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Properties of Transition Metals

Most of the transition metals exhibit a close-packed structure in which each atom has a coordination number of 12. Furthermore, these elements have relatively small atomic radii. The combined effect of closest packing and small atomic size results in strong metallic bonds. Therefore, [Pg.858]

Alfred Werner (1866-1919). Swiss chemist. Werner started as an Oiganic chemist but did his most notable work in coordination chemistry. For his theory of coordination compounds, Werner was awarded the Nobel Prize in Chemistiy in 1913. [Pg.858]

TABLE 22.1 Elecfir o GrrnliguratiiTrLS Other Propertie TransiScn Mctafe s n i file Fp umtJPeri i.xi H The trends in radii, electronegativi.y, and ionization energy for the first row of transition metals are somewhat different from those for [Pg.859]

Sc Ti V Cr Mn Fe Co Ni Cu main group elements. This is largely the effect of shiad tg of the 4s electrons by the 3d electrons. [Pg.859]

Electron configuration M 4s 3d 4s 3d 4s 3d 4s 3d 4s 3/ 4s 3d The electron configurations of the first-row transition metals and their ions were discussed in Section 6.9 and Section 7.5, respectively. [Pg.859]

Electron Configurations and Other IVopcrties of the Fourth-Period Transition Metals [Pg.923]

Student Annotation The oxidation state of 0 in each of these compounds is -2, making those of V, Cr, and Mn +5, +6, and +7, respectively [ Mt Section 4.4] [Pg.923]

Like other metals, transition metals are malleable, lustrous, and good conductors of electricity. However, a variety of physical and chemical properties distinguish the transition metals from other metals. There also is considerable variability in the properties of the transition metals themselves. This variability results from differences in their electron configurations. In this activity, you will discover how transition metals differ chemically from other metals. [Pg.17]

How can transition metals be distinguished chemically from other metals  [Pg.17]

96-well template 96-well microplate thin-stern pipettes (15) 0.1M KNO3 0.1MCa(NO3)2 0.1M NH4VO3 0.1MCr(NO3)2 0.1 M Mn(N03)2 [Pg.17]

Always wear safety goggles, gloves, and a lab apron. [Pg.17]

Several solutions are poisonous. HCI is corrosive, and HCI and NH3 will irritate the eyes, skin, and respiratory tract. [Pg.17]


The general understanding of the electronic structure and the bonding properties of transition-metal silicides is in terms of low-lying Si(3.s) and metal-d silicon-p hybridization. There are two dominant contributions to the bonding in transition-metal compounds, the decrease of the d band width and the covalent hybridization of atomic states. The former is caused by the increase in the distance between the transition-metal atoms due to the insertion of the silicon atoms, which decreases the d band broadening contribution to the stability of the lattice. [Pg.191]

INVESTIGATION OF GALVANO-MAGNETIC PROPERTIES OF TRANSITION METAL ALLOY SYSTEMS USING THE KUBO-GREENWOOD EQUATION... [Pg.283]

These compounds are generally believed to have square pyramidal structures (X-ray, PPr3) [157d] and have typical spectroscopic properties of transition-metal hydrides (IrHCl2(PBu2Me)2 i/(Ir—H) 1998 cm-1). [Pg.150]

W.W. Wendlandt and J.P. Smith, Thermal Properties of Transition Metal Ammine Complexes, Elsevier, Amsterdam, 1967. [Pg.317]

The magnetic properties of transition metal complexes. B. N. Figgis and J. Lewis, Prog. Inorg. [Pg.26]

The effect of inner orbital splitting on the thermodynamic properties of transition metal compounds and coordination complexes. P. George and D. S. McClure, Prog. Inorg. Chem., 1959,1, 381-463 (36). [Pg.26]

The angular overlap model for the description of the paramagnetic properties of transition metal complexes. A. Benici, C. Benelli and D. Gatteschi, Coord. Chem. Rev., 1984, 60,131 (204). [Pg.67]

Selected Chemical Properties of Transition-Metal Borides... [Pg.439]

Finally, we summarize some of the properties of transition-metal compounds and attempt to distinguish those which are characteristic of a transition-metal complex as opposed to any metal complex. [Pg.17]

The thermodynamic stability of coordination compounds is relatively easy to determine, and provides us with a valuable pool of data from which we may assess the importance of ligand-field and other effects upon the overall properties of transition-metal compounds. The bulk of this chapter will be concerned with the thermodynamic stability of transition-metal compounds, but we will briefly consider kinetic factors at the close. [Pg.145]

