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Antimony bond

Cyclic and Polymeric Substances Containing Antimony-Antimony Bonds. A number of oiganoantimony compounds containing rings of four, five, or six antimony atoms have been prepared. The first such compound to be adequately characterized, tetrakis-l,2,3,4-/f i-butyltetrastibetane [47191 -73-5], Cj H Sb, was obtained by the interaction of a dialkylstibide and iodine (70) ... [Pg.207]

Arsenic, Antimony and Bismuth Table 18 Sulfur-Antimony Bond Lengths and Angles... [Pg.266]

The antimony analogue of diars, o-phenylenebis(dimethylstibine), has been prepared, as has its phenyl analogue (equation 43).162 Attempts to prepare multidentate stibines have been unsuccessful, probably due to the weaknes of the carbon-antimony bond. For example, in the reaction of BunLi with o-C6H4(SbPh2)Br the nucleophile attacks the C—Sb as well as the C—Br bond.142... [Pg.1008]

Recently, Meinema el al. (86) reported that an alkyl-antimony bond of R3Sb (R = alkyl) is also cleaved by sodium in liquid ammonia. [Pg.197]

It was also found that the phenyl-antimony bonds of (CH3) (C6H5)2Sb were cleaved selectively by dry hydrogen chloride in chloroform to give CH3SbCl2 (40). This cleavage reaction was successfully applied to the preparation of new ligands,11 bis(diorganostibino) methanes (41), as follows ... [Pg.198]

In the reaction of R(C6H5)2Sb (R = C2HS, f-C3H7, C6H5CH2), cleavage of the alkyl-antimony bond took place (38). [Pg.198]

Dimethyl ditellurium and tetramethyldistibane formed, within a few minutes at 20° in an exothermic reaction dime thyIstibane methyl tellurium in quantitative yield2. The reaction with tetraethyldistibane is best carried out at — 40° to prevent cleavage of carbon-antimony bonds. [Pg.199]

Reaction of monoorganoantimony halides with metals gives compounds containing antimony-antimony bonds as shown in equation 126 and 127 . [Pg.782]


See other pages where Antimony bond is mentioned: [Pg.21]    [Pg.167]    [Pg.187]    [Pg.197]    [Pg.197]    [Pg.198]    [Pg.198]    [Pg.4872]    [Pg.4888]    [Pg.574]    [Pg.996]    [Pg.1030]    [Pg.25]    [Pg.59]    [Pg.574]   
See also in sourсe #XX -- [ Pg.802 ]

See also in sourсe #XX -- [ Pg.802 ]




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Antimony bond dissociation energies

Antimony bond type

Antimony carbon—arsenic bonds

Antimony carbon—bismuth bonds

Antimony complexes bonding

Antimony complexes double bonds

Antimony nitrogen—phosphorus bonds

Antimony-arsenic bonds

Antimony-arsenic bonds synthesis

Antimony-germanium bonds

Antimony-nitrogen bonds

Antimony-nitrogen bonds reactions with

Antimony—carbon bonds

Antimony—carbon bonds arsenic halides

Antimony—carbon bonds reactions with

Antimony—hydrogen bonds

Antimony—hydrogen bonds arsenic halides

Antimony—hydrogen bonds reactions with

Antimony—oxygen bonds

Antimony—oxygen bonds reactions with

Antimony—phosphorus bonds

Antimony—phosphorus bonds double

Antimony—phosphorus bonds reactions with

Antimony—phosphorus bonds synthesis

Antimony—silicon bonds

Antimony—silicon bonds reactions with

Antimony—sulfur bonds

Antimony—sulfur bonds reactions with

Arsenic antimony—hydrogen bonds

Bismuth—carbon bonds antimony halides

Bonded films antimony trioxide

Bonds antimony-halogen

Bonds antimony-metal

Boron antimony—hydrogen bonds

Halogen antimony—hydrogen bonds

Hydrogen antimony—oxygen bonds

Hydrogen antimony—sulfur bonds

Hydrogen carbon—antimony bonds

Nitrogen—phosphorus bonds antimony halides

Transition-metal carbon—antimony bonds

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