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GaCl

Signal registration was accomplished using the standard measurement scheme, consisting of 2 X 50 recordings with an illumination time of 17 s each. 10 g/L Ga as Ga(N03)s dissolved in 2 % v/v HNO3 / HCl was used as sample and deionized water as reference. [Pg.176]

Wavelength Relative Upper electronic Electronic Vibrational intensity energy transition transition [Pg.178]

Because of the use of the nitrous oxide/acetylene flame the modified measurement scheme with additional tungsten halogen lamp and emission correction was applied. The registration cycle consisted of 4 x 25 recordings with an individual illumination time of 12 s. [Pg.179]

A compilation of the characteristics of the NH bands can be found in Table 7.10. For recording the spectra the modified registration scheme was applied to eliminate the strong emissions coming from the nitrous oxide/acetylene flame. In total, 4 x 50 spectra were recorded with an illumination time of 12 s each. In the case of sample measurements the nitrous oxide/acetylene flame was turned on, while in the case of blank signal registration the flame was turned off. No additional solution was aspirated by the nebulizer to get the pure spectrum of the flame gases. [Pg.179]

Wavelength / nm Relative intensity Upper electronic energy lev Electronic transition Vibrational transition [Pg.180]


A very active, high yields but extensive intra- and intermolecular isomerisation AlCl, AlBr, A1L, GaCl, GaCl2, GaBr, Gal, ZrCl, HfCl, HfBr, Hfl, SbF, NbF, NbCl, TaF, TaCl, TaBr, MoF, and MoCl ... [Pg.564]

BeCl2, CdCl, ZnCl2, BF, BCl, BBr, GaCl, GaBr, TiCl, ZrCl, SnCl, SnBr, SbCl, SbCl, BiCl, FeCl, and UCl. ... [Pg.564]

Brmnsted-Lewis Superacids. Conjugate Friedel-Crafts acids prepared from ptotic and Lewis acids, such as HCl—AlCl and HCl—GaCl ate, indeed, supetacids with an estimated value of —15 to —16 and ate effective catalysts in hydrocarbon transformation (217). [Pg.565]

Gallium (I). Hahdes of Ga(I) ate known only in the vapor phase. Coordination complexes of GaCl and GaBt have been obtained with dioxane, morpholine, and acetylacetone. [Pg.162]

Gallium Halogenates. The anhydrous galhum(III) perchlorate [19854-31-0], Ga(Q0 2 is obtained by reaction of chlorine peroxide, 0120, on GaCl at —180° C (34). The product is a white sohd and is stable at room temperature. [Pg.162]

Dichloroethane reacts with toluene in the presence of Friedel-Crafts catalysts such as AIBr., AlCl, GaCl, and ZrCl (26). Ammonolysis of... [Pg.8]

Below dris temperature, mainly GaCls transports gallium, but above dris temperature, the monochloride will begin to predominate. [Pg.94]

Figure 4.1 Powder spectrum of [VO(mquin)2] in [GaCl(mquin)2] (bottom) 9.25 GHz (X-band), (top) 34.99 GHz (Q band). Figure 4.1 Powder spectrum of [VO(mquin)2] in [GaCl(mquin)2] (bottom) 9.25 GHz (X-band), (top) 34.99 GHz (Q band).
Very recently, von Hanisch et al. reported on the syntheses and crystal structures of cyclic and polycyclic GaSb compounds featuring low coordinated Sb centers.146 Reaction of Ph(w-Pr)2P -> GaCl3 with i-Pr3SiSb(SiMe3)2 yielded [Ph(n-Pr)2P -> Ga(Cl)SbSi(/-Pr)3]2 84 and [(GaCl)4(P( -Pr)2Ph)2(SbSi(/-Pr)3)4] 85, respectively147 (Scheme 20). [Pg.294]


See other pages where GaCl is mentioned: [Pg.2785]    [Pg.2902]    [Pg.560]    [Pg.561]    [Pg.564]    [Pg.159]    [Pg.159]    [Pg.162]    [Pg.162]    [Pg.162]    [Pg.162]    [Pg.162]    [Pg.162]    [Pg.162]    [Pg.164]    [Pg.233]    [Pg.67]    [Pg.67]    [Pg.231]    [Pg.263]    [Pg.330]    [Pg.108]    [Pg.382]    [Pg.383]    [Pg.383]    [Pg.383]    [Pg.383]    [Pg.383]    [Pg.383]    [Pg.423]    [Pg.423]    [Pg.423]    [Pg.423]    [Pg.157]    [Pg.55]    [Pg.1043]    [Pg.205]    [Pg.281]    [Pg.294]    [Pg.295]   


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GaCls

Gallium -chloride GaCl

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