Titlebook: Organosilicon Heteropolymers and Heterocompounds; S. N. Borisov,M. G. Voronkov,E. Ya. Lukevits Book 1970 Springer Science+Business Media N

Nutraceutical

書目名稱Organosilicon Heteropolymers and Heterocompounds影響因子(影響力)




書目名稱Organosilicon Heteropolymers and Heterocompounds影響因子(影響力)學(xué)科排名




書目名稱Organosilicon Heteropolymers and Heterocompounds網(wǎng)絡(luò)公開度




書目名稱Organosilicon Heteropolymers and Heterocompounds網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Organosilicon Heteropolymers and Heterocompounds被引頻次




書目名稱Organosilicon Heteropolymers and Heterocompounds被引頻次學(xué)科排名




書目名稱Organosilicon Heteropolymers and Heterocompounds年度引用




書目名稱Organosilicon Heteropolymers and Heterocompounds年度引用學(xué)科排名




書目名稱Organosilicon Heteropolymers and Heterocompounds讀者反饋




書目名稱Organosilicon Heteropolymers and Heterocompounds讀者反饋學(xué)科排名

fluoroscopy

spect of the growth of organosilicon chemistry. The extent of this field has developed so greatly in recent years that it now is desirable to reclassify parts to bring together hitherto frag- mented and relatively disparate sections. This has been accomplished by the presently available large units

背叛者

Organosilicon Compounds of Group I Elements,nd investigated its properties. Depending on the reaction conditions and the ratio of the starting reagents it was possible to obtain the lithium silicides Li.Si, Li.Si, and a mixture of them, Li.Si. [71, 564, 884, 942].

pulmonary

饒舌的人

Organosilicon Compounds of Elements of the Manganese Subgroup,s with an acetonitrile solution of silicon tetrachloride in the presence of mercuric chloride [1555]. There is the possibility that compounds of this type are obtained by the reaction of hydrates of manganese salts with dimethyldichlorosilane [1300].

異端

978-1-4615-8629-6Springer Science+Business Media New York 1970

discord

Organosilicon Compounds of Group III Elements,The simplest method of synthesizing tris(trialkylsilyl) borates is based on the reaction of trialkylchlorosilanes with boric acid [251]:.Thus, boiling boric acid with trialkylchlorosilanes for 12–15 hr gives tris(trialkylsilyl) borates in about 25% yield.

浪蕩子

Organosilicon Compounds of Group V Elements,The reaction of arsenic trichloride with triphenylchlorosilane in benzene in the presence of the calculated amount of 30% ammonium hydroxide forms crystalline tris(triphenylsilyl) arsenite [631]:.The yield of this compound is substantially affected by even slight variations in the rate of addition of AsCl. and the stirring rate.

frivolous

Aggressive

Organosilicon Compounds of Group IV Elements,ermasiloxanes, mainly of cyclic structure, containing 2–7.5% germanium [457, 1478]. The inorganic chain contains only about 40% of the amount of germanium introduced into the reaction. This is due to the higher stability (lower tendency for condensation) of dimethylgermanediol in an acid medium in comparison with dimethylsilanediol.