Fiacco Denise L, Hunt Sherri W, Leopold Kenneth R
Department of Chemistry, University of Minnesota, 207 Pleasant St., SE, Minneapolis, Minnesota 55455, USA.
J Am Chem Soc. 2002 Apr 24;124(16):4504-11. doi: 10.1021/ja012724w.
The complex H2SO4-H2O has been observed by rotational spectroscopy in a supersonic jet. A-type spectra for 18 isotopic forms have been analyzed, and the vibrationally averaged structure of the system has been determined. The complex forms a distorted, six-membered ring with the water unit acting as both a hydrogen bond donor and a hydrogen bond acceptor toward the sulfuric acid. One of the H2SO4 protons forms a short, direct hydrogen bond to the water oxygen, with an H...O distance of 1.645(5) A and an O-H...O angle of 165.2(4) degrees. Additionally, the orientation of the water suggests a weaker, secondary hydrogen bond between one of the H2O hydrogens and a nearby S=O oxygen on the sulfuric acid, with an O...H distance of 2.05(1) A and an O-H...O angle of 130.3(5) degrees. The experimentally determined structure is in excellent agreement with previously published DFT studies. Experiments with HOD in the jet reveal the formation of only isotopomers involving deuterium in the secondary hydrogen bond, providing direct experimental evidence for the secondary H...O interaction. Extensive isotopic substitution has also permitted a re-determination of the structure of the H2SO4 unit within the complex. The hydrogen-bonding OH bond of the sulfuric acid elongates by 0.07(2) A relative to that in free H2SO4, and the S=O bond involved in the secondary interaction stretches by 0.04(1) A. These changes reflect substantial distortion of the H2SO4 moiety in response to only a single water molecule, and prior to the proton transfer event. Spectral data indicate that the complex undergoes at least one, and probably more than one type of internal motion. Although the sulfuric acid in this work was produced from direct reaction of SO3 and water in the jet, experiments with H2(18)O indicate that about 2-3% of the acid is formed via processes not normally associated with the gas-phase hydration of SO3.
通过旋转光谱法在超声速射流中观测到了H₂SO₄ - H₂O络合物。已分析了18种同位素形式的A型光谱,并确定了该体系的振动平均结构。该络合物形成了一个扭曲的六元环,其中水单元既是硫酸的氢键供体,又是氢键受体。H₂SO₄的一个质子与水的氧原子形成了一个短的直接氢键,H…O距离为1.645(5) Å,O - H…O角度为165.2(4)度。此外,水的取向表明H₂O的一个氢原子与硫酸上附近的一个S = O氧原子之间存在较弱的二级氢键,O…H距离为2.05(1) Å,O - H…O角度为130.3(5)度。实验测定的结构与先前发表的密度泛函理论(DFT)研究结果高度吻合。在射流中使用HOD进行的实验表明,仅形成了在二级氢键中涉及氘的同位素异构体,为二级H…O相互作用提供了直接的实验证据。广泛的同位素取代还使得能够重新确定络合物中H₂SO₄单元的结构。硫酸的氢键合OH键相对于游离H₂SO₄中的键伸长了0.07(2) Å,参与二级相互作用的S = O键伸长了0.04(1) Å。这些变化反映了H₂SO₄部分在仅一个水分子作用下且在质子转移事件之前的显著扭曲。光谱数据表明该络合物经历了至少一种,可能不止一种类型的内部运动。尽管这项工作中的硫酸是由射流中SO₃与水的直接反应产生的,但使用H₂¹⁸O进行的实验表明,约2 - 3%的酸是通过通常与SO₃气相水合无关的过程形成的。