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Iv bonds

Table 16-IV. bonding orbitals, bonding capacity, and molecular shape... Table 16-IV. bonding orbitals, bonding capacity, and molecular shape...
Mo1 isocyanide complexes of the form [MoOX(CNR)4]Y (R = alkyl X=C1, Br Y = C1, Br, Brl2,13, PF6) have been prepared by several synthetic routes.125 These complexes contain a trans O—Mo—X arrangement, and in [MoOCl(CNMe)4](I3) the Mo—O, distance is 1.64(4),126 a length typical of the multiple terminal oxomolybdenum(IV) bond (Table 3). [Pg.1339]

Sulfation is the generation of an oxygen sulfur(IV) bond, where the oxygen is attached to the carbon backbone, in the most controlled manner possible, using some form of sulfur dioxide moiety. When sulfating alcohols, the reaction is strongly exothermic, Examples of feedstocks for such a process include alkenes, alcohols, or phenols. Unlike the sulfonates, which exhibit excellent stability to hydrolysis, the alcohol sulfates are readily susceptible to hydrolysis in acidic media, The sulfation of fatty alcohols and fatty polyalkoxylates has produced a substantial body of commercial detergents and emulsifiers. [Pg.1567]

IV. BOND CRITICAL POINT PROPERTIES OF THE ELECTRON DENSITY... [Pg.103]

In the case of inert cobalt(m) complexes it is possible to isolate the chelated products of the reaction. Let us return to the hydrolysis of the complex cations [Co(en)2(H2NCH2C02R)Cl]2+ (3.1), which contain a monodentate iV-bonded amino acid ester, that we encountered in Fig. 3-8. The chelate effect would be expected to favour the conversion of this to the chelated didentate AO-bonded ligand. However, the cobalt(iu) centre is kinetically inert and the chloride ligand is non-labile. When silver(i)... [Pg.52]

Refs. [i] Meyer B, Zhang S, Scholz F (1996) Fresenius J Anal Chem 356 267 [ii] Reddy SJ, Dostal A, Scholz F (1996) J Electroanal Chem 403 209 [Hi] Thiel A (1901) Z anorg allg Chem 24 1 [iv] Bond AM, Scholz F (1991) Langmuir 7 3197 [v] Kroger FA (1964) The chemistry of imperfect crystals. North-Holland, Amsterdam... [Pg.620]

J. D. Woollins, J. Chem. Soc., Dalton Trans. 1996, 2893 metallocycles with P, N, S/Se compounds iV-bonded to transition metals. [Pg.379]

A remarkable compound, comprising divalent and tetravalent tin atoms within one molecule, is the already mentioned triorganylstannylstannylene 27 the observed Sn(II)—Sn(IV) bond distance of 286.9 pm is much longer than the Sn(IV)—Sn(IV) bonds in distannanes responsible are the larger covalent radius of Sn(II) compared with Sn(rV) and the extremely bnlky Btp gronp present. It shonid be noted that a closely related donor-stabihzed stannylene is known which exhibits the same featnre,... [Pg.155]

Table IV Bond Energies in Selected Transition-Metal Systems... Table IV Bond Energies in Selected Transition-Metal Systems...
TABLE IV.- -Bond Energies OF Baughan AND Polanvi (Revised). [Pg.103]

Alkali metal salts of diethyl phosphite (122) act as nucleophiles or electron donors in their reaction with diethyl phosphorochloridate (123). Evidence was provided that formation of the direct P(IV)-P(IV) bond proceeds via a single electron transfer process (SET) from phosphite anion to phosphorochloridate (Scheme 34). ... [Pg.320]


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See also in sourсe #XX -- [ Pg.55 ]




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