## Abstract The multipleβchannel reactions SiH~3~ + SiH(CH~3~)~3~ β products are investigated by direct dynamics method. The minimum energy path (MEP) is calculated at the MP2/6β31+G(d,p) level, and energetic information is further refined by the MCβQCISD (singleβpoint) method. The rate constants f
Reaction of H and CH3, radicals with silanes. Evidence for SiH5 radical
β Scribed by L.C. Glasgow; G. Olbrich; P. Potzinger
- Publisher
- Elsevier Science
- Year
- 1972
- Tongue
- English
- Weight
- 429 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
β¦ Synopsis
The kinetic3 of [!-atom abstraction from silancs is shown to bc \vell described by th;: HEBO method cscqt for reaction (S): D + SiH4 -SiE-13 + ftD and Its isotopicanalogues.
In photochcm;.-nl csperiments ai -13O'C it is found that reaction (8) crln compc:c \vith (7): D f CrDj -+ C3Ds (k,/ks = 1.7) and must therefore be wry fast. Evidence from flow csperiments ;IS uell as CNDO/:! calculations support the hypothesis tfxt (8) proceeds via Ltn intermediate SiHs rxdiwl.
π SIMILAR VOLUMES
## Abstract The multipleβchannel reactions SiH~3~ + SiH~3~CH~3~ β products and SiH~3~ + SiH~2~(CH~3~)~2~ β products are investigated by direct dynamics method. The minimum energy path (MEP) is calculated at the MP2/6β31+G(d,p) level, and energetic information is further refined by the MCβQCISD meth
Laser Bash photolysis of DNOs/RSR'/R"H/Nr mixtures (R&HI, R'=CH, or C,H,, R"=n-hexyl or cyclohexyl) has been coupled with HDO detection by time-resolved tunable diode laser absorption spectroscopy to directly investigate the importance of C-H bond cleavage as the q-independent pathway for the atmosp
New determinations of the disproportionation and combination ratios between CFZH and CzH5 radicals yield (the hydrogen acceptor radical is given first) A(CF2H, CzH5) = 0.068 t\_ 0.008, and A(C2H5,CF2H) = 0.37 t\_ 0.01. A reevaluation of the existing data on CFHP and CF3 radicals leads t o t h e foll
Product distributions for the reactions of CH$ and CDf with methanol, methanol-da, and ethanol studied in a tandemkm CpdOtrOTl resonance mass SpeCtrOmeter are reported. The major reaction pathways may 5c rationalized in terms of 3x1 intermediate species havving a pro&mated ether structure. The react