Szczepaniak Urszula, Kołos Robert, Gronowski Marcin, Guillemin Jean-Claude, Crépin Claudine
Institut des Sciences Moléculaires d'Orsay (ISMO), UMR8214, CNRS, Univ. Paris-Sud, Université Paris-Saclay , F-91405 Orsay, France.
Institute of Physical Chemistry, Polish Academy of Sciences , Kasprzaka 44/52, PL-01-224 Warsaw, Poland.
J Phys Chem A. 2018 Jan 11;122(1):89-99. doi: 10.1021/acs.jpca.7b09728. Epub 2017 Dec 29.
This paper reports on UV-stimulated synthesis of methylcyanotriacetylene carried out in cryogenic rare gas matrixes via coupling of smaller precursors: propyne and cyanodiacetylene. The detection was possible due to the strong visible ã A' → X̃ A phosphorescence of CHCN, discovered in the course of this work. The ensuing measurements of electronic spectroscopy revealed the formally forbidden B̃ E-X̃ A system, as well as the allowed one Ẽ A-X̃ A, with origins at approximately 3.32 and 5.4 eV, respectively. It was also possible to revisit the spectroscopic characterization of cyanotriacetylene, HCN, formed in parallel to the title photoproduct. Spectral assignments were assisted with a density functional theory study.
本文报道了在低温稀有气体基质中通过较小前驱体丙炔和氰基二乙炔的偶联进行紫外线刺激合成甲基氰基三乙炔的过程。由于在本研究过程中发现的CHCN强烈的可见ã A'→X̃ A磷光,使得检测成为可能。随后的电子光谱测量揭示了形式上禁阻的B̃ E-X̃ A体系以及允许的Ẽ A-X̃ A体系,其起源分别约为3.32和5.4电子伏特。同时,也能够重新审视与标题光产物平行形成的氰基三乙炔HCN的光谱特征。光谱归属借助密度泛函理论研究得以辅助。