Bray KL (2001) High Pressure Probes of Electronic Structure and Luminescence Properties of Transition Metal and Lanthanide Systems. 213 1-94 Bronstein LM (2003) Nanoparticles Made in Mesoporous Solids. 226 55-89 Bronstrup M (2003) High Throughput Mass Spectrometry for Compound Characterization in Drug Discovery. 225 275-294... [Pg.231]

One of the properties of transition metal acyl complexes is their ability to lose CO, usually on heating or photolysis. This so-called decarbonylation often represents a special case of the reverse of the CO insertion in Eq. (8), where L = CO. [Pg.92]

In this chapter, we survey the diversity of transition metals, beginning with an overview. Then we describe the stmcture and bonding in transition metal complexes. We describe metallurgy, the processes by which pure metals are extracted from mineral ores. The chapter ends with a presentation of some properties of transition metals and their biological roles. [Pg.1429]

West, D.X., Padhye, S.B., Sonawane, P.B. Structural and Physical Correlations in the Biological Properties of Transitions Metal Heterocyclic Thiosemicarbazone and S-alkyldithiocarbazate Complexes. Vol. 76, pp. 1-50. [Pg.197]

Structural and Physical Correlations in the Biological Properties of Transition Metal Heterocyclic Thiosemicarbazone and S-alkyldithiocarbazate Complexes... [Pg.198]

I.B. Bersuker, Electronic Structure and Properties of Transition Metal Compounds. John Wiley and Sons, Inc., 1996. [Pg.252]

One-electron reduction or oxidation of organic compounds provides a useful method for the generation of anion radicals or cation radicals, respectively. These methods are used as key processes in radical reactions. Redox properties of transition metals can be utilized for the efficient one-electron reduction or oxidation (Scheme 1). In particular, the redox function of early transition metals including titanium, vanadium, and manganese has been of synthetic potential from this point of view [1-8]. The synthetic limitation exists in the use of a stoichiometric or excess amount of metallic reductants or oxidants to complete the reaction. Generally, the construction of a catalytic redox cycle for one-electron reduction is difficult to achieve. A catalytic system should be constructed to avoid the use of such amounts of expensive and/or toxic metallic reagents. [Pg.64]

Bella SD (2001) Second-order nonlinear optical properties of transition metal complexes. Chem Soc Rev 30 355-366... [Pg.260]

The information available is discussed in light of the effects of excitation energy and the environment on the photofragmentation process of several transition metal cluster complexes. The photochemical information provides a data base directly relevant to electronic structure theories currently used to understand and predict properties of transition metal complexes (1,18,19). [Pg.75]

Effect of the preparation method on physicochemical and catalytic Properties of transition metal M substituted Keggin type MPMoi2O40 heteropolyoxometalates... [Pg.241]

Properties of Transition Metal Complexes with Metal-Carbon Bonds in Aqueous... [Pg.653]

It must be emphasized that the duodectet rule (4.6) initially has no structural connotation, but is based on composition only. Indeed, the compositional regularity expressed by (4.6) encompasses both molecular species (such as the metal alkyls) and extended lattices (such as the oxides and halides) and therefore appears to transcend important structural classifications. Nevertheless, we expect (following Lewis) that such a rule of 12 may be associated with specific electronic configurations, bond connectivities, and geometrical propensities (perhaps quite different from those of octet-rule-conforming main-group atoms) that provide a useful qualitative model of the chemical and structural properties of transition metals. [Pg.367]


See other pages where Properties of Transition Metals is mentioned: [Pg.2219]    [Pg.2396]    [Pg.66]    [Pg.1206]    [Pg.49]    [Pg.17]    [Pg.17]    [Pg.19]    [Pg.44]    [Pg.257]    [Pg.1428]    [Pg.1429]    [Pg.1449]    [Pg.170]    [Pg.434]    [Pg.435]    [Pg.76]    [Pg.439]   


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Ground State Properties of Transition Metal Oxides

High temperature properties of transition metals

Magnetic properties of transition metal complexes

Magnetic properties of transition metal ions

Magnetic properties of transition-metal cluster

Optical properties of transition metal

Optical properties of transition metal complexes

Physical Properties of Transition Metal Formyl Complexes

Properties of Transition Metal Borides Ceramics

Properties of metals

Properties of the Transition Metals

Properties transitive

Spectral properties of transition-metal

Spectral properties of transition-metal complexes

The properties of perfluoro-alkyl and -aryl transition metal complexes

Transition metals properties

Transition properties

Transitivity properties

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