitrosyls. However, the contrasts in these chemistries are also noteworthy. 

This picture can qualitatively account for the g tensor anisotropy of nitrosyl complexes in which g = 2.08, gy = 2.01, and g == 2.00. However, gy is often less than 2 and is as small as 1.95 in proteins such as horseradish peroxidase. To explain the reduction in g from the free electron value along the y axis, it is necessary to postulate delocalization of the electron over the molecule. This can best be done by a complete molecular orbital description, but it is instructive to consider the formation of bonding and antibonding orbitals with dy character from the metal orbital and a p orbital from the nitrogen. The filled orbital would then contribute positively to the g value while admixture of the empty orbital would decrease the g value. Thus, the value of gy could be quite variable. The delocalization of the electron into ligand orbitals reduces the occupancy of the metal d/ orbital. This effectively reduces the coefficients of the wavefunction components which account for the g tensor anisotropy hence, the anisotropy is an order of magnitude less than might be expected for a pure ionic d complex in which the unpaired electron resides in the orbital. 

Molecular Rearrangements in Polynuclear Transition Metal Complexes, 16, 319 Multiply Bonded Germanium Species, 21, 241 Nitrogen Groups in Metal Carbonyl and Related Complexes, 10, 115 Nitrosyls, 7, 211... 

Table 1 summarizes the most important surface complexes formed when NO and CO are adsorbed on noble metal catalysts. According to the literature NO and CO are adsorbed as nitrites, nitrates and carbonates on alumina [2]. The most important surface complexes for CO and NO adsorption on rhodium are a gem-dicarbonyl (Rh(CO)2) and a linear Rh-NO complex [1]. However, tricarbonyl and bridged Rhx-CO complexes have been proposed to be formed and different kinds of linear Rh nitrosyl complexes are possible [1-4]. The adsorption of CO on R and Pd catalysts depends much on the oxidation stage of R and Pd [5]. CO adsorption on R forms mostly linear and bridged carbonyls [6-11]. NO is adsorbed linearly on R [12]. In the case of Pd the most common surface complexes are linear carbonyls [13], strong multilaterally-bonded carbonyls, bridged carbonyls [5,14,15] and triply-bonded CO [5]. Isocyanate, nitrous oxide or nitrogen dioxide are proposed to be coimected to the reaction mechanism of the NO-CO reactions [2,16-19]. 

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