Diamagnetic compounds

Molecular nitrogen (N2) can act as a ligand in certain coordination complexes. Predict the structure of [V(N2)g], which is isolated by condensing V with N2 at 25 K. Is this compound diamagnetic or paramagnetic What is the formula of the carbonyl compound of vanadium that has the same number of electrons ... 

Copper is known to exist in a -1-3 oxidation state, which is believed to be involved in some biological electron transfer reactions, (a) Would you expect this oxidation state of copper to be stable Explain, (b) Name the compound K3CUF6, and predict the geometry of the complex ion and its magnetic properties, (c) Most of the known Cu(III) compounds have square-planar geometry. Are these compounds diamagnetic or paramagnetic ... 

Section 3 Physical Constants of Organic Compounds Physical Constants of Organic Compounds Diamagnetic Susceptibility of Selected Organic Compounds... 

Ni(NH2NHCSNH2)JCl2 room, 3.02 in H3O solution crystalline compound diamagnetic 69A5... 

In contrast to the + 2 state, copper(I) compounds are less frequently coloured and are diamagnetic, as expected since the 3d level is full. However, the copper(I) ion, unlike copper(II), is unstable in aqueous solution where it disproportionates into copper(II) and copper(O) (i.e. copper metal). 

These compounds perform a dual function in synthesis procedures. The introduction of a complex anion assists in the stabilization of the desired product and the generation of unique intermediates by chloride displacement, eg, silver hexafluorophosphate, AgPF, forms adducts with neutral diamagnetic organometaHics which can act as controUed sources of highly reactive cations (29). Silver hexafluoroantimonate, AgSbF, is an electrophilic... 

Prussian Blue. Reaction of [Fe(CN)3] with an excess of aqueous h on(Ill) produces the finely divided, intensely blue precipitate Pmssian Blue [1403843-8] (tetrairon(Ill) tris(hexakiscyanoferrate)), Fe4[Fe(CN)3]. Pmssian Blue is identical to Turnbull s Blue, the name which originally was given to the material produced by reaction of [Fe(CN)3] with excess aqueous h on(Il). The soHd contains or has absorbed on its surface a large and variable number of water molecules, potassium ions (if present in the reaction), and h on(Ill) oxide. The h on(Il) centers are low spin and diamagnetic h on(Ill) centers are high spin. Variations of composition and properties result from variations in reaction conditions. Rapid precipitation in the presence of potassium ion affords a colloidal suspension of Pmssian Blue [25869-98-1] which has the approximate composition KFe[Fe(CN)3]. Pmssian Blue compounds are used as pigments in inks and paints and its formation on sensitized paper is utilized in the production of blueprints. 

Silver(III) Compounds. No simple silver(Ill) compounds exist. When mixtures of potassium or cesium haUdes are heated with silver hahdes ia a stream of fluorine gas, yellow KAgF [23739-18-6] or CsAgF [53585-89-0] respectively, are obtained. These compounds are diamagnetic and extremely sensitive to moisture (21). When Ag2S04 is treated with aqueous potassium persulfate ia the presence of ethylenedibiguanidinium sulfate, the relatively stable Ag(Ill)-ethylenebiguanide complex is formed. 

Vanadium, a typical transition element, displays weU-cliaractetized valence states of 2—5 in solid compounds and in solutions. Valence states of —1 and 0 may occur in solid compounds, eg, the carbonyl and certain complexes. In oxidation state 5, vanadium is diamagnetic and forms colorless, pale yeUow, or red compounds. In lower oxidation states, the presence of one or more 3d electrons, usually unpaired, results in paramagnetic and colored compounds. All compounds of vanadium having unpaired electrons are colored, but because the absorption spectra may be complex, a specific color does not necessarily correspond to a particular oxidation state. As an illustration, vanadium(IV) oxy salts are generally blue, whereas vanadium(IV) chloride is deep red. Differences over the valence range of 2—5 are shown in Table 2. The stmcture of vanadium compounds has been discussed (6,7). 

The dichalcogenides are hexagonal, the diamagnetic trichalcogenides are monoclinic. The compound sulfides BaZrS [12026-44-7], SrZrS ... 

The copper(I) ion, electronic stmcture [Ar]3t/ , is diamagnetic and colorless. Certain compounds such as cuprous oxide [1317-39-1] or cuprous sulfide [22205-45 ] are iatensely colored, however, because of metal-to-ligand charge-transfer bands. Copper(I) is isoelectronic with ziac(II) and has similar stereochemistry. The preferred configuration is tetrahedral. Liaear and trigonal planar stmctures are not uncommon, ia part because the stereochemistry about the metal is determined by steric as well as electronic requirements of the ligands (see Coordination compounds). 

Furazano[3,4-/]quinoxaline, 7,8-diphenyl-synthesis, 6, 412 Furazanothiophene synthesis, 6, 417 Furazans, 6, 393-426 biological activity, 6, 425 bond angles, 6, 396 bond lengths, 6, 396 coordination compounds, 6, 403 diamagnetic susceptibilities, 6, 395 dipole moments, 6, 395, 400 heats of combustion, 6, 400 heterocyclic ring reactions, 6, 400-403 IR spectra, 6, 398 isoxazoles from, 6, 81 mass spectra, 6, 399 microwave spectroscopy, 6, 395, 396 MO calculations, 6, 395 monosubstituted... 

The NMR spectrum of this compound shows a diamagnetic ring current of the type expected in an aromatic system. X-ray crystal structures of 1 and its carboxylic acid derivative 2 are shown in Fig. 9.2. Both reveal a pattern of bond lengths very similar to that in naphthalene (see p. 534). ... 

Two classes of charged radicals derived from ketones have been well studied. Ketyls are radical anions formed by one-electron reduction of carbonyl compounds. The formation of the benzophenone radical anion by reduction with sodium metal is an example. This radical anion is deep blue in color and is veiy reactive toward both oxygen and protons. Many detailed studies on the structure and spectral properties of this and related radical anions have been carried out. A common chemical reaction of the ketyl radicals is coupling to form a diamagnetic dianion. This occurs reversibly for simple aromatic ketyls. The dimerization is promoted by protonation of one or both of the ketyls because the electrostatic repulsion is then removed. The coupling process leads to reductive dimerization of carbonyl compounds, a reaction that will be discussed in detail in Section 5.5.3 of Part B. 

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