Carbonyl Complexes of the Transition Metals

Abstract

AbstractCarbon monoxide is a versatile ligand as it forms compounds with both transition metals and main group elements. Transition d metals of electronic configuration dn(0 < n < 10) form the most numerous class of these compounds, although recent progress has been made in expanding the area of existence toward main group, lanthanide (4f) and actinide (5f) metals. The most extensively studied series of carbonyl derivatives have the general formula [M(CO)n]m, withnrepresenting the coordination number of the central metal atom M, andmbeing the nuclearity of the system. In these compounds, the central metal atom is in the zero oxidation state. Starting from readily available inorganic derivatives in a positive oxidation state, the synthesis of these compounds normally requires a reducing agent capable of acting in the presence of carbon monoxide: in fact, only nickel metal, as a finely divided activated powder, is reactive toward CO leading to the corresponding derivative Ni(CO)4. The selection of the reducing agent varies as a function of the position of the metal M within the periodic table. There is a general trend of an increase in the nuclearitymtoward the end of the transition d series, the nuclearity being related to the bonding arrangements of the CO ligand, which may act as terminal, doubly bridging or triply bridging. Metal carbonyls are characterized by IR‐active vibrations around 2000 cm−1associated with the carbonyl groups. Vibrational spectra in solution give important information about: (a) the electronic distribution within the M–CO bond in terminally bonded carbonyl groups; (b) the molecular structure associated with the number of bands observed; (c) the type of bonding in dinuclear or polynuclear compounds. X‐ray diffraction data have been extensively used in order to define the molecular structure in the solid state. The metal–CO combinations span a wide range of oxidation states, derivatives being known for oxidation states from +III to −IV. Metal carbonyls undergo three types of reaction: (a) substitution of the carbonyl groups, whereby the oxidation state of the central metal atom remains unchanged, (b) oxidation, and (c) reduction. Carbonyl derivatives of early‐ and late transition metals present specific bonding and spectroscopic properties. Concerning the transition elements of groups 6–9, the M–CO bond dissociation enthalpy increases down the group, and is normally greater than the metal–metal bond enthalpy, the latter being estimated from the heat of atomization. From a mechanistic viewpoint, substitution and redox reactions have been studied extensively. A special case of substitution is the migratory carbonyl insertion, by which an M–R bond to a carbyl group R is converted by CO into the M–(CO)R sequence.