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In situ Alkylation of 4,4′‐Vinylenedipyridine for Inorganic‐Organic Iodides/Iodidomercurates

Solvothermal reactions of HgI2, 4,4′‐vinylenedipyridine, and HI in alcoholic solution (methanol, ethanol, or pentanol) gave rise to a family of organic‐inorganic hybrid complexes, formulated as [C14H16N2][I4]2– (1), [C16H20N2][HgI4] (2), and [C22H32N2][HgI4]4 (3). Single‐crystal X‐ray diffraction re...

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Published in:Zeitschrift für anorganische und allgemeine Chemie (1950) 2017-04, Vol.643 (7), p.483-487
Main Authors: Cui, Jian‐Qiu, Guo, Tian‐Shuo, Chu, Kai‐Bin, Wu, Chao, Yang, Gang, Song, Jun‐Ling, Zhang, Chi
Format: Article
Language:English
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Summary:Solvothermal reactions of HgI2, 4,4′‐vinylenedipyridine, and HI in alcoholic solution (methanol, ethanol, or pentanol) gave rise to a family of organic‐inorganic hybrid complexes, formulated as [C14H16N2][I4]2– (1), [C16H20N2][HgI4] (2), and [C22H32N2][HgI4]4 (3). Single‐crystal X‐ray diffraction reveals that all three compounds are discrete structures, including the inorganic anion [I4]2– or [HgI4]2– and an organic cation, where the resulting organic cations were generated in situ alkylation reactions of 4,4′‐vinylenedipyridine with alcohols, with cleavage of the alcoholic C–O bond followed by a one‐step in situ N‐alkylation reaction of 4,4′‐vinylenedipyridine in acidic HI solution. X‐ray powder diffraction (XRD), 1H NMR and 13C NMR, energy‐dispersive X‐ray (EDS), IR, as well as UV/Vis/NIR spectroscopy, elemental analysis, and thermogravimetric analysis (TGA) were used to characterize the complexes.
ISSN:0044-2313
1521-3749
DOI:10.1002/zaac.201600431