Titlebook: Ga Organogallium Compounds; Part 1 Jean-Claude Maire,Ulrich Krüerke,Christa Siebert,U Book 1986Latest edition Springer-Verlag Berlin Heidel

時(shí)間

書目名稱Ga Organogallium Compounds影響因子(影響力)




書目名稱Ga Organogallium Compounds影響因子(影響力)學(xué)科排名




書目名稱Ga Organogallium Compounds網(wǎng)絡(luò)公開度




書目名稱Ga Organogallium Compounds網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Ga Organogallium Compounds被引頻次




書目名稱Ga Organogallium Compounds被引頻次學(xué)科排名




書目名稱Ga Organogallium Compounds年度引用




書目名稱Ga Organogallium Compounds年度引用學(xué)科排名




書目名稱Ga Organogallium Compounds讀者反饋




書目名稱Ga Organogallium Compounds讀者反饋學(xué)科排名

笨拙處理

Organogallium Hydrides,5 Torr total pressure [3]). The composition of the colorless, highly viscous product was concluded from the supposedly quantitative thermal decomposition at 180°C to Ga(CH.)., H., and Ga metal [1, 2]. However, later workers were unable to isolate a uniform compound from the discharge. Their viscous

Inferior

左右連貫

Organogallium-Sulfur Compounds,rivatives contain potentially chelating ligands (Nos. 7 to 12 and No. 22), including chelating S N systems where it is impossible to distinguish between covalent and coordinative bonds to either the S or N atom. Derivatives of monothiocarboxylic acids, GaR.OC(S)R’. have already been described with t

哀悼

免除責(zé)任

免除責(zé)任

Organogallium-Boron Compounds,, Ga(CH.). was allowed to react with a fivefold excess of B.H. at -15°C for 3 h and was isolated in a 20 to 42% yield by trap-to-trap distillation of the volatiles in a vacuum system [6]. An 80% yield was obtained from the reaction of Ga(CH.).Cl with an excess of powdered LiBH. at -15°C with pumping

LARK

Synthesize

Compounds of Organogallium Anions,[GaR.]., and is followed by [GaR.X.]. anions (n = 1 to 3) where X stands for hydrogen, halogen, pseudohalogen, oxygen groups, etc. Finally, very extended subsections deal with organogallium pyrazolyl anions bonded to transition metal fragments via the second N atom of pyrazolyl, thus acting as anion

crease