Watson Peter D, Meizyte Gabriele, Pearcy Philip A J, Brewer Edward I, Green Alice E, Stace Anthony J, Mackenzie Stuart R
Department of Chemistry, Chemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford OX1 3TA, U.K.
School of Chemistry, University Park, University of Nottingham, Nottingham NG7 2RD, U.K.
J Phys Chem A. 2025 May 1;129(17):3867-3875. doi: 10.1021/acs.jpca.5c01377. Epub 2025 Apr 21.
Photofragmentation spectroscopy provides a powerful method for the determination of structures and bonding in isolated gas-phase clusters. Here we report infrared action spectra of mass-selected cationic nitric oxide clusters, (NO) ( = 3-8), and mixed NO(NO) clusters which are interpreted with the help of quantum chemical calculations. Despite the rich potential energy landscape which exhibits very many calculated low-energy isomers, clear structural motifs are observed. Important differences between our (NO) spectra and others published previously are interpreted in terms of the qualitatively different experimental techniques employed in the initial formation of the clusters in each study. Finally, spectra recorded in different fragmentation channels provide clear evidence for intracluster chemistry leading to the formation of mixed nitrous oxide/nitrogen dioxide/nitric oxide complexes, (NO)(NO)(NO).
光解离光谱法为确定孤立气相团簇中的结构和键合提供了一种强大的方法。在此,我们报告了质量选择的阳离子一氧化氮团簇(NO)( = 3 - 8)以及混合的NO(NO)团簇的红外作用光谱,并借助量子化学计算对其进行了解释。尽管势能面丰富,存在许多计算得到的低能异构体,但仍观察到了清晰的结构模式。我们的(NO)光谱与之前发表的其他光谱之间的重要差异,根据每项研究中团簇初始形成时所采用的定性不同的实验技术进行了解释。最后,在不同解离通道中记录的光谱为团簇内化学过程提供了明确证据,该过程导致形成了混合的一氧化二氮/二氧化氮/一氧化氮络合物(NO)(NO)(NO)。