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Fluorescent aminoarylcyclotetraphosphazenes

机译:荧光氨基芳基环四磷腈

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摘要

In the present work, octachlorocyclotetraphosphazatetraene (1), N _4P_4Cl_8, is reacted with aniline (2), 1-napthylamine (4) and 2-aminoanthracene (6) to give octakis(arylamino) cyclotetraphosphazenes (3, 5 and 7). These cyclotetraphosphazene compounds (3, 5 and 7) have been fully characterized by elemental analysis, mass (MS), FT-IR, ~1H and ~(31)P NMR spectroscopies. The molecular and crystal structures of 5 have been characterized by X-ray crystallography. The structure of 5 is monoclinic with the space group P21/c. The octakis(1-napthylamino)-(5) and octakis(2-aminoanthracene)-(7) cyclotetraphosphazene compounds have been synthesised for the first time in this study. The fluorescence properties of 3, 5 and 7 have been investigated in tetrahydrofuran (THF) and have been shown to have highly fluorescence behavior. This work also presents the quenching of arylamino substituted cyclotetraphosphazene derivatives (3, 5 and 7) by p-benzoquinone (BQ) or hydroquinone (HQ).
机译:在本工作中,将八氯环四磷腈酸酯(1)N _4P_4Cl_8与苯胺(2),1-萘胺(4)和2-氨基蒽(6)反应生成八(芳基氨基)环四磷腈(3、5和7)。这些环四磷腈化合物(3、5和7)已通过元素分析,质谱(MS),FT-IR,〜1H和〜(31)P NMR光谱进行了全面表征。 X射线晶体学表征了5的分子和晶体结构。 5的结构是单斜的,空间群为P21 / c。这项研究中首次合成了八(1-萘氨基)-(5)和八(2-氨基蒽)-(7)环四磷腈化合物。已经在四氢呋喃(THF)中研究了3、5和7的荧光特性,并且显示出具有很高的荧光特性。这项工作还提出了通过对苯醌(BQ)或对苯二酚(HQ)淬灭芳基氨基取代的环四磷腈衍生物(3、5和7)。

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