A Chemical Study of Photo-CVD of Silicon Nitride in Mercury-Sensitized Reactions Between Silane and Ammonia

1987 ◽  
Vol 101 ◽  
Author(s):  
Ching-Hsong Wu

ABSTRACTA photochemical system of mercury-sensitized reactions between silane and ammonia was studied to elucidate the gas-phase chemical processes involved in photo-CVD of silicon nitride. Several transient intermediates were detected and identified as silylated amines by the mass spectrometric isotope labeling method. These compounds containing both Si and N atoms appeared to be the precursors of silicon nitride. The chemical characteristics of silylated amines were studied under different experimental conditions. The reactivity and possible reaction paths for the formation of silylamine are discussed.

2000 ◽  
Vol 197 ◽  
pp. 237-250 ◽  
Author(s):  
B. R. Rowe ◽  
C. Rebrion Rowe ◽  
A. Canosa

A review of the most recent experimental results concerning reaction kinetics at low temperatures is presented, most of them having been obtained using the CRESU technique. Some astrochemical consequences are also highlighted.


2004 ◽  
Vol 109 (D23) ◽  
Author(s):  
J. B. Nowak ◽  
D. D. Parrish ◽  
J. A. Neuman ◽  
J. S. Holloway ◽  
O. R. Cooper ◽  
...  

2005 ◽  
Vol 70 (11) ◽  
pp. 1769-1786 ◽  
Author(s):  
Luc A. Vannier ◽  
Chunxiang Yao ◽  
František Tureček

A computational study at correlated levels of theory is reported to address the structures and energetics of transient radicals produced by hydrogen atom abstraction from C-1, C-2, C-3, C-4, C-5, O-1, O-3, and O-5 positions in 2-deoxyribofuranose in the gas phase and in aqueous solution. In general, the carbon-centered radicals are found to be thermodynamically and kinetically more stable than the oxygen-centered ones. The most stable gas-phase radical, 2-deoxyribofuranos-5-yl (5), is produced by H-atom abstraction from C-5 and stabilized by an intramolecular hydrogen bond between the O-5 hydroxy group and O-1. The order of radical stabilities is altered in aqueous solution due to different solvation free energies. These prefer conformers that lack intramolecular hydrogen bonds and expose O-H bonds to the solvent. Carbon-centered deoxyribose radicals can undergo competitive dissociations by loss of H atoms, OH radical, or by ring cleavages that all require threshold dissociation or transition state energies >100 kJ mol-1. This points to largely non-specific dissociations of 2-deoxyribose radicals when produced by exothermic hydrogen atom abstraction from the saccharide molecule. Oxygen-centered 2-deoxyribose radicals show only marginal thermodynamic and kinetic stability and are expected to readily fragment upon formation.


2006 ◽  
Vol 84 (5) ◽  
pp. 1128-1133 ◽  
Author(s):  
Alida Melse-Boonstra ◽  
Petra Verhoef ◽  
Clive E West ◽  
Johannes A van Rhijn ◽  
Richard B van Breemen ◽  
...  

1975 ◽  
Vol 6 (7) ◽  
pp. no-no
Author(s):  
JING CHAO ◽  
RANDOLPH C. WILHOIT ◽  
BRUNO J. ZWOLINSKI

2016 ◽  
Vol 26 (2) ◽  
pp. 157-159 ◽  
Author(s):  
Ning Luo ◽  
Hong Wen Jing ◽  
Zhan Guo Ma ◽  
Weidong Liu ◽  
Liangchi Zhang ◽  
...  

1988 ◽  
Vol 26 (2) ◽  
pp. 559-572 ◽  
Author(s):  
Youichi Nakayama ◽  
Takayuki Takahagi ◽  
Fusami Soeda ◽  
Kenji Hatada ◽  
Shoji Nagaoka ◽  
...  

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