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机构地区:[1]Key Laboratory of Photochemical Conversion and Optoelectronic Materials',Technical Institute of Physics and Chemistry,Chinese Academy of Sciences,Beijing 100190,China [2]College of Chemistry and Chemical Engineering,Yunnan Normal University,Kunming,Yunnan 650092,China
出 处:《Chinese Journal of Chemistry》2012年第8期1801-1806,共6页中国化学(英文版)
摘 要:Four new 1,8-naphthyridine derivatives were synthesized by reacting the parent molecules with aldehydes and characterized. Two of the compounds have completely new and unusual skeletons, and display red-fluorescence emissions and two-photon absorption. Their structures were determined using MS, 1D and 2D NMR, and density functional theory calculations. The structural investigations of 2-methyl-l,8-naphthyridine hydrochloride and hydrobromide showed that abundant hydrogen-bonds and π-π interactions lead to extended networks.Four new 1,8-naphthyridine derivatives were synthesized by reacting the parent molecules with aldehydes and characterized. Two of the compounds have completely new and unusual skeletons, and display red-fluorescence emissions and two-photon absorption. Their structures were determined using MS, 1D and 2D NMR, and density functional theory calculations. The structural investigations of 2-methyl-l,8-naphthyridine hydrochloride and hydrobromide showed that abundant hydrogen-bonds and π-π interactions lead to extended networks.
关 键 词:naphthyridine derivative red emission two-photon absorption structure DFT calculation
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