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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >New and efficient high Stokes shift fluorescent compounds: unsymmetrically substituted 1,2-bis-(5-phenyloxazol-2-yl)benzenes via microwave-assisted nucleophilic substitution of fluorine
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New and efficient high Stokes shift fluorescent compounds: unsymmetrically substituted 1,2-bis-(5-phenyloxazol-2-yl)benzenes via microwave-assisted nucleophilic substitution of fluorine

机译:新型高效的高斯托克斯频移荧光化合物:通过微波辅助的氟亲核取代反应不对称取代的1,2-双-(5-苯基恶唑-2-基)苯

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摘要

Two new unsymmetric derivatives of 1,2-bis-(5-phenyloxazol-2-yl)benzene (ortho-POPOP) were synthesized via microwave-assisted nucleophilic substitution of fluorine which appears to be significantly more efficient compared with conventional thermal activation. The compounds synthesized are characterized by high fluorescence Stokes shifts (6000-11,000 cm~(-1)) in solvents of various polarity, intermediate-to-high fluorescence quantum yields and lifetimes in the range of several nanoseconds.
机译:通过微波辅助的氟的亲核取代反应,合成了1,2-双-(5-苯基恶唑-2-基)苯的两个新的不对称衍生物(邻位POPOP),与常规的热活化方法相比,它的效率明显提高。合成的化合物的特征是在各种极性的溶剂中具有高的荧光斯托克斯位移(6000-11,000 cm〜(-1)),中等至高的荧光量子产率以及在几纳秒范围内的寿命。

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