Győző G. Lajgut, Tibor Pasinszki, Ana Torvisco, Melinda Krebsz
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引用次数: 0
Abstract
The 1,2,5-thiadiazole moiety serves as a valuable structural component in a diverse array of compounds and polymers, and small halogen-substituted derivatives may act as precursors in their synthesis. This study reports the first synthesis of 3,4-dibromo-1,2,5-thiadiazole (1) and 3,4-diiodo-1,2,5-thiadiazole (2), which were systematically characterized using mid-IR, Raman, UV–Vis, NMR, mass, and He I photoelectron spectroscopies. These analyses offered a comprehensive examination of the electronic and vibrational properties of the compounds. Vibrational spectroscopy indicates that solids 1 and 2 contain multiple crystalline phases. The solid-phase structure of 1 was determined using single-crystal X-ray diffraction. Depending on recrystallization conditions, 1 solidifies in either the triclinic P-1 or monoclinic P2/c space groups. 1 has sufficiently high vapor pressure for studying its thermal stability and decomposition in the gas-phase. Flash vacuum thermolysis of this compound yields quantitatively BrCN, NCCN, Br2, and sulfur above 800 °C. Additionally, a synthetic method for the novel 3-bromo-4-iodo-1,2,5-thiadiazole (3) has been established.
期刊介绍:
Research on Chemical Intermediates publishes current research articles and concise dynamic reviews on the properties, structures and reactivities of intermediate species in all the various domains of chemistry.
The journal also contains articles in related disciplines such as spectroscopy, molecular biology and biochemistry, atmospheric and environmental sciences, catalysis, photochemistry and photophysics. In addition, special issues dedicated to specific topics in the field are regularly published.