Generation of α-acetolactone and the acetoxyl diradical •CH2COO• in the gas phase

被引:47
作者
Schroder, D
Goldberg, N
Zummack, W
Schwarz, H
Poutsma, JC
Squires, RR
机构
[1] Tech Univ Berlin, Inst Organ Chem, D-10623 Berlin, Germany
[2] Cornell Univ, Dept Chem, Ithaca, NY 14853 USA
[3] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
关键词
collision activation; acetolactone; neutralization-reionization; biradicals;
D O I
10.1016/S0168-1176(97)00150-X
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
The formation of neutral [C-2,H-2,O-2] has been investigated by tandem mass spectrometry in a sector instrument and by energy-resolved collision-induced dissociation in a flowing afterglow-triple quadrupole apparatus. The neutral species are generated by two different methods: (i) neutralization of the distonic anion radical (CH2COO-)-C-. by collisional electron detachment and (ii) collision-induced loss of halides X-concomitant with formation of [C-2,H-2,O-2] from alpha-haloacetate ions XCH2COO-. The tandem mass spectrometry results suggest that neutralization of (CH2COO-)-C-. and high-energy collisional activation of alpha-haloacetate ions lead to a mixture of alpha-acetolactone, c-(CH2C(O)O), and the acetoxyl diradical, (CH2COO.)-C-.. Low-energy collisions with alpha-chloroacetate ions in the triple quadrupole analyzer produce alpha-acetolactone exclusively at the dissociation threshold. From the dissociation threshold measured for the appearance of Cl- from ClCH2COO- the heat of formation of acetolactone is determined to be Delta H-f,H-298 = -47.3 +/- 4.7 kcal/mol. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:71 / 82
页数:12
相关论文
共 63 条
[1]   CYCLIC PEROXIDES .23. BIS(TRIFLUOROMETHYL)ACETOLACTONE, A STABLE ALPHA-LACTONE [J].
ADAM, W ;
LIU, JC ;
RODRIGUE.O .
JOURNAL OF ORGANIC CHEMISTRY, 1973, 38 (12) :2269-2270
[2]   THEORETICAL-STUDY OF ALPHA-LACTONE, ACETOXYL DIRADICAL, AND THE GAS-PHASE DISSOCIATION OF THE CHLOROACETATE ANION [J].
ANTOLOVIC, D ;
SHINER, VJ ;
DAVIDSON, ER .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (05) :1375-1381
[3]   CHARGE INVERSION OF NEGATIVE-IONS IN TANDEM INSTRUMENTS [J].
BURSEY, MM .
MASS SPECTROMETRY REVIEWS, 1990, 9 (05) :555-574
[4]  
CASADEI MA, 1986, GAZZ CHIM ITAL, V116, P659
[5]   DOPPLER BROADENING IN BEAM EXPERIMENTS [J].
CHANTRY, PJ .
JOURNAL OF CHEMICAL PHYSICS, 1971, 55 (06) :2746-&
[6]   PHOTOCHEMICAL TRANSFORMATIONS .44. SYNTHESIS AND CHEMISTRY OF ALPHA-LACTONES [J].
CHAPMAN, OL ;
ADAM, W ;
WOJTKOWS.PW ;
RODRIQUE.O ;
RUCKTASC.R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1972, 94 (04) :1365-&
[7]   THE GENERATION OF OC2O-CENTER-DOT+ AND OC2O AND A STUDY OF IONIZED OC3O AND C2O BY TANDEM MASS-SPECTROMETRY [J].
CHEN, HW ;
HOLMES, JL .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1994, 133 (2-3) :111-119
[8]   THEORY OF TRANSLATIONALLY DRIVEN REACTIONS [J].
CHESNAVICH, WJ ;
BOWERS, MT .
JOURNAL OF PHYSICAL CHEMISTRY, 1979, 83 (08) :900-905
[9]   SEVERAL MECHANISMS IN THE ELIMINATION KINETICS OF OMEGA-CHLOROCARBOXYLIC ACIDS IN THE GAS-PHASE [J].
CHUCHANI, G ;
MARTIN, I ;
ROTINOV, A ;
DOMINGUEZ, RM ;
PEREZ, M .
JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, 1995, 8 (03) :133-138
[10]   ALPHA-LACTONES - SEMIEMPIRICAL SCF-MO STUDY [J].
CHUNG, CSC .
JOURNAL OF MOLECULAR STRUCTURE, 1976, 30 (01) :189-191