Reactions of Halogens/Interhalogens with Polypyridyl Substrates: The Case of 2,4,6‐Tris(2‐pyridyl)‐1,3,5‐triazine
Reactions of Halogens/Interhalogens with Polypyridyl Substrates: The Case of 2,4,6‐Tris(2‐pyridyl)‐1,3,5‐triazine
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卤素/卤间化合物与聚吡啶基底物的反应:以 2,4,6-Tris(2-吡啶基)-1,3,5-三嗪为例
DOI:
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发表时间:
2008
期刊:
影响因子:
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通讯作者:
G. Verani
中科院分区:
文献类型:
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作者:
M. Aragoni;M. Arca;F. Devillanova;M. Hursthouse;S. Huth;F. Isaia;V. Lippolis;A. Mancini;G. Verani
The reactions between 2,4,6-tris(2-pyridyl)-1,3,5-triazine (tptz) and halogens (Br2, I2) or interhalogens (ICl, IBr) yielded different products isolated in the solid state. (Htptz+)(Br3–), (Htptz+)(IBr2–), (H3tptz3+)(I3Br4–)(IBr2–)2, and (H3tptz3+)(ICl2–)3, obtained from the reactions between tptz and Br2, IBr, and ICl, were characterized by single-crystal X-ray diffraction and FT-Raman spectroscopy. All compounds are salts containing the protonated donor counterbalanced by polyhalide anions of various complexity. In particular, in (H3tptz3+)(I3Br4–)(IBr2–)2 the first example of a planar I3Br4– moiety can be observed. In the case of the reaction between tptz and I2, the elemental analysis of the product indicates a 1:1 molar ratio between tptz and I2, but the FT-Raman spectrum is not consistent with the formation of a simple adduct, clearly indicating the simultaneous presence of diiodine and symmetric triiodide. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)