CO-ORDINATION COMPOUNDS OF HYDRAZINE: PART II. THE INTERACTION OF TRIMETHYLBORANE AND TRIMETHYLALUMINUM WITH HYDRAZINE

1961 ◽  
Vol 39 (11) ◽  
pp. 2324-2329 ◽  
Author(s):  
W. G. Paterson ◽  
M. Onyszchuk

Trimethylborane and anhydrous hydrazine react at 25° in vacuum, yielding a 2:1 adduct, 2(CH3)3B•N2H4, which is stable at or below −78° and evolves trimethylborane slowly at higher temperatures, leaving a stable 1:1 adduct, (CH3)3B•N2H4 (m.p. 42–43°). The thermal decomposition of the latter at 150–160° is complex, producing nitrogen, methane, ammonia, a mixture of butane and the isomeric butenes, and a heterogeneous solid. At 25° diborane displaces trimethylborane from the 1:1 adduct and reacts with it to form 1,1-dimethyldiborane, in addition to hydrogen, methane, and a heterogeneous solid.Trimethylaluminum and hydrazine give a complex reaction in vacuum at 25°, but in diethyl ether solution the product was thought to be (CH3)2AlNHNHAl(CH3)2, which decomposes on being touched.

1992 ◽  
Vol 21 (7) ◽  
pp. 1149-1152 ◽  
Author(s):  
Yukihiro Yokoyama ◽  
Osamu Kikuchi
Keyword(s):  

2013 ◽  
Vol 734-737 ◽  
pp. 916-920 ◽  
Author(s):  
Jing Xia Chao ◽  
Ju Pei Xia ◽  
Chao Qin Yang ◽  
Zhao Shu Zhang ◽  
Xue Jiao Ren

The thermal decomposition process of K-feldspar-CaSO4-CaO system was studied by X-ray diffraction (XRD) analysis of the product which calcined at 1473K. The results show that KAlSi3O8 firstly is decomposed into KAlSi2O6 and released the SiO2, then has a complex reaction between KAlSi2O6 and CaO, which generated intermediates-K2SiO3 under the operating conditions. K2SiO3 is unstable and reacted with calcium sulfate to generate K2SO4. When the CaO amount is insufficient, the main products are KAlSi2O6 and 2CaOAl2O3SiO2, the potassium existed as K2S2O8; when n (CaO) / n (KAS6) 12:1, the products will further transfer into CaOSiO2 and 2CaO SiO2 and the potassium existed as K2SO4.


1989 ◽  
Vol 44 (10) ◽  
pp. 1329-1330
Author(s):  
Derek P. N. Satchell ◽  
Rosemary S. Satchell

Kinetic evidence is presented which strongly suggests that in the diethyl ether solution the aminolysis of p-nitrophenyl isothiocyanate proceeds via a mechanism involving a 1:1-addition intermediate which undergoes catalyzed prototropic rearrangement to the product (Baker-type mechanism).


It is of considerable interest to compare the velocities of homogeneous and heterogeneous gas reactions. In general homogeneous bimolecular reactions tend to become unimolecular in the presence of a catalyst, and the heat of activation falls to about one-half. This has been shown to be the case in the decomposition of nitrous oxide, hydrogen iodide, and ammonia. The question arises as to what is the effect of a catalyst on a homogeneous unimolecular reaction. The decomposition of gaseous diethyl ether was chosen for investigation on account of its simplicity; and an attempt has been made to compare the heterogeneous decomposition on the surface of platinum with that of the homogeneous reaction which has been investigated by Hinshelwood.


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