化学
氰
异氰
氰化物
基体隔离
金属
光解
红外光谱学
红外线的
金属羰基
霓虹灯
结晶学
物理化学
计算化学
无机化学
氩
光化学
立体化学
有机化学
物理
光学
作者
Han‐Gook Cho,Lester Andrews
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2021-04-15
卷期号:60 (9): 6421-6432
被引量:2
标识
DOI:10.1021/acs.inorgchem.1c00132
摘要
Reactions of group 11 metals with cyanogen, N≡C–C≡N, in excess argon and neon have been carried out, and the products were identified via examination of the matrix spectra and their variation upon photolysis, annealing, and isotopic substitutions. Density functional theory calculations provided helpful information for the plausible products and reaction paths. While M···NCCN and M···CNCN were observed in all three metal systems, the cyanide and isocyanide products (NCMCN, NCMNC, and CNMNC) were identified only in the Cu reactions, and M···C(N)CN was identified in the Cu and Au spectra. Intrinsic reaction coordinate calculation results along with the observed spectral variation upon photolysis and annealing suggest that Cu···C(N)CN was the pathway to cyanide and isocyanide. The product absorptions with exceptionally high C–N stretching frequencies in the Au system have been tentatively assigned to a cation [Au···NCCN+]. The group 11 metal cyanides and isocyanides that require two chemical bonds to the central metal are energetically favorable only in the lightest metal system.
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