Chemistry of protonated species on gaseous environments

被引:7
作者
Chiavarino, B [1 ]
Crestoni, ME [1 ]
Fornarini, S [1 ]
机构
[1] Univ Roma La Sapienza, Dipartimento Studi Chim & Tecnol Sostanze Biologi, I-00185 Rome, Italy
关键词
proton transfer; ion-molecule reactions; H/D exchange; radical cations; C3H7+ ions; gas-phase basicity; radiolysis; FT ICR mass spectrometry;
D O I
10.1002/poc.822
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An overview is presented of gas-phase studies on the structure and reactivity of protonated species from the authors' research. Specific problems have been addressed operating in different gaseous environments, either in radiolytic systems at atmospheric pressure, enabling the NMR characterization of the neutral end products of gas phase ion-molecule reactions, or in low-pressure FT-ICR mass spectrometry, where ions can be trapped and characterized by their reactivity or spectroscopic features. Proton transfer reactions have revealed the role of competing acidic sites leading to biologically relevant C7H7O radical species and of competing basic sites in substituted benzenes. Proton transfer reactions have also been used as a tool to form elusive cations, e.g. c-C3H7+, modulating the reaction energetics, and to unveil the structure and occurrence of degenerate isomerization processes within the benzenium ion. Copyright (C) 2004 John Wiley Sons, Ltd.
引用
收藏
页码:957 / 966
页数:10
相关论文
共 61 条
[1]   Structure and reactivity of protonated alpha,alpha,alpha-trifluorotoluene in the gas phase. A combined FT-ICR, radiolytic, and ab initio MO study [J].
Aschi, M ;
Chiavarino, B ;
Crestoni, ME ;
Fornarini, S .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (51) :19859-19863
[2]   Evaluation of the lifetime of gaseous ion-neutral complexes.: 1.: A chemical activation study [J].
Aschi, M ;
Attinà, M ;
Cacace, F ;
D'Arcangelo, G .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (16) :3982-3987
[3]   An alternative route to electrophilic substitution .2. Aromatic alkylation in the ion neutral complexes formed upon addition of gaseous arenium ions to olefins [J].
Aschi, M ;
Attina, M ;
Cacace, F .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (51) :12832-12839
[4]   AROMATIC-SUBSTITUTION IN THE GAS-PHASE - A COMPARATIVE-STUDY OF THE ALKYLATION OF BENZENE AND TOLUENE WITH C3H7+ IONS FROM THE PROTONATION OF CYCLOPROPANE AND PROPENE [J].
ATTINA, M ;
CACACE, F ;
GIACOMELLO, P .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1980, 102 (14) :4768-4772
[5]  
Baciocchi E, 1999, CHEM-EUR J, V5, P1785, DOI 10.1002/(SICI)1521-3765(19990604)5:6<1785::AID-CHEM1785>3.0.CO
[6]  
2-0
[7]  
Baciocchi E, 2002, CHEM-EUR J, V8, P532, DOI 10.1002/1521-3765(20020118)8:2<532::AID-CHEM532>3.3.CO
[8]  
2-K
[9]   -OH-induced shift from carbon to oxygen acidity in the side-chain deprotonation of 2-, 3- and 4-methoxybenzyl alcohol radical cations in aqueous solution:: results from pulse radiolysis and DFT calculations [J].
Baciocchi, E ;
Bietti, M ;
Ercolani, G ;
Steenken, S .
TETRAHEDRON, 2003, 59 (05) :613-618
[10]   Mechanistic aspects of β-bond-cleavage reactions of aromatic radical cations [J].
Baciocchi, E ;
Bietti, M ;
Lanzalunga, O .
ACCOUNTS OF CHEMICAL RESEARCH, 2000, 33 (04) :243-251