| Literature DB >> 29131927 |
Mei Lu1, Yijin Su2, Pengyi Zhao1, Xiaohan Ye2, Yi Cai1, Xiaodong Shi2, Eric Masson1, Fengyao Li1, J Larry Campbell3, Hao Chen1.
Abstract
Gold-catalyzed alkyne hydration was studied by using in situ reacting mass spectrometry (MS) technology. By monitoring the reaction process in solution under different conditions (regular and very diluted catalyst concentrations, different pH values) and examining the reaction occurrence in the early reaction stage (1-2 ms after mixing) with MS, we collected a series of experimental evidence to support that the bis-gold complex is a potential key reaction intermediate. Furthermore, both experimental and computational studies confirmed that the σ,π-bis-gold complexes are not active intermediates toward nucleophilic addition. Instead, formation of geminally diaurated complex C is crucial for this catalytic process.Entities:
Keywords: desorption electrospray ionization mass spectrometry (DESI-MS); gold catalysis; hydration; mass spectrometry
Year: 2018 PMID: 29131927 PMCID: PMC6139295 DOI: 10.1002/chem.201703666
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236