Propargyl from the reaction of singlet methylene with acetylene

被引:30
作者
Adamson, JD
Morter, CL
DeSain, JD
Glass, GP
Curl, RF
机构
[1] RICE UNIV,DEPT CHEM,HOUSTON,TX 77251
[2] RICE UNIV,RICE QUANTUM INST,HOUSTON,TX 77251
关键词
D O I
10.1021/jp952147w
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 technique of infrared kinetic spectroscopy has been used to study the production of propargyl radical from the reaction of singlet methylene with acetylene. The rate constant for this product channel was determined to be (3.5 +/- 0.7) x 10(-10) cm(3) molecule(-1) s(-1) at 295 K, measured relative to the known rate for (CH2)-C-1 with H-2 or CH4. Methylene was produced in the singlet state by excimer laser photolysis of ketene at 308 nm in the presence of acetylene and either H-2 or CH4. Reaction of (CH2)-C-1 with acetylene produces propargyl, and reaction of (CH2)-C-1 with either H-2 or CH4 produces CH3. The intensity of a propargyl infrared absorption line was compared with that of a methyl infrared absorption line, and the rate of formation of propargyl was determined from the ratio of these two intensities and the known rate of reaction of singlet methylene with H-2 (or CH4) to produce CH3. The relative peak infrared absorption cross sections of methyl and propargyl were calibrated under the conditions of the experiment by photolyzing crotyl bromide at 193 nm to produce methyl and propargyl in equal concentrations.
引用
收藏
页码:2125 / 2128
页数:4
相关论文
共 24 条
[1]   FORMATION OF C6H6 ISOMERS BY RECOMBINATION OF PROPYNYL IN THE SYSTEM SODIUM VAPOR PROPYNYLHALIDE [J].
ALKEMADE, U ;
HOMANN, KH .
ZEITSCHRIFT FUR PHYSIKALISCHE CHEMIE NEUE FOLGE, 1989, 161 :19-34
[2]   DIFFERENCE FREQUENCY LASER SPECTROSCOPY OF THE UPSILON-3-BAND OF THE CH3 RADICAL [J].
AMANO, T ;
BERNATH, PF ;
YAMADA, C ;
ENDO, Y ;
HIROTA, E .
JOURNAL OF CHEMICAL PHYSICS, 1982, 77 (11) :5284-5287
[3]   EVALUATED KINETIC DATA FOR COMBUSTION MODELING [J].
BAULCH, DL ;
COBOS, CJ ;
COX, RA ;
ESSER, C ;
FRANK, P ;
JUST, T ;
KERR, JA ;
PILLING, MJ ;
TROE, J ;
WALKER, RW ;
WARNATZ, J .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1992, 21 (03) :411-734
[4]  
BOHLAND T, 1985, BER BUNSEN PHYS CHEM, V89, P1013, DOI 10.1002/bbpc.19850890917
[5]   FORMATION MECHANISMS OF AROMATIC-COMPOUNDS IN ALIPHATIC FLAMES [J].
COLE, JA ;
BITTNER, JD ;
LONGWELL, JP ;
HOWARD, JB .
COMBUSTION AND FLAME, 1984, 56 (01) :51-70
[6]  
COLKET MB, 1987, 21ST S INT COMB, P851
[7]   DETAILED MODELING OF PAH PROFILES IN A SOOTING LOW-PRESSURE ACETYLENE FLAME [J].
FRENKLACH, M ;
WARNATZ, J .
COMBUSTION SCIENCE AND TECHNOLOGY, 1987, 51 (4-6) :265-283
[8]  
Frenklach M., 1984, P COMBUST INST, P887, DOI DOI 10.1016/S0082-0784(85)80578-6
[9]   FORMATION OF SMALL AROMATIC-MOLECULES IN A SOOTING ETHYLENE FLAME [J].
HARRIS, SJ ;
WEINER, AM ;
BLINT, RJ .
COMBUSTION AND FLAME, 1988, 72 (01) :91-109
[10]   METHYLENE SINGLET TRIPLET ENERGY SPLITTING BY MOLECULAR-BEAM PHOTO-DISSOCIATION OF KETENE [J].
HAYDEN, CC ;
NEUMARK, DM ;
SHOBATAKE, K ;
SPARKS, RK ;
LEE, YT .
JOURNAL OF CHEMICAL PHYSICS, 1982, 76 (07) :3607-3613