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机构地区:[1]College of Pharmacy, Nankai University [2]State Key Laboratory of Elemento-organic Chemistry,Nankai University
出 处:《Chinese Journal of Structural Chemistry》2009年第8期1008-1012,共5页结构化学(英文)
基 金:supported by Tianjin Municipal Science and Technology Commission (09JCYBJC09200);National Key Basic Research and Development Program of China (973 Program, 2007CB914803)
摘 要:A novel alkynyl substituted N-aryl-1,8-naphthalimide II (C20H11NO2) was synthesized for the discovery and evaluation of new fluorescence probes, and was characterized by X-ray crystal diffraction. It crystallizes in monoclinic, space group P21/n with a = 15.898(3), b = 5.0102(10), c = 17.962(4)A, β = 92.97(3)°, V = 1428.7(5) A^3, Z = 4, Mr = 297.30, Dc = 1.382 g/cm^3, F(000) = 616,/J = 0.090 mm^-1, S = 1.011, the final R = 0.0542 and wR = 0.1204 for 1669 observed reflections with I 〉 2σ(I) and 212 variable parameters. Hydrogen-bounding and n-stacking interactions were discussed. The influence of acetylene group on the fluorescence properties was also investigated. In comparison with N-phenyl-1,8-naphthalimide I (C18H11NO2), few new structure characters and fluorescence properties of the title compound have been found.A novel alkynyl substituted N-aryl-1,8-naphthalimide II (C20H11NO2) was synthesized for the discovery and evaluation of new fluorescence probes, and was characterized by X-ray crystal diffraction. It crystallizes in monoclinic, space group P21/n with a = 15.898(3), b = 5.0102(10), c = 17.962(4)A, β = 92.97(3)°, V = 1428.7(5) A^3, Z = 4, Mr = 297.30, Dc = 1.382 g/cm^3, F(000) = 616,/J = 0.090 mm^-1, S = 1.011, the final R = 0.0542 and wR = 0.1204 for 1669 observed reflections with I 〉 2σ(I) and 212 variable parameters. Hydrogen-bounding and n-stacking interactions were discussed. The influence of acetylene group on the fluorescence properties was also investigated. In comparison with N-phenyl-1,8-naphthalimide I (C18H11NO2), few new structure characters and fluorescence properties of the title compound have been found.
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