Spectroscopy in the Ultraviolet and Visible Regions As Studied by Solution-Phase and Vapor-Phase Photoabsorption in the Ultraviolet and Visible Regions†

1996 ◽  
Vol 15 (22) ◽  
pp. 4747-4754 ◽  
Author(s):  
Jennifer C. Green ◽  
Sergey Yu. Ketkov
Keyword(s):  
1981 ◽  
Vol 59 (9) ◽  
pp. 1368-1374 ◽  
Author(s):  
Dennis D. Tanner ◽  
Tomoki C-S. Ruo ◽  
Hideki Takiguchi ◽  
Andre Guillaume

The relative rates of transfer of the cyclopentyl radical with molecular bromine and hydrogen bromide (k2′/k−1′) and with hydrogen tribromide and hydrogen bromide (k3′/k−1′) have been determined. The relative transfer rates are compared with the analogous values previously reported for the reactions of cyclohexyl radicals (k2/k−1 and k3/k−1). Utilizing the values of k2′/k−1 and k2/k−1 the competitive vapor phase rates of bromine atom abstraction of hydrogen from the two substrates could be obtained. An expression using a combination of the five sets of relative rate constants was used to determine the effect of competitive cage reversal which occurs in the solution phase bromination of the two substrate radicals with caged hydrogen bromide. For two structurally similar radicals, cage reversal (internal return) was found to affect the relative rates of bromination by 30%, while the relative transfer rates, although differing each by a factor of two, fortuitously nearly cancel each other's effect.The effect of both internal and external reversal reactions on the relative rates of bromination of structurally dissimilar substrates, halogenated alkanes and their parent hydrocarbons, is discussed.


1998 ◽  
Vol 563 (1-2) ◽  
pp. 209-217 ◽  
Author(s):  
Sergey Yu Ketkov ◽  
Richard D Ernst ◽  
Lothar Stahl ◽  
Wimonrat Trakarnpruk

1984 ◽  
Vol 62 (11) ◽  
pp. 2310-2316 ◽  
Author(s):  
Dennis D. Tanner ◽  
Tomoki C. S. Ruo ◽  
Yoshio Kosugi ◽  
Alan Potter

The solution phase photobromination of 2-bromobutane yields 2,2-dibromobutane, meso-2,3-dibromobutane, dl-2,3-dibromobutane, small amounts of 1,2-dibromobutane, and 2,2,3-tribromobutane. However, in the corresponding vapor phase bromination these products appear along with other polybrominated products. The yield of these polybromides increases with temperature. The increase in yield of the polyhalogenated materials is rationalized by considering the thermal instability of the β-bromoalkyl radical, which eliminates a bromine atom to form the corresponding alkene. It is demonstrated that in the vapor phase allylic bromination competes successfully with bromine addition. Reaction schemes are suggested to explain the formation of polybromides. An explanation is also offered for the discrepancy between these results and those of previously reported vapor phase work.


Author(s):  
S. McKernan ◽  
C. B. Carter ◽  
D. Bour ◽  
J. R. Shealy

The growth of ternary III-V semiconductors by organo-metallic vapor phase epitaxy (OMVPE) is widely practiced. It has been generally assumed that the resulting structure is the same as that of the corresponding binary semiconductors, but with the two different cation or anion species randomly distributed on their appropriate sublattice sites. Recently several different ternary semiconductors including AlxGa1-xAs, Gaxln-1-xAs and Gaxln1-xP1-6 have been observed in ordered states. A common feature of these ordered compounds is that they contain a relatively high density of defects. This is evident in electron diffraction patterns from these materials where streaks, which are typically parallel to the growth direction, are associated with the extra reflections arising from the ordering. However, where the (Ga,ln)P epilayer is reasonably well ordered the streaking is extremely faint, and the intensity of the ordered spot at 1/2(111) is much greater than that at 1/2(111). In these cases it is possible to image relatively clearly many of the defects found in the ordered structure.


Author(s):  
R.W. Carpenter ◽  
Changhai Li ◽  
David J. Smith

Binary Nb-Hf alloys exhibit a wide bcc solid solution phase field at temperatures above the Hfα→ß transition (2023K) and a two phase bcc+hcp field at lower temperatures. The β solvus exhibits a small slope above about 1500K, suggesting the possible existence of a miscibility gap. An earlier investigation showed that two morphological forms of precipitate occur during the bcc→hcp transformation. The equilibrium morphology is rod-type with axes along <113> bcc. The crystallographic habit of the rod precipitate follows the Burgers relations: {110}||{0001}, <112> || <1010>. The earlier metastable form, transition α, occurs as thin discs with {100} habit. The {100} discs induce large strains in the matrix. Selected area diffraction examination of regions ∼2 microns in diameter containing many disc precipitates showed that, a diffuse intensity distribution whose symmetry resembled the distribution of equilibrium α Bragg spots was associated with the disc precipitate.


1999 ◽  
Author(s):  
C. Joseph ◽  
D. Campbell ◽  
J. Suggs ◽  
J. Moore ◽  
N. Hartman
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document