PHOTODISSOCIATION OF DIMETHYLNITRAMINE AT 248 NM

被引:24
作者
MCQUAID, MJ
MIZIOLEK, AW
SAUSA, RC
MERROW, CN
机构
[1] USA,BALLIST RES LAB,SLCBR-IB-I,ABERDEEN PROVING GROUND,MD 21005
[2] USA,CTR CHEM RES DEV & ENGN,ABERDEEN PROVING GROUND,MD 21010
关键词
D O I
10.1021/j100160a018
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The production of OH A2-SIGMA+, OH X2-PI(i), NO2 A2B2, NO2 X2A1, and NO X2-PI following dimethylnitramine (DMNA) photolysis at 248 nm has been investigated by using laser-induced fluorescence and emission spectroscopies. NO2 A2B2, NO2 X2A1, and OH X2-PI(i) are formed via monophotonic, unimolecular pathways. The quantum yields for NO2 X2A1 and OH X2-PI(i), production are estimated to be 0.15 and 0.004, respectively. The unimolecular production of NO X2-PI (upsilon" = 0) was not observed, implying its quantum yield is < 0.001. OH A2-SIGMA+ is formed via a two-photon, unimolecular process. These results are compared with previous studies investigating the thermal and photochemical decomposition of DMNA.
引用
收藏
页码:2713 / 2718
页数:6
相关论文
共 29 条
[11]  
KORSUNSK.BL, 1967, DOKL AKAD NAUK SSSR+, V174, P1126
[12]  
KORSUNSKII BL, 1964, DOKL AKAD NAUK SSSR+, V155, P402
[13]   INFRARED MULTIPHOTON DECOMPOSITION OF DIMETHYLNITRAMINE [J].
LAZAROU, YG ;
PAPAGIANNAKOPOULOS, P .
JOURNAL OF PHYSICAL CHEMISTRY, 1990, 94 (18) :7114-7119
[14]  
LLOYD SA, 1985, J ENERG MATER, V3, P187
[15]   PULSED LASER PYROLYSIS OF DIMETHYLNITRAMINE AND DIMETHYLNITROSAMINE [J].
MCMILLEN, DF ;
NIGENDA, SE ;
GONZALEZ, AC ;
GOLDEN, DM .
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 1987, 43 (02) :237-239
[16]  
MCQUAID MJ, UNPUB APPL SPECTROSC
[17]  
MELIUS CF, 1986, 21ST S INT COMB, P1953
[18]   PICOSECOND LASER STUDY OF THE COLLISIONLESS PHOTODISSOCIATION OF DIMETHYLNITRAMINE AT 266 NM [J].
MIALOCO, JC ;
STEPHENSON, JC .
CHEMICAL PHYSICS LETTERS, 1986, 123 (05) :390-393
[19]  
NIGENDA SE, 1989, J PHYS CHEM-US, V94, P1124
[20]  
Okabe H., 1978, PHOTOCHEMISTRY SMALL