Chemistry Department, University of Utah, 315 S. 1400 E. Rm 2020, Salt Lake City, Utah 84112, USA.
J Chem Phys. 2011 Jan 14;134(2):024310. doi: 10.1063/1.3514899.
Reactions of the late third-row transition metal cation Au(+) with H(2), D(2), and HD are examined using guided ion beam tandem mass spectrometry. A flow tube ion source produces Au(+) in its (1)S (5d(10)) electronic ground state level. Corresponding state-specific reaction cross sections for forming AuH(+) and AuD(+) as a function of kinetic energy are obtained and analyzed to give a 0 K bond dissociation energy of D(0)(Au(+)-H) = 2.13 ± 0.11 eV. Quantum chemical calculations at the B3LYP∕HW+∕6-311+G(3p) and B3LYP∕Def2TZVPP levels performed here show good agreement with the experimental bond energy. Theory also provides the electronic structures of these species and the reactive potential energy surfaces. We also compare this third-row transition metal system with previous results for analogous reactions of the first-row and second-row congeners, Cu(+) and Ag(+). We find that Au(+) has a stronger M(+)-H bond, which can be explained by the lanthanide contraction and relativistic effects that alter the relative size of the valence s and d orbitals. Results from reactions with HD provide insight into the reaction mechanism and indicate that ground state Au(+) reacts largely via a direct mechanism, in concordance with the behavior of the lighter group 11 metal ions, but includes more statistical behavior than these metals as well.
使用导向离子束串联质谱法研究了 late third-row 过渡金属阳离子 Au(+)与 H(2)、D(2)和 HD 的反应。流管离子源产生处于 (1)S (5d(10))电子基态能级的 Au(+)。获得了形成 AuH(+)和 AuD(+)的相应态特定反应截面,并对其进行了分析,得出 0 K 时 Au(+)-H 的键离解能 D(0)(Au(+)-H) = 2.13 ± 0.11 eV。在此处执行的 B3LYP∕HW+∕6-311+G(3p)和 B3LYP∕Def2TZVPP 能级的量子化学计算与实验键能吻合良好。理论还提供了这些物种的电子结构和反应势能面。我们还将这个第三排过渡金属系统与之前类似的第一排和第二排同族体 Cu(+)和 Ag(+)的反应结果进行了比较。我们发现 Au(+)具有更强的 M(+)-H 键,这可以通过镧系收缩和相对论效应来解释,这些效应改变了价 s 和 d 轨道的相对大小。与 HD 的反应结果提供了对反应机制的深入了解,并表明基态 Au(+)主要通过直接机制反应,与较轻的第 11 族金属离子的行为一致,但也比这些金属具有更多的统计行为。