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Organotins hydrogen halides

Organotin halides can also be obtained from oxides or hydroxides on reaction with hydrogen halides (or ammonium halides) (equation 61) and from tin-tin bonded species on reaction with halogens (equation 62). [Pg.4882]

Trimethyltin chloride and other organotin halides react with water to produce hydrogen halides. Organotin hydrides react with water to produce hydrogen gas, which is flammable and explosive. [Pg.412]

Another type of divalent organotin n complex has been reported by Noltes et al. (228,229). The cyclopentadienyltin halides LXIXa,b precipitate upon mixing concentrated THF solutions of stannocene with the tin dihalides [Eq. (38)]. The complex LXIXa can also be obtained by the reaction of LXVIIIa with hydrogen chloride in THF [Eq. (39)] (228). Similarly, the pentamethylcyclopentadienyltin compounds LXIXc,d have been prepared from decamethylstannocene LXVIIIc and the appropriate carboxylic acid [Eq. (40)] (230). [Pg.274]

Organotin hydrides are advantageous as reductants in terms of their facile availability, stability, and reactivity. - Almost all tin hydrides are liquids, and stoichiometric tin-hydrogen bonds can be used. In general, the tin hydride reductions have been performed under radical conditions using initiators such as azobisisobutyroni-trile (AIBN), triethylborane, and UV irradiation. The reduction of organic halides and pseudohalides by tri- -... [Pg.342]

Cellulose can be modified with organostannane chlorides, such as dibutyl or triphenyl derivatives [91,92], or with organotin halides in the presence of bisethylenediamine copper(II) hydroxide [93]. Epoxy-activated cellulose was prepared by reacting cellulose acetate fibers with sodium methoxide, followed by reacting it with epichlorohydrin in DMSO. This epoxy-activated cellulose has proved to be a useful intermediate to react with substances containing active hydrogen, such as amine, amino acid, or carboxylic acids [94], as shown in Fig. 3. Epoxidized cellulose has also been converted to a thiol derivative via reduction of a thiosulfate intermediate [95], and sulfoethylcellu-[ose has been obtained from sodium chloroethanesulfonate [96]. Cellulose... [Pg.109]


See other pages where Organotins hydrogen halides is mentioned: [Pg.513]    [Pg.45]    [Pg.53]    [Pg.45]    [Pg.4882]    [Pg.361]    [Pg.4881]    [Pg.135]    [Pg.108]    [Pg.395]    [Pg.404]    [Pg.492]    [Pg.525]    [Pg.540]    [Pg.278]    [Pg.439]    [Pg.454]    [Pg.278]    [Pg.1579]    [Pg.1619]    [Pg.67]    [Pg.1307]    [Pg.1309]    [Pg.265]    [Pg.1579]    [Pg.1619]    [Pg.492]    [Pg.544]    [Pg.606]    [Pg.258]    [Pg.524]   
See also in sourсe #XX -- [ Pg.2 , Pg.2 , Pg.3 , Pg.3 , Pg.5 , Pg.6 ]




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Hydrogen halides

Hydrogenation, halides

Organotin halides

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