The Interplay Between Hydrogen Bonding and Coulombic Forces in Determining the Structure of Sulfuric Acid-Amine Clusters

被引:37
|
作者
Waller, Sarah E. [1 ]
Yang, Yi [1 ]
Castracane, Eleanor [1 ]
Racow, Emily E. [1 ]
Kreinbihl, John J. [1 ]
Nickson, Kathleen A. [1 ]
Johnson, Christopher J. [1 ]
机构
[1] SUNY Stony Brook, Dept Chem, 100 Nicolls Rd, Stony Brook, NY 11794 USA
来源
基金
美国国家科学基金会;
关键词
SECONDARY ORGANIC AEROSOL; PARTICLE FORMATION; VIBRATIONAL SPECTROSCOPY; MASS-SPECTROMETRY; MOLECULAR COMPOSITION; MATRIX-ISOLATION; BONDED CLUSTERS; ION-TRAP; DIMETHYLAMINE; AMMONIA;
D O I
10.1021/acs.jpclett.8b00161
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
Acid-base cluster chemistry drives atmospheric new particle formation (NPF), but the details of the growth mechanisms are difficult to experimentally probe. Clusters of ammonia, alkylamines, and sulfuric acid, species fundamental to NPF, are probed by infrared spectroscopy. These spectra show that substitution of amines for ammonia, which is linked to accelerated growth, induces profound structural rearrangement in clusters with initial compositions (NH4+)(n+1)(HSO4-)(n) (1 <= n <= 3). This rearrangement is driven by the loss of N-H hydrogen bond donors, yielding direct bisulfate-bisulfate hydrogen bonds, and its onset with respect to cluster composition indicates that more substituted amines induce rearrangement at smaller sizes. A simple model counting hydrogen bond donors and acceptors explains these observations. The presence of direct hydrogen bonds between formal anions shows that hydrogen bonding can compete with Coulombic forces in determining cluster structure. These results suggest that NPF mechanisms may be highly dependent on amine identity.
引用
收藏
页码:1216 / 1222
页数:13
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