ChemInform Abstract: β-ELIMINATION FROM TRANSITION METAL AMIDES

1978 ◽  
Vol 9 (19) ◽  
Author(s):  
S. E. DIAMOND ◽  
F. MARES
1988 ◽  
Vol 27 (10) ◽  
pp. 1782-1786 ◽  
Author(s):  
R. A. Andersen ◽  
Knut Faegri ◽  
Jennifer C. Green ◽  
Arne Haaland ◽  
M. F. Lappert ◽  
...  

1999 ◽  
Vol 54 (11) ◽  
pp. 1450-1456 ◽  
Author(s):  
Benno Bildstein ◽  
Michael Malaun ◽  
Holger Kopacka ◽  
Klaus Wurst

The reactivity of diferrocenylamine has been investigated aiming at the preparation of novel diferrocenylamino compounds, including nitrenium salts, amino radicals, transition metal amides, carbamato ligands, and others. However, diferrocenylamine is unexpectedly difficult to derivatize; only simple metalation by butyl lithium, alkylation by iodomethane, and chloroformylation by phosgene were possible. X-ray crystal structures are reported for the starting diferrocenylamine, and for the derivatives diferrocenylmethylamine and N,N diferrocenylcarbamoylchloride.


1999 ◽  
Vol 575 ◽  
Author(s):  
Yuhong Huang ◽  
C. T. Chu ◽  
Qiang Wei ◽  
Haixing Zheng

ABSTRACTTransition metal nitrides and carbonitride materials were fabricated via sol-gel technology. The transition metal amides were sythesized by two methods: chemical route and electrolysis. The transition metal amides were then further polymerized, sintering to high temperature in an inert or reduced atmosphere. Transition metal nitrides and carbonitrides powders with surface area up to 160 m2/g were obtained. The resultant electrode material showed high specific capacitance as crystalline ruthenium oxide.


ChemInform ◽  
1988 ◽  
Vol 19 (36) ◽  
Author(s):  
R. A. ANDERSEN ◽  
K. JUN. FAEGRI ◽  
J. C. GREEN ◽  
A. HAALAND ◽  
M. F. LAPPERT ◽  
...  

1999 ◽  
Vol 57 (8) ◽  
pp. 698-707 ◽  
Author(s):  
Satoshi HAMURA ◽  
Hideo NAGASHIMA

Sign in / Sign up

Export Citation Format

Share Document