Water dimer proton affinity from the kinetic method: dissociation energy of the water dimer

被引:60
作者
Goebbert, DJ [1 ]
Wenthold, PG [1 ]
机构
[1] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
关键词
kinetic method; proton affinity; water dimer; hydrogen bond energy;
D O I
10.1255/ejms.684
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 proton affinity of water dimer was measured, using the kinetic method with nitrile reference bases, to be 808 +/- 6 kJ mol(-1). The difference between the measured value and the proton affinity of a single water molecule (690 +/- 4 kJ mol(-1)) reflects the difference in solvation energy for two neutral water molecules (the hydrogen bond energy of water dimer), and the energy for solvation of hydronium cation and water. Using the measured proton affinity of the dimer along with ancillary data yields an experimental value of the hydrogen bond energy of neutral water dimer, 18 9 kJ mol(-1), in good agreement with previous experimental and theoretical values. The proton affinity of the dimer measured by using alcohol references is ca 100 kJ mol(-1) too low, likely because the structure of the protonated cluster is not well-suited for kinetic method measurements. These results highlight the importance of choosing reference bases that form cluster ions consisting of a proton bound complex between the water dimer and the reference base.
引用
收藏
页码:837 / 845
页数:9
相关论文
共 39 条
[1]   Entropy measurements and the kinetic method: A statistically meaningful approach [J].
Armentrout, PB .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2000, 11 (05) :371-379
[2]   Ab initio studies of methanol, methanethiol and methylamine dimer [J].
Bakó, I ;
Pálinkás, G .
JOURNAL OF MOLECULAR STRUCTURE-THEOCHEM, 2002, 594 (03) :179-184
[3]   Application of the kinetic method to bifunctional bases MIKE and CID-MIKE test cases [J].
Bouchoux, G ;
Djazi, F ;
Gaillard, F ;
Vierezet, D .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2003, 227 (03) :479-496
[4]   THE HYDROGEN-BOND, AND THE STRUCTURE AND PROPERTIES OF H2O AND (H2O)2 [J].
BUCKINGHAM, AD .
JOURNAL OF MOLECULAR STRUCTURE, 1991, 250 (2-4) :111-118
[5]   Proton affinities of simple amines; entropies and enthalpies of activation and their effect on the kinetic method for evaluating proton affinities [J].
Cao, J ;
Aubry, C ;
Holmes, JL .
JOURNAL OF PHYSICAL CHEMISTRY A, 2000, 104 (44) :10045-10052
[6]   The determination of proton affinities of secondary alcohols from the dissociation of proton-bound molecular trios. A new application of the kinetic method [J].
Cao, J ;
Holmes, JL .
EUROPEAN JOURNAL OF MASS SPECTROMETRY, 2001, 7 (03) :243-247
[7]   Li+, Na+, and K+ binding to the DNA and RNA nucleobases. Bond energies and attachment sites from the dissociation of metal ion-bound heterodimers [J].
Cerda, BA ;
Wesdemiotis, C .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (47) :11884-11892
[8]   Na+ binding to cyclic and linear dipeptides.: Bond energies, entropies of Na+ complexation, and attachment sites from the dissociation of Na+-bound heterodimers and ab initio calculations [J].
Cerda, BA ;
Hoyau, S ;
Ohanessian, G ;
Wesdemiotis, C .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (10) :2437-2448
[9]   Gas phase copper(I) ion affinities of valine, lysine, and arginine based on the dissociation of Cu+-bound heterodimers at varying internal energies [J].
Cerda, BA ;
Wesdemiotis, C .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 1999, 185 :107-116
[10]   COLLISION ENERGY-DEPENDENCE OF PROTON-BOUND DIMER DISSOCIATION - ENTROPY EFFECTS, PROTON AFFINITIES, AND INTRAMOLECULAR HYDROGEN-BONDING IN PROTONATED PEPTIDES [J].
CHENG, XH ;
WU, ZC ;
FENSELAU, C .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (11) :4844-4848