TY - JOUR
T1 - H-Bonding of Sulfuric Acid with Its Decomposition Products
T2 - An Infrared Matrix Isolation and Computational Study of the H2SO4·H2O·SO3 Complex
AU - Rozenberg, Mark
AU - Loewenschuss, Aharon
AU - Nielsen, Claus J.
N1 - Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/5/26
Y1 - 2016/5/26
N2 - The FTIR matrix isolation spectra of H2SO4 vapors show a group of bands with synchronous growth of their relative intensities which is independent of the water species content of the matrix layer. Their frequency positions indicate that the species they represent is H-bonded and composed of all three components (H2SO4, H2O, and SO3) involved in the vapor decomposition equilibrium of the acid molecule. Structure, stabilization energies, and vibrational frequencies of several H-bonded complexes between these components were considered in B3LYP calculations employing Dunnings correlation-consistent aug-cc-pVTZ basis sets. Correlations between spectral shifts, bond lengths, and H-bond energies were also considered. The best fitting complex is a ring structured 1:1:1 H2SO4·H2O·SO3. The indications are that the complex is formed in the vapor phase and not after deposition. The atmospheric significance may be in its ability to serve as a H-bonding nucleation center even without the presence of additional contaminants.
AB - The FTIR matrix isolation spectra of H2SO4 vapors show a group of bands with synchronous growth of their relative intensities which is independent of the water species content of the matrix layer. Their frequency positions indicate that the species they represent is H-bonded and composed of all three components (H2SO4, H2O, and SO3) involved in the vapor decomposition equilibrium of the acid molecule. Structure, stabilization energies, and vibrational frequencies of several H-bonded complexes between these components were considered in B3LYP calculations employing Dunnings correlation-consistent aug-cc-pVTZ basis sets. Correlations between spectral shifts, bond lengths, and H-bond energies were also considered. The best fitting complex is a ring structured 1:1:1 H2SO4·H2O·SO3. The indications are that the complex is formed in the vapor phase and not after deposition. The atmospheric significance may be in its ability to serve as a H-bonding nucleation center even without the presence of additional contaminants.
UR - http://www.scopus.com/inward/record.url?scp=84973402116&partnerID=8YFLogxK
U2 - 10.1021/acs.jpca.6b00635
DO - 10.1021/acs.jpca.6b00635
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AN - SCOPUS:84973402116
SN - 1089-5639
VL - 120
SP - 3450
EP - 3455
JO - Journal of Physical Chemistry A
JF - Journal of Physical Chemistry A
IS - 20
ER -